Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9465 |
| ensemblid | ENSG00000118507.19 |
| hgncid | 377 |
| symbol | AKAP7 |
| name | A-kinase anchoring protein 7 |
| refseq_nuc | NM_016377.4 |
| refseq_prot | NP_057461.2 |
| ensembl_nuc | ENST00000431975.7 |
| ensembl_prot | ENSP00000405252.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 131135467 |
| end | 131283532 |
| strand | + |
| ver | v1.2 |
| region | chr6:131135467-131283532 |
| region5000 | chr6:131130467-131288532 |
| regionname0 | AKAP7_chr6_131135467_131283532 |
| regionname5000 | AKAP7_chr6_131130467_131288532 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 348 | 223 | 51 | 31 | 114 | 7 | 18 | 99 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0002 | 0/0 | 348 | 50 | 15 | 17 | 1 | 7 | 10 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0003 | 0/0 | 348 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0004 | 0/0 | 348 | 7 | 0 | 5 | 0 | 2 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0005 | 0/0 | 348 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0006 | 0/0 | 348 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0007 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0008 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0009 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0010 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| a0011 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | MERPE others(343): Show |
chr6 | 131130467 | 131288532 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1044 | 223 | 51 | 31 | 114 | 7 | 18 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0002c0002 | 0/0 | 1044 | 50 | 15 | 17 | 1 | 7 | 10 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0003c0003 | 0/0 | 1044 | 10 | 10 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0004c0004 | 0/0 | 1044 | 7 | 0 | 5 | 0 | 2 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0005c0005 | 0/0 | 1044 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0006c0006 | 0/0 | 1044 | 4 | 3 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0007c0009 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0008c0007 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0009c0011 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0010c0010 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 | ||
| a0011c0008 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | ATGGA others(1039): Show |
chr6 | 131130467 | 131288532 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3150 | 69 | 7 | 19 | 29 | 1 | 11 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0002 | 0/0 | 3150 | 40 | 2 | 3 | 28 | 3 | 4 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0003 | 0/0 | 3150 | 27 | 4 | 2 | 15 | 3 | 3 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0004 | 0/0 | 3148 | 26 | 0 | 2 | 24 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0005 | 0/0 | 3148 | 9 | 9 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0006 | 0/0 | 3148 | 9 | 0 | 1 | 8 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0007 | 0/0 | 3148 | 6 | 6 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0008 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3142): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0009 | 0/0 | 3148 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0010 | 0/0 | 3147 | 3 | 2 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3142): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0011 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0012 | 0/0 | 3148 | 3 | 0 | 2 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0013 | 0/0 | 3150 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0016 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3154): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0018 | 0/0 | 3163 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3158): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0019 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3160): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0020 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0021 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0022 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0023 | 0/0 | 3147 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3142): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0025 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0026 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0028 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3203): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0030 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0031 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3142): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0033 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0034 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0038 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0040 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0041 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0001c0001t0042 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0001 | 0/0 | 3150 | 22 | 4 | 8 | 1 | 5 | 4 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0002 | 0/0 | 3150 | 8 | 1 | 4 | 0 | 0 | 3 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0003 | 0/0 | 3150 | 10 | 1 | 4 | 0 | 2 | 3 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0015 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3154): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0017 | 0/0 | 3157 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3152): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0020 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0024 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0027 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0036 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0037 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0002c0002t0039 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0003c0003t0007 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0003c0003t0008 | 0/0 | 3147 | 6 | 6 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3142): Show |
chr6 | 131130467 | 131288532 |
| a0003c0003t0010 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3142): Show |
chr6 | 131130467 | 131288532 |
| a0003c0003t0019 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3160): Show |
chr6 | 131130467 | 131288532 |
| a0003c0003t0032 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3142): Show |
chr6 | 131130467 | 131288532 |
| a0004c0004t0001 | 0/0 | 3150 | 5 | 0 | 4 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0004c0004t0003 | 0/0 | 3150 | 2 | 0 | 1 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0005c0005t0005 | 0/0 | 3148 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0005c0005t0011 | 0/0 | 3148 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0006c0006t0014 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3154): Show |
chr6 | 131130467 | 131288532 |
| a0006c0006t0016 | 0/0 | 3159 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3154): Show |
chr6 | 131130467 | 131288532 |
| a0006c0006t0035 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0007c0009t0005 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0008c0007t0029 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0009c0011t0004 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| a0010c0010t0002 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3145): Show |
chr6 | 131130467 | 131288532 |
| a0011c0008t0006 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | CTGGC others(3143): Show |
chr6 | 131130467 | 131288532 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0006g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0010g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0012g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0013g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0013g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0013g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0018g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0018g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0019g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0020g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0021g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0021g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0022g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0022g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0023g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0023g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0025g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0026g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0028g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0030g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0031g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0033g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0034g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0038g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0040g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0041g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0001c0001t0042g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0017g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0020g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0024g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0027g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0036g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0037g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0002c0002t0039g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0019g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0003c0003t0032g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0004c0004t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0005c0005t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0006c0006t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0006c0006t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0006c0006t0016g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0006c0006t0035g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0007c0009t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0008c0007t0029g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0009c0011t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0010c0010t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| a0011c0008t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0001 | g0216 | EUR | GBR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0053 | EUR | GBR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0248 | EUR | GBR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0181 | EUR | GBR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | FIN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00280 | hp2 | a0002 | c0002 | t0003 | g0114 | EUR | FIN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0107 | EUR | FIN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00323 | hp2 | a0004 | c0004 | t0003 | g0055 | EUR | FIN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00609 | hp2 | a0001 | c0001 | t0013 | g0112 | EAS | CHS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00741 | hp1 | a0001 | c0001 | t0038 | g0166 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0244 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01071 | hp2 | a0004 | c0004 | t0001 | g0001 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01169 | hp2 | a0004 | c0004 | t0001 | g0001 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0235 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01175 | hp2 | a0002 | c0002 | t0003 | g0071 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0245 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01255 | hp1 | a0004 | c0004 | t0001 | g0131 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01256 | hp2 | a0002 | c0002 | t0003 | g0133 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0137 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01261 | hp2 | a0002 | c0002 | t0039 | g0080 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0109 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0270 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0115 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0134 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0269 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0135 | EUR | IBS | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01884 | hp1 | a0002 | c0002 | t0015 | g0003 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0282 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01891 | hp1 | a0005 | c0005 | t0005 | g0098 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01891 | hp2 | a0003 | c0003 | t0032 | g0290 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0082 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01978 | hp1 | a0004 | c0004 | t0001 | g0129 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01978 | hp2 | a0001 | c0001 | t0012 | g0058 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01993 | hp1 | a0004 | c0004 | t0003 | g0167 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0254 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02145 | hp2 | a0005 | c0005 | t0011 | g0165 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02155 | hp1 | a0001 | c0001 | t0042 | g0212 | EAS | CDX | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | CDX | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02257 | hp1 | a0002 | c0002 | t0015 | g0004 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02257 | hp2 | a0002 | c0002 | t0036 | g0221 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02258 | hp1 | a0001 | c0001 | t0041 | g0159 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02258 | hp2 | a0007 | c0009 | t0005 | g0230 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02280 | hp2 | a0002 | c0002 | t0017 | g0010 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0061 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02300 | hp1 | a0001 | c0001 | t0012 | g0060 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02451 | hp2 | a0001 | c0001 | t0022 | g0086 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0163 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0070 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0243 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02622 | hp2 | a0002 | c0002 | t0003 | g0120 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02647 | hp1 | a0003 | c0003 | t0008 | g0148 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0184 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02717 | hp2 | a0005 | c0005 | t0005 | g0097 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02723 | hp1 | a0001 | c0001 | t0034 | g0219 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02809 | hp1 | a0001 | c0001 | t0020 | g0117 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02809 | hp2 | a0002 | c0002 | t0017 | g0005 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0009 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02818 | hp2 | a0003 | c0003 | t0008 | g0146 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0218 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0102 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02897 | hp1 | a0001 | c0001 | t0033 | g0101 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0095 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02922 | hp2 | a0003 | c0003 | t0019 | g0242 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02970 | hp1 | a0003 | c0003 | t0008 | g0149 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0265 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0076 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03041 | hp2 | a0001 | c0001 | t0023 | g0175 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03098 | hp1 | a0001 | c0001 | t0023 | g0174 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0092 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0291 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03130 | hp2 | a0001 | c0001 | t0040 | g0081 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03139 | hp2 | a0001 | c0001 | t0021 | g0223 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03195 | hp1 | a0003 | c0003 | t0007 | g0228 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03195 | hp2 | a0002 | c0002 | t0024 | g0100 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03209 | hp2 | a0002 | c0002 | t0020 | g0150 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03225 | hp1 | a0003 | c0003 | t0008 | g0144 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03225 | hp2 | a0006 | c0006 | t0014 | g0007 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0136 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03453 | hp1 | a0002 | c0002 | t0027 | g0231 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03453 | hp2 | a0005 | c0005 | t0005 | g0099 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03490 | hp1 | a0002 | c0002 | t0003 | g0051 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0049 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03516 | hp1 | a0008 | c0007 | t0029 | g0227 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0281 | AFR | ESN | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03540 | hp1 | a0001 | c0001 | t0031 | g0285 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03540 | hp2 | a0003 | c0003 | t0008 | g0147 | AFR | GWD | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03579 | hp1 | a0001 | c0001 | t0028 | g0236 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0142 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0288 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0121 | SAS | BEB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | BEB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0273 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0074 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0064 | SAS | STU | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0220 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | CHB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18906 | hp2 | a0006 | c0006 | t0014 | g0006 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0297 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0298 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18946 | hp1 | a0009 | c0011 | t0004 | g0197 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18969 | hp1 | a0001 | c0001 | t0013 | g0201 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18970 | hp2 | a0001 | c0001 | t0013 | g0210 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18977 | hp2 | a0010 | c0010 | t0002 | g0249 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18978 | hp2 | a0001 | c0001 | t0012 | g0062 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18981 | hp1 | a0011 | c0008 | t0006 | g0002 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18986 | hp2 | a0001 | c0001 | t0025 | g0067 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0292 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0293 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19043 | hp2 | a0002 | c0002 | t0037 | g0162 | AFR | LWK | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19062 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19083 | hp1 | a0001 | c0001 | t0018 | g0240 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19085 | hp1 | a0001 | c0001 | t0030 | g0296 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19087 | hp2 | a0001 | c0001 | t0019 | g0239 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19091 | hp1 | a0001 | c0001 | t0018 | g0241 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0185 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0087 | AFR | YRI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20129 | hp1 | a0001 | c0001 | t0026 | g0123 | AFR | ASW | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20129 | hp2 | a0006 | c0006 | t0035 | g0217 | AFR | ASW | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0052 | EUR | TSI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0138 | EUR | TSI | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0233 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG01123 | hp2 | a0006 | c0006 | t0016 | g0008 | AMR | CLM | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02109 | hp1 | a0005 | c0005 | t0011 | g0140 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0251 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02559 | hp1 | a0003 | c0003 | t0010 | g0083 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | ACB | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0277 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0075 | AFR | MSL | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | USA | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| HG06807 | hp2 | a0003 | c0003 | t0008 | g0145 | AFR | USA | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0094 | AFR | USA | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | USA | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0104 | REF | REF | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0103 | REF | REF | AKAP7_chr6_131130467_131288532 | AKAP7 | chr6 | 131130467 | 131288532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131145341 | G | A | 2 | a0006 a0008 |
5 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
missense_variant | MODERATE | c.76G>A | p.Glu26Lys | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/8 | 373/3150 | 76/1047 | 26/348 | chr6 | 131145341 | |||
| chr6:131145366 | C | T | 1 | a0009 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.101C>T | p.Ser34Phe | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/8 | 398/3150 | 101/1047 | 34/348 | chr6 | 131145366 | |||
| chr6:131165133 | G | A | 1 | a0011 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.344G>A | p.Arg115Gln | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/8 | 641/3150 | 344/1047 | 115/348 | chr6 | 131165133 | |||
| chr6:131165197 | A | C | 1 | a0008 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.408A>C | p.Leu136Phe | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/8 | 705/3150 | 408/1047 | 136/348 | chr6 | 131165197 | |||
| chr6:131169123 | G | T | 1 | a0003 | 10 | HG01891.hp2 HG02559.hp1 HG02647.hp1 others(7): Show |
missense_variant | MODERATE | c.439G>T | p.Ala147Ser | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/8 | 736/3150 | 439/1047 | 147/348 | chr6 | 131169123 | |||
| chr6:131169171 | C | T | 1 | a0010 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.487C>T | p.His163Tyr | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/8 | 784/3150 | 487/1047 | 163/348 | chr6 | 131169171 | |||
| chr6:131199502 | G | C | 1 | a0005 | 5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
missense_variant | MODERATE | c.631G>C | p.Gly211Arg | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/8 | 928/3150 | 631/1047 | 211/348 | chr6 | 131199502 | |||
| chr6:131199515 | G | A | 1 | a0002 | 50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
missense_variant | MODERATE | c.644G>A | p.Ser215Asn | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/8 | 941/3150 | 644/1047 | 215/348 | chr6 | 131199515 | |||
| chr6:131199551 | A | G | 1 | a0004 | 7 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(4): Show |
missense_variant | MODERATE | c.680A>G | p.Lys227Arg | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/8 | 977/3150 | 680/1047 | 227/348 | chr6 | 131199551 | |||
| chr6:131219733 | C | T | 1 | a0007 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.775C>T | p.Arg259Cys | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/8 | 1072/3150 | 775/1047 | 259/348 | chr6 | 131219733 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131135512 | C | T | 1 | a0001c0001t0042 | 1 | HG02155.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-252C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | chr6 | 131135512 | |||||||
| chr6:131135513 | T | C | 9 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(6): Show |
48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-251T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 251 | chr6 | 131135513 | ||||||
| chr6:131135516 | G | GGCTGCCG others(8): Show |
3 | a0001c0001t0018 a0001c0001t0019 a0003c0003t0019 |
4 | HG02922.hp2 NA19083.hp1 NA19087.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-239_-225dupCGCCGC others(9): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 224 | INFO_REALIGN_3_PRIME | chr6 | 131135516 | |||||
| chr6:131135516 | G | GGCTGCCG others(53): Show |
1 | a0001c0001t0028 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-225_-224insCGCCGC others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 224 | INFO_REALIGN_3_PRIME | chr6 | 131135516 | |||||
| chr6:131135517 | G | A | 1 | a0002c0002t0027 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-247G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 247 | chr6 | 131135517 | ||||||
| chr6:131135529 | G | GCTGCTGC others(2): Show |
5 | a0001c0001t0016 a0002c0002t0015 a0002c0002t0017 others(2): Show |
8 | HG01123.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-227_-226insCCTGCT others(3): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 226 | INFO_REALIGN_3_PRIME | chr6 | 131135529 | |||||
| chr6:131135593 | G | C | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(12): Show |
75 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(72): Show |
5_prime_UTR_variant | MODIFIER | c.-171G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 171 | chr6 | 131135593 | ||||||
| chr6:131135639 | G | C | 2 | a0001c0001t0020 a0002c0002t0020 |
2 | HG02809.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-125G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 125 | chr6 | 131135639 | ||||||
| chr6:131135722 | G | A | 9 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0021 others(6): Show |
18 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-42G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/8 | 42 | chr6 | 131135722 | ||||||
| chr6:131281804 | C | T | 1 | a0002c0002t0037 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 78 | chr6 | 131281804 | ||||||
| chr6:131281828 | T | C | 4 | a0001c0001t0033 a0001c0001t0038 a0006c0006t0014 others(1): Show |
5 | HG00741.hp1 HG02897.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*102T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 102 | chr6 | 131281828 | ||||||
| chr6:131281939 | T | C | 2 | a0001c0001t0021 a0001c0001t0022 |
4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*213T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 213 | chr6 | 131281939 | ||||||
| chr6:131281950 | T | C | 3 | a0001c0001t0034 a0002c0002t0015 a0002c0002t0024 |
4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*224T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 224 | chr6 | 131281950 | ||||||
| chr6:131281969 | C | T | 4 | a0001c0001t0041 a0002c0002t0017 a0002c0002t0027 others(1): Show |
5 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 243 | chr6 | 131281969 | ||||||
| chr6:131282226 | AGT | A | 20 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(17): Show |
76 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*505delTG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 504 | INFO_REALIGN_3_PRIME | chr6 | 131282226 | |||||
| chr6:131282303 | A | G | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0012 others(3): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*577A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 577 | chr6 | 131282303 | ||||||
| chr6:131282408 | CTAT | C | 7 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0023 others(4): Show |
15 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*684_*686delATT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 684 | INFO_REALIGN_3_PRIME | chr6 | 131282408 | |||||
| chr6:131282802 | A | G | 15 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0009 others(12): Show |
35 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1076A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1076 | chr6 | 131282802 | ||||||
| chr6:131283137 | A | T | 1 | a0001c0001t0026 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1411 | chr6 | 131283137 | ||||||
| chr6:131283244 | G | T | 1 | a0001c0001t0023 | 2 | HG03041.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1518G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1518 | chr6 | 131283244 | ||||||
| chr6:131283291 | G | A | 3 | a0001c0001t0013 a0001c0001t0025 a0001c0001t0030 |
5 | HG00609.hp2 NA18969.hp1 NA18970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1565G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1565 | chr6 | 131283291 | ||||||
| chr6:131283303 | A | T | 1 | a0003c0003t0032 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1577 | chr6 | 131283303 | ||||||
| chr6:131283409 | C | T | 1 | a0002c0002t0039 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1683C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 8/8 | 1683 | chr6 | 131283409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131135842 | C | T | 73 | a0001c0001t0002g0232 a0001c0001t0002g0234 a0001c0001t0002g0237 others(70): Show |
73 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.19+60C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131135842 | |||||||
| chr6:131136155 | T | C | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
37 | HG00408.hp1 HG01074.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.19+373T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136155 | |||||||
| chr6:131136157 | C | G | 3 | a0002c0002t0001g0229 a0002c0002t0027g0231 a0007c0009t0005g0230 |
3 | HG02055.hp1 HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.19+375C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136157 | |||||||
| chr6:131136226 | A | G | 2 | a0003c0003t0007g0228 a0008c0007t0029g0227 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+444A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136226 | |||||||
| chr6:131136381 | G | A | 8 | a0001c0001t0016g0009 a0002c0002t0015g0003 a0002c0002t0015g0004 others(5): Show |
8 | HG01123.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+599G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136381 | |||||||
| chr6:131136517 | A | G | 143 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(140): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.19+735A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136517 | |||||||
| chr6:131136597 | G | A | 1 | a0001c0001t0007g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19+815G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136597 | |||||||
| chr6:131136645 | T | G | 193 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.19+863T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136645 | |||||||
| chr6:131136806 | T | TCAA | 3 | a0001c0001t0022g0095 a0002c0002t0001g0096 a0002c0002t0002g0244 |
3 | HG00741.hp2 HG01071.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.19+1024_19+1025ins others(3): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131136806 | |||||||
| chr6:131137137 | A | AT | 11 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0001g0226 others(8): Show |
12 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.19+1366dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131137137 | ||||||
| chr6:131137254 | A | G | 62 | a0001c0001t0001g0161 a0001c0001t0001g0186 a0001c0001t0001g0187 others(59): Show |
63 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.19+1472A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137254 | |||||||
| chr6:131137331 | G | A | 1 | a0002c0002t0002g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19+1549G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137331 | |||||||
| chr6:131137381 | TCTCTTTT others(26): Show |
T | 3 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 |
3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19+1604_19+1636del others(33): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131137381 | ||||||
| chr6:131137384 | C | CT | 14 | a0001c0001t0001g0042 a0001c0001t0005g0094 a0001c0001t0010g0184 others(11): Show |
14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+1616dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131137384 | ||||||
| chr6:131137386 | T | C | 1 | a0001c0001t0004g0206 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.19+1604T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137386 | |||||||
| chr6:131137466 | T | G | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+1684T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137466 | |||||||
| chr6:131137476 | A | G | 1 | a0002c0002t0001g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19+1694A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137476 | |||||||
| chr6:131137487 | A | G | 1 | a0002c0002t0001g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.19+1705A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137487 | |||||||
| chr6:131137499 | C | T | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0005g0090 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+1717C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137499 | |||||||
| chr6:131137502 | C | G | 5 | a0001c0001t0009g0185 a0001c0001t0009g0222 a0001c0001t0021g0220 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+1720C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137502 | |||||||
| chr6:131137842 | A | G | 84 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0152 others(81): Show |
85 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.19+2060A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137842 | |||||||
| chr6:131137848 | A | G | 29 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0152 others(26): Show |
29 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.19+2066A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137848 | |||||||
| chr6:131137945 | C | T | 11 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0152 others(8): Show |
11 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+2163C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131137945 | |||||||
| chr6:131138046 | T | C | 81 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0152 others(78): Show |
81 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.19+2264T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138046 | |||||||
| chr6:131138073 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.19+2291A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138073 | |||||||
| chr6:131138108 | C | A | 2 | a0001c0001t0005g0141 a0001c0001t0009g0142 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.19+2326C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138108 | |||||||
| chr6:131138592 | C | A | 2 | a0001c0001t0003g0040 a0001c0001t0003g0041 |
2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.19+2810C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138592 | |||||||
| chr6:131138767 | C | T | 57 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0126 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.19+2985C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138767 | |||||||
| chr6:131138877 | TA | T | 37 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(34): Show |
37 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.19+3096delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138877 | |||||||
| chr6:131138907 | T | C | 5 | a0006c0006t0014g0006 a0006c0006t0014g0007 a0006c0006t0016g0008 others(2): Show |
5 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+3125T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131138907 | |||||||
| chr6:131139445 | C | G | 80 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0152 others(77): Show |
80 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.19+3663C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139445 | |||||||
| chr6:131139627 | A | AGT | 81 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0152 others(78): Show |
81 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.19+3847_19+3848dup others(2): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131139627 | ||||||
| chr6:131139788 | G | C | 137 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0084 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+4006G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139788 | |||||||
| chr6:131139794 | T | C | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.19+4012T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139794 | |||||||
| chr6:131139899 | A | T | 5 | a0001c0001t0009g0185 a0001c0001t0009g0222 a0001c0001t0021g0220 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4117A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139899 | |||||||
| chr6:131139902 | C | T | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+4120C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131139902 | |||||||
| chr6:131139976 | ACT | A | 4 | a0001c0001t0001g0042 a0001c0001t0005g0157 a0001c0001t0041g0159 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4196_19+4197del others(2): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131139976 | ||||||
| chr6:131140063 | C | G | 41 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(38): Show |
41 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.19+4281C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140063 | |||||||
| chr6:131140098 | A | G | 1 | a0001c0001t0003g0073 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.19+4316A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140098 | |||||||
| chr6:131140161 | G | C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
8 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+4379G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140161 | |||||||
| chr6:131140165 | A | G | 41 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(38): Show |
41 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.19+4383A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140165 | |||||||
| chr6:131140174 | A | T | 1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.19+4392A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140174 | |||||||
| chr6:131140198 | C | T | 25 | a0001c0001t0001g0079 a0001c0001t0007g0243 a0001c0001t0007g0281 others(22): Show |
25 | HG00140.hp2 HG01074.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.19+4416C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140198 | |||||||
| chr6:131140266 | A | AT | 14 | a0001c0001t0002g0299 a0001c0001t0009g0185 a0001c0001t0009g0222 others(11): Show |
14 | HG01123.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.19+4496dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131140266 | ||||||
| chr6:131140266 | AT | A | 78 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(75): Show |
79 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.19+4496delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131140266 | ||||||
| chr6:131140273 | T | G | 2 | a0002c0002t0001g0229 a0007c0009t0005g0230 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.19+4491T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140273 | |||||||
| chr6:131140331 | G | A | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19+4549G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140331 | |||||||
| chr6:131140436 | C | T | 39 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(36): Show |
39 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.19+4654C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140436 | |||||||
| chr6:131140619 | A | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-4666A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140619 | |||||||
| chr6:131140695 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.20-4590G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140695 | |||||||
| chr6:131140827 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0211 a0001c0001t0042g0212 |
3 | HG02155.hp1 NA19001.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.20-4458A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140827 | |||||||
| chr6:131140844 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02155.hp2 NA18941.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-4441A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131140844 | |||||||
| chr6:131141014 | G | T | 8 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-4271G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141014 | |||||||
| chr6:131141070 | CTTAA | C | 5 | a0006c0006t0014g0006 a0006c0006t0014g0007 a0006c0006t0016g0008 others(2): Show |
5 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-4206_20-4203del others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131141070 | ||||||
| chr6:131141159 | C | T | 27 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(24): Show |
27 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.20-4126C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141159 | |||||||
| chr6:131141574 | G | C | 1 | a0001c0001t0002g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.20-3711G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141574 | |||||||
| chr6:131141671 | T | G | 48 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(45): Show |
49 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.20-3614T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141671 | |||||||
| chr6:131141777 | T | C | 1 | a0002c0002t0001g0115 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.20-3508T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141777 | |||||||
| chr6:131141899 | C | CT | 22 | a0001c0001t0001g0156 a0001c0001t0002g0271 a0001c0001t0002g0274 others(19): Show |
22 | HG01256.hp1 HG02559.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.20-3367dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131141899 | ||||||
| chr6:131141899 | CTT | C | 6 | a0001c0001t0003g0125 a0001c0001t0009g0185 a0001c0001t0009g0222 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-3368_20-3367del others(2): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131141899 | ||||||
| chr6:131141902 | T | TC | 44 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(41): Show |
44 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.20-3383_20-3382ins others(1): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131141902 | |||||||
| chr6:131142213 | C | T | 13 | a0001c0001t0002g0301 a0001c0001t0007g0277 a0001c0001t0038g0166 others(10): Show |
14 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.20-3072C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142213 | |||||||
| chr6:131142284 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.20-3001C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142284 | |||||||
| chr6:131142291 | A | G | 1 | a0002c0002t0003g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.20-2994A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142291 | |||||||
| chr6:131142416 | G | T | 175 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(172): Show |
176 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.20-2869G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142416 | |||||||
| chr6:131142448 | A | G | 1 | a0001c0001t0005g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.20-2837A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142448 | |||||||
| chr6:131142451 | G | T | 2 | a0002c0002t0003g0070 a0002c0002t0003g0071 |
2 | HG01175.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.20-2834G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142451 | |||||||
| chr6:131142482 | G | A | 41 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(38): Show |
41 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.20-2803G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142482 | |||||||
| chr6:131142540 | A | G | 2 | a0002c0002t0001g0229 a0007c0009t0005g0230 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.20-2745A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142540 | |||||||
| chr6:131142615 | C | T | 1 | a0002c0002t0003g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.20-2670C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142615 | |||||||
| chr6:131142800 | G | C | 1 | a0010c0010t0002g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.20-2485G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131142800 | |||||||
| chr6:131143229 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.20-2056A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143229 | |||||||
| chr6:131143269 | T | TA | 9 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-2014dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143269 | ||||||
| chr6:131143525 | T | G | 4 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0017g0005 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1760T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143525 | |||||||
| chr6:131143534 | C | A | 1 | a0001c0001t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20-1751C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143534 | |||||||
| chr6:131143626 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20-1659G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143626 | |||||||
| chr6:131143738 | CT | C | 15 | a0001c0001t0001g0126 a0001c0001t0001g0152 a0001c0001t0002g0272 others(12): Show |
16 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.20-1534delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143738 | ||||||
| chr6:131143740 | TTTTTTTT others(5): Show |
T | 4 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0180 others(1): Show |
4 | HG00140.hp2 HG01074.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1538_20-1527del others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143740 | ||||||
| chr6:131143745 | T | A | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20-1540T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143745 | |||||||
| chr6:131143745 | T | TTA | 42 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(39): Show |
42 | HG01074.hp1 HG01175.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-1539_20-1538ins others(2): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143745 | ||||||
| chr6:131143752 | A | T | 1 | a0002c0002t0003g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.20-1533A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143752 | |||||||
| chr6:131143759 | A | T | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.20-1526A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143759 | |||||||
| chr6:131143805 | G | A | 1 | a0001c0001t0021g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.20-1480G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143805 | |||||||
| chr6:131143902 | C | G | 1 | a0002c0002t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.20-1383C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143902 | |||||||
| chr6:131143905 | G | GCGGCCTT others(1): Show |
80 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0028 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.20-1377_20-1370dup others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131143905 | ||||||
| chr6:131143906 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0013g0210 |
2 | NA18955.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.20-1379C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143906 | |||||||
| chr6:131143913 | C | T | 4 | a0002c0002t0002g0291 a0003c0003t0007g0228 a0003c0003t0019g0242 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-1372C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131143913 | |||||||
| chr6:131144290 | C | G | 22 | a0001c0001t0002g0301 a0001c0001t0002g0302 a0001c0001t0003g0143 others(19): Show |
23 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.20-995C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144290 | |||||||
| chr6:131144609 | T | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02155.hp2 NA18941.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-676T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144609 | |||||||
| chr6:131144609 | T | G | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.20-676T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144609 | |||||||
| chr6:131144610 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02155.hp2 NA18941.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-675T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144610 | |||||||
| chr6:131144848 | G | T | 42 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(39): Show |
42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-437G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131144848 | |||||||
| chr6:131145105 | TAG | T | 5 | a0006c0006t0014g0006 a0006c0006t0014g0007 a0006c0006t0016g0008 others(2): Show |
5 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-177_20-176delAG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 131145105 | ||||||
| chr6:131145256 | C | A | 2 | a0001c0001t0002g0294 a0001c0001t0004g0026 |
2 | HG01943.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.20-29C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 1/7 | chr6 | 131145256 | |||||||
| chr6:131145656 | A | G | 2 | a0001c0001t0007g0277 a0001c0001t0008g0218 |
2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.151+240A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131145656 | |||||||
| chr6:131145848 | C | T | 40 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(37): Show |
40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+432C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131145848 | |||||||
| chr6:131145918 | A | C | 48 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(45): Show |
48 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.151+502A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131145918 | |||||||
| chr6:131145967 | G | C | 174 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(171): Show |
175 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.151+551G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131145967 | |||||||
| chr6:131146094 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.151+678C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146094 | |||||||
| chr6:131146466 | A | T | 3 | a0001c0001t0005g0224 a0001c0001t0007g0281 a0001c0001t0007g0282 |
3 | HG01884.hp2 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.151+1050A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146466 | |||||||
| chr6:131146608 | A | T | 5 | a0001c0001t0002g0301 a0001c0001t0038g0166 a0004c0004t0001g0001 others(2): Show |
6 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+1192A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146608 | |||||||
| chr6:131146657 | G | T | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.151+1241G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146657 | |||||||
| chr6:131146813 | A | G | 42 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(39): Show |
42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.151+1397A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131146813 | |||||||
| chr6:131147018 | T | G | 122 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(119): Show |
123 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.151+1602T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147018 | |||||||
| chr6:131147361 | G | A | 17 | a0001c0001t0002g0302 a0001c0001t0003g0143 a0001c0001t0003g0151 others(14): Show |
17 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.151+1945G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147361 | |||||||
| chr6:131147395 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.151+1979C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147395 | |||||||
| chr6:131147461 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | NA18977.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.151+2045G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147461 | |||||||
| chr6:131147937 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.151+2521C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131147937 | |||||||
| chr6:131148008 | T | C | 8 | a0001c0001t0003g0125 a0001c0001t0009g0185 a0001c0001t0009g0222 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+2592T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148008 | |||||||
| chr6:131148089 | C | T | 2 | a0001c0001t0005g0141 a0001c0001t0009g0142 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151+2673C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148089 | |||||||
| chr6:131148312 | G | T | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.151+2896G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148312 | |||||||
| chr6:131148321 | G | T | 178 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(175): Show |
179 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.151+2905G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148321 | |||||||
| chr6:131148344 | A | G | 6 | a0001c0001t0003g0125 a0001c0001t0009g0185 a0001c0001t0009g0222 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+2928A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148344 | |||||||
| chr6:131148471 | T | C | 1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.151+3055T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148471 | |||||||
| chr6:131148471 | TC | T | 149 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.151+3064delC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131148471 | ||||||
| chr6:131148471 | TCC | T | 26 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(23): Show |
26 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.151+3063_151+3064d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131148471 | ||||||
| chr6:131148586 | C | T | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.151+3170C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148586 | |||||||
| chr6:131148713 | G | T | 1 | a0001c0001t0010g0082 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.151+3297G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148713 | |||||||
| chr6:131148765 | C | T | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.151+3349C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131148765 | |||||||
| chr6:131148943 | CT | C | 40 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(37): Show |
40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+3530delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131148943 | ||||||
| chr6:131149096 | C | T | 82 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0028 others(79): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.151+3680C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149096 | |||||||
| chr6:131149393 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.151+3977G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149393 | |||||||
| chr6:131149401 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+3985G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149401 | |||||||
| chr6:131149517 | C | T | 48 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(45): Show |
48 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.151+4101C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149517 | |||||||
| chr6:131149615 | A | T | 5 | a0001c0001t0001g0170 a0001c0001t0002g0237 a0002c0002t0001g0096 others(2): Show |
5 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+4199A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149615 | |||||||
| chr6:131149699 | T | C | 40 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(37): Show |
40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+4283T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149699 | |||||||
| chr6:131149709 | A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.151+4293A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131149709 | |||||||
| chr6:131150053 | C | T | 42 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(39): Show |
42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.151+4637C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150053 | |||||||
| chr6:131150154 | T | C | 1 | a0005c0005t0011g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.151+4738T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150154 | |||||||
| chr6:131150172 | C | A | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.151+4756C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150172 | |||||||
| chr6:131150252 | G | A | 26 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(23): Show |
26 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.151+4836G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150252 | |||||||
| chr6:131150769 | T | C | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.151+5353T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131150769 | |||||||
| chr6:131151008 | A | G | 42 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(39): Show |
42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.151+5592A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151008 | |||||||
| chr6:131151165 | C | T | 6 | a0002c0002t0001g0158 a0006c0006t0014g0006 a0006c0006t0014g0007 others(3): Show |
6 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5749C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151165 | |||||||
| chr6:131151249 | G | A | 1 | a0006c0006t0016g0008 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.151+5833G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151249 | |||||||
| chr6:131151381 | G | GT | 21 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0001g0226 others(18): Show |
22 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+5979dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131151381 | ||||||
| chr6:131151381 | G | GTT | 29 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(26): Show |
29 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.151+5978_151+5979d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131151381 | ||||||
| chr6:131151381 | G | GTTT | 6 | a0001c0001t0001g0089 a0002c0002t0001g0092 a0002c0002t0015g0003 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5977_151+5979d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131151381 | ||||||
| chr6:131151583 | A | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(6): Show |
9 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+6167A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151583 | |||||||
| chr6:131151904 | A | G | 40 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(37): Show |
40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+6488A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131151904 | |||||||
| chr6:131152032 | C | T | 8 | a0001c0001t0003g0125 a0001c0001t0009g0185 a0001c0001t0009g0222 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+6616C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152032 | |||||||
| chr6:131152089 | G | GC | 26 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(23): Show |
26 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.151+6674dupC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131152089 | ||||||
| chr6:131152221 | T | C | 9 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(6): Show |
9 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+6805T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152221 | |||||||
| chr6:131152461 | A | G | 4 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0017g0005 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+7045A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152461 | |||||||
| chr6:131152622 | G | A | 2 | a0001c0001t0001g0079 a0002c0002t0001g0136 |
2 | HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.151+7206G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152622 | |||||||
| chr6:131152660 | C | G | 1 | a0001c0001t0003g0044 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.151+7244C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152660 | |||||||
| chr6:131152689 | A | T | 172 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(169): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.151+7273A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152689 | |||||||
| chr6:131152738 | A | G | 42 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(39): Show |
42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.152-7321A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152738 | |||||||
| chr6:131152826 | C | CA | 14 | a0001c0001t0001g0085 a0001c0001t0001g0126 a0001c0001t0001g0153 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-7213dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131152826 | ||||||
| chr6:131152858 | C | G | 173 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(170): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.152-7201C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152858 | |||||||
| chr6:131152935 | TG | T | 40 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(37): Show |
40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-7122delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131152935 | ||||||
| chr6:131152998 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.152-7061C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131152998 | |||||||
| chr6:131153077 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152-6982C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153077 | |||||||
| chr6:131153107 | A | G | 1 | a0002c0002t0001g0121 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152-6952A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153107 | |||||||
| chr6:131153108 | C | T | 1 | a0002c0002t0001g0121 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152-6951C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153108 | |||||||
| chr6:131153129 | C | CA | 9 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0001g0226 others(6): Show |
9 | HG01891.hp1 HG01978.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-6915dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153129 | ||||||
| chr6:131153129 | C | CAA | 29 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(26): Show |
30 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.152-6916_152-6915d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153129 | ||||||
| chr6:131153129 | C | CAAA | 19 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0007g0277 others(16): Show |
19 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-6917_152-6915d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153129 | ||||||
| chr6:131153406 | A | G | 56 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.152-6653A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153406 | |||||||
| chr6:131153621 | G | T | 5 | a0001c0001t0010g0082 a0002c0002t0002g0291 a0003c0003t0007g0228 others(2): Show |
5 | HG01891.hp2 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-6438G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153621 | |||||||
| chr6:131153670 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152-6389G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131153670 | |||||||
| chr6:131153755 | ATATCT | A | 3 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0006g0298 |
3 | HG00597.hp1 NA18943.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.152-6297_152-6293d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153755 | ||||||
| chr6:131153935 | TGTG | T | 40 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(37): Show |
40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-6119_152-6117d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131153935 | ||||||
| chr6:131154041 | C | G | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.152-6018C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154041 | |||||||
| chr6:131154090 | T | C | 190 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(187): Show |
190 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.152-5969T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154090 | |||||||
| chr6:131154112 | G | A | 27 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(24): Show |
27 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-5947G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154112 | |||||||
| chr6:131154179 | G | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-5880G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154179 | |||||||
| chr6:131154211 | A | AC | 4 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0017g0005 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-5848_152-5847i others(3): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154211 | |||||||
| chr6:131154212 | A | C | 40 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(37): Show |
40 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-5847A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154212 | |||||||
| chr6:131154369 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.152-5690C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154369 | |||||||
| chr6:131154468 | G | GT | 15 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0034 others(12): Show |
15 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-5569dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131154468 | ||||||
| chr6:131154468 | GT | G | 86 | a0001c0001t0001g0085 a0001c0001t0001g0124 a0001c0001t0001g0127 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.152-5569delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131154468 | ||||||
| chr6:131154468 | GTT | G | 40 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(37): Show |
40 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.152-5570_152-5569d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131154468 | ||||||
| chr6:131154468 | GTTT | G | 6 | a0001c0001t0003g0125 a0001c0001t0009g0185 a0001c0001t0009g0222 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-5571_152-5569d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131154468 | ||||||
| chr6:131154513 | G | C | 175 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(172): Show |
175 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.152-5546G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154513 | |||||||
| chr6:131154627 | T | A | 1 | a0001c0001t0003g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.152-5432T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154627 | |||||||
| chr6:131154802 | C | A | 175 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(172): Show |
175 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.152-5257C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154802 | |||||||
| chr6:131154866 | A | G | 23 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0010g0082 others(20): Show |
23 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-5193A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154866 | |||||||
| chr6:131154951 | T | G | 8 | a0001c0001t0003g0125 a0001c0001t0009g0185 a0001c0001t0009g0222 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-5108T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131154951 | |||||||
| chr6:131155019 | AT | A | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.152-5028delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131155019 | ||||||
| chr6:131155109 | A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152-4950A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155109 | |||||||
| chr6:131155149 | G | A | 1 | a0003c0003t0007g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-4910G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155149 | |||||||
| chr6:131155259 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.152-4800C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155259 | |||||||
| chr6:131155379 | C | G | 2 | a0002c0002t0001g0229 a0007c0009t0005g0230 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.152-4680C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155379 | |||||||
| chr6:131155388 | A | G | 27 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(24): Show |
27 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-4671A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155388 | |||||||
| chr6:131155445 | G | A | 1 | a0001c0001t0006g0292 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.152-4614G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155445 | |||||||
| chr6:131155790 | C | T | 48 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(45): Show |
48 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.152-4269C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131155790 | |||||||
| chr6:131156118 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-3941C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131156118 | |||||||
| chr6:131156132 | T | C | 17 | a0001c0001t0002g0302 a0001c0001t0003g0143 a0001c0001t0003g0151 others(14): Show |
17 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.152-3927T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131156132 | |||||||
| chr6:131156589 | A | G | 40 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(37): Show |
40 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-3470A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131156589 | |||||||
| chr6:131157017 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.152-3042C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157017 | |||||||
| chr6:131157022 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.152-3037G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157022 | |||||||
| chr6:131157055 | A | G | 1 | a0001c0001t0012g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.152-3004A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157055 | |||||||
| chr6:131157065 | A | G | 1 | a0001c0001t0012g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.152-2994A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157065 | |||||||
| chr6:131157068 | C | T | 1 | a0001c0001t0008g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.152-2991C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157068 | |||||||
| chr6:131157113 | T | C | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152-2946T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157113 | |||||||
| chr6:131157244 | G | A | 3 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 |
3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152-2815G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157244 | |||||||
| chr6:131157298 | T | C | 21 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0001g0226 others(18): Show |
21 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.152-2761T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157298 | |||||||
| chr6:131157420 | A | G | 1 | a0001c0001t0004g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152-2639A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157420 | |||||||
| chr6:131157448 | G | A | 138 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(135): Show |
138 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.152-2611G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157448 | |||||||
| chr6:131157486 | A | G | 1 | a0001c0001t0002g0279 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.152-2573A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157486 | |||||||
| chr6:131157596 | C | G | 175 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(172): Show |
175 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.152-2463C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157596 | |||||||
| chr6:131157668 | A | G | 3 | a0001c0001t0004g0194 a0001c0001t0018g0240 a0001c0001t0018g0241 |
3 | NA18973.hp2 NA19083.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.152-2391A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157668 | |||||||
| chr6:131157680 | A | G | 16 | a0001c0001t0002g0302 a0001c0001t0003g0143 a0001c0001t0003g0151 others(13): Show |
16 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-2379A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157680 | |||||||
| chr6:131157686 | A | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-2373A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157686 | |||||||
| chr6:131157697 | A | G | 4 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0017g0005 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-2362A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131157697 | |||||||
| chr6:131158033 | C | T | 1 | a0001c0001t0006g0254 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152-2026C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158033 | |||||||
| chr6:131158189 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.152-1870A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158189 | |||||||
| chr6:131158327 | CCTT | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0003g0074 |
3 | HG02602.hp2 HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.152-1728_152-1726d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131158327 | ||||||
| chr6:131158474 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.152-1585T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158474 | |||||||
| chr6:131158610 | C | T | 17 | a0001c0001t0002g0302 a0001c0001t0003g0143 a0001c0001t0003g0151 others(14): Show |
17 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.152-1449C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158610 | |||||||
| chr6:131158652 | T | A | 27 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(24): Show |
27 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-1407T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158652 | |||||||
| chr6:131158804 | G | T | 1 | a0001c0001t0003g0057 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.152-1255G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131158804 | |||||||
| chr6:131158915 | T | TA | 50 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(47): Show |
50 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.152-1130dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131158915 | ||||||
| chr6:131158915 | TA | T | 41 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(38): Show |
41 | HG00741.hp1 HG01081.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.152-1130delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131158915 | ||||||
| chr6:131159047 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.152-1012C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159047 | |||||||
| chr6:131159087 | ATTTTATT | A | 148 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0025 others(145): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.152-954_152-948del others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131159087 | ||||||
| chr6:131159117 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152-942G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159117 | |||||||
| chr6:131159125 | C | A | 18 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(15): Show |
18 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-934C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159125 | |||||||
| chr6:131159132 | C | T | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.152-927C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159132 | |||||||
| chr6:131159194 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.152-865T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159194 | |||||||
| chr6:131159279 | G | A | 1 | a0001c0001t0003g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.152-780G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159279 | |||||||
| chr6:131159283 | C | T | 3 | a0002c0002t0001g0180 a0002c0002t0001g0181 a0002c0002t0002g0235 |
3 | HG00140.hp2 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.152-776C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159283 | |||||||
| chr6:131159295 | G | A | 3 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0024g0100 |
3 | HG01884.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.152-764G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159295 | |||||||
| chr6:131159299 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-760T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159299 | |||||||
| chr6:131159329 | G | A | 1 | a0001c0001t0007g0277 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152-730G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159329 | |||||||
| chr6:131159339 | C | T | 46 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(43): Show |
46 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(43): Show |
intron_variant | MODIFIER | c.152-720C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159339 | |||||||
| chr6:131159340 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.152-719G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159340 | |||||||
| chr6:131159354 | A | G | 5 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-705A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159354 | |||||||
| chr6:131159367 | A | G | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152-692A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159367 | |||||||
| chr6:131159396 | G | T | 93 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0028 others(90): Show |
93 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.152-663G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159396 | |||||||
| chr6:131159407 | A | T | 9 | a0001c0001t0001g0156 a0001c0001t0001g0164 a0001c0001t0001g0225 others(6): Show |
9 | HG01256.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-652A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159407 | |||||||
| chr6:131159433 | A | G | 32 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(29): Show |
32 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.152-626A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159433 | |||||||
| chr6:131159859 | T | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | NA18952.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.152-200T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | chr6 | 131159859 | |||||||
| chr6:131159990 | G | GT | 40 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0079 others(37): Show |
40 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.152-60dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 131159990 | ||||||
| chr6:131160254 | CA | C | 254 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(251): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.291+58delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131160254 | ||||||
| chr6:131160443 | G | T | 3 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 |
3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291+245G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160443 | |||||||
| chr6:131160516 | C | T | 41 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(38): Show |
41 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.291+318C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160516 | |||||||
| chr6:131160530 | C | T | 101 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0028 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.291+332C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160530 | |||||||
| chr6:131160699 | G | C | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.291+501G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160699 | |||||||
| chr6:131160903 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0005g0157 a0001c0001t0041g0159 |
3 | HG02258.hp1 HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.291+705C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160903 | |||||||
| chr6:131160918 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.291+720A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160918 | |||||||
| chr6:131160987 | T | C | 151 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.291+789T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131160987 | |||||||
| chr6:131160996 | A | AT | 256 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.291+800dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131160996 | ||||||
| chr6:131161000 | C | T | 41 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(38): Show |
41 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.291+802C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161000 | |||||||
| chr6:131161149 | A | C | 101 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0028 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.291+951A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161149 | |||||||
| chr6:131161601 | T | C | 253 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(250): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.291+1403T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161601 | |||||||
| chr6:131161613 | C | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(28): Show |
31 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.291+1415C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161613 | |||||||
| chr6:131161644 | C | CA | 20 | a0001c0001t0001g0012 a0001c0001t0001g0124 a0001c0001t0001g0127 others(17): Show |
21 | HG00099.hp1 HG01071.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.291+1486dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | C | CAA | 25 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0024 others(22): Show |
25 | HG00544.hp2 HG01081.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.291+1485_291+1486d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | C | CAAA | 12 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0179 others(9): Show |
12 | HG01943.hp2 HG02155.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.291+1484_291+1486d others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | C | CAAAA | 13 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0089 others(10): Show |
13 | HG00408.hp2 HG01109.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.291+1483_291+1486d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | C | CAAAAAAA | 6 | a0001c0001t0002g0302 a0001c0001t0003g0078 a0001c0001t0003g0151 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+1480_291+1486d others(9): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0005g0094 a0001c0001t0011g0163 |
2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.291+1477_291+1486d others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0153 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.291+1475_291+1486d others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0155 others(3): Show |
6 | HG01106.hp1 HG01192.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+1474_291+1486d others(15): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0154 a0001c0001t0001g0225 |
2 | HG01099.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.291+1473_291+1486d others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CA | C | 8 | a0001c0001t0003g0050 a0001c0001t0003g0054 a0001c0001t0007g0277 others(5): Show |
8 | HG00280.hp1 HG00323.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+1486delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAA | C | 15 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0132 others(12): Show |
15 | HG00408.hp1 HG00597.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.291+1483_291+1486d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAA | C | 43 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(40): Show |
43 | HG00280.hp2 HG00558.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.291+1482_291+1486d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAA | C | 36 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0111 others(33): Show |
36 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.291+1481_291+1486d others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAAA others(3): Show |
C | 30 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0003g0052 others(27): Show |
30 | HG01074.hp1 HG01074.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.291+1477_291+1486d others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0001g0181 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.291+1476_291+1486d others(13): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0003g0053 a0002c0002t0003g0120 |
2 | HG00099.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.291+1475_291+1486d others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAAA others(8): Show |
C | 2 | a0002c0002t0001g0229 a0007c0009t0005g0230 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.291+1472_291+1486d others(17): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0006g0284 |
3 | NA18970.hp1 NA18991.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.291+1471_291+1486d others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAAA others(10): Show |
C | 16 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(13): Show |
16 | HG00597.hp1 HG01884.hp2 HG03098.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+1470_291+1486d others(19): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0004g0039 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.291+1469_291+1486d others(20): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161644 | CAAAAAAA others(14): Show |
C | 4 | a0001c0001t0001g0079 a0005c0005t0005g0097 a0005c0005t0005g0098 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+1466_291+1486d others(23): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131161644 | ||||||
| chr6:131161866 | A | G | 1 | a0001c0001t0012g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.291+1668A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131161866 | |||||||
| chr6:131162143 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0002g0264 |
2 | HG00609.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.291+1945C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162143 | |||||||
| chr6:131162528 | T | C | 3 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0007g0286 |
3 | HG02622.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.291+2330T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162528 | |||||||
| chr6:131162529 | A | G | 1 | a0002c0002t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.291+2331A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162529 | |||||||
| chr6:131162569 | A | T | 1 | a0002c0002t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.291+2371A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162569 | |||||||
| chr6:131162638 | G | A | 102 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.291+2440G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162638 | |||||||
| chr6:131162699 | C | T | 42 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(39): Show |
42 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.292-2382C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162699 | |||||||
| chr6:131162978 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.292-2103C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131162978 | |||||||
| chr6:131163005 | G | GCT | 101 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.292-2061_292-2060d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131163005 | ||||||
| chr6:131163210 | G | GTAATGTT others(26): Show |
1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.292-1866_292-1834d others(35): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131163210 | ||||||
| chr6:131163739 | T | A | 1 | a0001c0001t0040g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.292-1342T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131163739 | |||||||
| chr6:131163789 | TG | T | 3 | a0004c0004t0001g0001 a0004c0004t0001g0216 a0004c0004t0003g0167 |
4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1287delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 131163789 | ||||||
| chr6:131163836 | GA | G | 3 | a0001c0001t0007g0243 a0001c0001t0021g0223 a0002c0002t0001g0092 |
3 | HG02615.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.292-1244delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131163836 | |||||||
| chr6:131163901 | C | T | 6 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(3): Show |
6 | HG01884.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1180C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131163901 | |||||||
| chr6:131163964 | G | A | 110 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(107): Show |
110 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.292-1117G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131163964 | |||||||
| chr6:131164203 | T | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-878T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164203 | |||||||
| chr6:131164267 | T | C | 6 | a0001c0001t0038g0166 a0004c0004t0001g0001 a0004c0004t0001g0129 others(3): Show |
7 | HG00099.hp1 HG00741.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-814T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164267 | |||||||
| chr6:131164480 | T | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0004g0178 others(1): Show |
4 | NA18979.hp1 NA19056.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-601T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164480 | |||||||
| chr6:131164621 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.292-460A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164621 | |||||||
| chr6:131164692 | G | T | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292-389G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164692 | |||||||
| chr6:131164901 | C | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(24): Show |
27 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.292-180C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 3/7 | chr6 | 131164901 | |||||||
| chr6:131165253 | A | G | 1 | a0002c0002t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.428+36A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165253 | |||||||
| chr6:131165326 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.428+109T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165326 | |||||||
| chr6:131165528 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.428+311C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165528 | |||||||
| chr6:131165563 | A | G | 1 | a0001c0001t0028g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.428+346A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165563 | |||||||
| chr6:131165571 | TC | T | 4 | a0002c0002t0027g0231 a0005c0005t0005g0097 a0005c0005t0005g0098 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+355delC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165571 | |||||||
| chr6:131165733 | C | G | 1 | a0001c0001t0012g0058 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.428+516C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165733 | |||||||
| chr6:131165808 | A | G | 15 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(12): Show |
15 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.428+591A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165808 | |||||||
| chr6:131165894 | T | C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.428+677T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131165894 | |||||||
| chr6:131166177 | G | A | 1 | a0001c0001t0012g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.428+960G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166177 | |||||||
| chr6:131166365 | C | CTG | 6 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0154 others(3): Show |
6 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+1156_428+1157d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131166365 | ||||||
| chr6:131166373 | G | T | 41 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0079 others(38): Show |
41 | HG00140.hp2 HG00408.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.428+1156G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166373 | |||||||
| chr6:131166374 | T | G | 41 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0079 others(38): Show |
41 | HG00140.hp2 HG00408.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.428+1157T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166374 | |||||||
| chr6:131166543 | G | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0132 |
2 | NA18965.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.428+1326G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166543 | |||||||
| chr6:131166585 | C | A | 2 | a0001c0001t0005g0077 a0002c0002t0027g0231 |
2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.428+1368C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166585 | |||||||
| chr6:131166953 | T | TA | 102 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.428+1743dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131166953 | ||||||
| chr6:131166996 | G | A | 2 | a0001c0001t0008g0218 a0001c0001t0010g0184 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428+1779G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131166996 | |||||||
| chr6:131167375 | G | A | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429-1738G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131167375 | |||||||
| chr6:131167455 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.429-1658T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131167455 | |||||||
| chr6:131167702 | C | T | 173 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(170): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.429-1411C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131167702 | |||||||
| chr6:131167960 | G | A | 173 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(170): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.429-1153G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131167960 | |||||||
| chr6:131168077 | G | A | 2 | a0002c0002t0001g0122 a0008c0007t0029g0227 |
2 | HG01109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.429-1036G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168077 | |||||||
| chr6:131168096 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.429-1017T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168096 | |||||||
| chr6:131168201 | T | C | 226 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.429-912T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168201 | |||||||
| chr6:131168223 | A | G | 256 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(253): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.429-890A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168223 | |||||||
| chr6:131168272 | A | G | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-841A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168272 | |||||||
| chr6:131168426 | GA | G | 14 | a0001c0001t0002g0302 a0001c0001t0003g0143 a0001c0001t0003g0151 others(11): Show |
14 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.429-686delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168426 | |||||||
| chr6:131168550 | T | C | 128 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(125): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.429-563T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168550 | |||||||
| chr6:131168616 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.429-497G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | chr6 | 131168616 | |||||||
| chr6:131168875 | C | CT | 4 | a0002c0002t0020g0150 a0005c0005t0005g0097 a0005c0005t0005g0098 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-235dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131168875 | ||||||
| chr6:131169052 | AT | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-58delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131169052 | ||||||
| chr6:131169089 | GA | G | 21 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0164 others(18): Show |
21 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.429-19delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 131169089 | ||||||
| chr6:131169332 | T | C | 154 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(151): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.589+59T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169332 | |||||||
| chr6:131169391 | T | G | 1 | a0001c0001t0040g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.589+118T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169391 | |||||||
| chr6:131169403 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.589+130G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169403 | |||||||
| chr6:131169407 | C | A | 1 | a0002c0002t0020g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589+134C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169407 | |||||||
| chr6:131169440 | A | C | 4 | a0001c0001t0007g0277 a0002c0002t0015g0003 a0002c0002t0015g0004 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+167A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169440 | |||||||
| chr6:131169447 | T | A | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+174T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169447 | |||||||
| chr6:131169482 | A | G | 5 | a0004c0004t0001g0001 a0004c0004t0001g0129 a0004c0004t0001g0131 others(2): Show |
6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+209A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169482 | |||||||
| chr6:131169806 | T | TA | 4 | a0002c0002t0020g0150 a0005c0005t0005g0097 a0005c0005t0005g0098 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+534dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131169806 | ||||||
| chr6:131169900 | A | G | 1 | a0001c0001t0002g0276 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.589+627A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169900 | |||||||
| chr6:131169904 | G | A | 1 | a0001c0001t0010g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.589+631G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131169904 | |||||||
| chr6:131170095 | A | C | 1 | a0001c0001t0003g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.589+822A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170095 | |||||||
| chr6:131170152 | T | G | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589+879T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170152 | |||||||
| chr6:131170153 | G | C | 38 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(35): Show |
38 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.589+880G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170153 | |||||||
| chr6:131170183 | A | T | 154 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(151): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.589+910A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170183 | |||||||
| chr6:131170290 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0004g0178 others(1): Show |
4 | NA18979.hp1 NA19056.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.589+1017A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170290 | |||||||
| chr6:131170300 | A | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0154 others(3): Show |
6 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+1027A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170300 | |||||||
| chr6:131170308 | AAG | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0179 others(17): Show |
20 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.589+1037_589+1038d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131170308 | ||||||
| chr6:131170310 | GA | G | 206 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(203): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.589+1047delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131170310 | ||||||
| chr6:131170311 | A | G | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0179 others(17): Show |
20 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.589+1038A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170311 | |||||||
| chr6:131170334 | A | G | 38 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(35): Show |
38 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.589+1061A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170334 | |||||||
| chr6:131170367 | GA | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0179 others(16): Show |
19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+1104delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131170367 | ||||||
| chr6:131170428 | A | C | 1 | a0001c0001t0003g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.589+1155A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170428 | |||||||
| chr6:131170441 | T | G | 2 | a0001c0001t0006g0002 a0011c0008t0006g0002 |
2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.589+1168T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170441 | |||||||
| chr6:131170711 | T | A | 3 | a0001c0001t0001g0023 a0001c0001t0002g0267 a0001c0001t0002g0275 |
3 | HG00544.hp1 HG02155.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.589+1438T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170711 | |||||||
| chr6:131170963 | G | A | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.589+1690G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131170963 | |||||||
| chr6:131171177 | G | T | 3 | a0002c0002t0001g0064 a0002c0002t0001g0121 a0002c0002t0002g0288 |
3 | HG03669.hp2 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.589+1904G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171177 | |||||||
| chr6:131171218 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.589+1945A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171218 | |||||||
| chr6:131171323 | T | C | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589+2050T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171323 | |||||||
| chr6:131171604 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0004g0178 others(1): Show |
4 | NA18979.hp1 NA19056.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.589+2331G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171604 | |||||||
| chr6:131171608 | T | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0179 others(16): Show |
19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+2335T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171608 | |||||||
| chr6:131171725 | A | C | 50 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(47): Show |
50 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.589+2452A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171725 | |||||||
| chr6:131171823 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.589+2550T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131171823 | |||||||
| chr6:131172063 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.589+2790G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172063 | |||||||
| chr6:131172078 | A | G | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.589+2805A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172078 | |||||||
| chr6:131172109 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.589+2836C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172109 | |||||||
| chr6:131172206 | A | G | 153 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.589+2933A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172206 | |||||||
| chr6:131172229 | T | C | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+2956T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172229 | |||||||
| chr6:131172269 | C | T | 11 | a0001c0001t0001g0042 a0001c0001t0001g0085 a0001c0001t0001g0088 others(8): Show |
11 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+2996C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172269 | |||||||
| chr6:131172283 | G | A | 1 | a0001c0001t0040g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.589+3010G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172283 | |||||||
| chr6:131172351 | T | C | 6 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0005g0094 others(3): Show |
6 | HG01952.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+3078T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172351 | |||||||
| chr6:131172510 | A | C | 155 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(152): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.589+3237A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172510 | |||||||
| chr6:131172638 | T | C | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+3365T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172638 | |||||||
| chr6:131172654 | A | C | 2 | a0003c0003t0008g0148 a0003c0003t0008g0149 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.589+3381A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172654 | |||||||
| chr6:131172781 | T | C | 8 | a0001c0001t0005g0157 a0001c0001t0007g0282 a0001c0001t0009g0222 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+3508T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172781 | |||||||
| chr6:131172962 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.589+3689C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131172962 | |||||||
| chr6:131173076 | C | A | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.589+3803C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173076 | |||||||
| chr6:131173126 | G | A | 8 | a0001c0001t0002g0302 a0001c0001t0003g0143 a0001c0001t0003g0151 others(5): Show |
8 | HG02572.hp2 HG02622.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+3853G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173126 | |||||||
| chr6:131173133 | G | A | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+3860G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173133 | |||||||
| chr6:131173155 | C | T | 128 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(125): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.589+3882C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173155 | |||||||
| chr6:131173200 | CA | C | 169 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(166): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.589+3943delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131173200 | ||||||
| chr6:131173300 | A | G | 2 | a0001c0001t0007g0251 a0001c0001t0009g0102 |
2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.589+4027A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173300 | |||||||
| chr6:131173301 | T | A | 14 | a0001c0001t0002g0302 a0001c0001t0003g0143 a0001c0001t0003g0151 others(11): Show |
14 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.589+4028T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173301 | |||||||
| chr6:131173326 | T | C | 14 | a0001c0001t0002g0302 a0001c0001t0003g0143 a0001c0001t0003g0151 others(11): Show |
14 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.589+4053T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173326 | |||||||
| chr6:131173339 | C | A | 255 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(252): Show |
256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.589+4066C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173339 | |||||||
| chr6:131173376 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.589+4103A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131173376 | |||||||
| chr6:131173772 | C | CTTAG | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.589+4500_589+4503d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131173772 | ||||||
| chr6:131174028 | T | C | 1 | a0001c0001t0028g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.589+4755T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174028 | |||||||
| chr6:131174175 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.589+4902T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174175 | |||||||
| chr6:131174360 | T | C | 3 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 |
3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.589+5087T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174360 | |||||||
| chr6:131174432 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.589+5159A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174432 | |||||||
| chr6:131174457 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.589+5184C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174457 | |||||||
| chr6:131174466 | G | A | 3 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 |
3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.589+5193G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174466 | |||||||
| chr6:131174469 | G | T | 1 | a0001c0001t0004g0209 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.589+5196G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174469 | |||||||
| chr6:131174532 | A | G | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+5259A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174532 | |||||||
| chr6:131174556 | A | G | 1 | a0002c0002t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589+5283A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174556 | |||||||
| chr6:131174587 | C | T | 8 | a0001c0001t0005g0157 a0001c0001t0007g0282 a0001c0001t0009g0222 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+5314C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174587 | |||||||
| chr6:131174713 | C | T | 8 | a0001c0001t0005g0157 a0001c0001t0007g0282 a0001c0001t0009g0222 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+5440C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174713 | |||||||
| chr6:131174909 | GAACCCTG others(24): Show |
G | 25 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0164 others(22): Show |
25 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.589+5637_589+5667d others(33): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174909 | |||||||
| chr6:131174913 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0003g0074 |
2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.589+5640C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131174913 | |||||||
| chr6:131174979 | AT | A | 8 | a0001c0001t0005g0157 a0001c0001t0007g0282 a0001c0001t0009g0222 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+5708delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131174979 | ||||||
| chr6:131175109 | C | T | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+5836C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175109 | |||||||
| chr6:131175220 | T | C | 12 | a0001c0001t0001g0042 a0001c0001t0001g0085 a0001c0001t0001g0088 others(9): Show |
12 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.589+5947T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175220 | |||||||
| chr6:131175506 | G | C | 1 | a0002c0002t0020g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589+6233G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175506 | |||||||
| chr6:131175511 | G | T | 1 | a0001c0001t0003g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.589+6238G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175511 | |||||||
| chr6:131175579 | A | G | 226 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.589+6306A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175579 | |||||||
| chr6:131175792 | T | C | 2 | a0001c0001t0003g0143 a0001c0001t0003g0151 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.589+6519T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175792 | |||||||
| chr6:131175912 | G | A | 1 | a0001c0001t0003g0044 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.589+6639G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175912 | |||||||
| chr6:131175936 | G | T | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+6663G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175936 | |||||||
| chr6:131175941 | T | C | 2 | a0001c0001t0008g0218 a0001c0001t0010g0184 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.589+6668T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175941 | |||||||
| chr6:131175961 | T | C | 4 | a0002c0002t0001g0158 a0006c0006t0014g0006 a0006c0006t0016g0008 others(1): Show |
4 | HG01123.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+6688T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131175961 | |||||||
| chr6:131176079 | A | G | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+6806A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176079 | |||||||
| chr6:131176285 | G | GT | 8 | a0001c0001t0001g0161 a0001c0001t0002g0271 a0001c0001t0004g0033 others(5): Show |
8 | HG03098.hp2 NA18955.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.589+7024dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131176285 | ||||||
| chr6:131176285 | GT | G | 8 | a0001c0001t0005g0157 a0001c0001t0007g0282 a0001c0001t0009g0222 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+7024delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131176285 | ||||||
| chr6:131176717 | C | T | 1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.589+7444C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176717 | |||||||
| chr6:131176718 | G | A | 8 | a0001c0001t0005g0157 a0001c0001t0007g0282 a0001c0001t0009g0222 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+7445G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176718 | |||||||
| chr6:131176817 | C | A | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+7544C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176817 | |||||||
| chr6:131176857 | C | A | 2 | a0001c0001t0004g0208 a0001c0001t0006g0298 |
2 | HG00597.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.589+7584C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176857 | |||||||
| chr6:131176889 | C | G | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.589+7616C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131176889 | |||||||
| chr6:131177088 | T | G | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+7815T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177088 | |||||||
| chr6:131177224 | G | T | 1 | a0002c0002t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589+7951G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177224 | |||||||
| chr6:131177400 | C | G | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+8127C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177400 | |||||||
| chr6:131177460 | T | C | 1 | a0002c0002t0003g0109 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.589+8187T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177460 | |||||||
| chr6:131177463 | G | A | 200 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.589+8190G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177463 | |||||||
| chr6:131177469 | G | A | 51 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(48): Show |
51 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.589+8196G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177469 | |||||||
| chr6:131177663 | G | A | 3 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 |
3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.589+8390G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177663 | |||||||
| chr6:131177758 | C | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0154 others(3): Show |
6 | HG01099.hp2 HG01106.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+8485C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177758 | |||||||
| chr6:131177823 | C | T | 5 | a0004c0004t0001g0001 a0004c0004t0001g0129 a0004c0004t0001g0131 others(2): Show |
6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+8550C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131177823 | |||||||
| chr6:131177850 | ACCTCTTC others(3): Show |
A | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+8581_589+8590d others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131177850 | ||||||
| chr6:131178055 | G | T | 38 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(35): Show |
38 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.589+8782G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178055 | |||||||
| chr6:131178226 | C | T | 8 | a0001c0001t0005g0157 a0001c0001t0007g0282 a0001c0001t0009g0222 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+8953C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178226 | |||||||
| chr6:131178237 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0003g0106 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.589+8964T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178237 | |||||||
| chr6:131178302 | G | A | 225 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(222): Show |
226 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.589+9029G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178302 | |||||||
| chr6:131178306 | T | C | 1 | a0002c0002t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.589+9033T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178306 | |||||||
| chr6:131178379 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.589+9106G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178379 | |||||||
| chr6:131178499 | A | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0179 others(16): Show |
19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+9226A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178499 | |||||||
| chr6:131178658 | A | G | 1 | a0001c0001t0013g0112 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.589+9385A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178658 | |||||||
| chr6:131178763 | C | T | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0179 others(16): Show |
19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+9490C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178763 | |||||||
| chr6:131178812 | G | A | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589+9539G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178812 | |||||||
| chr6:131178876 | A | G | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.589+9603A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178876 | |||||||
| chr6:131178973 | A | G | 2 | a0001c0001t0006g0002 a0011c0008t0006g0002 |
2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.589+9700A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178973 | |||||||
| chr6:131178990 | G | T | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.589+9717G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131178990 | |||||||
| chr6:131179041 | C | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0179 others(16): Show |
19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+9768C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179041 | |||||||
| chr6:131179166 | C | T | 131 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.589+9893C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179166 | |||||||
| chr6:131179168 | GT | G | 155 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(152): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.589+9905delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131179168 | ||||||
| chr6:131179187 | G | T | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0179 others(16): Show |
19 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+9914G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179187 | |||||||
| chr6:131179215 | C | G | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589+9942C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179215 | |||||||
| chr6:131179258 | C | T | 43 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.589+9985C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179258 | |||||||
| chr6:131179463 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0002g0255 a0001c0001t0002g0256 |
3 | HG01496.hp1 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.589+10190C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179463 | |||||||
| chr6:131179529 | C | T | 1 | a0001c0001t0007g0277 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.589+10256C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179529 | |||||||
| chr6:131179597 | C | T | 4 | a0001c0001t0007g0277 a0002c0002t0015g0003 a0002c0002t0015g0004 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+10324C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179597 | |||||||
| chr6:131179602 | AG | A | 38 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0211 others(35): Show |
38 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.589+10331delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131179602 | ||||||
| chr6:131179868 | CAAAT | C | 36 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0164 others(33): Show |
36 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.589+10622_589+1062 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131179868 | ||||||
| chr6:131179895 | A | T | 190 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(187): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.589+10622A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179895 | |||||||
| chr6:131179896 | T | A | 191 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(188): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.589+10623T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179896 | |||||||
| chr6:131179896 | T | TAATA | 6 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+10637_589+1064 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131179896 | ||||||
| chr6:131179899 | T | A | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+10626T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179899 | |||||||
| chr6:131179900 | A | T | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589+10627A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131179900 | |||||||
| chr6:131180025 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.589+10752G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180025 | |||||||
| chr6:131180072 | C | T | 2 | a0006c0006t0016g0008 a0006c0006t0035g0217 |
2 | HG01123.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.589+10799C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180072 | |||||||
| chr6:131180231 | T | G | 1 | a0001c0001t0002g0276 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.589+10958T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180231 | |||||||
| chr6:131180250 | C | T | 2 | a0001c0001t0005g0224 a0001c0001t0007g0281 |
2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.589+10977C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180250 | |||||||
| chr6:131180463 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.589+11190C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180463 | |||||||
| chr6:131180493 | C | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.589+11220C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180493 | |||||||
| chr6:131180664 | C | T | 1 | a0007c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.589+11391C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180664 | |||||||
| chr6:131180694 | A | G | 42 | a0001c0001t0001g0215 a0001c0001t0002g0272 a0001c0001t0004g0026 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+11421A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180694 | |||||||
| chr6:131180750 | A | G | 20 | a0001c0001t0005g0075 a0001c0001t0005g0157 a0001c0001t0007g0243 others(17): Show |
20 | HG01123.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.589+11477A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180750 | |||||||
| chr6:131180812 | ACTTT | A | 22 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(19): Show |
22 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.589+11544_589+1154 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131180812 | ||||||
| chr6:131180832 | TTG | T | 18 | a0001c0001t0005g0090 a0002c0002t0001g0065 a0002c0002t0001g0091 others(15): Show |
18 | HG00140.hp2 HG01071.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.589+11561_589+1156 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131180832 | ||||||
| chr6:131180834 | G | T | 2 | a0002c0002t0017g0010 a0002c0002t0036g0221 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.589+11561G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180834 | |||||||
| chr6:131180834 | GT | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(179): Show |
183 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.589+11575delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131180834 | ||||||
| chr6:131180847 | TTA | T | 30 | a0001c0001t0002g0248 a0001c0001t0005g0075 a0001c0001t0005g0076 others(27): Show |
30 | HG00140.hp1 HG00323.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.589+11575_589+1157 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180847 | |||||||
| chr6:131180848 | TA | T | 4 | a0001c0001t0021g0223 a0001c0001t0022g0086 a0001c0001t0022g0095 others(1): Show |
4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+11577delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131180848 | ||||||
| chr6:131180849 | A | T | 21 | a0001c0001t0005g0090 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.589+11576A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180849 | |||||||
| chr6:131180866 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0010g0087 a0006c0006t0014g0007 |
3 | HG02280.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.589+11593A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180866 | |||||||
| chr6:131180945 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.589+11672G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131180945 | |||||||
| chr6:131181048 | G | GC | 127 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.589+11777dupC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131181048 | ||||||
| chr6:131181081 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0010g0087 a0001c0001t0034g0219 others(1): Show |
4 | HG02280.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+11808G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181081 | |||||||
| chr6:131181190 | C | A | 6 | a0001c0001t0002g0232 a0001c0001t0002g0279 a0001c0001t0002g0300 others(3): Show |
6 | HG00099.hp2 HG01978.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+11917C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181190 | |||||||
| chr6:131181199 | A | G | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.589+11926A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181199 | |||||||
| chr6:131181388 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0002g0261 |
2 | NA18955.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.589+12115C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181388 | |||||||
| chr6:131181395 | A | T | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.589+12122A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181395 | |||||||
| chr6:131181453 | T | G | 11 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0157 others(8): Show |
11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+12180T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181453 | |||||||
| chr6:131181488 | G | A | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+12215G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181488 | |||||||
| chr6:131181506 | A | T | 16 | a0001c0001t0001g0042 a0001c0001t0007g0286 a0001c0001t0009g0142 others(13): Show |
16 | HG01952.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.589+12233A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181506 | |||||||
| chr6:131181522 | G | C | 17 | a0002c0002t0001g0065 a0002c0002t0001g0091 a0002c0002t0001g0096 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.589+12249G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181522 | |||||||
| chr6:131181538 | T | C | 17 | a0002c0002t0001g0065 a0002c0002t0001g0091 a0002c0002t0001g0096 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.589+12265T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181538 | |||||||
| chr6:131181631 | T | C | 91 | a0001c0001t0002g0248 a0001c0001t0004g0026 a0001c0001t0004g0033 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.589+12358T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181631 | |||||||
| chr6:131181728 | C | T | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+12455C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181728 | |||||||
| chr6:131181759 | T | C | 52 | a0001c0001t0002g0248 a0001c0001t0005g0075 a0001c0001t0005g0076 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.589+12486T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181759 | |||||||
| chr6:131181894 | C | T | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589+12621C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131181894 | |||||||
| chr6:131182027 | GA | G | 4 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0007g0277 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+12755delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182027 | |||||||
| chr6:131182125 | G | GA | 46 | a0001c0001t0002g0248 a0002c0002t0001g0027 a0002c0002t0001g0064 others(43): Show |
46 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.589+12862dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131182125 | ||||||
| chr6:131182160 | A | G | 1 | a0002c0002t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589+12887A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182160 | |||||||
| chr6:131182243 | A | G | 1 | a0001c0001t0003g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.589+12970A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182243 | |||||||
| chr6:131182509 | C | T | 29 | a0001c0001t0002g0302 a0001c0001t0005g0075 a0001c0001t0005g0076 others(26): Show |
29 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.589+13236C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182509 | |||||||
| chr6:131182669 | G | A | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+13396G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182669 | |||||||
| chr6:131182758 | C | A | 1 | a0001c0001t0004g0199 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.589+13485C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182758 | |||||||
| chr6:131182816 | CT | C | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+13552delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131182816 | ||||||
| chr6:131182817 | T | C | 1 | a0002c0002t0001g0115 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.589+13544T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131182817 | |||||||
| chr6:131183147 | A | G | 3 | a0001c0001t0002g0246 a0001c0001t0002g0295 a0001c0001t0002g0299 |
3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.589+13874A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183147 | |||||||
| chr6:131183163 | CT | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0002g0280 others(1): Show |
4 | NA18981.hp2 NA19006.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+13892delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131183163 | ||||||
| chr6:131183235 | A | G | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.589+13962A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183235 | |||||||
| chr6:131183261 | T | C | 23 | a0001c0001t0002g0248 a0001c0001t0034g0219 a0002c0002t0001g0027 others(20): Show |
23 | HG00140.hp1 HG00323.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.589+13988T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183261 | |||||||
| chr6:131183360 | T | C | 51 | a0001c0001t0002g0248 a0001c0001t0005g0075 a0001c0001t0005g0076 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.589+14087T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183360 | |||||||
| chr6:131183436 | G | A | 5 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(2): Show |
5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.589+14163G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183436 | |||||||
| chr6:131183711 | T | C | 60 | a0001c0001t0002g0248 a0001c0001t0005g0075 a0001c0001t0005g0076 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.589+14438T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131183711 | |||||||
| chr6:131184003 | A | C | 1 | a0001c0001t0004g0026 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.589+14730A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184003 | |||||||
| chr6:131184091 | G | T | 16 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(13): Show |
16 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.589+14818G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184091 | |||||||
| chr6:131184185 | C | T | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.589+14912C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184185 | |||||||
| chr6:131184293 | T | G | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.589+15020T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184293 | |||||||
| chr6:131184310 | A | AG | 55 | a0001c0001t0002g0248 a0001c0001t0005g0075 a0001c0001t0005g0076 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.589+15043dupG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131184310 | ||||||
| chr6:131184313 | G | A | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.589+15040G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184313 | |||||||
| chr6:131184315 | G | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.589+15042G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184315 | |||||||
| chr6:131184391 | C | T | 130 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(127): Show |
131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.590-15070C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184391 | |||||||
| chr6:131184501 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0124 |
2 | NA18941.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.590-14960G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184501 | |||||||
| chr6:131184605 | A | G | 134 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.590-14856A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184605 | |||||||
| chr6:131184779 | G | A | 1 | a0001c0001t0005g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.590-14682G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184779 | |||||||
| chr6:131184844 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.590-14617A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184844 | |||||||
| chr6:131184920 | A | C | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.590-14541A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131184920 | |||||||
| chr6:131185025 | C | T | 50 | a0001c0001t0002g0248 a0001c0001t0034g0219 a0002c0002t0001g0027 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.590-14436C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185025 | |||||||
| chr6:131185157 | A | G | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590-14304A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185157 | |||||||
| chr6:131185533 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.590-13928A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185533 | |||||||
| chr6:131185738 | C | G | 3 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0024g0100 |
3 | HG01884.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.590-13723C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185738 | |||||||
| chr6:131185784 | A | G | 50 | a0001c0001t0002g0248 a0001c0001t0034g0219 a0002c0002t0001g0027 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.590-13677A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185784 | |||||||
| chr6:131185814 | A | C | 55 | a0001c0001t0002g0248 a0001c0001t0005g0075 a0001c0001t0005g0076 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.590-13647A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131185814 | |||||||
| chr6:131186131 | G | A | 255 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.590-13330G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186131 | |||||||
| chr6:131186370 | G | A | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-13091G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186370 | |||||||
| chr6:131186429 | A | AT | 6 | a0002c0002t0037g0162 a0005c0005t0005g0097 a0005c0005t0005g0098 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-13022dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131186429 | ||||||
| chr6:131186429 | A | G | 1 | a0001c0001t0002g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.590-13032A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186429 | |||||||
| chr6:131186481 | C | G | 22 | a0001c0001t0002g0248 a0002c0002t0001g0027 a0002c0002t0001g0064 others(19): Show |
22 | HG00140.hp1 HG00323.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.590-12980C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186481 | |||||||
| chr6:131186558 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.590-12903T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186558 | |||||||
| chr6:131186626 | A | G | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-12835A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131186626 | |||||||
| chr6:131186804 | GA | G | 20 | a0002c0002t0001g0065 a0002c0002t0001g0091 a0002c0002t0001g0096 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-12655delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131186804 | ||||||
| chr6:131187062 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.590-12399A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187062 | |||||||
| chr6:131187142 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.590-12319T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187142 | |||||||
| chr6:131187153 | A | G | 3 | a0004c0004t0001g0001 a0004c0004t0001g0216 a0004c0004t0003g0167 |
4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-12308A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187153 | |||||||
| chr6:131187234 | T | A | 245 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.590-12227T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187234 | |||||||
| chr6:131187255 | A | T | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.590-12206A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187255 | |||||||
| chr6:131187304 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0010g0087 a0006c0006t0014g0007 |
3 | HG02280.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.590-12157A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187304 | |||||||
| chr6:131187749 | A | G | 4 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-11712A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187749 | |||||||
| chr6:131187756 | A | G | 20 | a0002c0002t0001g0065 a0002c0002t0001g0091 a0002c0002t0001g0096 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-11705A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187756 | |||||||
| chr6:131187956 | A | G | 55 | a0001c0001t0002g0248 a0001c0001t0005g0075 a0001c0001t0005g0076 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.590-11505A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131187956 | |||||||
| chr6:131188128 | A | G | 1 | a0002c0002t0020g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.590-11333A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131188128 | |||||||
| chr6:131188166 | A | G | 1 | a0006c0006t0014g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.590-11295A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131188166 | |||||||
| chr6:131188237 | C | CAT | 255 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.590-11222_590-1122 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188237 | ||||||
| chr6:131188494 | TACTC | T | 9 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.590-10965_590-1096 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188494 | ||||||
| chr6:131188529 | TTTG | T | 3 | a0001c0001t0007g0243 a0001c0001t0041g0159 a0002c0002t0027g0231 |
3 | HG02258.hp1 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.590-10917_590-1091 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188529 | ||||||
| chr6:131188602 | A | G | 6 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0224 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-10859A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131188602 | |||||||
| chr6:131188710 | T | C | 5 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(2): Show |
5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-10751T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131188710 | |||||||
| chr6:131188717 | C | CT | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(49): Show |
52 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.590-10728dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188717 | ||||||
| chr6:131188717 | CT | C | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-10728delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131188717 | ||||||
| chr6:131189495 | AAG | A | 133 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.590-9965_590-9964d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131189495 | |||||||
| chr6:131189515 | A | G | 1 | a0001c0001t0002g0279 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.590-9946A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131189515 | |||||||
| chr6:131189647 | A | G | 1 | a0004c0004t0003g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.590-9814A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131189647 | |||||||
| chr6:131189661 | G | A | 1 | a0009c0011t0004g0197 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.590-9800G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131189661 | |||||||
| chr6:131190048 | T | C | 1 | a0007c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.590-9413T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190048 | |||||||
| chr6:131190063 | C | T | 92 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.590-9398C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190063 | |||||||
| chr6:131190107 | T | C | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-9354T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190107 | |||||||
| chr6:131190127 | C | G | 11 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0157 others(8): Show |
11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-9334C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190127 | |||||||
| chr6:131190149 | A | G | 21 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(18): Show |
21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.590-9312A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190149 | |||||||
| chr6:131190232 | T | G | 50 | a0001c0001t0034g0219 a0002c0002t0001g0027 a0002c0002t0001g0064 others(47): Show |
50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.590-9229T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190232 | |||||||
| chr6:131190290 | C | G | 10 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-9171C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190290 | |||||||
| chr6:131190365 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-9096G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190365 | |||||||
| chr6:131190413 | C | T | 51 | a0001c0001t0034g0219 a0001c0001t0041g0159 a0002c0002t0001g0027 others(48): Show |
51 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.590-9048C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190413 | |||||||
| chr6:131190534 | C | G | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-8927C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190534 | |||||||
| chr6:131190846 | T | G | 1 | a0001c0001t0004g0205 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.590-8615T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190846 | |||||||
| chr6:131190994 | C | G | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-8467C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131190994 | |||||||
| chr6:131191061 | C | A | 8 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0153 others(5): Show |
8 | HG01099.hp2 HG01192.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.590-8400C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191061 | |||||||
| chr6:131191066 | G | A | 3 | a0001c0001t0007g0282 a0001c0001t0028g0236 a0006c0006t0016g0008 |
3 | HG01123.hp2 HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.590-8395G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191066 | |||||||
| chr6:131191105 | A | G | 50 | a0001c0001t0034g0219 a0002c0002t0001g0027 a0002c0002t0001g0064 others(47): Show |
50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.590-8356A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191105 | |||||||
| chr6:131191205 | A | T | 2 | a0001c0001t0007g0243 a0001c0001t0041g0159 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.590-8256A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191205 | |||||||
| chr6:131191233 | A | G | 1 | a0003c0003t0008g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.590-8228A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191233 | |||||||
| chr6:131191618 | A | C | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-7843A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191618 | |||||||
| chr6:131191839 | C | T | 1 | a0001c0001t0010g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.590-7622C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191839 | |||||||
| chr6:131191845 | G | GT | 31 | a0001c0001t0002g0300 a0001c0001t0003g0151 a0002c0002t0001g0065 others(28): Show |
31 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.590-7599dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131191845 | ||||||
| chr6:131191936 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.590-7525G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131191936 | |||||||
| chr6:131192265 | A | G | 2 | a0002c0002t0001g0121 a0002c0002t0002g0288 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.590-7196A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192265 | |||||||
| chr6:131192342 | G | A | 2 | a0001c0001t0023g0174 a0001c0001t0023g0175 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.590-7119G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192342 | |||||||
| chr6:131192427 | A | G | 1 | a0001c0001t0002g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.590-7034A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192427 | |||||||
| chr6:131192521 | T | C | 296 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.590-6940T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192521 | |||||||
| chr6:131192545 | A | G | 9 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.590-6916A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131192545 | |||||||
| chr6:131193194 | A | G | 1 | a0001c0001t0006g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.590-6267A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193194 | |||||||
| chr6:131193218 | T | C | 5 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(2): Show |
5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-6243T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193218 | |||||||
| chr6:131193306 | T | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590-6155T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193306 | |||||||
| chr6:131193328 | A | G | 54 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(51): Show |
54 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.590-6133A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193328 | |||||||
| chr6:131193432 | G | T | 23 | a0002c0002t0001g0065 a0002c0002t0001g0091 a0002c0002t0001g0096 others(20): Show |
23 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.590-6029G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193432 | |||||||
| chr6:131193615 | G | A | 2 | a0001c0001t0005g0157 a0001c0001t0007g0251 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.590-5846G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193615 | |||||||
| chr6:131193722 | AT | A | 3 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0024g0100 |
3 | HG01884.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.590-5738delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193722 | |||||||
| chr6:131193754 | G | A | 134 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.590-5707G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131193754 | |||||||
| chr6:131194092 | C | G | 1 | a0001c0001t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.590-5369C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194092 | |||||||
| chr6:131194106 | G | A | 11 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0157 others(8): Show |
11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-5355G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194106 | |||||||
| chr6:131194149 | C | CT | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-5304dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131194149 | ||||||
| chr6:131194283 | T | C | 49 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0065 others(46): Show |
49 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.590-5178T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194283 | |||||||
| chr6:131194355 | T | C | 9 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.590-5106T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194355 | |||||||
| chr6:131194364 | T | C | 5 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(2): Show |
5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-5097T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194364 | |||||||
| chr6:131194404 | T | A | 4 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(1): Show |
4 | HG00741.hp1 HG01891.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-5057T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194404 | |||||||
| chr6:131194406 | A | T | 4 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(1): Show |
4 | HG00741.hp1 HG01891.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-5055A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194406 | |||||||
| chr6:131194535 | A | G | 11 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0157 others(8): Show |
11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-4926A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194535 | |||||||
| chr6:131194610 | A | G | 109 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(106): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.590-4851A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194610 | |||||||
| chr6:131194614 | C | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-4847C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194614 | |||||||
| chr6:131194827 | G | A | 2 | a0002c0002t0001g0121 a0002c0002t0002g0288 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.590-4634G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194827 | |||||||
| chr6:131194901 | T | A | 20 | a0002c0002t0001g0065 a0002c0002t0001g0091 a0002c0002t0001g0096 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-4560T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131194901 | |||||||
| chr6:131195109 | C | T | 254 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.590-4352C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195109 | |||||||
| chr6:131195300 | C | T | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-4161C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195300 | |||||||
| chr6:131195469 | A | G | 1 | a0002c0002t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.590-3992A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195469 | |||||||
| chr6:131195521 | C | G | 1 | a0001c0001t0005g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.590-3940C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195521 | |||||||
| chr6:131195895 | C | T | 5 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(2): Show |
5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-3566C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195895 | |||||||
| chr6:131195954 | A | G | 4 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-3507A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131195954 | |||||||
| chr6:131196267 | C | CT | 136 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.590-3178dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131196267 | ||||||
| chr6:131196292 | G | A | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-3169G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196292 | |||||||
| chr6:131196329 | A | G | 1 | a0001c0001t0023g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.590-3132A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196329 | |||||||
| chr6:131196389 | C | T | 2 | a0002c0002t0001g0134 a0002c0002t0001g0135 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.590-3072C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196389 | |||||||
| chr6:131196405 | A | G | 1 | a0002c0002t0020g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.590-3056A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196405 | |||||||
| chr6:131196452 | C | T | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-3009C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196452 | |||||||
| chr6:131196554 | G | A | 21 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(18): Show |
21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.590-2907G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196554 | |||||||
| chr6:131196626 | A | C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-2835A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196626 | |||||||
| chr6:131196678 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.590-2783A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196678 | |||||||
| chr6:131196687 | T | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-2774T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196687 | |||||||
| chr6:131196690 | A | C | 1 | a0001c0001t0005g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.590-2771A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196690 | |||||||
| chr6:131196695 | A | G | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-2766A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196695 | |||||||
| chr6:131196740 | T | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-2721T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196740 | |||||||
| chr6:131196761 | A | G | 255 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.590-2700A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196761 | |||||||
| chr6:131196955 | T | C | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.590-2506T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131196955 | |||||||
| chr6:131197097 | T | C | 11 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0157 others(8): Show |
11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-2364T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197097 | |||||||
| chr6:131197140 | C | G | 1 | a0001c0001t0002g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.590-2321C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197140 | |||||||
| chr6:131197459 | A | G | 1 | a0001c0001t0006g0298 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.590-2002A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197459 | |||||||
| chr6:131197583 | A | T | 1 | a0001c0001t0008g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.590-1878A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197583 | |||||||
| chr6:131197732 | A | G | 1 | a0002c0002t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.590-1729A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197732 | |||||||
| chr6:131197754 | T | C | 136 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.590-1707T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131197754 | |||||||
| chr6:131198090 | C | T | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.590-1371C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198090 | |||||||
| chr6:131198096 | G | A | 5 | a0004c0004t0001g0001 a0004c0004t0001g0129 a0004c0004t0001g0131 others(2): Show |
6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-1365G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198096 | |||||||
| chr6:131198199 | A | G | 8 | a0001c0001t0001g0046 a0001c0001t0003g0040 a0001c0001t0003g0041 others(5): Show |
8 | NA18943.hp1 NA18951.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.590-1262A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198199 | |||||||
| chr6:131198229 | T | C | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.590-1232T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198229 | |||||||
| chr6:131198523 | A | G | 2 | a0001c0001t0007g0243 a0001c0001t0041g0159 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.590-938A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198523 | |||||||
| chr6:131198555 | T | C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590-906T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198555 | |||||||
| chr6:131198560 | A | G | 11 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0157 others(8): Show |
11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-901A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198560 | |||||||
| chr6:131198592 | G | A | 1 | a0001c0001t0002g0258 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.590-869G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198592 | |||||||
| chr6:131198851 | C | A | 1 | a0001c0001t0003g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.590-610C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198851 | |||||||
| chr6:131198895 | TCTTA | T | 5 | a0001c0001t0005g0141 a0001c0001t0009g0185 a0001c0001t0021g0223 others(2): Show |
5 | HG02922.hp1 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-562_590-559del others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 131198895 | ||||||
| chr6:131198980 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.590-481A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198980 | |||||||
| chr6:131198984 | G | C | 254 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.590-477G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131198984 | |||||||
| chr6:131199038 | G | A | 2 | a0001c0001t0007g0243 a0001c0001t0041g0159 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.590-423G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131199038 | |||||||
| chr6:131199149 | A | G | 255 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.590-312A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131199149 | |||||||
| chr6:131199298 | G | T | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-163G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131199298 | |||||||
| chr6:131199367 | A | G | 20 | a0002c0002t0001g0065 a0002c0002t0001g0091 a0002c0002t0001g0096 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-94A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 5/7 | chr6 | 131199367 | |||||||
| chr6:131199597 | G | T | 1 | a0001c0001t0002g0274 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.702+24G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199597 | |||||||
| chr6:131199754 | T | C | 9 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+181T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199754 | |||||||
| chr6:131199827 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.702+254C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199827 | |||||||
| chr6:131199854 | C | A | 21 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(18): Show |
21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+281C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199854 | |||||||
| chr6:131199947 | C | G | 1 | a0001c0001t0002g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.702+374C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131199947 | |||||||
| chr6:131200234 | G | A | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.702+661G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200234 | |||||||
| chr6:131200414 | C | T | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.702+841C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200414 | |||||||
| chr6:131200564 | G | A | 20 | a0002c0002t0001g0065 a0002c0002t0001g0091 a0002c0002t0001g0096 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.702+991G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200564 | |||||||
| chr6:131200688 | T | C | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.702+1115T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200688 | |||||||
| chr6:131200690 | A | G | 97 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(94): Show |
97 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.702+1117A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200690 | |||||||
| chr6:131200807 | C | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.702+1234C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200807 | |||||||
| chr6:131200821 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.702+1248A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200821 | |||||||
| chr6:131200853 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.702+1280G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200853 | |||||||
| chr6:131200881 | T | C | 1 | a0001c0001t0002g0259 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.702+1308T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200881 | |||||||
| chr6:131200969 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.702+1396G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131200969 | |||||||
| chr6:131201072 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.702+1499T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201072 | |||||||
| chr6:131201269 | A | G | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.702+1696A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201269 | |||||||
| chr6:131201342 | C | T | 21 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(18): Show |
21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+1769C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201342 | |||||||
| chr6:131201352 | A | G | 12 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0157 others(9): Show |
12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+1779A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201352 | |||||||
| chr6:131201372 | A | G | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+1799A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201372 | |||||||
| chr6:131201434 | A | G | 5 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(2): Show |
5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+1861A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201434 | |||||||
| chr6:131201472 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.702+1899C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201472 | |||||||
| chr6:131201659 | T | C | 8 | a0001c0001t0002g0302 a0001c0001t0005g0093 a0001c0001t0005g0224 others(5): Show |
8 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.702+2086T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201659 | |||||||
| chr6:131201766 | T | A | 1 | a0007c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.702+2193T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201766 | |||||||
| chr6:131201786 | G | A | 3 | a0002c0002t0001g0180 a0002c0002t0001g0181 a0002c0002t0002g0235 |
3 | HG00140.hp2 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.702+2213G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201786 | |||||||
| chr6:131201835 | T | C | 10 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(7): Show |
10 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.702+2262T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201835 | |||||||
| chr6:131201861 | A | G | 136 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.702+2288A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201861 | |||||||
| chr6:131201932 | T | C | 98 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(95): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.702+2359T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201932 | |||||||
| chr6:131201933 | A | G | 1 | a0001c0001t0003g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.702+2360A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131201933 | |||||||
| chr6:131202024 | T | G | 1 | a0002c0002t0001g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.702+2451T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202024 | |||||||
| chr6:131202046 | C | A | 9 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2473C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202046 | |||||||
| chr6:131202088 | G | A | 92 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.702+2515G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202088 | |||||||
| chr6:131202303 | G | A | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.702+2730G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202303 | |||||||
| chr6:131202394 | A | T | 134 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.702+2821A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202394 | |||||||
| chr6:131202526 | T | C | 255 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.702+2953T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202526 | |||||||
| chr6:131202568 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.702+2995C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202568 | |||||||
| chr6:131202595 | C | T | 124 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.702+3022C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202595 | |||||||
| chr6:131202689 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.702+3116G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202689 | |||||||
| chr6:131202733 | C | T | 1 | a0001c0001t0009g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.702+3160C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131202733 | |||||||
| chr6:131202762 | TAATAA | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | NA18964.hp1 NA18982.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.702+3206_702+3210d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131202762 | ||||||
| chr6:131203037 | G | A | 1 | a0001c0001t0005g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.702+3464G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203037 | |||||||
| chr6:131203198 | C | T | 1 | a0001c0001t0002g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.702+3625C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203198 | |||||||
| chr6:131203218 | A | G | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.702+3645A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203218 | |||||||
| chr6:131203374 | C | T | 10 | a0001c0001t0010g0082 a0001c0001t0023g0174 a0001c0001t0023g0175 others(7): Show |
10 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+3801C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203374 | |||||||
| chr6:131203478 | G | A | 32 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(29): Show |
32 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.702+3905G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203478 | |||||||
| chr6:131203854 | C | T | 12 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(9): Show |
12 | NA18612.hp1 NA18942.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+4281C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203854 | |||||||
| chr6:131203859 | A | G | 3 | a0001c0001t0002g0246 a0001c0001t0002g0295 a0001c0001t0002g0299 |
3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.702+4286A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131203859 | |||||||
| chr6:131204108 | C | T | 15 | a0001c0001t0001g0042 a0001c0001t0007g0286 a0001c0001t0010g0082 others(12): Show |
15 | HG01952.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+4535C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204108 | |||||||
| chr6:131204402 | A | C | 2 | a0001c0001t0008g0218 a0001c0001t0010g0184 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.702+4829A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204402 | |||||||
| chr6:131204415 | C | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.702+4842C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204415 | |||||||
| chr6:131204544 | A | G | 55 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(52): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+4971A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204544 | |||||||
| chr6:131204749 | G | A | 55 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(52): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+5176G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204749 | |||||||
| chr6:131204754 | C | T | 1 | a0002c0002t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.702+5181C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204754 | |||||||
| chr6:131204843 | G | A | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.702+5270G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131204843 | |||||||
| chr6:131205046 | TA | T | 9 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(6): Show |
9 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.702+5478delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131205046 | ||||||
| chr6:131205365 | A | G | 120 | a0001c0001t0002g0302 a0001c0001t0004g0026 a0001c0001t0004g0033 others(117): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.702+5792A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131205365 | |||||||
| chr6:131205383 | C | T | 1 | a0010c0010t0002g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.702+5810C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131205383 | |||||||
| chr6:131205448 | C | T | 2 | a0001c0001t0007g0282 a0001c0001t0028g0236 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.702+5875C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131205448 | |||||||
| chr6:131205449 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.702+5876C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131205449 | |||||||
| chr6:131206197 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.702+6624A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206197 | |||||||
| chr6:131206332 | A | G | 9 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+6759A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206332 | |||||||
| chr6:131206565 | A | G | 1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.702+6992A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206565 | |||||||
| chr6:131206607 | T | A | 2 | a0002c0002t0001g0177 a0002c0002t0002g0265 |
2 | HG02074.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.702+7034T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206607 | |||||||
| chr6:131206647 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.702+7074G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206647 | |||||||
| chr6:131206775 | G | A | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(184): Show |
187 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.702+7202G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206775 | |||||||
| chr6:131206786 | C | CATCT | 26 | a0001c0001t0003g0057 a0001c0001t0005g0157 a0001c0001t0007g0243 others(23): Show |
26 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.702+7234_702+7237d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131206786 | ||||||
| chr6:131206790 | T | C | 1 | a0003c0003t0032g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.702+7217T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206790 | |||||||
| chr6:131206809 | C | T | 1 | a0001c0001t0003g0050 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.702+7236C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131206809 | |||||||
| chr6:131207130 | C | T | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.702+7557C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207130 | |||||||
| chr6:131207318 | A | AT | 53 | a0001c0001t0001g0084 a0001c0001t0001g0153 a0001c0001t0001g0154 others(50): Show |
53 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.702+7760dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207318 | ||||||
| chr6:131207318 | AT | A | 21 | a0001c0001t0002g0238 a0001c0001t0003g0073 a0001c0001t0004g0061 others(18): Show |
21 | HG00323.hp2 HG01993.hp2 HG02293.hp1 others(18): Show |
intron_variant | MODIFIER | c.702+7760delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207318 | ||||||
| chr6:131207421 | A | G | 1 | a0002c0002t0039g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.702+7848A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207421 | |||||||
| chr6:131207491 | A | AT | 11 | a0001c0001t0001g0034 a0001c0001t0001g0139 a0001c0001t0001g0179 others(8): Show |
11 | HG01123.hp2 HG01943.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.702+7944dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATATATTT others(9): Show |
1 | a0002c0002t0020g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.702+7919_702+7920i others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0006g0253 a0001c0001t0022g0086 a0005c0005t0005g0097 |
3 | HG02451.hp2 HG02717.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.702+7935_702+7944d others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(4): Show |
20 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0004g0198 others(17): Show |
20 | HG00408.hp2 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.702+7934_702+7944d others(13): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(5): Show |
15 | a0001c0001t0004g0061 a0001c0001t0004g0168 a0001c0001t0004g0169 others(12): Show |
15 | HG01993.hp2 HG02257.hp1 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+7933_702+7944d others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(6): Show |
12 | a0001c0001t0004g0026 a0001c0001t0004g0035 a0001c0001t0004g0036 others(9): Show |
12 | HG00597.hp1 HG01516.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+7932_702+7944d others(15): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(7): Show |
5 | a0001c0001t0004g0033 a0001c0001t0004g0038 a0001c0001t0004g0206 others(2): Show |
5 | NA18953.hp1 NA18965.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+7931_702+7944d others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(8): Show |
3 | a0001c0001t0004g0178 a0001c0001t0004g0190 a0002c0002t0002g0265 |
3 | HG03017.hp2 NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.702+7930_702+7944d others(17): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0012g0058 a0002c0002t0001g0136 a0002c0002t0001g0158 others(1): Show |
4 | HG01978.hp2 HG02074.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+7929_702+7944d others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(10): Show |
14 | a0001c0001t0001g0084 a0001c0001t0001g0154 a0002c0002t0001g0096 others(11): Show |
14 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.702+7928_702+7944d others(19): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(11): Show |
17 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0065 others(14): Show |
17 | HG01109.hp2 HG01123.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.702+7927_702+7944d others(20): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(12): Show |
2 | a0002c0002t0001g0160 a0002c0002t0002g0245 |
2 | HG01243.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.702+7926_702+7944d others(21): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.702+7925_702+7944d others(22): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(14): Show |
1 | a0002c0002t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.702+7924_702+7944d others(23): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(15): Show |
1 | a0002c0002t0001g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.702+7923_702+7944d others(24): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | A | ATTTTTTT others(16): Show |
1 | a0002c0002t0039g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.702+7922_702+7944d others(25): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | AT | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0116 others(13): Show |
16 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.702+7944delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | ATT | A | 6 | a0001c0001t0005g0093 a0001c0001t0005g0224 a0001c0001t0007g0277 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+7943_702+7944d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207491 | ATTTT | A | 6 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(3): Show |
6 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+7941_702+7944d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131207491 | ||||||
| chr6:131207493 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.702+7920T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207493 | |||||||
| chr6:131207517 | T | TTTTTTTT others(4): Show |
1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.702+7944_702+7945i others(13): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207517 | |||||||
| chr6:131207517 | T | TTTTTTTT others(5): Show |
3 | a0002c0002t0017g0005 a0002c0002t0017g0010 a0002c0002t0036g0221 |
3 | HG02257.hp2 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.702+7944_702+7945i others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207517 | |||||||
| chr6:131207517 | T | TTTTTTTT others(14): Show |
1 | a0002c0002t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.702+7944_702+7945i others(23): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207517 | |||||||
| chr6:131207728 | G | A | 1 | a0001c0001t0003g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702+8155G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207728 | |||||||
| chr6:131207802 | C | T | 3 | a0004c0004t0001g0001 a0004c0004t0001g0216 a0004c0004t0003g0167 |
4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+8229C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207802 | |||||||
| chr6:131207962 | C | T | 12 | a0001c0001t0005g0094 a0001c0001t0007g0286 a0001c0001t0010g0082 others(9): Show |
12 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+8389C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207962 | |||||||
| chr6:131207963 | G | A | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+8390G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131207963 | |||||||
| chr6:131208500 | T | G | 3 | a0001c0001t0001g0023 a0001c0001t0002g0267 a0001c0001t0002g0275 |
3 | HG00544.hp1 HG02155.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.702+8927T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131208500 | |||||||
| chr6:131209010 | C | T | 5 | a0001c0001t0005g0093 a0001c0001t0005g0224 a0001c0001t0007g0277 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+9437C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209010 | |||||||
| chr6:131209150 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.702+9577A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209150 | |||||||
| chr6:131209173 | AT | A | 22 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(19): Show |
22 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.702+9611delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131209173 | ||||||
| chr6:131209180 | T | A | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+9607T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209180 | |||||||
| chr6:131209241 | A | G | 1 | a0001c0001t0003g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702+9668A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209241 | |||||||
| chr6:131209257 | T | G | 1 | a0007c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.702+9684T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209257 | |||||||
| chr6:131209293 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
4 | NA18943.hp1 NA18951.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+9720C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209293 | |||||||
| chr6:131209388 | C | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.702+9815C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209388 | |||||||
| chr6:131209441 | G | A | 24 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.702+9868G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209441 | |||||||
| chr6:131209733 | G | GT | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-9923dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131209733 | ||||||
| chr6:131209740 | G | C | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.703-9921G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209740 | |||||||
| chr6:131209811 | A | G | 2 | a0006c0006t0014g0006 a0006c0006t0014g0007 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.703-9850A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209811 | |||||||
| chr6:131209844 | A | T | 5 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(2): Show |
5 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-9817A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209844 | |||||||
| chr6:131209876 | C | T | 62 | a0001c0001t0001g0084 a0001c0001t0005g0075 a0001c0001t0005g0076 others(59): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.703-9785C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131209876 | |||||||
| chr6:131210046 | A | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0003g0045 |
3 | NA19006.hp2 NA19065.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.703-9615A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210046 | |||||||
| chr6:131210097 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703-9564T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210097 | |||||||
| chr6:131210166 | A | T | 62 | a0001c0001t0001g0084 a0001c0001t0005g0075 a0001c0001t0005g0076 others(59): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.703-9495A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210166 | |||||||
| chr6:131210172 | C | T | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.703-9489C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210172 | |||||||
| chr6:131210330 | G | A | 2 | a0002c0002t0001g0177 a0002c0002t0002g0265 |
2 | HG02074.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.703-9331G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210330 | |||||||
| chr6:131210606 | C | T | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-9055C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210606 | |||||||
| chr6:131210710 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.703-8951C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210710 | |||||||
| chr6:131210928 | T | G | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.703-8733T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131210928 | |||||||
| chr6:131211505 | C | T | 3 | a0002c0002t0001g0091 a0002c0002t0003g0133 a0002c0002t0003g0137 |
3 | HG01255.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.703-8156C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211505 | |||||||
| chr6:131211523 | T | C | 62 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(59): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.703-8138T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211523 | |||||||
| chr6:131211547 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.703-8114C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211547 | |||||||
| chr6:131211601 | T | TA | 15 | a0001c0001t0001g0046 a0001c0001t0001g0213 a0001c0001t0003g0040 others(12): Show |
15 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(12): Show |
intron_variant | MODIFIER | c.703-8047dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211601 | ||||||
| chr6:131211646 | A | G | 2 | a0001c0001t0005g0094 a0001c0001t0007g0286 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.703-8015A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211646 | |||||||
| chr6:131211729 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0073 |
3 | NA18980.hp2 NA19058.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.703-7932C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211729 | |||||||
| chr6:131211772 | C | CA | 114 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0084 others(111): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.703-7868dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211772 | ||||||
| chr6:131211772 | C | CAA | 11 | a0001c0001t0004g0168 a0001c0001t0004g0195 a0001c0001t0004g0208 others(8): Show |
11 | HG00408.hp2 HG00597.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.703-7869_703-7868d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211772 | ||||||
| chr6:131211772 | C | CAAAAA | 6 | a0001c0001t0005g0093 a0001c0001t0005g0224 a0001c0001t0007g0277 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-7872_703-7868d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211772 | ||||||
| chr6:131211772 | CAAAAAAA | C | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
44 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.703-7874_703-7868d others(9): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131211772 | ||||||
| chr6:131211819 | A | G | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.703-7842A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211819 | |||||||
| chr6:131211853 | G | A | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.703-7808G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131211853 | |||||||
| chr6:131212156 | C | A | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.703-7505C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212156 | |||||||
| chr6:131212173 | T | G | 16 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(13): Show |
16 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.703-7488T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212173 | |||||||
| chr6:131212216 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.703-7445T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212216 | |||||||
| chr6:131212248 | G | T | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-7413G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212248 | |||||||
| chr6:131212257 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.703-7404C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212257 | |||||||
| chr6:131212357 | T | C | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-7304T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212357 | |||||||
| chr6:131212454 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.703-7207T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212454 | |||||||
| chr6:131212466 | T | C | 1 | a0002c0002t0001g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.703-7195T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212466 | |||||||
| chr6:131212521 | C | T | 2 | a0001c0001t0004g0208 a0001c0001t0006g0298 |
2 | HG00597.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.703-7140C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212521 | |||||||
| chr6:131212542 | C | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.703-7119C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212542 | |||||||
| chr6:131212550 | T | C | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-7111T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212550 | |||||||
| chr6:131212681 | A | C | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.703-6980A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212681 | |||||||
| chr6:131212821 | T | A | 2 | a0001c0001t0001g0171 a0001c0001t0003g0059 |
2 | HG01081.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.703-6840T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131212821 | |||||||
| chr6:131213163 | T | G | 1 | a0001c0001t0004g0195 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.703-6498T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213163 | |||||||
| chr6:131213234 | T | C | 120 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0225 others(117): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.703-6427T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213234 | |||||||
| chr6:131213263 | T | A | 58 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0002c0002t0001g0027 others(55): Show |
58 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.703-6398T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213263 | |||||||
| chr6:131213321 | C | T | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-6340C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213321 | |||||||
| chr6:131213569 | G | A | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-6092G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213569 | |||||||
| chr6:131213902 | T | C | 200 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(197): Show |
200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.703-5759T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213902 | |||||||
| chr6:131213973 | G | A | 2 | a0001c0001t0006g0002 a0011c0008t0006g0002 |
2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.703-5688G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131213973 | |||||||
| chr6:131214118 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-5543G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214118 | |||||||
| chr6:131214201 | G | C | 1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.703-5460G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214201 | |||||||
| chr6:131214356 | C | A | 15 | a0001c0001t0001g0042 a0001c0001t0005g0094 a0001c0001t0007g0286 others(12): Show |
15 | HG01952.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-5305C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214356 | |||||||
| chr6:131214477 | T | A | 10 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0193 others(7): Show |
10 | HG02155.hp1 NA18946.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.703-5184T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214477 | |||||||
| chr6:131214840 | G | A | 1 | a0001c0001t0040g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703-4821G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214840 | |||||||
| chr6:131214899 | C | G | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703-4762C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131214899 | |||||||
| chr6:131215012 | TG | T | 43 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.703-4647delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131215012 | ||||||
| chr6:131215111 | A | AT | 17 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(14): Show |
17 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.703-4541dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131215111 | ||||||
| chr6:131215143 | G | A | 3 | a0001c0001t0002g0246 a0001c0001t0002g0295 a0001c0001t0002g0299 |
3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.703-4518G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131215143 | |||||||
| chr6:131215353 | C | A | 3 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0024g0100 |
3 | HG01884.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.703-4308C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131215353 | |||||||
| chr6:131215935 | T | C | 24 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.703-3726T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131215935 | |||||||
| chr6:131215952 | A | G | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.703-3709A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131215952 | |||||||
| chr6:131216086 | A | G | 10 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.703-3575A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216086 | |||||||
| chr6:131216468 | T | C | 3 | a0001c0001t0001g0225 a0002c0002t0020g0150 a0006c0006t0035g0217 |
3 | HG03209.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.703-3193T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216468 | |||||||
| chr6:131216666 | G | C | 1 | a0001c0001t0003g0040 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.703-2995G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216666 | |||||||
| chr6:131216747 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0003g0041 |
2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.703-2914C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216747 | |||||||
| chr6:131216828 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.703-2833T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131216828 | |||||||
| chr6:131217045 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.703-2616A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217045 | |||||||
| chr6:131217237 | T | G | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.703-2424T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217237 | |||||||
| chr6:131217332 | G | A | 168 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(165): Show |
168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.703-2329G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217332 | |||||||
| chr6:131217448 | A | G | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-2213A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217448 | |||||||
| chr6:131217474 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0010g0087 a0006c0006t0014g0007 |
3 | HG02280.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.703-2187A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217474 | |||||||
| chr6:131217520 | A | G | 7 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(4): Show |
7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-2141A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217520 | |||||||
| chr6:131217548 | C | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.703-2113C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217548 | |||||||
| chr6:131217614 | T | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703-2047T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217614 | |||||||
| chr6:131217621 | T | C | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-2040T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217621 | |||||||
| chr6:131217674 | G | A | 2 | a0001c0001t0023g0174 a0001c0001t0023g0175 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.703-1987G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217674 | |||||||
| chr6:131217788 | C | T | 3 | a0004c0004t0001g0001 a0004c0004t0001g0216 a0004c0004t0003g0167 |
4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1873C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217788 | |||||||
| chr6:131217812 | C | A | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.703-1849C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217812 | |||||||
| chr6:131217979 | T | C | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-1682T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131217979 | |||||||
| chr6:131218057 | A | G | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.703-1604A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218057 | |||||||
| chr6:131218234 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.703-1427C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218234 | |||||||
| chr6:131218277 | C | T | 1 | a0001c0001t0006g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.703-1384C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218277 | |||||||
| chr6:131218453 | GA | G | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.703-1203delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131218453 | ||||||
| chr6:131218478 | G | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703-1183G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218478 | |||||||
| chr6:131218520 | A | T | 2 | a0001c0001t0003g0040 a0001c0001t0003g0041 |
2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.703-1141A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218520 | |||||||
| chr6:131218561 | T | C | 3 | a0001c0001t0001g0226 a0001c0001t0016g0009 a0001c0001t0033g0101 |
3 | HG02818.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.703-1100T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218561 | |||||||
| chr6:131218578 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-1083A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218578 | |||||||
| chr6:131218675 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.703-986C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218675 | |||||||
| chr6:131218711 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.703-950T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218711 | |||||||
| chr6:131218834 | G | A | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-827G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218834 | |||||||
| chr6:131218909 | T | C | 4 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-752T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218909 | |||||||
| chr6:131218950 | A | G | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.703-711A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131218950 | |||||||
| chr6:131219289 | C | CA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0002g0237 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-353dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131219289 | ||||||
| chr6:131219289 | CA | C | 57 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(54): Show |
57 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(54): Show |
intron_variant | MODIFIER | c.703-353delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 131219289 | ||||||
| chr6:131219586 | A | T | 177 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.703-75A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 6/7 | chr6 | 131219586 | |||||||
| chr6:131219826 | A | G | 10 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+18A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131219826 | |||||||
| chr6:131219916 | A | G | 1 | a0001c0001t0002g0294 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.850+108A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131219916 | |||||||
| chr6:131220118 | T | C | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+310T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220118 | |||||||
| chr6:131220172 | T | C | 1 | a0001c0001t0005g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.850+364T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220172 | |||||||
| chr6:131220269 | T | C | 1 | a0002c0002t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850+461T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220269 | |||||||
| chr6:131220298 | G | A | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.850+490G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220298 | |||||||
| chr6:131220473 | A | T | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+665A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220473 | |||||||
| chr6:131220498 | T | A | 3 | a0001c0001t0001g0226 a0001c0001t0016g0009 a0001c0001t0033g0101 |
3 | HG02818.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.850+690T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131220498 | |||||||
| chr6:131221098 | A | C | 62 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(59): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.850+1290A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221098 | |||||||
| chr6:131221361 | A | T | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+1553A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221361 | |||||||
| chr6:131221397 | A | G | 6 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+1589A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221397 | |||||||
| chr6:131221400 | G | A | 2 | a0001c0001t0007g0243 a0001c0001t0009g0222 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+1592G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221400 | |||||||
| chr6:131221448 | C | A | 2 | a0005c0005t0011g0140 a0005c0005t0011g0165 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.850+1640C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221448 | |||||||
| chr6:131221503 | T | G | 1 | a0001c0001t0002g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.850+1695T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221503 | |||||||
| chr6:131221799 | C | T | 2 | a0002c0002t0003g0049 a0002c0002t0003g0051 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.850+1991C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221799 | |||||||
| chr6:131221942 | A | G | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+2134A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131221942 | |||||||
| chr6:131222297 | G | A | 1 | a0007c0009t0005g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.850+2489G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222297 | |||||||
| chr6:131222321 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.850+2513C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222321 | |||||||
| chr6:131222383 | C | T | 5 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(2): Show |
5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2575C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222383 | |||||||
| chr6:131222435 | G | A | 5 | a0004c0004t0001g0001 a0004c0004t0001g0129 a0004c0004t0001g0131 others(2): Show |
6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+2627G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222435 | |||||||
| chr6:131222543 | A | T | 5 | a0001c0001t0005g0093 a0001c0001t0005g0224 a0001c0001t0007g0277 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2735A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222543 | |||||||
| chr6:131222555 | A | G | 1 | a0001c0001t0008g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850+2747A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222555 | |||||||
| chr6:131222624 | A | G | 1 | a0003c0003t0019g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.850+2816A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222624 | |||||||
| chr6:131222926 | C | A | 2 | a0001c0001t0007g0243 a0001c0001t0009g0222 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+3118C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131222926 | |||||||
| chr6:131223207 | A | G | 12 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(9): Show |
12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+3399A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131223207 | |||||||
| chr6:131223564 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0152 others(2): Show |
5 | HG01074.hp1 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+3756C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131223564 | |||||||
| chr6:131223620 | A | G | 10 | a0001c0001t0010g0082 a0001c0001t0023g0174 a0001c0001t0023g0175 others(7): Show |
10 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.850+3812A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131223620 | |||||||
| chr6:131223864 | A | G | 1 | a0001c0001t0020g0117 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850+4056A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131223864 | |||||||
| chr6:131224118 | C | T | 2 | a0006c0006t0014g0006 a0006c0006t0014g0007 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850+4310C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224118 | |||||||
| chr6:131224225 | T | C | 1 | a0002c0002t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.850+4417T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224225 | |||||||
| chr6:131224251 | A | G | 1 | a0002c0002t0001g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.850+4443A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224251 | |||||||
| chr6:131224414 | C | T | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.850+4606C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224414 | |||||||
| chr6:131224418 | G | A | 4 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(1): Show |
4 | HG00741.hp1 HG01891.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+4610G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224418 | |||||||
| chr6:131224464 | A | G | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+4656A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224464 | |||||||
| chr6:131224598 | A | G | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+4790A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224598 | |||||||
| chr6:131224708 | T | A | 15 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(12): Show |
15 | HG00741.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.850+4900T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224708 | |||||||
| chr6:131224709 | GTAAAGTT others(7): Show |
G | 15 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(12): Show |
15 | HG00741.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.850+4902_850+4915d others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224709 | |||||||
| chr6:131224715 | T | G | 2 | a0001c0001t0031g0285 a0003c0003t0032g0290 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4907T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224715 | |||||||
| chr6:131224716 | T | A | 2 | a0001c0001t0031g0285 a0003c0003t0032g0290 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4908T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224716 | |||||||
| chr6:131224718 | C | T | 2 | a0001c0001t0031g0285 a0003c0003t0032g0290 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4910C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224718 | |||||||
| chr6:131224721 | G | C | 2 | a0001c0001t0031g0285 a0003c0003t0032g0290 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4913G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224721 | |||||||
| chr6:131224728 | C | T | 2 | a0001c0001t0031g0285 a0003c0003t0032g0290 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4920C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224728 | |||||||
| chr6:131224729 | A | T | 2 | a0001c0001t0031g0285 a0003c0003t0032g0290 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4921A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224729 | |||||||
| chr6:131224730 | C | CT | 36 | a0001c0001t0001g0079 a0001c0001t0001g0111 a0001c0001t0001g0211 others(33): Show |
36 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.850+4951dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131224730 | ||||||
| chr6:131224730 | C | T | 2 | a0001c0001t0031g0285 a0003c0003t0032g0290 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.850+4922C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224730 | |||||||
| chr6:131224730 | CT | C | 96 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(93): Show |
96 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.850+4951delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131224730 | ||||||
| chr6:131224730 | CTT | C | 36 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0002g0289 others(33): Show |
36 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.850+4950_850+4951d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131224730 | ||||||
| chr6:131224730 | CTTTTT | C | 6 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(3): Show |
6 | HG02922.hp1 HG03139.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+4947_850+4951d others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131224730 | ||||||
| chr6:131224830 | A | C | 2 | a0001c0001t0008g0218 a0001c0001t0010g0184 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850+5022A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131224830 | |||||||
| chr6:131225244 | G | A | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+5436G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131225244 | |||||||
| chr6:131225888 | A | T | 81 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.850+6080A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131225888 | |||||||
| chr6:131225991 | A | G | 1 | a0001c0001t0002g0256 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.850+6183A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131225991 | |||||||
| chr6:131226119 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+6311G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226119 | |||||||
| chr6:131226201 | A | G | 81 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.850+6393A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226201 | |||||||
| chr6:131226244 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.850+6436A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226244 | |||||||
| chr6:131226324 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.850+6516A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226324 | |||||||
| chr6:131226352 | T | C | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+6544T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226352 | |||||||
| chr6:131226438 | C | T | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+6630C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226438 | |||||||
| chr6:131226440 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.850+6632C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226440 | |||||||
| chr6:131226705 | T | A | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+6897T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226705 | |||||||
| chr6:131226763 | TTTTG | T | 6 | a0002c0002t0002g0244 a0005c0005t0005g0097 a0005c0005t0005g0098 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+6972_850+6975d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131226763 | ||||||
| chr6:131226950 | A | G | 1 | a0001c0001t0025g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.850+7142A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131226950 | |||||||
| chr6:131227163 | G | A | 12 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(9): Show |
12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+7355G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227163 | |||||||
| chr6:131227256 | T | C | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+7448T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227256 | |||||||
| chr6:131227297 | A | C | 1 | a0001c0001t0003g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.850+7489A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227297 | |||||||
| chr6:131227389 | G | C | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.850+7581G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227389 | |||||||
| chr6:131227539 | A | G | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+7731A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227539 | |||||||
| chr6:131227731 | A | G | 12 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(9): Show |
12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+7923A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227731 | |||||||
| chr6:131227920 | T | C | 105 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0004g0026 others(102): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.850+8112T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227920 | |||||||
| chr6:131227961 | T | G | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+8153T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131227961 | |||||||
| chr6:131228027 | G | C | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+8219G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228027 | |||||||
| chr6:131228048 | C | T | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+8240C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228048 | |||||||
| chr6:131228095 | T | C | 1 | a0001c0001t0002g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.850+8287T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228095 | |||||||
| chr6:131228193 | G | A | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+8385G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228193 | |||||||
| chr6:131228707 | C | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+8899C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228707 | |||||||
| chr6:131228729 | T | G | 12 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(9): Show |
12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+8921T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228729 | |||||||
| chr6:131228735 | G | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+8927G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131228735 | |||||||
| chr6:131229009 | G | A | 7 | a0002c0002t0001g0091 a0002c0002t0001g0096 a0002c0002t0002g0244 others(4): Show |
7 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+9201G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229009 | |||||||
| chr6:131229057 | C | T | 5 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(2): Show |
5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+9249C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229057 | |||||||
| chr6:131229063 | T | TAA | 10 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+9256_850+9257i others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131229063 | ||||||
| chr6:131229107 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.850+9299C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229107 | |||||||
| chr6:131229439 | C | T | 24 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.850+9631C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229439 | |||||||
| chr6:131229551 | G | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+9743G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229551 | |||||||
| chr6:131229586 | T | A | 6 | a0001c0001t0007g0251 a0001c0001t0031g0285 a0001c0001t0038g0166 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+9778T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131229586 | |||||||
| chr6:131230098 | C | T | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+10290C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230098 | |||||||
| chr6:131230104 | G | A | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+10296G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230104 | |||||||
| chr6:131230303 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.850+10495A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230303 | |||||||
| chr6:131230455 | G | A | 69 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(66): Show |
69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.850+10647G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230455 | |||||||
| chr6:131230502 | G | T | 12 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(9): Show |
12 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+10694G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230502 | |||||||
| chr6:131230635 | G | A | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+10827G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230635 | |||||||
| chr6:131230950 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.850+11142T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131230950 | |||||||
| chr6:131231230 | T | C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+11422T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231230 | |||||||
| chr6:131231361 | G | GT | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+11562dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131231361 | ||||||
| chr6:131231617 | C | T | 1 | a0004c0004t0003g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.850+11809C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231617 | |||||||
| chr6:131231710 | A | G | 20 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(17): Show |
20 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.850+11902A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231710 | |||||||
| chr6:131231731 | A | G | 10 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+11923A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231731 | |||||||
| chr6:131231760 | A | G | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+11952A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231760 | |||||||
| chr6:131231831 | C | T | 156 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(153): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.850+12023C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231831 | |||||||
| chr6:131231884 | G | T | 5 | a0001c0001t0004g0200 a0001c0001t0004g0202 a0001c0001t0004g0203 others(2): Show |
5 | HG01978.hp2 NA18941.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+12076G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231884 | |||||||
| chr6:131231984 | C | T | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+12176C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131231984 | |||||||
| chr6:131232062 | A | T | 1 | a0010c0010t0002g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.850+12254A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232062 | |||||||
| chr6:131232066 | G | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+12258G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232066 | |||||||
| chr6:131232078 | A | G | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+12270A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232078 | |||||||
| chr6:131232123 | G | A | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+12315G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232123 | |||||||
| chr6:131232132 | A | G | 5 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(2): Show |
5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+12324A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232132 | |||||||
| chr6:131232552 | C | G | 56 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.850+12744C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232552 | |||||||
| chr6:131232682 | A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+12874A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232682 | |||||||
| chr6:131232846 | A | G | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+13038A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131232846 | |||||||
| chr6:131232969 | T | TAA | 170 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.850+13162_850+1316 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131232969 | ||||||
| chr6:131233018 | A | G | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+13210A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233018 | |||||||
| chr6:131233044 | C | T | 78 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(75): Show |
78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.850+13236C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233044 | |||||||
| chr6:131233142 | T | TA | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+13341dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131233142 | ||||||
| chr6:131233151 | C | T | 177 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.850+13343C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233151 | |||||||
| chr6:131233295 | G | C | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+13487G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233295 | |||||||
| chr6:131233327 | T | G | 1 | a0003c0003t0007g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.850+13519T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233327 | |||||||
| chr6:131233413 | A | T | 194 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(191): Show |
194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.850+13605A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233413 | |||||||
| chr6:131233422 | G | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+13614G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233422 | |||||||
| chr6:131233428 | A | G | 3 | a0001c0001t0002g0246 a0001c0001t0002g0295 a0001c0001t0002g0299 |
3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.850+13620A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233428 | |||||||
| chr6:131233604 | A | T | 1 | a0001c0001t0010g0082 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.850+13796A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233604 | |||||||
| chr6:131233769 | A | G | 21 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(18): Show |
21 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+13961A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131233769 | |||||||
| chr6:131234162 | A | G | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+14354A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234162 | |||||||
| chr6:131234251 | T | C | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+14443T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234251 | |||||||
| chr6:131234483 | G | C | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+14675G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234483 | |||||||
| chr6:131234509 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.850+14701C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234509 | |||||||
| chr6:131234519 | G | A | 2 | a0002c0002t0001g0121 a0002c0002t0002g0288 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.850+14711G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234519 | |||||||
| chr6:131234533 | G | C | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.850+14725G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234533 | |||||||
| chr6:131234710 | A | G | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+14902A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234710 | |||||||
| chr6:131234804 | C | T | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+14996C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131234804 | |||||||
| chr6:131235055 | C | G | 1 | a0001c0001t0003g0053 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.850+15247C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235055 | |||||||
| chr6:131235240 | T | C | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+15432T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235240 | |||||||
| chr6:131235255 | A | G | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+15447A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235255 | |||||||
| chr6:131235319 | T | G | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+15511T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235319 | |||||||
| chr6:131235377 | A | G | 3 | a0001c0001t0001g0225 a0002c0002t0020g0150 a0006c0006t0035g0217 |
3 | HG03209.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.850+15569A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235377 | |||||||
| chr6:131235398 | T | A | 2 | a0001c0001t0004g0178 a0001c0001t0004g0190 |
2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.850+15590T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235398 | |||||||
| chr6:131235616 | T | C | 55 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(52): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.850+15808T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235616 | |||||||
| chr6:131235636 | T | G | 1 | a0001c0001t0010g0082 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.850+15828T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235636 | |||||||
| chr6:131235710 | T | C | 2 | a0001c0001t0021g0223 a0001c0001t0022g0095 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.850+15902T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131235710 | |||||||
| chr6:131236063 | A | C | 1 | a0001c0001t0002g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.850+16255A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236063 | |||||||
| chr6:131236065 | T | G | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+16257T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236065 | |||||||
| chr6:131236117 | A | G | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+16309A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236117 | |||||||
| chr6:131236165 | G | C | 172 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(169): Show |
172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.850+16357G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236165 | |||||||
| chr6:131236249 | G | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+16441G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236249 | |||||||
| chr6:131236287 | A | G | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.850+16479A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236287 | |||||||
| chr6:131236295 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.850+16487T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236295 | |||||||
| chr6:131236323 | C | T | 65 | a0001c0001t0001g0084 a0001c0001t0001g0116 a0001c0001t0001g0119 others(62): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.850+16515C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236323 | |||||||
| chr6:131236324 | G | A | 1 | a0001c0001t0005g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.850+16516G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236324 | |||||||
| chr6:131236377 | T | G | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.850+16569T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236377 | |||||||
| chr6:131236431 | G | A | 1 | a0003c0003t0008g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.850+16623G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236431 | |||||||
| chr6:131236483 | A | T | 7 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(4): Show |
7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+16675A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236483 | |||||||
| chr6:131236852 | C | G | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+17044C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236852 | |||||||
| chr6:131236919 | C | G | 50 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(47): Show |
50 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.850+17111C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236919 | |||||||
| chr6:131236921 | G | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+17113G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236921 | |||||||
| chr6:131236922 | G | T | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+17114G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236922 | |||||||
| chr6:131236937 | A | G | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+17129A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236937 | |||||||
| chr6:131236975 | T | C | 3 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0056 |
3 | NA18943.hp1 NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.850+17167T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131236975 | |||||||
| chr6:131237076 | G | T | 1 | a0002c0002t0002g0273 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.850+17268G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237076 | |||||||
| chr6:131237104 | T | G | 1 | a0001c0001t0040g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850+17296T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237104 | |||||||
| chr6:131237117 | G | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0170 |
3 | HG01074.hp1 HG01169.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.850+17309G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237117 | |||||||
| chr6:131237453 | A | G | 7 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(4): Show |
7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+17645A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237453 | |||||||
| chr6:131237514 | C | T | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+17706C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237514 | |||||||
| chr6:131237550 | T | A | 1 | a0001c0001t0022g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.850+17742T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237550 | |||||||
| chr6:131237584 | G | A | 4 | a0001c0001t0004g0168 a0001c0001t0004g0169 a0001c0001t0004g0204 others(1): Show |
4 | NA18946.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+17776G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237584 | |||||||
| chr6:131237586 | C | T | 4 | a0001c0001t0004g0168 a0001c0001t0004g0169 a0001c0001t0004g0204 others(1): Show |
4 | NA18946.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+17778C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237586 | |||||||
| chr6:131237612 | A | G | 18 | a0001c0001t0004g0061 a0001c0001t0004g0168 a0001c0001t0004g0169 others(15): Show |
18 | HG00408.hp2 HG01993.hp2 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.850+17804A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237612 | |||||||
| chr6:131237669 | C | G | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+17861C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237669 | |||||||
| chr6:131237738 | G | A | 2 | a0001c0001t0007g0243 a0001c0001t0009g0222 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+17930G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237738 | |||||||
| chr6:131237759 | C | T | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.850+17951C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237759 | |||||||
| chr6:131237826 | A | G | 1 | a0001c0001t0006g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.850+18018A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237826 | |||||||
| chr6:131237852 | A | T | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+18044A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237852 | |||||||
| chr6:131237926 | G | A | 20 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(17): Show |
20 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.850+18118G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237926 | |||||||
| chr6:131237956 | T | C | 1 | a0002c0002t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850+18148T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131237956 | |||||||
| chr6:131238302 | T | G | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+18494T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238302 | |||||||
| chr6:131238327 | T | C | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+18519T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238327 | |||||||
| chr6:131238431 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0124 |
2 | NA18941.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.850+18623G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238431 | |||||||
| chr6:131238446 | G | A | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+18638G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238446 | |||||||
| chr6:131238654 | T | C | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+18846T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238654 | |||||||
| chr6:131238661 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850+18853T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238661 | |||||||
| chr6:131238684 | C | A | 1 | a0002c0002t0003g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.850+18876C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238684 | |||||||
| chr6:131238684 | C | G | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+18876C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238684 | |||||||
| chr6:131238742 | T | C | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+18934T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238742 | |||||||
| chr6:131238842 | A | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(168): Show |
171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.850+19034A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238842 | |||||||
| chr6:131238844 | G | A | 1 | a0002c0002t0001g0177 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.850+19036G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238844 | |||||||
| chr6:131238873 | C | T | 2 | a0001c0001t0025g0067 a0002c0002t0003g0109 |
2 | HG01496.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.850+19065C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131238873 | |||||||
| chr6:131239089 | T | G | 2 | a0001c0001t0007g0282 a0001c0001t0028g0236 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.850+19281T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239089 | |||||||
| chr6:131239129 | C | A | 1 | a0001c0001t0033g0101 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.850+19321C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239129 | |||||||
| chr6:131239233 | G | A | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+19425G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239233 | |||||||
| chr6:131239266 | C | T | 2 | a0001c0001t0008g0218 a0001c0001t0010g0184 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850+19458C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239266 | |||||||
| chr6:131239314 | A | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(168): Show |
171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.850+19506A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239314 | |||||||
| chr6:131239358 | A | G | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+19550A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239358 | |||||||
| chr6:131239419 | C | T | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+19611C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239419 | |||||||
| chr6:131239420 | G | A | 1 | a0001c0001t0007g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.850+19612G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239420 | |||||||
| chr6:131239449 | T | G | 126 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0225 others(123): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.850+19641T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239449 | |||||||
| chr6:131239463 | G | T | 1 | a0001c0001t0003g0057 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.850+19655G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239463 | |||||||
| chr6:131239468 | G | A | 43 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.850+19660G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239468 | |||||||
| chr6:131239513 | G | T | 2 | a0001c0001t0007g0243 a0001c0001t0009g0222 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+19705G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239513 | |||||||
| chr6:131239556 | G | T | 2 | a0001c0001t0021g0223 a0001c0001t0022g0095 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.850+19748G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239556 | |||||||
| chr6:131239588 | T | C | 3 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 |
3 | HG03579.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.850+19780T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239588 | |||||||
| chr6:131239722 | G | A | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+19914G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239722 | |||||||
| chr6:131239735 | C | T | 1 | a0001c0001t0004g0204 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.850+19927C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239735 | |||||||
| chr6:131239738 | G | T | 2 | a0006c0006t0014g0006 a0006c0006t0014g0007 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850+19930G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239738 | |||||||
| chr6:131239876 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.850+20068T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239876 | |||||||
| chr6:131239907 | T | C | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.850+20099T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239907 | |||||||
| chr6:131239927 | C | T | 2 | a0002c0002t0001g0065 a0002c0002t0001g0136 |
2 | HG02004.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.850+20119C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239927 | |||||||
| chr6:131239979 | C | T | 7 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(4): Show |
7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+20171C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131239979 | |||||||
| chr6:131240068 | C | T | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850+20260C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240068 | |||||||
| chr6:131240141 | T | C | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+20333T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240141 | |||||||
| chr6:131240204 | G | A | 2 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
2 | NA18941.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.850+20396G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240204 | |||||||
| chr6:131240221 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0152 others(2): Show |
5 | HG01074.hp1 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+20413G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240221 | |||||||
| chr6:131240233 | A | C | 2 | a0001c0001t0007g0282 a0001c0001t0028g0236 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.850+20425A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240233 | |||||||
| chr6:131240300 | G | A | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+20492G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240300 | |||||||
| chr6:131240491 | C | A | 2 | a0002c0002t0001g0134 a0002c0002t0001g0135 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.850+20683C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240491 | |||||||
| chr6:131240514 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.850+20706A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240514 | |||||||
| chr6:131240522 | A | T | 3 | a0001c0001t0002g0246 a0001c0001t0002g0295 a0001c0001t0002g0299 |
3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.850+20714A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240522 | |||||||
| chr6:131240699 | G | A | 1 | a0002c0002t0036g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850+20891G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240699 | |||||||
| chr6:131240702 | G | A | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+20894G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240702 | |||||||
| chr6:131240799 | G | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0078 |
2 | HG02486.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.850+20991G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240799 | |||||||
| chr6:131240856 | G | A | 7 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(4): Show |
7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+21048G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240856 | |||||||
| chr6:131240889 | C | T | 1 | a0001c0001t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.850+21081C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240889 | |||||||
| chr6:131240890 | G | A | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+21082G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240890 | |||||||
| chr6:131240942 | C | T | 5 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(2): Show |
5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+21134C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131240942 | |||||||
| chr6:131241161 | T | C | 1 | a0001c0001t0003g0044 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.850+21353T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241161 | |||||||
| chr6:131241382 | A | T | 1 | a0006c0006t0014g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.850+21574A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241382 | |||||||
| chr6:131241437 | C | G | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.850+21629C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241437 | |||||||
| chr6:131241451 | A | G | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(39): Show |
42 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.850+21643A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241451 | |||||||
| chr6:131241525 | G | C | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+21717G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241525 | |||||||
| chr6:131241569 | T | TTA | 3 | a0004c0004t0001g0001 a0004c0004t0001g0216 a0004c0004t0003g0167 |
4 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+21769_850+2177 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241569 | ||||||
| chr6:131241569 | T | TTATA | 16 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(13): Show |
16 | HG01175.hp2 HG01192.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.850+21767_850+2177 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241569 | ||||||
| chr6:131241569 | T | TTATATA | 4 | a0002c0002t0001g0107 a0002c0002t0001g0110 a0002c0002t0003g0049 others(1): Show |
4 | HG00323.hp1 HG01981.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21765_850+2177 others(10): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241569 | ||||||
| chr6:131241577 | A | ATG | 21 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(18): Show |
21 | HG00323.hp2 HG01081.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.850+21819_850+2182 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | ||||||
| chr6:131241577 | A | ATGTG | 14 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0139 others(11): Show |
14 | HG01169.hp1 HG01952.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.850+21817_850+2182 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | ||||||
| chr6:131241577 | A | ATGTGTG | 7 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0088 others(4): Show |
7 | HG02145.hp1 HG02486.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+21815_850+2182 others(10): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | ||||||
| chr6:131241577 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0002g0258 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.850+21811_850+2182 others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | ||||||
| chr6:131241577 | A | G | 6 | a0001c0001t0003g0066 a0001c0001t0041g0159 a0005c0005t0005g0097 others(3): Show |
6 | HG00558.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+21769A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241577 | |||||||
| chr6:131241577 | ATG | A | 32 | a0001c0001t0001g0079 a0001c0001t0001g0113 a0001c0001t0001g0126 others(29): Show |
32 | HG00544.hp2 HG01192.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.850+21819_850+2182 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | ||||||
| chr6:131241577 | ATGTG | A | 6 | a0001c0001t0001g0105 a0001c0001t0002g0234 a0001c0001t0002g0279 others(3): Show |
6 | HG00099.hp2 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+21817_850+2182 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | ||||||
| chr6:131241577 | ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0008g0218 a0001c0001t0010g0184 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850+21809_850+2182 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241577 | ||||||
| chr6:131241579 | G | A | 40 | a0001c0001t0001g0084 a0001c0001t0002g0248 a0001c0001t0003g0073 others(37): Show |
40 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.850+21771G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241579 | |||||||
| chr6:131241581 | G | A | 4 | a0002c0002t0001g0122 a0002c0002t0001g0177 a0002c0002t0002g0265 others(1): Show |
4 | HG01109.hp2 HG02074.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+21773G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241581 | |||||||
| chr6:131241599 | G | GTGTGTGT others(29): Show |
1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.850+21814_850+2181 others(40): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241599 | ||||||
| chr6:131241599 | G | GTGTGTGT others(31): Show |
4 | a0001c0001t0004g0203 a0001c0001t0006g0002 a0001c0001t0011g0163 others(1): Show |
4 | HG02572.hp1 NA18941.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21816_850+2181 others(42): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241599 | ||||||
| chr6:131241599 | G | GTGTGTGT others(33): Show |
2 | a0001c0001t0005g0093 a0001c0001t0007g0277 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.850+21818_850+2181 others(44): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241599 | ||||||
| chr6:131241601 | G | GTGTGTGT others(49): Show |
1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+21808_850+2180 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241601 | ||||||
| chr6:131241601 | G | GTGTGTGT others(55): Show |
2 | a0006c0006t0014g0006 a0006c0006t0014g0007 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850+21814_850+2181 others(66): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241601 | ||||||
| chr6:131241607 | G | GTATATAT others(15): Show |
21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+21800_850+2180 others(26): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241607 | ||||||
| chr6:131241607 | G | GTGTGTGT others(17): Show |
1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+21808_850+2180 others(28): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241607 | ||||||
| chr6:131241609 | GTGTGTGT others(13): Show |
G | 4 | a0001c0001t0021g0220 a0001c0001t0021g0223 a0001c0001t0022g0086 others(1): Show |
4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+21803_850+2182 others(24): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241609 | ||||||
| chr6:131241611 | GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 |
3 | HG03579.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.850+21805_850+2182 others(22): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241611 | ||||||
| chr6:131241616 | TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0002g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.850+21809_850+2181 others(15): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241616 | |||||||
| chr6:131241623 | G | GTATATAT others(3): Show |
19 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.850+21816_850+2181 others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241623 | ||||||
| chr6:131241623 | G | GTATATAT others(5): Show |
1 | a0002c0002t0002g0235 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.850+21816_850+2181 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241623 | ||||||
| chr6:131241625 | G | A | 28 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0004g0203 others(25): Show |
28 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.850+21817G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241625 | |||||||
| chr6:131241625 | G | GTATACGT others(31): Show |
1 | a0002c0002t0024g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850+21818_850+2181 others(42): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | ||||||
| chr6:131241625 | G | GTATACGT others(33): Show |
6 | a0001c0001t0001g0046 a0001c0001t0002g0261 a0001c0001t0002g0275 others(3): Show |
6 | HG02155.hp2 HG02293.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+21818_850+2181 others(44): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | ||||||
| chr6:131241625 | G | GTATACGT others(59): Show |
1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.850+21818_850+2181 others(70): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | ||||||
| chr6:131241625 | G | GTATATAC others(61): Show |
1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+21818_850+2181 others(72): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | ||||||
| chr6:131241625 | G | GTATATAT others(41): Show |
1 | a0005c0005t0011g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.850+21818_850+2181 others(52): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241625 | ||||||
| chr6:131241627 | G | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0084 others(55): Show |
58 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.850+21819G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241627 | |||||||
| chr6:131241627 | G | GTATACGT others(31): Show |
2 | a0001c0001t0007g0243 a0001c0001t0009g0222 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850+21823_850+2182 others(42): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTATACGT others(33): Show |
2 | a0001c0001t0005g0157 a0001c0001t0005g0224 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.850+21823_850+2182 others(44): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTATACGT others(35): Show |
10 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0003g0040 others(7): Show |
10 | HG00280.hp1 HG01993.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+21823_850+2182 others(46): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTATACGT others(61): Show |
1 | a0003c0003t0032g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.850+21823_850+2182 others(72): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTATATAC others(41): Show |
1 | a0002c0002t0001g0158 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.850+21825_850+2182 others(52): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTATATAT others(43): Show |
5 | a0002c0002t0001g0122 a0002c0002t0001g0177 a0002c0002t0002g0265 others(2): Show |
5 | HG01109.hp2 HG02074.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+21827_850+2182 others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTATATAT others(43): Show |
3 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 |
3 | HG01891.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.850+21827_850+2182 others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTATAC others(35): Show |
2 | a0002c0002t0015g0003 a0002c0002t0015g0004 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.850+21820_850+2182 others(46): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTATAC others(37): Show |
27 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0028 others(24): Show |
27 | HG00408.hp2 HG00597.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(48): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTATAT others(45): Show |
6 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0110 others(3): Show |
6 | HG01192.hp2 HG01981.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(56): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTAT others(37): Show |
1 | a0001c0001t0007g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(48): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTAT others(39): Show |
23 | a0001c0001t0001g0013 a0001c0001t0001g0124 a0001c0001t0001g0127 others(20): Show |
23 | HG00558.hp2 HG00609.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(50): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTAT others(41): Show |
1 | a0001c0001t0003g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(52): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTAT others(45): Show |
1 | a0002c0002t0001g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(56): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTAT others(47): Show |
4 | a0002c0002t0001g0107 a0002c0002t0001g0121 a0002c0002t0002g0273 others(1): Show |
4 | HG00323.hp1 HG01175.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTAT others(47): Show |
1 | a0005c0005t0011g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(39): Show |
2 | a0001c0001t0007g0281 a0001c0001t0040g0081 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.850+21820_850+2182 others(50): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(41): Show |
10 | a0001c0001t0001g0031 a0001c0001t0002g0267 a0001c0001t0003g0047 others(7): Show |
10 | HG00544.hp1 HG01943.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(52): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(47): Show |
1 | a0001c0001t0001g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(49): Show |
1 | a0002c0002t0001g0115 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(53): Show |
1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(64): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(43): Show |
3 | a0001c0001t0001g0012 a0001c0001t0004g0200 a0001c0001t0006g0293 |
3 | HG01433.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.850+21820_850+2182 others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(49): Show |
1 | a0006c0006t0035g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(49): Show |
1 | a0002c0002t0017g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(49): Show |
1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(45): Show |
1 | a0001c0001t0005g0076 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(56): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(51): Show |
1 | a0002c0002t0002g0291 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(62): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(47): Show |
1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(43): Show |
1 | a0001c0001t0007g0282 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(54): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(45): Show |
4 | a0001c0001t0001g0018 a0001c0001t0004g0033 a0001c0001t0004g0178 others(1): Show |
4 | HG01099.hp1 NA18970.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21820_850+2182 others(56): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(53): Show |
1 | a0002c0002t0036g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(64): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(49): Show |
1 | a0002c0002t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(47): Show |
1 | a0009c0011t0004g0197 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(53): Show |
1 | a0002c0002t0020g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(64): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(49): Show |
2 | a0001c0001t0005g0077 a0001c0001t0009g0102 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(55): Show |
1 | a0002c0002t0001g0229 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(66): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(47): Show |
1 | a0001c0001t0028g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(58): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(49): Show |
1 | a0003c0003t0007g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.850+21820_850+2182 others(60): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(57): Show |
1 | a0002c0002t0017g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(68): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241627 | G | GTGTGTGT others(51): Show |
1 | a0001c0001t0005g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.850+21820_850+2182 others(62): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131241627 | ||||||
| chr6:131241629 | A | G | 4 | a0001c0001t0001g0089 a0001c0001t0003g0143 a0001c0001t0003g0151 others(1): Show |
4 | HG02145.hp1 HG02572.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+21821A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241629 | |||||||
| chr6:131241836 | A | T | 2 | a0001c0001t0005g0157 a0001c0001t0007g0251 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.850+22028A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131241836 | |||||||
| chr6:131242137 | A | G | 1 | a0001c0001t0040g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850+22329A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242137 | |||||||
| chr6:131242152 | A | G | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.850+22344A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242152 | |||||||
| chr6:131242226 | G | A | 2 | a0001c0001t0005g0157 a0001c0001t0007g0251 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.850+22418G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242226 | |||||||
| chr6:131242376 | A | G | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+22568A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242376 | |||||||
| chr6:131242437 | G | A | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.850+22629G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242437 | |||||||
| chr6:131242648 | C | T | 56 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.850+22840C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242648 | |||||||
| chr6:131242672 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.850+22864C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242672 | |||||||
| chr6:131242810 | A | G | 5 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(2): Show |
5 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+23002A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131242810 | |||||||
| chr6:131242982 | ATTTAGAG others(17): Show |
A | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+23180_850+2320 others(28): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131242982 | ||||||
| chr6:131243225 | C | T | 2 | a0002c0002t0001g0229 a0002c0002t0002g0291 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.850+23417C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243225 | |||||||
| chr6:131243451 | A | T | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+23643A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243451 | |||||||
| chr6:131243511 | A | T | 1 | a0001c0001t0002g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.850+23703A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243511 | |||||||
| chr6:131243653 | C | T | 1 | a0003c0003t0008g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.850+23845C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243653 | |||||||
| chr6:131243726 | T | C | 12 | a0001c0001t0008g0218 a0001c0001t0010g0082 a0001c0001t0010g0184 others(9): Show |
12 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.850+23918T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243726 | |||||||
| chr6:131243958 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.850+24150A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243958 | |||||||
| chr6:131243970 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.850+24162C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131243970 | |||||||
| chr6:131243999 | C | CT | 83 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0002g0238 others(80): Show |
83 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.850+24204dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131243999 | ||||||
| chr6:131243999 | CT | C | 8 | a0002c0002t0015g0003 a0002c0002t0015g0004 a0002c0002t0024g0100 others(5): Show |
9 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.850+24204delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131243999 | ||||||
| chr6:131244011 | T | C | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.850+24203T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244011 | |||||||
| chr6:131244013 | C | T | 61 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(58): Show |
61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.850+24205C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244013 | |||||||
| chr6:131244323 | G | A | 4 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+24515G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244323 | |||||||
| chr6:131244327 | A | G | 1 | a0001c0001t0022g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.850+24519A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244327 | |||||||
| chr6:131244620 | A | G | 1 | a0001c0001t0040g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850+24812A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244620 | |||||||
| chr6:131244657 | G | C | 1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.850+24849G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244657 | |||||||
| chr6:131244708 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+24900G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244708 | |||||||
| chr6:131244743 | T | C | 1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.850+24935T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244743 | |||||||
| chr6:131244777 | T | A | 17 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(14): Show |
17 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.850+24969T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244777 | |||||||
| chr6:131244822 | G | T | 63 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.850+25014G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131244822 | |||||||
| chr6:131244836 | GA | G | 9 | a0001c0001t0005g0157 a0001c0001t0007g0251 a0002c0002t0001g0091 others(6): Show |
9 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.850+25037delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131244836 | ||||||
| chr6:131245402 | G | T | 2 | a0001c0001t0023g0174 a0001c0001t0023g0175 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.850+25594G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245402 | |||||||
| chr6:131245412 | G | GT | 11 | a0001c0001t0001g0019 a0001c0001t0002g0258 a0001c0001t0002g0272 others(8): Show |
11 | HG00609.hp2 HG01081.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.850+25615dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131245412 | ||||||
| chr6:131245412 | GT | G | 55 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0031g0285 others(52): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.850+25615delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131245412 | ||||||
| chr6:131245423 | T | G | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+25615T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245423 | |||||||
| chr6:131245424 | G | T | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+25616G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245424 | |||||||
| chr6:131245439 | G | GT | 7 | a0001c0001t0002g0247 a0003c0003t0010g0083 a0005c0005t0005g0097 others(4): Show |
7 | HG00597.hp2 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+25642dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131245439 | ||||||
| chr6:131245440 | T | G | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850+25632T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245440 | |||||||
| chr6:131245458 | T | C | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.850+25650T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245458 | |||||||
| chr6:131245468 | G | A | 7 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(4): Show |
7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+25660G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245468 | |||||||
| chr6:131245523 | C | T | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+25715C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245523 | |||||||
| chr6:131245591 | G | A | 177 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.850+25783G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245591 | |||||||
| chr6:131245631 | C | T | 6 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(3): Show |
6 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+25823C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245631 | |||||||
| chr6:131245644 | A | T | 3 | a0001c0001t0013g0201 a0001c0001t0013g0210 a0001c0001t0030g0296 |
3 | NA18969.hp1 NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.850+25836A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245644 | |||||||
| chr6:131245747 | G | A | 1 | a0001c0001t0006g0254 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.850+25939G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245747 | |||||||
| chr6:131245859 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.850+26051C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245859 | |||||||
| chr6:131245883 | T | C | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+26075T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245883 | |||||||
| chr6:131245905 | C | T | 1 | a0002c0002t0039g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.850+26097C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245905 | |||||||
| chr6:131245934 | A | G | 1 | a0001c0001t0031g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.850+26126A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131245934 | |||||||
| chr6:131246009 | C | T | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.850+26201C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246009 | |||||||
| chr6:131246056 | A | T | 56 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.850+26248A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246056 | |||||||
| chr6:131246074 | T | G | 23 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(20): Show |
23 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.850+26266T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246074 | |||||||
| chr6:131246094 | A | AAT | 22 | a0001c0001t0001g0024 a0001c0001t0001g0105 a0001c0001t0001g0108 others(19): Show |
22 | HG00558.hp1 HG01109.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.850+26309_850+2631 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131246094 | ||||||
| chr6:131246094 | A | AATAT | 6 | a0001c0001t0004g0036 a0001c0001t0004g0207 a0002c0002t0001g0092 others(3): Show |
6 | HG02257.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+26307_850+2631 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131246094 | ||||||
| chr6:131246094 | AAT | A | 94 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0088 others(91): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.850+26309_850+2631 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131246094 | ||||||
| chr6:131246101 | A | G | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.850+26293A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246101 | |||||||
| chr6:131246525 | T | C | 1 | a0001c0001t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.850+26717T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246525 | |||||||
| chr6:131246648 | G | A | 2 | a0001c0001t0008g0218 a0001c0001t0010g0184 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.850+26840G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246648 | |||||||
| chr6:131246962 | A | AC | 82 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.850+27154_850+2715 others(5): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131246962 | |||||||
| chr6:131247269 | G | GTA | 11 | a0001c0001t0001g0085 a0001c0001t0001g0105 a0001c0001t0001g0108 others(8): Show |
12 | HG01071.hp2 HG01109.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+27505_850+2750 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | G | GTATA | 4 | a0001c0001t0002g0287 a0001c0001t0003g0063 a0004c0004t0001g0129 others(1): Show |
4 | HG01106.hp1 HG01255.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+27503_850+2750 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | G | GTATATA | 4 | a0001c0001t0001g0031 a0001c0001t0002g0248 a0001c0001t0004g0196 others(1): Show |
4 | HG00140.hp1 NA18963.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+27501_850+2750 others(10): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | G | GTATATAT others(1): Show |
5 | a0001c0001t0001g0019 a0001c0001t0002g0264 a0001c0001t0026g0123 others(2): Show |
5 | HG00099.hp1 HG00609.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+27499_850+2750 others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0034 a0001c0001t0001g0119 a0001c0001t0002g0268 |
3 | HG03704.hp1 NA18942.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.850+27497_850+2750 others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.850+27493_850+2750 others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | G | GTGTATAT others(5): Show |
1 | a0001c0001t0001g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.850+27462_850+2746 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTA | G | 27 | a0001c0001t0001g0130 a0001c0001t0001g0152 a0001c0001t0001g0191 others(24): Show |
27 | HG00323.hp2 HG00609.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.850+27505_850+2750 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATA | G | 31 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0032 others(28): Show |
31 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.850+27503_850+2750 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATA | G | 33 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.850+27501_850+2750 others(10): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(1): Show |
G | 17 | a0001c0001t0001g0025 a0001c0001t0001g0170 a0001c0001t0002g0238 others(14): Show |
17 | HG01074.hp1 HG01169.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.850+27499_850+2750 others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(3): Show |
G | 5 | a0001c0001t0001g0014 a0001c0001t0005g0094 a0001c0001t0007g0286 others(2): Show |
5 | HG02004.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+27497_850+2750 others(14): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(5): Show |
G | 7 | a0001c0001t0003g0059 a0001c0001t0023g0174 a0001c0001t0023g0175 others(4): Show |
7 | HG01071.hp1 HG01081.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+27495_850+2750 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(7): Show |
G | 34 | a0001c0001t0001g0084 a0001c0001t0001g0128 a0001c0001t0001g0132 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.850+27493_850+2750 others(18): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(9): Show |
G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(36): Show |
39 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.850+27491_850+2750 others(20): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(11): Show |
G | 10 | a0001c0001t0002g0234 a0001c0001t0005g0093 a0001c0001t0005g0224 others(7): Show |
10 | HG01884.hp2 HG02074.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+27489_850+2750 others(22): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(13): Show |
G | 18 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(15): Show |
18 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.850+27487_850+2750 others(24): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(15): Show |
G | 4 | a0001c0001t0001g0225 a0002c0002t0020g0150 a0002c0002t0037g0162 others(1): Show |
4 | HG03209.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+27485_850+2750 others(26): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(17): Show |
G | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+27483_850+2750 others(28): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(19): Show |
G | 7 | a0003c0003t0008g0144 a0003c0003t0008g0145 a0003c0003t0008g0146 others(4): Show |
7 | HG02559.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+27481_850+2750 others(30): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(21): Show |
G | 1 | a0001c0001t0020g0117 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.850+27479_850+2750 others(32): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247269 | GTATATAT others(23): Show |
G | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.850+27477_850+2750 others(34): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131247269 | ||||||
| chr6:131247271 | A | G | 8 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
8 | HG01981.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+27463A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247271 | |||||||
| chr6:131247275 | A | G | 1 | a0010c0010t0002g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.850+27467A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247275 | |||||||
| chr6:131247277 | A | G | 2 | a0001c0001t0004g0194 a0005c0005t0011g0140 |
2 | HG02109.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.850+27469A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247277 | |||||||
| chr6:131247279 | A | G | 6 | a0001c0001t0002g0256 a0001c0001t0005g0075 a0001c0001t0005g0076 others(3): Show |
6 | HG01496.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+27471A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247279 | |||||||
| chr6:131247281 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.850+27473A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247281 | |||||||
| chr6:131247283 | A | G | 4 | a0001c0001t0003g0059 a0002c0002t0001g0096 a0002c0002t0002g0245 others(1): Show |
4 | HG01071.hp1 HG01081.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+27475A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247283 | |||||||
| chr6:131247285 | A | G | 29 | a0001c0001t0001g0084 a0001c0001t0001g0128 a0001c0001t0001g0132 others(26): Show |
29 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.850+27477A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247285 | |||||||
| chr6:131247287 | A | G | 34 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
34 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.850+27479A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247287 | |||||||
| chr6:131247289 | A | G | 3 | a0001c0001t0003g0106 a0002c0002t0001g0177 a0002c0002t0002g0265 |
3 | HG02074.hp2 HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.850+27481A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247289 | |||||||
| chr6:131247291 | A | G | 18 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(15): Show |
18 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.850+27483A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247291 | |||||||
| chr6:131247292 | TATATATA others(16): Show |
T | 5 | a0001c0001t0031g0285 a0003c0003t0032g0290 a0006c0006t0014g0006 others(2): Show |
5 | HG01891.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+27485_850+2750 others(27): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247292 | |||||||
| chr6:131247293 | A | G | 4 | a0001c0001t0001g0225 a0002c0002t0020g0150 a0002c0002t0037g0162 others(1): Show |
4 | HG03209.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+27485A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247293 | |||||||
| chr6:131247294 | TATATATA others(14): Show |
T | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+27487_850+2750 others(25): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247294 | |||||||
| chr6:131247316 | T | G | 7 | a0001c0001t0009g0185 a0001c0001t0031g0285 a0001c0001t0038g0166 others(4): Show |
7 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+27508T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247316 | |||||||
| chr6:131247344 | G | T | 2 | a0006c0006t0014g0006 a0006c0006t0014g0007 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.850+27536G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247344 | |||||||
| chr6:131247453 | G | C | 10 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+27645G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247453 | |||||||
| chr6:131247515 | G | A | 1 | a0001c0001t0022g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.850+27707G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247515 | |||||||
| chr6:131247558 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.850+27750G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247558 | |||||||
| chr6:131247653 | C | T | 1 | a0001c0001t0003g0050 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.850+27845C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247653 | |||||||
| chr6:131247698 | A | G | 25 | a0001c0001t0001g0084 a0001c0001t0005g0075 a0001c0001t0005g0076 others(22): Show |
25 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.850+27890A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247698 | |||||||
| chr6:131247784 | T | C | 179 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(176): Show |
179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.850+27976T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131247784 | |||||||
| chr6:131248596 | A | G | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+28788A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131248596 | |||||||
| chr6:131248698 | T | C | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.850+28890T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131248698 | |||||||
| chr6:131248938 | C | G | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+29130C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131248938 | |||||||
| chr6:131248968 | A | G | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+29160A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131248968 | |||||||
| chr6:131249113 | A | C | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+29305A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249113 | |||||||
| chr6:131249130 | A | G | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+29322A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249130 | |||||||
| chr6:131249364 | A | T | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+29556A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249364 | |||||||
| chr6:131249556 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0003g0072 |
2 | HG01943.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.850+29748G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249556 | |||||||
| chr6:131249601 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.850+29793A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249601 | |||||||
| chr6:131249924 | G | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+30116G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131249924 | |||||||
| chr6:131250008 | A | G | 5 | a0004c0004t0001g0001 a0004c0004t0001g0129 a0004c0004t0001g0131 others(2): Show |
6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+30200A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250008 | |||||||
| chr6:131250129 | G | T | 45 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0004g0168 others(42): Show |
45 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.850+30321G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250129 | |||||||
| chr6:131250245 | G | A | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+30437G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250245 | |||||||
| chr6:131250270 | A | T | 1 | a0001c0001t0003g0057 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.850+30462A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250270 | |||||||
| chr6:131250276 | T | A | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+30468T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250276 | |||||||
| chr6:131250418 | G | T | 1 | a0001c0001t0002g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.850+30610G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250418 | |||||||
| chr6:131250548 | A | G | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+30740A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250548 | |||||||
| chr6:131250591 | T | C | 1 | a0001c0001t0010g0082 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.850+30783T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131250591 | |||||||
| chr6:131251028 | T | C | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-30502T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251028 | |||||||
| chr6:131251107 | A | G | 1 | a0001c0001t0006g0254 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.851-30423A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251107 | |||||||
| chr6:131251207 | G | T | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-30323G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251207 | |||||||
| chr6:131251270 | G | T | 2 | a0001c0001t0006g0002 a0011c0008t0006g0002 |
2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.851-30260G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251270 | |||||||
| chr6:131251498 | G | A | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.851-30032G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251498 | |||||||
| chr6:131251568 | T | TA | 163 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.851-29952dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131251568 | ||||||
| chr6:131251637 | G | T | 1 | a0001c0001t0002g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.851-29893G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251637 | |||||||
| chr6:131251738 | T | C | 3 | a0001c0001t0005g0094 a0001c0001t0007g0286 a0007c0009t0005g0230 |
3 | HG02258.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.851-29792T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251738 | |||||||
| chr6:131251959 | G | A | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.851-29571G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131251959 | |||||||
| chr6:131252024 | C | T | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-29506C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252024 | |||||||
| chr6:131252156 | T | C | 1 | a0001c0001t0002g0276 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.851-29374T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252156 | |||||||
| chr6:131252293 | A | G | 196 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(193): Show |
196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.851-29237A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252293 | |||||||
| chr6:131252601 | G | A | 1 | a0001c0001t0003g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.851-28929G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252601 | |||||||
| chr6:131252732 | A | T | 60 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.851-28798A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252732 | |||||||
| chr6:131252770 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.851-28760T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252770 | |||||||
| chr6:131252822 | G | A | 1 | a0002c0002t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.851-28708G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131252822 | |||||||
| chr6:131253135 | T | G | 1 | a0001c0001t0002g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.851-28395T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253135 | |||||||
| chr6:131253246 | A | AT | 14 | a0001c0001t0005g0157 a0001c0001t0005g0224 a0001c0001t0007g0243 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.851-28277dupT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253246 | ||||||
| chr6:131253347 | G | A | 48 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(45): Show |
48 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.851-28183G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253347 | |||||||
| chr6:131253351 | T | C | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851-28179T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253351 | |||||||
| chr6:131253357 | T | C | 2 | a0001c0001t0023g0174 a0001c0001t0023g0175 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.851-28173T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253357 | |||||||
| chr6:131253586 | T | G | 1 | a0001c0001t0003g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.851-27944T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253586 | |||||||
| chr6:131253659 | C | CTTAT | 43 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0079 others(40): Show |
43 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.851-27838_851-2783 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | ||||||
| chr6:131253659 | C | CTTATTTA others(1): Show |
9 | a0001c0001t0002g0295 a0001c0001t0002g0299 a0001c0001t0004g0026 others(6): Show |
9 | HG00544.hp2 HG01943.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-27842_851-2783 others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | ||||||
| chr6:131253659 | CTTATTTA others(1): Show |
C | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.851-27842_851-2783 others(12): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | ||||||
| chr6:131253659 | CTTATTTA others(5): Show |
C | 14 | a0001c0001t0005g0093 a0001c0001t0005g0157 a0001c0001t0005g0224 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.851-27846_851-2783 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | ||||||
| chr6:131253659 | CTTATTTA others(9): Show |
C | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-27850_851-2783 others(20): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131253659 | ||||||
| chr6:131253929 | G | A | 50 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(47): Show |
50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-27601G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131253929 | |||||||
| chr6:131254052 | T | A | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-27478T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254052 | |||||||
| chr6:131254128 | CTG | C | 11 | a0001c0001t0008g0218 a0001c0001t0010g0184 a0001c0001t0023g0174 others(8): Show |
11 | HG02559.hp1 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.851-27400_851-2739 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131254128 | ||||||
| chr6:131254210 | C | T | 8 | a0001c0001t0001g0029 a0001c0001t0001g0126 a0001c0001t0001g0176 others(5): Show |
8 | HG00408.hp1 HG02074.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.851-27320C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254210 | |||||||
| chr6:131254471 | A | T | 3 | a0001c0001t0005g0094 a0001c0001t0007g0286 a0007c0009t0005g0230 |
3 | HG02258.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.851-27059A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254471 | |||||||
| chr6:131254492 | C | T | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-27038C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254492 | |||||||
| chr6:131254506 | A | G | 1 | a0002c0002t0003g0071 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.851-27024A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131254506 | |||||||
| chr6:131255088 | A | G | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-26442A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255088 | |||||||
| chr6:131255487 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.851-26043C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255487 | |||||||
| chr6:131255498 | A | C | 1 | a0001c0001t0041g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851-26032A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255498 | |||||||
| chr6:131255539 | T | G | 55 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(52): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.851-25991T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255539 | |||||||
| chr6:131255844 | C | T | 1 | a0001c0001t0040g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.851-25686C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131255844 | |||||||
| chr6:131256047 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.851-25483G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256047 | |||||||
| chr6:131256061 | C | T | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-25469C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256061 | |||||||
| chr6:131256162 | A | G | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(159): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.851-25368A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256162 | |||||||
| chr6:131256191 | G | A | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.851-25339G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256191 | |||||||
| chr6:131256551 | T | A | 4 | a0001c0001t0001g0046 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
4 | NA18943.hp1 NA18951.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-24979T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256551 | |||||||
| chr6:131256624 | T | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0126 others(6): Show |
9 | HG00408.hp1 HG02074.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.851-24906T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256624 | |||||||
| chr6:131256629 | G | A | 7 | a0002c0002t0001g0091 a0002c0002t0001g0096 a0002c0002t0002g0244 others(4): Show |
7 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-24901G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256629 | |||||||
| chr6:131256640 | ACT | A | 46 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(43): Show |
46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.851-24887_851-2488 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256640 | ||||||
| chr6:131256649 | T | C | 3 | a0001c0001t0001g0225 a0002c0002t0020g0150 a0006c0006t0035g0217 |
3 | HG03209.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.851-24881T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256649 | |||||||
| chr6:131256653 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.851-24877G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256653 | |||||||
| chr6:131256708 | C | CATT | 22 | a0001c0001t0001g0029 a0001c0001t0001g0088 a0001c0001t0001g0089 others(19): Show |
22 | HG00408.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.851-24796_851-2479 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | ||||||
| chr6:131256708 | C | CATTATTA others(2): Show |
27 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.851-24802_851-2479 others(13): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | ||||||
| chr6:131256708 | C | CATTATTA others(5): Show |
18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
18 | HG00280.hp1 HG01081.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.851-24805_851-2479 others(16): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | ||||||
| chr6:131256708 | C | CATTATTA others(8): Show |
1 | a0001c0001t0003g0048 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.851-24808_851-2479 others(19): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | ||||||
| chr6:131256708 | CATT | C | 95 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0004g0026 others(92): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.851-24796_851-2479 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131256708 | ||||||
| chr6:131256752 | CAGG | C | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24777_851-2477 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256752 | |||||||
| chr6:131256756 | T | G | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24774T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256756 | |||||||
| chr6:131256780 | T | G | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24750T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256780 | |||||||
| chr6:131256781 | C | T | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24749C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256781 | |||||||
| chr6:131256782 | C | T | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24748C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256782 | |||||||
| chr6:131256783 | T | TGAGC | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24747_851-2474 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256783 | |||||||
| chr6:131256784 | C | T | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24746C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256784 | |||||||
| chr6:131256786 | C | A | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.851-24744C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256786 | |||||||
| chr6:131256810 | G | T | 2 | a0002c0002t0001g0121 a0002c0002t0002g0288 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.851-24720G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256810 | |||||||
| chr6:131256945 | C | CTTGAAAC others(10): Show |
44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-24585_851-2458 others(21): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256945 | |||||||
| chr6:131256946 | C | G | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-24584C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256946 | |||||||
| chr6:131256947 | C | A | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-24583C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131256947 | |||||||
| chr6:131257201 | G | A | 1 | a0001c0001t0002g0279 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.851-24329G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257201 | |||||||
| chr6:131257367 | C | CA | 61 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(58): Show |
61 | HG00280.hp1 HG00558.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.851-24141dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131257367 | ||||||
| chr6:131257367 | C | CAA | 41 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0002g0267 others(38): Show |
41 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.851-24142_851-2414 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131257367 | ||||||
| chr6:131257367 | CA | C | 49 | a0001c0001t0001g0019 a0001c0001t0001g0084 a0001c0001t0001g0225 others(46): Show |
49 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.851-24141delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131257367 | ||||||
| chr6:131257367 | CAA | C | 9 | a0001c0001t0005g0090 a0002c0002t0001g0115 a0002c0002t0001g0134 others(6): Show |
9 | HG00140.hp2 HG01074.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.851-24142_851-2414 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131257367 | ||||||
| chr6:131257537 | C | T | 50 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(47): Show |
50 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.851-23993C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257537 | |||||||
| chr6:131257541 | C | T | 7 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(4): Show |
7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-23989C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257541 | |||||||
| chr6:131257545 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.851-23985T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257545 | |||||||
| chr6:131257764 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0003g0057 |
3 | NA18962.hp2 NA19006.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.851-23766G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131257764 | |||||||
| chr6:131258294 | G | A | 44 | a0001c0001t0001g0031 a0001c0001t0004g0026 a0001c0001t0004g0033 others(41): Show |
44 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-23236G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131258294 | |||||||
| chr6:131258663 | G | C | 4 | a0001c0001t0001g0046 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
4 | NA18943.hp1 NA18951.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-22867G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131258663 | |||||||
| chr6:131259160 | A | G | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-22370A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259160 | |||||||
| chr6:131259483 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.851-22047G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259483 | |||||||
| chr6:131259794 | A | C | 1 | a0001c0001t0019g0239 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.851-21736A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259794 | |||||||
| chr6:131259802 | T | A | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-21728T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259802 | |||||||
| chr6:131259818 | T | C | 2 | a0001c0001t0008g0218 a0001c0001t0010g0184 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.851-21712T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259818 | |||||||
| chr6:131259828 | C | A | 7 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 others(4): Show |
7 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-21702C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259828 | |||||||
| chr6:131259920 | G | A | 7 | a0001c0001t0002g0272 a0001c0001t0031g0285 a0001c0001t0038g0166 others(4): Show |
7 | HG00741.hp1 HG01891.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-21610G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259920 | |||||||
| chr6:131259933 | A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-21597A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131259933 | |||||||
| chr6:131259949 | G | GC | 61 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(58): Show |
61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.851-21577dupC | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131259949 | ||||||
| chr6:131260000 | A | C | 172 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(169): Show |
172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.851-21530A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260000 | |||||||
| chr6:131260072 | G | A | 50 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(47): Show |
50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-21458G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260072 | |||||||
| chr6:131260072 | G | T | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-21458G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260072 | |||||||
| chr6:131260267 | G | A | 3 | a0001c0001t0005g0157 a0001c0001t0007g0251 a0002c0002t0037g0162 |
3 | HG02486.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.851-21263G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260267 | |||||||
| chr6:131260488 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.851-21042C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260488 | |||||||
| chr6:131260577 | A | C | 1 | a0001c0001t0016g0009 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.851-20953A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260577 | |||||||
| chr6:131260729 | A | T | 5 | a0002c0002t0001g0092 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-20801A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260729 | |||||||
| chr6:131260882 | A | C | 57 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(54): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.851-20648A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260882 | |||||||
| chr6:131260919 | C | T | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.851-20611C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260919 | |||||||
| chr6:131260956 | G | A | 6 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0003c0003t0032g0290 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-20574G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260956 | |||||||
| chr6:131260994 | T | C | 177 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.851-20536T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131260994 | |||||||
| chr6:131261042 | CAA | C | 3 | a0001c0001t0005g0094 a0001c0001t0007g0286 a0007c0009t0005g0230 |
3 | HG02258.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.851-20486_851-2048 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131261042 | ||||||
| chr6:131261057 | G | A | 47 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.851-20473G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261057 | |||||||
| chr6:131261078 | C | T | 3 | a0001c0001t0013g0201 a0001c0001t0013g0210 a0001c0001t0030g0296 |
3 | NA18969.hp1 NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.851-20452C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261078 | |||||||
| chr6:131261209 | C | CA | 119 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(116): Show |
119 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.851-20305dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131261209 | ||||||
| chr6:131261209 | CA | C | 21 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(18): Show |
21 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.851-20305delA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131261209 | ||||||
| chr6:131261230 | A | G | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-20300A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261230 | |||||||
| chr6:131261249 | A | C | 1 | a0001c0001t0022g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.851-20281A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261249 | |||||||
| chr6:131261306 | C | T | 12 | a0001c0001t0008g0218 a0001c0001t0010g0082 a0001c0001t0010g0184 others(9): Show |
12 | HG01952.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.851-20224C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261306 | |||||||
| chr6:131261317 | CACTT | C | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-20210_851-2020 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131261317 | ||||||
| chr6:131261541 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.851-19989T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261541 | |||||||
| chr6:131261689 | C | T | 43 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.851-19841C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261689 | |||||||
| chr6:131261690 | G | A | 1 | a0004c0004t0003g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.851-19840G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261690 | |||||||
| chr6:131261761 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.851-19769A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261761 | |||||||
| chr6:131261796 | G | A | 46 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(43): Show |
46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.851-19734G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131261796 | |||||||
| chr6:131262330 | G | C | 13 | a0001c0001t0005g0093 a0001c0001t0005g0141 a0001c0001t0005g0224 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.851-19200G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262330 | |||||||
| chr6:131262559 | A | T | 1 | a0001c0001t0002g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.851-18971A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262559 | |||||||
| chr6:131262611 | T | A | 47 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(44): Show |
47 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.851-18919T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262611 | |||||||
| chr6:131262612 | T | A | 47 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(44): Show |
47 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.851-18918T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262612 | |||||||
| chr6:131262613 | A | T | 2 | a0001c0001t0001g0154 a0004c0004t0003g0167 |
2 | HG01099.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.851-18917A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262613 | |||||||
| chr6:131262616 | A | AAT | 4 | a0001c0001t0031g0285 a0001c0001t0038g0166 a0006c0006t0014g0006 others(1): Show |
4 | HG00741.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-18913_851-1891 others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131262616 | ||||||
| chr6:131262618 | A | T | 108 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0004g0026 others(105): Show |
108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.851-18912A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262618 | |||||||
| chr6:131262804 | T | C | 2 | a0002c0002t0001g0134 a0002c0002t0001g0135 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.851-18726T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131262804 | |||||||
| chr6:131263192 | A | G | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-18338A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263192 | |||||||
| chr6:131263325 | G | A | 1 | a0002c0002t0003g0070 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.851-18205G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263325 | |||||||
| chr6:131263508 | T | C | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-18022T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263508 | |||||||
| chr6:131263670 | G | A | 25 | a0001c0001t0001g0225 a0001c0001t0041g0159 a0002c0002t0001g0027 others(22): Show |
25 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.851-17860G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263670 | |||||||
| chr6:131263776 | A | T | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-17754A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263776 | |||||||
| chr6:131263832 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.851-17698C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263832 | |||||||
| chr6:131263833 | G | A | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.851-17697G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263833 | |||||||
| chr6:131263986 | T | G | 57 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(54): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.851-17544T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131263986 | |||||||
| chr6:131264009 | A | G | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.851-17521A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264009 | |||||||
| chr6:131264102 | G | A | 2 | a0002c0002t0017g0010 a0002c0002t0036g0221 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.851-17428G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264102 | |||||||
| chr6:131264111 | C | T | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
46 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.851-17419C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264111 | |||||||
| chr6:131264159 | G | A | 57 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0090 others(54): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.851-17371G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264159 | |||||||
| chr6:131264361 | A | G | 1 | a0002c0002t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.851-17169A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264361 | |||||||
| chr6:131264515 | A | G | 1 | a0001c0001t0010g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.851-17015A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264515 | |||||||
| chr6:131264571 | CATAA | C | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-16951_851-1694 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131264571 | ||||||
| chr6:131264587 | T | G | 2 | a0001c0001t0001g0032 a0001c0001t0002g0252 |
2 | NA18953.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.851-16943T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264587 | |||||||
| chr6:131264763 | C | T | 1 | a0002c0002t0027g0231 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.851-16767C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131264763 | |||||||
| chr6:131265004 | G | A | 5 | a0001c0001t0007g0243 a0001c0001t0009g0222 a0002c0002t0015g0003 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-16526G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265004 | |||||||
| chr6:131265160 | A | G | 18 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(15): Show |
18 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.851-16370A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265160 | |||||||
| chr6:131265161 | G | T | 18 | a0002c0002t0001g0027 a0002c0002t0001g0064 a0002c0002t0001g0107 others(15): Show |
18 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.851-16369G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265161 | |||||||
| chr6:131265403 | G | A | 1 | a0001c0001t0010g0082 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.851-16127G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265403 | |||||||
| chr6:131265694 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.851-15836A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265694 | |||||||
| chr6:131265795 | A | G | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.851-15735A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265795 | |||||||
| chr6:131265847 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0137 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.851-15683C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265847 | |||||||
| chr6:131265962 | C | A | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-15568C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131265962 | |||||||
| chr6:131266017 | A | G | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.851-15513A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266017 | |||||||
| chr6:131266099 | G | A | 1 | a0001c0001t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.851-15431G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266099 | |||||||
| chr6:131266173 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.851-15357T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266173 | |||||||
| chr6:131266684 | TTTG | T | 4 | a0001c0001t0021g0220 a0001c0001t0021g0223 a0001c0001t0022g0086 others(1): Show |
4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-14822_851-1482 others(7): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131266684 | ||||||
| chr6:131266704 | TG | T | 84 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0018 others(81): Show |
84 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.851-14825delG | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266704 | |||||||
| chr6:131266705 | G | T | 59 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0001g0225 others(56): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.851-14825G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266705 | |||||||
| chr6:131266708 | G | T | 146 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.851-14822G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266708 | |||||||
| chr6:131266717 | C | T | 4 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-14813C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131266717 | |||||||
| chr6:131267064 | C | CA | 61 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0005g0075 others(58): Show |
61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.851-14461dupA | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131267064 | ||||||
| chr6:131267442 | G | A | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-14088G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267442 | |||||||
| chr6:131267573 | A | C | 194 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(191): Show |
194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.851-13957A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267573 | |||||||
| chr6:131267603 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851-13927C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267603 | |||||||
| chr6:131267936 | A | G | 3 | a0001c0001t0002g0246 a0001c0001t0002g0295 a0001c0001t0002g0299 |
3 | HG00544.hp2 NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.851-13594A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267936 | |||||||
| chr6:131267988 | A | T | 1 | a0002c0002t0001g0158 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.851-13542A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131267988 | |||||||
| chr6:131268013 | G | A | 4 | a0001c0001t0004g0061 a0001c0001t0006g0254 a0001c0001t0012g0060 others(1): Show |
4 | HG01993.hp2 HG02293.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-13517G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268013 | |||||||
| chr6:131268032 | G | T | 3 | a0001c0001t0002g0257 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | NA18946.hp2 NA18955.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.851-13498G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268032 | |||||||
| chr6:131268097 | G | T | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
45 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.851-13433G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268097 | |||||||
| chr6:131268102 | T | A | 3 | a0002c0002t0017g0005 a0002c0002t0017g0010 a0002c0002t0036g0221 |
3 | HG02257.hp2 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.851-13428T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268102 | |||||||
| chr6:131268154 | A | G | 16 | a0001c0001t0005g0093 a0001c0001t0005g0141 a0001c0001t0005g0157 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.851-13376A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268154 | |||||||
| chr6:131268155 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851-13375A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268155 | |||||||
| chr6:131268173 | T | C | 4 | a0001c0001t0034g0219 a0002c0002t0015g0003 a0002c0002t0015g0004 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-13357T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268173 | |||||||
| chr6:131268174 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.851-13356T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268174 | |||||||
| chr6:131268197 | G | A | 2 | a0001c0001t0002g0246 a0001c0001t0002g0299 |
2 | NA18959.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.851-13333G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268197 | |||||||
| chr6:131268263 | A | C | 1 | a0001c0001t0018g0240 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.851-13267A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268263 | |||||||
| chr6:131268299 | T | G | 21 | a0001c0001t0001g0084 a0002c0002t0001g0065 a0002c0002t0001g0091 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.851-13231T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268299 | |||||||
| chr6:131268366 | G | A | 111 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(108): Show |
111 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.851-13164G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268366 | |||||||
| chr6:131268382 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0193 others(3): Show |
6 | HG02155.hp1 NA18952.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-13148T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268382 | |||||||
| chr6:131268471 | T | G | 3 | a0001c0001t0001g0225 a0002c0002t0020g0150 a0006c0006t0035g0217 |
3 | HG03209.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.851-13059T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268471 | |||||||
| chr6:131268475 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-13055A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268475 | |||||||
| chr6:131268503 | G | C | 4 | a0001c0001t0021g0220 a0001c0001t0021g0223 a0001c0001t0022g0086 others(1): Show |
4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-13027G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268503 | |||||||
| chr6:131268572 | A | G | 1 | a0001c0001t0004g0026 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.851-12958A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268572 | |||||||
| chr6:131268647 | G | A | 15 | a0001c0001t0001g0130 a0001c0001t0008g0218 a0001c0001t0010g0082 others(12): Show |
15 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.851-12883G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268647 | |||||||
| chr6:131268711 | A | G | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-12819A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131268711 | |||||||
| chr6:131269247 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0003g0059 |
2 | HG01081.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.851-12283G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269247 | |||||||
| chr6:131269305 | C | T | 7 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0005g0224 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-12225C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269305 | |||||||
| chr6:131269327 | C | T | 1 | a0001c0001t0010g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.851-12203C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269327 | |||||||
| chr6:131269588 | A | G | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-11942A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269588 | |||||||
| chr6:131269626 | G | A | 76 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(73): Show |
76 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.851-11904G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269626 | |||||||
| chr6:131269746 | G | A | 4 | a0001c0001t0005g0093 a0001c0001t0007g0277 a0001c0001t0011g0163 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-11784G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269746 | |||||||
| chr6:131269789 | A | G | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-11741A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269789 | |||||||
| chr6:131269817 | A | T | 104 | a0001c0001t0001g0225 a0001c0001t0003g0125 a0001c0001t0004g0026 others(101): Show |
104 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.851-11713A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131269817 | |||||||
| chr6:131270053 | C | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-11477C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270053 | |||||||
| chr6:131270217 | C | A | 1 | a0001c0001t0002g0258 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.851-11313C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270217 | |||||||
| chr6:131270359 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.851-11171C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270359 | |||||||
| chr6:131270360 | G | A | 8 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.851-11170G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270360 | |||||||
| chr6:131270491 | A | T | 1 | a0002c0002t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.851-11039A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270491 | |||||||
| chr6:131270845 | A | G | 1 | a0002c0002t0001g0158 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.851-10685A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270845 | |||||||
| chr6:131270967 | A | G | 4 | a0001c0001t0038g0166 a0006c0006t0014g0006 a0006c0006t0014g0007 others(1): Show |
4 | HG00741.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-10563A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131270967 | |||||||
| chr6:131271227 | T | A | 1 | a0001c0001t0004g0204 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.851-10303T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271227 | |||||||
| chr6:131271255 | GTTCT | G | 4 | a0001c0001t0021g0220 a0001c0001t0021g0223 a0001c0001t0022g0086 others(1): Show |
4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-10272_851-1026 others(8): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131271255 | ||||||
| chr6:131271379 | C | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0193 others(2): Show |
5 | HG02155.hp1 NA18952.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-10151C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271379 | |||||||
| chr6:131271386 | T | G | 17 | a0001c0001t0005g0093 a0001c0001t0005g0141 a0001c0001t0005g0157 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.851-10144T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271386 | |||||||
| chr6:131271423 | T | C | 5 | a0004c0004t0001g0001 a0004c0004t0001g0129 a0004c0004t0001g0131 others(2): Show |
6 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-10107T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271423 | |||||||
| chr6:131271722 | T | C | 24 | a0001c0001t0001g0225 a0002c0002t0001g0027 a0002c0002t0001g0064 others(21): Show |
24 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.851-9808T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271722 | |||||||
| chr6:131271816 | A | G | 1 | a0001c0001t0002g0295 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.851-9714A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271816 | |||||||
| chr6:131271838 | C | A | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.851-9692C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271838 | |||||||
| chr6:131271907 | C | G | 66 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(63): Show |
66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.851-9623C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131271907 | |||||||
| chr6:131272010 | A | G | 50 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(47): Show |
50 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-9520A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272010 | |||||||
| chr6:131272027 | G | A | 1 | a0001c0001t0021g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.851-9503G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272027 | |||||||
| chr6:131272079 | T | C | 22 | a0001c0001t0005g0093 a0001c0001t0005g0141 a0001c0001t0005g0157 others(19): Show |
22 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.851-9451T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272079 | |||||||
| chr6:131272277 | A | G | 3 | a0002c0002t0001g0092 a0002c0002t0001g0229 a0002c0002t0002g0291 |
3 | HG02055.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.851-9253A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272277 | |||||||
| chr6:131272324 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.851-9206T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272324 | |||||||
| chr6:131272367 | A | C | 4 | a0001c0001t0038g0166 a0006c0006t0014g0006 a0006c0006t0014g0007 others(1): Show |
4 | HG00741.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-9163A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272367 | |||||||
| chr6:131272449 | G | T | 2 | a0002c0002t0001g0177 a0002c0002t0002g0265 |
2 | HG02074.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.851-9081G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272449 | |||||||
| chr6:131272730 | A | C | 1 | a0008c0007t0029g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.851-8800A>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272730 | |||||||
| chr6:131272841 | G | T | 1 | a0001c0001t0012g0060 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.851-8689G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272841 | |||||||
| chr6:131272852 | T | C | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-8678T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272852 | |||||||
| chr6:131272864 | G | T | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-8666G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131272864 | |||||||
| chr6:131273027 | T | C | 4 | a0001c0001t0005g0157 a0001c0001t0007g0251 a0001c0001t0007g0282 others(1): Show |
4 | HG01884.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-8503T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273027 | |||||||
| chr6:131273096 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-8434G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273096 | |||||||
| chr6:131273182 | G | A | 9 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(6): Show |
9 | HG01978.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-8348G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273182 | |||||||
| chr6:131273239 | C | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(168): Show |
171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.851-8291C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273239 | |||||||
| chr6:131273488 | T | G | 51 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(48): Show |
51 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(48): Show |
intron_variant | MODIFIER | c.851-8042T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273488 | |||||||
| chr6:131273606 | C | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-7924C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273606 | |||||||
| chr6:131273722 | C | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-7808C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273722 | |||||||
| chr6:131273782 | T | C | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.851-7748T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273782 | |||||||
| chr6:131273833 | T | G | 1 | a0002c0002t0001g0115 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.851-7697T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273833 | |||||||
| chr6:131273940 | CT | C | 45 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(42): Show |
45 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.851-7573delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131273940 | ||||||
| chr6:131273988 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-7542G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131273988 | |||||||
| chr6:131274168 | C | G | 16 | a0001c0001t0005g0093 a0001c0001t0005g0141 a0001c0001t0005g0157 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.851-7362C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274168 | |||||||
| chr6:131274369 | TCTTC | T | 4 | a0001c0001t0034g0219 a0002c0002t0015g0003 a0002c0002t0015g0004 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-7155_851-7152d others(6): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131274369 | ||||||
| chr6:131274459 | C | G | 50 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(47): Show |
50 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-7071C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274459 | |||||||
| chr6:131274496 | T | G | 3 | a0001c0001t0005g0141 a0001c0001t0009g0142 a0001c0001t0009g0185 |
3 | HG03579.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.851-7034T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274496 | |||||||
| chr6:131274498 | T | C | 52 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(49): Show |
52 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(49): Show |
intron_variant | MODIFIER | c.851-7032T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274498 | |||||||
| chr6:131274897 | ACT | A | 6 | a0001c0001t0005g0093 a0001c0001t0005g0224 a0001c0001t0007g0277 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-6630_851-6629d others(4): Show |
AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131274897 | ||||||
| chr6:131274912 | G | A | 1 | a0002c0002t0020g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.851-6618G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131274912 | |||||||
| chr6:131275663 | C | T | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.851-5867C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131275663 | |||||||
| chr6:131275767 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.851-5763G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131275767 | |||||||
| chr6:131276014 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.851-5516C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276014 | |||||||
| chr6:131276180 | A | G | 5 | a0005c0005t0005g0097 a0005c0005t0005g0098 a0005c0005t0005g0099 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-5350A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276180 | |||||||
| chr6:131276229 | T | C | 41 | a0001c0001t0001g0225 a0001c0001t0005g0093 a0001c0001t0005g0141 others(38): Show |
41 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.851-5301T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276229 | |||||||
| chr6:131276236 | G | A | 171 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(168): Show |
171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.851-5294G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276236 | |||||||
| chr6:131276350 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.851-5180A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276350 | |||||||
| chr6:131276357 | T | C | 50 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(47): Show |
50 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-5173T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276357 | |||||||
| chr6:131276534 | A | G | 2 | a0001c0001t0006g0002 a0011c0008t0006g0002 |
2 | NA18981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.851-4996A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276534 | |||||||
| chr6:131276539 | A | G | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-4991A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276539 | |||||||
| chr6:131276753 | C | A | 1 | a0002c0002t0037g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851-4777C>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276753 | |||||||
| chr6:131276829 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.851-4701G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276829 | |||||||
| chr6:131276849 | C | T | 72 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(69): Show |
72 | HG00408.hp2 HG00597.hp1 HG01884.hp2 others(69): Show |
intron_variant | MODIFIER | c.851-4681C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276849 | |||||||
| chr6:131276890 | A | G | 2 | a0001c0001t0031g0285 a0003c0003t0032g0290 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.851-4640A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276890 | |||||||
| chr6:131276976 | A | G | 1 | a0002c0002t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.851-4554A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131276976 | |||||||
| chr6:131277048 | T | A | 1 | a0001c0001t0005g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-4482T>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131277048 | |||||||
| chr6:131277151 | G | A | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.851-4379G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131277151 | |||||||
| chr6:131277543 | G | A | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.851-3987G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131277543 | |||||||
| chr6:131277919 | C | G | 14 | a0001c0001t0008g0218 a0001c0001t0010g0082 a0001c0001t0010g0184 others(11): Show |
14 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.851-3611C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131277919 | |||||||
| chr6:131278031 | G | C | 10 | a0001c0001t0005g0090 a0001c0001t0005g0094 a0001c0001t0007g0286 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-3499G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278031 | |||||||
| chr6:131278046 | G | A | 50 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(47): Show |
50 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.851-3484G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278046 | |||||||
| chr6:131278081 | T | C | 10 | a0001c0001t0005g0090 a0001c0001t0005g0094 a0001c0001t0007g0286 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-3449T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278081 | |||||||
| chr6:131278181 | G | A | 1 | a0001c0001t0038g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.851-3349G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278181 | |||||||
| chr6:131278364 | C | G | 1 | a0001c0001t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.851-3166C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278364 | |||||||
| chr6:131278490 | G | A | 76 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(73): Show |
76 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.851-3040G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278490 | |||||||
| chr6:131278546 | T | C | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.851-2984T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278546 | |||||||
| chr6:131278582 | A | G | 60 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(57): Show |
60 | HG00408.hp2 HG00597.hp1 HG01891.hp1 others(57): Show |
intron_variant | MODIFIER | c.851-2948A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278582 | |||||||
| chr6:131278912 | G | A | 5 | a0001c0001t0005g0090 a0001c0001t0005g0094 a0001c0001t0007g0286 others(2): Show |
5 | HG02258.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-2618G>A | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131278912 | |||||||
| chr6:131279033 | GT | G | 4 | a0001c0001t0021g0220 a0001c0001t0021g0223 a0001c0001t0022g0086 others(1): Show |
4 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-2494delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 131279033 | ||||||
| chr6:131279048 | A | G | 169 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.851-2482A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131279048 | |||||||
| chr6:131279100 | A | G | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.851-2430A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131279100 | |||||||
| chr6:131279321 | T | G | 8 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.851-2209T>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131279321 | |||||||
| chr6:131279546 | C | T | 5 | a0001c0001t0005g0090 a0001c0001t0005g0094 a0001c0001t0007g0286 others(2): Show |
5 | HG02258.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-1984C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131279546 | |||||||
| chr6:131280082 | C | G | 10 | a0001c0001t0005g0090 a0001c0001t0005g0094 a0001c0001t0007g0286 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-1448C>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280082 | |||||||
| chr6:131280206 | T | C | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG02559.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.851-1324T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280206 | |||||||
| chr6:131280573 | C | T | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-957C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280573 | |||||||
| chr6:131280650 | C | T | 1 | a0001c0001t0002g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.851-880C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280650 | |||||||
| chr6:131280656 | C | T | 3 | a0001c0001t0038g0166 a0006c0006t0014g0006 a0006c0006t0014g0007 |
3 | HG00741.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.851-874C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280656 | |||||||
| chr6:131280685 | C | T | 42 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0035 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG01943.hp1 others(39): Show |
intron_variant | MODIFIER | c.851-845C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280685 | |||||||
| chr6:131280697 | T | C | 1 | a0001c0001t0003g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.851-833T>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280697 | |||||||
| chr6:131280927 | A | T | 16 | a0001c0001t0005g0093 a0001c0001t0005g0141 a0001c0001t0005g0157 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.851-603A>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280927 | |||||||
| chr6:131280974 | AT | A | 5 | a0001c0001t0041g0159 a0002c0002t0017g0005 a0002c0002t0017g0010 others(2): Show |
5 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-555delT | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131280974 | |||||||
| chr6:131281073 | G | C | 1 | a0002c0002t0020g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.851-457G>C | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131281073 | |||||||
| chr6:131281396 | A | G | 3 | a0001c0001t0038g0166 a0006c0006t0014g0006 a0006c0006t0014g0007 |
3 | HG00741.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.851-134A>G | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131281396 | |||||||
| chr6:131281460 | C | T | 1 | a0001c0001t0034g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.851-70C>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131281460 | |||||||
| chr6:131281462 | G | T | 6 | a0001c0001t0005g0093 a0001c0001t0005g0224 a0001c0001t0007g0277 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-68G>T | AKAP7 | ENSG00000118507.19 | transcript | ENST00000431975.7 | protein_coding | 7/7 | chr6 | 131281462 |