Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10096 |
| ensemblid | ENSG00000115091.12 |
| hgncid | 170 |
| symbol | ACTR3 |
| name | actin related protein 3 |
| refseq_nuc | NM_005721.5 |
| refseq_prot | NP_005712.1 |
| ensembl_nuc | ENST00000263238.7 |
| ensembl_prot | ENSP00000263238.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 113890089 |
| end | 113962596 |
| strand | + |
| ver | v1.2 |
| region | chr2:113890089-113962596 |
| region5000 | chr2:113885089-113967596 |
| regionname0 | ACTR3_chr2_113890089_113962596 |
| regionname5000 | ACTR3_chr2_113885089_113967596 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 418 | 389 | 87 | 62 | 188 | 12 | 38 | 148 | ACTR3_chr2_113885089_113967596 | ACTR3 | MAGRL others(413): Show |
chr2 | 113885089 | 113967596 |
| a0002 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | MAGRL others(413): Show |
chr2 | 113885089 | 113967596 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1254 | 387 | 86 | 62 | 188 | 11 | 38 | ACTR3_chr2_113885089_113967596 | ACTR3 | ATGGC others(1249): Show |
chr2 | 113885089 | 113967596 | ||
| a0001c0002 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | ATGGC others(1249): Show |
chr2 | 113885089 | 113967596 | ||
| a0001c0003 | 0/0 | 1254 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | ATGGC others(1249): Show |
chr2 | 113885089 | 113967596 | ||
| a0002c0004 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | ATGGC others(1249): Show |
chr2 | 113885089 | 113967596 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6588 | 103 | 19 | 11 | 61 | 0 | 12 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0002 | 0/1 | 6589 | 64 | 2 | 22 | 17 | 6 | 16 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0003 | 1/0 | 6589 | 54 | 4 | 6 | 41 | 1 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0004 | 0/0 | 6590 | 42 | 4 | 1 | 29 | 3 | 5 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6585): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0005 | 0/0 | 6588 | 16 | 6 | 2 | 8 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0006 | 0/0 | 6589 | 12 | 6 | 5 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0007 | 0/0 | 6588 | 11 | 11 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0008 | 0/0 | 6589 | 11 | 0 | 10 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0009 | 0/0 | 6589 | 11 | 10 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0010 | 0/0 | 6589 | 5 | 5 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0011 | 0/0 | 6594 | 5 | 0 | 0 | 5 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6589): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0012 | 0/0 | 6589 | 5 | 5 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0013 | 0/0 | 6588 | 5 | 4 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0014 | 0/0 | 6589 | 4 | 0 | 0 | 4 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0015 | 0/0 | 6584 | 4 | 4 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6579): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0016 | 0/0 | 6590 | 4 | 0 | 0 | 4 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6585): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0017 | 0/0 | 6588 | 4 | 0 | 0 | 3 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0018 | 0/0 | 6588 | 3 | 0 | 0 | 3 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0019 | 0/0 | 6589 | 2 | 0 | 1 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0020 | 0/0 | 6590 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6585): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0021 | 0/0 | 6588 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0022 | 0/0 | 6590 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6585): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0023 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0024 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0025 | 0/0 | 6589 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0026 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0027 | 0/0 | 6589 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0028 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0029 | 0/0 | 6589 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0030 | 0/0 | 6589 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0031 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0032 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0033 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0034 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0035 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0036 | 0/0 | 6590 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6585): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0037 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6583): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0038 | 0/0 | 6589 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0001t0039 | 0/0 | 6589 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0002t0010 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0001c0003t0002 | 0/0 | 6589 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| a0002c0004t0006 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | GTTGC others(6584): Show |
chr2 | 113885089 | 113967596 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0017 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0010 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0001 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0008g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0008g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0011g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0011g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0011g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0013g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0013g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0013g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0014g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0014g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0014g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0015g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0015g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0015g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0016g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0016g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0016g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0016g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0017g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0017g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0017g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0017g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0018g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0018g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0018g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0019g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0019g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0020g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0020g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0021g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0021g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0022g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0023g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0024g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0025g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0026g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0027g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0028g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0029g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0030g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0031g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0032g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0033g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0034g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0035g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0036g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0037g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0038g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0001t0039g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0002t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| a0002c0004t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0134 | EUR | GBR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | FIN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00544 | hp1 | a0001 | c0001 | t0018 | g0315 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0327 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00733 | hp1 | a0001 | c0001 | t0029 | g0094 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0113 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0220 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01070 | hp2 | a0001 | c0001 | t0019 | g0172 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0323 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0211 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0126 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01257 | hp2 | a0001 | c0001 | t0025 | g0157 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0117 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0182 | EUR | IBS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | IBS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0056 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01928 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0080 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0116 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0325 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01993 | hp1 | a0001 | c0001 | t0008 | g0004 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0215 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02129 | hp2 | a0001 | c0001 | t0019 | g0042 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0321 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02165 | hp1 | a0001 | c0001 | t0014 | g0005 | EAS | CDX | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0127 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02258 | hp2 | a0001 | c0001 | t0013 | g0206 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0344 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02451 | hp1 | a0001 | c0001 | t0026 | g0003 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02451 | hp2 | a0001 | c0001 | t0013 | g0205 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0031 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0109 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02622 | hp2 | a0001 | c0002 | t0010 | g0022 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0193 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0340 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0151 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02809 | hp2 | a0001 | c0001 | t0028 | g0061 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0337 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0063 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0192 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0060 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0329 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0194 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0057 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0195 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0059 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0150 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0210 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0214 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0223 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0125 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0218 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03453 | hp2 | a0001 | c0001 | t0035 | g0347 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0341 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0328 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03516 | hp1 | a0001 | c0001 | t0023 | g0217 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03540 | hp2 | a0001 | c0001 | t0024 | g0343 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0345 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03688 | hp1 | a0001 | c0001 | t0030 | g0111 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0135 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03831 | hp2 | a0001 | c0001 | t0036 | g0041 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03834 | hp1 | a0001 | c0001 | t0039 | g0106 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG04204 | hp1 | a0001 | c0001 | t0017 | g0294 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | YRI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0342 | AFR | YRI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | CHB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | CHB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | CHB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18941 | hp2 | a0001 | c0001 | t0014 | g0005 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18942 | hp1 | a0001 | c0001 | t0020 | g0147 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18945 | hp2 | a0001 | c0001 | t0011 | g0028 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18947 | hp1 | a0001 | c0001 | t0022 | g0046 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18953 | hp1 | a0001 | c0001 | t0038 | g0292 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18957 | hp2 | a0001 | c0001 | t0016 | g0149 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18960 | hp1 | a0001 | c0001 | t0016 | g0148 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0339 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18973 | hp1 | a0001 | c0001 | t0018 | g0297 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18981 | hp1 | a0001 | c0001 | t0011 | g0028 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18981 | hp2 | a0001 | c0001 | t0016 | g0152 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18986 | hp1 | a0001 | c0001 | t0014 | g0096 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18986 | hp2 | a0001 | c0001 | t0033 | g0027 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18988 | hp2 | a0001 | c0001 | t0037 | g0023 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18992 | hp1 | a0001 | c0001 | t0011 | g0301 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18993 | hp1 | a0001 | c0001 | t0021 | g0293 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0335 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18995 | hp1 | a0001 | c0001 | t0017 | g0284 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18997 | hp1 | a0001 | c0001 | t0018 | g0311 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18998 | hp2 | a0001 | c0001 | t0031 | g0007 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19002 | hp2 | a0001 | c0001 | t0032 | g0296 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19005 | hp2 | a0001 | c0001 | t0011 | g0286 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19006 | hp2 | a0001 | c0001 | t0027 | g0168 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | LWK | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19043 | hp1 | a0002 | c0004 | t0006 | g0224 | AFR | LWK | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0338 | AFR | LWK | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19055 | hp2 | a0001 | c0001 | t0017 | g0306 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19065 | hp1 | a0001 | c0001 | t0016 | g0019 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19077 | hp2 | a0001 | c0001 | t0011 | g0307 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19078 | hp2 | a0001 | c0001 | t0021 | g0316 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19082 | hp1 | a0001 | c0001 | t0014 | g0099 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19086 | hp1 | a0001 | c0001 | t0017 | g0283 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19086 | hp2 | a0001 | c0001 | t0008 | g0083 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19091 | hp1 | a0001 | c0001 | t0020 | g0131 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0062 | AFR | YRI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0216 | AFR | YRI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0330 | AFR | ASW | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ASW | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0124 | EUR | TSI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0191 | EUR | TSI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0221 | EUR | TSI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0174 | EUR | TSI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | GIH | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | GIH | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0208 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0058 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | USA | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0336 | AFR | USA | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0209 | AFR | USA | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| NA20300 | hp2 | a0001 | c0001 | t0034 | g0346 | AFR | USA | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0156 | REF | REF | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0010 | REF | REF | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113931368 | A | G | 1 | a0002 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.404A>G | p.Asn135Ser | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/12 | 595/6589 | 404/1257 | 135/418 | chr2 | 113931368 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113942200 | T | C | 1 | a0001c0002 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.699T>C | p.Tyr233Tyr | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/12 | 890/6589 | 699/1257 | 233/418 | chr2 | 113942200 | |||
| chr2:113951842 | G | A | 1 | a0001c0003 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.1074G>A | p.Leu358Leu | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/12 | 1265/6589 | 1074/1257 | 358/418 | chr2 | 113951842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113890251 | G | GGCAGCA | 1 | a0001c0001t0011 | 5 | NA18945.hp2 NA18981.hp1 NA18992.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-18_-13dupCAGCAG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/12 | 12 | INFO_REALIGN_3_PRIME | chr2 | 113890251 | |||||
| chr2:113957745 | A | G | 1 | a0001c0001t0039 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 290 | chr2 | 113957745 | ||||||
| chr2:113957753 | A | G | 2 | a0001c0001t0017 a0001c0001t0038 |
5 | HG04204.hp1 NA18953.hp1 NA18995.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*298A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 298 | chr2 | 113957753 | ||||||
| chr2:113957767 | T | C | 1 | a0001c0001t0022 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 312 | chr2 | 113957767 | ||||||
| chr2:113957867 | C | CA | 3 | a0001c0001t0006 a0001c0001t0023 a0002c0004t0006 |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*415dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 416 | INFO_REALIGN_3_PRIME | chr2 | 113957867 | |||||
| chr2:113957892 | A | G | 1 | a0001c0001t0037 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 437 | chr2 | 113957892 | ||||||
| chr2:113957899 | T | C | 1 | a0001c0001t0024 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*444T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 444 | chr2 | 113957899 | ||||||
| chr2:113957956 | G | A | 11 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0014 others(8): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*501G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 501 | chr2 | 113957956 | ||||||
| chr2:113958093 | G | A | 1 | a0001c0001t0020 | 2 | NA18942.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*638G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 638 | chr2 | 113958093 | ||||||
| chr2:113958133 | G | A | 1 | a0001c0001t0025 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*678G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 678 | chr2 | 113958133 | ||||||
| chr2:113958173 | T | C | 1 | a0001c0001t0030 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 718 | chr2 | 113958173 | ||||||
| chr2:113958366 | G | T | 1 | a0001c0001t0016 | 4 | NA18957.hp2 NA18960.hp1 NA18981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*911G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 911 | chr2 | 113958366 | ||||||
| chr2:113958407 | T | C | 1 | a0001c0001t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 952 | chr2 | 113958407 | ||||||
| chr2:113958601 | GT | G | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(16): Show |
174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1158delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1158 | INFO_REALIGN_3_PRIME | chr2 | 113958601 | |||||
| chr2:113958613 | T | A | 3 | a0001c0001t0006 a0001c0001t0023 a0002c0004t0006 |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1158T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1158 | chr2 | 113958613 | ||||||
| chr2:113958730 | T | C | 1 | a0001c0001t0008 | 11 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1275T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1275 | chr2 | 113958730 | ||||||
| chr2:113958788 | G | A | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(17): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1333G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1333 | chr2 | 113958788 | ||||||
| chr2:113958834 | A | G | 2 | a0001c0001t0026 a0001c0001t0029 |
2 | HG00733.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1379A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1379 | chr2 | 113958834 | ||||||
| chr2:113958871 | A | G | 3 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0024 |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1416A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1416 | chr2 | 113958871 | ||||||
| chr2:113958971 | T | C | 1 | a0001c0001t0027 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1516T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1516 | chr2 | 113958971 | ||||||
| chr2:113959039 | A | G | 1 | a0001c0001t0005 | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1584A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1584 | chr2 | 113959039 | ||||||
| chr2:113959343 | A | C | 8 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0013 others(5): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1888A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1888 | chr2 | 113959343 | ||||||
| chr2:113959407 | C | T | 1 | a0001c0001t0033 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1952C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1952 | chr2 | 113959407 | ||||||
| chr2:113959408 | G | A | 1 | a0001c0001t0019 | 2 | HG01070.hp2 HG02129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1953G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1953 | chr2 | 113959408 | ||||||
| chr2:113959507 | G | A | 1 | a0001c0001t0031 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2052G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 2052 | chr2 | 113959507 | ||||||
| chr2:113960037 | G | A | 1 | a0001c0001t0029 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2582G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 2582 | chr2 | 113960037 | ||||||
| chr2:113960225 | G | C | 1 | a0001c0001t0032 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2770G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 2770 | chr2 | 113960225 | ||||||
| chr2:113960324 | G | A | 2 | a0001c0001t0010 a0001c0002t0010 |
6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2869G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 2869 | chr2 | 113960324 | ||||||
| chr2:113960466 | A | G | 3 | a0001c0001t0006 a0001c0001t0023 a0002c0004t0006 |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3011A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3011 | chr2 | 113960466 | ||||||
| chr2:113960705 | A | G | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03453.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3250A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3250 | chr2 | 113960705 | ||||||
| chr2:113960731 | A | G | 1 | a0001c0001t0036 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3276A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3276 | chr2 | 113960731 | ||||||
| chr2:113960776 | C | G | 3 | a0001c0001t0006 a0001c0001t0023 a0002c0004t0006 |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3321C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3321 | chr2 | 113960776 | ||||||
| chr2:113960794 | C | T | 3 | a0001c0001t0006 a0001c0001t0023 a0002c0004t0006 |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3339C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3339 | chr2 | 113960794 | ||||||
| chr2:113960895 | A | G | 1 | a0001c0001t0021 | 2 | NA18993.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3440A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3440 | chr2 | 113960895 | ||||||
| chr2:113960925 | A | G | 1 | a0001c0001t0035 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3470A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3470 | chr2 | 113960925 | ||||||
| chr2:113961316 | C | G | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0016 others(3): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3861C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3861 | chr2 | 113961316 | ||||||
| chr2:113961449 | A | G | 1 | a0001c0001t0028 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3994A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3994 | chr2 | 113961449 | ||||||
| chr2:113961456 | C | T | 1 | a0001c0001t0008 | 11 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4001C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4001 | chr2 | 113961456 | ||||||
| chr2:113961690 | A | G | 1 | a0001c0001t0023 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4235A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4235 | chr2 | 113961690 | ||||||
| chr2:113961782 | G | A | 1 | a0001c0001t0013 | 5 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4327G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4327 | chr2 | 113961782 | ||||||
| chr2:113961874 | A | G | 9 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0019 others(6): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*4419A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4419 | chr2 | 113961874 | ||||||
| chr2:113961913 | CTAAG | C | 1 | a0001c0001t0015 | 4 | HG02615.hp1 HG02818.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4460_*4463delAAGT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4460 | INFO_REALIGN_3_PRIME | chr2 | 113961913 | |||||
| chr2:113962362 | T | C | 1 | a0001c0001t0018 | 3 | HG00544.hp1 NA18973.hp1 NA18997.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4907T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4907 | chr2 | 113962362 | ||||||
| chr2:113962402 | T | C | 1 | a0001c0001t0014 | 4 | HG02165.hp1 NA18941.hp2 NA18986.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4947T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4947 | chr2 | 113962402 | ||||||
| chr2:113962555 | A | AT | 5 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(2): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5102dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 5103 | INFO_REALIGN_3_PRIME | chr2 | 113962555 | |||||
| chr2:113962570 | C | A | 1 | a0001c0001t0029 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5115C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 5115 | chr2 | 113962570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113890346 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG00609.hp1 NA18951.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+23G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890346 | |||||||
| chr2:113890359 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.44+36G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890359 | |||||||
| chr2:113890368 | A | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44+45A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890368 | |||||||
| chr2:113890394 | C | T | 6 | a0001c0001t0007g0340 a0001c0001t0007g0341 a0001c0001t0007g0342 others(3): Show |
6 | HG02280.hp2 HG02723.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+71C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890394 | |||||||
| chr2:113890495 | C | T | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+172C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890495 | |||||||
| chr2:113890504 | C | T | 111 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(108): Show |
116 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.44+181C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890504 | |||||||
| chr2:113890535 | C | G | 1 | a0001c0001t0001g0320 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.44+212C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890535 | |||||||
| chr2:113891295 | A | G | 1 | a0001c0001t0035g0347 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.44+972A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891295 | |||||||
| chr2:113891323 | G | T | 165 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(162): Show |
174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+1000G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891323 | |||||||
| chr2:113891456 | AGAGAATA others(4): Show |
A | 1 | a0001c0001t0002g0040 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.44+1134_44+1144del others(11): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891456 | |||||||
| chr2:113891499 | G | C | 165 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(162): Show |
174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+1176G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891499 | |||||||
| chr2:113891519 | G | T | 165 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(162): Show |
174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+1196G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891519 | |||||||
| chr2:113891573 | T | TA | 134 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(131): Show |
141 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.44+1250_44+1251ins others(1): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891573 | |||||||
| chr2:113891615 | C | CT | 6 | a0001c0001t0001g0319 a0001c0001t0004g0201 a0001c0001t0004g0202 others(3): Show |
6 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+1302dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113891615 | ||||||
| chr2:113891643 | T | C | 1 | a0001c0001t0005g0321 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.44+1320T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891643 | |||||||
| chr2:113891790 | C | T | 2 | a0001c0001t0001g0318 a0001c0001t0002g0200 |
2 | HG02015.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.44+1467C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891790 | |||||||
| chr2:113891962 | T | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44+1639T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891962 | |||||||
| chr2:113892328 | G | A | 165 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(162): Show |
174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+2005G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892328 | |||||||
| chr2:113892589 | G | A | 1 | a0001c0001t0036g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.44+2266G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892589 | |||||||
| chr2:113892679 | T | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+2356T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892679 | |||||||
| chr2:113892911 | A | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.44+2588A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892911 | |||||||
| chr2:113892992 | A | G | 1 | a0001c0001t0002g0198 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.44+2669A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892992 | |||||||
| chr2:113893141 | T | C | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44+2818T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893141 | |||||||
| chr2:113893190 | A | T | 1 | a0001c0001t0002g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.44+2867A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893190 | |||||||
| chr2:113893256 | CG | C | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+2934delG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893256 | |||||||
| chr2:113893288 | TTTTG | T | 134 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(131): Show |
141 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.44+2985_44+2988del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113893288 | ||||||
| chr2:113893388 | G | C | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+3065G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893388 | |||||||
| chr2:113893398 | A | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.44+3075A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893398 | |||||||
| chr2:113893468 | C | A | 165 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(162): Show |
174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+3145C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893468 | |||||||
| chr2:113893581 | C | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.44+3258C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893581 | |||||||
| chr2:113893584 | G | C | 10 | a0001c0001t0004g0043 a0001c0001t0004g0044 a0001c0001t0004g0045 others(7): Show |
10 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+3261G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893584 | |||||||
| chr2:113893607 | A | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+3284A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893607 | |||||||
| chr2:113893657 | G | A | 8 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(5): Show |
10 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+3334G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893657 | |||||||
| chr2:113893783 | A | T | 1 | a0001c0001t0004g0196 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.44+3460A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893783 | |||||||
| chr2:113893807 | C | T | 1 | a0001c0001t0015g0338 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.44+3484C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893807 | |||||||
| chr2:113893827 | A | G | 6 | a0001c0001t0010g0022 a0001c0001t0010g0192 a0001c0001t0010g0193 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+3504A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893827 | |||||||
| chr2:113893851 | G | A | 1 | a0001c0001t0006g0223 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44+3528G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893851 | |||||||
| chr2:113893949 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.44+3626C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893949 | |||||||
| chr2:113894080 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.44+3757A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894080 | |||||||
| chr2:113894089 | G | C | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44+3766G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894089 | |||||||
| chr2:113894093 | C | CT | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01884.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+3783dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113894093 | ||||||
| chr2:113894093 | CT | C | 51 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(48): Show |
54 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.44+3783delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113894093 | ||||||
| chr2:113894143 | G | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.44+3820G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894143 | |||||||
| chr2:113894175 | C | T | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+3852C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894175 | |||||||
| chr2:113894188 | G | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+3865G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894188 | |||||||
| chr2:113894279 | G | T | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.44+3956G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894279 | |||||||
| chr2:113894295 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+3972G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894295 | |||||||
| chr2:113894300 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.44+3977C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894300 | |||||||
| chr2:113894302 | A | G | 37 | a0001c0001t0002g0021 a0001c0001t0002g0053 a0001c0001t0002g0158 others(34): Show |
38 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.44+3979A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894302 | |||||||
| chr2:113894363 | G | A | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.44+4040G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894363 | |||||||
| chr2:113894434 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.44+4111T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894434 | |||||||
| chr2:113894552 | T | C | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.44+4229T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894552 | |||||||
| chr2:113894600 | TTG | T | 51 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(48): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.44+4281_44+4282del others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113894600 | ||||||
| chr2:113894621 | G | A | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44+4298G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894621 | |||||||
| chr2:113894891 | C | T | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.44+4568C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894891 | |||||||
| chr2:113894980 | C | CA | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.44+4666dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113894980 | ||||||
| chr2:113895058 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.44+4735T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895058 | |||||||
| chr2:113895059 | T | C | 1 | a0001c0001t0003g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.44+4736T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895059 | |||||||
| chr2:113895059 | T | TC | 32 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0185 others(29): Show |
36 | HG00544.hp2 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.44+4746dupC | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113895059 | ||||||
| chr2:113895059 | TC | T | 134 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(131): Show |
142 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+4746delC | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113895059 | ||||||
| chr2:113895069 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44+4746C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895069 | |||||||
| chr2:113895070 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44+4747A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895070 | |||||||
| chr2:113895077 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+4754T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895077 | |||||||
| chr2:113895493 | A | ACCC | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.44+5172_44+5174dup others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113895493 | ||||||
| chr2:113895623 | G | A | 6 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0058 others(3): Show |
6 | HG01884.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+5300G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895623 | |||||||
| chr2:113895697 | T | A | 55 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.44+5374T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895697 | |||||||
| chr2:113895706 | G | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+5383G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895706 | |||||||
| chr2:113895708 | G | A | 6 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0058 others(3): Show |
6 | HG01884.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+5385G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895708 | |||||||
| chr2:113895721 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.44+5398C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895721 | |||||||
| chr2:113895801 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.44+5478A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895801 | |||||||
| chr2:113895808 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.44+5485C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895808 | |||||||
| chr2:113895932 | C | CACTGCAT others(6): Show |
1 | a0001c0001t0002g0184 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.44+5613_44+5625dup others(13): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113895932 | ||||||
| chr2:113896008 | GCCA | G | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(38): Show |
44 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.44+5689_44+5691del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113896008 | ||||||
| chr2:113896238 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.44+5915A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896238 | |||||||
| chr2:113896294 | A | T | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.44+5971A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896294 | |||||||
| chr2:113896408 | A | AGG | 10 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(7): Show |
10 | HG01099.hp1 HG01167.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+6086_44+6087dup others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113896408 | ||||||
| chr2:113896439 | C | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+6116C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896439 | |||||||
| chr2:113896625 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.44+6302G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896625 | |||||||
| chr2:113896875 | A | C | 1 | a0001c0001t0002g0108 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.44+6552A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896875 | |||||||
| chr2:113896950 | G | A | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+6627G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896950 | |||||||
| chr2:113897171 | G | A | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+6848G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897171 | |||||||
| chr2:113897373 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+7050A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897373 | |||||||
| chr2:113897515 | GTTATTT | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.44+7195_44+7200del others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897515 | ||||||
| chr2:113897515 | GTTATTTT | G | 112 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(109): Show |
118 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.44+7195_44+7201del others(7): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897515 | ||||||
| chr2:113897518 | A | AT | 13 | a0001c0001t0003g0078 a0001c0001t0004g0019 a0001c0001t0004g0049 others(10): Show |
13 | HG00438.hp2 HG00621.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.44+7221dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897518 | ||||||
| chr2:113897518 | AT | A | 57 | a0001c0001t0002g0178 a0001c0001t0002g0198 a0001c0001t0003g0002 others(54): Show |
68 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.44+7221delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897518 | ||||||
| chr2:113897518 | ATT | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(62): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.44+7220_44+7221del others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897518 | ||||||
| chr2:113897522 | T | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0310 a0001c0001t0001g0313 others(1): Show |
4 | HG03688.hp2 NA18955.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+7199T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897522 | |||||||
| chr2:113897523 | T | A | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.44+7200T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897523 | |||||||
| chr2:113897524 | T | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(109): Show |
118 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.44+7201T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897524 | |||||||
| chr2:113897525 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.44+7202T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897525 | |||||||
| chr2:113897613 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.44+7290G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897613 | |||||||
| chr2:113897652 | G | A | 1 | a0001c0001t0005g0335 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.44+7329G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897652 | |||||||
| chr2:113897827 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0015g0031 a0001c0001t0015g0336 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+7504A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897827 | |||||||
| chr2:113898009 | G | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+7686G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898009 | |||||||
| chr2:113898024 | G | A | 55 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.44+7701G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898024 | |||||||
| chr2:113898239 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+7916A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898239 | |||||||
| chr2:113898513 | T | C | 1 | a0001c0001t0003g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.44+8190T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898513 | |||||||
| chr2:113898544 | A | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+8221A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898544 | |||||||
| chr2:113898556 | T | C | 1 | a0001c0001t0001g0320 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.44+8233T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898556 | |||||||
| chr2:113898599 | A | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.44+8276A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898599 | |||||||
| chr2:113898698 | C | T | 1 | a0001c0003t0002g0124 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.44+8375C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898698 | |||||||
| chr2:113898725 | A | T | 1 | a0001c0001t0002g0107 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.44+8402A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898725 | |||||||
| chr2:113898751 | A | G | 1 | a0001c0001t0003g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.44+8428A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898751 | |||||||
| chr2:113898878 | G | A | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+8555G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898878 | |||||||
| chr2:113898927 | T | G | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.44+8604T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898927 | |||||||
| chr2:113898934 | G | T | 3 | a0001c0001t0003g0089 a0001c0001t0003g0120 a0001c0001t0003g0121 |
3 | NA18940.hp1 NA18959.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.44+8611G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898934 | |||||||
| chr2:113899008 | A | G | 2 | a0001c0001t0004g0050 a0001c0001t0004g0051 |
2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.44+8685A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899008 | |||||||
| chr2:113899263 | T | C | 8 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(5): Show |
10 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+8940T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899263 | |||||||
| chr2:113899295 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44+8972T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899295 | |||||||
| chr2:113899327 | A | G | 55 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.44+9004A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899327 | |||||||
| chr2:113899352 | A | G | 5 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0187 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+9029A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899352 | |||||||
| chr2:113899379 | T | TA | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+9063dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113899379 | ||||||
| chr2:113899392 | G | T | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44+9069G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899392 | |||||||
| chr2:113899506 | G | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+9183G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899506 | |||||||
| chr2:113899619 | G | C | 1 | a0001c0001t0001g0032 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.44+9296G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899619 | |||||||
| chr2:113899761 | G | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.44+9438G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899761 | |||||||
| chr2:113899774 | T | C | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+9451T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899774 | |||||||
| chr2:113899808 | G | A | 2 | a0001c0001t0002g0187 a0001c0001t0002g0189 |
2 | HG00733.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.44+9485G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899808 | |||||||
| chr2:113899877 | C | G | 1 | a0001c0001t0001g0312 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.44+9554C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899877 | |||||||
| chr2:113899898 | G | A | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.44+9575G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899898 | |||||||
| chr2:113900340 | G | A | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.44+10017G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113900340 | |||||||
| chr2:113900525 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+10202G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113900525 | |||||||
| chr2:113900676 | A | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.44+10353A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113900676 | |||||||
| chr2:113900838 | G | A | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.44+10515G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113900838 | |||||||
| chr2:113901037 | T | C | 1 | a0001c0001t0004g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.44+10714T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901037 | |||||||
| chr2:113901085 | C | T | 1 | a0001c0001t0021g0316 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.44+10762C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901085 | |||||||
| chr2:113901226 | G | C | 2 | a0001c0001t0012g0056 a0001c0001t0012g0057 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.44+10903G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901226 | |||||||
| chr2:113901286 | A | T | 1 | a0001c0001t0001g0030 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.44+10963A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901286 | |||||||
| chr2:113901315 | G | T | 1 | a0001c0001t0001g0030 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.44+10992G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901315 | |||||||
| chr2:113901334 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+11011G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901334 | |||||||
| chr2:113901420 | A | C | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+11097A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901420 | |||||||
| chr2:113901507 | A | G | 4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+11184A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901507 | |||||||
| chr2:113901568 | A | C | 3 | a0001c0001t0004g0201 a0001c0001t0004g0203 a0001c0001t0004g0204 |
3 | HG02145.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.44+11245A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901568 | |||||||
| chr2:113901633 | A | G | 130 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(127): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+11310A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901633 | |||||||
| chr2:113901707 | T | C | 10 | a0001c0001t0009g0008 a0001c0001t0009g0062 a0001c0001t0009g0063 others(7): Show |
11 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+11384T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901707 | |||||||
| chr2:113901867 | A | G | 1 | a0001c0001t0009g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45-11305A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901867 | |||||||
| chr2:113901989 | A | G | 1 | a0001c0001t0003g0119 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45-11183A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901989 | |||||||
| chr2:113902061 | G | A | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-11111G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902061 | |||||||
| chr2:113902072 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.45-11100A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902072 | |||||||
| chr2:113902132 | C | G | 4 | a0001c0001t0006g0223 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02109.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-11040C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902132 | |||||||
| chr2:113902137 | T | A | 1 | a0001c0001t0006g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45-11035T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902137 | |||||||
| chr2:113902146 | C | A | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-11026C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902146 | |||||||
| chr2:113902257 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.45-10915C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902257 | |||||||
| chr2:113902304 | G | A | 1 | a0001c0001t0003g0065 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.45-10868G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902304 | |||||||
| chr2:113902377 | T | C | 1 | a0001c0001t0003g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.45-10795T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902377 | |||||||
| chr2:113902387 | T | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(113): Show |
121 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.45-10785T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902387 | |||||||
| chr2:113902456 | A | G | 1 | a0001c0001t0005g0331 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.45-10716A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902456 | |||||||
| chr2:113902517 | T | C | 2 | a0001c0001t0003g0009 a0001c0001t0003g0066 |
3 | NA18992.hp2 NA19005.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.45-10655T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902517 | |||||||
| chr2:113902599 | G | GT | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.45-10562dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113902599 | ||||||
| chr2:113902626 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45-10546G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902626 | |||||||
| chr2:113902660 | C | T | 1 | a0001c0001t0006g0006 | 3 | HG00639.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.45-10512C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902660 | |||||||
| chr2:113902692 | C | T | 2 | a0001c0001t0006g0225 a0001c0001t0006g0226 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.45-10480C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902692 | |||||||
| chr2:113902709 | C | T | 51 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(48): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.45-10463C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902709 | |||||||
| chr2:113902716 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.45-10456C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902716 | |||||||
| chr2:113902809 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45-10363A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902809 | |||||||
| chr2:113902818 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45-10354T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902818 | |||||||
| chr2:113902841 | C | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-10331C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902841 | |||||||
| chr2:113902846 | G | A | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.45-10326G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902846 | |||||||
| chr2:113903012 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.45-10160C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903012 | |||||||
| chr2:113903042 | C | G | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.45-10130C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903042 | |||||||
| chr2:113903097 | C | A | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.45-10075C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903097 | |||||||
| chr2:113903114 | C | T | 6 | a0001c0001t0010g0022 a0001c0001t0010g0192 a0001c0001t0010g0193 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-10058C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903114 | |||||||
| chr2:113903117 | G | C | 1 | a0001c0001t0005g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45-10055G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903117 | |||||||
| chr2:113903127 | A | G | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.45-10045A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903127 | |||||||
| chr2:113903173 | C | T | 1 | a0001c0001t0004g0154 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.45-9999C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903173 | |||||||
| chr2:113903192 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0003g0110 |
2 | NA18997.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.45-9980G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903192 | |||||||
| chr2:113903438 | C | T | 1 | a0001c0001t0028g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45-9734C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903438 | |||||||
| chr2:113903442 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.45-9730C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903442 | |||||||
| chr2:113903510 | C | T | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-9662C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903510 | |||||||
| chr2:113903537 | CT | C | 144 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(141): Show |
149 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.45-9618delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113903537 | ||||||
| chr2:113903537 | CTT | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0006g0006 others(9): Show |
15 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.45-9619_45-9618del others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113903537 | ||||||
| chr2:113903724 | C | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-9448C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903724 | |||||||
| chr2:113903836 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.45-9336C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903836 | |||||||
| chr2:113903957 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-9215T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903957 | |||||||
| chr2:113904020 | C | T | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-9152C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904020 | |||||||
| chr2:113904032 | T | C | 3 | a0001c0001t0002g0159 a0001c0001t0002g0186 a0001c0001t0002g0198 |
3 | HG01261.hp2 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.45-9140T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904032 | |||||||
| chr2:113904051 | G | A | 5 | a0001c0001t0005g0321 a0001c0001t0005g0323 a0001c0001t0005g0324 others(2): Show |
5 | HG01167.hp1 HG01981.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-9121G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904051 | |||||||
| chr2:113904081 | C | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-9091C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904081 | |||||||
| chr2:113904111 | C | T | 6 | a0001c0001t0003g0015 a0001c0001t0003g0084 a0001c0001t0003g0085 others(3): Show |
7 | NA18946.hp2 NA18960.hp2 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-9061C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904111 | |||||||
| chr2:113904135 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-9037C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904135 | |||||||
| chr2:113904659 | A | G | 1 | a0001c0001t0003g0119 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45-8513A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904659 | |||||||
| chr2:113904773 | G | A | 3 | a0001c0001t0003g0084 a0001c0001t0003g0085 a0001c0001t0003g0118 |
3 | NA19000.hp1 NA19080.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.45-8399G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904773 | |||||||
| chr2:113904933 | C | G | 1 | a0001c0001t0001g0309 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.45-8239C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904933 | |||||||
| chr2:113904937 | A | G | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45-8235A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904937 | |||||||
| chr2:113905114 | C | T | 1 | a0001c0001t0005g0330 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.45-8058C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905114 | |||||||
| chr2:113905154 | T | C | 4 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0009g0128 others(1): Show |
4 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-8018T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905154 | |||||||
| chr2:113905196 | G | A | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.45-7976G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905196 | |||||||
| chr2:113905275 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-7897G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905275 | |||||||
| chr2:113905371 | A | G | 41 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(38): Show |
46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.45-7801A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905371 | |||||||
| chr2:113905422 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.45-7750G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905422 | |||||||
| chr2:113905427 | G | A | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.45-7745G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905427 | |||||||
| chr2:113905464 | C | CA | 6 | a0001c0001t0001g0231 a0001c0001t0001g0275 a0001c0001t0002g0187 others(3): Show |
6 | HG02738.hp2 HG03098.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-7693dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113905464 | ||||||
| chr2:113905464 | CA | C | 25 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(22): Show |
25 | HG01099.hp1 HG01167.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.45-7693delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113905464 | ||||||
| chr2:113905632 | G | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-7540G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905632 | |||||||
| chr2:113905849 | T | TTAA | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.45-7323_45-7322ins others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905849 | |||||||
| chr2:113905965 | A | G | 2 | a0001c0001t0016g0148 a0001c0001t0016g0149 |
2 | NA18957.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.45-7207A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905965 | |||||||
| chr2:113906378 | C | G | 1 | a0002c0004t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.45-6794C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906378 | |||||||
| chr2:113906739 | A | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-6433A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906739 | |||||||
| chr2:113906852 | G | A | 51 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(48): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.45-6320G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906852 | |||||||
| chr2:113906899 | G | A | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-6273G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906899 | |||||||
| chr2:113906993 | G | C | 1 | a0001c0001t0001g0310 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.45-6179G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906993 | |||||||
| chr2:113907023 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-6149A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907023 | |||||||
| chr2:113907191 | A | G | 1 | a0001c0001t0011g0307 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.45-5981A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907191 | |||||||
| chr2:113907499 | T | A | 1 | a0001c0001t0001g0317 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.45-5673T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907499 | |||||||
| chr2:113907547 | C | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.45-5625C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907547 | |||||||
| chr2:113907654 | A | G | 1 | a0001c0001t0006g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45-5518A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907654 | |||||||
| chr2:113907856 | C | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-5316C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907856 | |||||||
| chr2:113907971 | T | A | 6 | a0001c0001t0010g0022 a0001c0001t0010g0192 a0001c0001t0010g0193 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-5201T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907971 | |||||||
| chr2:113907971 | TC | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(71): Show |
79 | HG00408.hp2 HG00639.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.45-5196delC | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113907971 | ||||||
| chr2:113907975 | C | CA | 42 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(39): Show |
45 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.45-5197_45-5196ins others(1): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907975 | |||||||
| chr2:113907975 | C | CAA | 7 | a0001c0001t0001g0034 a0001c0001t0001g0285 a0001c0001t0011g0286 others(4): Show |
7 | HG04184.hp2 NA18995.hp1 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.45-5197_45-5196ins others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907975 | |||||||
| chr2:113907976 | C | A | 70 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(67): Show |
74 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.45-5196C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907976 | |||||||
| chr2:113907976 | C | CA | 23 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0158 others(20): Show |
23 | HG01106.hp1 HG01169.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.45-5170dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113907976 | ||||||
| chr2:113907976 | CA | C | 49 | a0001c0001t0002g0108 a0001c0001t0002g0178 a0001c0001t0003g0079 others(46): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.45-5170delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113907976 | ||||||
| chr2:113907977 | A | C | 34 | a0001c0001t0002g0017 a0001c0001t0002g0040 a0001c0001t0002g0102 others(31): Show |
41 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.45-5195A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907977 | |||||||
| chr2:113907978 | A | C | 1 | a0001c0001t0008g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.45-5194A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907978 | |||||||
| chr2:113908003 | G | A | 6 | a0001c0001t0002g0160 a0001c0001t0002g0165 a0001c0001t0002g0166 others(3): Show |
6 | NA18947.hp2 NA18984.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-5169G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908003 | |||||||
| chr2:113908156 | C | G | 6 | a0001c0001t0007g0212 a0001c0001t0013g0205 a0001c0001t0013g0206 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-5016C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908156 | |||||||
| chr2:113908244 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-4928G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908244 | |||||||
| chr2:113908251 | G | GT | 8 | a0001c0001t0001g0263 a0001c0001t0002g0167 a0001c0001t0002g0180 others(5): Show |
8 | HG03453.hp2 HG03831.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-4906dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113908251 | ||||||
| chr2:113908251 | GT | G | 64 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(61): Show |
69 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.45-4906delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113908251 | ||||||
| chr2:113908275 | A | T | 1 | a0001c0001t0010g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.45-4897A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908275 | |||||||
| chr2:113908366 | G | A | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0023g0217 |
3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45-4806G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908366 | |||||||
| chr2:113908387 | G | T | 17 | a0001c0001t0004g0043 a0001c0001t0004g0044 a0001c0001t0004g0045 others(14): Show |
17 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.45-4785G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908387 | |||||||
| chr2:113908434 | T | G | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.45-4738T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908434 | |||||||
| chr2:113908557 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-4615A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908557 | |||||||
| chr2:113908637 | A | G | 1 | a0001c0001t0015g0337 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45-4535A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908637 | |||||||
| chr2:113908663 | C | T | 4 | a0001c0001t0004g0201 a0001c0001t0004g0202 a0001c0001t0004g0203 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-4509C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908663 | |||||||
| chr2:113908769 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45-4403C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908769 | |||||||
| chr2:113908773 | C | T | 19 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(16): Show |
19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-4399C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908773 | |||||||
| chr2:113908791 | G | A | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-4381G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908791 | |||||||
| chr2:113909114 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.45-4058T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909114 | |||||||
| chr2:113909185 | A | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-3987A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909185 | |||||||
| chr2:113909335 | T | C | 1 | a0001c0001t0004g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.45-3837T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909335 | |||||||
| chr2:113909475 | C | T | 1 | a0001c0001t0036g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.45-3697C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909475 | |||||||
| chr2:113909606 | TTTG | T | 50 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(47): Show |
55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.45-3551_45-3549del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113909606 | ||||||
| chr2:113909609 | G | T | 10 | a0001c0001t0005g0321 a0001c0001t0005g0323 a0001c0001t0005g0324 others(7): Show |
10 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-3563G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909609 | |||||||
| chr2:113909621 | G | GT | 64 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
66 | HG00408.hp2 HG00544.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.45-3538dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113909621 | ||||||
| chr2:113909642 | T | A | 1 | a0001c0001t0012g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45-3530T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909642 | |||||||
| chr2:113909700 | GAA | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-3467_45-3466del others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113909700 | ||||||
| chr2:113909703 | A | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.45-3469A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909703 | |||||||
| chr2:113909917 | C | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-3255C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909917 | |||||||
| chr2:113909979 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45-3193G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909979 | |||||||
| chr2:113910039 | G | T | 1 | a0001c0001t0002g0184 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.45-3133G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910039 | |||||||
| chr2:113910055 | A | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-3117A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910055 | |||||||
| chr2:113910056 | TG | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-3113delG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113910056 | ||||||
| chr2:113910139 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.45-3033G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910139 | |||||||
| chr2:113910147 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45-3025C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910147 | |||||||
| chr2:113910236 | C | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-2936C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910236 | |||||||
| chr2:113910238 | A | G | 2 | a0001c0001t0003g0070 a0001c0001t0003g0114 |
2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.45-2934A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910238 | |||||||
| chr2:113910254 | CAGAGTTT others(2): Show |
C | 19 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(16): Show |
19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-2913_45-2905del others(9): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113910254 | ||||||
| chr2:113910310 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.45-2862C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910310 | |||||||
| chr2:113910330 | G | A | 6 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0058 others(3): Show |
6 | HG01884.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-2842G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910330 | |||||||
| chr2:113910334 | A | G | 1 | a0001c0001t0010g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.45-2838A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910334 | |||||||
| chr2:113910338 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0333 a0001c0001t0001g0334 |
4 | HG01891.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-2834C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910338 | |||||||
| chr2:113910515 | T | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-2657T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910515 | |||||||
| chr2:113910743 | C | G | 1 | a0001c0001t0001g0033 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.45-2429C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910743 | |||||||
| chr2:113910746 | A | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.45-2426A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910746 | |||||||
| chr2:113910765 | A | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-2407A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910765 | |||||||
| chr2:113910837 | T | C | 1 | a0001c0001t0028g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45-2335T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910837 | |||||||
| chr2:113910907 | T | A | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0023g0217 |
3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45-2265T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910907 | |||||||
| chr2:113911072 | G | A | 2 | a0001c0001t0004g0129 a0001c0001t0004g0130 |
2 | NA18940.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.45-2100G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911072 | |||||||
| chr2:113911108 | A | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.45-2064A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911108 | |||||||
| chr2:113911115 | G | A | 1 | a0001c0001t0003g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.45-2057G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911115 | |||||||
| chr2:113911227 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.45-1945G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911227 | |||||||
| chr2:113911294 | G | GT | 24 | a0001c0001t0001g0280 a0001c0001t0001g0320 a0001c0001t0002g0187 others(21): Show |
24 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.45-1866dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911294 | ||||||
| chr2:113911307 | A | T | 1 | a0001c0001t0003g0082 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.45-1865A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911307 | |||||||
| chr2:113911419 | C | CT | 114 | a0001c0001t0001g0287 a0001c0001t0002g0160 a0001c0001t0003g0002 others(111): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.45-1735dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911419 | ||||||
| chr2:113911419 | C | CTT | 61 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(58): Show |
65 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-1736_45-1735dup others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911419 | ||||||
| chr2:113911419 | C | CTTT | 75 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(72): Show |
78 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.45-1737_45-1735dup others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911419 | ||||||
| chr2:113911419 | C | CTTTT | 6 | a0001c0001t0001g0259 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG01884.hp1 HG02148.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-1738_45-1735dup others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911419 | ||||||
| chr2:113911442 | C | T | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45-1730C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911442 | |||||||
| chr2:113911475 | A | C | 1 | a0001c0001t0007g0340 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.45-1697A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911475 | |||||||
| chr2:113911524 | A | G | 1 | a0001c0001t0007g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45-1648A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911524 | |||||||
| chr2:113911542 | C | A | 1 | a0001c0001t0007g0342 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.45-1630C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911542 | |||||||
| chr2:113911609 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.45-1563G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911609 | |||||||
| chr2:113911780 | A | T | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-1392A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911780 | |||||||
| chr2:113911805 | C | T | 4 | a0001c0001t0006g0223 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02109.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-1367C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911805 | |||||||
| chr2:113911822 | C | T | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.45-1350C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911822 | |||||||
| chr2:113911945 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-1227T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911945 | |||||||
| chr2:113912047 | T | G | 1 | a0001c0001t0004g0143 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.45-1125T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912047 | |||||||
| chr2:113912093 | C | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-1079C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912093 | |||||||
| chr2:113912129 | G | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0011 others(46): Show |
62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.45-1043G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912129 | |||||||
| chr2:113912147 | G | A | 296 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(293): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.45-1025G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912147 | |||||||
| chr2:113912184 | A | AT | 7 | a0001c0001t0003g0067 a0001c0001t0006g0006 a0001c0001t0006g0220 others(4): Show |
9 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-977dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113912184 | ||||||
| chr2:113912241 | A | G | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.45-931A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912241 | |||||||
| chr2:113912355 | A | T | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-817A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912355 | |||||||
| chr2:113912368 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.45-804C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912368 | |||||||
| chr2:113912446 | T | C | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-726T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912446 | |||||||
| chr2:113912469 | G | A | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-703G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912469 | |||||||
| chr2:113912889 | T | C | 3 | a0001c0001t0004g0201 a0001c0001t0004g0203 a0001c0001t0004g0204 |
3 | HG02145.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.45-283T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912889 | |||||||
| chr2:113912895 | TAGA | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-274_45-272delAA others(1): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113912895 | ||||||
| chr2:113912917 | GACCTTGA others(14): Show |
G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-252_45-232delCT others(19): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113912917 | ||||||
| chr2:113913389 | CTATT | C | 4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+163_100+166del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913389 | |||||||
| chr2:113913530 | A | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100+303A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913530 | |||||||
| chr2:113913560 | A | T | 1 | a0001c0001t0001g0312 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.100+333A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913560 | |||||||
| chr2:113913568 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100+341A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913568 | |||||||
| chr2:113913739 | G | C | 1 | a0001c0001t0007g0340 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+512G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913739 | |||||||
| chr2:113913785 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.100+558C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913785 | |||||||
| chr2:113913920 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+693G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913920 | |||||||
| chr2:113913955 | A | G | 31 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.100+728A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913955 | |||||||
| chr2:113913956 | T | G | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.100+729T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913956 | |||||||
| chr2:113914026 | C | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+799C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914026 | |||||||
| chr2:113914112 | A | AT | 351 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(348): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.100+887dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914112 | ||||||
| chr2:113914199 | A | ATAGGAAT | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.100+973_100+974ins others(7): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914199 | ||||||
| chr2:113914255 | C | G | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.100+1028C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914255 | |||||||
| chr2:113914334 | C | T | 1 | a0001c0001t0004g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100+1107C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914334 | |||||||
| chr2:113914336 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.100+1109G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914336 | |||||||
| chr2:113914340 | C | T | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+1113C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914340 | |||||||
| chr2:113914350 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+1123C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914350 | |||||||
| chr2:113914351 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100+1124G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914351 | |||||||
| chr2:113914353 | C | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+1126C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914353 | |||||||
| chr2:113914383 | C | T | 1 | a0002c0004t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100+1156C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914383 | |||||||
| chr2:113914474 | G | A | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.100+1247G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914474 | |||||||
| chr2:113914529 | C | T | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+1302C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914529 | |||||||
| chr2:113914614 | C | CA | 27 | a0001c0001t0001g0031 a0001c0001t0002g0159 a0001c0001t0003g0066 others(24): Show |
30 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+1406dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914614 | ||||||
| chr2:113914614 | C | CAA | 5 | a0001c0001t0001g0030 a0001c0001t0001g0333 a0001c0001t0001g0334 others(2): Show |
6 | HG01891.hp1 HG02559.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+1405_100+1406d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914614 | ||||||
| chr2:113914614 | CA | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(125): Show |
133 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.100+1406delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914614 | ||||||
| chr2:113914630 | A | AG | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+1403_100+1404i others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914630 | |||||||
| chr2:113914630 | A | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100+1403A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914630 | |||||||
| chr2:113914727 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.100+1500A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914727 | |||||||
| chr2:113914763 | A | C | 1 | a0001c0001t0001g0303 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.100+1536A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914763 | |||||||
| chr2:113914909 | A | T | 1 | a0001c0001t0001g0256 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.100+1682A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914909 | |||||||
| chr2:113915013 | A | T | 265 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(262): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.100+1786A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915013 | |||||||
| chr2:113915120 | G | A | 130 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(127): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.101-1764G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915120 | |||||||
| chr2:113915151 | C | T | 2 | a0001c0001t0002g0092 a0001c0001t0002g0101 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.101-1733C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915151 | |||||||
| chr2:113915194 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.101-1690A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915194 | |||||||
| chr2:113915231 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.101-1653A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915231 | |||||||
| chr2:113915307 | C | T | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0023g0217 |
3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.101-1577C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915307 | |||||||
| chr2:113915504 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.101-1380A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915504 | |||||||
| chr2:113915650 | C | T | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.101-1234C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915650 | |||||||
| chr2:113915663 | G | C | 3 | a0001c0001t0003g0009 a0001c0001t0003g0066 a0001c0001t0003g0074 |
4 | NA18945.hp1 NA18992.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-1221G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915663 | |||||||
| chr2:113915853 | A | G | 3 | a0001c0001t0002g0091 a0001c0001t0002g0100 a0001c0001t0002g0108 |
3 | NA19058.hp2 NA19078.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.101-1031A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915853 | |||||||
| chr2:113915967 | A | G | 7 | a0001c0001t0001g0199 a0001c0001t0001g0309 a0001c0001t0001g0310 others(4): Show |
8 | HG02083.hp2 NA18945.hp2 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-917A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915967 | |||||||
| chr2:113916099 | A | T | 130 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(127): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.101-785A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916099 | |||||||
| chr2:113916170 | G | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.101-714G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916170 | |||||||
| chr2:113916225 | C | T | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0023g0217 |
3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.101-659C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916225 | |||||||
| chr2:113916237 | G | A | 1 | a0001c0001t0003g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.101-647G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916237 | |||||||
| chr2:113916238 | T | TAC | 3 | a0001c0001t0003g0011 a0001c0001t0003g0067 a0001c0001t0003g0110 |
4 | NA18942.hp2 NA18997.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-644_101-643dup others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113916238 | ||||||
| chr2:113916587 | C | T | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.101-297C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916587 | |||||||
| chr2:113916591 | G | T | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.101-293G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916591 | |||||||
| chr2:113916618 | A | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.101-266A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916618 | |||||||
| chr2:113916847 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.101-37A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916847 | |||||||
| chr2:113917099 | A | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+91A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113917099 | |||||||
| chr2:113917310 | CT | C | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.225+309delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113917310 | ||||||
| chr2:113917333 | A | G | 1 | a0001c0001t0023g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.225+325A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113917333 | |||||||
| chr2:113917679 | C | T | 41 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(38): Show |
46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.225+671C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113917679 | |||||||
| chr2:113918039 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.225+1031A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918039 | |||||||
| chr2:113918272 | G | A | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.225+1264G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918272 | |||||||
| chr2:113918386 | C | CT | 20 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0187 others(17): Show |
22 | HG00639.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.225+1393dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113918386 | ||||||
| chr2:113918386 | C | CTT | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.225+1392_225+1393d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113918386 | ||||||
| chr2:113918386 | CT | C | 13 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0266 others(10): Show |
13 | HG01167.hp2 HG01943.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+1393delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113918386 | ||||||
| chr2:113918408 | A | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+1400A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918408 | |||||||
| chr2:113918558 | G | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.225+1550G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918558 | |||||||
| chr2:113918639 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.225+1631C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918639 | |||||||
| chr2:113918807 | A | G | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.225+1799A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918807 | |||||||
| chr2:113918815 | T | C | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.225+1807T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918815 | |||||||
| chr2:113919076 | A | G | 1 | a0001c0001t0002g0163 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.225+2068A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919076 | |||||||
| chr2:113919100 | G | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+2092G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919100 | |||||||
| chr2:113919153 | T | C | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.225+2145T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919153 | |||||||
| chr2:113919173 | A | G | 11 | a0001c0001t0004g0020 a0001c0001t0004g0129 a0001c0001t0004g0130 others(8): Show |
12 | HG02080.hp1 HG02523.hp2 NA18939.hp2 others(9): Show |
intron_variant | MODIFIER | c.225+2165A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919173 | |||||||
| chr2:113919393 | G | A | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.225+2385G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919393 | |||||||
| chr2:113919465 | A | C | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225+2457A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919465 | |||||||
| chr2:113919602 | A | T | 1 | a0001c0001t0006g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.225+2594A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919602 | |||||||
| chr2:113919756 | A | AT | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+2753dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113919756 | ||||||
| chr2:113919809 | A | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.225+2801A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919809 | |||||||
| chr2:113919815 | GCTCA | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+2814_225+2817d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113919815 | ||||||
| chr2:113919874 | G | A | 51 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(48): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.225+2866G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919874 | |||||||
| chr2:113919969 | G | A | 19 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(16): Show |
19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.225+2961G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919969 | |||||||
| chr2:113919982 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.225+2974G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919982 | |||||||
| chr2:113919999 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+2991C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919999 | |||||||
| chr2:113920084 | G | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+3076G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920084 | |||||||
| chr2:113920112 | T | C | 4 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0009g0128 others(1): Show |
4 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+3104T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920112 | |||||||
| chr2:113920220 | G | C | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.225+3212G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920220 | |||||||
| chr2:113920251 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.225+3243T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920251 | |||||||
| chr2:113920427 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.225+3419T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920427 | |||||||
| chr2:113920719 | T | C | 1 | a0001c0001t0006g0223 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.225+3711T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920719 | |||||||
| chr2:113920725 | T | C | 1 | a0001c0001t0004g0045 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.225+3717T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920725 | |||||||
| chr2:113920868 | T | C | 4 | a0001c0001t0005g0327 a0001c0001t0005g0331 a0001c0001t0005g0332 others(1): Show |
4 | HG00609.hp2 NA18961.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+3860T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920868 | |||||||
| chr2:113920976 | A | G | 1 | a0001c0001t0004g0196 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.225+3968A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920976 | |||||||
| chr2:113921124 | C | T | 1 | a0001c0001t0007g0342 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.225+4116C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921124 | |||||||
| chr2:113921173 | G | A | 130 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(127): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.225+4165G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921173 | |||||||
| chr2:113921318 | G | GT | 9 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0312 others(6): Show |
9 | HG01109.hp1 HG04184.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+4325dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113921318 | ||||||
| chr2:113921320 | T | C | 3 | a0001c0001t0001g0231 a0001c0001t0001g0238 a0001c0001t0001g0240 |
3 | NA18946.hp1 NA18953.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.225+4312T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921320 | |||||||
| chr2:113921408 | G | C | 1 | a0001c0001t0002g0161 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.225+4400G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921408 | |||||||
| chr2:113921603 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0035 |
2 | NA18951.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.225+4595G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921603 | |||||||
| chr2:113921721 | G | A | 1 | a0001c0001t0010g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.225+4713G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921721 | |||||||
| chr2:113921845 | C | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+4837C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921845 | |||||||
| chr2:113921847 | G | A | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+4839G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921847 | |||||||
| chr2:113921874 | A | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.225+4866A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921874 | |||||||
| chr2:113922167 | A | G | 1 | a0001c0001t0005g0335 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.225+5159A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922167 | |||||||
| chr2:113922182 | T | C | 1 | a0001c0001t0004g0202 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.226-5163T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922182 | |||||||
| chr2:113922221 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.226-5124C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922221 | |||||||
| chr2:113922314 | A | G | 1 | a0001c0001t0027g0168 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.226-5031A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922314 | |||||||
| chr2:113922410 | T | C | 5 | a0001c0001t0001g0031 a0001c0001t0015g0031 a0001c0001t0015g0336 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-4935T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922410 | |||||||
| chr2:113922418 | A | G | 35 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0043 others(32): Show |
36 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.226-4927A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922418 | |||||||
| chr2:113922463 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.226-4882C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922463 | |||||||
| chr2:113922535 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.226-4810A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922535 | |||||||
| chr2:113922640 | CT | C | 296 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(293): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.226-4702delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113922640 | ||||||
| chr2:113922668 | C | T | 1 | a0001c0001t0036g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.226-4677C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922668 | |||||||
| chr2:113922845 | T | C | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.226-4500T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922845 | |||||||
| chr2:113922892 | A | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-4453A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922892 | |||||||
| chr2:113923071 | C | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.226-4274C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923071 | |||||||
| chr2:113923181 | A | G | 1 | a0001c0001t0003g0013 | 2 | HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.226-4164A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923181 | |||||||
| chr2:113923279 | T | C | 1 | a0001c0001t0008g0116 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.226-4066T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923279 | |||||||
| chr2:113923305 | C | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.226-4040C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923305 | |||||||
| chr2:113923318 | ATTTG | A | 100 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(97): Show |
104 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.226-3995_226-3992d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113923318 | ||||||
| chr2:113923318 | ATTTGTTT others(1): Show |
A | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.226-3999_226-3992d others(10): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113923318 | ||||||
| chr2:113923350 | G | GTTT | 5 | a0001c0001t0001g0031 a0001c0001t0015g0031 a0001c0001t0015g0336 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-3992_226-3990d others(5): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113923350 | ||||||
| chr2:113923350 | G | T | 263 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(260): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.226-3995G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923350 | |||||||
| chr2:113923351 | T | A | 4 | a0001c0001t0006g0223 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02109.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-3994T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923351 | |||||||
| chr2:113923422 | C | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0114 |
2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.226-3923C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923422 | |||||||
| chr2:113923436 | T | C | 154 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(151): Show |
161 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.226-3909T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923436 | |||||||
| chr2:113923490 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.226-3855C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923490 | |||||||
| chr2:113923626 | T | C | 296 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(293): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.226-3719T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923626 | |||||||
| chr2:113923627 | G | A | 1 | a0001c0001t0005g0335 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.226-3718G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923627 | |||||||
| chr2:113923631 | G | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.226-3714G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923631 | |||||||
| chr2:113923699 | C | T | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226-3646C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923699 | |||||||
| chr2:113923732 | CT | C | 119 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.226-3599delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113923732 | ||||||
| chr2:113924001 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-3344G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924001 | |||||||
| chr2:113924004 | C | T | 1 | a0001c0001t0032g0296 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.226-3341C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924004 | |||||||
| chr2:113924027 | C | T | 2 | a0001c0001t0004g0050 a0001c0001t0004g0051 |
2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.226-3318C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924027 | |||||||
| chr2:113924054 | C | CT | 14 | a0001c0001t0003g0086 a0001c0001t0006g0006 a0001c0001t0006g0216 others(11): Show |
16 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-3274dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924054 | ||||||
| chr2:113924054 | CT | C | 121 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(118): Show |
127 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.226-3274delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924054 | ||||||
| chr2:113924054 | CTT | C | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-3275_226-3274d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924054 | ||||||
| chr2:113924081 | G | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(109): Show |
117 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.226-3264G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924081 | |||||||
| chr2:113924201 | C | T | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.226-3144C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924201 | |||||||
| chr2:113924228 | C | T | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-3117C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924228 | |||||||
| chr2:113924233 | C | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-3112C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924233 | |||||||
| chr2:113924423 | C | T | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.226-2922C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924423 | |||||||
| chr2:113924424 | G | A | 1 | a0001c0001t0009g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.226-2921G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924424 | |||||||
| chr2:113924563 | T | C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0102 others(4): Show |
9 | HG01069.hp1 HG01070.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-2782T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924563 | |||||||
| chr2:113924709 | A | T | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-2636A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924709 | |||||||
| chr2:113924840 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-2505C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924840 | |||||||
| chr2:113924887 | C | CTATT | 34 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(31): Show |
40 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.226-2432_226-2429d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924887 | ||||||
| chr2:113924887 | C | CTATTTAT others(5): Show |
1 | a0001c0001t0002g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.226-2440_226-2429d others(14): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924887 | ||||||
| chr2:113924887 | CTATT | C | 129 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(126): Show |
134 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.226-2432_226-2429d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924887 | ||||||
| chr2:113925127 | C | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-2218C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925127 | |||||||
| chr2:113925194 | C | CT | 10 | a0001c0001t0002g0105 a0001c0001t0002g0177 a0001c0001t0002g0187 others(7): Show |
10 | HG01361.hp2 HG02145.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.226-2133dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113925194 | ||||||
| chr2:113925194 | C | CTT | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.226-2134_226-2133d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113925194 | ||||||
| chr2:113925194 | CT | C | 121 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(118): Show |
127 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.226-2133delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113925194 | ||||||
| chr2:113925195 | T | C | 11 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(8): Show |
13 | HG00639.hp1 HG00738.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.226-2150T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925195 | |||||||
| chr2:113925303 | C | T | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-2042C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925303 | |||||||
| chr2:113925451 | C | T | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226-1894C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925451 | |||||||
| chr2:113925485 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0285 others(6): Show |
10 | HG02015.hp1 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-1860C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925485 | |||||||
| chr2:113925513 | A | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-1832A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925513 | |||||||
| chr2:113925559 | A | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.226-1786A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925559 | |||||||
| chr2:113925672 | A | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.226-1673A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925672 | |||||||
| chr2:113925728 | C | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-1617C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925728 | |||||||
| chr2:113925731 | A | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226-1614A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925731 | |||||||
| chr2:113925741 | G | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.226-1604G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925741 | |||||||
| chr2:113925937 | C | T | 79 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(76): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.226-1408C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925937 | |||||||
| chr2:113925938 | G | A | 5 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0220 others(2): Show |
7 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-1407G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925938 | |||||||
| chr2:113926233 | C | T | 112 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(109): Show |
117 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.226-1112C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926233 | |||||||
| chr2:113926453 | A | C | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-892A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926453 | |||||||
| chr2:113926548 | A | G | 4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-797A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926548 | |||||||
| chr2:113926729 | A | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.226-616A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926729 | |||||||
| chr2:113926774 | G | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.226-571G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926774 | |||||||
| chr2:113926786 | A | G | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-559A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926786 | |||||||
| chr2:113926894 | C | G | 4 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0009g0128 others(1): Show |
4 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-451C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926894 | |||||||
| chr2:113926895 | AATT | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0011 others(46): Show |
62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.226-446_226-444del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113926895 | ||||||
| chr2:113926937 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-408G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926937 | |||||||
| chr2:113927148 | CATCT | C | 5 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0058 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-196_226-193del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113927148 | |||||||
| chr2:113927173 | A | T | 1 | a0001c0001t0023g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-172A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113927173 | |||||||
| chr2:113927271 | T | C | 51 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(48): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.226-74T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113927271 | |||||||
| chr2:113927535 | T | C | 1 | a0001c0001t0002g0123 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.336+80T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927535 | |||||||
| chr2:113927680 | A | T | 1 | a0001c0001t0001g0302 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.336+225A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927680 | |||||||
| chr2:113927699 | A | C | 3 | a0001c0001t0006g0225 a0001c0001t0006g0226 a0002c0004t0006g0224 |
3 | HG02109.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.336+244A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927699 | |||||||
| chr2:113927699 | A | T | 1 | a0001c0001t0006g0223 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.336+244A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927699 | |||||||
| chr2:113927798 | A | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.336+343A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927798 | |||||||
| chr2:113927832 | A | G | 1 | a0001c0001t0003g0071 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.336+377A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927832 | |||||||
| chr2:113928026 | AT | A | 19 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(16): Show |
19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.336+581delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113928026 | ||||||
| chr2:113928044 | C | A | 302 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(299): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.336+589C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928044 | |||||||
| chr2:113928133 | A | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.336+678A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928133 | |||||||
| chr2:113928141 | A | G | 2 | a0001c0001t0004g0048 a0001c0001t0004g0052 |
2 | HG00544.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.336+686A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928141 | |||||||
| chr2:113928513 | GGGTTT | G | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.336+1061_336+1065d others(7): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113928513 | ||||||
| chr2:113928703 | AT | A | 347 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(344): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.336+1260delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113928703 | ||||||
| chr2:113928773 | A | G | 1 | a0001c0001t0004g0146 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.336+1318A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928773 | |||||||
| chr2:113928857 | T | C | 3 | a0001c0001t0004g0201 a0001c0001t0004g0203 a0001c0001t0004g0204 |
3 | HG02145.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.336+1402T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928857 | |||||||
| chr2:113928879 | G | A | 1 | a0001c0001t0005g0331 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.336+1424G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928879 | |||||||
| chr2:113928884 | C | T | 1 | a0001c0001t0005g0332 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.336+1429C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928884 | |||||||
| chr2:113928946 | G | A | 4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.336+1491G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928946 | |||||||
| chr2:113928954 | A | G | 4 | a0001c0001t0004g0201 a0001c0001t0004g0202 a0001c0001t0004g0203 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+1499A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928954 | |||||||
| chr2:113929108 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0038 |
2 | NA18955.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.336+1653G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929108 | |||||||
| chr2:113929113 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.336+1658A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929113 | |||||||
| chr2:113929130 | G | GT | 116 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(113): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.336+1685dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113929130 | ||||||
| chr2:113929130 | GT | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.336+1685delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113929130 | ||||||
| chr2:113929141 | G | T | 5 | a0001c0001t0017g0283 a0001c0001t0017g0284 a0001c0001t0017g0294 others(2): Show |
5 | HG04204.hp1 NA18953.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+1686G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929141 | |||||||
| chr2:113929147 | G | T | 1 | a0001c0001t0007g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.336+1692G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929147 | |||||||
| chr2:113929190 | T | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.336+1735T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929190 | |||||||
| chr2:113929192 | G | A | 1 | a0001c0001t0007g0342 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.336+1737G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929192 | |||||||
| chr2:113929289 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.336+1834C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929289 | |||||||
| chr2:113929359 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.336+1904T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929359 | |||||||
| chr2:113929540 | G | T | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.337-1761G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929540 | |||||||
| chr2:113929541 | C | T | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.337-1760C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929541 | |||||||
| chr2:113929551 | G | C | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.337-1750G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929551 | |||||||
| chr2:113929641 | G | A | 6 | a0001c0001t0002g0169 a0001c0001t0002g0182 a0001c0001t0002g0183 others(3): Show |
6 | HG00733.hp2 HG01069.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-1660G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929641 | |||||||
| chr2:113929751 | A | G | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.337-1550A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929751 | |||||||
| chr2:113929826 | G | A | 1 | a0001c0001t0008g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.337-1475G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929826 | |||||||
| chr2:113929861 | TA | T | 5 | a0001c0001t0002g0021 a0001c0001t0002g0164 a0001c0001t0002g0176 others(2): Show |
6 | HG01361.hp1 HG01433.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-1439delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929861 | |||||||
| chr2:113929906 | T | C | 27 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(24): Show |
29 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.337-1395T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929906 | |||||||
| chr2:113929924 | C | T | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.337-1377C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929924 | |||||||
| chr2:113929938 | C | T | 1 | a0001c0001t0004g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.337-1363C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929938 | |||||||
| chr2:113930004 | G | A | 351 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(348): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.337-1297G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930004 | |||||||
| chr2:113930028 | T | C | 2 | a0001c0001t0009g0125 a0001c0001t0009g0155 |
2 | HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.337-1273T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930028 | |||||||
| chr2:113930325 | A | T | 6 | a0001c0001t0010g0022 a0001c0001t0010g0192 a0001c0001t0010g0193 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-976A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930325 | |||||||
| chr2:113930504 | AT | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.337-792delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113930504 | ||||||
| chr2:113930578 | C | T | 10 | a0001c0001t0009g0008 a0001c0001t0009g0062 a0001c0001t0009g0063 others(7): Show |
11 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.337-723C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930578 | |||||||
| chr2:113930798 | A | C | 1 | a0001c0001t0009g0125 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.337-503A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930798 | |||||||
| chr2:113930800 | A | G | 2 | a0001c0001t0006g0225 a0001c0001t0006g0226 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.337-501A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930800 | |||||||
| chr2:113930923 | A | G | 1 | a0001c0001t0001g0319 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.337-378A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930923 | |||||||
| chr2:113930961 | A | G | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0023g0217 |
3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.337-340A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930961 | |||||||
| chr2:113931090 | A | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(13): Show |
17 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.337-211A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113931090 | |||||||
| chr2:113931139 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.337-162C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113931139 | |||||||
| chr2:113931470 | C | CT | 134 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(131): Show |
141 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.432+87dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113931470 | ||||||
| chr2:113931906 | C | T | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.432+510C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113931906 | |||||||
| chr2:113931969 | C | A | 1 | a0001c0001t0010g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.432+573C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113931969 | |||||||
| chr2:113931979 | T | A | 1 | a0001c0001t0011g0286 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.432+583T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113931979 | |||||||
| chr2:113932034 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.432+638T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932034 | |||||||
| chr2:113932124 | C | T | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.432+728C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932124 | |||||||
| chr2:113932292 | T | C | 3 | a0001c0001t0009g0008 a0001c0001t0009g0062 a0001c0001t0009g0109 |
4 | HG02257.hp1 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+896T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932292 | |||||||
| chr2:113932311 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.432+915G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932311 | |||||||
| chr2:113932402 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.432+1006A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932402 | |||||||
| chr2:113932432 | A | G | 12 | a0001c0001t0004g0140 a0001c0001t0007g0207 a0001c0001t0007g0208 others(9): Show |
12 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.432+1036A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932432 | |||||||
| chr2:113932469 | C | T | 1 | a0001c0001t0005g0328 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.432+1073C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932469 | |||||||
| chr2:113932498 | G | A | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.432+1102G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932498 | |||||||
| chr2:113932645 | C | T | 1 | a0001c0001t0009g0125 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.432+1249C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932645 | |||||||
| chr2:113932696 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0015g0031 a0001c0001t0015g0336 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+1300G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932696 | |||||||
| chr2:113932701 | T | C | 1 | a0001c0001t0035g0347 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.432+1305T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932701 | |||||||
| chr2:113932804 | T | C | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.432+1408T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932804 | |||||||
| chr2:113932807 | T | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.432+1411T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932807 | |||||||
| chr2:113932833 | G | A | 4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+1437G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932833 | |||||||
| chr2:113933079 | G | A | 44 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(41): Show |
49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.433-1200G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933079 | |||||||
| chr2:113933124 | C | T | 5 | a0001c0001t0005g0029 a0001c0001t0005g0322 a0001c0001t0005g0328 others(2): Show |
6 | HG02145.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-1155C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933124 | |||||||
| chr2:113933154 | T | C | 4 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0009g0128 others(1): Show |
4 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1125T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933154 | |||||||
| chr2:113933165 | C | T | 1 | a0001c0001t0003g0112 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.433-1114C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933165 | |||||||
| chr2:113933171 | C | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.433-1108C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933171 | |||||||
| chr2:113933365 | C | T | 49 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0011 others(46): Show |
62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.433-914C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933365 | |||||||
| chr2:113933366 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.433-913G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933366 | |||||||
| chr2:113933521 | AAAAG | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.433-755_433-752del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933521 | ||||||
| chr2:113933650 | TAAG | T | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-628_433-626del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933650 | |||||||
| chr2:113933677 | A | AT | 67 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(64): Show |
71 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.433-582dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | ||||||
| chr2:113933677 | A | ATT | 60 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(57): Show |
62 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.433-583_433-582dup others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | ||||||
| chr2:113933677 | A | ATTT | 6 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0253 others(3): Show |
6 | HG03453.hp2 NA18943.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.433-584_433-582dup others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | ||||||
| chr2:113933677 | A | ATTTT | 19 | a0001c0001t0006g0216 a0001c0001t0006g0218 a0001c0001t0006g0219 others(16): Show |
19 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.433-585_433-582dup others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | ||||||
| chr2:113933677 | A | ATTTTT | 9 | a0001c0001t0006g0006 a0001c0001t0006g0222 a0001c0001t0006g0223 others(6): Show |
11 | HG00639.hp1 HG00738.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-586_433-582dup others(5): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | ||||||
| chr2:113933677 | AT | A | 10 | a0001c0001t0002g0102 a0001c0001t0003g0119 a0001c0001t0004g0138 others(7): Show |
10 | HG01070.hp1 HG01884.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-582delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | ||||||
| chr2:113933714 | C | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0102 others(4): Show |
9 | HG01069.hp1 HG01070.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-565C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933714 | |||||||
| chr2:113933765 | C | T | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-514C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933765 | |||||||
| chr2:113933870 | C | T | 1 | a0001c0001t0010g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.433-409C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933870 | |||||||
| chr2:113933881 | C | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.433-398C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933881 | |||||||
| chr2:113933932 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-347G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933932 | |||||||
| chr2:113934029 | A | G | 1 | a0001c0001t0015g0336 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433-250A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113934029 | |||||||
| chr2:113934232 | G | GT | 61 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(58): Show |
66 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.433-35dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113934232 | ||||||
| chr2:113934254 | C | T | 1 | a0001c0001t0003g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.433-25C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113934254 | |||||||
| chr2:113934419 | T | C | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+33T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934419 | |||||||
| chr2:113934420 | G | T | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+34G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934420 | |||||||
| chr2:113934422 | A | T | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+36A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934422 | |||||||
| chr2:113934424 | T | C | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+38T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934424 | |||||||
| chr2:113934427 | C | G | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+41C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934427 | |||||||
| chr2:113934428 | A | T | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+42A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934428 | |||||||
| chr2:113934429 | C | G | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+43C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934429 | |||||||
| chr2:113934432 | C | G | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+46C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934432 | |||||||
| chr2:113934435 | G | T | 1 | a0001c0001t0003g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+49G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934435 | |||||||
| chr2:113934583 | G | A | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.540+197G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934583 | |||||||
| chr2:113934658 | G | A | 1 | a0001c0001t0005g0325 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.540+272G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934658 | |||||||
| chr2:113934960 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.540+574A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934960 | |||||||
| chr2:113935010 | A | T | 1 | a0001c0001t0007g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.540+624A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935010 | |||||||
| chr2:113935017 | G | A | 55 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.540+631G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935017 | |||||||
| chr2:113935035 | C | CT | 51 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(48): Show |
54 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.540+663dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113935035 | ||||||
| chr2:113935153 | C | T | 1 | a0001c0001t0009g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.540+767C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935153 | |||||||
| chr2:113935237 | C | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.540+851C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935237 | |||||||
| chr2:113935249 | G | GT | 112 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(109): Show |
117 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.540+864dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113935249 | ||||||
| chr2:113935254 | G | T | 1 | a0001c0001t0034g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.540+868G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935254 | |||||||
| chr2:113935455 | A | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.540+1069A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935455 | |||||||
| chr2:113935543 | T | A | 1 | a0001c0001t0009g0125 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.540+1157T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935543 | |||||||
| chr2:113935564 | T | C | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.540+1178T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935564 | |||||||
| chr2:113935698 | A | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.540+1312A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935698 | |||||||
| chr2:113935749 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+1363G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935749 | |||||||
| chr2:113935941 | A | C | 10 | a0001c0001t0005g0321 a0001c0001t0005g0323 a0001c0001t0005g0324 others(7): Show |
10 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.540+1555A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935941 | |||||||
| chr2:113936022 | G | A | 1 | a0001c0001t0002g0016 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.540+1636G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936022 | |||||||
| chr2:113936032 | C | T | 2 | a0001c0001t0006g0219 a0001c0001t0023g0217 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.540+1646C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936032 | |||||||
| chr2:113936209 | C | G | 1 | a0001c0001t0004g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.540+1823C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936209 | |||||||
| chr2:113936302 | C | CA | 52 | a0001c0001t0002g0103 a0001c0001t0002g0182 a0001c0001t0002g0183 others(49): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.540+1938dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | ||||||
| chr2:113936302 | C | CAA | 19 | a0001c0001t0002g0040 a0001c0001t0002g0187 a0001c0001t0004g0047 others(16): Show |
19 | HG01256.hp1 HG02056.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.540+1937_540+1938d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | ||||||
| chr2:113936302 | C | CAAA | 13 | a0001c0001t0004g0201 a0001c0001t0007g0207 a0001c0001t0007g0212 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+1936_540+1938d others(5): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | ||||||
| chr2:113936302 | C | CAAAA | 6 | a0001c0001t0010g0022 a0001c0001t0010g0192 a0001c0001t0010g0193 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+1935_540+1938d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | ||||||
| chr2:113936302 | CA | C | 51 | a0001c0001t0001g0031 a0001c0001t0001g0230 a0001c0001t0001g0232 others(48): Show |
53 | HG00639.hp2 HG01106.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.540+1938delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | ||||||
| chr2:113936302 | CAA | C | 108 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(105): Show |
114 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.540+1937_540+1938d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | ||||||
| chr2:113936302 | CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+1931_540+1938d others(10): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | ||||||
| chr2:113936338 | G | GT | 4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1953dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936338 | ||||||
| chr2:113936349 | T | G | 302 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(299): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.540+1963T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936349 | |||||||
| chr2:113936546 | A | G | 10 | a0001c0001t0005g0321 a0001c0001t0005g0323 a0001c0001t0005g0324 others(7): Show |
10 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.540+2160A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936546 | |||||||
| chr2:113936628 | A | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.540+2242A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936628 | |||||||
| chr2:113936632 | T | C | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+2246T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936632 | |||||||
| chr2:113936737 | G | T | 5 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0220 others(2): Show |
7 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+2351G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936737 | |||||||
| chr2:113936871 | A | G | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540+2485A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936871 | |||||||
| chr2:113936980 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.540+2594A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936980 | |||||||
| chr2:113937087 | T | G | 2 | a0001c0001t0003g0012 a0001c0001t0003g0088 |
3 | NA18962.hp2 NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.540+2701T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937087 | |||||||
| chr2:113937253 | A | G | 221 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(218): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.541-2706A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937253 | |||||||
| chr2:113937350 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.541-2609C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937350 | |||||||
| chr2:113937479 | C | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.541-2480C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937479 | |||||||
| chr2:113937599 | G | A | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.541-2360G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937599 | |||||||
| chr2:113937810 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.541-2149G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937810 | |||||||
| chr2:113937820 | A | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.541-2139A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937820 | |||||||
| chr2:113937991 | A | G | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.541-1968A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937991 | |||||||
| chr2:113937998 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-1961C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937998 | |||||||
| chr2:113938320 | C | T | 4 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-1639C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113938320 | |||||||
| chr2:113938323 | TA | T | 6 | a0001c0001t0010g0022 a0001c0001t0010g0192 a0001c0001t0010g0193 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-1634delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113938323 | ||||||
| chr2:113938340 | C | T | 2 | a0001c0001t0010g0192 a0001c0001t0010g0193 |
2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.541-1619C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113938340 | |||||||
| chr2:113938358 | T | C | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.541-1601T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113938358 | |||||||
| chr2:113938410 | CTTTATAA others(3): Show |
C | 3 | a0001c0001t0001g0239 a0001c0001t0001g0254 a0001c0001t0001g0261 |
3 | HG02723.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.541-1544_541-1535d others(12): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113938410 | ||||||
| chr2:113938952 | ATTTG | A | 4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-1003_541-1000d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113938952 | ||||||
| chr2:113939029 | C | CT | 11 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(8): Show |
13 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-918dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113939029 | ||||||
| chr2:113939141 | A | C | 1 | a0001c0001t0001g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.541-818A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939141 | |||||||
| chr2:113939149 | G | A | 65 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(62): Show |
67 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.541-810G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939149 | |||||||
| chr2:113939273 | C | A | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.541-686C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939273 | |||||||
| chr2:113939273 | C | T | 2 | a0001c0001t0004g0151 a0002c0004t0006g0224 |
2 | HG02738.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.541-686C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939273 | |||||||
| chr2:113939321 | C | T | 1 | a0001c0001t0004g0196 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.541-638C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939321 | |||||||
| chr2:113939455 | C | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0272 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.541-504C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939455 | |||||||
| chr2:113939560 | G | T | 1 | a0001c0001t0001g0303 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.541-399G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939560 | |||||||
| chr2:113939669 | T | C | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.541-290T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939669 | |||||||
| chr2:113939788 | C | G | 55 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.541-171C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939788 | |||||||
| chr2:113939939 | A | G | 6 | a0001c0001t0004g0001 a0001c0001t0004g0134 a0001c0001t0004g0135 others(3): Show |
10 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-20A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939939 | |||||||
| chr2:113940407 | AT | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+306delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940407 | |||||||
| chr2:113940761 | G | T | 1 | a0002c0004t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.684+659G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940761 | |||||||
| chr2:113940820 | A | AT | 66 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(63): Show |
70 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.684+733dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 113940820 | ||||||
| chr2:113940820 | AT | A | 18 | a0001c0001t0002g0173 a0001c0001t0007g0207 a0001c0001t0007g0208 others(15): Show |
18 | HG01243.hp1 HG01952.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.684+733delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 113940820 | ||||||
| chr2:113940892 | C | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.684+790C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940892 | |||||||
| chr2:113940932 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.684+830C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940932 | |||||||
| chr2:113940935 | G | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+833G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940935 | |||||||
| chr2:113940994 | G | A | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+892G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940994 | |||||||
| chr2:113941065 | C | T | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.684+963C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941065 | |||||||
| chr2:113941114 | T | C | 19 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(16): Show |
19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+1012T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941114 | |||||||
| chr2:113941344 | T | C | 1 | a0001c0001t0007g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.685-842T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941344 | |||||||
| chr2:113941402 | A | G | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.685-784A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941402 | |||||||
| chr2:113941414 | A | G | 31 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.685-772A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941414 | |||||||
| chr2:113941691 | G | A | 5 | a0001c0001t0005g0321 a0001c0001t0005g0323 a0001c0001t0005g0324 others(2): Show |
5 | HG01167.hp1 HG01981.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-495G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941691 | |||||||
| chr2:113942083 | GT | G | 24 | a0001c0001t0005g0321 a0001c0001t0005g0323 a0001c0001t0005g0324 others(21): Show |
26 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.685-91delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 113942083 | ||||||
| chr2:113942363 | A | AT | 11 | a0001c0001t0009g0008 a0001c0001t0009g0062 a0001c0001t0009g0063 others(8): Show |
12 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.858+12dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113942363 | ||||||
| chr2:113942453 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.858+94G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113942453 | |||||||
| chr2:113942470 | GTTT | G | 4 | a0001c0001t0004g0201 a0001c0001t0004g0202 a0001c0001t0004g0203 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+114_858+116del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113942470 | ||||||
| chr2:113942478 | GA | G | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.858+123delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113942478 | ||||||
| chr2:113942600 | A | T | 1 | a0001c0001t0003g0114 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.858+241A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113942600 | |||||||
| chr2:113943080 | C | T | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.858+721C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943080 | |||||||
| chr2:113943210 | A | T | 1 | a0001c0001t0004g0135 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.858+851A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943210 | |||||||
| chr2:113943275 | T | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(44): Show |
49 | HG00408.hp2 HG01099.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.858+916T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943275 | |||||||
| chr2:113943464 | A | C | 19 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(16): Show |
19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.858+1105A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943464 | |||||||
| chr2:113943565 | T | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.858+1206T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943565 | |||||||
| chr2:113943615 | A | G | 1 | a0001c0001t0006g0223 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.858+1256A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943615 | |||||||
| chr2:113943646 | A | G | 1 | a0001c0001t0005g0331 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.858+1287A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943646 | |||||||
| chr2:113943671 | G | A | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.858+1312G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943671 | |||||||
| chr2:113943770 | G | A | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.858+1411G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943770 | |||||||
| chr2:113943802 | A | G | 55 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.858+1443A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943802 | |||||||
| chr2:113943821 | C | T | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG01069.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.858+1462C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943821 | |||||||
| chr2:113943879 | G | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.858+1520G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943879 | |||||||
| chr2:113943892 | G | A | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.858+1533G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943892 | |||||||
| chr2:113943952 | C | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.858+1593C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943952 | |||||||
| chr2:113944200 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.858+1841T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944200 | |||||||
| chr2:113944376 | C | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.858+2017C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944376 | |||||||
| chr2:113944466 | G | T | 1 | a0001c0001t0004g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.858+2107G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944466 | |||||||
| chr2:113944554 | C | T | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.858+2195C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944554 | |||||||
| chr2:113944580 | C | G | 4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.858+2221C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944580 | |||||||
| chr2:113944584 | T | TA | 134 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(131): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.858+2253dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | ||||||
| chr2:113944584 | T | TAA | 25 | a0001c0001t0001g0199 a0001c0001t0001g0285 a0001c0001t0001g0288 others(22): Show |
25 | HG00438.hp1 HG01243.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.858+2252_858+2253d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | ||||||
| chr2:113944584 | T | TAAA | 6 | a0001c0001t0002g0162 a0001c0001t0002g0170 a0001c0001t0002g0173 others(3): Show |
6 | HG01106.hp1 HG01433.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.858+2251_858+2253d others(5): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | ||||||
| chr2:113944584 | TA | T | 28 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
29 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(26): Show |
intron_variant | MODIFIER | c.858+2253delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | ||||||
| chr2:113944584 | TAA | T | 54 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0228 others(51): Show |
56 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.858+2252_858+2253d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | ||||||
| chr2:113944622 | C | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.858+2263C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944622 | |||||||
| chr2:113944635 | G | A | 29 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(26): Show |
31 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.858+2276G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944635 | |||||||
| chr2:113944655 | G | A | 29 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(26): Show |
31 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.858+2296G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944655 | |||||||
| chr2:113944692 | G | A | 1 | a0001c0001t0005g0335 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.858+2333G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944692 | |||||||
| chr2:113944923 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.858+2564T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944923 | |||||||
| chr2:113945013 | C | A | 1 | a0001c0001t0002g0173 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.858+2654C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945013 | |||||||
| chr2:113945014 | C | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.858+2655C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945014 | |||||||
| chr2:113945160 | G | A | 4 | a0001c0001t0006g0223 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02109.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+2801G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945160 | |||||||
| chr2:113945227 | A | G | 221 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(218): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.858+2868A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945227 | |||||||
| chr2:113945238 | C | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.858+2879C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945238 | |||||||
| chr2:113945625 | T | G | 6 | a0001c0001t0004g0001 a0001c0001t0004g0134 a0001c0001t0004g0135 others(3): Show |
10 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.858+3266T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945625 | |||||||
| chr2:113946131 | A | G | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.858+3772A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946131 | |||||||
| chr2:113946257 | A | G | 2 | a0001c0001t0004g0048 a0001c0001t0004g0052 |
2 | HG00544.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.858+3898A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946257 | |||||||
| chr2:113946366 | G | T | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.858+4007G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946366 | |||||||
| chr2:113946389 | T | C | 1 | a0001c0001t0006g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.858+4030T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946389 | |||||||
| chr2:113946501 | A | G | 1 | a0001c0001t0006g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.858+4142A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946501 | |||||||
| chr2:113946733 | G | T | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0023g0217 |
3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.858+4374G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946733 | |||||||
| chr2:113946745 | A | G | 1 | a0001c0001t0003g0071 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.858+4386A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946745 | |||||||
| chr2:113946765 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0053 a0001c0001t0002g0158 others(28): Show |
32 | HG00438.hp1 HG01070.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.858+4406C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946765 | |||||||
| chr2:113946921 | C | A | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.859-4558C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946921 | |||||||
| chr2:113947073 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.859-4406C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947073 | |||||||
| chr2:113947090 | C | T | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.859-4389C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947090 | |||||||
| chr2:113947156 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.859-4323C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947156 | |||||||
| chr2:113947427 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.859-4052G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947427 | |||||||
| chr2:113947471 | G | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0091 a0001c0001t0002g0093 others(6): Show |
10 | HG02083.hp1 HG02165.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.859-4008G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947471 | |||||||
| chr2:113947509 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.859-3970G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947509 | |||||||
| chr2:113947517 | T | C | 1 | a0001c0001t0006g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859-3962T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947517 | |||||||
| chr2:113947572 | T | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.859-3907T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947572 | |||||||
| chr2:113947597 | C | A | 3 | a0001c0001t0004g0138 a0001c0001t0004g0140 a0001c0001t0004g0141 |
3 | HG02523.hp2 NA18989.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.859-3882C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947597 | |||||||
| chr2:113947633 | A | T | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.859-3846A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947633 | |||||||
| chr2:113947669 | A | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.859-3810A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947669 | |||||||
| chr2:113947853 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.859-3626A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947853 | |||||||
| chr2:113947897 | G | A | 6 | a0001c0001t0007g0340 a0001c0001t0007g0341 a0001c0001t0007g0342 others(3): Show |
6 | HG02280.hp2 HG02723.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-3582G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947897 | |||||||
| chr2:113947958 | G | C | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.859-3521G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947958 | |||||||
| chr2:113948092 | T | C | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.859-3387T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948092 | |||||||
| chr2:113948118 | T | G | 1 | a0001c0001t0007g0342 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.859-3361T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948118 | |||||||
| chr2:113948153 | G | A | 1 | a0001c0001t0015g0336 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.859-3326G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948153 | |||||||
| chr2:113948187 | G | T | 7 | a0001c0001t0004g0019 a0001c0001t0004g0133 a0001c0001t0004g0137 others(4): Show |
7 | NA18747.hp2 NA18941.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.859-3292G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948187 | |||||||
| chr2:113948228 | C | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.859-3251C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948228 | |||||||
| chr2:113948376 | C | T | 5 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0058 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-3103C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948376 | |||||||
| chr2:113948461 | G | A | 302 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(299): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.859-3018G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948461 | |||||||
| chr2:113948959 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.859-2520T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948959 | |||||||
| chr2:113948973 | C | CTACTGTC others(3946): Show |
1 | a0001c0001t0001g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3955): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3947): Show |
1 | a0001c0001t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3956): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3943): Show |
2 | a0001c0001t0001g0237 a0001c0001t0001g0318 |
2 | HG02015.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3945): Show |
6 | a0001c0001t0001g0248 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
6 | HG00408.hp2 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3947): Show |
1 | a0001c0001t0001g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3956): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3946): Show |
1 | a0001c0001t0001g0261 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3955): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3945): Show |
1 | a0001c0001t0001g0239 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3944): Show |
9 | a0001c0001t0001g0024 a0001c0001t0001g0227 a0001c0001t0001g0233 others(6): Show |
10 | HG02074.hp1 HG02148.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3953): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3945): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0246 |
2 | HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3945): Show |
1 | a0001c0001t0001g0263 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3944): Show |
1 | a0001c0001t0001g0243 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3953): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3943): Show |
26 | a0001c0001t0001g0007 a0001c0001t0001g0228 a0001c0001t0001g0231 others(23): Show |
27 | HG01099.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3943): Show |
1 | a0001c0001t0001g0249 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3943): Show |
1 | a0001c0001t0001g0320 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3942): Show |
3 | a0001c0001t0001g0230 a0001c0001t0001g0271 a0001c0001t0001g0273 |
3 | HG01168.hp1 HG02080.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3951): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3944): Show |
1 | a0001c0001t0001g0229 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3953): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3946): Show |
1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3955): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3945): Show |
1 | a0001c0001t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3939): Show |
2 | a0001c0001t0001g0023 a0001c0001t0037g0023 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3948): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3947): Show |
1 | a0001c0001t0001g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3956): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3964): Show |
1 | a0001c0001t0001g0298 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3973): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3968): Show |
3 | a0001c0001t0001g0026 a0001c0001t0001g0287 a0001c0001t0001g0299 |
4 | HG00408.hp1 HG02040.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3977): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3964): Show |
2 | a0001c0001t0001g0289 a0001c0001t0001g0295 |
2 | HG02071.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3973): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3962): Show |
12 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0035 others(9): Show |
13 | HG02015.hp1 HG02074.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3962): Show |
1 | a0001c0001t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3964): Show |
1 | a0001c0001t0001g0313 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3973): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3960): Show |
2 | a0001c0001t0017g0294 a0001c0001t0038g0292 |
2 | HG04204.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3969): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3962): Show |
20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
21 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3962): Show |
1 | a0001c0001t0001g0036 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3962): Show |
1 | a0001c0001t0001g0302 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3963): Show |
1 | a0001c0001t0001g0199 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3972): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3952): Show |
1 | a0001c0001t0007g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3961): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3960): Show |
1 | a0001c0001t0001g0317 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3969): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3962): Show |
1 | a0001c0001t0001g0309 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3950): Show |
3 | a0001c0001t0013g0211 a0001c0001t0013g0214 a0001c0001t0013g0215 |
3 | HG01243.hp1 HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3959): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3949): Show |
1 | a0001c0001t0013g0205 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3958): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3948): Show |
1 | a0001c0001t0013g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3957): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3950): Show |
1 | a0001c0001t0007g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3959): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3950): Show |
1 | a0001c0001t0007g0212 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3959): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3949): Show |
1 | a0001c0001t0007g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3958): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3949): Show |
1 | a0001c0001t0007g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3958): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3948): Show |
2 | a0001c0001t0007g0207 a0001c0001t0007g0208 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3957): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3948): Show |
4 | a0001c0001t0007g0340 a0001c0001t0007g0342 a0001c0001t0007g0344 others(1): Show |
4 | HG02280.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3957): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3941): Show |
1 | a0001c0001t0007g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3950): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3952): Show |
4 | a0001c0001t0005g0029 a0001c0001t0005g0328 a0001c0001t0005g0329 others(1): Show |
5 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3961): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3952): Show |
2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3961): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3952): Show |
1 | a0001c0001t0001g0030 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3961): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3963): Show |
1 | a0001c0001t0001g0305 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3972): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3963): Show |
1 | a0001c0001t0032g0296 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3972): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3953): Show |
2 | a0001c0001t0005g0332 a0001c0001t0005g0339 |
2 | NA18961.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3956): Show |
1 | a0001c0001t0006g0223 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3965): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3954): Show |
1 | a0002c0004t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3963): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3953): Show |
6 | a0001c0001t0005g0321 a0001c0001t0005g0323 a0001c0001t0005g0325 others(3): Show |
6 | HG01167.hp1 HG01981.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3954): Show |
1 | a0001c0001t0005g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3963): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3953): Show |
1 | a0001c0001t0005g0327 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3939): Show |
2 | a0001c0001t0004g0203 a0001c0001t0004g0204 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3948): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3953): Show |
2 | a0001c0001t0006g0225 a0001c0001t0006g0226 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3954): Show |
1 | a0001c0001t0006g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3963): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3955): Show |
4 | a0001c0001t0006g0006 a0001c0001t0006g0220 a0001c0001t0006g0221 others(1): Show |
6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3964): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3945): Show |
1 | a0001c0001t0009g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3939): Show |
36 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(33): Show |
41 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3948): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3943): Show |
8 | a0001c0001t0009g0008 a0001c0001t0009g0062 a0001c0001t0009g0063 others(5): Show |
9 | HG01243.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3943): Show |
1 | a0001c0001t0009g0125 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3955): Show |
1 | a0001c0001t0006g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3964): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3953): Show |
1 | a0001c0001t0006g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3931): Show |
2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3940): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3940): Show |
1 | a0001c0001t0004g0143 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3949): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3940): Show |
1 | a0001c0001t0004g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3949): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3956): Show |
1 | a0001c0001t0005g0324 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3965): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3940): Show |
2 | a0001c0001t0004g0129 a0001c0001t0004g0201 |
2 | HG02145.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3949): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3940): Show |
3 | a0001c0001t0004g0050 a0001c0001t0004g0052 a0001c0001t0036g0041 |
3 | HG00544.hp2 HG02027.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3949): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3956): Show |
1 | a0001c0001t0023g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3965): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948973 | C | CTACTGTC others(3951): Show |
5 | a0001c0001t0001g0031 a0001c0001t0015g0031 a0001c0001t0015g0336 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3960): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | |||||||
| chr2:113948974 | A | T | 221 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(218): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.859-2505A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948974 | |||||||
| chr2:113949051 | C | T | 54 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(51): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.859-2428C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949051 | |||||||
| chr2:113949089 | G | C | 3 | a0001c0001t0001g0241 a0001c0001t0001g0263 a0001c0001t0001g0276 |
3 | NA18984.hp2 NA18991.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.859-2390G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949089 | |||||||
| chr2:113949377 | C | CA | 71 | a0001c0001t0002g0091 a0001c0001t0002g0182 a0001c0001t0002g0187 others(68): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.859-2086dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113949377 | ||||||
| chr2:113949377 | CA | C | 11 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0069 others(8): Show |
13 | HG02965.hp2 NA18940.hp1 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.859-2086delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113949377 | ||||||
| chr2:113949393 | A | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0265 |
2 | HG01943.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.859-2086A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949393 | |||||||
| chr2:113949393 | AG | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.859-2085delG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949393 | |||||||
| chr2:113949394 | G | A | 4 | a0001c0001t0001g0199 a0001c0001t0001g0230 a0001c0001t0001g0251 others(1): Show |
4 | HG01943.hp1 HG02080.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-2085G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949394 | |||||||
| chr2:113949394 | G | GA | 131 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(128): Show |
138 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.859-2074dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113949394 | ||||||
| chr2:113949397 | A | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.859-2082A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949397 | |||||||
| chr2:113949406 | G | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.859-2073G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949406 | |||||||
| chr2:113949474 | A | T | 302 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(299): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.859-2005A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949474 | |||||||
| chr2:113949476 | GTC | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.859-1998_859-1997d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113949476 | ||||||
| chr2:113949484 | A | G | 112 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(109): Show |
117 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.859-1995A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949484 | |||||||
| chr2:113949668 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.859-1811C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949668 | |||||||
| chr2:113949810 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0333 a0001c0001t0001g0334 |
4 | HG01891.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-1669G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949810 | |||||||
| chr2:113949970 | G | A | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.859-1509G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949970 | |||||||
| chr2:113949977 | T | A | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.859-1502T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949977 | |||||||
| chr2:113950023 | T | C | 1 | a0001c0001t0011g0301 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.859-1456T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950023 | |||||||
| chr2:113950118 | T | C | 5 | a0001c0001t0001g0031 a0001c0001t0015g0031 a0001c0001t0015g0336 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-1361T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950118 | |||||||
| chr2:113950144 | T | C | 75 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(72): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.859-1335T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950144 | |||||||
| chr2:113950444 | C | T | 75 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(72): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.859-1035C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950444 | |||||||
| chr2:113950489 | C | T | 45 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(42): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.859-990C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950489 | |||||||
| chr2:113950530 | G | T | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.859-949G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950530 | |||||||
| chr2:113950716 | T | C | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.859-763T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950716 | |||||||
| chr2:113950826 | AAAAG | A | 69 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.859-647_859-644del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113950826 | ||||||
| chr2:113950833 | A | G | 1 | a0001c0001t0032g0296 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.859-646A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950833 | |||||||
| chr2:113950857 | C | T | 5 | a0001c0001t0005g0029 a0001c0001t0005g0322 a0001c0001t0005g0328 others(2): Show |
6 | HG02145.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-622C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950857 | |||||||
| chr2:113950861 | G | A | 1 | a0001c0001t0004g0141 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.859-618G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950861 | |||||||
| chr2:113950954 | C | T | 2 | a0001c0001t0004g0145 a0001c0001t0007g0342 |
2 | HG02040.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.859-525C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950954 | |||||||
| chr2:113951017 | C | T | 31 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(28): Show |
33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.859-462C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951017 | |||||||
| chr2:113951021 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0245 a0001c0001t0001g0319 |
4 | NA18944.hp1 NA19057.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-458A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951021 | |||||||
| chr2:113951021 | A | T | 5 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG01099.hp1 HG01167.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-458A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951021 | |||||||
| chr2:113951031 | C | A | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.859-448C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951031 | |||||||
| chr2:113951151 | C | T | 296 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(293): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.859-328C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951151 | |||||||
| chr2:113951358 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.859-121A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951358 | |||||||
| chr2:113951594 | T | C | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0023g0217 |
3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.951+23T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 9/11 | chr2 | 113951594 | |||||||
| chr2:113951899 | A | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.1077+54A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113951899 | |||||||
| chr2:113951963 | A | G | 1 | a0001c0001t0009g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1077+118A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113951963 | |||||||
| chr2:113952011 | AT | A | 8 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(5): Show |
10 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+169delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113952011 | ||||||
| chr2:113952087 | A | T | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.1077+242A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952087 | |||||||
| chr2:113952104 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0015g0031 a0001c0001t0015g0336 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+259A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952104 | |||||||
| chr2:113952255 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1077+410C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952255 | |||||||
| chr2:113952290 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0035 |
2 | NA18951.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1077+445C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952290 | |||||||
| chr2:113952448 | C | T | 1 | a0001c0001t0002g0016 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1077+603C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952448 | |||||||
| chr2:113952743 | C | A | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1077+898C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952743 | |||||||
| chr2:113952839 | C | G | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077+994C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952839 | |||||||
| chr2:113952883 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1077+1038C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952883 | |||||||
| chr2:113952941 | A | C | 2 | a0001c0001t0002g0053 a0001c0001t0002g0200 |
2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1077+1096A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952941 | |||||||
| chr2:113953066 | C | T | 1 | a0001c0001t0004g0143 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1077+1221C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953066 | |||||||
| chr2:113953284 | G | A | 8 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(5): Show |
10 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+1439G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953284 | |||||||
| chr2:113953352 | T | C | 7 | a0001c0001t0002g0095 a0001c0001t0002g0169 a0001c0001t0002g0182 others(4): Show |
7 | HG00733.hp2 HG01069.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+1507T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953352 | |||||||
| chr2:113953417 | C | T | 1 | a0001c0001t0018g0297 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1077+1572C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953417 | |||||||
| chr2:113953516 | G | A | 1 | a0001c0001t0019g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1077+1671G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953516 | |||||||
| chr2:113953533 | C | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.1077+1688C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953533 | |||||||
| chr2:113953611 | C | A | 1 | a0001c0001t0007g0212 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1077+1766C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953611 | |||||||
| chr2:113953679 | GGTGT | G | 49 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0011 others(46): Show |
62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077+1839_1077+184 others(8): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113953679 | ||||||
| chr2:113953684 | G | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0011 others(46): Show |
62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077+1839G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953684 | |||||||
| chr2:113953685 | T | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0011 others(46): Show |
62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077+1840T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953685 | |||||||
| chr2:113953686 | G | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0011 others(46): Show |
62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077+1841G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953686 | |||||||
| chr2:113953687 | T | TAC | 51 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(48): Show |
54 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1077+1857_1077+185 others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113953687 | ||||||
| chr2:113953687 | T | TACAC | 3 | a0001c0001t0017g0283 a0001c0001t0017g0284 a0001c0001t0017g0306 |
3 | NA18995.hp1 NA19055.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1077+1855_1077+185 others(8): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113953687 | ||||||
| chr2:113953736 | A | G | 1 | a0001c0001t0003g0013 | 2 | HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1078-1887A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953736 | |||||||
| chr2:113953853 | C | T | 2 | a0001c0001t0034g0346 a0001c0001t0035g0347 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1078-1770C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953853 | |||||||
| chr2:113953878 | A | G | 1 | a0002c0004t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1078-1745A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953878 | |||||||
| chr2:113953929 | T | A | 1 | a0001c0001t0001g0303 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1078-1694T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953929 | |||||||
| chr2:113953946 | T | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1078-1677T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953946 | |||||||
| chr2:113954054 | G | A | 1 | a0001c0001t0028g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1078-1569G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954054 | |||||||
| chr2:113954073 | G | A | 15 | a0001c0001t0005g0029 a0001c0001t0005g0321 a0001c0001t0005g0322 others(12): Show |
16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078-1550G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954073 | |||||||
| chr2:113954141 | G | A | 1 | a0001c0001t0006g0225 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1482G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954141 | |||||||
| chr2:113954302 | TAA | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.1078-1320_1078-131 others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954302 | |||||||
| chr2:113954333 | TG | T | 14 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(11): Show |
16 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078-1289delG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954333 | |||||||
| chr2:113954347 | A | G | 6 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0058 others(3): Show |
6 | HG01884.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-1276A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954347 | |||||||
| chr2:113954418 | A | T | 296 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(293): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1078-1205A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954418 | |||||||
| chr2:113954483 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0034g0346 a0001c0001t0035g0347 |
3 | HG03453.hp2 NA18984.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1078-1140A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954483 | |||||||
| chr2:113954581 | A | AT | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(12): Show |
16 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078-1029dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113954581 | ||||||
| chr2:113954733 | G | A | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-890G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954733 | |||||||
| chr2:113954767 | T | C | 17 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0001c0001t0007g0209 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-856T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954767 | |||||||
| chr2:113954810 | A | C | 1 | a0001c0001t0007g0340 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1078-813A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954810 | |||||||
| chr2:113955367 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1078-256A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955367 | |||||||
| chr2:113955400 | T | C | 296 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(293): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1078-223T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955400 | |||||||
| chr2:113955592 | A | G | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078-31A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955592 | |||||||
| chr2:113955609 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1078-14A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955609 | |||||||
| chr2:113955611 | G | A | 12 | a0001c0001t0006g0006 a0001c0001t0006g0216 a0001c0001t0006g0218 others(9): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078-12G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955611 | |||||||
| chr2:113955773 | C | T | 1 | a0001c0001t0007g0340 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1161+67C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113955773 | |||||||
| chr2:113955789 | C | A | 1 | a0001c0001t0002g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1161+83C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113955789 | |||||||
| chr2:113955807 | G | A | 1 | a0001c0001t0003g0118 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1161+101G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113955807 | |||||||
| chr2:113956377 | A | AT | 17 | a0001c0001t0004g0048 a0001c0001t0005g0029 a0001c0001t0005g0321 others(14): Show |
18 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.1161+687dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 113956377 | ||||||
| chr2:113956377 | AT | A | 16 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0246 others(13): Show |
16 | HG00639.hp2 HG00733.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1161+687delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 113956377 | ||||||
| chr2:113956481 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1161+775T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956481 | |||||||
| chr2:113956576 | C | G | 1 | a0001c0001t0006g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1162-784C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956576 | |||||||
| chr2:113956803 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(163): Show |
175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.1162-557T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956803 | |||||||
| chr2:113956836 | T | G | 1 | a0001c0001t0001g0258 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1162-524T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956836 | |||||||
| chr2:113956852 | T | C | 63 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(60): Show |
65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.1162-508T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956852 | |||||||
| chr2:113956866 | T | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0333 others(20): Show |
25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1162-494T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956866 | |||||||
| chr2:113957265 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1162-95T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113957265 | |||||||
| chr2:113957278 | A | G | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1162-82A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113957278 |