| geneid | 88 |
|---|---|
| ensemblid | ENSG00000077522.15 |
| hgncid | 164 |
| symbol | ACTN2 |
| name | actinin alpha 2 |
| refseq_nuc | NM_001103.4 |
| refseq_prot | NP_001094.1 |
| ensembl_nuc | ENST00000366578.6 |
| ensembl_prot | ENSP00000355537.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 236686499 |
| end | 236764631 |
| strand | + |
| ver | v1.2 |
| region | chr1:236686499-236764631 |
| region5000 | chr1:236681499-236769631 |
| regionname0 | ACTN2_chr1_236686499_236764631 |
| regionname5000 | ACTN2_chr1_236681499_236769631 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 894 | 320 | 88 | 61 | 121 | 12 | 36 | 96 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002 | 0/0 | 894 | 16 | 0 | 0 | 16 | 0 | 0 | 11 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0003 | 0/0 | 894 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0004 | 0/0 | 894 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0005 | 0/0 | 57 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0006 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0007 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0008 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2685 | 184 | 32 | 36 | 82 | 6 | 27 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0002 | 0/0 | 2685 | 64 | 18 | 9 | 28 | 4 | 5 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0003 | 0/0 | 2685 | 20 | 7 | 9 | 3 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0004 | 0/0 | 2685 | 17 | 16 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0005 | 0/0 | 2685 | 9 | 0 | 0 | 9 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0006 | 0/0 | 2685 | 6 | 2 | 0 | 3 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0007 | 0/0 | 2685 | 5 | 5 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0008 | 0/0 | 2685 | 5 | 0 | 0 | 5 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0009 | 0/0 | 2685 | 3 | 0 | 0 | 2 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0010 | 0/0 | 2685 | 3 | 1 | 2 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0011 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0012 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0013 | 0/0 | 2685 | 2 | 1 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0014 | 1/0 | 2685 | 2 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0015 | 0/0 | 2685 | 2 | 0 | 2 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0016 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0017 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0018 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0019 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0020 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0021 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0022 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0023 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0024 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0025 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0026 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0027 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0028 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0029 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0030 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0031 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0032 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| c0033 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2188 | 93 | 1 | 28 | 43 | 5 | 15 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0002 | 0/0 | 2188 | 68 | 27 | 8 | 23 | 4 | 6 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0003 | 0/0 | 2188 | 49 | 1 | 4 | 34 | 1 | 9 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0004 | 1/0 | 2188 | 45 | 18 | 1 | 24 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0005 | 0/0 | 2188 | 27 | 27 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0006 | 0/0 | 2195 | 10 | 0 | 7 | 2 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0007 | 0/0 | 2185 | 9 | 0 | 4 | 5 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0008 | 0/0 | 2195 | 5 | 2 | 0 | 2 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0009 | 0/0 | 2188 | 5 | 4 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0010 | 0/0 | 2188 | 4 | 0 | 1 | 0 | 1 | 2 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0011 | 0/0 | 2188 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0012 | 0/0 | 2188 | 3 | 0 | 2 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0013 | 0/0 | 2188 | 3 | 0 | 0 | 3 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0014 | 0/0 | 2188 | 3 | 2 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0015 | 0/0 | 2195 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0016 | 0/0 | 2195 | 2 | 0 | 2 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0017 | 0/0 | 2195 | 2 | 1 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0018 | 0/0 | 2188 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0019 | 0/0 | 2188 | 2 | 0 | 0 | 0 | 0 | 2 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0020 | 0/0 | 2195 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0021 | 0/0 | 2195 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0022 | 0/0 | 2195 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0023 | 0/0 | 2188 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0024 | 0/0 | 2188 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0025 | 0/0 | 2188 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| t0026 | 0/0 | 2188 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0333 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2685 | 184 | 32 | 36 | 82 | 6 | 27 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0002 | 0/0 | 2685 | 64 | 18 | 9 | 28 | 4 | 5 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003 | 0/0 | 2685 | 20 | 7 | 9 | 3 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0004 | 0/0 | 2685 | 17 | 16 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0006 | 0/0 | 2685 | 6 | 2 | 0 | 3 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0007 | 0/0 | 2685 | 5 | 5 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0009 | 0/0 | 2685 | 3 | 0 | 0 | 2 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0010 | 0/0 | 2685 | 3 | 1 | 2 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0011 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0013 | 0/0 | 2685 | 2 | 1 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0014 | 1/0 | 2685 | 2 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0015 | 0/0 | 2685 | 2 | 0 | 2 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0016 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0018 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0021 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0024 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0025 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0027 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0028 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0029 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0030 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0031 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002c0005 | 0/0 | 2685 | 9 | 0 | 0 | 9 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002c0008 | 0/0 | 2685 | 5 | 0 | 0 | 5 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002c0019 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002c0020 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0003c0012 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0004c0026 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0004c0032 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0005c0033 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0006c0022 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0007c0023 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0008c0017 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4872 | 87 | 1 | 26 | 42 | 4 | 13 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0002 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0003 | 0/0 | 4872 | 42 | 1 | 3 | 30 | 0 | 8 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0004 | 0/0 | 4872 | 24 | 13 | 1 | 9 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0005 | 0/0 | 4872 | 4 | 4 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0006 | 0/0 | 4879 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0009 | 0/0 | 4872 | 5 | 4 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0010 | 0/0 | 4872 | 4 | 0 | 1 | 0 | 1 | 2 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0011 | 0/0 | 4872 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0012 | 0/0 | 4872 | 3 | 0 | 2 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0014 | 0/0 | 4872 | 3 | 2 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0015 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0017 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0018 | 0/0 | 4872 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0019 | 0/0 | 4872 | 2 | 0 | 0 | 0 | 0 | 2 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0001t0025 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0002t0002 | 0/0 | 4872 | 52 | 18 | 5 | 20 | 4 | 5 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0002t0007 | 0/0 | 4869 | 9 | 0 | 4 | 5 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0002t0013 | 0/0 | 4872 | 3 | 0 | 0 | 3 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003t0001 | 0/0 | 4872 | 2 | 0 | 2 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003t0002 | 0/0 | 4872 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003t0003 | 0/0 | 4872 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003t0005 | 0/0 | 4872 | 5 | 5 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003t0006 | 0/0 | 4879 | 7 | 0 | 5 | 2 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003t0020 | 0/0 | 4879 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003t0021 | 0/0 | 4879 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0003t0022 | 0/0 | 4879 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0004t0002 | 0/0 | 4872 | 3 | 2 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0004t0005 | 0/0 | 4872 | 14 | 14 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0006t0002 | 0/0 | 4872 | 3 | 2 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0006t0008 | 0/0 | 4879 | 3 | 0 | 0 | 2 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0007t0004 | 0/0 | 4872 | 4 | 4 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0007t0015 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0009t0003 | 0/0 | 4872 | 3 | 0 | 0 | 2 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0010t0002 | 0/0 | 4872 | 3 | 1 | 2 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0011t0004 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0011t0005 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0013t0002 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0013t0023 | 0/0 | 4872 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0014t0002 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0014t0004 | 1/0 | 4872 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0015t0016 | 0/0 | 4879 | 2 | 0 | 2 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0016t0003 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0018t0006 | 0/0 | 4879 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0021t0001 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0024t0003 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0025t0006 | 0/0 | 4879 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0027t0001 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0028t0026 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0029t0005 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0030t0002 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0001c0031t0005 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002c0005t0004 | 0/0 | 4872 | 9 | 0 | 0 | 9 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002c0008t0004 | 0/0 | 4872 | 5 | 0 | 0 | 5 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002c0019t0004 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0002c0020t0002 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0003c0012t0008 | 0/0 | 4879 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0004c0026t0005 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0004c0032t0017 | 0/0 | 4879 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0005c0033t0003 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0006c0022t0001 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0007c0023t0001 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| a0008c0017t0024 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | copy fasta | chr1 | 236681499 | 236769631 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0333 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0009g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0010g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0010g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0012g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0012g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0012g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0014g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0014g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0017g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0018g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0018g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0019g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0019g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0001t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0007g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0013g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0013g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0002t0013g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0020g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0021g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0003t0022g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0004t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0006t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0006t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0006t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0006t0008g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0006t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0006t0008g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0007t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0007t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0007t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0007t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0007t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0009t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0009t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0009t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0010t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0010t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0010t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0011t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0011t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0013t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0013t0023g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0014t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0014t0004g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0015t0016g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0015t0016g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0016t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0018t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0021t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0024t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0025t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0027t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0028t0026g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0029t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0030t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0001c0031t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0005t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0008t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0008t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0008t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0008t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0008t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0019t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0002c0020t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0003c0012t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0003c0012t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0004c0026t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0004c0032t0017g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0005c0033t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0006c0022t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0007c0023t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| a0008c0017t0024g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0233 | EUR | GBR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0342 | EUR | GBR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0017 | EUR | GBR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0182 | EUR | FIN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00323 | hp1 | a0001 | c0009 | t0003 | g0012 | EUR | FIN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0214 | EUR | FIN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00639 | hp2 | a0001 | c0003 | t0006 | g0126 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00642 | hp2 | a0001 | c0002 | t0007 | g0176 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0329 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0196 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01106 | hp2 | a0001 | c0010 | t0002 | g0164 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01109 | hp1 | a0001 | c0013 | t0023 | g0095 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0152 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01168 | hp1 | a0001 | c0010 | t0002 | g0160 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01168 | hp2 | a0001 | c0015 | t0016 | g0113 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01169 | hp2 | a0001 | c0015 | t0016 | g0115 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0247 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01192 | hp1 | a0004 | c0032 | t0017 | g0094 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01243 | hp1 | a0001 | c0003 | t0022 | g0093 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01243 | hp2 | a0001 | c0004 | t0002 | g0064 | AMR | PUR | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01258 | hp1 | a0001 | c0001 | t0012 | g0109 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01261 | hp1 | a0001 | c0003 | t0003 | g0058 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0263 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0043 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01433 | hp1 | a0001 | c0003 | t0006 | g0124 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01516 | hp1 | a0001 | c0027 | t0001 | g0311 | EUR | IBS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01516 | hp2 | a0001 | c0001 | t0012 | g0019 | EUR | IBS | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01884 | hp1 | a0001 | c0006 | t0002 | g0049 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0235 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01891 | hp2 | a0001 | c0003 | t0005 | g0048 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01928 | hp2 | a0001 | c0002 | t0007 | g0034 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01934 | hp1 | a0001 | c0002 | t0007 | g0201 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01943 | hp1 | a0001 | c0002 | t0007 | g0298 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0133 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0135 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0129 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01978 | hp2 | a0001 | c0018 | t0006 | g0123 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01981 | hp2 | a0001 | c0001 | t0014 | g0086 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02015 | hp1 | a0002 | c0008 | t0004 | g0296 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02027 | hp1 | a0001 | c0002 | t0013 | g0325 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02055 | hp2 | a0001 | c0011 | t0005 | g0100 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02080 | hp1 | a0001 | c0001 | t0025 | g0010 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02080 | hp2 | a0002 | c0008 | t0004 | g0277 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02083 | hp2 | a0002 | c0005 | t0004 | g0008 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02129 | hp1 | a0002 | c0019 | t0004 | g0002 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02132 | hp1 | a0002 | c0005 | t0004 | g0306 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02148 | hp1 | a0001 | c0003 | t0006 | g0130 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02257 | hp1 | a0004 | c0026 | t0005 | g0076 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02257 | hp2 | a0001 | c0014 | t0002 | g0052 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02273 | hp1 | a0001 | c0003 | t0006 | g0131 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02280 | hp1 | a0001 | c0001 | t0018 | g0088 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02451 | hp1 | a0001 | c0001 | t0018 | g0303 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02451 | hp2 | a0001 | c0004 | t0005 | g0061 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02523 | hp2 | a0001 | c0002 | t0013 | g0239 | EAS | KHV | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02572 | hp1 | a0001 | c0031 | t0005 | g0053 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0302 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0271 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02615 | hp2 | a0001 | c0007 | t0004 | g0070 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0051 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02630 | hp1 | a0001 | c0003 | t0005 | g0172 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02717 | hp1 | a0001 | c0004 | t0005 | g0065 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02717 | hp2 | a0001 | c0004 | t0005 | g0081 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02723 | hp2 | a0001 | c0010 | t0002 | g0183 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0223 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0339 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02809 | hp1 | a0001 | c0003 | t0005 | g0068 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02809 | hp2 | a0001 | c0013 | t0002 | g0054 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02818 | hp1 | a0001 | c0007 | t0004 | g0112 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02886 | hp2 | a0003 | c0012 | t0008 | g0098 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02895 | hp1 | a0001 | c0001 | t0015 | g0116 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02897 | hp2 | a0001 | c0011 | t0004 | g0101 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02922 | hp1 | a0001 | c0004 | t0005 | g0197 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02922 | hp2 | a0001 | c0004 | t0005 | g0120 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0192 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02965 | hp2 | a0001 | c0003 | t0005 | g0047 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02970 | hp1 | a0001 | c0029 | t0005 | g0107 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0082 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02976 | hp1 | a0001 | c0004 | t0005 | g0057 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0181 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0299 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03041 | hp1 | a0001 | c0004 | t0005 | g0063 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0084 | AFR | GWD | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03098 | hp1 | a0008 | c0017 | t0024 | g0099 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0193 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0194 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03130 | hp2 | a0001 | c0004 | t0005 | g0163 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03139 | hp1 | a0001 | c0007 | t0004 | g0085 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0090 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03225 | hp1 | a0001 | c0004 | t0005 | g0198 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03225 | hp2 | a0001 | c0004 | t0005 | g0199 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03239 | hp2 | a0001 | c0001 | t0019 | g0252 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03453 | hp1 | a0001 | c0028 | t0026 | g0106 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03453 | hp2 | a0001 | c0004 | t0005 | g0060 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03490 | hp1 | a0001 | c0001 | t0010 | g0045 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03490 | hp2 | a0001 | c0025 | t0006 | g0121 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03492 | hp1 | a0001 | c0016 | t0003 | g0108 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03492 | hp2 | a0001 | c0001 | t0010 | g0046 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03516 | hp1 | a0001 | c0001 | t0017 | g0097 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03516 | hp2 | a0001 | c0003 | t0005 | g0050 | AFR | ESN | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03579 | hp1 | a0001 | c0004 | t0005 | g0056 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0162 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03654 | hp1 | a0007 | c0023 | t0001 | g0332 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0213 | SAS | STU | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0272 | SAS | STU | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03704 | hp1 | a0001 | c0006 | t0008 | g0127 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03710 | hp1 | a0001 | c0001 | t0019 | g0250 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | BEB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | BEB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0243 | SAS | BEB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0137 | SAS | BEB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | STU | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | STU | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG04184 | hp2 | a0006 | c0022 | t0001 | g0203 | SAS | BEB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG04204 | hp1 | a0001 | c0003 | t0020 | g0122 | SAS | STU | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | YRI | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0170 | AFR | YRI | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | CHB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18747 | hp2 | a0001 | c0003 | t0006 | g0132 | EAS | CHB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | YRI | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18906 | hp2 | a0003 | c0012 | t0008 | g0092 | AFR | YRI | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18939 | hp2 | a0002 | c0008 | t0004 | g0168 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18940 | hp1 | a0001 | c0030 | t0002 | g0267 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18940 | hp2 | a0002 | c0020 | t0002 | g0007 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18945 | hp1 | a0001 | c0002 | t0007 | g0209 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18953 | hp2 | a0002 | c0008 | t0004 | g0025 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18960 | hp1 | a0001 | c0003 | t0021 | g0125 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18963 | hp1 | a0001 | c0002 | t0013 | g0161 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18963 | hp2 | a0001 | c0002 | t0007 | g0326 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18964 | hp2 | a0001 | c0006 | t0008 | g0128 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18967 | hp1 | a0001 | c0024 | t0003 | g0014 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18969 | hp1 | a0001 | c0006 | t0008 | g0344 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18972 | hp1 | a0001 | c0002 | t0007 | g0300 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18979 | hp2 | a0002 | c0008 | t0004 | g0027 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18983 | hp1 | a0002 | c0005 | t0004 | g0305 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18991 | hp2 | a0001 | c0002 | t0007 | g0323 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18993 | hp2 | a0002 | c0005 | t0004 | g0035 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18995 | hp1 | a0001 | c0003 | t0006 | g0134 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19000 | hp1 | a0002 | c0005 | t0004 | g0009 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19007 | hp2 | a0001 | c0002 | t0007 | g0241 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19010 | hp1 | a0002 | c0005 | t0004 | g0294 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0118 | AFR | LWK | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19030 | hp2 | a0001 | c0004 | t0002 | g0062 | AFR | LWK | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | LWK | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0240 | AFR | LWK | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19060 | hp2 | a0001 | c0021 | t0001 | g0254 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19063 | hp1 | a0002 | c0005 | t0004 | g0297 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19063 | hp2 | a0005 | c0033 | t0003 | g0169 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19068 | hp1 | a0001 | c0009 | t0003 | g0013 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19072 | hp1 | a0001 | c0009 | t0003 | g0038 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19072 | hp2 | a0002 | c0005 | t0004 | g0256 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19082 | hp2 | a0002 | c0005 | t0004 | g0257 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19088 | hp1 | a0001 | c0006 | t0002 | g0150 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0283 | AFR | YRI | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | YRI | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0089 | AFR | ASW | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA20129 | hp2 | a0001 | c0004 | t0005 | g0177 | AFR | ASW | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA20805 | hp1 | a0001 | c0001 | t0010 | g0044 | EUR | TSI | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | TSI | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01123 | hp1 | a0001 | c0001 | t0012 | g0337 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG01123 | hp2 | a0001 | c0003 | t0006 | g0136 | AMR | CLM | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0187 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0091 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02486 | hp2 | a0001 | c0006 | t0002 | g0171 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | ACB | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0067 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | MSL | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG06807 | hp1 | a0001 | c0004 | t0005 | g0077 | AFR | USA | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | USA | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0273 | AFR | USA | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0073 | AFR | USA | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA21309 | hp1 | a0001 | c0007 | t0015 | g0096 | AFR | LWK | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| NA21309 | hp2 | a0001 | c0007 | t0004 | g0083 | AFR | LWK | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0333 | REF | REF | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| homoSapiens_grch38 | hp1 | a0001 | c0014 | t0004 | g0066 | REF | REF | ACTN2_chr1_236681499_236769631 | ACTN2 | chr1 | 236681499 | 236769631 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:236717900
|
A | C | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.169A>C | p.Thr57Pro | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 344/4872 | 169/2685 | 57/894 | chr1 | 236717900 | ||
| chr1:236717903
|
C | T | 1 | a0005 | 1 | NA19063.hp2 | stop_gained | HIGH | c.172C>T | p.Gln58* | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 347/4872 | 172/2685 | 58/894 | chr1 | 236717903 | ||
| chr1:236717906
|
A | G | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.175A>G | p.Ile59Val | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 350/4872 | 175/2685 | 59/894 | chr1 | 236717906 | ||
| chr1:236717908
|
T | G | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.177T>G | p.Ile59Met | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 352/4872 | 177/2685 | 59/894 | chr1 | 236717908 | ||
| chr1:236717912
|
A | T | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.181A>T | p.Asn61Tyr | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 356/4872 | 181/2685 | 61/894 | chr1 | 236717912 | ||
| chr1:236717916
|
T | C | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.185T>C | p.Ile62Thr | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 360/4872 | 185/2685 | 62/894 | chr1 | 236717916 | ||
| chr1:236717918
|
G | A | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.187G>A | p.Glu63Lys | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 362/4872 | 187/2685 | 63/894 | chr1 | 236717918 | ||
| chr1:236717919
|
A | G | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.188A>G | p.Glu63Gly | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 363/4872 | 188/2685 | 63/894 | chr1 | 236717919 | ||
| chr1:236717921
|
G | C | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.190G>C | p.Glu64Gln | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 365/4872 | 190/2685 | 64/894 | chr1 | 236717921 | ||
| chr1:236717922
|
A | C | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.191A>C | p.Glu64Ala | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 366/4872 | 191/2685 | 64/894 | chr1 | 236717922 | ||
| chr1:236717926
|
C | G | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.195C>G | p.Asp65Glu | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 370/4872 | 195/2685 | 65/894 | chr1 | 236717926 | ||
| chr1:236717927
|
T | G | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.196T>G | p.Phe66Val | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 371/4872 | 196/2685 | 66/894 | chr1 | 236717927 | ||
| chr1:236717930
|
A | T | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.199A>T | p.Arg67Trp | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 374/4872 | 199/2685 | 67/894 | chr1 | 236717930 | ||
| chr1:236717932
|
G | C | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.201G>C | p.Arg67Ser | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 376/4872 | 201/2685 | 67/894 | chr1 | 236717932 | ||
| chr1:236717935
|
T | A | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.204T>A | p.Asn68Lys | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 379/4872 | 204/2685 | 68/894 | chr1 | 236717935 | ||
| chr1:236717939
|
C | A | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.208C>A | p.Leu70Ile | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 383/4872 | 208/2685 | 70/894 | chr1 | 236717939 | ||
| chr1:236717940
|
T | A | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.209T>A | p.Leu70His | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 384/4872 | 209/2685 | 70/894 | chr1 | 236717940 | ||
| chr1:236717944
|
G | C | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.213G>C | p.Lys71Asn | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 388/4872 | 213/2685 | 71/894 | chr1 | 236717944 | ||
| chr1:236717946
|
T | A | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.215T>A | p.Leu72His | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 390/4872 | 215/2685 | 72/894 | chr1 | 236717946 | ||
| chr1:236717949
|
T | C | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.218T>C | p.Met73Thr | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 393/4872 | 218/2685 | 73/894 | chr1 | 236717949 | ||
| chr1:236717950
|
G | A | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.219G>A | p.Met73Ile | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 394/4872 | 219/2685 | 73/894 | chr1 | 236717950 | ||
| chr1:236717952
|
T | G | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.221T>G | p.Leu74Arg | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 396/4872 | 221/2685 | 74/894 | chr1 | 236717952 | ||
| chr1:236717958
|
T | A | 1 | a0005 | 1 | NA19063.hp2 | stop_gained | HIGH | c.227T>A | p.Leu76* | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 402/4872 | 227/2685 | 76/894 | chr1 | 236717958 | ||
| chr1:236717960
|
G | C | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.229G>C | p.Glu77Gln | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 404/4872 | 229/2685 | 77/894 | chr1 | 236717960 | ||
| chr1:236717964
|
T | G | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.233T>G | p.Val78Gly | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 408/4872 | 233/2685 | 78/894 | chr1 | 236717964 | ||
| chr1:236744668
|
C | T | 1 | a0003 | 2 | HG02886.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1298C>T | p.Ser433Leu | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/21 | 1473/4872 | 1298/2685 | 433/894 | chr1 | 236744668 | ||
| chr1:236744682
|
C | T | 1 | a0008 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1312C>T | p.Arg438Trp | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/21 | 1487/4872 | 1312/2685 | 438/894 | chr1 | 236744682 | ||
| chr1:236747683
|
G | A | 1 | a0002 | 16 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.1423G>A | p.Asp475Asn | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/21 | 1598/4872 | 1423/2685 | 475/894 | chr1 | 236747683 | ||
| chr1:236747712
|
G | C | 1 | a0006 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1452G>C | p.Gln484His | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/21 | 1627/4872 | 1452/2685 | 484/894 | chr1 | 236747712 | ||
| chr1:236751623
|
A | G | 1 | a0004 | 2 | HG01192.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.1810A>G | p.Met604Val | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/21 | 1985/4872 | 1810/2685 | 604/894 | chr1 | 236751623 | ||
| chr1:236751636
|
G | A | 1 | a0007 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.1823G>A | p.Arg608Gln | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/21 | 1998/4872 | 1823/2685 | 608/894 | chr1 | 236751636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:236686691
|
C | A | 1 | a0001c0016 | 1 | HG03492.hp1 | synonymous_variant | LOW | c.18C>A | p.Pro6Pro | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/21 | 193/4872 | 18/2685 | 6/894 | chr1 | 236686691 | ||
| chr1:236717902
|
C | T | 1 | a0005c0033 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.171C>T | p.Thr57Thr | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 346/4872 | 171/2685 | 57/894 | chr1 | 236717902 | ||
| chr1:236717917
|
C | T | 1 | a0001c0015 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.186C>T | p.Ile62Ile | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 361/4872 | 186/2685 | 62/894 | chr1 | 236717917 | ||
| chr1:236717941
|
T | A | 1 | a0005c0033 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.210T>A | p.Leu70Leu | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 385/4872 | 210/2685 | 70/894 | chr1 | 236717941 | ||
| chr1:236717947
|
C | A | 1 | a0005c0033 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.216C>A | p.Leu72Leu | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/21 | 391/4872 | 216/2685 | 72/894 | chr1 | 236717947 | ||
| chr1:236719003
|
T | C | 29 | a0001c0001a0001c0002a0001c0003others(26): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
synonymous_variant | LOW | c.351T>C | p.Ile117Ile | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/21 | 526/4872 | 351/2685 | 117/894 | chr1 | 236719003 | ||
| chr1:236720121
|
C | T | 23 | a0001c0001a0001c0002a0001c0004others(20): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
synonymous_variant | LOW | c.378C>T | p.Asn126Asn | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/21 | 553/4872 | 378/2685 | 126/894 | chr1 | 236720121 | ||
| chr1:236735642
|
G | C | 5 | a0001c0009a0001c0021a0002c0005others(2): Show | 15 | HG00323.hp1 HG02083.hp2 HG02129.hp1 others(12): Show |
synonymous_variant | LOW | c.705G>C | p.Val235Val | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/21 | 880/4872 | 705/2685 | 235/894 | chr1 | 236735642 | ||
| chr1:236737208
|
G | A | 2 | a0001c0011a0008c0017 | 3 | HG02055.hp2 HG02897.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.870G>A | p.Ala290Ala | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/21 | 1045/4872 | 870/2685 | 290/894 | chr1 | 236737208 | ||
| chr1:236739343
|
C | T | 1 | a0001c0030 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.918C>T | p.Asn306Asn | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/21 | 1093/4872 | 918/2685 | 306/894 | chr1 | 236739343 | ||
| chr1:236739352
|
C | T | 1 | a0001c0029 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.927C>T | p.Pro309Pro | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/21 | 1102/4872 | 927/2685 | 309/894 | chr1 | 236739352 | ||
| chr1:236744666
|
G | A | 5 | a0001c0007a0001c0010a0001c0029others(2): Show | 12 | HG01106.hp2 HG01168.hp1 HG02572.hp1 others(9): Show |
synonymous_variant | LOW | c.1296G>A | p.Ala432Ala | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/21 | 1471/4872 | 1296/2685 | 432/894 | chr1 | 236744666 | ||
| chr1:236744741
|
C | T | 1 | a0001c0028 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1371C>T | p.Arg457Arg | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/21 | 1546/4872 | 1371/2685 | 457/894 | chr1 | 236744741 | ||
| chr1:236744753
|
C | T | 1 | a0001c0027 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.1383C>T | p.Ile461Ile | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/21 | 1558/4872 | 1383/2685 | 461/894 | chr1 | 236744753 | ||
| chr1:236751607
|
G | A | 1 | a0002c0019 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.1794G>A | p.Pro598Pro | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/21 | 1969/4872 | 1794/2685 | 598/894 | chr1 | 236751607 | ||
| chr1:236754039
|
C | A | 1 | a0001c0029 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1932C>A | p.Ala644Ala | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/21 | 2107/4872 | 1932/2685 | 644/894 | chr1 | 236754039 | ||
| chr1:236755120
|
C | T | 1 | a0008c0017 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.2076C>T | p.Ile692Ile | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/21 | 2251/4872 | 2076/2685 | 692/894 | chr1 | 236755120 | ||
| chr1:236755183
|
G | A | 1 | a0001c0004 | 17 | HG01243.hp2 HG02451.hp2 HG02717.hp1 others(14): Show |
synonymous_variant | LOW | c.2139G>A | p.Thr713Thr | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/21 | 2314/4872 | 2139/2685 | 713/894 | chr1 | 236755183 | ||
| chr1:236755192
|
G | A | 1 | a0001c0021 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.2148G>A | p.Thr716Thr | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/21 | 2323/4872 | 2148/2685 | 716/894 | chr1 | 236755192 | ||
| chr1:236757542
|
G | A | 1 | a0001c0024 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.2211G>A | p.Glu737Glu | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/21 | 2386/4872 | 2211/2685 | 737/894 | chr1 | 236757542 | ||
| chr1:236757566
|
A | G | 1 | a0001c0025 | 1 | HG03490.hp2 | synonymous_variant | LOW | c.2235A>G | p.Arg745Arg | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/21 | 2410/4872 | 2235/2685 | 745/894 | chr1 | 236757566 | ||
| chr1:236762544
|
G | A | 7 | a0001c0002a0001c0006a0001c0010others(4): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
synonymous_variant | LOW | c.2610G>A | p.Ser870Ser | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 2785/4872 | 2610/2685 | 870/894 | chr1 | 236762544 | ||
| chr1:236762592
|
C | T | 1 | a0001c0018 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.2658C>T | p.Ser886Ser | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 2833/4872 | 2658/2685 | 886/894 | chr1 | 236762592 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:236686571
|
G | GCGCCCGC | 14 | a0001c0001t0006a0001c0001t0015a0001c0001t0017others(11): Show | 24 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-84_-78dupCGCCGCC | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/21 | 77 | INFO_REALIGN_3_PRIME | chr1 | 236686571 | ||||
| chr1:236686631
|
C | G | 1 | a0001c0001t0019 | 2 | HG03239.hp2 HG03710.hp1 |
5_prime_UTR_variant | MODIFIER | c.-43C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/21 | 43 | chr1 | 236686631 | |||||
| chr1:236686652
|
C | T | 1 | a0001c0001t0010 | 4 | HG01361.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-22C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/21 | 22 | chr1 | 236686652 | |||||
| chr1:236762665
|
C | T | 1 | a0001c0028t0026 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*46C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 46 | chr1 | 236762665 | |||||
| chr1:236762730
|
A | G | 13 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(10): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*111A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 111 | chr1 | 236762730 | |||||
| chr1:236763042
|
A | G | 3 | a0001c0001t0014a0001c0001t0017a0004c0032t0017 | 5 | HG01192.hp1 HG01981.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*423A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 423 | chr1 | 236763042 | |||||
| chr1:236763066
|
C | G | 15 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(12): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*447C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 447 | chr1 | 236763066 | |||||
| chr1:236763145
|
T | C | 33 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(30): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*526T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 526 | chr1 | 236763145 | |||||
| chr1:236763319
|
A | G | 2 | a0001c0001t0012a0001c0003t0020 | 4 | HG01123.hp1 HG01258.hp1 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*700A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 700 | chr1 | 236763319 | |||||
| chr1:236763343
|
G | C | 16 | a0001c0001t0002a0001c0001t0011a0001c0001t0018others(13): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*724G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 724 | chr1 | 236763343 | |||||
| chr1:236763367
|
A | G | 14 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(11): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*748A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 748 | chr1 | 236763367 | |||||
| chr1:236763437
|
G | A | 1 | a0001c0001t0025 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*818G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 818 | chr1 | 236763437 | |||||
| chr1:236763573
|
G | A | 7 | a0001c0001t0003a0001c0003t0003a0001c0003t0021others(4): Show | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*954G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 954 | chr1 | 236763573 | |||||
| chr1:236763598
|
C | A | 1 | a0001c0028t0026 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 979 | chr1 | 236763598 | |||||
| chr1:236763706
|
G | A | 3 | a0001c0001t0009a0001c0001t0015a0001c0007t0015 | 7 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1087G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 1087 | chr1 | 236763706 | |||||
| chr1:236763735
|
G | A | 1 | a0001c0003t0021 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1116G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 1116 | chr1 | 236763735 | |||||
| chr1:236764154
|
C | T | 1 | a0001c0013t0023 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1535C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 1535 | chr1 | 236764154 | |||||
| chr1:236764538
|
C | G | 1 | a0001c0001t0018 | 2 | HG02280.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1919C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 1919 | chr1 | 236764538 | |||||
| chr1:236764546
|
GTAT | G | 1 | a0001c0002t0007 | 9 | HG00642.hp2 HG01928.hp2 HG01934.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1932_*1934delATT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 21/21 | 1932 | INFO_REALIGN_3_PRIME | chr1 | 236764546 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:236686956
|
A | G | 96 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0258others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.126+157A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236686956 | ||||||
| chr1:236687096
|
C | T | 1 | a0001c0002t0002g0248 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.126+297C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687096 | ||||||
| chr1:236687130
|
G | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.126+331G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687130 | ||||||
| chr1:236687245
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.126+446T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687245 | ||||||
| chr1:236687346
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.126+547A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687346 | ||||||
| chr1:236687450
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.126+651T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687450 | ||||||
| chr1:236687558
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.126+759A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687558 | ||||||
| chr1:236687641
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+842A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687641 | ||||||
| chr1:236687692
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.126+893G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687692 | ||||||
| chr1:236687808
|
C | G | 8 | a0001c0003t0002g0051a0001c0003t0005g0047a0001c0003t0005g0048others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+1009C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236687808 | ||||||
| chr1:236688121
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+1322G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236688121 | ||||||
| chr1:236688185
|
G | GT | 18 | a0001c0001t0006g0135a0001c0002t0002g0247a0001c0003t0001g0129others(15): Show | 18 | HG00639.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+1395dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236688185 | |||||
| chr1:236688195
|
A | T | 25 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+1396A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236688195 | ||||||
| chr1:236688376
|
C | CT | 13 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(10): Show | 13 | HG01168.hp2 HG01169.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+1589dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236688376 | |||||
| chr1:236688376
|
C | CTT | 16 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(13): Show | 16 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+1588_126+1589d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236688376 | |||||
| chr1:236688505
|
G | A | 24 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(21): Show | 24 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+1706G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236688505 | ||||||
| chr1:236688592
|
A | G | 1 | a0001c0007t0004g0112 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.126+1793A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236688592 | ||||||
| chr1:236688835
|
G | A | 23 | a0001c0001t0004g0069a0001c0001t0004g0071a0001c0001t0004g0074others(20): Show | 23 | HG01981.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+2036G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236688835 | ||||||
| chr1:236688850
|
A | G | 25 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+2051A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236688850 | ||||||
| chr1:236688982
|
A | T | 109 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0001g0251others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.126+2183A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236688982 | ||||||
| chr1:236689012
|
A | G | 2 | a0001c0001t0004g0119a0001c0001t0009g0118 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.126+2213A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689012 | ||||||
| chr1:236689080
|
A | T | 25 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+2281A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689080 | ||||||
| chr1:236689128
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0019g0250a0001c0001t0019g0252 | 3 | HG03239.hp2 HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.126+2329G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689128 | ||||||
| chr1:236689300
|
GAT | G | 17 | a0001c0001t0001g0230a0001c0001t0001g0236a0001c0001t0003g0234others(14): Show | 17 | HG00099.hp2 HG00423.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.126+2539_126+2540d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATAT | G | 33 | a0001c0001t0001g0205a0001c0001t0001g0211a0001c0001t0001g0219others(30): Show | 33 | HG00323.hp2 HG00438.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.126+2537_126+2540d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATAT | G | 27 | a0001c0001t0001g0184a0001c0001t0001g0188a0001c0001t0001g0190others(24): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.126+2535_126+2540d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATATA others(1): Show |
G | 7 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0175others(4): Show | 7 | HG00642.hp2 HG03831.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+2533_126+2540d others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATATA others(3): Show |
G | 2 | a0001c0003t0005g0172a0001c0006t0002g0171 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.126+2531_126+2540d others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATATA others(5): Show |
G | 2 | a0001c0003t0002g0170a0001c0004t0005g0056 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.126+2529_126+2540d others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATATA others(7): Show |
G | 2 | a0001c0001t0005g0055a0001c0003t0005g0047 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.126+2527_126+2540d others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATATA others(9): Show |
G | 1 | a0001c0001t0001g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.126+2525_126+2540d others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATATA others(11): Show |
G | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.126+2523_126+2540d others(20): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATATA others(13): Show |
G | 23 | a0001c0001t0004g0069a0001c0001t0004g0071a0001c0001t0004g0074others(20): Show | 23 | HG01981.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+2521_126+2540d others(22): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689300
|
GATATATA others(15): Show |
G | 33 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(30): Show | 33 | HG00609.hp1 HG00741.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.126+2519_126+2540d others(24): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689300 | |||||
| chr1:236689303
|
A | G | 1 | a0001c0001t0011g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.126+2504A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689303 | ||||||
| chr1:236689304
|
T | G | 1 | a0001c0002t0002g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.126+2505T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689304 | ||||||
| chr1:236689315
|
A | C | 1 | a0001c0004t0005g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126+2516A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689315 | ||||||
| chr1:236689317
|
A | C | 23 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(20): Show | 23 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.126+2518A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689317 | ||||||
| chr1:236689318
|
TATATATA others(15): Show |
T | 1 | a0001c0004t0005g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126+2521_126+2542d others(24): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689318 | |||||
| chr1:236689319
|
A | C | 1 | a0001c0025t0006g0121 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.126+2520A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689319 | ||||||
| chr1:236689320
|
TATATATA others(13): Show |
T | 29 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0004g0102others(26): Show | 29 | HG00639.hp2 HG01081.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.126+2523_126+2542d others(22): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689320 | |||||
| chr1:236689322
|
TATATATA others(11): Show |
T | 96 | a0001c0001t0001g0110a0001c0001t0001g0251a0001c0001t0001g0258others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.126+2525_126+2542d others(20): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689322 | |||||
| chr1:236689324
|
TATATATA others(9): Show |
T | 7 | a0001c0001t0001g0338a0001c0001t0001g0341a0001c0001t0001g0342others(4): Show | 7 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+2527_126+2542d others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689324 | |||||
| chr1:236689338
|
T | C | 16 | a0001c0001t0010g0043a0001c0001t0010g0044a0001c0001t0010g0045others(13): Show | 16 | HG01109.hp1 HG01192.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+2539T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689338 | ||||||
| chr1:236689338
|
T | TATATATA others(3): Show |
1 | a0001c0013t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.126+2540_126+2541i others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689338 | |||||
| chr1:236689358
|
T | A | 95 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0258others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.126+2559T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689358 | ||||||
| chr1:236689358
|
T | TTATA | 25 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+2570_126+2573d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236689358 | |||||
| chr1:236689434
|
G | A | 1 | a0001c0021t0001g0254 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.126+2635G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689434 | ||||||
| chr1:236689709
|
G | A | 7 | a0001c0001t0004g0069a0001c0001t0004g0071a0001c0001t0009g0073others(4): Show | 7 | HG02559.hp1 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+2910G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689709 | ||||||
| chr1:236689777
|
G | T | 1 | a0001c0001t0004g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+2978G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689777 | ||||||
| chr1:236689813
|
C | T | 23 | a0001c0001t0004g0069a0001c0001t0004g0071a0001c0001t0004g0074others(20): Show | 23 | HG01981.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+3014C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689813 | ||||||
| chr1:236689867
|
G | A | 109 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0001g0251others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.126+3068G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689867 | ||||||
| chr1:236689927
|
C | T | 23 | a0001c0001t0004g0069a0001c0001t0004g0071a0001c0001t0004g0074others(20): Show | 23 | HG01981.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+3128C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689927 | ||||||
| chr1:236689970
|
G | A | 1 | a0001c0002t0007g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.126+3171G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689970 | ||||||
| chr1:236689985
|
G | A | 17 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(14): Show | 17 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.126+3186G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689985 | ||||||
| chr1:236689988
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.126+3189G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689988 | ||||||
| chr1:236689992
|
C | T | 23 | a0001c0001t0004g0069a0001c0001t0004g0071a0001c0001t0004g0074others(20): Show | 23 | HG01981.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+3193C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236689992 | ||||||
| chr1:236690022
|
C | T | 1 | a0001c0001t0004g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.126+3223C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690022 | ||||||
| chr1:236690023
|
G | A | 2 | a0001c0003t0005g0172a0001c0006t0002g0171 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.126+3224G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690023 | ||||||
| chr1:236690038
|
A | G | 25 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+3239A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690038 | ||||||
| chr1:236690047
|
T | C | 1 | a0001c0004t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+3248T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690047 | ||||||
| chr1:236690130
|
C | T | 1 | a0001c0002t0002g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.126+3331C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690130 | ||||||
| chr1:236690233
|
T | C | 25 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+3434T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690233 | ||||||
| chr1:236690235
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.126+3436G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690235 | ||||||
| chr1:236690250
|
C | G | 4 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+3451C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690250 | ||||||
| chr1:236690283
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.126+3484C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690283 | ||||||
| chr1:236690324
|
T | C | 1 | a0001c0001t0003g0202 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.126+3525T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690324 | ||||||
| chr1:236690325
|
C | T | 1 | a0001c0001t0003g0202 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.126+3526C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690325 | ||||||
| chr1:236690327
|
T | C | 1 | a0001c0001t0003g0202 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.126+3528T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690327 | ||||||
| chr1:236690349
|
T | C | 25 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+3550T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690349 | ||||||
| chr1:236690448
|
C | T | 1 | a0001c0001t0003g0040 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.126+3649C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690448 | ||||||
| chr1:236690543
|
T | G | 1 | a0001c0001t0003g0202 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.126+3744T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690543 | ||||||
| chr1:236690656
|
C | T | 1 | a0001c0001t0018g0088 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+3857C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690656 | ||||||
| chr1:236690726
|
G | A | 25 | a0001c0001t0001g0114a0001c0001t0004g0117a0001c0001t0004g0119others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+3927G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690726 | ||||||
| chr1:236690809
|
T | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(329): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.126+4010T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690809 | ||||||
| chr1:236690811
|
G | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(216): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.126+4012G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690811 | ||||||
| chr1:236690814
|
C | T | 1 | a0001c0001t0003g0336 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.126+4015C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236690814 | ||||||
| chr1:236690935
|
C | CT | 6 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0202others(3): Show | 6 | HG02083.hp1 NA18939.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+4156dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236690935 | |||||
| chr1:236690935
|
CT | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.126+4156delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236690935 | |||||
| chr1:236690935
|
CTT | C | 12 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(9): Show | 12 | HG00741.hp2 HG01168.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+4155_126+4156d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236690935 | |||||
| chr1:236691028
|
C | CCCGGGTT others(106): Show |
1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+4333_126+4334i others(115): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236691028 | |||||
| chr1:236691146
|
G | A | 1 | a0001c0002t0002g0228 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.126+4347G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691146 | ||||||
| chr1:236691172
|
T | C | 1 | a0001c0001t0003g0202 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.126+4373T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691172 | ||||||
| chr1:236691200
|
C | G | 4 | a0001c0003t0002g0170a0001c0003t0005g0172a0001c0004t0002g0240others(1): Show | 4 | HG02486.hp2 HG02630.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+4401C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691200 | ||||||
| chr1:236691276
|
G | A | 1 | a0001c0001t0005g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+4477G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691276 | ||||||
| chr1:236691332
|
G | A | 23 | a0001c0001t0004g0069a0001c0001t0004g0071a0001c0001t0004g0074others(20): Show | 23 | HG01981.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+4533G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691332 | ||||||
| chr1:236691364
|
C | T | 5 | a0001c0001t0004g0178a0001c0001t0004g0200a0001c0001t0005g0181others(2): Show | 5 | HG02572.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+4565C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691364 | ||||||
| chr1:236691631
|
C | T | 1 | a0001c0001t0015g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126+4832C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691631 | ||||||
| chr1:236691670
|
G | A | 342 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(339): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.126+4871G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691670 | ||||||
| chr1:236691673
|
T | C | 99 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0258others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.126+4874T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691673 | ||||||
| chr1:236691832
|
C | T | 23 | a0001c0001t0004g0069a0001c0001t0004g0071a0001c0001t0004g0074others(20): Show | 23 | HG01981.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+5033C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691832 | ||||||
| chr1:236691867
|
G | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | NA18941.hp1 NA18942.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5068G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691867 | ||||||
| chr1:236691872
|
A | G | 12 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0003g0104others(9): Show | 12 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+5073A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691872 | ||||||
| chr1:236691888
|
C | T | 9 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(6): Show | 9 | HG00738.hp1 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+5089C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691888 | ||||||
| chr1:236691932
|
A | G | 2 | a0001c0001t0004g0037a0001c0001t0011g0036 | 2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.126+5133A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236691932 | ||||||
| chr1:236692335
|
A | T | 35 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(32): Show | 35 | HG00609.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.126+5536A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692335 | ||||||
| chr1:236692468
|
C | T | 2 | a0001c0004t0005g0197a0001c0004t0005g0198 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.126+5669C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692468 | ||||||
| chr1:236692547
|
G | A | 17 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(14): Show | 17 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.126+5748G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692547 | ||||||
| chr1:236692614
|
A | G | 17 | a0001c0001t0017g0097a0001c0003t0002g0051a0001c0003t0005g0047others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.126+5815A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692614 | ||||||
| chr1:236692744
|
G | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+5945G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692744 | ||||||
| chr1:236692745
|
C | G | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+5946C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692745 | ||||||
| chr1:236692797
|
A | AG | 332 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(329): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.126+5999dupG | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236692797 | |||||
| chr1:236692813
|
A | G | 2 | a0001c0002t0007g0326a0001c0002t0013g0325 | 2 | HG02027.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.126+6014A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692813 | ||||||
| chr1:236692856
|
A | G | 1 | a0001c0002t0002g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+6057A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692856 | ||||||
| chr1:236692985
|
G | C | 2 | a0001c0001t0017g0097a0001c0007t0015g0096 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.126+6186G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236692985 | ||||||
| chr1:236693001
|
C | T | 1 | a0001c0001t0003g0324 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.126+6202C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693001 | ||||||
| chr1:236693177
|
G | GCA | 41 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0148others(38): Show | 41 | HG00609.hp1 HG00642.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+6415_126+6416d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
G | GCACA | 59 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(56): Show | 59 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.126+6413_126+6416d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
G | GCACACA | 7 | a0001c0001t0001g0205a0001c0001t0003g0173a0001c0001t0004g0204others(4): Show | 7 | HG00280.hp1 HG01255.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+6411_126+6416d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCA | G | 5 | a0001c0001t0001g0225a0001c0001t0004g0117a0001c0001t0004g0119others(2): Show | 5 | HG02647.hp2 HG02683.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+6415_126+6416d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCACA | G | 35 | a0001c0001t0001g0114a0001c0001t0004g0074a0001c0001t0004g0075others(32): Show | 35 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+6413_126+6416d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCACACA | G | 19 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0003g0104others(16): Show | 19 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.126+6411_126+6416d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCACACAC others(1): Show |
G | 10 | a0001c0001t0001g0253a0001c0001t0001g0262a0001c0001t0015g0116others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+6409_126+6416d others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCACACAC others(3): Show |
G | 100 | a0001c0001t0001g0244a0001c0001t0001g0251a0001c0001t0001g0258others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.126+6407_126+6416d others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCACACAC others(5): Show |
G | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0343 | 3 | HG00438.hp1 HG04115.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.126+6405_126+6416d others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCACACAC others(7): Show |
G | 3 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322 | 3 | HG00639.hp1 HG01081.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.126+6403_126+6416d others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCACACAC others(9): Show |
G | 1 | a0002c0019t0004g0002 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.126+6401_126+6416d others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693177
|
GCACACAC others(11): Show |
G | 40 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(37): Show | 40 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.126+6399_126+6416d others(20): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236693177 | |||||
| chr1:236693181
|
A | G | 1 | a0001c0003t0020g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.126+6382A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693181 | ||||||
| chr1:236693183
|
A | G | 15 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(12): Show | 15 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+6384A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693183 | ||||||
| chr1:236693205
|
A | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+6406A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693205 | ||||||
| chr1:236693205
|
A | T | 1 | a0001c0002t0007g0323 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.126+6406A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693205 | ||||||
| chr1:236693227
|
A | G | 1 | a0001c0003t0002g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.126+6428A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693227 | ||||||
| chr1:236693299
|
G | T | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+6500G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693299 | ||||||
| chr1:236693324
|
A | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(40): Show | 43 | HG00140.hp2 HG00323.hp1 HG01516.hp2 others(40): Show |
intron_variant | MODIFIER | c.126+6525A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693324 | ||||||
| chr1:236693436
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.126+6637G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693436 | ||||||
| chr1:236693769
|
C | T | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG00140.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.126+6970C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693769 | ||||||
| chr1:236693812
|
G | C | 4 | a0001c0001t0004g0075a0001c0001t0018g0088a0001c0004t0005g0077others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7013G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236693812 | ||||||
| chr1:236694034
|
C | T | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+7235C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236694034 | ||||||
| chr1:236694035
|
T | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+7236T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236694035 | ||||||
| chr1:236694203
|
A | AT | 18 | a0001c0001t0006g0135a0001c0001t0015g0116a0001c0003t0001g0129others(15): Show | 18 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+7415dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236694203 | |||||
| chr1:236694203
|
AT | A | 10 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0078others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+7415delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236694203 | |||||
| chr1:236694220
|
C | CT | 10 | a0001c0001t0001g0114a0001c0001t0001g0335a0001c0001t0004g0246others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+7437dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236694220 | |||||
| chr1:236694255
|
C | T | 29 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0003g0104others(26): Show | 29 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.126+7456C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236694255 | ||||||
| chr1:236694308
|
C | T | 1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+7509C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236694308 | ||||||
| chr1:236694379
|
C | T | 1 | a0001c0001t0003g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.126+7580C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236694379 | ||||||
| chr1:236694634
|
G | A | 298 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0103others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.126+7835G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236694634 | ||||||
| chr1:236694780
|
C | T | 2 | a0001c0001t0004g0069a0001c0001t0009g0091 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.126+7981C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236694780 | ||||||
| chr1:236694787
|
G | A | 1 | a0008c0017t0024g0099 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.126+7988G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236694787 | ||||||
| chr1:236695185
|
G | A | 3 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118 | 3 | HG02647.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.126+8386G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236695185 | ||||||
| chr1:236695212
|
C | CA | 221 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0041others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.126+8429dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236695212 | |||||
| chr1:236695212
|
C | CAA | 10 | a0001c0001t0001g0184a0001c0001t0001g0265a0001c0001t0001g0320others(7): Show | 10 | HG01255.hp1 HG01433.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+8428_126+8429d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236695212 | |||||
| chr1:236695212
|
CA | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 13 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+8429delA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236695212 | |||||
| chr1:236695310
|
G | A | 1 | a0001c0001t0003g0266 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.126+8511G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236695310 | ||||||
| chr1:236695375
|
C | CA | 13 | a0001c0001t0003g0039a0001c0001t0003g0104a0001c0001t0003g0105others(10): Show | 13 | HG00609.hp2 HG01169.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+8593dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236695375 | |||||
| chr1:236695454
|
C | A | 13 | a0001c0001t0003g0238a0001c0001t0004g0059a0001c0001t0004g0102others(10): Show | 13 | HG01243.hp2 HG01261.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+8655C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236695454 | ||||||
| chr1:236695563
|
T | TC | 147 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0103others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.126+8773dupC | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236695563 | |||||
| chr1:236695563
|
T | TCC | 51 | a0001c0001t0001g0114a0001c0001t0001g0211a0001c0001t0001g0230others(48): Show | 51 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.126+8772_126+8773d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236695563 | |||||
| chr1:236695572
|
CT | C | 16 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(13): Show | 16 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+8774delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236695572 | ||||||
| chr1:236695573
|
T | C | 282 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0103others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.126+8774T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236695573 | ||||||
| chr1:236695638
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0004g0030 | 2 | NA18973.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.126+8839C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236695638 | ||||||
| chr1:236695987
|
A | G | 2 | a0001c0001t0001g0103a0001c0007t0004g0112 | 2 | HG01081.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.126+9188A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236695987 | ||||||
| chr1:236695997
|
C | T | 4 | a0001c0001t0015g0116a0001c0004t0005g0120a0001c0015t0016g0113others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+9198C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236695997 | ||||||
| chr1:236696111
|
A | G | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9312A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696111 | ||||||
| chr1:236696112
|
G | A | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9313G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696112 | ||||||
| chr1:236696178
|
G | A | 1 | a0001c0002t0007g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.126+9379G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696178 | ||||||
| chr1:236696261
|
C | T | 1 | a0001c0002t0002g0179 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.126+9462C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696261 | ||||||
| chr1:236696316
|
T | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9517T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696316 | ||||||
| chr1:236696317
|
C | T | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9518C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696317 | ||||||
| chr1:236696317
|
CA | C | 279 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0103others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.126+9534delA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236696317 | |||||
| chr1:236696318
|
A | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9519A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696318 | ||||||
| chr1:236696427
|
G | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9628G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696427 | ||||||
| chr1:236696430
|
A | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9631A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696430 | ||||||
| chr1:236696431
|
T | A | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9632T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696431 | ||||||
| chr1:236696432
|
C | T | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+9633C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696432 | ||||||
| chr1:236696472
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.126+9673T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696472 | ||||||
| chr1:236696534
|
G | C | 1 | a0001c0001t0005g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+9735G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696534 | ||||||
| chr1:236696574
|
C | T | 1 | a0001c0001t0017g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.126+9775C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696574 | ||||||
| chr1:236696666
|
A | AT | 21 | a0001c0001t0001g0110a0001c0001t0001g0195a0001c0001t0001g0224others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+9885dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236696666 | |||||
| chr1:236696666
|
AT | A | 119 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0114others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.126+9885delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236696666 | |||||
| chr1:236696735
|
G | A | 1 | a0001c0007t0004g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126+9936G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696735 | ||||||
| chr1:236696860
|
T | G | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+10061T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236696860 | ||||||
| chr1:236696962
|
ATTG | A | 71 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.126+10168_126+1017 others(7): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236696962 | |||||
| chr1:236697015
|
C | T | 3 | a0001c0002t0002g0278a0001c0002t0002g0309a0001c0002t0002g0310 | 3 | NA18990.hp1 NA19064.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.126+10216C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697015 | ||||||
| chr1:236697208
|
C | T | 2 | a0001c0002t0002g0223a0001c0002t0002g0237 | 2 | HG02132.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.126+10409C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697208 | ||||||
| chr1:236697312
|
C | A | 2 | a0001c0001t0003g0174a0001c0001t0003g0175 | 2 | NA18943.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.126+10513C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697312 | ||||||
| chr1:236697416
|
C | T | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126+10617C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697416 | ||||||
| chr1:236697479
|
A | G | 2 | a0001c0001t0001g0159a0001c0010t0002g0160 | 2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.126+10680A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697479 | ||||||
| chr1:236697493
|
C | A | 298 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0103others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.126+10694C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697493 | ||||||
| chr1:236697749
|
C | T | 16 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(13): Show | 16 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+10950C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697749 | ||||||
| chr1:236697760
|
C | CT | 69 | a0001c0001t0001g0110a0001c0001t0001g0139a0001c0001t0001g0141others(66): Show | 69 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.126+10979dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236697760 | |||||
| chr1:236697760
|
CT | C | 7 | a0001c0001t0001g0317a0001c0001t0004g0078a0001c0001t0014g0084others(4): Show | 7 | HG01071.hp1 HG02132.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+10979delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236697760 | |||||
| chr1:236697782
|
G | C | 16 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(13): Show | 16 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+10983G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697782 | ||||||
| chr1:236697850
|
G | A | 36 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(33): Show | 36 | HG00609.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.126+11051G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697850 | ||||||
| chr1:236697931
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(33): Show | 36 | HG00323.hp1 HG01071.hp2 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.126+11132C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697931 | ||||||
| chr1:236697934
|
A | AT | 244 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0103others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.126+11154dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236697934 | |||||
| chr1:236697934
|
A | ATT | 28 | a0001c0001t0001g0308a0001c0001t0003g0147a0001c0001t0003g0202others(25): Show | 28 | HG01106.hp1 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.126+11153_126+1115 others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236697934 | |||||
| chr1:236697946
|
T | TA | 3 | a0001c0003t0002g0170a0001c0003t0005g0172a0001c0006t0002g0171 | 3 | HG02486.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.126+11147_126+1114 others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236697946 | ||||||
| chr1:236698063
|
C | T | 261 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0103others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.126+11264C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698063 | ||||||
| chr1:236698069
|
C | T | 2 | a0001c0001t0005g0055a0001c0004t0005g0065 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.126+11270C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698069 | ||||||
| chr1:236698116
|
T | A | 4 | a0001c0001t0010g0043a0001c0001t0010g0044a0001c0001t0010g0045others(1): Show | 4 | HG01361.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+11317T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698116 | ||||||
| chr1:236698224
|
T | A | 2 | a0001c0001t0001g0103a0001c0007t0004g0112 | 2 | HG01081.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.126+11425T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698224 | ||||||
| chr1:236698224
|
T | TA | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.126+11437dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236698224 | |||||
| chr1:236698328
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.126+11529T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698328 | ||||||
| chr1:236698357
|
G | A | 334 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(331): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.126+11558G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698357 | ||||||
| chr1:236698505
|
G | A | 298 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0103others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.126+11706G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698505 | ||||||
| chr1:236698621
|
C | T | 51 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(48): Show | 51 | HG00609.hp1 HG00741.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.126+11822C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698621 | ||||||
| chr1:236698642
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.126+11843G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698642 | ||||||
| chr1:236698783
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.126+11984T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698783 | ||||||
| chr1:236698968
|
G | A | 1 | a0001c0001t0003g0021 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.126+12169G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698968 | ||||||
| chr1:236698991
|
C | T | 1 | a0001c0001t0001g0319 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.126+12192C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698991 | ||||||
| chr1:236698994
|
A | G | 1 | a0006c0022t0001g0203 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.126+12195A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236698994 | ||||||
| chr1:236699012
|
C | A | 16 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(13): Show | 16 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+12213C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699012 | ||||||
| chr1:236699105
|
A | T | 1 | a0002c0005t0004g0306 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.126+12306A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699105 | ||||||
| chr1:236699152
|
T | G | 1 | a0001c0003t0005g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.126+12353T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699152 | ||||||
| chr1:236699190
|
A | G | 1 | a0001c0004t0005g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126+12391A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699190 | ||||||
| chr1:236699258
|
A | G | 1 | a0002c0008t0004g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.126+12459A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699258 | ||||||
| chr1:236699395
|
A | G | 6 | a0001c0001t0001g0304a0001c0001t0001g0319a0001c0001t0003g0268others(3): Show | 6 | HG00438.hp1 NA18944.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+12596A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699395 | ||||||
| chr1:236699569
|
T | G | 2 | a0001c0028t0026g0106a0001c0029t0005g0107 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.126+12770T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699569 | ||||||
| chr1:236699628
|
C | T | 3 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118 | 3 | HG02647.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.126+12829C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699628 | ||||||
| chr1:236699817
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.126+13018C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699817 | ||||||
| chr1:236699818
|
G | A | 3 | a0001c0003t0022g0093a0003c0012t0008g0092a0003c0012t0008g0098 | 3 | HG01243.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+13019G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699818 | ||||||
| chr1:236699912
|
A | G | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+13113A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699912 | ||||||
| chr1:236699913
|
G | A | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+13114G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236699913 | ||||||
| chr1:236700117
|
A | T | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+13318A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700117 | ||||||
| chr1:236700189
|
T | C | 3 | a0001c0002t0007g0176a0001c0002t0007g0201a0001c0002t0007g0209 | 3 | HG00642.hp2 HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.126+13390T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700189 | ||||||
| chr1:236700228
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | NA19011.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.126+13429A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700228 | ||||||
| chr1:236700313
|
G | T | 92 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.126+13514G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700313 | ||||||
| chr1:236700412
|
G | A | 1 | a0001c0001t0003g0279 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.126+13613G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700412 | ||||||
| chr1:236700427
|
C | T | 1 | a0001c0002t0013g0325 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.126+13628C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700427 | ||||||
| chr1:236700470
|
G | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+13671G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700470 | ||||||
| chr1:236700471
|
C | G | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+13672C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700471 | ||||||
| chr1:236700531
|
C | T | 30 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(27): Show | 30 | HG00609.hp1 HG00741.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.126+13732C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700531 | ||||||
| chr1:236700651
|
A | G | 68 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.126+13852A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700651 | ||||||
| chr1:236700722
|
C | T | 3 | a0001c0001t0001g0011a0001c0009t0003g0012a0001c0009t0003g0013 | 3 | HG00323.hp1 NA18964.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.126+13923C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700722 | ||||||
| chr1:236700723
|
G | T | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+13924G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236700723 | ||||||
| chr1:236701057
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.126+14258G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701057 | ||||||
| chr1:236701085
|
C | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.126+14286C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701085 | ||||||
| chr1:236701159
|
C | T | 96 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.126+14360C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701159 | ||||||
| chr1:236701258
|
T | C | 11 | a0001c0003t0002g0051a0001c0003t0005g0047a0001c0003t0005g0048others(8): Show | 11 | HG01109.hp1 HG01192.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+14459T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701258 | ||||||
| chr1:236701286
|
G | C | 11 | a0001c0003t0002g0051a0001c0003t0005g0047a0001c0003t0005g0048others(8): Show | 11 | HG01109.hp1 HG01192.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+14487G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701286 | ||||||
| chr1:236701314
|
G | A | 213 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0031others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.126+14515G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701314 | ||||||
| chr1:236701368
|
GA | G | 3 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118 | 3 | HG02647.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.126+14570delA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701368 | ||||||
| chr1:236701377
|
G | GTA | 6 | a0001c0001t0005g0055a0001c0001t0011g0090a0001c0001t0015g0116others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+14586_126+1458 others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236701377 | |||||
| chr1:236701504
|
C | T | 1 | a0001c0001t0003g0336 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.126+14705C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701504 | ||||||
| chr1:236701529
|
T | C | 27 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(24): Show | 27 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.126+14730T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701529 | ||||||
| chr1:236701720
|
A | T | 67 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.126+14921A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701720 | ||||||
| chr1:236701904
|
G | A | 1 | a0001c0001t0003g0336 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.126+15105G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701904 | ||||||
| chr1:236701916
|
G | A | 1 | a0001c0028t0026g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.126+15117G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701916 | ||||||
| chr1:236701928
|
A | C | 2 | a0001c0001t0004g0037a0001c0001t0011g0036 | 2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.126+15129A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701928 | ||||||
| chr1:236701942
|
G | C | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+15143G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701942 | ||||||
| chr1:236701943
|
C | G | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.126+15144C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236701943 | ||||||
| chr1:236702064
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.126+15265G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236702064 | ||||||
| chr1:236702132
|
T | TA | 6 | a0001c0001t0018g0303a0001c0002t0002g0271a0001c0002t0002g0283others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+15340dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236702132 | |||||
| chr1:236702268
|
G | A | 42 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0103others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.126+15469G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236702268 | ||||||
| chr1:236702653
|
A | T | 343 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.127-15205A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236702653 | ||||||
| chr1:236702708
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0003g0020a0001c0001t0004g0003others(16): Show | 19 | HG00323.hp1 HG02083.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-15150A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236702708 | ||||||
| chr1:236702723
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01071.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.127-15135G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236702723 | ||||||
| chr1:236702760
|
T | C | 1 | a0001c0007t0004g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.127-15098T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236702760 | ||||||
| chr1:236703252
|
T | G | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-14606T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703252 | ||||||
| chr1:236703413
|
C | T | 2 | a0001c0002t0002g0223a0001c0002t0002g0237 | 2 | HG02132.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.127-14445C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703413 | ||||||
| chr1:236703414
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127-14444G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703414 | ||||||
| chr1:236703423
|
G | T | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-14435G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703423 | ||||||
| chr1:236703433
|
C | CT | 27 | a0001c0001t0001g0184a0001c0001t0001g0221a0001c0001t0001g0276others(24): Show | 27 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-14401dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236703433 | |||||
| chr1:236703433
|
CT | C | 46 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0251others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.127-14401delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236703433 | |||||
| chr1:236703434
|
T | A | 7 | a0001c0001t0001g0103a0001c0001t0004g0178a0001c0001t0004g0200others(4): Show | 7 | HG01081.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-14424T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703434 | ||||||
| chr1:236703515
|
G | T | 1 | a0001c0001t0015g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-14343G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703515 | ||||||
| chr1:236703536
|
C | T | 27 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(24): Show | 27 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-14322C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703536 | ||||||
| chr1:236703561
|
A | G | 2 | a0001c0001t0017g0097a0001c0007t0015g0096 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-14297A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703561 | ||||||
| chr1:236703662
|
CT | C | 26 | a0001c0001t0003g0238a0001c0001t0003g0272a0001c0001t0003g0340others(23): Show | 26 | HG01243.hp2 HG01261.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.127-14183delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236703662 | |||||
| chr1:236703700
|
A | T | 2 | a0001c0001t0017g0097a0001c0007t0015g0096 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-14158A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703700 | ||||||
| chr1:236703837
|
G | A | 2 | a0003c0012t0008g0092a0003c0012t0008g0098 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-14021G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236703837 | ||||||
| chr1:236704012
|
A | C | 2 | a0001c0001t0017g0097a0001c0007t0015g0096 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-13846A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704012 | ||||||
| chr1:236704071
|
G | A | 4 | a0001c0001t0015g0116a0001c0015t0016g0113a0001c0015t0016g0115others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-13787G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704071 | ||||||
| chr1:236704094
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.127-13764C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704094 | ||||||
| chr1:236704285
|
C | T | 1 | a0001c0001t0011g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.127-13573C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704285 | ||||||
| chr1:236704327
|
T | C | 3 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118 | 3 | HG02647.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.127-13531T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704327 | ||||||
| chr1:236704557
|
T | C | 1 | a0001c0001t0004g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.127-13301T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704557 | ||||||
| chr1:236704722
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.127-13136G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704722 | ||||||
| chr1:236704723
|
C | G | 1 | a0001c0001t0001g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.127-13135C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704723 | ||||||
| chr1:236704725
|
C | T | 3 | a0001c0001t0015g0116a0001c0015t0016g0113a0001c0015t0016g0115 | 3 | HG01168.hp2 HG01169.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.127-13133C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704725 | ||||||
| chr1:236704833
|
C | T | 5 | a0001c0013t0002g0054a0001c0013t0023g0095a0001c0014t0002g0052others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-13025C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704833 | ||||||
| chr1:236704878
|
T | C | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(1): Show | 4 | HG01099.hp2 HG01258.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-12980T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704878 | ||||||
| chr1:236704900
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.127-12958A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236704900 | ||||||
| chr1:236705020
|
C | T | 5 | a0001c0013t0002g0054a0001c0013t0023g0095a0001c0014t0002g0052others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-12838C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705020 | ||||||
| chr1:236705051
|
A | C | 1 | a0001c0001t0003g0249 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.127-12807A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705051 | ||||||
| chr1:236705110
|
A | C | 1 | a0001c0002t0002g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-12748A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705110 | ||||||
| chr1:236705207
|
A | AAT | 3 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118 | 3 | HG02647.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.127-12639_127-1263 others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236705207 | |||||
| chr1:236705221
|
A | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.127-12637A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705221 | ||||||
| chr1:236705301
|
GAAAGAC | G | 3 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118 | 3 | HG02647.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.127-12556_127-1255 others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705301 | ||||||
| chr1:236705377
|
A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0041others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.127-12481A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705377 | ||||||
| chr1:236705388
|
T | C | 1 | a0001c0001t0003g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.127-12470T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705388 | ||||||
| chr1:236705433
|
A | G | 103 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.127-12425A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705433 | ||||||
| chr1:236705522
|
GGT | G | 9 | a0001c0001t0003g0020a0001c0001t0004g0003a0001c0001t0004g0015others(6): Show | 9 | HG02622.hp1 HG03486.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-12334_127-1233 others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236705522 | |||||
| chr1:236705658
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0017g0097a0001c0007t0015g0096 | 3 | HG03195.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-12200G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705658 | ||||||
| chr1:236705666
|
A | C | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12192A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705666 | ||||||
| chr1:236705669
|
G | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12189G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705669 | ||||||
| chr1:236705671
|
T | C | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12187T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705671 | ||||||
| chr1:236705672
|
T | A | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12186T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705672 | ||||||
| chr1:236705674
|
T | A | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12184T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705674 | ||||||
| chr1:236705675
|
T | G | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12183T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705675 | ||||||
| chr1:236705676
|
C | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12182C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705676 | ||||||
| chr1:236705677
|
C | G | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12181C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705677 | ||||||
| chr1:236705678
|
C | A | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12180C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705678 | ||||||
| chr1:236705685
|
A | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-12173A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236705685 | ||||||
| chr1:236706111
|
CT | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.127-11735delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236706111 | |||||
| chr1:236706154
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.127-11704T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706154 | ||||||
| chr1:236706428
|
A | G | 1 | a0001c0002t0007g0300 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.127-11430A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706428 | ||||||
| chr1:236706446
|
G | T | 1 | a0001c0001t0001g0308 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.127-11412G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706446 | ||||||
| chr1:236706636
|
A | T | 3 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118 | 3 | HG02647.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.127-11222A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706636 | ||||||
| chr1:236706668
|
C | G | 1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.127-11190C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706668 | ||||||
| chr1:236706798
|
C | G | 1 | a0001c0001t0011g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.127-11060C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706798 | ||||||
| chr1:236706856
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0003g0138 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.127-11002C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706856 | ||||||
| chr1:236706946
|
C | T | 343 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.127-10912C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706946 | ||||||
| chr1:236706955
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.127-10903G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236706955 | ||||||
| chr1:236707015
|
G | A | 7 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG00673.hp2 NA18941.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-10843G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707015 | ||||||
| chr1:236707142
|
T | A | 1 | a0001c0007t0004g0112 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-10716T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707142 | ||||||
| chr1:236707288
|
C | T | 19 | a0001c0001t0001g0011a0001c0001t0003g0020a0001c0001t0004g0003others(16): Show | 19 | HG00323.hp1 HG02083.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-10570C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707288 | ||||||
| chr1:236707305
|
A | C | 1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-10553A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707305 | ||||||
| chr1:236707306
|
G | T | 1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-10552G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707306 | ||||||
| chr1:236707311
|
G | T | 1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-10547G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707311 | ||||||
| chr1:236707315
|
C | T | 1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-10543C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707315 | ||||||
| chr1:236707316
|
C | G | 1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-10542C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707316 | ||||||
| chr1:236707317
|
T | A | 1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-10541T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707317 | ||||||
| chr1:236707319
|
C | G | 1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-10539C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707319 | ||||||
| chr1:236707412
|
T | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0244 | 2 | HG01934.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.127-10446T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707412 | ||||||
| chr1:236707500
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.127-10358A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707500 | ||||||
| chr1:236707659
|
CTTTTCTT others(5): Show |
C | 105 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.127-10185_127-1017 others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236707659 | |||||
| chr1:236707709
|
CT | C | 95 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(92): Show | 95 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.127-10129delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236707709 | |||||
| chr1:236707709
|
CTT | C | 70 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0139others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.127-10130_127-1012 others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236707709 | |||||
| chr1:236707709
|
CTTT | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.127-10131_127-1012 others(7): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236707709 | |||||
| chr1:236707709
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0009g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127-10141_127-1012 others(17): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236707709 | |||||
| chr1:236707814
|
C | T | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-10044C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707814 | ||||||
| chr1:236707868
|
C | T | 5 | a0001c0013t0002g0054a0001c0013t0023g0095a0001c0014t0002g0052others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-9990C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707868 | ||||||
| chr1:236707991
|
G | A | 44 | a0001c0001t0003g0238a0001c0001t0004g0059a0001c0001t0006g0135others(41): Show | 44 | HG00639.hp2 HG01123.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-9867G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236707991 | ||||||
| chr1:236708028
|
G | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 49 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.127-9830G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708028 | ||||||
| chr1:236708078
|
A | G | 1 | a0006c0022t0001g0203 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127-9780A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708078 | ||||||
| chr1:236708222
|
G | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 68 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.127-9636G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708222 | ||||||
| chr1:236708223
|
C | T | 1 | a0001c0004t0002g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-9635C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708223 | ||||||
| chr1:236708323
|
G | A | 3 | a0001c0001t0015g0116a0001c0015t0016g0113a0001c0015t0016g0115 | 3 | HG01168.hp2 HG01169.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.127-9535G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708323 | ||||||
| chr1:236708672
|
G | A | 17 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(14): Show | 17 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-9186G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708672 | ||||||
| chr1:236708718
|
G | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.127-9140G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708718 | ||||||
| chr1:236708811
|
T | C | 2 | a0001c0001t0002g0156a0001c0001t0003g0138 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.127-9047T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708811 | ||||||
| chr1:236708858
|
C | T | 4 | a0001c0004t0002g0064a0001c0004t0005g0060a0001c0004t0005g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-9000C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708858 | ||||||
| chr1:236708932
|
C | T | 1 | a0001c0001t0003g0339 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.127-8926C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236708932 | ||||||
| chr1:236709066
|
T | G | 1 | a0001c0001t0003g0022 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.127-8792T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709066 | ||||||
| chr1:236709111
|
C | T | 1 | a0006c0022t0001g0203 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127-8747C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709111 | ||||||
| chr1:236709112
|
G | A | 18 | a0001c0001t0001g0011a0001c0001t0003g0020a0001c0001t0004g0003others(15): Show | 18 | HG00323.hp1 HG02083.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-8746G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709112 | ||||||
| chr1:236709125
|
G | C | 1 | a0001c0004t0005g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-8733G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709125 | ||||||
| chr1:236709132
|
C | T | 27 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(24): Show | 27 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-8726C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709132 | ||||||
| chr1:236709175
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.127-8683A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709175 | ||||||
| chr1:236709218
|
C | CTG | 15 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0154others(12): Show | 15 | HG00609.hp1 HG01243.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.127-8638_127-8637d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709218 | |||||
| chr1:236709218
|
C | CTGTG | 7 | a0001c0001t0001g0145a0001c0001t0002g0156a0001c0001t0003g0138others(4): Show | 7 | HG01261.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-8637_127-8636i others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709218 | |||||
| chr1:236709220
|
G | GTA | 16 | a0001c0001t0001g0041a0001c0001t0001g0222a0001c0001t0001g0224others(13): Show | 16 | HG00323.hp2 HG00438.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-8603_127-8602d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTATA | 13 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0244others(10): Show | 13 | HG00099.hp2 HG00544.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-8605_127-8602d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTATATA | 7 | a0001c0001t0003g0202a0001c0001t0010g0045a0001c0001t0010g0046others(4): Show | 7 | HG02132.hp2 HG03130.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-8607_127-8602d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0184a0001c0001t0001g0230a0001c0001t0004g0226others(4): Show | 7 | HG00423.hp1 HG01099.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-8609_127-8602d others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0003g0234a0001c0002t0002g0218a0001c0002t0007g0323 | 3 | NA18949.hp2 NA18991.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.127-8611_127-8602d others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTGTGTA | 4 | a0001c0003t0002g0170a0001c0011t0004g0101a0001c0011t0005g0100others(1): Show | 4 | HG02055.hp2 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-8637_127-8636i others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTGTGTGT others(3): Show |
5 | a0001c0003t0005g0047a0001c0003t0005g0048a0001c0003t0005g0050others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-8637_127-8636i others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTGTGTGT others(5): Show |
1 | a0001c0003t0002g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.127-8637_127-8636i others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTGTGTGT others(7): Show |
2 | a0003c0012t0008g0092a0003c0012t0008g0098 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-8637_127-8636i others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTGTGTGT others(5): Show |
1 | a0001c0003t0006g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.127-8637_127-8636i others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTGTGTGT others(7): Show |
12 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0006g0124others(9): Show | 12 | HG01433.hp1 HG01952.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-8637_127-8636i others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTGTGTGT others(9): Show |
2 | a0001c0003t0006g0136a0001c0003t0020g0122 | 2 | HG01123.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.127-8637_127-8636i others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0006g0135 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.127-8637_127-8636i others(20): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
GTA | G | 8 | a0001c0001t0001g0225a0001c0001t0004g0074a0001c0001t0004g0078others(5): Show | 8 | HG01106.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-8603_127-8602d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
GTATA | G | 10 | a0001c0001t0001g0205a0001c0001t0003g0021a0001c0001t0003g0026others(7): Show | 10 | HG01255.hp2 HG01891.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-8605_127-8602d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
GTATATA | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(19): Show | 22 | HG00544.hp1 HG00609.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-8607_127-8602d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
GTATATAT others(1): Show |
G | 12 | a0001c0001t0014g0082a0001c0001t0014g0084a0001c0001t0014g0086others(9): Show | 12 | HG01981.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-8609_127-8602d others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
GTATATAT others(3): Show |
G | 16 | a0001c0001t0001g0011a0001c0001t0003g0020a0001c0001t0004g0003others(13): Show | 16 | HG00323.hp1 HG02083.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-8611_127-8602d others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709220
|
GTATATAT others(5): Show |
G | 6 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0004g0028others(3): Show | 6 | HG02083.hp1 NA18939.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-8613_127-8602d others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709220 | |||||
| chr1:236709222
|
A | G | 35 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(32): Show | 35 | HG00609.hp1 HG00673.hp2 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.127-8636A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709222 | ||||||
| chr1:236709224
|
A | G | 22 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(19): Show | 22 | HG00673.hp2 HG01106.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-8634A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709224 | ||||||
| chr1:236709239
|
TATATATA others(11): Show |
T | 1 | a0001c0002t0002g0189 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.127-8617_127-8600d others(20): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709239 | |||||
| chr1:236709242
|
A | G | 7 | a0001c0003t0002g0170a0001c0003t0003g0058a0001c0003t0005g0172others(4): Show | 7 | HG01261.hp1 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-8616A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709242 | ||||||
| chr1:236709249
|
T | TATATATA others(5): Show |
2 | a0001c0002t0002g0212a0001c0002t0002g0229 | 2 | NA18944.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.127-8602_127-8601i others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709249 | |||||
| chr1:236709251
|
T | C | 6 | a0001c0001t0003g0272a0001c0001t0009g0091a0001c0002t0002g0255others(3): Show | 6 | HG02080.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-8607T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709251 | ||||||
| chr1:236709251
|
T | TACAC | 4 | a0001c0001t0001g0006a0001c0001t0001g0312a0001c0001t0019g0250others(1): Show | 4 | HG02129.hp2 HG03239.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-8606_127-8605i others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709251 | |||||
| chr1:236709253
|
T | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0157a0001c0001t0001g0158others(34): Show | 37 | HG01169.hp1 HG01243.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-8605T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709253 | ||||||
| chr1:236709253
|
T | TAC | 4 | a0001c0001t0001g0258a0001c0001t0001g0264a0001c0001t0001g0318others(1): Show | 4 | HG00741.hp2 HG04115.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-8604_127-8603i others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709253 | |||||
| chr1:236709253
|
T | TACAC | 40 | a0001c0001t0001g0159a0001c0001t0001g0269a0001c0001t0001g0275others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.127-8604_127-8603i others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709253 | |||||
| chr1:236709253
|
TATAC | T | 3 | a0001c0001t0001g0103a0001c0015t0016g0113a0001c0015t0016g0115 | 3 | HG01081.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.127-8603_127-8600d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709253 | |||||
| chr1:236709255
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.127-8603T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709255 | ||||||
| chr1:236709255
|
T | TACACAC | 35 | a0001c0001t0001g0031a0001c0001t0001g0251a0001c0001t0001g0253others(32): Show | 35 | HG00280.hp2 HG00738.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-8591_127-8586d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TACACACA others(1): Show |
4 | a0001c0001t0003g0173a0001c0001t0004g0295a0001c0001t0017g0097others(1): Show | 4 | HG03516.hp1 HG03831.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-8593_127-8586d others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TATACACA others(1): Show |
6 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0274others(3): Show | 6 | HG00738.hp2 HG01258.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-8602_127-8601i others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TATACACA others(3): Show |
2 | a0001c0001t0003g0104a0001c0016t0003g0108 | 2 | HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.127-8602_127-8601i others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TATATAC | 3 | a0001c0001t0001g0190a0001c0001t0001g0236a0001c0001t0001g0261 | 3 | HG02523.hp1 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.127-8602_127-8601i others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TATATACA others(3): Show |
8 | a0001c0001t0001g0018a0001c0001t0004g0178a0001c0001t0004g0200others(5): Show | 8 | HG01258.hp1 HG01516.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-8602_127-8601i others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TATATACA others(5): Show |
1 | a0001c0002t0002g0302 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.127-8602_127-8601i others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0288a0001c0001t0004g0102 | 2 | HG03195.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.127-8602_127-8601i others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TATATATA others(7): Show |
3 | a0001c0004t0005g0199a0001c0007t0004g0112a0001c0027t0001g0311 | 3 | HG01516.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.127-8602_127-8601i others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709255
|
T | TATATATA others(9): Show |
2 | a0001c0001t0001g0317a0001c0002t0002g0313 | 2 | HG00621.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.127-8602_127-8601i others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709255 | |||||
| chr1:236709257
|
C | CATATAT | 22 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0002g0051others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-8600_127-8599i others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709257 | |||||
| chr1:236709257
|
C | T | 37 | a0001c0001t0001g0188a0001c0001t0001g0195a0001c0001t0001g0221others(34): Show | 37 | HG00280.hp1 HG00621.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-8601C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709257 | ||||||
| chr1:236709259
|
C | T | 47 | a0001c0001t0001g0188a0001c0001t0003g0238a0001c0001t0004g0059others(44): Show | 47 | HG00280.hp1 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.127-8599C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709259 | ||||||
| chr1:236709261
|
C | T | 46 | a0001c0001t0001g0188a0001c0001t0003g0238a0001c0001t0004g0059others(43): Show | 46 | HG00280.hp1 HG00621.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.127-8597C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709261 | ||||||
| chr1:236709263
|
C | T | 19 | a0001c0001t0003g0238a0001c0001t0004g0059a0001c0002t0002g0182others(16): Show | 19 | HG00280.hp1 HG01243.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-8595C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709263 | ||||||
| chr1:236709265
|
C | T | 2 | a0001c0002t0002g0182a0001c0004t0005g0061 | 2 | HG00280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.127-8593C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709265 | ||||||
| chr1:236709273
|
T | C | 25 | a0001c0001t0001g0103a0001c0001t0001g0188a0001c0001t0001g0221others(22): Show | 25 | HG00280.hp1 HG00621.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.127-8585T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709273 | ||||||
| chr1:236709275
|
T | C | 6 | a0001c0001t0001g0188a0001c0001t0001g0289a0001c0001t0001g0312others(3): Show | 6 | HG00280.hp1 HG00621.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-8583T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709275 | ||||||
| chr1:236709277
|
T | C | 3 | a0001c0001t0001g0188a0001c0001t0003g0339a0001c0002t0002g0182 | 3 | HG00280.hp1 HG00621.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.127-8581T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709277 | ||||||
| chr1:236709278
|
ATGTATAT others(5): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.127-8578_127-8567d others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709278 | |||||
| chr1:236709279
|
T | C | 1 | a0001c0002t0002g0182 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127-8579T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709279 | ||||||
| chr1:236709280
|
G | A | 13 | a0001c0001t0001g0259a0001c0001t0001g0280a0001c0001t0001g0289others(10): Show | 13 | HG00280.hp1 HG02015.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-8578G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709280 | ||||||
| chr1:236709281
|
T | C | 3 | a0001c0002t0002g0182a0001c0002t0002g0220a0001c0004t0005g0061 | 3 | HG00280.hp1 HG02451.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.127-8577T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709281 | ||||||
| chr1:236709288
|
A | G | 1 | a0001c0001t0003g0339 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.127-8570A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709288 | ||||||
| chr1:236709290
|
G | A | 1 | a0001c0001t0003g0339 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.127-8568G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709290 | ||||||
| chr1:236709307
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.127-8551C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709307 | ||||||
| chr1:236709318
|
A | G | 77 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(74): Show | 77 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.127-8540A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709318 | ||||||
| chr1:236709329
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.127-8529T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709329 | ||||||
| chr1:236709341
|
C | T | 3 | a0001c0011t0004g0101a0001c0011t0005g0100a0008c0017t0024g0099 | 3 | HG02055.hp2 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-8517C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709341 | ||||||
| chr1:236709344
|
G | GTA | 52 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(49): Show | 52 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.127-8501_127-8500d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709344 | |||||
| chr1:236709344
|
G | GTATA | 18 | a0001c0001t0003g0238a0001c0001t0004g0059a0001c0003t0002g0170others(15): Show | 18 | HG01243.hp2 HG01261.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-8503_127-8500d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709344 | |||||
| chr1:236709344
|
G | GTATATA | 3 | a0001c0001t0005g0055a0001c0001t0011g0090a0001c0004t0005g0065 | 3 | HG02109.hp2 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.127-8505_127-8500d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709344 | |||||
| chr1:236709344
|
G | GTATATAT others(29): Show |
1 | a0001c0003t0002g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.127-8500_127-8499i others(38): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709344 | |||||
| chr1:236709358
|
A | ATATACG | 3 | a0001c0001t0015g0116a0001c0015t0016g0113a0001c0015t0016g0115 | 3 | HG01168.hp2 HG01169.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.127-8500_127-8499i others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709358 | ||||||
| chr1:236709359
|
C | T | 3 | a0001c0001t0015g0116a0001c0015t0016g0113a0001c0015t0016g0115 | 3 | HG01168.hp2 HG01169.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.127-8499C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709359 | ||||||
| chr1:236709368
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.127-8490G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709368 | ||||||
| chr1:236709368
|
G | GTA | 74 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(71): Show | 74 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.127-8478_127-8477d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709368 | |||||
| chr1:236709427
|
G | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.127-8431G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709427 | ||||||
| chr1:236709456
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-8402G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709456 | ||||||
| chr1:236709480
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127-8378T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709480 | ||||||
| chr1:236709486
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0017g0097a0001c0007t0015g0096 | 3 | HG03195.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-8372G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709486 | ||||||
| chr1:236709516
|
G | A | 1 | a0001c0016t0003g0108 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.127-8342G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709516 | ||||||
| chr1:236709529
|
G | A | 100 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.127-8329G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709529 | ||||||
| chr1:236709548
|
T | C | 3 | a0001c0001t0004g0102a0001c0001t0017g0097a0001c0007t0015g0096 | 3 | HG03195.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-8310T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709548 | ||||||
| chr1:236709587
|
GGAA | G | 6 | a0001c0001t0005g0055a0001c0001t0011g0090a0001c0001t0015g0116others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-8269_127-8267d others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236709587 | |||||
| chr1:236709607
|
A | G | 1 | a0001c0001t0004g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.127-8251A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709607 | ||||||
| chr1:236709670
|
C | T | 8 | a0001c0003t0002g0051a0001c0003t0005g0047a0001c0003t0005g0048others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-8188C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709670 | ||||||
| chr1:236709854
|
C | A | 9 | a0001c0001t0004g0059a0001c0004t0002g0062a0001c0004t0002g0064others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-8004C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709854 | ||||||
| chr1:236709945
|
T | C | 101 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.127-7913T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236709945 | ||||||
| chr1:236710004
|
T | C | 101 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.127-7854T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710004 | ||||||
| chr1:236710115
|
C | T | 3 | a0001c0003t0003g0058a0001c0003t0005g0172a0001c0006t0002g0171 | 3 | HG01261.hp1 HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.127-7743C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710115 | ||||||
| chr1:236710197
|
A | C | 1 | a0001c0002t0007g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.127-7661A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710197 | ||||||
| chr1:236710335
|
T | A | 1 | a0001c0001t0001g0258 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-7523T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710335 | ||||||
| chr1:236710375
|
C | T | 17 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(14): Show | 17 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-7483C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710375 | ||||||
| chr1:236710376
|
G | A | 6 | a0001c0001t0005g0055a0001c0001t0011g0090a0001c0001t0015g0116others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-7482G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710376 | ||||||
| chr1:236710471
|
G | C | 1 | a0001c0001t0004g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.127-7387G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710471 | ||||||
| chr1:236710594
|
G | C | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-7264G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710594 | ||||||
| chr1:236710597
|
C | A | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-7261C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710597 | ||||||
| chr1:236710601
|
G | A | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-7257G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710601 | ||||||
| chr1:236710602
|
G | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-7256G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710602 | ||||||
| chr1:236710603
|
C | G | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-7255C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710603 | ||||||
| chr1:236710605
|
C | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-7253C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710605 | ||||||
| chr1:236710638
|
G | A | 44 | a0001c0001t0003g0238a0001c0001t0004g0059a0001c0001t0006g0135others(41): Show | 44 | HG00639.hp2 HG01123.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-7220G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710638 | ||||||
| chr1:236710720
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.127-7138A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710720 | ||||||
| chr1:236710805
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.127-7053C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710805 | ||||||
| chr1:236710823
|
G | A | 335 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(332): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.127-7035G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710823 | ||||||
| chr1:236710838
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.127-7020C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710838 | ||||||
| chr1:236710906
|
G | A | 1 | a0001c0002t0002g0220 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127-6952G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710906 | ||||||
| chr1:236710923
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-6935C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710923 | ||||||
| chr1:236710961
|
C | T | 1 | a0001c0004t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-6897C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710961 | ||||||
| chr1:236710985
|
A | C | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-6873A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710985 | ||||||
| chr1:236710992
|
G | A | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-6866G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710992 | ||||||
| chr1:236710995
|
G | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-6863G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710995 | ||||||
| chr1:236710997
|
C | A | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-6861C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710997 | ||||||
| chr1:236710998
|
A | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-6860A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236710998 | ||||||
| chr1:236711000
|
A | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-6858A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711000 | ||||||
| chr1:236711001
|
G | T | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-6857G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711001 | ||||||
| chr1:236711163
|
A | C | 5 | a0001c0001t0004g0178a0001c0001t0004g0200a0001c0001t0005g0181others(2): Show | 5 | HG02572.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-6695A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711163 | ||||||
| chr1:236711166
|
G | T | 1 | a0001c0001t0006g0135 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.127-6692G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711166 | ||||||
| chr1:236711215
|
G | T | 3 | a0001c0001t0005g0055a0001c0001t0011g0090a0001c0004t0005g0065 | 3 | HG02109.hp2 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.127-6643G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711215 | ||||||
| chr1:236711371
|
G | C | 1 | a0001c0003t0002g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-6487G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711371 | ||||||
| chr1:236711531
|
G | A | 3 | a0001c0001t0015g0116a0001c0015t0016g0113a0001c0015t0016g0115 | 3 | HG01168.hp2 HG01169.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.127-6327G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711531 | ||||||
| chr1:236711542
|
A | T | 2 | a0001c0001t0001g0260a0001c0001t0003g0299 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.127-6316A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711542 | ||||||
| chr1:236711611
|
A | G | 1 | a0001c0004t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-6247A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711611 | ||||||
| chr1:236711678
|
T | C | 1 | a0001c0001t0004g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.127-6180T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711678 | ||||||
| chr1:236711996
|
G | C | 12 | a0001c0001t0001g0259a0001c0001t0001g0280a0001c0001t0001g0289others(9): Show | 12 | HG02015.hp1 HG02027.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-5862G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236711996 | ||||||
| chr1:236712013
|
A | C | 3 | a0001c0001t0005g0151a0001c0001t0009g0152a0001c0002t0002g0162 | 3 | HG01109.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.127-5845A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712013 | ||||||
| chr1:236712111
|
C | T | 2 | a0001c0001t0003g0026a0001c0001t0003g0039 | 2 | NA19009.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.127-5747C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712111 | ||||||
| chr1:236712340
|
T | C | 67 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.127-5518T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712340 | ||||||
| chr1:236712360
|
C | T | 1 | a0001c0001t0003g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.127-5498C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712360 | ||||||
| chr1:236712471
|
C | T | 107 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.127-5387C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712471 | ||||||
| chr1:236712540
|
G | GTAATATC others(60): Show |
1 | a0001c0002t0002g0310 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.127-5317_127-5251d others(69): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236712540 | |||||
| chr1:236712563
|
G | A | 2 | a0001c0001t0017g0097a0001c0007t0015g0096 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-5295G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712563 | ||||||
| chr1:236712651
|
C | T | 101 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.127-5207C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712651 | ||||||
| chr1:236712657
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.127-5201A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712657 | ||||||
| chr1:236712724
|
A | C | 1 | a0001c0002t0007g0323 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.127-5134A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712724 | ||||||
| chr1:236712785
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.127-5073G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712785 | ||||||
| chr1:236712799
|
T | C | 74 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(71): Show | 74 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.127-5059T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712799 | ||||||
| chr1:236712800
|
T | C | 7 | a0001c0001t0003g0238a0001c0001t0004g0059a0001c0004t0002g0064others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-5058T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712800 | ||||||
| chr1:236712813
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.127-5045A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712813 | ||||||
| chr1:236712877
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.127-4981T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712877 | ||||||
| chr1:236712920
|
CT | C | 172 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0103others(169): Show | 172 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.127-4924delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236712920 | |||||
| chr1:236712920
|
CTT | C | 43 | a0001c0001t0001g0018a0001c0001t0001g0110a0001c0001t0001g0190others(40): Show | 43 | HG00140.hp2 HG00738.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-4925_127-4924d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236712920 | |||||
| chr1:236712920
|
CTTT | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 26 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.127-4926_127-4924d others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236712920 | |||||
| chr1:236712957
|
C | A | 107 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.127-4901C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236712957 | ||||||
| chr1:236713044
|
G | C | 5 | a0001c0013t0002g0054a0001c0013t0023g0095a0001c0014t0002g0052others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-4814G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713044 | ||||||
| chr1:236713082
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.127-4776G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713082 | ||||||
| chr1:236713183
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.127-4675C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713183 | ||||||
| chr1:236713226
|
C | CT | 93 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0184others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.127-4619dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713226 | |||||
| chr1:236713226
|
CT | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0110a0001c0001t0003g0104others(9): Show | 12 | HG00140.hp2 HG00738.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-4619delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713226 | |||||
| chr1:236713291
|
G | C | 101 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.127-4567G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713291 | ||||||
| chr1:236713337
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.127-4521T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713337 | ||||||
| chr1:236713403
|
T | G | 5 | a0001c0013t0002g0054a0001c0013t0023g0095a0001c0014t0002g0052others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-4455T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713403 | ||||||
| chr1:236713462
|
A | G | 2 | a0001c0001t0001g0320a0001c0001t0001g0322 | 2 | HG01081.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.127-4396A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713462 | ||||||
| chr1:236713469
|
C | A | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-4389C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713469 | ||||||
| chr1:236713541
|
G | A | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-4317G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713541 | ||||||
| chr1:236713565
|
G | C | 1 | a0001c0002t0002g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-4293G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713565 | ||||||
| chr1:236713573
|
A | AG | 92 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(89): Show | 92 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.127-4282dupG | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713573 | |||||
| chr1:236713577
|
A | G | 3 | a0001c0001t0003g0339a0001c0001t0025g0010a0001c0002t0007g0298 | 3 | HG01943.hp1 HG02080.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.127-4281A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713577 | ||||||
| chr1:236713584
|
A | G | 93 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(90): Show | 93 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.127-4274A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713584 | ||||||
| chr1:236713593
|
T | TCTGTGTG others(60): Show |
3 | a0001c0001t0005g0055a0001c0001t0011g0090a0001c0004t0005g0065 | 3 | HG02109.hp2 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.127-4252_127-4251i others(69): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(396): Show |
2 | a0001c0001t0003g0104a0001c0016t0003g0108 | 2 | HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.127-3905_127-3904i others(405): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(1468): Show |
1 | a0001c0002t0002g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-3905_127-3904i others(1477): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(2474): Show |
2 | a0001c0004t0005g0081a0001c0007t0004g0083 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.127-3905_127-3904i others(2483): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(2541): Show |
1 | a0001c0002t0002g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127-3905_127-3904i others(2550): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(3614): Show |
1 | a0001c0001t0001g0001 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.127-3905_127-3904i others(3623): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(2273): Show |
1 | a0001c0001t0001g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.127-3905_127-3904i others(2282): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(2474): Show |
1 | a0001c0001t0014g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.127-3905_127-3904i others(2483): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(2541): Show |
8 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0078others(5): Show | 8 | HG01981.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-3905_127-3904i others(2550): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(2742): Show |
1 | a0001c0002t0002g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-3905_127-3904i others(2751): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(2876): Show |
1 | a0001c0001t0001g0005 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.127-3905_127-3904i others(2885): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(1870): Show |
1 | a0001c0001t0003g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.127-3905_127-3904i others(1879): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(3679): Show |
1 | a0001c0001t0004g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.127-3905_127-3904i others(3688): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713593
|
T | TCTGTGTG others(1803): Show |
1 | a0001c0001t0005g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.127-3436_127-3435i others(1812): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713593 | |||||
| chr1:236713605
|
T | TGTATACA others(3748): Show |
1 | a0001c0001t0004g0293 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.127-4039_127-4038i others(3757): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713605 | |||||
| chr1:236713672
|
T | TGTATACA others(60): Show |
63 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.127-4120_127-4119i others(69): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713672 | |||||
| chr1:236713672
|
T | TGTATACA others(998): Show |
1 | a0001c0002t0007g0323 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.127-4120_127-4119i others(1007): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713672 | |||||
| chr1:236713684
|
T | TACCACTG others(61): Show |
1 | a0001c0001t0004g0295 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.127-4173_127-4106d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713684 | |||||
| chr1:236713714
|
A | AGCTTCAT others(60): Show |
1 | a0001c0002t0002g0220 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127-4120_127-4119i others(69): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713714 | |||||
| chr1:236713739
|
T | C | 1 | a0001c0001t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.127-4119T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236713739 | ||||||
| chr1:236713751
|
T | TACCACTG others(61): Show |
32 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0269others(29): Show | 32 | HG00642.hp1 HG01099.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-4106_127-4039d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713751 | |||||
| chr1:236713806
|
T | TGTATACA others(3614): Show |
1 | a0001c0001t0003g0174 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.127-4039_127-4038i others(3623): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713806 | |||||
| chr1:236713818
|
T | TA | 69 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.127-4039dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713818 | |||||
| chr1:236713818
|
T | TACCACTG others(61): Show |
57 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.127-4039_127-3972d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713818 | |||||
| chr1:236713818
|
T | TACCACTG others(61): Show |
1 | a0001c0002t0007g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.127-3983_127-3982i others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713818 | |||||
| chr1:236713828
|
G | GGGATATG others(193): Show |
1 | a0001c0001t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.127-3962_127-3961i others(202): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713828 | |||||
| chr1:236713885
|
T | TA | 5 | a0001c0001t0010g0044a0001c0002t0002g0218a0001c0002t0002g0229others(2): Show | 5 | HG02723.hp2 HG02922.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-3972dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713885 | |||||
| chr1:236713885
|
T | TACCACTG others(61): Show |
42 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0018others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.127-3972_127-3905d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713885 | |||||
| chr1:236713885
|
T | TACCACTG others(1536): Show |
1 | a0001c0001t0003g0023 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127-3905_127-3904i others(1545): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713885 | |||||
| chr1:236713897
|
G | GATATGCA others(61): Show |
1 | a0001c0024t0003g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.127-3905_127-3904i others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713897 | |||||
| chr1:236713935
|
G | GTTTATGT others(61): Show |
1 | a0001c0001t0004g0295 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.127-3905_127-3904i others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713935 | |||||
| chr1:236713935
|
G | GTTTATGT others(194): Show |
1 | a0001c0002t0002g0255 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.127-3895_127-3894i others(203): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713935 | |||||
| chr1:236713935
|
G | GTTTATGT others(195): Show |
1 | a0001c0001t0003g0143 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.127-3857_127-3856i others(204): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713935 | |||||
| chr1:236713952
|
T | TA | 6 | a0001c0001t0003g0039a0001c0001t0003g0111a0001c0001t0004g0246others(3): Show | 6 | HG00609.hp2 HG01891.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-3905dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713952 | |||||
| chr1:236713952
|
T | TACCACTG others(61): Show |
6 | a0001c0001t0001g0320a0001c0001t0003g0166a0001c0001t0003g0167others(3): Show | 6 | HG01255.hp1 HG02083.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-3905_127-3838d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713952 | |||||
| chr1:236713987
|
C | CATTCCTC others(60): Show |
27 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(24): Show | 27 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-3805_127-3804i others(69): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713987 | |||||
| chr1:236713997
|
T | TGTGTGTT others(3546): Show |
1 | a0002c0005t0004g0305 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.127-3771_127-3770i others(3555): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713997 | |||||
| chr1:236713997
|
T | TGTGTGTT others(3479): Show |
1 | a0001c0001t0001g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.127-3771_127-3770i others(3488): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236713997 | |||||
| chr1:236714002
|
G | GTTTATGT others(61): Show |
28 | a0001c0001t0001g0264a0001c0001t0001g0269a0001c0001t0001g0286others(25): Show | 28 | HG00642.hp1 HG01099.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-3838_127-3837i others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714002 | |||||
| chr1:236714007
|
T | TGTATACA others(3280): Show |
1 | a0001c0001t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.127-3838_127-3837i others(3289): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714007 | |||||
| chr1:236714019
|
T | TACCACTG others(128): Show |
1 | a0001c0004t0005g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.127-3790_127-3789i others(137): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714019 | |||||
| chr1:236714019
|
T | TACCACTG others(61): Show |
4 | a0001c0001t0001g0321a0001c0001t0001g0338a0001c0001t0009g0118others(1): Show | 4 | HG00639.hp1 HG01169.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-3838_127-3771d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714019 | |||||
| chr1:236714019
|
T | TACCACTG others(399): Show |
1 | a0001c0001t0011g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.127-3771_127-3770i others(408): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714019 | |||||
| chr1:236714030
|
G | GGATATGC others(466): Show |
1 | a0001c0001t0005g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.127-3771_127-3770i others(475): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714030 | |||||
| chr1:236714064
|
T | TGTGTGTT others(3479): Show |
1 | a0001c0001t0001g0342 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127-3771_127-3770i others(3488): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714064 | |||||
| chr1:236714069
|
G | C | 2 | a0001c0001t0001g0262a0001c0004t0005g0197 | 2 | HG02735.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.127-3789G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714069 | ||||||
| chr1:236714069
|
G | GTTTATGT others(61): Show |
106 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0114others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.127-3771_127-3770i others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714069 | |||||
| chr1:236714074
|
T | C | 1 | a0001c0001t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.127-3784T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714074 | ||||||
| chr1:236714078
|
T | TACACAGA others(61): Show |
1 | a0001c0001t0001g0236 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.127-3771_127-3770i others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714078 | |||||
| chr1:236714086
|
T | TA | 19 | a0001c0001t0001g0006a0001c0001t0001g0253a0001c0001t0001g0258others(16): Show | 19 | HG00099.hp1 HG00741.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-3771dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714086 | |||||
| chr1:236714086
|
T | TACCACTG others(62): Show |
1 | a0001c0002t0002g0218 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.127-3725_127-3724i others(71): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714086 | |||||
| chr1:236714097
|
G | C | 1 | a0001c0001t0011g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.127-3761G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714097 | ||||||
| chr1:236714136
|
G | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0253a0001c0001t0001g0259others(9): Show | 12 | HG00099.hp1 HG01884.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-3722G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714136 | ||||||
| chr1:236714136
|
G | GTTTATGT others(61): Show |
3 | a0001c0001t0010g0044a0001c0002t0002g0229a0001c0010t0002g0183 | 3 | HG02723.hp2 NA19089.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.127-3704_127-3703i others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714136 | |||||
| chr1:236714140
|
A | ATGTATAC others(398): Show |
1 | a0001c0004t0005g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127-3664_127-3663i others(407): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714140 | |||||
| chr1:236714153
|
T | TACCACTG others(61): Show |
2 | a0001c0001t0003g0143a0001c0001t0004g0295 | 2 | NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.127-3704_127-3637d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714153 | |||||
| chr1:236714197
|
C | T | 1 | a0001c0010t0002g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.127-3661C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714197 | ||||||
| chr1:236714198
|
T | TGTGTGTT others(3076): Show |
1 | a0001c0001t0001g0320 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-3570_127-3569i others(3085): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714198 | |||||
| chr1:236714208
|
T | C | 1 | a0001c0002t0007g0323 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.127-3650T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714208 | ||||||
| chr1:236714220
|
T | TA | 25 | a0001c0001t0003g0020a0001c0001t0003g0238a0001c0001t0004g0003others(22): Show | 25 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-3637dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714220 | |||||
| chr1:236714220
|
T | TAACCACT others(129): Show |
1 | a0001c0004t0005g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-3637_127-3636i others(138): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714220 | |||||
| chr1:236714220
|
T | TACCACTG others(61): Show |
18 | a0001c0001t0001g0264a0001c0001t0001g0286a0001c0001t0001g0291others(15): Show | 18 | HG01099.hp2 HG01943.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-3637_127-3570d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714220 | |||||
| chr1:236714220
|
T | TACCACTG others(331): Show |
1 | a0001c0001t0017g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127-3503_127-3502i others(340): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714220 | |||||
| chr1:236714265
|
T | TGTGTGTT others(2673): Show |
1 | a0001c0001t0001g0258 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-3584_127-3583i others(2682): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714265 | |||||
| chr1:236714265
|
T | TGTGTGTT others(3143): Show |
1 | a0001c0027t0001g0311 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.127-3570_127-3569i others(3152): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714265 | |||||
| chr1:236714265
|
T | TGTGTGTT others(3143): Show |
1 | a0001c0001t0001g0341 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.127-3570_127-3569i others(3152): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714265 | |||||
| chr1:236714265
|
T | TGTGTGTT others(3143): Show |
1 | a0001c0002t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127-3570_127-3569i others(3152): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714265 | |||||
| chr1:236714265
|
T | TGTGTGTT others(3210): Show |
1 | a0001c0001t0003g0279 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.127-3570_127-3569i others(3219): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714265 | |||||
| chr1:236714265
|
T | TGTGTGTT others(3143): Show |
1 | a0001c0001t0001g0287 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.127-3570_127-3569i others(3152): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714265 | |||||
| chr1:236714265
|
T | TGTGTGTT others(2876): Show |
1 | a0001c0001t0001g0269 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.127-3570_127-3569i others(2885): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714265 | |||||
| chr1:236714265
|
T | TGTGTGTT others(2540): Show |
1 | a0006c0022t0001g0203 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127-3570_127-3569i others(2549): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714265 | |||||
| chr1:236714266
|
G | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0292 | 2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.127-3592G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714266 | ||||||
| chr1:236714276
|
G | A | 1 | a0001c0003t0005g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127-3582G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714276 | ||||||
| chr1:236714280
|
A | G | 1 | a0001c0002t0007g0323 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.127-3578A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714280 | ||||||
| chr1:236714287
|
T | TA | 8 | a0001c0001t0001g0307a0001c0001t0001g0333a0001c0001t0003g0020others(5): Show | 8 | HG01243.hp1 HG02970.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-3570dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714287 | |||||
| chr1:236714287
|
T | TACCACTG others(61): Show |
92 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0159others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.127-3570_127-3503d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714287 | |||||
| chr1:236714354
|
T | TA | 48 | a0001c0001t0001g0011a0001c0001t0001g0114a0001c0001t0001g0259others(45): Show | 48 | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.127-3503dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714354 | |||||
| chr1:236714354
|
T | TACCACTG others(61): Show |
2 | a0001c0001t0004g0295a0001c0002t0002g0229 | 2 | NA19084.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.127-3503_127-3436d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714354 | |||||
| chr1:236714421
|
T | TA | 23 | a0001c0001t0001g0006a0001c0001t0001g0253a0001c0001t0001g0260others(20): Show | 23 | HG00099.hp1 HG01081.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-3436dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714421 | |||||
| chr1:236714421
|
T | TAACCACT others(671): Show |
1 | a0001c0006t0002g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.127-3436_127-3435i others(680): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714421 | |||||
| chr1:236714421
|
T | TACCACTG others(61): Show |
2 | a0001c0001t0010g0044a0001c0004t0005g0065 | 2 | HG02717.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.127-3436_127-3369d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714421 | |||||
| chr1:236714476
|
T | C | 1 | a0001c0001t0001g0338 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.127-3382T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714476 | ||||||
| chr1:236714488
|
T | TA | 6 | a0001c0001t0004g0102a0001c0001t0011g0090a0001c0001t0017g0097others(3): Show | 6 | HG03195.hp1 HG03195.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-3369dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714488 | |||||
| chr1:236714488
|
T | TAACCACT others(1144): Show |
3 | a0001c0001t0003g0020a0001c0001t0004g0003a0001c0001t0004g0015 | 3 | NA18939.hp1 NA18952.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.127-3369_127-3368i others(1153): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714488 | |||||
| chr1:236714488
|
T | TAACCACT others(1414): Show |
7 | a0001c0001t0001g0011a0001c0009t0003g0012a0001c0009t0003g0013others(4): Show | 7 | HG00323.hp1 HG02083.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-3369_127-3368i others(1423): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714488 | |||||
| chr1:236714488
|
T | TACCACTG others(61): Show |
56 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.127-3369_127-3302d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714488 | |||||
| chr1:236714543
|
T | C | 1 | a0001c0001t0001g0338 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.127-3315T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714543 | ||||||
| chr1:236714543
|
T | TGTATACA others(328): Show |
1 | a0001c0001t0001g0307 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.127-3225_127-3224i others(337): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714543 | |||||
| chr1:236714543
|
T | TGTATACA others(328): Show |
1 | a0007c0023t0001g0332 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127-3182_127-3181i others(337): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714543 | |||||
| chr1:236714548
|
A | G | 1 | a0001c0004t0005g0198 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127-3310A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714548 | ||||||
| chr1:236714555
|
T | TA | 40 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0141others(37): Show | 40 | HG00323.hp1 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.127-3302dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714555 | |||||
| chr1:236714555
|
T | TAACCACT others(1482): Show |
1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.127-3302_127-3301i others(1491): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714555 | |||||
| chr1:236714555
|
T | TAACCACT others(1482): Show |
6 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0037others(3): Show | 6 | HG02622.hp1 HG03486.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-3302_127-3301i others(1491): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714555 | |||||
| chr1:236714555
|
T | TACCACTG others(61): Show |
1 | a0001c0002t0002g0229 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.127-3302_127-3235d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714555 | |||||
| chr1:236714555
|
T | TACCACTG others(605): Show |
1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.127-3235_127-3234i others(614): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714555 | |||||
| chr1:236714555
|
T | TACCACTG others(7247): Show |
1 | a0004c0032t0017g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(7256): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714555 | |||||
| chr1:236714557
|
C | CCACTGAA others(194): Show |
1 | a0001c0002t0002g0218 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.127-3168_127-3167i others(203): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714557 | |||||
| chr1:236714577
|
A | T | 1 | a0001c0001t0017g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127-3281A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714577 | ||||||
| chr1:236714582
|
G | A | 7 | a0001c0003t0002g0170a0001c0003t0003g0058a0001c0003t0005g0172others(4): Show | 7 | HG01261.hp1 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-3276G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714582 | ||||||
| chr1:236714605
|
G | GTTTATGT others(61): Show |
1 | a0001c0001t0004g0295 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.127-3235_127-3234i others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714605 | |||||
| chr1:236714610
|
T | C | 5 | a0001c0001t0001g0286a0001c0001t0001g0338a0001c0001t0003g0143others(2): Show | 5 | HG01099.hp2 HG01169.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-3248T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714610 | ||||||
| chr1:236714610
|
T | TGTATACA others(60): Show |
1 | a0001c0002t0007g0298 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.127-3182_127-3181i others(69): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714610 | |||||
| chr1:236714610
|
T | TGTATACA others(194): Show |
9 | a0001c0001t0001g0291a0001c0001t0001g0312a0001c0001t0001g0319others(6): Show | 9 | HG02080.hp2 HG02602.hp2 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-3182_127-3181i others(203): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714610 | |||||
| chr1:236714610
|
T | TGTATACA others(194): Show |
1 | a0002c0005t0004g0306 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.127-3182_127-3181i others(203): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714610 | |||||
| chr1:236714610
|
T | TGTATACA others(328): Show |
1 | a0001c0001t0001g0331 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-3115_127-3114i others(337): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714610 | |||||
| chr1:236714621
|
A | AGAACCAC others(265): Show |
2 | a0001c0001t0005g0055a0001c0004t0005g0065 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.127-3237_127-3236i others(274): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714621 | ||||||
| chr1:236714622
|
T | A | 2 | a0001c0001t0005g0055a0001c0004t0005g0065 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.127-3236T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714622 | ||||||
| chr1:236714622
|
T | TA | 7 | a0001c0001t0004g0246a0001c0002t0002g0245a0001c0002t0007g0201others(4): Show | 7 | HG01891.hp1 HG01934.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-3235dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714622 | |||||
| chr1:236714622
|
T | TACCACTG others(332): Show |
1 | a0001c0001t0011g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.127-3170_127-3169i others(341): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714622 | |||||
| chr1:236714622
|
T | TACCACTG others(61): Show |
2 | a0001c0001t0010g0044a0001c0004t0005g0198 | 2 | HG03225.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.127-3235_127-3168d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714622 | |||||
| chr1:236714624
|
C | CCACTGAA others(395): Show |
1 | a0001c0001t0001g0333 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.127-3182_127-3181i others(404): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714624 | |||||
| chr1:236714632
|
G | C | 1 | a0001c0002t0007g0323 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.127-3226G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714632 | ||||||
| chr1:236714671
|
T | A | 1 | a0001c0002t0002g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-3187T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714671 | ||||||
| chr1:236714677
|
T | C | 9 | a0001c0001t0001g0264a0001c0001t0001g0286a0001c0001t0003g0143others(6): Show | 9 | HG01099.hp2 HG01361.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-3181T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714677 | ||||||
| chr1:236714677
|
T | TGTATACA others(194): Show |
29 | a0001c0001t0001g0031a0001c0001t0001g0251a0001c0001t0001g0265others(26): Show | 29 | HG00438.hp1 HG00639.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-3115_127-3114i others(203): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714677 | |||||
| chr1:236714677
|
T | TGTATACA others(261): Show |
7 | a0001c0001t0001g0114a0001c0001t0001g0285a0001c0001t0001g0288others(4): Show | 7 | HG00280.hp2 HG01496.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-3115_127-3114i others(270): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714677 | |||||
| chr1:236714677
|
T | TGTATACA others(462): Show |
1 | a0001c0001t0003g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127-3115_127-3114i others(471): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714677 | |||||
| chr1:236714677
|
T | TGTATACA others(195): Show |
1 | a0001c0002t0007g0300 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.127-3115_127-3114i others(204): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714677 | |||||
| chr1:236714682
|
A | G | 1 | a0001c0001t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.127-3176A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714682 | ||||||
| chr1:236714685
|
C | G | 1 | a0001c0002t0002g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-3173C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714685 | ||||||
| chr1:236714689
|
T | TA | 30 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(27): Show | 30 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-3168dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TAACCACT others(874): Show |
1 | a0001c0001t0006g0135 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.127-3168_127-3167i others(883): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TAACCACT others(939): Show |
1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-3168_127-3167i others(948): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TAACCACT others(2617): Show |
1 | a0001c0001t0003g0149 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.127-3168_127-3167i others(2626): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TACCACTG others(3162): Show |
1 | a0001c0003t0005g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.127-3101_127-3100i others(3171): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TACCACTG others(3229): Show |
5 | a0001c0003t0002g0051a0001c0003t0005g0047a0001c0003t0005g0050others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-3101_127-3100i others(3238): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TACCACTG others(3229): Show |
2 | a0003c0012t0008g0092a0003c0012t0008g0098 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-3101_127-3100i others(3238): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TACCACTG others(6843): Show |
1 | a0001c0031t0005g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(6852): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TACCACTG others(7112): Show |
1 | a0001c0013t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(7121): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714689
|
T | TACCACTG others(7377): Show |
1 | a0001c0014t0002g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(7386): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714689 | |||||
| chr1:236714701
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.127-3157G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714701 | ||||||
| chr1:236714728
|
C | CCTCACTG others(194): Show |
1 | a0001c0002t0002g0313 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.127-3115_127-3114i others(203): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714728 | |||||
| chr1:236714728
|
C | CCTCACTG others(194): Show |
1 | a0001c0001t0003g0266 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.127-3115_127-3114i others(203): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714728 | |||||
| chr1:236714744
|
T | C | 15 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0001g0286others(12): Show | 15 | HG00741.hp1 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-3114T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714744 | ||||||
| chr1:236714744
|
T | TGTATACA others(194): Show |
5 | a0001c0001t0001g0316a0001c0001t0019g0252a0001c0030t0002g0267others(2): Show | 5 | HG03239.hp2 NA18940.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-3048_127-3047i others(203): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714744 | |||||
| chr1:236714749
|
A | G | 58 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0188others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.127-3109A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714749 | ||||||
| chr1:236714756
|
T | TA | 21 | a0001c0001t0001g0011a0001c0001t0003g0020a0001c0001t0003g0149others(18): Show | 21 | HG00323.hp1 HG01243.hp1 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-3101dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714756 | |||||
| chr1:236714756
|
T | TACCACTG others(61): Show |
1 | a0001c0002t0007g0298 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.127-3101_127-3034d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714756 | |||||
| chr1:236714756
|
T | TACCACTG others(128): Show |
9 | a0001c0001t0001g0184a0001c0001t0001g0236a0001c0001t0001g0261others(6): Show | 9 | HG01099.hp1 HG01361.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-3101_127-2967d others(137): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714756 | |||||
| chr1:236714756
|
T | TACCACTG others(2608): Show |
1 | a0001c0007t0004g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2617): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714756 | |||||
| chr1:236714756
|
T | TACCACTG others(5167): Show |
1 | a0001c0013t0023g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5176): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714756 | |||||
| chr1:236714757
|
ACCACTGA others(59): Show |
A | 1 | a0001c0001t0004g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.127-3100_127-3035d others(68): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714757 | ||||||
| chr1:236714805
|
T | A | 1 | a0001c0002t0002g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-3053T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714805 | ||||||
| chr1:236714811
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0159a0001c0001t0001g0259others(14): Show | 17 | HG00741.hp1 HG01099.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-3047T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714811 | ||||||
| chr1:236714816
|
A | G | 3 | a0001c0002t0002g0137a0001c0002t0002g0229a0001c0002t0002g0232 | 3 | HG02280.hp2 HG03927.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.127-3042A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714816 | ||||||
| chr1:236714823
|
T | TA | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0042others(17): Show | 20 | HG01071.hp2 HG01943.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.127-3034dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TAACCACT others(1342): Show |
1 | a0001c0001t0004g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.127-3034_127-3033i others(1351): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(61): Show |
48 | a0001c0001t0001g0041a0001c0001t0001g0188a0001c0001t0001g0190others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.127-3034_127-2967d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(128): Show |
1 | a0001c0002t0002g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-3034_127-2900d others(137): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4553): Show |
1 | a0001c0001t0003g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.127-2833_127-2832i others(4562): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(1871): Show |
4 | a0001c0001t0009g0073a0001c0001t0011g0067a0001c0002t0002g0072others(1): Show | 4 | HG02615.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-2833_127-2832i others(1880): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4352): Show |
1 | a0001c0002t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4361): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4486): Show |
1 | a0001c0001t0003g0039 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4495): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4486): Show |
1 | a0001c0001t0003g0022 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4495): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4485): Show |
6 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0003g0026others(3): Show | 6 | HG00544.hp1 HG01928.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(4494): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4484): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0334a0001c0001t0003g0021 | 3 | HG01928.hp1 HG02148.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(4493): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4418): Show |
1 | a0001c0001t0003g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4427): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4552): Show |
2 | a0001c0001t0003g0166a0002c0008t0004g0168 | 2 | HG02083.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(4561): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4284): Show |
1 | a0001c0024t0003g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4293): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4551): Show |
1 | a0001c0001t0003g0167 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4560): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4483): Show |
2 | a0001c0001t0003g0024a0002c0008t0004g0025 | 2 | NA18953.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(4492): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(4617): Show |
1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4626): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(195): Show |
1 | a0001c0002t0007g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.127-2976_127-2975i others(204): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714823
|
T | TACCACTG others(129): Show |
1 | a0001c0002t0002g0229 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.127-3012_127-3011i others(138): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714823 | |||||
| chr1:236714873
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127-2985G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714873 | ||||||
| chr1:236714878
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0159a0001c0001t0001g0253others(15): Show | 18 | HG00099.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-2980T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714878 | ||||||
| chr1:236714883
|
A | G | 3 | a0001c0001t0010g0044a0001c0001t0017g0097a0001c0004t0005g0198 | 3 | HG03225.hp1 HG03516.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.127-2975A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714883 | ||||||
| chr1:236714890
|
T | TA | 20 | a0001c0001t0001g0011a0001c0001t0003g0020a0001c0001t0003g0173others(17): Show | 20 | HG00323.hp1 HG02083.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.127-2967dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TAACCACT others(1883): Show |
1 | a0001c0001t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.127-2967_127-2966i others(1892): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TAACCACT others(2352): Show |
1 | a0001c0001t0001g0342 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127-2967_127-2966i others(2361): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TAACCACT others(5032): Show |
1 | a0001c0002t0002g0217 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.127-2967_127-2966i others(5041): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TAACCACT others(1880): Show |
1 | a0001c0007t0015g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.127-2967_127-2966i others(1889): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5434): Show |
1 | a0002c0005t0004g0306 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(7913): Show |
1 | a0007c0023t0001g0332 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(7922): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5971): Show |
1 | a0001c0001t0001g0307 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5980): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(10459): Show |
1 | a0001c0001t0001g0333 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(10468): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5836): Show |
3 | a0001c0021t0001g0254a0002c0005t0004g0256a0002c0005t0004g0294 | 3 | NA19010.hp1 NA19060.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.127-2914_127-2913i others(5845): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5297): Show |
1 | a0001c0001t0001g0322 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5306): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5836): Show |
1 | a0001c0001t0003g0299 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5845): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5836): Show |
1 | a0001c0001t0001g0006 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5845): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5836): Show |
1 | a0001c0001t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5845): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5836): Show |
1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5845): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5835): Show |
1 | a0001c0001t0001g0253 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5844): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5836): Show |
1 | a0001c0001t0001g0259 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5845): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5836): Show |
1 | a0001c0001t0001g0280 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5845): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5769): Show |
1 | a0001c0002t0002g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5778): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5837): Show |
1 | a0001c0001t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.127-2914_127-2913i others(5846): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5769): Show |
1 | a0001c0002t0002g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-2900_127-2899i others(5778): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(1477): Show |
1 | a0001c0002t0007g0323 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.127-2900_127-2899i others(1486): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5434): Show |
1 | a0002c0008t0004g0277 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.127-2847_127-2846i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5434): Show |
1 | a0001c0001t0001g0338 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.127-2847_127-2846i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5702): Show |
1 | a0001c0002t0002g0302 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.127-2847_127-2846i others(5711): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5367): Show |
3 | a0001c0002t0002g0278a0001c0002t0002g0309a0001c0002t0002g0310 | 3 | NA18990.hp1 NA19064.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.127-2847_127-2846i others(5376): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5434): Show |
2 | a0001c0001t0001g0319a0001c0001t0003g0268 | 2 | NA18979.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.127-2847_127-2846i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5434): Show |
1 | a0001c0001t0001g0291 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.127-2847_127-2846i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5434): Show |
1 | a0001c0001t0001g0312 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.127-2847_127-2846i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(7972): Show |
1 | a0001c0001t0001g0331 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-2847_127-2846i others(7981): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5569): Show |
1 | a0001c0001t0004g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.127-2833_127-2832i others(5578): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(13782): Show |
1 | a0001c0001t0005g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(13791): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(10765): Show |
1 | a0001c0001t0011g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(10774): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(10618): Show |
1 | a0001c0004t0005g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(10627): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(396): Show |
1 | a0001c0002t0002g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(405): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(530): Show |
6 | a0001c0001t0001g0018a0001c0001t0001g0110a0001c0001t0003g0105others(3): Show | 6 | HG00140.hp2 HG00738.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(539): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(597): Show |
1 | a0001c0001t0012g0337 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(606): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(2483): Show |
2 | a0001c0001t0004g0069a0001c0001t0009g0091 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(2492): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(2416): Show |
23 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(20): Show | 23 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(2425): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(2416): Show |
1 | a0001c0002t0002g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2425): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5433): Show |
1 | a0001c0002t0002g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127-2842_127-2841i others(5442): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5500): Show |
1 | a0001c0002t0002g0192 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-2842_127-2841i others(5509): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5098): Show |
1 | a0001c0001t0001g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.127-2842_127-2841i others(5107): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(4897): Show |
3 | a0001c0001t0001g0236a0001c0001t0001g0261a0001c0002t0002g0231 | 3 | HG02523.hp1 NA18942.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.127-2842_127-2841i others(4906): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(4964): Show |
1 | a0001c0001t0010g0043 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.127-2842_127-2841i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5835): Show |
1 | a0001c0002t0002g0223 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.127-2842_127-2841i others(5844): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(5903): Show |
1 | a0001c0002t0002g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-2909_127-2908i others(5912): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(2150): Show |
1 | a0001c0001t0003g0174 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.127-2909_127-2908i others(2159): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714890
|
T | TACCACTG others(2419): Show |
1 | a0002c0005t0004g0305 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.127-2919_127-2918i others(2428): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714890 | |||||
| chr1:236714950
|
A | G | 1 | a0001c0010t0002g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.127-2908A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236714950 | ||||||
| chr1:236714957
|
T | TA | 28 | a0001c0001t0001g0011a0001c0001t0003g0020a0001c0001t0004g0003others(25): Show | 28 | HG00323.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.127-2900dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TAACCACT others(2023): Show |
1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-2900_127-2899i others(2032): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TAACCACT others(3750): Show |
1 | a0001c0007t0004g0112 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-2900_127-2899i others(3759): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TAACCACT others(2542): Show |
1 | a0001c0001t0001g0103 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.127-2900_127-2899i others(2551): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TAACCACT others(3213): Show |
1 | a0001c0004t0005g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127-2900_127-2899i others(3222): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TAACCACT others(3615): Show |
3 | a0001c0001t0004g0200a0001c0001t0005g0181a0001c0002t0002g0179 | 3 | HG02572.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.127-2900_127-2899i others(3624): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(61): Show |
2 | a0001c0001t0006g0135a0001c0003t0022g0093 | 2 | HG01243.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.127-2900_127-2833d others(70): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(1345): Show |
1 | a0001c0006t0008g0128 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(1354): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(5647): Show |
1 | a0001c0001t0009g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5656): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(4713): Show |
1 | a0001c0004t0005g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4722): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(5713): Show |
1 | a0001c0001t0004g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5722): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(1412): Show |
1 | a0001c0003t0020g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(1421): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(2760): Show |
1 | a0001c0011t0004g0101 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2769): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(1540): Show |
3 | a0001c0001t0015g0116a0001c0015t0016g0113a0001c0015t0016g0115 | 3 | HG01168.hp2 HG01169.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(1549): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(1479): Show |
12 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0006g0124others(9): Show | 12 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(1488): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(3164): Show |
1 | a0001c0003t0005g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(3173): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(2827): Show |
1 | a0001c0001t0003g0238 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2836): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(3164): Show |
2 | a0001c0003t0003g0058a0001c0006t0002g0171 | 2 | HG01261.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(3173): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(2827): Show |
11 | a0001c0003t0002g0170a0001c0004t0002g0062a0001c0004t0002g0064others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(2836): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(2691): Show |
1 | a0001c0001t0004g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2700): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(1546): Show |
1 | a0001c0006t0008g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(1555): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714957
|
T | TACCACTG others(4435): Show |
1 | a0001c0001t0004g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4444): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714957 | |||||
| chr1:236714972
|
A | ATGCAAGA others(4484): Show |
1 | a0001c0001t0003g0040 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4493): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236714972 | |||||
| chr1:236715026
|
C | CCACTGAA others(5236): Show |
1 | a0001c0002t0007g0300 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5245): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5569): Show |
1 | a0002c0005t0004g0257 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5578): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5635): Show |
1 | a0001c0001t0001g0316 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5644): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(6105): Show |
1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(6114): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5568): Show |
1 | a0002c0005t0004g0297 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5577): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(8047): Show |
1 | a0001c0001t0001g0330 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(8056): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(8114): Show |
1 | a0001c0001t0001g0327 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(8123): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5568): Show |
1 | a0001c0001t0019g0252 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5577): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(8114): Show |
1 | a0001c0001t0001g0335 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(8123): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5433): Show |
1 | a0001c0001t0003g0143 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5442): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(8047): Show |
1 | a0001c0001t0003g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(8056): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0002t0013g0239 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5366): Show |
1 | a0001c0001t0003g0324 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5375): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0002t0013g0325 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5434): Show |
1 | a0001c0001t0001g0321 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0002t0002g0313 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0019g0250 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0001g0308 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5568): Show |
1 | a0001c0001t0003g0284 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5577): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0001g0285 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(8047): Show |
1 | a0001c0001t0001g0328 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(8056): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0001g0288 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0001g0318 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(9054): Show |
1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(9063): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(8383): Show |
1 | a0001c0001t0001g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(8392): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0003g0343 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
7 | a0001c0001t0001g0031a0001c0001t0001g0265a0001c0001t0001g0274others(4): Show | 7 | HG01433.hp2 NA18950.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5498): Show |
1 | a0001c0001t0003g0207 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5507): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5434): Show |
1 | a0001c0002t0002g0314 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0001g0304 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5502): Show |
1 | a0001c0001t0003g0339 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5511): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5497): Show |
1 | a0001c0001t0001g0315 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5506): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5434): Show |
1 | a0001c0001t0003g0249 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0001g0290 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0001g0317 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
3 | a0001c0001t0001g0289a0001c0001t0003g0340a0001c0001t0025g0010 | 3 | HG02080.hp1 NA19065.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0002c0008t0004g0296 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0025t0006g0121 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(1880): Show |
1 | a0001c0001t0004g0293 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(1889): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(2081): Show |
1 | a0001c0001t0001g0320 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2090): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5300): Show |
1 | a0001c0010t0002g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5309): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5635): Show |
1 | a0001c0001t0003g0175 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5644): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0002t0002g0255 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0001t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(1477): Show |
1 | a0001c0001t0017g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(1486): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5300): Show |
1 | a0001c0001t0003g0272 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5309): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(6238): Show |
1 | a0001c0001t0004g0295 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(6247): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5635): Show |
1 | a0001c0001t0001g0286 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5644): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5501): Show |
1 | a0001c0002t0002g0273 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5510): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(6171): Show |
1 | a0001c0002t0007g0298 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(6180): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4829): Show |
2 | a0001c0001t0001g0159a0001c0010t0002g0160 | 2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(4838): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(2481): Show |
2 | a0001c0001t0018g0303a0001c0002t0002g0283 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(2490): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(3960): Show |
1 | a0001c0002t0007g0326 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(3969): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5032): Show |
1 | a0001c0004t0005g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5041): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0004t0005g0198 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4830): Show |
1 | a0001c0001t0010g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4839): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5031): Show |
1 | a0001c0001t0004g0204 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5040): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5567): Show |
1 | a0001c0002t0002g0191 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5576): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5567): Show |
4 | a0001c0002t0002g0189a0001c0002t0002g0193a0001c0002t0002g0194others(1): Show | 4 | HG01106.hp1 HG02145.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(5576): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4961): Show |
1 | a0001c0002t0002g0218 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4970): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5165): Show |
1 | a0001c0002t0002g0216 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5174): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4829): Show |
1 | a0001c0001t0004g0208 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4838): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5031): Show |
1 | a0001c0001t0004g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5040): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5031): Show |
1 | a0001c0002t0002g0182 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5040): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0001t0001g0222 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4897): Show |
1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4906): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(7180): Show |
1 | a0001c0001t0001g0188 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(7189): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5098): Show |
1 | a0001c0004t0005g0177 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5107): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5165): Show |
1 | a0001c0002t0002g0247 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5174): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5165): Show |
1 | a0001c0002t0002g0233 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5174): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5165): Show |
1 | a0001c0002t0002g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5174): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0002t0007g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0002t0002g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0001t0001g0225 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0002t0007g0209 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0001t0003g0202 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
12 | a0001c0001t0001g0041a0001c0001t0001g0190a0001c0001t0001g0219others(9): Show | 12 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0002t0002g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4828): Show |
1 | a0001c0002t0007g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4837): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0001t0001g0195 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(6979): Show |
1 | a0001c0001t0001g0205 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(6988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(6979): Show |
1 | a0001c0001t0001g0211 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(6988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5098): Show |
1 | a0001c0002t0002g0220 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5107): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5031): Show |
2 | a0001c0001t0010g0045a0001c0001t0010g0046 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.127-2793_127-2792i others(5040): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5969): Show |
1 | a0001c0002t0002g0248 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5978): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5902): Show |
1 | a0001c0002t0002g0237 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5911): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4963): Show |
1 | a0001c0001t0001g0224 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4972): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(4964): Show |
1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(4973): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(7313): Show |
1 | a0001c0002t0002g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(7322): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(5166): Show |
1 | a0001c0001t0009g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(5175): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(2553): Show |
1 | a0006c0022t0001g0203 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2562): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(2553): Show |
6 | a0001c0001t0001g0258a0001c0001t0001g0287a0001c0001t0001g0301others(3): Show | 6 | HG00741.hp2 HG01175.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-2793_127-2792i others(2562): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(2485): Show |
1 | a0001c0001t0001g0341 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2494): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | CCACTGAA others(2419): Show |
1 | a0001c0001t0001g0269 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.127-2793_127-2792i others(2428): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715026 | |||||
| chr1:236715026
|
C | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0184a0001c0001t0001g0236others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-2832C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715026 | ||||||
| chr1:236715027
|
C | T | 4 | a0001c0003t0005g0047a0001c0003t0005g0048a0001c0003t0005g0050others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-2831C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715027 | ||||||
| chr1:236715119
|
C | T | 277 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0031others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.127-2739C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715119 | ||||||
| chr1:236715155
|
CT | C | 110 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0184others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.127-2689delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715155 | |||||
| chr1:236715155
|
CTT | C | 25 | a0001c0001t0006g0135a0001c0003t0001g0129a0001c0003t0001g0133others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-2690_127-2689d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715155 | |||||
| chr1:236715169
|
T | A | 6 | a0001c0003t0002g0051a0001c0003t0005g0047a0001c0003t0005g0048others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-2689T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715169 | ||||||
| chr1:236715218
|
A | T | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-2640A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715218 | ||||||
| chr1:236715218
|
ACAT | A | 6 | a0001c0001t0001g0031a0001c0001t0001g0265a0001c0001t0001g0274others(3): Show | 6 | NA18952.hp2 NA19003.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-2639_127-2637d others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715218 | ||||||
| chr1:236715220
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 49 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.127-2638A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715220 | ||||||
| chr1:236715224
|
G | A | 57 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0059others(54): Show | 57 | HG00639.hp2 HG01081.hp2 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.127-2634G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715224 | ||||||
| chr1:236715229
|
C | T | 9 | a0001c0001t0003g0020a0001c0001t0004g0003a0001c0001t0004g0015others(6): Show | 9 | HG02622.hp1 HG03486.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-2629C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715229 | ||||||
| chr1:236715240
|
T | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 61 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.127-2618T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715240 | ||||||
| chr1:236715244
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0003g0020a0001c0001t0004g0003others(16): Show | 19 | HG00323.hp1 HG02083.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-2614T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715244 | ||||||
| chr1:236715246
|
T | C | 2 | a0001c0015t0016g0113a0001c0015t0016g0115 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.127-2612T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715246 | ||||||
| chr1:236715283
|
C | T | 3 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0009g0118 | 3 | HG02647.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.127-2575C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715283 | ||||||
| chr1:236715294
|
C | G | 101 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0114others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.127-2564C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715294 | ||||||
| chr1:236715308
|
T | TC | 47 | a0001c0001t0001g0103a0001c0001t0001g0244a0001c0001t0003g0238others(44): Show | 47 | HG00639.hp2 HG01081.hp2 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.127-2544dupC | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715308 | |||||
| chr1:236715317
|
C | G | 2 | a0003c0012t0008g0092a0003c0012t0008g0098 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-2541C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715317 | ||||||
| chr1:236715338
|
A | G | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.127-2520A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715338 | ||||||
| chr1:236715339
|
T | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.127-2519T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715339 | ||||||
| chr1:236715357
|
C | G | 57 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0059others(54): Show | 57 | HG00639.hp2 HG01081.hp2 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.127-2501C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715357 | ||||||
| chr1:236715386
|
A | G | 18 | a0001c0001t0003g0238a0001c0001t0004g0059a0001c0003t0002g0170others(15): Show | 18 | HG01243.hp2 HG01261.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-2472A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715386 | ||||||
| chr1:236715440
|
A | G | 2 | a0003c0012t0008g0092a0003c0012t0008g0098 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-2418A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715440 | ||||||
| chr1:236715445
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.127-2413T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715445 | ||||||
| chr1:236715454
|
A | G | 3 | a0001c0001t0005g0055a0001c0001t0011g0090a0001c0004t0005g0065 | 3 | HG02109.hp2 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.127-2404A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715454 | ||||||
| chr1:236715471
|
A | T | 1 | a0001c0003t0006g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.127-2387A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715471 | ||||||
| chr1:236715487
|
A | G | 85 | a0001c0001t0001g0103a0001c0001t0001g0139a0001c0001t0001g0141others(82): Show | 85 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.127-2371A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715487 | ||||||
| chr1:236715517
|
C | G | 5 | a0001c0013t0002g0054a0001c0013t0023g0095a0001c0014t0002g0052others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-2341C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715517 | ||||||
| chr1:236715688
|
G | A | 1 | a0001c0002t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.127-2170G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715688 | ||||||
| chr1:236715695
|
C | G | 1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-2163C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715695 | ||||||
| chr1:236715825
|
A | G | 4 | a0001c0003t0021g0125a0001c0006t0002g0150a0001c0006t0008g0128others(1): Show | 4 | NA18960.hp1 NA18964.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-2033A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236715825 | ||||||
| chr1:236715951
|
AAAAATAA others(4): Show |
A | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.127-1902_127-1892d others(13): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236715951 | |||||
| chr1:236716032
|
C | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.127-1826C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716032 | ||||||
| chr1:236716096
|
CTTCT | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.127-1759_127-1756d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236716096 | |||||
| chr1:236716099
|
CT | C | 186 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0031others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.127-1742delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236716099 | |||||
| chr1:236716102
|
T | C | 16 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0006g0124others(13): Show | 16 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-1756T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716102 | ||||||
| chr1:236716191
|
C | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.127-1667C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716191 | ||||||
| chr1:236716255
|
T | C | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-1603T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716255 | ||||||
| chr1:236716329
|
A | G | 6 | a0001c0001t0003g0238a0001c0001t0004g0178a0001c0001t0004g0200others(3): Show | 6 | HG02572.hp2 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-1529A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716329 | ||||||
| chr1:236716432
|
A | C | 1 | a0001c0031t0005g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.127-1426A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716432 | ||||||
| chr1:236716437
|
G | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0021others(47): Show | 50 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.127-1421G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716437 | ||||||
| chr1:236716493
|
A | G | 24 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(21): Show | 24 | HG00609.hp1 HG00673.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.127-1365A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716493 | ||||||
| chr1:236716545
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.127-1313G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716545 | ||||||
| chr1:236716682
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.127-1176G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716682 | ||||||
| chr1:236716835
|
A | AT | 27 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(24): Show | 27 | HG00609.hp1 HG00673.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-1006dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236716835 | |||||
| chr1:236716835
|
A | ATT | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0242others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.127-1007_127-1006d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236716835 | |||||
| chr1:236716835
|
A | ATTT | 55 | a0001c0001t0001g0018a0001c0001t0001g0103a0001c0001t0001g0110others(52): Show | 55 | HG00140.hp2 HG00738.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.127-1008_127-1006d others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236716835 | |||||
| chr1:236716835
|
A | ATTTT | 190 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.127-1009_127-1006d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236716835 | |||||
| chr1:236716835
|
A | ATTTTT | 26 | a0001c0001t0001g0114a0001c0001t0001g0224a0001c0001t0001g0304others(23): Show | 26 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.127-1010_127-1006d others(7): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236716835 | |||||
| chr1:236716877
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01071.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.127-981C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716877 | ||||||
| chr1:236716904
|
G | C | 1 | a0001c0002t0007g0034 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.127-954G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716904 | ||||||
| chr1:236716915
|
A | G | 24 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(21): Show | 24 | HG00609.hp1 HG00673.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.127-943A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716915 | ||||||
| chr1:236716921
|
G | A | 1 | a0001c0001t0003g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127-937G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236716921 | ||||||
| chr1:236717055
|
G | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0242others(47): Show | 50 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.127-803G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236717055 | ||||||
| chr1:236717078
|
GC | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.127-777delC | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 236717078 | |||||
| chr1:236717259
|
C | T | 15 | a0001c0001t0003g0020a0001c0001t0004g0003a0001c0001t0004g0015others(12): Show | 15 | HG02622.hp1 HG02970.hp1 HG03139.hp2 others(12): Show |
intron_variant | MODIFIER | c.127-599C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236717259 | ||||||
| chr1:236717262
|
A | G | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-596A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236717262 | ||||||
| chr1:236717384
|
C | T | 6 | a0001c0001t0003g0238a0001c0001t0004g0178a0001c0001t0004g0200others(3): Show | 6 | HG02572.hp2 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-474C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236717384 | ||||||
| chr1:236717554
|
A | T | 1 | a0001c0001t0001g0338 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.127-304A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236717554 | ||||||
| chr1:236717587
|
A | G | 7 | a0001c0003t0002g0170a0001c0003t0003g0058a0001c0003t0005g0172others(4): Show | 7 | HG01261.hp1 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-271A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | chr1 | 236717587 | ||||||
| chr1:236717975
|
T | C | 1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | splice_region_variant&intron_variant | LOW | c.241+3T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236717975 | ||||||
| chr1:236717978
|
T | A | 1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | splice_region_variant&intron_variant | LOW | c.241+6T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236717978 | ||||||
| chr1:236717979
|
G | T | 1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | splice_region_variant&intron_variant | LOW | c.241+7G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236717979 | ||||||
| chr1:236717980
|
T | C | 1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | splice_region_variant&intron_variant | LOW | c.241+8T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236717980 | ||||||
| chr1:236717982
|
A | T | 1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.241+10A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236717982 | ||||||
| chr1:236717983
|
T | C | 1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.241+11T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236717983 | ||||||
| chr1:236717985
|
T | G | 1 | a0005c0033t0003g0169 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.241+13T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236717985 | ||||||
| chr1:236718103
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.241+131C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718103 | ||||||
| chr1:236718107
|
T | C | 31 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0002g0051others(28): Show | 31 | HG00639.hp2 HG01123.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.241+135T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718107 | ||||||
| chr1:236718274
|
G | T | 24 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(21): Show | 24 | HG00609.hp1 HG00673.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.241+302G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718274 | ||||||
| chr1:236718403
|
T | A | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.241+431T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718403 | ||||||
| chr1:236718403
|
T | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.241+431T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718403 | ||||||
| chr1:236718448
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.242-446T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718448 | ||||||
| chr1:236718484
|
G | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(64): Show | 67 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.242-410G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718484 | ||||||
| chr1:236718493
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0282 | 2 | HG00673.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.242-401A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718493 | ||||||
| chr1:236718810
|
G | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.242-84G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2/20 | chr1 | 236718810 | ||||||
| chr1:236719109
|
C | T | 8 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0330others(5): Show | 8 | HG00738.hp1 HG01496.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+96C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719109 | ||||||
| chr1:236719151
|
G | A | 2 | a0001c0004t0005g0197a0001c0004t0005g0198 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.361+138G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719151 | ||||||
| chr1:236719250
|
A | G | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.361+237A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719250 | ||||||
| chr1:236719451
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.361+438G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719451 | ||||||
| chr1:236719454
|
C | T | 1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.361+441C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719454 | ||||||
| chr1:236719604
|
C | T | 40 | a0001c0001t0004g0059a0001c0002t0002g0232a0001c0002t0002g0235others(37): Show | 40 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.362-501C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719604 | ||||||
| chr1:236719768
|
C | T | 16 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(13): Show | 16 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.362-337C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719768 | ||||||
| chr1:236719849
|
C | T | 16 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(13): Show | 16 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.362-256C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719849 | ||||||
| chr1:236719861
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.362-244A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719861 | ||||||
| chr1:236719940
|
T | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.362-165T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719940 | ||||||
| chr1:236719941
|
G | A | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.362-164G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236719941 | ||||||
| chr1:236720077
|
C | T | 1 | a0001c0002t0013g0161 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.362-28C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3/20 | chr1 | 236720077 | ||||||
| chr1:236720264
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.448+73G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236720264 | ||||||
| chr1:236720386
|
G | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.448+195G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236720386 | ||||||
| chr1:236720471
|
T | C | 2 | a0001c0001t0004g0213a0001c0002t0002g0243 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448+280T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236720471 | ||||||
| chr1:236720494
|
A | G | 3 | a0001c0001t0004g0102a0001c0001t0017g0097a0001c0007t0015g0096 | 3 | HG03195.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.448+303A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236720494 | ||||||
| chr1:236720525
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.448+334T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236720525 | ||||||
| chr1:236720796
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.448+605G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236720796 | ||||||
| chr1:236720835
|
T | C | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.448+644T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236720835 | ||||||
| chr1:236720897
|
A | G | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.448+706A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236720897 | ||||||
| chr1:236720919
|
TGTAATCC others(1): Show |
T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.448+732_448+739del others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236720919 | |||||
| chr1:236721006
|
C | CTGGTTTT | 4 | a0001c0001t0004g0102a0001c0004t0002g0062a0001c0004t0002g0064others(1): Show | 4 | HG01243.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+818_448+824dup others(7): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721006 | |||||
| chr1:236721014
|
T | TG | 31 | a0001c0001t0001g0031a0001c0001t0001g0205a0001c0001t0001g0221others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.448+824dupG | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721014 | |||||
| chr1:236721015
|
G | GGT | 39 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0195others(36): Show | 39 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTT | 9 | a0001c0001t0001g0304a0001c0001t0001g0308a0001c0001t0004g0246others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(3): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTT | 4 | a0001c0001t0003g0153a0001c0001t0003g0268a0001c0001t0003g0343others(1): Show | 4 | HG00438.hp1 HG03471.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(3): Show |
4 | a0001c0001t0001g0103a0001c0001t0015g0116a0001c0001t0019g0252others(1): Show | 4 | HG01081.hp2 HG01361.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(4): Show |
7 | a0001c0001t0004g0117a0001c0001t0009g0091a0001c0001t0019g0250others(4): Show | 7 | HG01943.hp1 HG02129.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(11): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(5): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0029others(10): Show | 13 | HG01071.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(6): Show |
23 | a0001c0001t0001g0042a0001c0001t0001g0244a0001c0001t0003g0167others(20): Show | 23 | HG00323.hp1 HG01934.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(13): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(7): Show |
16 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0280others(13): Show | 16 | HG00544.hp1 HG02004.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(14): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(8): Show |
12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0291others(9): Show | 12 | HG00423.hp2 HG01169.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(15): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(9): Show |
5 | a0001c0001t0001g0001a0001c0001t0003g0020a0001c0001t0003g0026others(2): Show | 5 | HG01952.hp2 HG02622.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(10): Show |
8 | a0001c0001t0001g0242a0001c0001t0001g0281a0001c0001t0003g0022others(5): Show | 8 | HG00609.hp2 HG01433.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(17): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(11): Show |
2 | a0001c0001t0003g0021a0001c0001t0003g0039 | 2 | NA19009.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.448+824_448+825ins others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(12): Show |
3 | a0001c0001t0004g0003a0001c0002t0007g0300a0004c0026t0005g0076 | 3 | HG02257.hp1 NA18939.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.448+824_448+825ins others(19): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(16): Show |
5 | a0001c0001t0001g0269a0001c0001t0001g0316a0001c0001t0001g0319others(2): Show | 5 | HG02027.hp2 NA18973.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(23): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(17): Show |
6 | a0001c0001t0001g0006a0001c0001t0003g0174a0001c0001t0003g0175others(3): Show | 6 | HG02129.hp2 HG03688.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(24): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(18): Show |
6 | a0001c0001t0001g0264a0001c0001t0001g0318a0001c0001t0001g0341others(3): Show | 6 | HG00642.hp1 HG04115.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(25): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(19): Show |
2 | a0001c0001t0001g0258a0001c0001t0001g0262 | 2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.448+824_448+825ins others(26): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(20): Show |
1 | a0001c0001t0001g0188 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.448+824_448+825ins others(27): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(21): Show |
3 | a0001c0001t0001g0011a0001c0001t0003g0143a0001c0001t0018g0303 | 3 | HG02451.hp1 NA18964.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.448+824_448+825ins others(28): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(22): Show |
6 | a0001c0001t0001g0288a0001c0001t0001g0327a0001c0001t0001g0328others(3): Show | 6 | HG00738.hp1 HG01978.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(29): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(23): Show |
4 | a0001c0001t0001g0287a0001c0001t0001g0330a0001c0001t0001g0331others(1): Show | 4 | HG01258.hp2 HG01496.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(30): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(25): Show |
1 | a0001c0001t0004g0295 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.448+824_448+825ins others(32): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(26): Show |
2 | a0001c0001t0001g0320a0001c0001t0001g0342 | 2 | HG00140.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.448+824_448+825ins others(33): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(27): Show |
3 | a0001c0001t0001g0253a0001c0001t0001g0321a0001c0001t0003g0339 | 3 | HG00639.hp1 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.448+824_448+825ins others(34): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(28): Show |
4 | a0001c0001t0001g0285a0001c0001t0001g0292a0001c0001t0001g0322others(1): Show | 4 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+824_448+825ins others(35): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
G | GGTTTTTT others(36): Show |
1 | a0001c0001t0003g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.448+824_448+825ins others(43): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721015 | ||||||
| chr1:236721015
|
GTTTTTTG others(2): Show |
G | 6 | a0001c0001t0004g0293a0001c0021t0001g0254a0002c0005t0004g0257others(3): Show | 6 | HG02132.hp1 HG03654.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.448+831_448+839del others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721015 | |||||
| chr1:236721015
|
GTTTTTTG others(3): Show |
G | 3 | a0002c0005t0004g0256a0002c0005t0004g0297a0002c0008t0004g0277 | 3 | HG02080.hp2 NA19063.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.448+831_448+840del others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721015 | |||||
| chr1:236721015
|
GTTTTTTG others(5): Show |
G | 1 | a0001c0002t0002g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.448+831_448+842del others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721015 | |||||
| chr1:236721015
|
GTTTTTTG others(6): Show |
G | 1 | a0001c0001t0003g0279 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.448+831_448+843del others(13): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721015 | |||||
| chr1:236721015
|
GTTTTTTG others(8): Show |
G | 2 | a0001c0001t0001g0286a0001c0001t0004g0226 | 2 | HG01099.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.448+831_448+845del others(15): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721015 | |||||
| chr1:236721015
|
GTTTTTTG others(11): Show |
G | 2 | a0001c0001t0004g0213a0001c0002t0002g0243 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448+831_448+848del others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721015 | |||||
| chr1:236721016
|
T | G | 92 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0110others(89): Show | 92 | HG00140.hp2 HG00609.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.448+825T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721016 | ||||||
| chr1:236721020
|
TTG | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0110a0001c0001t0001g0114others(6): Show | 9 | HG00140.hp2 HG00738.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.448+831_448+832del others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721020 | |||||
| chr1:236721021
|
TG | T | 6 | a0001c0001t0001g0301a0001c0001t0012g0019a0001c0001t0012g0109others(3): Show | 6 | HG01123.hp1 HG01258.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+831delG | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721021 | ||||||
| chr1:236721022
|
G | GT | 19 | a0001c0003t0001g0129a0001c0003t0002g0170a0001c0003t0005g0047others(16): Show | 19 | HG01123.hp2 HG01192.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.448+854dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721022 | |||||
| chr1:236721022
|
G | GTT | 14 | a0001c0003t0001g0133a0001c0003t0002g0051a0001c0003t0003g0058others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.448+853_448+854dup others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721022 | |||||
| chr1:236721022
|
G | GTTTT | 16 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(13): Show | 16 | HG00609.hp1 HG02015.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.448+851_448+854dup others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721022 | |||||
| chr1:236721022
|
G | GTTTTT | 7 | a0001c0001t0001g0282a0001c0001t0003g0147a0001c0001t0003g0155others(4): Show | 7 | HG00673.hp2 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.448+850_448+854dup others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721022 | |||||
| chr1:236721022
|
G | GTTTTTT | 12 | a0001c0001t0001g0148a0001c0001t0004g0059a0001c0001t0005g0055others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.448+849_448+854dup others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236721022 | |||||
| chr1:236721022
|
G | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.448+831G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721022 | ||||||
| chr1:236721024
|
T | G | 1 | a0001c0010t0002g0164 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.448+833T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721024 | ||||||
| chr1:236721025
|
T | G | 6 | a0001c0001t0004g0293a0001c0021t0001g0254a0002c0005t0004g0257others(3): Show | 6 | HG02132.hp1 HG03654.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.448+834T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721025 | ||||||
| chr1:236721026
|
T | G | 3 | a0002c0005t0004g0256a0002c0005t0004g0297a0002c0008t0004g0277 | 3 | HG02080.hp2 NA19063.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.448+835T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721026 | ||||||
| chr1:236721028
|
T | G | 1 | a0001c0002t0002g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.448+837T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721028 | ||||||
| chr1:236721029
|
T | G | 1 | a0001c0001t0003g0279 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.448+838T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721029 | ||||||
| chr1:236721031
|
T | G | 2 | a0001c0001t0001g0286a0001c0001t0004g0226 | 2 | HG01099.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.448+840T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721031 | ||||||
| chr1:236721034
|
T | G | 2 | a0001c0001t0004g0213a0001c0002t0002g0243 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448+843T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721034 | ||||||
| chr1:236721051
|
G | A | 17 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(14): Show | 17 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.448+860G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721051 | ||||||
| chr1:236721173
|
G | A | 1 | a0001c0002t0002g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.448+982G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721173 | ||||||
| chr1:236721195
|
T | A | 16 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(13): Show | 16 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.448+1004T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721195 | ||||||
| chr1:236721213
|
A | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.448+1022A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721213 | ||||||
| chr1:236721216
|
C | T | 1 | a0002c0005t0004g0305 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.448+1025C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721216 | ||||||
| chr1:236721420
|
T | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.448+1229T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721420 | ||||||
| chr1:236721438
|
T | C | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.448+1247T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721438 | ||||||
| chr1:236721491
|
C | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.448+1300C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721491 | ||||||
| chr1:236721581
|
A | C | 1 | a0001c0002t0002g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.448+1390A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721581 | ||||||
| chr1:236721929
|
C | T | 24 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0002g0051others(21): Show | 24 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.448+1738C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236721929 | ||||||
| chr1:236722273
|
G | A | 8 | a0001c0001t0004g0059a0001c0002t0002g0235a0001c0004t0002g0064others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.448+2082G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236722273 | ||||||
| chr1:236722470
|
A | G | 1 | a0001c0003t0006g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.448+2279A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236722470 | ||||||
| chr1:236722493
|
G | T | 1 | a0001c0016t0003g0108 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.448+2302G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236722493 | ||||||
| chr1:236722549
|
C | G | 16 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(13): Show | 16 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.448+2358C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236722549 | ||||||
| chr1:236722549
|
C | T | 16 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0006g0124others(13): Show | 16 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.448+2358C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236722549 | ||||||
| chr1:236722634
|
C | CA | 33 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.448+2460dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236722634 | |||||
| chr1:236722634
|
C | CAA | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.448+2459_448+2460d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236722634 | |||||
| chr1:236722634
|
C | CAAA | 11 | a0001c0001t0004g0204a0001c0001t0004g0227a0001c0001t0004g0293others(8): Show | 11 | HG02080.hp1 HG02080.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.448+2458_448+2460d others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236722634 | |||||
| chr1:236722634
|
CA | C | 30 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0002g0051others(27): Show | 30 | HG00639.hp2 HG01123.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.448+2460delA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236722634 | |||||
| chr1:236722744
|
T | C | 337 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.448+2553T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236722744 | ||||||
| chr1:236722811
|
G | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | HG01928.hp1 HG01943.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+2620G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236722811 | ||||||
| chr1:236723013
|
G | A | 1 | a0001c0004t0005g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.448+2822G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723013 | ||||||
| chr1:236723018
|
A | G | 1 | a0001c0001t0011g0067 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.448+2827A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723018 | ||||||
| chr1:236723059
|
C | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.448+2868C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723059 | ||||||
| chr1:236723085
|
G | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.449-2848G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723085 | ||||||
| chr1:236723163
|
A | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.449-2770A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723163 | ||||||
| chr1:236723195
|
C | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.449-2738C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723195 | ||||||
| chr1:236723201
|
C | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.449-2732C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723201 | ||||||
| chr1:236723231
|
A | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.449-2702A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723231 | ||||||
| chr1:236723264
|
C | A | 1 | a0002c0019t0004g0002 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.449-2669C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723264 | ||||||
| chr1:236723272
|
A | G | 1 | a0008c0017t0024g0099 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-2661A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723272 | ||||||
| chr1:236723339
|
A | G | 306 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.449-2594A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723339 | ||||||
| chr1:236723447
|
G | T | 1 | a0001c0001t0004g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.449-2486G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723447 | ||||||
| chr1:236723662
|
G | T | 1 | a0001c0001t0003g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.449-2271G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723662 | ||||||
| chr1:236723941
|
G | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.449-1992G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236723941 | ||||||
| chr1:236724008
|
T | C | 1 | a0001c0024t0003g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.449-1925T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724008 | ||||||
| chr1:236724059
|
C | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.449-1874C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724059 | ||||||
| chr1:236724061
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.449-1872A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724061 | ||||||
| chr1:236724207
|
G | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.449-1726G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724207 | ||||||
| chr1:236724325
|
A | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(64): Show | 67 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.449-1608A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724325 | ||||||
| chr1:236724370
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.449-1563G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724370 | ||||||
| chr1:236724516
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0017g0097a0001c0007t0015g0096 | 3 | HG03195.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.449-1417G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724516 | ||||||
| chr1:236724626
|
G | A | 1 | a0001c0002t0002g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.449-1307G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724626 | ||||||
| chr1:236724781
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.449-1152C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724781 | ||||||
| chr1:236724788
|
C | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.449-1145C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724788 | ||||||
| chr1:236724835
|
T | G | 10 | a0001c0001t0004g0059a0001c0002t0002g0232a0001c0002t0002g0235others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.449-1098T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724835 | ||||||
| chr1:236724838
|
CT | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.449-1073delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236724838 | |||||
| chr1:236724838
|
CTT | C | 6 | a0001c0001t0001g0184a0001c0001t0005g0055a0001c0001t0011g0090others(3): Show | 6 | HG02109.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-1074_449-1073d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236724838 | |||||
| chr1:236724949
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.449-984T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236724949 | ||||||
| chr1:236725042
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.449-891T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236725042 | ||||||
| chr1:236725454
|
C | T | 16 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(13): Show | 16 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.449-479C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236725454 | ||||||
| chr1:236725463
|
A | G | 16 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(13): Show | 16 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.449-470A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236725463 | ||||||
| chr1:236725634
|
A | AAT | 16 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(13): Show | 16 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.449-299_449-298ins others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236725634 | ||||||
| chr1:236725634
|
A | T | 1 | a0001c0009t0003g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.449-299A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236725634 | ||||||
| chr1:236725636
|
T | A | 17 | a0001c0001t0001g0103a0001c0001t0003g0238a0001c0001t0004g0069others(14): Show | 17 | HG01081.hp2 HG01106.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.449-297T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236725636 | ||||||
| chr1:236725636
|
T | TA | 286 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.449-290dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr1 | 236725636 | |||||
| chr1:236725811
|
G | C | 31 | a0001c0003t0001g0129a0001c0003t0001g0133a0001c0003t0002g0051others(28): Show | 31 | HG00639.hp2 HG01123.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.449-122G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4/20 | chr1 | 236725811 | ||||||
| chr1:236726030
|
C | T | 2 | a0001c0001t0004g0119a0001c0001t0009g0118 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.536+10C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726030 | ||||||
| chr1:236726072
|
G | A | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.536+52G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726072 | ||||||
| chr1:236726243
|
G | A | 5 | a0001c0001t0005g0055a0001c0001t0011g0090a0001c0004t0002g0062others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.536+223G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726243 | ||||||
| chr1:236726267
|
A | G | 1 | a0001c0002t0002g0191 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.536+247A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726267 | ||||||
| chr1:236726290
|
G | A | 8 | a0001c0001t0004g0059a0001c0002t0002g0235a0001c0004t0002g0064others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.536+270G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726290 | ||||||
| chr1:236726389
|
C | A | 1 | a0006c0022t0001g0203 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.536+369C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726389 | ||||||
| chr1:236726389
|
C | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0032others(44): Show | 47 | HG00621.hp2 HG01081.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.536+369C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726389 | ||||||
| chr1:236726427
|
T | A | 1 | a0001c0001t0005g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.536+407T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726427 | ||||||
| chr1:236726481
|
T | C | 1 | a0001c0013t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.536+461T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726481 | ||||||
| chr1:236726815
|
T | C | 1 | a0001c0001t0001g0307 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.536+795T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236726815 | ||||||
| chr1:236727185
|
GA | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.537-483delA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 236727185 | |||||
| chr1:236727481
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.537-197A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236727481 | ||||||
| chr1:236727514
|
AGAT | A | 29 | a0001c0001t0004g0059a0001c0003t0001g0129a0001c0003t0001g0133others(26): Show | 29 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.537-161_537-159del others(3): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr1 | 236727514 | |||||
| chr1:236727535
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.537-143G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 5/20 | chr1 | 236727535 | ||||||
| chr1:236727961
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0292a0001c0001t0003g0105 | 3 | HG00099.hp1 HG01496.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.615+205G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236727961 | ||||||
| chr1:236727973
|
C | A | 2 | a0001c0001t0004g0213a0001c0002t0002g0243 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.615+217C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236727973 | ||||||
| chr1:236728107
|
A | G | 9 | a0001c0001t0004g0069a0001c0001t0004g0117a0001c0001t0004g0178others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.615+351A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728107 | ||||||
| chr1:236728143
|
C | CT | 100 | a0001c0001t0001g0190a0001c0001t0001g0195a0001c0001t0001g0205others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.615+405dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 236728143 | |||||
| chr1:236728143
|
CT | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.615+405delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 236728143 | |||||
| chr1:236728174
|
C | T | 6 | a0001c0003t0002g0170a0001c0003t0003g0058a0001c0003t0005g0172others(3): Show | 6 | HG01261.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.615+418C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728174 | ||||||
| chr1:236728225
|
G | C | 2 | a0001c0001t0004g0074a0001c0001t0004g0078 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.615+469G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728225 | ||||||
| chr1:236728236
|
C | T | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.615+480C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728236 | ||||||
| chr1:236728300
|
C | T | 1 | a0001c0021t0001g0254 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.615+544C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728300 | ||||||
| chr1:236728439
|
G | T | 1 | a0001c0024t0003g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.615+683G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728439 | ||||||
| chr1:236728596
|
T | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.615+840T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728596 | ||||||
| chr1:236728617
|
G | GT | 24 | a0001c0001t0001g0158a0001c0001t0001g0224a0001c0001t0001g0317others(21): Show | 24 | HG00423.hp2 HG00621.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.615+870dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 236728617 | |||||
| chr1:236728633
|
GC | G | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.615+878delC | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728633 | ||||||
| chr1:236728700
|
T | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.615+944T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728700 | ||||||
| chr1:236728726
|
T | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0242others(42): Show | 45 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.615+970T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728726 | ||||||
| chr1:236728726
|
T | G | 130 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0103others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.615+970T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728726 | ||||||
| chr1:236728938
|
T | A | 305 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.615+1182T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728938 | ||||||
| chr1:236728940
|
T | C | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.615+1184T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236728940 | ||||||
| chr1:236729266
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0103a0001c0001t0001g0301others(6): Show | 9 | HG00140.hp2 HG01081.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.615+1510G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236729266 | ||||||
| chr1:236729279
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.615+1523G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236729279 | ||||||
| chr1:236729349
|
G | A | 2 | a0001c0001t0004g0102a0001c0007t0015g0096 | 2 | HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.615+1593G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236729349 | ||||||
| chr1:236729355
|
A | G | 4 | a0001c0001t0009g0091a0001c0001t0015g0116a0001c0015t0016g0113others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+1599A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236729355 | ||||||
| chr1:236729364
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.615+1608A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236729364 | ||||||
| chr1:236729426
|
C | T | 6 | a0001c0003t0005g0047a0001c0003t0005g0048a0001c0003t0005g0050others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1670C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236729426 | ||||||
| chr1:236729764
|
G | C | 1 | a0001c0001t0001g0330 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.616-1469G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236729764 | ||||||
| chr1:236729835
|
C | A | 4 | a0001c0003t0002g0170a0001c0003t0003g0058a0001c0003t0005g0172others(1): Show | 4 | HG01261.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-1398C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236729835 | ||||||
| chr1:236730031
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.616-1202C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730031 | ||||||
| chr1:236730050
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.616-1183C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730050 | ||||||
| chr1:236730168
|
A | G | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.616-1065A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730168 | ||||||
| chr1:236730271
|
C | CT | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.616-947dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 236730271 | |||||
| chr1:236730271
|
CT | C | 27 | a0001c0001t0001g0110a0001c0001t0004g0102a0001c0001t0012g0019others(24): Show | 27 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.616-947delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 236730271 | |||||
| chr1:236730276
|
T | A | 3 | a0001c0002t0007g0326a0001c0002t0013g0239a0001c0002t0013g0325 | 3 | HG02027.hp1 HG02523.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.616-957T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730276 | ||||||
| chr1:236730295
|
C | T | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.616-938C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730295 | ||||||
| chr1:236730299
|
G | A | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(171): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.616-934G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730299 | ||||||
| chr1:236730379
|
GTGTTTCA others(1): Show |
G | 20 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(17): Show | 20 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.616-850_616-843del others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 236730379 | |||||
| chr1:236730462
|
C | T | 2 | a0001c0001t0004g0102a0001c0007t0015g0096 | 2 | HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.616-771C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730462 | ||||||
| chr1:236730698
|
A | G | 6 | a0001c0003t0005g0047a0001c0003t0005g0048a0001c0003t0005g0050others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-535A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730698 | ||||||
| chr1:236730785
|
A | G | 6 | a0001c0003t0005g0047a0001c0003t0005g0048a0001c0003t0005g0050others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-448A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | chr1 | 236730785 | ||||||
| chr1:236731347
|
G | A | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(171): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.697+33G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236731347 | ||||||
| chr1:236731418
|
G | A | 1 | a0001c0001t0003g0210 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.697+104G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236731418 | ||||||
| chr1:236731633
|
T | G | 5 | a0001c0001t0003g0238a0001c0001t0004g0075a0001c0001t0004g0200others(2): Show | 5 | HG01106.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.697+319T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236731633 | ||||||
| chr1:236731700
|
A | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0110a0001c0001t0001g0265others(26): Show | 29 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.697+386A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236731700 | ||||||
| chr1:236731721
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.697+407T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236731721 | ||||||
| chr1:236731789
|
A | G | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(171): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.697+475A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236731789 | ||||||
| chr1:236731905
|
C | CT | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+596dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr1 | 236731905 | |||||
| chr1:236731960
|
T | C | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+646T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236731960 | ||||||
| chr1:236731985
|
T | G | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.697+671T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236731985 | ||||||
| chr1:236732141
|
C | T | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+827C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732141 | ||||||
| chr1:236732203
|
G | A | 2 | a0001c0015t0016g0113a0001c0015t0016g0115 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.697+889G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732203 | ||||||
| chr1:236732271
|
G | A | 1 | a0006c0022t0001g0203 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.697+957G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732271 | ||||||
| chr1:236732374
|
C | G | 1 | a0001c0001t0001g0328 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.697+1060C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732374 | ||||||
| chr1:236732425
|
C | CTTTTTAT | 153 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.697+1138_697+1144d others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr1 | 236732425 | |||||
| chr1:236732431
|
A | C | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+1117A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732431 | ||||||
| chr1:236732437
|
T | TTTA | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+1123_697+1124i others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732437 | ||||||
| chr1:236732438
|
A | T | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+1124A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732438 | ||||||
| chr1:236732553
|
T | C | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(194): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.697+1239T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732553 | ||||||
| chr1:236732615
|
G | GT | 6 | a0001c0001t0005g0055a0001c0001t0011g0067a0001c0001t0011g0090others(3): Show | 6 | HG02109.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.697+1308dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr1 | 236732615 | |||||
| chr1:236732869
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0341a0001c0010t0002g0160 | 3 | HG00642.hp1 HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.697+1555G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732869 | ||||||
| chr1:236732892
|
C | T | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+1578C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732892 | ||||||
| chr1:236732893
|
T | C | 1 | a0001c0004t0005g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.697+1579T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732893 | ||||||
| chr1:236732999
|
C | G | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(194): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.697+1685C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236732999 | ||||||
| chr1:236733017
|
A | G | 1 | a0001c0003t0002g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.697+1703A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733017 | ||||||
| chr1:236733109
|
C | G | 1 | a0001c0001t0001g0259 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.697+1795C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733109 | ||||||
| chr1:236733185
|
A | G | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+1871A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733185 | ||||||
| chr1:236733206
|
G | A | 48 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0242others(45): Show | 48 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.697+1892G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733206 | ||||||
| chr1:236733283
|
G | A | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+1969G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733283 | ||||||
| chr1:236733319
|
C | T | 71 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0195others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.697+2005C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733319 | ||||||
| chr1:236733360
|
G | A | 80 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0195others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.697+2046G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733360 | ||||||
| chr1:236733398
|
T | C | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.697+2084T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733398 | ||||||
| chr1:236733404
|
C | T | 1 | a0001c0003t0022g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.697+2090C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733404 | ||||||
| chr1:236733502
|
T | G | 2 | a0001c0001t0004g0246a0001c0002t0002g0245 | 2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.698-2133T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733502 | ||||||
| chr1:236733546
|
C | A | 1 | a0001c0002t0002g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.698-2089C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733546 | ||||||
| chr1:236733621
|
C | A | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.698-2014C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733621 | ||||||
| chr1:236733631
|
G | A | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.698-2004G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733631 | ||||||
| chr1:236733737
|
A | G | 1 | a0001c0001t0003g0210 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.698-1898A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733737 | ||||||
| chr1:236733948
|
C | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.698-1687C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733948 | ||||||
| chr1:236733952
|
G | T | 28 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(25): Show | 28 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.698-1683G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236733952 | ||||||
| chr1:236734076
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(224): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.698-1559C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734076 | ||||||
| chr1:236734080
|
A | G | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.698-1555A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734080 | ||||||
| chr1:236734139
|
C | T | 1 | a0001c0001t0004g0204 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.698-1496C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734139 | ||||||
| chr1:236734207
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0242others(44): Show | 47 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.698-1428C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734207 | ||||||
| chr1:236734289
|
T | G | 6 | a0001c0001t0005g0055a0001c0001t0011g0067a0001c0001t0011g0090others(3): Show | 6 | HG02109.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.698-1346T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734289 | ||||||
| chr1:236734333
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.698-1302A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734333 | ||||||
| chr1:236734386
|
G | C | 1 | a0001c0004t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.698-1249G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734386 | ||||||
| chr1:236734567
|
T | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0103others(55): Show | 58 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.698-1068T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734567 | ||||||
| chr1:236734597
|
T | C | 5 | a0001c0001t0005g0055a0001c0001t0011g0067a0001c0001t0011g0090others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-1038T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734597 | ||||||
| chr1:236734612
|
C | T | 1 | a0001c0016t0003g0108 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.698-1023C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734612 | ||||||
| chr1:236734626
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0103a0001c0001t0001g0301others(7): Show | 10 | HG00140.hp2 HG01081.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.698-1009G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734626 | ||||||
| chr1:236734735
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.698-900T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734735 | ||||||
| chr1:236734811
|
G | A | 11 | a0001c0001t0004g0059a0001c0004t0002g0064a0001c0004t0005g0056others(8): Show | 11 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.698-824G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734811 | ||||||
| chr1:236734863
|
A | C | 100 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.698-772A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734863 | ||||||
| chr1:236734887
|
G | A | 30 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(27): Show | 30 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.698-748G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734887 | ||||||
| chr1:236734990
|
G | A | 1 | a0001c0003t0020g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.698-645G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236734990 | ||||||
| chr1:236735076
|
T | C | 1 | a0001c0002t0002g0233 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.698-559T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236735076 | ||||||
| chr1:236735095
|
G | A | 29 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(26): Show | 29 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.698-540G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236735095 | ||||||
| chr1:236735363
|
G | A | 1 | a0001c0002t0002g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.698-272G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236735363 | ||||||
| chr1:236735383
|
AG | A | 29 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(26): Show | 29 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.698-248delG | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr1 | 236735383 | |||||
| chr1:236735389
|
G | C | 1 | a0001c0001t0005g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.698-246G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | chr1 | 236735389 | ||||||
| chr1:236735589
|
G | GGT | 3 | a0001c0001t0001g0269a0001c0001t0005g0181a0002c0005t0004g0257 | 3 | HG02976.hp2 NA18973.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.698-34_698-33dupTG | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr1 | 236735589 | |||||
| chr1:236735742
|
G | A | 73 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0195others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.783+22G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236735742 | ||||||
| chr1:236735746
|
T | A | 1 | a0001c0002t0002g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.783+26T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236735746 | ||||||
| chr1:236735869
|
A | G | 1 | a0001c0001t0017g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.783+149A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236735869 | ||||||
| chr1:236736022
|
G | A | 29 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(26): Show | 29 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.783+302G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736022 | ||||||
| chr1:236736043
|
A | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.783+323A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736043 | ||||||
| chr1:236736083
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.783+363G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736083 | ||||||
| chr1:236736133
|
C | T | 3 | a0001c0003t0003g0058a0001c0003t0005g0172a0001c0006t0002g0171 | 3 | HG01261.hp1 HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.783+413C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736133 | ||||||
| chr1:236736169
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.783+449G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736169 | ||||||
| chr1:236736298
|
T | C | 5 | a0001c0001t0003g0238a0001c0001t0004g0075a0001c0001t0004g0200others(2): Show | 5 | HG01106.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.783+578T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736298 | ||||||
| chr1:236736401
|
G | A | 20 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(17): Show | 20 | HG00609.hp1 HG00673.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.783+681G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736401 | ||||||
| chr1:236736458
|
A | G | 1 | a0001c0001t0004g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784-664A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736458 | ||||||
| chr1:236736599
|
TC | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.784-518delC | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 236736599 | |||||
| chr1:236736687
|
G | T | 1 | a0001c0002t0002g0248 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.784-435G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736687 | ||||||
| chr1:236736718
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.784-404G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736718 | ||||||
| chr1:236736961
|
C | T | 1 | a0002c0005t0004g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.784-161C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236736961 | ||||||
| chr1:236737062
|
A | G | 1 | a0001c0001t0001g0312 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.784-60A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236737062 | ||||||
| chr1:236737077
|
A | G | 8 | a0001c0002t0002g0180a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG01106.hp1 HG01175.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-45A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 8/20 | chr1 | 236737077 | ||||||
| chr1:236737297
|
G | GTATA | 5 | a0001c0001t0001g0041a0001c0001t0001g0141a0001c0001t0001g0144others(2): Show | 5 | HG00673.hp2 NA18941.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATA | 6 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0145others(3): Show | 6 | HG03239.hp2 HG03710.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(5): Show |
3 | a0001c0001t0004g0178a0001c0002t0002g0179a0001c0004t0005g0199 | 3 | HG03225.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.876+83_876+84insTA others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(7): Show |
1 | a0001c0003t0006g0134 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.876+83_876+84insTA others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0110a0001c0003t0006g0132a0006c0022t0001g0203 | 3 | HG00738.hp2 HG04184.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.876+83_876+84insTA others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0289 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.876+83_876+84insTA others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(15): Show |
8 | a0001c0001t0001g0320a0001c0001t0001g0322a0001c0001t0001g0342others(5): Show | 8 | HG00140.hp1 HG01081.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(20): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(17): Show |
10 | a0001c0001t0001g0114a0001c0001t0001g0259a0001c0001t0001g0288others(7): Show | 10 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(22): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(19): Show |
19 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0265others(16): Show | 19 | HG00099.hp1 HG01106.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(24): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(21): Show |
11 | a0001c0001t0001g0188a0001c0001t0001g0276a0001c0001t0001g0290others(8): Show | 11 | HG00621.hp2 HG01123.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(26): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(23): Show |
8 | a0001c0001t0001g0287a0001c0001t0001g0328a0001c0002t0007g0298others(5): Show | 8 | HG00639.hp2 HG01258.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(28): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(25): Show |
6 | a0001c0001t0001g0307a0001c0001t0004g0295a0001c0003t0002g0051others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(30): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(27): Show |
9 | a0001c0001t0001g0219a0001c0001t0001g0258a0001c0001t0001g0304others(6): Show | 9 | HG00438.hp1 HG00741.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(32): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(29): Show |
11 | a0001c0001t0001g0033a0001c0001t0001g0338a0001c0001t0003g0284others(8): Show | 11 | HG00738.hp1 HG01169.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(34): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(31): Show |
12 | a0001c0001t0001g0042a0001c0001t0001g0253a0001c0001t0001g0260others(9): Show | 12 | HG00639.hp1 HG01943.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(36): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(33): Show |
7 | a0001c0001t0001g0032a0001c0001t0001g0158a0001c0001t0001g0327others(4): Show | 7 | HG01123.hp1 HG01168.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(38): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(35): Show |
6 | a0001c0001t0001g0001a0001c0001t0001g0264a0001c0001t0001g0285others(3): Show | 6 | HG00280.hp2 HG00673.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(40): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(37): Show |
3 | a0001c0001t0001g0286a0001c0001t0003g0174a0001c0003t0006g0130 | 3 | HG01099.hp2 HG02148.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.876+83_876+84insTA others(42): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(39): Show |
5 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0001g0333others(2): Show | 5 | HG00642.hp1 HG02129.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(44): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(41): Show |
2 | a0001c0001t0001g0157a0001c0001t0001g0251 | 2 | HG03669.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.876+83_876+84insTA others(46): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(43): Show |
1 | a0001c0001t0001g0318 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.876+83_876+84insTA others(48): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(45): Show |
3 | a0001c0001t0001g0225a0001c0001t0001g0262a0001c0003t0020g0122 | 3 | HG02683.hp2 HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.876+83_876+84insTA others(50): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATATAT others(47): Show |
2 | a0001c0001t0003g0143a0001c0001t0012g0019 | 2 | HG01516.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.876+83_876+84insTA others(52): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATGTAT others(27): Show |
4 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0003g0147others(1): Show | 4 | HG00609.hp1 NA18967.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+83_876+84insTA others(32): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATGTAT others(31): Show |
1 | a0001c0001t0003g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.876+83_876+84insTA others(36): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737297
|
G | GTATTATA others(30): Show |
1 | a0001c0001t0003g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.876+83_876+84insTA others(35): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737297 | ||||||
| chr1:236737298
|
C | CAT | 16 | a0001c0001t0004g0003a0001c0001t0004g0015a0001c0001t0004g0071others(13): Show | 16 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.876+103_876+104dup others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737298 | |||||
| chr1:236737298
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0103 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.876+93_876+104dupA others(11): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737298 | |||||
| chr1:236737298
|
C | CATATATA others(29): Show |
1 | a0001c0001t0004g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.876+104_876+105ins others(36): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737298 | |||||
| chr1:236737298
|
C | CATATATA others(31): Show |
2 | a0001c0001t0001g0301a0001c0001t0002g0156 | 2 | HG02683.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.876+104_876+105ins others(38): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737298 | |||||
| chr1:236737298
|
C | CATATATA others(37): Show |
1 | a0001c0002t0002g0302 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.876+104_876+105ins others(44): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737298 | |||||
| chr1:236737298
|
C | CATATATA others(39): Show |
2 | a0001c0001t0003g0104a0001c0002t0002g0017 | 2 | HG00140.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.876+104_876+105ins others(46): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737298 | |||||
| chr1:236737298
|
C | CATATATA others(41): Show |
1 | a0001c0001t0001g0018 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.876+104_876+105ins others(48): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737298 | |||||
| chr1:236737298
|
C | CATATATA others(43): Show |
1 | a0001c0002t0002g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.876+104_876+105ins others(50): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737298 | |||||
| chr1:236737298
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(167): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.876+84C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737298 | ||||||
| chr1:236737299
|
A | T | 8 | a0001c0001t0005g0151a0001c0001t0009g0152a0001c0003t0005g0047others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.876+85A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737299 | ||||||
| chr1:236737315
|
A | ATATATAT others(39): Show |
1 | a0001c0004t0005g0061 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.876+104_876+105ins others(46): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737315 | |||||
| chr1:236737315
|
A | ATATATAT others(35): Show |
1 | a0001c0004t0002g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.876+104_876+105ins others(42): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737315 | |||||
| chr1:236737315
|
A | ATATATAT others(29): Show |
4 | a0001c0004t0005g0056a0001c0004t0005g0077a0001c0004t0005g0120others(1): Show | 4 | HG01192.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+104_876+105ins others(36): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737315 | |||||
| chr1:236737315
|
A | ATATATAT others(27): Show |
2 | a0001c0001t0004g0059a0001c0004t0005g0060 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.876+104_876+105ins others(34): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737315 | |||||
| chr1:236737315
|
A | ATATATAT others(21): Show |
1 | a0001c0014t0002g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.876+104_876+105ins others(28): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737315 | |||||
| chr1:236737315
|
A | ATATATAT others(13): Show |
1 | a0001c0013t0023g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.876+104_876+105ins others(20): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737315 | |||||
| chr1:236737318
|
T | TATATATA others(34): Show |
1 | a0001c0001t0004g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.876+104_876+105ins others(41): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737318 | ||||||
| chr1:236737318
|
T | TATATATA others(36): Show |
1 | a0001c0001t0003g0268 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.876+104_876+105ins others(43): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737318 | ||||||
| chr1:236737319
|
T | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0327 | 2 | HG02004.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.876+105T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737319 | ||||||
| chr1:236737320
|
T | A | 1 | a0001c0001t0004g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.876+106T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737320 | ||||||
| chr1:236737328
|
T | C | 1 | a0001c0001t0004g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.876+114T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737328 | ||||||
| chr1:236737436
|
C | T | 3 | a0001c0009t0003g0012a0001c0009t0003g0013a0001c0009t0003g0038 | 3 | HG00323.hp1 NA19068.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.876+222C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737436 | ||||||
| chr1:236737527
|
CT | C | 20 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(17): Show | 20 | HG00609.hp1 HG00673.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.876+314delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737527 | ||||||
| chr1:236737548
|
G | GT | 128 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.876+346dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236737548 | |||||
| chr1:236737548
|
G | T | 1 | a0001c0002t0002g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.876+334G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737548 | ||||||
| chr1:236737601
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.876+387T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737601 | ||||||
| chr1:236737663
|
C | T | 1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.876+449C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737663 | ||||||
| chr1:236737675
|
G | A | 22 | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.876+461G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737675 | ||||||
| chr1:236737857
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.876+643C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737857 | ||||||
| chr1:236737863
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.876+649A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737863 | ||||||
| chr1:236737869
|
G | A | 20 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(17): Show | 20 | HG00609.hp1 HG00673.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.876+655G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737869 | ||||||
| chr1:236737968
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.876+754A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236737968 | ||||||
| chr1:236738002
|
CTTTGT | C | 30 | a0001c0001t0001g0110a0001c0001t0005g0151a0001c0001t0009g0152others(27): Show | 30 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.876+807_876+811del others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236738002 | |||||
| chr1:236738075
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.876+861T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738075 | ||||||
| chr1:236738082
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.876+868G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738082 | ||||||
| chr1:236738099
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.876+885C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738099 | ||||||
| chr1:236738102
|
A | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.876+888A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738102 | ||||||
| chr1:236738114
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.876+900A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738114 | ||||||
| chr1:236738212
|
G | T | 24 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(21): Show | 24 | HG00609.hp1 HG00673.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.876+998G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738212 | ||||||
| chr1:236738225
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.876+1011C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738225 | ||||||
| chr1:236738226
|
C | T | 6 | a0001c0001t0004g0178a0001c0002t0002g0179a0001c0004t0005g0199others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.876+1012C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738226 | ||||||
| chr1:236738255
|
C | T | 1 | a0001c0001t0015g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.876+1041C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738255 | ||||||
| chr1:236738276
|
C | T | 5 | a0001c0001t0003g0111a0001c0001t0003g0249a0001c0001t0011g0067others(2): Show | 5 | HG00609.hp2 HG02027.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-1026C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738276 | ||||||
| chr1:236738299
|
G | A | 1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.877-1003G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738299 | ||||||
| chr1:236738518
|
A | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.877-784A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738518 | ||||||
| chr1:236738549
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.877-753C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738549 | ||||||
| chr1:236738552
|
G | A | 4 | a0001c0001t0004g0117a0001c0002t0002g0079a0001c0002t0002g0162others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.877-750G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738552 | ||||||
| chr1:236738611
|
T | G | 5 | a0001c0001t0004g0071a0001c0001t0004g0074a0001c0001t0004g0078others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-691T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738611 | ||||||
| chr1:236738695
|
A | G | 1 | a0001c0004t0005g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.877-607A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738695 | ||||||
| chr1:236738735
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.877-567T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738735 | ||||||
| chr1:236738772
|
A | T | 1 | a0001c0002t0002g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.877-530A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738772 | ||||||
| chr1:236738850
|
T | A | 1 | a0001c0001t0003g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.877-452T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236738850 | ||||||
| chr1:236739064
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.877-238C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236739064 | ||||||
| chr1:236739108
|
C | T | 1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.877-194C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236739108 | ||||||
| chr1:236739203
|
T | C | 8 | a0001c0001t0005g0151a0001c0001t0009g0152a0001c0003t0005g0047others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.877-99T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236739203 | ||||||
| chr1:236739232
|
ATT | A | 25 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(22): Show | 25 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.877-59_877-58delTT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 236739232 | |||||
| chr1:236739260
|
C | G | 25 | a0001c0001t0001g0041a0001c0001t0001g0139a0001c0001t0001g0141others(22): Show | 25 | HG00609.hp1 HG00673.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.877-42C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236739260 | ||||||
| chr1:236739260
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.877-42C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236739260 | ||||||
| chr1:236739294
|
C | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
splice_region_variant&intron_variant | LOW | c.877-8C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | chr1 | 236739294 | ||||||
| chr1:236739565
|
A | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1107+33A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236739565 | ||||||
| chr1:236739618
|
A | G | 1 | a0001c0001t0009g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1107+86A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236739618 | ||||||
| chr1:236739655
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1107+123T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236739655 | ||||||
| chr1:236739887
|
G | A | 1 | a0001c0002t0002g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1107+355G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236739887 | ||||||
| chr1:236740199
|
C | T | 1 | a0001c0002t0002g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1107+667C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740199 | ||||||
| chr1:236740262
|
C | T | 2 | a0001c0007t0004g0085a0001c0031t0005g0053 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1107+730C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740262 | ||||||
| chr1:236740275
|
G | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1107+743G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740275 | ||||||
| chr1:236740387
|
G | T | 72 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0195others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1107+855G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740387 | ||||||
| chr1:236740394
|
G | A | 1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1107+862G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740394 | ||||||
| chr1:236740491
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1107+959C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740491 | ||||||
| chr1:236740526
|
C | CATTTTT | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1107+1013_1107+101 others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 236740526 | |||||
| chr1:236740526
|
C | CATTTTTA others(5): Show |
1 | a0001c0001t0001g0308 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1107+1007_1107+101 others(16): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 236740526 | |||||
| chr1:236740526
|
C | CATTTTTA others(11): Show |
1 | a0001c0001t0001g0312 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1107+1001_1107+101 others(22): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 236740526 | |||||
| chr1:236740556
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1107+1024A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740556 | ||||||
| chr1:236740565
|
C | T | 1 | a0001c0002t0002g0192 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1107+1033C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740565 | ||||||
| chr1:236740575
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1107+1043C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740575 | ||||||
| chr1:236740681
|
C | T | 1 | a0001c0013t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1107+1149C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740681 | ||||||
| chr1:236740689
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1107+1157C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740689 | ||||||
| chr1:236740745
|
C | T | 1 | a0001c0031t0005g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1107+1213C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740745 | ||||||
| chr1:236740825
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1107+1293A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740825 | ||||||
| chr1:236740835
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1107+1303G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740835 | ||||||
| chr1:236740870
|
C | T | 149 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0103others(146): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1107+1338C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236740870 | ||||||
| chr1:236741016
|
G | C | 2 | a0001c0001t0004g0075a0001c0010t0002g0164 | 2 | HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1107+1484G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741016 | ||||||
| chr1:236741169
|
T | G | 1 | a0002c0005t0004g0294 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1107+1637T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741169 | ||||||
| chr1:236741254
|
C | T | 15 | a0001c0001t0001g0018a0001c0001t0001g0103a0001c0001t0001g0301others(12): Show | 15 | HG00140.hp2 HG01081.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1108-1642C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741254 | ||||||
| chr1:236741259
|
C | T | 5 | a0001c0001t0004g0069a0001c0001t0004g0117a0001c0002t0002g0079others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-1637C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741259 | ||||||
| chr1:236741635
|
G | T | 1 | a0001c0001t0005g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1108-1261G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741635 | ||||||
| chr1:236741677
|
C | T | 3 | a0001c0001t0014g0082a0001c0001t0014g0084a0001c0001t0014g0086 | 3 | HG01981.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1108-1219C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741677 | ||||||
| chr1:236741690
|
T | A | 66 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0032others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1108-1206T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741690 | ||||||
| chr1:236741793
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0031others(60): Show | 63 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1108-1103T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741793 | ||||||
| chr1:236741865
|
G | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0103a0001c0001t0002g0156others(23): Show | 26 | HG00140.hp2 HG00673.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1108-1031G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741865 | ||||||
| chr1:236741934
|
G | C | 1 | a0001c0007t0015g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1108-962G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741934 | ||||||
| chr1:236741974
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1108-922G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741974 | ||||||
| chr1:236741986
|
C | G | 7 | a0001c0001t0005g0151a0001c0001t0009g0152a0001c0003t0005g0047others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1108-910C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741986 | ||||||
| chr1:236741986
|
C | T | 1 | a0001c0010t0002g0160 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1108-910C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236741986 | ||||||
| chr1:236742000
|
C | G | 1 | a0001c0002t0002g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1108-896C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742000 | ||||||
| chr1:236742010
|
G | A | 62 | a0001c0001t0001g0114a0001c0001t0001g0184a0001c0001t0001g0195others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1108-886G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742010 | ||||||
| chr1:236742153
|
C | T | 7 | a0001c0001t0005g0151a0001c0001t0009g0152a0001c0003t0005g0047others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1108-743C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742153 | ||||||
| chr1:236742214
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1108-682T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742214 | ||||||
| chr1:236742285
|
T | TGGGAACG | 86 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0031others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1108-605_1108-604i others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 236742285 | |||||
| chr1:236742427
|
A | C | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1108-469A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742427 | ||||||
| chr1:236742470
|
C | T | 2 | a0001c0001t0003g0104a0001c0016t0003g0108 | 2 | HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1108-426C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742470 | ||||||
| chr1:236742535
|
T | TA | 13 | a0001c0001t0004g0037a0001c0001t0004g0071a0001c0001t0004g0074others(10): Show | 13 | HG01361.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1108-352dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 236742535 | |||||
| chr1:236742544
|
AC | A | 25 | a0001c0001t0001g0018a0001c0001t0001g0103a0001c0001t0002g0156others(22): Show | 25 | HG00140.hp2 HG01081.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1108-351delC | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742544 | ||||||
| chr1:236742595
|
G | T | 2 | a0001c0001t0005g0055a0001c0002t0002g0245 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1108-301G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742595 | ||||||
| chr1:236742666
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1108-230C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | chr1 | 236742666 | ||||||
| chr1:236743138
|
C | T | 1 | a0001c0010t0002g0160 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1255+95C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743138 | ||||||
| chr1:236743151
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1255+108G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743151 | ||||||
| chr1:236743212
|
A | G | 3 | a0001c0001t0019g0250a0001c0001t0019g0252a0001c0006t0008g0127 | 3 | HG03239.hp2 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1255+169A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743212 | ||||||
| chr1:236743234
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1255+191C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743234 | ||||||
| chr1:236743364
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0110others(17): Show | 20 | HG00673.hp2 HG00738.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1255+321G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743364 | ||||||
| chr1:236743507
|
A | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0018others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1255+464A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743507 | ||||||
| chr1:236743569
|
C | CT | 7 | a0001c0001t0003g0238a0001c0001t0004g0075a0001c0001t0004g0178others(4): Show | 7 | HG02145.hp1 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255+541dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr1 | 236743569 | |||||
| chr1:236743569
|
CT | C | 18 | a0001c0001t0001g0141a0001c0001t0001g0154a0001c0001t0004g0059others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1255+541delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr1 | 236743569 | |||||
| chr1:236743586
|
G | A | 331 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1255+543G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743586 | ||||||
| chr1:236743692
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1255+649A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743692 | ||||||
| chr1:236743868
|
G | A | 1 | a0002c0020t0002g0007 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1256-758G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743868 | ||||||
| chr1:236743957
|
T | C | 4 | a0001c0001t0004g0117a0001c0002t0002g0079a0001c0002t0002g0162others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-669T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236743957 | ||||||
| chr1:236744055
|
G | A | 1 | a0001c0010t0002g0160 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1256-571G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236744055 | ||||||
| chr1:236744060
|
C | T | 4 | a0001c0001t0004g0117a0001c0002t0002g0079a0001c0002t0002g0162others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-566C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236744060 | ||||||
| chr1:236744164
|
C | G | 2 | a0001c0002t0002g0089a0001c0002t0002g0232 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1256-462C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236744164 | ||||||
| chr1:236744246
|
C | G | 1 | a0001c0002t0002g0218 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1256-380C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236744246 | ||||||
| chr1:236744294
|
G | C | 44 | a0001c0001t0001g0041a0001c0001t0001g0110a0001c0001t0001g0141others(41): Show | 44 | HG00438.hp1 HG00673.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1256-332G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236744294 | ||||||
| chr1:236744461
|
A | G | 1 | a0001c0003t0006g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1256-165A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236744461 | ||||||
| chr1:236744511
|
C | G | 1 | a0001c0010t0002g0160 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1256-115C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236744511 | ||||||
| chr1:236744547
|
G | A | 29 | a0001c0001t0001g0041a0001c0001t0001g0110a0001c0001t0001g0141others(26): Show | 29 | HG00438.hp1 HG00673.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1256-79G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | chr1 | 236744547 | ||||||
| chr1:236744794
|
C | G | 1 | a0001c0001t0003g0299 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1406+18C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236744794 | ||||||
| chr1:236744844
|
T | C | 7 | a0001c0010t0002g0160a0001c0010t0002g0164a0001c0011t0004g0101others(4): Show | 7 | HG01106.hp2 HG01168.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1406+68T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236744844 | ||||||
| chr1:236744899
|
A | C | 9 | a0001c0001t0003g0299a0001c0001t0010g0044a0001c0001t0010g0045others(6): Show | 9 | HG03017.hp2 HG03490.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.1406+123A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236744899 | ||||||
| chr1:236745016
|
C | A | 1 | a0001c0001t0003g0210 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1406+240C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745016 | ||||||
| chr1:236745172
|
C | T | 11 | a0001c0001t0004g0059a0001c0004t0002g0064a0001c0004t0005g0056others(8): Show | 11 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1406+396C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745172 | ||||||
| chr1:236745241
|
T | C | 1 | a0001c0004t0005g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1406+465T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745241 | ||||||
| chr1:236745306
|
T | C | 2 | a0001c0004t0005g0177a0001c0010t0002g0183 | 2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1406+530T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745306 | ||||||
| chr1:236745327
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0211a0001c0027t0001g0311 | 3 | HG01255.hp2 HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1406+551G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745327 | ||||||
| chr1:236745359
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1406+583A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745359 | ||||||
| chr1:236745389
|
G | C | 1 | a0001c0001t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1406+613G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745389 | ||||||
| chr1:236745422
|
G | A | 1 | a0001c0002t0002g0313 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1406+646G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745422 | ||||||
| chr1:236745486
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1406+710G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745486 | ||||||
| chr1:236745501
|
G | A | 1 | a0001c0001t0004g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1406+725G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745501 | ||||||
| chr1:236745890
|
A | G | 6 | a0001c0001t0005g0151a0001c0001t0009g0152a0001c0003t0005g0047others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406+1114A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745890 | ||||||
| chr1:236745960
|
A | G | 2 | a0001c0001t0003g0299a0001c0006t0008g0127 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1406+1184A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745960 | ||||||
| chr1:236745970
|
T | A | 1 | a0001c0025t0006g0121 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1406+1194T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745970 | ||||||
| chr1:236745974
|
T | C | 1 | a0001c0002t0002g0243 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1406+1198T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745974 | ||||||
| chr1:236745979
|
C | G | 1 | a0001c0025t0006g0121 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1406+1203C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745979 | ||||||
| chr1:236745993
|
A | C | 8 | a0001c0001t0001g0141a0001c0001t0001g0154a0001c0001t0003g0147others(5): Show | 8 | HG00438.hp1 HG01243.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.1406+1217A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236745993 | ||||||
| chr1:236746023
|
A | G | 2 | a0001c0010t0002g0164a0001c0029t0005g0107 | 2 | HG01106.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1406+1247A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746023 | ||||||
| chr1:236746032
|
G | A | 1 | a0001c0001t0014g0084 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1406+1256G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746032 | ||||||
| chr1:236746043
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1406+1267G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746043 | ||||||
| chr1:236746080
|
G | T | 1 | a0002c0008t0004g0277 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1406+1304G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746080 | ||||||
| chr1:236746090
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1406+1314C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746090 | ||||||
| chr1:236746091
|
G | A | 1 | a0001c0001t0003g0299 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1406+1315G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746091 | ||||||
| chr1:236746097
|
C | T | 1 | a0001c0002t0002g0072 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1406+1321C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746097 | ||||||
| chr1:236746114
|
C | G | 1 | a0001c0001t0001g0139 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1406+1338C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746114 | ||||||
| chr1:236746165
|
C | CA | 8 | a0001c0001t0004g0028a0001c0007t0004g0070a0001c0007t0004g0083others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1406+1407dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 236746165 | |||||
| chr1:236746165
|
C | CAA | 16 | a0001c0001t0001g0041a0001c0001t0001g0110a0001c0001t0001g0141others(13): Show | 16 | HG00438.hp1 HG00673.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1406+1406_1406+140 others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 236746165 | |||||
| chr1:236746165
|
CA | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1406+1407delA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 236746165 | |||||
| chr1:236746165
|
CAA | C | 56 | a0001c0001t0001g0018a0001c0001t0001g0275a0001c0001t0002g0156others(53): Show | 56 | HG00140.hp2 HG01109.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.1406+1406_1406+140 others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 236746165 | |||||
| chr1:236746180
|
A | G | 1 | a0001c0001t0003g0272 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1406+1404A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746180 | ||||||
| chr1:236746228
|
G | T | 1 | a0001c0003t0006g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1407-1439G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746228 | ||||||
| chr1:236746313
|
T | G | 1 | a0001c0002t0002g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1407-1354T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746313 | ||||||
| chr1:236746620
|
C | A | 1 | a0001c0002t0002g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1407-1047C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746620 | ||||||
| chr1:236746646
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1407-1021T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746646 | ||||||
| chr1:236746706
|
CA | C | 19 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0003g0104others(16): Show | 19 | HG00639.hp2 HG01123.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1407-945delA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 236746706 | |||||
| chr1:236746814
|
C | T | 2 | a0001c0001t0009g0187a0001c0001t0017g0097 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1407-853C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236746814 | ||||||
| chr1:236747001
|
G | A | 3 | a0001c0002t0002g0278a0001c0002t0002g0309a0001c0002t0002g0310 | 3 | NA18990.hp1 NA19064.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1407-666G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747001 | ||||||
| chr1:236747003
|
G | A | 23 | a0001c0001t0001g0041a0001c0001t0001g0141a0001c0001t0001g0144others(20): Show | 23 | HG00438.hp1 HG00673.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1407-664G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747003 | ||||||
| chr1:236747086
|
C | T | 6 | a0001c0002t0002g0079a0001c0002t0002g0087a0001c0002t0002g0162others(3): Show | 6 | HG02257.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407-581C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747086 | ||||||
| chr1:236747243
|
T | A | 1 | a0001c0001t0003g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1407-424T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747243 | ||||||
| chr1:236747332
|
A | G | 1 | a0001c0001t0018g0303 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1407-335A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747332 | ||||||
| chr1:236747365
|
T | G | 3 | a0001c0001t0004g0178a0001c0002t0002g0072a0001c0002t0002g0179 | 3 | HG06807.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1407-302T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747365 | ||||||
| chr1:236747480
|
C | T | 1 | a0001c0002t0002g0248 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1407-187C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747480 | ||||||
| chr1:236747517
|
ACTGT | A | 15 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(12): Show | 15 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1407-147_1407-144d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 236747517 | |||||
| chr1:236747539
|
A | G | 28 | a0001c0001t0002g0156a0001c0001t0003g0104a0001c0001t0003g0173others(25): Show | 28 | HG00140.hp2 HG00673.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1407-128A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747539 | ||||||
| chr1:236747563
|
T | C | 125 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0141others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1407-104T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747563 | ||||||
| chr1:236747572
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1407-95T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | chr1 | 236747572 | ||||||
| chr1:236747790
|
C | T | 2 | a0001c0007t0004g0070a0001c0011t0004g0101 | 2 | HG02615.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1515+15C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236747790 | ||||||
| chr1:236747822
|
C | T | 27 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(24): Show | 27 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1515+47C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236747822 | ||||||
| chr1:236747837
|
A | G | 51 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0141others(48): Show | 51 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1515+62A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236747837 | ||||||
| chr1:236747921
|
G | T | 52 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(49): Show | 52 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1515+146G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236747921 | ||||||
| chr1:236748023
|
G | A | 1 | a0001c0004t0005g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1515+248G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748023 | ||||||
| chr1:236748043
|
C | T | 78 | a0001c0001t0001g0184a0001c0001t0001g0205a0001c0001t0001g0211others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1515+268C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748043 | ||||||
| chr1:236748127
|
G | C | 3 | a0001c0001t0009g0187a0004c0026t0005g0076a0004c0032t0017g0094 | 3 | HG01192.hp1 HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1515+352G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748127 | ||||||
| chr1:236748156
|
T | C | 20 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0003t0020g0122others(17): Show | 20 | HG01258.hp1 HG01516.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.1515+381T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748156 | ||||||
| chr1:236748269
|
G | C | 1 | a0001c0003t0021g0125 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1515+494G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748269 | ||||||
| chr1:236748369
|
T | C | 3 | a0001c0002t0002g0089a0001c0010t0002g0164a0001c0010t0002g0183 | 3 | HG01106.hp2 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1515+594T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748369 | ||||||
| chr1:236748403
|
A | G | 3 | a0001c0001t0005g0080a0001c0007t0004g0085a0001c0031t0005g0053 | 3 | HG02572.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1515+628A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748403 | ||||||
| chr1:236748419
|
A | C | 15 | a0001c0001t0003g0238a0001c0001t0004g0069a0001c0001t0004g0075others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1515+644A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748419 | ||||||
| chr1:236748451
|
C | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1516-673C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748451 | ||||||
| chr1:236748523
|
C | T | 4 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0003t0020g0122others(1): Show | 4 | HG01258.hp1 HG01516.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516-601C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748523 | ||||||
| chr1:236748558
|
G | A | 15 | a0001c0001t0003g0238a0001c0001t0004g0069a0001c0001t0004g0075others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1516-566G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748558 | ||||||
| chr1:236748701
|
G | C | 16 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(13): Show | 16 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1516-423G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748701 | ||||||
| chr1:236748757
|
T | C | 74 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0141others(71): Show | 74 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.1516-367T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748757 | ||||||
| chr1:236748918
|
T | A | 1 | a0001c0002t0002g0273 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1516-206T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748918 | ||||||
| chr1:236748919
|
G | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1516-205G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748919 | ||||||
| chr1:236748986
|
G | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1516-138G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236748986 | ||||||
| chr1:236749015
|
C | T | 1 | a0001c0018t0006g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1516-109C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 13/20 | chr1 | 236749015 | ||||||
| chr1:236749297
|
A | G | 84 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0141others(81): Show | 84 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.1656+33A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749297 | ||||||
| chr1:236749356
|
G | T | 62 | a0001c0001t0003g0104a0001c0001t0003g0173a0001c0001t0003g0174others(59): Show | 62 | HG00673.hp1 HG01106.hp2 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.1656+92G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749356 | ||||||
| chr1:236749423
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1656+159G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749423 | ||||||
| chr1:236749522
|
C | T | 30 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(27): Show | 30 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1656+258C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749522 | ||||||
| chr1:236749539
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1656+275A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749539 | ||||||
| chr1:236749560
|
G | A | 1 | a0001c0016t0003g0108 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1656+296G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749560 | ||||||
| chr1:236749586
|
C | T | 1 | a0001c0004t0005g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1656+322C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749586 | ||||||
| chr1:236749715
|
C | T | 77 | a0001c0001t0001g0184a0001c0001t0001g0205a0001c0001t0001g0211others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1656+451C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749715 | ||||||
| chr1:236749816
|
A | G | 3 | a0001c0002t0002g0223a0001c0002t0002g0237a0001c0002t0002g0248 | 3 | HG01071.hp1 HG02132.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1656+552A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749816 | ||||||
| chr1:236749913
|
G | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1656+649G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749913 | ||||||
| chr1:236749936
|
A | G | 3 | a0001c0002t0002g0089a0001c0010t0002g0164a0001c0010t0002g0183 | 3 | HG01106.hp2 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1656+672A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749936 | ||||||
| chr1:236749980
|
C | T | 1 | a0001c0003t0003g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1656+716C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749980 | ||||||
| chr1:236749987
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1656+723G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236749987 | ||||||
| chr1:236750047
|
T | C | 12 | a0001c0001t0005g0055a0001c0002t0002g0072a0001c0002t0002g0089others(9): Show | 12 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1656+783T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750047 | ||||||
| chr1:236750200
|
T | C | 72 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0141others(69): Show | 72 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.1656+936T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750200 | ||||||
| chr1:236750219
|
T | C | 4 | a0001c0004t0002g0062a0001c0004t0002g0240a0001c0015t0016g0113others(1): Show | 4 | HG01168.hp2 HG01169.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+955T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750219 | ||||||
| chr1:236750405
|
C | T | 15 | a0001c0001t0003g0238a0001c0001t0004g0069a0001c0001t0004g0075others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1657-1065C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750405 | ||||||
| chr1:236750445
|
A | G | 17 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0024others(14): Show | 17 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.1657-1025A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750445 | ||||||
| chr1:236750542
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1657-928C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750542 | ||||||
| chr1:236750543
|
A | G | 2 | a0001c0001t0004g0102a0001c0001t0004g0119 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1657-927A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750543 | ||||||
| chr1:236750608
|
C | T | 1 | a0001c0030t0002g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1657-862C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750608 | ||||||
| chr1:236750638
|
G | A | 2 | a0001c0001t0004g0075a0001c0001t0004g0200 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1657-832G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750638 | ||||||
| chr1:236750713
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1657-757A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750713 | ||||||
| chr1:236750920
|
CT | C | 15 | a0001c0001t0003g0238a0001c0001t0004g0069a0001c0001t0004g0075others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1657-549delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236750920 | ||||||
| chr1:236751077
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0328 | 2 | HG00741.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1657-393G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236751077 | ||||||
| chr1:236751089
|
C | CA | 13 | a0001c0001t0004g0071a0001c0001t0004g0074a0001c0001t0004g0078others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1657-355dupA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 236751089 | |||||
| chr1:236751089
|
CA | C | 69 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0144others(66): Show | 69 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1657-355delA | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 236751089 | |||||
| chr1:236751089
|
CAA | C | 98 | a0001c0001t0001g0018a0001c0001t0001g0141a0001c0001t0001g0184others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1657-356_1657-355d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 236751089 | |||||
| chr1:236751089
|
CAAA | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1657-357_1657-355d others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 236751089 | |||||
| chr1:236751221
|
A | AT | 13 | a0001c0001t0003g0238a0001c0001t0004g0069a0001c0001t0011g0036others(10): Show | 13 | HG01109.hp1 HG01243.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1657-243dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 236751221 | |||||
| chr1:236751266
|
G | A | 4 | a0001c0001t0004g0246a0001c0001t0009g0091a0001c0001t0015g0116others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657-204G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236751266 | ||||||
| chr1:236751276
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1657-194C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236751276 | ||||||
| chr1:236751310
|
G | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1657-160G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236751310 | ||||||
| chr1:236751438
|
ATTGT | A | 3 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0003t0020g0122 | 3 | HG01258.hp1 HG01516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1657-29_1657-26del others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 236751438 | |||||
| chr1:236751439
|
T | C | 1 | a0001c0004t0005g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1657-31T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | chr1 | 236751439 | ||||||
| chr1:236751907
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1839+255G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236751907 | ||||||
| chr1:236751908
|
T | C | 1 | a0004c0026t0005g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1839+256T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236751908 | ||||||
| chr1:236752015
|
T | C | 6 | a0001c0001t0005g0055a0001c0003t0002g0170a0001c0011t0005g0100others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1839+363T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752015 | ||||||
| chr1:236752298
|
T | C | 2 | a0001c0001t0004g0075a0001c0001t0004g0200 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1839+646T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752298 | ||||||
| chr1:236752367
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1839+715G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752367 | ||||||
| chr1:236752378
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1839+726A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752378 | ||||||
| chr1:236752508
|
T | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1839+856T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752508 | ||||||
| chr1:236752586
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1839+934C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752586 | ||||||
| chr1:236752594
|
C | A | 4 | a0001c0002t0002g0089a0001c0010t0002g0164a0001c0010t0002g0183others(1): Show | 4 | HG01106.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839+942C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752594 | ||||||
| chr1:236752596
|
G | T | 2 | a0001c0010t0002g0164a0001c0010t0002g0183 | 2 | HG01106.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1839+944G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752596 | ||||||
| chr1:236752636
|
C | T | 20 | a0001c0001t0017g0097a0001c0002t0002g0072a0001c0002t0002g0179others(17): Show | 20 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1839+984C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752636 | ||||||
| chr1:236752643
|
G | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1839+991G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752643 | ||||||
| chr1:236752743
|
AGGTTTCA others(7): Show |
A | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1839+1094_1839+110 others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr1 | 236752743 | |||||
| chr1:236752784
|
G | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1839+1132G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752784 | ||||||
| chr1:236752840
|
G | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1840-1107G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752840 | ||||||
| chr1:236752876
|
G | T | 1 | a0001c0001t0003g0279 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1840-1071G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752876 | ||||||
| chr1:236752930
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1840-1017G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752930 | ||||||
| chr1:236752968
|
T | G | 1 | a0001c0013t0023g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1840-979T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236752968 | ||||||
| chr1:236753052
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1840-895G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236753052 | ||||||
| chr1:236753105
|
G | A | 1 | a0001c0001t0018g0303 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1840-842G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236753105 | ||||||
| chr1:236753114
|
G | T | 1 | a0001c0001t0018g0303 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1840-833G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236753114 | ||||||
| chr1:236753312
|
A | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1840-635A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236753312 | ||||||
| chr1:236753736
|
T | C | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1840-211T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 15/20 | chr1 | 236753736 | ||||||
| chr1:236754141
|
G | A | 1 | a0001c0003t0002g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1974+60G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754141 | ||||||
| chr1:236754200
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1974+119C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754200 | ||||||
| chr1:236754217
|
C | T | 3 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0003t0020g0122 | 3 | HG01258.hp1 HG01516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1974+136C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754217 | ||||||
| chr1:236754303
|
G | T | 1 | a0001c0001t0017g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1974+222G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754303 | ||||||
| chr1:236754425
|
T | C | 40 | a0001c0001t0001g0184a0001c0001t0003g0238a0001c0001t0004g0037others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1974+344T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754425 | ||||||
| chr1:236754528
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1974+447T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754528 | ||||||
| chr1:236754547
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1974+466T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754547 | ||||||
| chr1:236754568
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1975-451G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754568 | ||||||
| chr1:236754579
|
T | C | 1 | a0001c0009t0003g0012 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1975-440T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754579 | ||||||
| chr1:236754680
|
AC | A | 9 | a0001c0003t0002g0170a0001c0004t0005g0056a0001c0004t0005g0060others(6): Show | 9 | HG02451.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1975-334delC | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr1 | 236754680 | |||||
| chr1:236754701
|
A | G | 10 | a0001c0001t0004g0074a0001c0001t0004g0078a0001c0001t0009g0073others(7): Show | 10 | HG01109.hp2 HG01192.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1975-318A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754701 | ||||||
| chr1:236754705
|
T | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1975-314T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754705 | ||||||
| chr1:236754911
|
C | T | 3 | a0001c0006t0002g0150a0001c0006t0008g0128a0001c0006t0008g0344 | 3 | NA18964.hp2 NA18969.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1975-108C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754911 | ||||||
| chr1:236754952
|
G | A | 1 | a0001c0001t0003g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1975-67G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754952 | ||||||
| chr1:236754996
|
G | C | 1 | a0001c0014t0002g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1975-23G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236754996 | ||||||
| chr1:236755013
|
C | T | 1 | a0001c0002t0007g0300 | 1 | NA18972.hp1 | splice_region_variant&intron_variant | LOW | c.1975-6C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 16/20 | chr1 | 236755013 | ||||||
| chr1:236755444
|
C | A | 8 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+246C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755444 | ||||||
| chr1:236755570
|
T | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2154+372T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755570 | ||||||
| chr1:236755597
|
G | A | 17 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0008others(14): Show | 17 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2154+399G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755597 | ||||||
| chr1:236755603
|
T | G | 3 | a0001c0001t0003g0210a0001c0001t0003g0234a0001c0024t0003g0014 | 3 | NA18949.hp2 NA18967.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.2154+405T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755603 | ||||||
| chr1:236755607
|
C | T | 17 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0008others(14): Show | 17 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2154+409C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755607 | ||||||
| chr1:236755624
|
T | C | 3 | a0001c0001t0003g0210a0001c0001t0003g0234a0001c0024t0003g0014 | 3 | NA18949.hp2 NA18967.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.2154+426T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755624 | ||||||
| chr1:236755628
|
G | GGTT | 3 | a0001c0001t0003g0210a0001c0001t0003g0234a0001c0024t0003g0014 | 3 | NA18949.hp2 NA18967.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.2154+430_2154+431i others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755628 | ||||||
| chr1:236755629
|
ATAATATA others(35): Show |
A | 3 | a0002c0005t0004g0297a0002c0008t0004g0025a0002c0008t0004g0168 | 3 | NA18939.hp2 NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2154+437_2154+478d others(44): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755629 | |||||
| chr1:236755631
|
A | AATAGAGT | 6 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0009others(3): Show | 6 | HG02080.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+436_2154+437i others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755631 | |||||
| chr1:236755631
|
A | AGAGTATA others(683): Show |
1 | a0001c0024t0003g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2154+433_2154+434i others(692): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755631 | ||||||
| chr1:236755631
|
A | AGAGTATA others(683): Show |
2 | a0001c0001t0003g0210a0001c0001t0003g0234 | 2 | NA18949.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2154+433_2154+434i others(692): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755631 | ||||||
| chr1:236755631
|
AATATACT others(84): Show |
A | 8 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(5): Show | 8 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+437_2154+527d others(93): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755631 | |||||
| chr1:236755649
|
C | T | 2 | a0001c0001t0017g0097a0004c0032t0017g0094 | 2 | HG01192.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2154+451C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755649 | ||||||
| chr1:236755650
|
A | G | 3 | a0001c0001t0003g0210a0001c0001t0003g0234a0001c0024t0003g0014 | 3 | NA18949.hp2 NA18967.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.2154+452A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755650 | ||||||
| chr1:236755658
|
C | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0234a0001c0024t0003g0014 | 3 | NA18949.hp2 NA18967.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.2154+460C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755658 | ||||||
| chr1:236755694
|
G | T | 9 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0009others(6): Show | 9 | HG02080.hp2 HG03195.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2154+496G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755694 | ||||||
| chr1:236755695
|
GCCCGCTG others(41): Show |
G | 2 | a0001c0010t0002g0164a0001c0010t0002g0183 | 2 | HG01106.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2154+498_2154+545d others(50): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755695 | ||||||
| chr1:236755699
|
G | A | 3 | a0002c0005t0004g0297a0002c0008t0004g0025a0002c0008t0004g0168 | 3 | NA18939.hp2 NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2154+501G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755699 | ||||||
| chr1:236755707
|
T | C | 25 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0009g0073others(22): Show | 25 | HG01109.hp2 HG01891.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.2154+509T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755707 | ||||||
| chr1:236755707
|
TGTTAGAA others(238): Show |
T | 3 | a0001c0001t0005g0055a0001c0001t0005g0080a0001c0031t0005g0053 | 3 | HG02109.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2154+524_2154+768d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755707 | |||||
| chr1:236755707
|
TGTTAGAA others(875): Show |
T | 1 | a0008c0017t0024g0099 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2154+524_2155-883d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755707 | |||||
| chr1:236755708
|
G | GTTAGAAC others(42): Show |
2 | a0001c0001t0018g0088a0001c0001t0018g0303 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2154+523_2154+524i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755708 | |||||
| chr1:236755708
|
GTTAGAAC others(728): Show |
G | 78 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0002t0002g0016others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2154+524_2155-1030 others(3): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755708 | |||||
| chr1:236755717
|
CTGGTTAT others(140): Show |
C | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2154+594_2154+740d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755717 | |||||
| chr1:236755722
|
T | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.2154+524T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755722 | ||||||
| chr1:236755743
|
T | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2154+545T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755743 | ||||||
| chr1:236755748
|
G | A | 8 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(5): Show | 8 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+550G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755748 | ||||||
| chr1:236755756
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2154+558T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755756 | ||||||
| chr1:236755756
|
TGTTAGAA others(189): Show |
T | 15 | a0001c0001t0004g0102a0001c0001t0004g0119a0001c0001t0009g0073others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.2154+594_2154+789d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755756 | |||||
| chr1:236755757
|
G | A | 6 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0009others(3): Show | 6 | HG02080.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+559G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755757 | ||||||
| chr1:236755757
|
G | GTTAGAAC others(42): Show |
1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2154+593_2154+594i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755757 | |||||
| chr1:236755757
|
G | GTTAGAAC others(140): Show |
2 | a0001c0001t0003g0105a0001c0001t0003g0272 | 2 | HG01496.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2154+593_2154+594i others(149): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755757 | |||||
| chr1:236755766
|
C | G | 8 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+568C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755766 | ||||||
| chr1:236755771
|
A | AATAGAGT others(777): Show |
1 | a0001c0001t0003g0021 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2154+593_2154+594i others(786): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755771 | |||||
| chr1:236755771
|
A | AATAGAGT others(777): Show |
1 | a0001c0001t0003g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2154+593_2154+594i others(786): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755771 | |||||
| chr1:236755771
|
A | AATAGAGT others(777): Show |
36 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(33): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.2154+593_2154+594i others(786): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755771 | |||||
| chr1:236755771
|
A | AATAGAGT others(777): Show |
2 | a0001c0001t0003g0104a0001c0001t0003g0299 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2154+593_2154+594i others(786): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755771 | |||||
| chr1:236755771
|
A | AATAGAGT others(777): Show |
1 | a0001c0001t0003g0268 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2154+593_2154+594i others(786): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755771 | |||||
| chr1:236755771
|
A | AATAGAGT others(777): Show |
1 | a0001c0003t0021g0125 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2154+593_2154+594i others(786): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755771 | |||||
| chr1:236755771
|
A | AATAGAGT others(189): Show |
1 | a0001c0028t0026g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2154+606_2154+607i others(198): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755771 | |||||
| chr1:236755771
|
A | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2154+573A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755771 | ||||||
| chr1:236755792
|
T | G | 10 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(7): Show | 10 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2154+594T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755792 | ||||||
| chr1:236755805
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2154+607T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755805 | ||||||
| chr1:236755806
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2154+608G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755806 | ||||||
| chr1:236755820
|
A | T | 2 | a0001c0010t0002g0164a0001c0010t0002g0183 | 2 | HG01106.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2154+622A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755820 | ||||||
| chr1:236755820
|
AATAGAGT others(42): Show |
A | 1 | a0001c0002t0002g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2154+666_2154+714d others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755820 | |||||
| chr1:236755841
|
T | G | 14 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0011g0067others(11): Show | 14 | HG01891.hp2 HG02080.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2154+643T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755841 | ||||||
| chr1:236755845
|
C | T | 1 | a0001c0003t0021g0125 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2154+647C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755845 | ||||||
| chr1:236755852
|
ACTGTTAG others(39): Show |
A | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2154+656_2154+701d others(48): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755852 | |||||
| chr1:236755852
|
ACTGTTAG others(333): Show |
A | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2154+656_2154+995d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755852 | |||||
| chr1:236755854
|
T | C | 31 | a0001c0001t0003g0021a0001c0001t0005g0151a0001c0001t0005g0181others(28): Show | 31 | HG01106.hp2 HG01891.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.2154+656T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755854 | ||||||
| chr1:236755855
|
G | A | 10 | a0001c0010t0002g0164a0001c0010t0002g0183a0002c0005t0004g0008others(7): Show | 10 | HG01106.hp2 HG02015.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.2154+657G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755855 | ||||||
| chr1:236755864
|
G | C | 74 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(71): Show | 74 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.2154+666G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755864 | ||||||
| chr1:236755869
|
T | A | 66 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2154+671T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755869 | ||||||
| chr1:236755890
|
T | G | 9 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0009others(6): Show | 9 | HG02080.hp2 HG03195.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2154+692T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755890 | ||||||
| chr1:236755895
|
G | A | 3 | a0001c0001t0018g0088a0001c0001t0018g0303a0001c0029t0005g0107 | 3 | HG02280.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2154+697G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755895 | ||||||
| chr1:236755901
|
ACTG | A | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2154+704_2154+706d others(5): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755901 | ||||||
| chr1:236755903
|
T | C | 19 | a0001c0001t0011g0067a0001c0001t0011g0090a0001c0001t0017g0097others(16): Show | 19 | HG01192.hp1 HG02015.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.2154+705T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755903 | ||||||
| chr1:236755904
|
G | A | 6 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0009others(3): Show | 6 | HG02080.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+706G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755904 | ||||||
| chr1:236755912
|
C | G | 45 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(42): Show | 45 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2154+714C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755912 | ||||||
| chr1:236755933
|
G | A | 8 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+735G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755933 | ||||||
| chr1:236755939
|
G | T | 45 | a0001c0001t0003g0105a0001c0001t0003g0272a0001c0001t0005g0151others(42): Show | 45 | HG01106.hp2 HG01123.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.2154+741G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755939 | ||||||
| chr1:236755944
|
G | A | 6 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0009others(3): Show | 6 | HG02080.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+746G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755944 | ||||||
| chr1:236755952
|
C | T | 82 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(79): Show | 82 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.2154+754C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755952 | ||||||
| chr1:236755953
|
G | A | 3 | a0002c0005t0004g0297a0002c0008t0004g0025a0002c0008t0004g0168 | 3 | NA18939.hp2 NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2154+755G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755953 | ||||||
| chr1:236755962
|
C | G | 11 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0118others(8): Show | 11 | HG01109.hp2 HG01981.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2154+764C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755962 | ||||||
| chr1:236755967
|
A | AATAGAGT others(42): Show |
2 | a0001c0001t0018g0088a0001c0001t0018g0303 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2154+789_2154+790i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236755967 | |||||
| chr1:236755967
|
A | T | 19 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0009g0073others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.2154+769A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755967 | ||||||
| chr1:236755988
|
G | T | 89 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(86): Show | 89 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.2154+790G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755988 | ||||||
| chr1:236755992
|
C | T | 43 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(40): Show | 43 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.2154+794C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755992 | ||||||
| chr1:236755993
|
G | A | 4 | a0001c0007t0004g0070a0002c0005t0004g0297a0002c0008t0004g0025others(1): Show | 4 | HG02615.hp2 NA18939.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154+795G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236755993 | ||||||
| chr1:236756001
|
T | C | 19 | a0001c0001t0004g0015a0001c0001t0011g0036a0001c0001t0017g0097others(16): Show | 19 | HG01106.hp2 HG01192.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.2154+803T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756001 | ||||||
| chr1:236756001
|
TGTTAGAA others(581): Show |
T | 3 | a0001c0001t0005g0055a0001c0001t0005g0080a0001c0031t0005g0053 | 3 | HG02109.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2154+839_2155-862d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756001 | |||||
| chr1:236756002
|
G | A | 12 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(9): Show | 12 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.2154+804G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756002 | ||||||
| chr1:236756011
|
C | G | 1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2154+813C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756011 | ||||||
| chr1:236756016
|
A | T | 11 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0017g0097others(8): Show | 11 | HG01192.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2154+818A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756016 | ||||||
| chr1:236756037
|
G | GGCCCGCT others(336): Show |
1 | a0001c0001t0003g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2154+851_2154+852i others(345): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756037 | |||||
| chr1:236756037
|
G | T | 96 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(93): Show | 96 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2154+839G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756037 | ||||||
| chr1:236756042
|
G | A | 12 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(9): Show | 12 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.2154+844G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756042 | ||||||
| chr1:236756050
|
C | CGTTAGAA others(434): Show |
2 | a0001c0009t0003g0013a0001c0009t0003g0038 | 2 | NA19068.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2154+1056_2154+105 others(445): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756050 | |||||
| chr1:236756050
|
C | T | 25 | a0001c0001t0003g0272a0001c0001t0005g0151a0001c0001t0005g0181others(22): Show | 25 | HG01192.hp1 HG01891.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.2154+852C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756050 | ||||||
| chr1:236756051
|
G | A | 24 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(21): Show | 24 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2154+853G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756051 | ||||||
| chr1:236756060
|
C | G | 8 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+862C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756060 | ||||||
| chr1:236756065
|
A | T | 26 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0009g0073others(23): Show | 26 | HG01106.hp2 HG01109.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2154+867A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756065 | ||||||
| chr1:236756080
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2154+882G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756080 | ||||||
| chr1:236756086
|
T | G | 9 | a0001c0029t0005g0107a0002c0005t0004g0008a0002c0005t0004g0256others(6): Show | 9 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.2154+888T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756086 | ||||||
| chr1:236756091
|
G | A | 13 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0011g0067others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2154+893G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756091 | ||||||
| chr1:236756099
|
T | C | 12 | a0001c0001t0003g0021a0001c0001t0017g0097a0001c0029t0005g0107others(9): Show | 12 | HG01192.hp1 HG02015.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.2154+901T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756099 | ||||||
| chr1:236756100
|
G | A | 8 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(5): Show | 8 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+902G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756100 | ||||||
| chr1:236756109
|
C | G | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2154+911C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756109 | ||||||
| chr1:236756114
|
A | T | 2 | a0001c0001t0011g0036a0001c0029t0005g0107 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2154+916A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756114 | ||||||
| chr1:236756129
|
G | A | 13 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0118others(10): Show | 13 | HG01109.hp2 HG01981.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2154+931G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756129 | ||||||
| chr1:236756135
|
T | G | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2154+937T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756135 | ||||||
| chr1:236756140
|
G | A | 31 | a0001c0001t0011g0067a0001c0001t0011g0090a0001c0001t0012g0019others(28): Show | 31 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.2154+942G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756140 | ||||||
| chr1:236756148
|
T | C | 6 | a0001c0001t0003g0272a0001c0001t0017g0097a0001c0002t0002g0089others(3): Show | 6 | HG01106.hp2 HG01192.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154+950T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756148 | ||||||
| chr1:236756158
|
G | C | 37 | a0001c0001t0003g0272a0001c0001t0009g0073a0001c0001t0009g0091others(34): Show | 37 | HG01106.hp2 HG01109.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.2154+960G>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756158 | ||||||
| chr1:236756163
|
T | A | 23 | a0001c0001t0011g0036a0001c0001t0011g0067a0001c0001t0011g0090others(20): Show | 23 | HG01106.hp2 HG01192.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.2154+965T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756163 | ||||||
| chr1:236756178
|
G | A | 4 | a0002c0005t0004g0009a0002c0005t0004g0035a0002c0005t0004g0305others(1): Show | 4 | HG02080.hp2 NA18983.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154+980G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756178 | ||||||
| chr1:236756184
|
T | TGCCCGCT others(91): Show |
17 | a0001c0001t0003g0023a0001c0001t0003g0104a0001c0001t0003g0111others(14): Show | 17 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.2154+1056_2154+105 others(102): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756184 | |||||
| chr1:236756195
|
ACTG | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2154+998_2154+1000 others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756195 | ||||||
| chr1:236756197
|
T | C | 17 | a0001c0001t0003g0272a0001c0001t0005g0151a0001c0001t0005g0181others(14): Show | 17 | HG01106.hp2 HG01192.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2154+999T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756197 | ||||||
| chr1:236756198
|
G | A | 3 | a0001c0001t0003g0272a0001c0001t0011g0067a0001c0001t0011g0090 | 3 | HG03195.hp1 HG03471.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2154+1000G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756198 | ||||||
| chr1:236756212
|
A | T | 19 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0118others(16): Show | 19 | HG01109.hp2 HG01192.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.2154+1014A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756212 | ||||||
| chr1:236756227
|
G | A | 7 | a0002c0005t0004g0009a0002c0005t0004g0035a0002c0005t0004g0297others(4): Show | 7 | HG02080.hp2 NA18939.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154+1029G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756227 | ||||||
| chr1:236756233
|
T | G | 8 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1035T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756233 | ||||||
| chr1:236756233
|
T | TGCCCGCT others(42): Show |
27 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0024others(24): Show | 27 | HG00673.hp1 HG00738.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.2154+1056_2154+105 others(53): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756233 | |||||
| chr1:236756238
|
G | A | 6 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0009others(3): Show | 6 | HG02080.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+1040G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756238 | ||||||
| chr1:236756246
|
T | C | 20 | a0001c0001t0003g0272a0001c0001t0004g0037a0001c0001t0004g0059others(17): Show | 20 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.2154+1048T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756246 | ||||||
| chr1:236756247
|
G | A | 7 | a0001c0001t0004g0037a0001c0001t0004g0059a0001c0001t0004g0075others(4): Show | 7 | HG02145.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154+1049G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756247 | ||||||
| chr1:236756255
|
C | G | 2 | a0001c0009t0003g0013a0001c0009t0003g0038 | 2 | NA19068.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2154+1057C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756255 | ||||||
| chr1:236756256
|
C | G | 13 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0118others(10): Show | 13 | HG01109.hp2 HG01981.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2154+1058C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756256 | ||||||
| chr1:236756261
|
A | T | 19 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0118others(16): Show | 19 | HG01106.hp2 HG01109.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.2154+1063A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756261 | ||||||
| chr1:236756276
|
G | A | 11 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.2154+1078G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756276 | ||||||
| chr1:236756282
|
T | G | 7 | a0001c0009t0003g0013a0001c0009t0003g0038a0001c0029t0005g0107others(4): Show | 7 | HG02080.hp2 HG02970.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154+1084T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756282 | ||||||
| chr1:236756282
|
TGCCCGCT others(483): Show |
T | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 90 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.2154+1112_2155-687 others(3): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756282 | |||||
| chr1:236756287
|
G | A | 35 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0118others(32): Show | 35 | HG01109.hp2 HG01243.hp2 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.2154+1089G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756287 | ||||||
| chr1:236756295
|
T | C | 11 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0017g0097others(8): Show | 11 | HG01192.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2154+1097T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756295 | ||||||
| chr1:236756295
|
T | TGTTAGAA others(630): Show |
1 | a0001c0001t0004g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2155-1143_2155-114 others(641): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756295 | |||||
| chr1:236756305
|
C | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0211others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.2154+1107C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756305 | ||||||
| chr1:236756310
|
A | T | 50 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0211others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.2154+1112A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756310 | ||||||
| chr1:236756319
|
T | C | 4 | a0002c0005t0004g0009a0002c0005t0004g0035a0002c0005t0004g0305others(1): Show | 4 | HG02080.hp2 NA18983.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154+1121T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756319 | ||||||
| chr1:236756325
|
G | A | 8 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(5): Show | 8 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1127G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756325 | ||||||
| chr1:236756331
|
T | G | 4 | a0001c0001t0003g0272a0002c0005t0004g0297a0002c0008t0004g0025others(1): Show | 4 | HG03688.hp2 NA18939.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154+1133T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756331 | ||||||
| chr1:236756335
|
C | CGCTGCCA others(42): Show |
24 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0026others(21): Show | 24 | HG00673.hp1 HG00738.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.2155-1128_2155-112 others(53): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756335 | |||||
| chr1:236756335
|
C | CGCTGCCA others(924): Show |
1 | a0001c0001t0003g0021 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2155-1128_2155-112 others(935): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756335 | |||||
| chr1:236756335
|
C | T | 17 | a0001c0001t0003g0023a0001c0001t0003g0104a0001c0001t0003g0111others(14): Show | 17 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.2154+1137C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756335 | ||||||
| chr1:236756336
|
G | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0211others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.2154+1138G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756336 | ||||||
| chr1:236756344
|
T | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0028a0001c0001t0004g0069others(12): Show | 15 | HG01106.hp2 HG02257.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2155-1142T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756344 | ||||||
| chr1:236756344
|
T | TGTTAGAA others(42): Show |
1 | a0001c0007t0004g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2155-1128_2155-112 others(53): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756344 | |||||
| chr1:236756344
|
TGTTAGAA others(140): Show |
T | 15 | a0001c0004t0002g0064a0001c0004t0005g0056a0001c0004t0005g0057others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.2155-1127_2155-981 others(3): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756344 | |||||
| chr1:236756354
|
C | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0211others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2155-1132C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756354 | ||||||
| chr1:236756359
|
T | A | 75 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(72): Show | 75 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.2155-1127T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756359 | ||||||
| chr1:236756359
|
TATAGAGT others(532): Show |
T | 7 | a0001c0003t0006g0124a0001c0003t0006g0126a0001c0003t0006g0130others(4): Show | 7 | HG00639.hp2 HG01123.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.2155-1093_2155-555 others(3): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756359 | |||||
| chr1:236756368
|
T | C | 3 | a0002c0005t0004g0297a0002c0008t0004g0025a0002c0008t0004g0168 | 3 | NA18939.hp2 NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2155-1118T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756368 | ||||||
| chr1:236756369
|
A | ATACTGCA others(42): Show |
4 | a0001c0001t0004g0071a0001c0001t0004g0074a0001c0001t0004g0078others(1): Show | 4 | HG02559.hp1 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-1092_2155-104 others(53): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756369 | |||||
| chr1:236756369
|
A | G | 2 | a0001c0001t0004g0069a0001c0007t0004g0083 | 2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-1117A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756369 | ||||||
| chr1:236756374
|
G | A | 6 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0009others(3): Show | 6 | HG02080.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155-1112G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756374 | ||||||
| chr1:236756380
|
T | G | 8 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(5): Show | 8 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2155-1106T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756380 | ||||||
| chr1:236756385
|
G | A | 10 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0008others(7): Show | 10 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.2155-1101G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756385 | ||||||
| chr1:236756393
|
C | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0211others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2155-1093C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756393 | ||||||
| chr1:236756394
|
G | A | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2155-1092G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756394 | ||||||
| chr1:236756394
|
GTTAGAAC others(42): Show |
G | 34 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0211others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.2155-1078_2155-103 others(53): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756394 | |||||
| chr1:236756394
|
GTTAGAAC others(140): Show |
G | 1 | a0001c0001t0012g0337 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2155-1078_2155-932 others(3): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756394 | |||||
| chr1:236756403
|
C | G | 3 | a0001c0002t0002g0089a0001c0010t0002g0164a0001c0010t0002g0183 | 3 | HG01106.hp2 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2155-1083C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756403 | ||||||
| chr1:236756408
|
T | A | 76 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(73): Show | 76 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.2155-1078T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756408 | ||||||
| chr1:236756417
|
T | C | 8 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(5): Show | 8 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2155-1069T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756417 | ||||||
| chr1:236756418
|
G | A | 90 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(87): Show | 90 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2155-1068G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756418 | ||||||
| chr1:236756423
|
G | A | 3 | a0002c0005t0004g0297a0002c0008t0004g0025a0002c0008t0004g0168 | 3 | NA18939.hp2 NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2155-1063G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756423 | ||||||
| chr1:236756429
|
T | G | 4 | a0001c0001t0017g0097a0001c0001t0018g0088a0001c0001t0018g0303others(1): Show | 4 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2155-1057T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756429 | ||||||
| chr1:236756433
|
C | CGCTGCCA others(875): Show |
1 | a0001c0024t0003g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2155-1045_2155-104 others(886): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756433 | |||||
| chr1:236756433
|
C | CGCTGCCA others(875): Show |
1 | a0001c0001t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2155-1045_2155-104 others(886): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756433 | |||||
| chr1:236756442
|
C | CGTTAGAA others(189): Show |
1 | a0001c0001t0003g0272 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2155-1044_2155-104 others(200): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756442 | ||||||
| chr1:236756442
|
C | T | 71 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2155-1044C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756442 | ||||||
| chr1:236756443
|
A | G | 85 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(82): Show | 85 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2155-1043A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756443 | ||||||
| chr1:236756452
|
C | G | 2 | a0001c0001t0017g0097a0004c0032t0017g0094 | 2 | HG01192.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2155-1034C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756452 | ||||||
| chr1:236756457
|
A | AATAGAGT others(1071): Show |
1 | a0001c0028t0026g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2155-883_2155-882i others(1080): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756457 | |||||
| chr1:236756457
|
A | AATAGAGT others(42): Show |
39 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(36): Show | 39 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.2155-996_2155-995i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756457 | |||||
| chr1:236756457
|
A | T | 5 | a0001c0001t0017g0097a0002c0005t0004g0297a0002c0008t0004g0025others(2): Show | 5 | HG01192.hp1 HG03516.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-1029A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756457 | ||||||
| chr1:236756472
|
G | A | 8 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(5): Show | 8 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2155-1014G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756472 | ||||||
| chr1:236756478
|
T | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0184others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.2155-1008T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756478 | ||||||
| chr1:236756482
|
C | T | 2 | a0001c0009t0003g0013a0001c0009t0003g0038 | 2 | NA19068.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2155-1004C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756482 | ||||||
| chr1:236756483
|
G | GCTGCCAC others(42): Show |
2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2155-996_2155-995i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756483 | |||||
| chr1:236756491
|
C | T | 76 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(73): Show | 76 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.2155-995C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756491 | ||||||
| chr1:236756501
|
C | G | 8 | a0001c0001t0004g0075a0001c0001t0004g0200a0001c0002t0002g0089others(5): Show | 8 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.2155-985C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756501 | ||||||
| chr1:236756506
|
A | T | 94 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0004g0075others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2155-980A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756506 | ||||||
| chr1:236756521
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2155-965G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756521 | ||||||
| chr1:236756527
|
T | G | 7 | a0002c0005t0004g0009a0002c0005t0004g0035a0002c0005t0004g0297others(4): Show | 7 | HG02080.hp2 NA18939.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.2155-959T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756527 | ||||||
| chr1:236756527
|
TGCCCGCT others(189): Show |
T | 2 | a0001c0001t0004g0075a0001c0001t0004g0200 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2155-946_2155-751d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756527 | |||||
| chr1:236756540
|
C | T | 96 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(93): Show | 96 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2155-946C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756540 | ||||||
| chr1:236756540
|
CGTTAGAA others(434): Show |
C | 19 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0211others(16): Show | 19 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.2155-931_2155-491d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756540 | |||||
| chr1:236756541
|
G | A | 82 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0002t0002g0016others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2155-945G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756541 | ||||||
| chr1:236756541
|
G | GTTAGAAC others(42): Show |
1 | a0001c0003t0002g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2155-932_2155-931i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756541 | |||||
| chr1:236756549
|
C | CGTGGTTA others(91): Show |
1 | a0001c0001t0003g0266 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2155-937_2155-936i others(100): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756549 | ||||||
| chr1:236756549
|
C | G | 39 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(36): Show | 39 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.2155-937C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756549 | ||||||
| chr1:236756550
|
C | G | 4 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0017g0097others(1): Show | 4 | HG01192.hp1 HG01258.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-936C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756550 | ||||||
| chr1:236756555
|
A | T | 6 | a0001c0001t0011g0067a0001c0001t0011g0090a0001c0001t0012g0019others(3): Show | 6 | HG01192.hp1 HG01258.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2155-931A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756555 | ||||||
| chr1:236756570
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2155-916G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756570 | ||||||
| chr1:236756571
|
C | T | 1 | a0001c0003t0005g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2155-915C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756571 | ||||||
| chr1:236756576
|
T | G | 55 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(52): Show | 55 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.2155-910T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756576 | ||||||
| chr1:236756576
|
T | TGCCCGCT others(140): Show |
1 | a0001c0001t0003g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2155-898_2155-897i others(149): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756576 | |||||
| chr1:236756581
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2155-905G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756581 | ||||||
| chr1:236756589
|
C | T | 162 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0003g0021others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.2155-897C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756589 | ||||||
| chr1:236756590
|
G | A | 3 | a0002c0005t0004g0297a0002c0008t0004g0025a0002c0008t0004g0168 | 3 | NA18939.hp2 NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2155-896G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756590 | ||||||
| chr1:236756599
|
C | G | 7 | a0001c0001t0003g0021a0001c0001t0003g0234a0001c0001t0003g0272others(4): Show | 7 | HG01106.hp2 HG02723.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.2155-887C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756599 | ||||||
| chr1:236756604
|
A | T | 10 | a0001c0001t0003g0021a0001c0001t0003g0234a0001c0001t0003g0272others(7): Show | 10 | HG01106.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2155-882A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756604 | ||||||
| chr1:236756604
|
AATAGAGT others(42): Show |
A | 3 | a0002c0005t0004g0297a0002c0008t0004g0025a0002c0008t0004g0168 | 3 | NA18939.hp2 NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2155-833_2155-785d others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756604 | |||||
| chr1:236756625
|
T | G | 11 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0008others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.2155-861T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756625 | ||||||
| chr1:236756625
|
TGCCCGCT others(91): Show |
T | 4 | a0002c0005t0004g0009a0002c0005t0004g0035a0002c0005t0004g0305others(1): Show | 4 | HG02080.hp2 NA18983.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-848_2155-751d others(100): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756625 | |||||
| chr1:236756630
|
G | A | 80 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0011g0067others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2155-856G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756630 | ||||||
| chr1:236756638
|
C | T | 153 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0003g0021others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2155-848C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756638 | ||||||
| chr1:236756639
|
G | A | 8 | a0002c0005t0004g0008a0002c0005t0004g0256a0002c0005t0004g0257others(5): Show | 8 | HG02015.hp1 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2155-847G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756639 | ||||||
| chr1:236756648
|
C | G | 96 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0012g0337others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.2155-838C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756648 | ||||||
| chr1:236756653
|
T | A | 51 | a0001c0001t0003g0021a0001c0001t0003g0234a0001c0001t0003g0272others(48): Show | 51 | HG01106.hp2 HG01109.hp2 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.2155-833T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756653 | ||||||
| chr1:236756674
|
T | G | 19 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(16): Show | 19 | HG01891.hp2 HG02015.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.2155-812T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756674 | ||||||
| chr1:236756674
|
TGCCCGCT others(91): Show |
T | 1 | a0001c0001t0012g0109 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2155-799_2155-702d others(100): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756674 | |||||
| chr1:236756687
|
C | T | 160 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0003g0021others(157): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.2155-799C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756687 | ||||||
| chr1:236756687
|
CGTTAGAA others(483): Show |
C | 11 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0118others(8): Show | 11 | HG01109.hp2 HG01981.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2155-763_2155-274d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756687 | |||||
| chr1:236756688
|
G | A | 14 | a0001c0001t0004g0037a0001c0001t0004g0059a0001c0001t0004g0117others(11): Show | 14 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2155-798G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756688 | ||||||
| chr1:236756696
|
C | CCTGGTAA others(42): Show |
2 | a0001c0009t0003g0013a0001c0009t0003g0038 | 2 | NA19068.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2155-764_2155-763i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756696 | |||||
| chr1:236756696
|
C | G | 4 | a0001c0001t0003g0021a0001c0001t0003g0234a0001c0001t0003g0272others(1): Show | 4 | HG03688.hp2 NA18949.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2155-790C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756696 | ||||||
| chr1:236756697
|
C | G | 2 | a0001c0001t0017g0097a0004c0032t0017g0094 | 2 | HG01192.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2155-789C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756697 | ||||||
| chr1:236756702
|
A | T | 14 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0011g0036others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2155-784A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756702 | ||||||
| chr1:236756723
|
G | T | 92 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(89): Show | 92 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2155-763G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756723 | ||||||
| chr1:236756728
|
G | A | 15 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(12): Show | 15 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2155-758G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756728 | ||||||
| chr1:236756728
|
G | GCTGCCAC others(140): Show |
7 | a0001c0001t0005g0181a0001c0003t0005g0047a0001c0003t0005g0048others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2155-721_2155-720i others(149): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756728 | |||||
| chr1:236756736
|
T | C | 7 | a0001c0001t0004g0119a0001c0001t0011g0036a0001c0001t0012g0019others(4): Show | 7 | HG01192.hp1 HG01516.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2155-750T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756736 | ||||||
| chr1:236756737
|
G | A | 2 | a0001c0001t0012g0019a0008c0017t0024g0099 | 2 | HG01516.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2155-749G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756737 | ||||||
| chr1:236756746
|
C | A | 75 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0002t0002g0016others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2155-740C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756746 | ||||||
| chr1:236756746
|
C | G | 8 | a0001c0001t0017g0097a0001c0002t0002g0072a0001c0002t0002g0089others(5): Show | 8 | HG01106.hp2 HG01109.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2155-740C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756746 | ||||||
| chr1:236756751
|
A | T | 83 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0017g0097others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2155-735A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756751 | ||||||
| chr1:236756766
|
G | A | 1 | a0001c0001t0005g0151 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2155-720G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756766 | ||||||
| chr1:236756772
|
G | T | 181 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0003g0021others(178): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.2155-714G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756772 | ||||||
| chr1:236756776
|
C | T | 38 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(35): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2155-710C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756776 | ||||||
| chr1:236756776
|
C | TGCTGCCA others(1022): Show |
1 | a0001c0001t0003g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2155-711_2155-710i others(1031): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756776 | ||||||
| chr1:236756777
|
G | A | 15 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(12): Show | 15 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2155-709G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756777 | ||||||
| chr1:236756785
|
T | C | 10 | a0001c0001t0004g0102a0001c0001t0004g0119a0001c0001t0004g0178others(7): Show | 10 | HG01106.hp2 HG01243.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2155-701T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756785 | ||||||
| chr1:236756786
|
G | A | 2 | a0001c0010t0002g0164a0001c0010t0002g0183 | 2 | HG01106.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2155-700G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756786 | ||||||
| chr1:236756795
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(118): Show | 121 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.2155-691C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756795 | ||||||
| chr1:236756800
|
T | A | 148 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0003g0022others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.2155-686T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756800 | ||||||
| chr1:236756800
|
T | AATAGAGT others(826): Show |
1 | a0001c0001t0003g0210 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2155-687_2155-686i others(835): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756800 | ||||||
| chr1:236756813
|
C | A | 1 | a0001c0003t0002g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2155-673C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756813 | ||||||
| chr1:236756815
|
G | A | 15 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(12): Show | 15 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2155-671G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756815 | ||||||
| chr1:236756821
|
T | G | 6 | a0001c0001t0004g0102a0001c0001t0004g0119a0001c0001t0011g0036others(3): Show | 6 | HG02622.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2155-665T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756821 | ||||||
| chr1:236756825
|
C | CGCTGCCA others(434): Show |
1 | a0001c0001t0003g0324 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2155-653_2155-652i others(443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756825 | |||||
| chr1:236756825
|
C | CGCTGCCA others(91): Show |
2 | a0001c0009t0003g0013a0001c0009t0003g0038 | 2 | NA19068.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2155-653_2155-652i others(100): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756825 | |||||
| chr1:236756825
|
C | CGCTGCCA others(42): Show |
1 | a0001c0001t0003g0272 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2155-653_2155-652i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756825 | |||||
| chr1:236756826
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 90 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.2155-660G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756826 | ||||||
| chr1:236756826
|
G | GCTGCCAC others(42): Show |
1 | a0001c0001t0005g0151 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2155-653_2155-652i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756826 | |||||
| chr1:236756834
|
C | CGTTAGAA others(336): Show |
1 | a0001c0003t0002g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2155-604_2155-603i others(345): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756834 | |||||
| chr1:236756834
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(257): Show | 260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2155-652C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756834 | ||||||
| chr1:236756835
|
G | A | 4 | a0001c0001t0011g0067a0001c0001t0011g0090a0001c0001t0012g0109others(1): Show | 4 | HG01123.hp1 HG01258.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2155-651G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756835 | ||||||
| chr1:236756844
|
C | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2155-642C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756844 | ||||||
| chr1:236756849
|
T | A | 84 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(81): Show | 84 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.2155-637T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756849 | ||||||
| chr1:236756849
|
T | AATAGAGT others(777): Show |
1 | a0001c0009t0003g0012 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2155-638_2155-637i others(786): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756849 | ||||||
| chr1:236756864
|
GCAGAGTG others(287): Show |
G | 3 | a0001c0003t0020g0122a0001c0015t0016g0113a0001c0015t0016g0115 | 3 | HG01168.hp2 HG01169.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2155-603_2155-310d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756864 | |||||
| chr1:236756870
|
T | G | 11 | a0001c0001t0005g0181a0001c0001t0012g0109a0001c0001t0012g0337others(8): Show | 11 | HG01123.hp1 HG01258.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2155-616T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756870 | ||||||
| chr1:236756870
|
T | TGCCCGCT others(91): Show |
1 | a0001c0001t0005g0151 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2155-604_2155-603i others(100): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756870 | |||||
| chr1:236756883
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(240): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.2155-603C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756883 | ||||||
| chr1:236756884
|
G | A | 8 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2155-602G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756884 | ||||||
| chr1:236756884
|
G | GTTAGAAC others(483): Show |
1 | a0001c0001t0004g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2155-540_2155-539i others(492): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756884 | |||||
| chr1:236756898
|
A | AATAGAGT others(42): Show |
1 | a0001c0029t0005g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2155-568_2155-567i others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756898 | |||||
| chr1:236756898
|
A | AATAGAGT others(728): Show |
1 | a0001c0001t0003g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2155-545_2155-544i others(737): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756898 | |||||
| chr1:236756898
|
A | T | 17 | a0001c0001t0018g0088a0001c0001t0018g0303a0002c0005t0004g0008others(14): Show | 17 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2155-588A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756898 | ||||||
| chr1:236756907
|
T | C | 1 | a0001c0013t0023g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2155-579T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756907 | ||||||
| chr1:236756913
|
GCAGAGTG others(238): Show |
G | 1 | a0001c0001t0012g0019 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2155-518_2155-274d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756913 | |||||
| chr1:236756919
|
T | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(108): Show | 111 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.2155-567T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756919 | ||||||
| chr1:236756923
|
C | CGCTGCCA others(336): Show |
1 | a0001c0001t0003g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2155-545_2155-544i others(345): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756923 | |||||
| chr1:236756923
|
C | CGCTGCCA others(875): Show |
1 | a0001c0001t0003g0339 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2155-545_2155-544i others(884): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756923 | |||||
| chr1:236756923
|
C | CGCTGCCA others(826): Show |
34 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(31): Show | 34 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2155-545_2155-544i others(835): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756923 | |||||
| chr1:236756923
|
C | T | 2 | a0001c0001t0003g0021a0001c0024t0003g0014 | 2 | NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2155-563C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756923 | ||||||
| chr1:236756924
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2155-562G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756924 | ||||||
| chr1:236756932
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(99): Show | 102 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.2155-554T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756932 | ||||||
| chr1:236756942
|
C | G | 4 | a0001c0001t0004g0075a0001c0001t0004g0200a0001c0001t0012g0109others(1): Show | 4 | HG01123.hp1 HG01258.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.2155-544C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756942 | ||||||
| chr1:236756947
|
A | T | 6 | a0001c0001t0004g0075a0001c0001t0004g0200a0001c0001t0012g0109others(3): Show | 6 | HG01123.hp1 HG01192.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155-539A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756947 | ||||||
| chr1:236756962
|
G | A | 4 | a0001c0001t0011g0067a0001c0001t0011g0090a0001c0001t0018g0088others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2155-524G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756962 | ||||||
| chr1:236756968
|
G | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(261): Show | 264 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2155-518G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756968 | ||||||
| chr1:236756972
|
C | T | 1 | a0001c0009t0003g0012 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2155-514C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756972 | ||||||
| chr1:236756981
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(122): Show | 125 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(122): Show |
intron_variant | MODIFIER | c.2155-505T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756981 | ||||||
| chr1:236756981
|
TGTTAGAA others(140): Show |
T | 4 | a0001c0001t0004g0075a0001c0001t0004g0200a0001c0001t0012g0109others(1): Show | 4 | HG01123.hp1 HG01258.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.2155-416_2155-270d others(2): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236756981 | |||||
| chr1:236756982
|
G | A | 15 | a0001c0004t0002g0064a0001c0004t0005g0056a0001c0004t0005g0057others(12): Show | 15 | HG01243.hp2 HG02451.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.2155-504G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756982 | ||||||
| chr1:236756990
|
C | G | 1 | a0001c0001t0003g0324 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2155-496C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756990 | ||||||
| chr1:236756991
|
C | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.2155-495C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756991 | ||||||
| chr1:236756996
|
T | A | 70 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(67): Show | 70 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2155-490T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236756996 | ||||||
| chr1:236757011
|
A | ACAGAGTG others(434): Show |
5 | a0001c0001t0004g0037a0001c0001t0004g0059a0001c0001t0004g0117others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2155-442_2155-441i others(443): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236757011 | |||||
| chr1:236757011
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.2155-475A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757011 | ||||||
| chr1:236757017
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2155-469T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757017 | ||||||
| chr1:236757021
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2155-465C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757021 | ||||||
| chr1:236757022
|
G | A | 17 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0008others(14): Show | 17 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2155-464G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757022 | ||||||
| chr1:236757030
|
T | C | 9 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0003t0005g0047others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2155-456T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757030 | ||||||
| chr1:236757030
|
T | TGTTAGAA others(924): Show |
2 | a0001c0001t0018g0088a0001c0001t0018g0303 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2155-447_2155-446i others(933): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236757030 | |||||
| chr1:236757066
|
T | G | 13 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0017g0097others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2155-420T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757066 | ||||||
| chr1:236757070
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2155-416T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757070 | ||||||
| chr1:236757079
|
T | C | 2 | a0001c0001t0004g0003a0001c0001t0004g0028 | 2 | NA18939.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2155-407T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757079 | ||||||
| chr1:236757088
|
C | G | 46 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(43): Show | 46 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.2155-398C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757088 | ||||||
| chr1:236757089
|
C | G | 93 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0002t0002g0016others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2155-397C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757089 | ||||||
| chr1:236757094
|
A | T | 93 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0002t0002g0016others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2155-392A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757094 | ||||||
| chr1:236757109
|
GCAGAGGG others(42): Show |
G | 2 | a0001c0001t0017g0097a0004c0032t0017g0094 | 2 | HG01192.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2155-371_2155-323d others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236757109 | |||||
| chr1:236757115
|
G | T | 148 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0003g0021others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.2155-371G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757115 | ||||||
| chr1:236757115
|
GGCCCGCT others(42): Show |
G | 15 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(12): Show | 15 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2155-358_2155-310d others(51): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236757115 | |||||
| chr1:236757119
|
C | T | 3 | a0001c0001t0001g0301a0001c0001t0001g0333a0001c0001t0004g0015 | 3 | HG04184.hp1 NA18952.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2155-367C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757119 | ||||||
| chr1:236757128
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2155-358C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757128 | ||||||
| chr1:236757138
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2155-348C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757138 | ||||||
| chr1:236757143
|
T | A | 153 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0003g0021others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2155-343T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757143 | ||||||
| chr1:236757158
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2155-328A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757158 | ||||||
| chr1:236757164
|
T | G | 104 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0004g0075others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2155-322T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757164 | ||||||
| chr1:236757168
|
C | CGCTGCCA others(385): Show |
2 | a0001c0009t0003g0013a0001c0009t0003g0038 | 2 | NA19068.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2155-295_2155-294i others(394): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236757168 | |||||
| chr1:236757168
|
C | CGCTGCCA others(385): Show |
1 | a0001c0001t0003g0272 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2155-295_2155-294i others(394): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr1 | 236757168 | |||||
| chr1:236757168
|
C | T | 52 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(49): Show | 52 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.2155-318C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757168 | ||||||
| chr1:236757177
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2155-309T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757177 | ||||||
| chr1:236757192
|
A | T | 1 | a0001c0001t0003g0324 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2155-294A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757192 | ||||||
| chr1:236757234
|
C | A | 1 | a0001c0002t0002g0179 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2155-252C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757234 | ||||||
| chr1:236757241
|
T | A | 11 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0118others(8): Show | 11 | HG01109.hp2 HG01981.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2155-245T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 17/20 | chr1 | 236757241 | ||||||
| chr1:236757660
|
A | G | 2 | a0001c0001t0017g0097a0004c0032t0017g0094 | 2 | HG01192.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2301+28A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236757660 | ||||||
| chr1:236757698
|
G | T | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2301+66G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236757698 | ||||||
| chr1:236757733
|
A | T | 1 | a0002c0008t0004g0027 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2301+101A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236757733 | ||||||
| chr1:236757880
|
A | G | 47 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(44): Show | 47 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.2301+248A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236757880 | ||||||
| chr1:236757993
|
C | A | 2 | a0001c0001t0003g0023a0001c0001t0003g0029 | 2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2301+361C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236757993 | ||||||
| chr1:236758007
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2301+375A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758007 | ||||||
| chr1:236758040
|
A | G | 2 | a0001c0003t0002g0170a0001c0028t0026g0106 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2301+408A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758040 | ||||||
| chr1:236758100
|
A | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2301+468A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758100 | ||||||
| chr1:236758118
|
G | T | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2301+486G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758118 | ||||||
| chr1:236758184
|
C | T | 2 | a0001c0003t0002g0170a0001c0028t0026g0106 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2301+552C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758184 | ||||||
| chr1:236758232
|
A | T | 125 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0004g0075others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2301+600A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758232 | ||||||
| chr1:236758266
|
T | C | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2301+634T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758266 | ||||||
| chr1:236758289
|
C | CTTTTTTT others(16): Show |
2 | a0001c0004t0005g0197a0001c0015t0016g0115 | 2 | HG01169.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2301+669_2301+670i others(25): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758289 | |||||
| chr1:236758289
|
C | CTTTTTTT others(17): Show |
12 | a0001c0004t0005g0057a0001c0004t0005g0060a0001c0004t0005g0061others(9): Show | 12 | HG01168.hp2 HG02451.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2301+669_2301+670i others(26): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758289 | |||||
| chr1:236758289
|
C | CTTTTTTT others(18): Show |
3 | a0001c0004t0002g0064a0001c0004t0005g0056a0001c0004t0005g0081 | 3 | HG01243.hp2 HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2301+669_2301+670i others(27): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758289 | |||||
| chr1:236758289
|
C | CTTTTTTT others(19): Show |
1 | a0001c0003t0020g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2301+669_2301+670i others(28): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758289 | |||||
| chr1:236758289
|
CT | C | 133 | a0001c0001t0001g0184a0001c0001t0001g0286a0001c0001t0002g0156others(130): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2301+669delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758289 | |||||
| chr1:236758302
|
A | T | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2301+670A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758302 | ||||||
| chr1:236758303
|
A | T | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2301+671A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758303 | ||||||
| chr1:236758325
|
C | CG | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2301+693_2301+694i others(3): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758325 | ||||||
| chr1:236758326
|
A | C | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2301+694A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758326 | ||||||
| chr1:236758346
|
C | T | 1 | a0001c0004t0002g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2301+714C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758346 | ||||||
| chr1:236758347
|
A | G | 22 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(19): Show | 22 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.2301+715A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758347 | ||||||
| chr1:236758348
|
T | G | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2301+716T>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758348 | ||||||
| chr1:236758371
|
C | T | 19 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0009g0073others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.2301+739C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758371 | ||||||
| chr1:236758408
|
C | G | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2301+776C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758408 | ||||||
| chr1:236758442
|
T | C | 2 | a0001c0003t0002g0170a0001c0028t0026g0106 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2301+810T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758442 | ||||||
| chr1:236758448
|
G | A | 7 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | NA18941.hp1 NA18942.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.2301+816G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758448 | ||||||
| chr1:236758452
|
A | AT | 19 | a0001c0001t0001g0242a0001c0001t0003g0234a0001c0001t0017g0097others(16): Show | 19 | HG01192.hp1 HG01978.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.2301+837dupT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758452 | |||||
| chr1:236758452
|
AT | A | 29 | a0001c0001t0004g0102a0001c0001t0004g0119a0001c0001t0005g0055others(26): Show | 29 | HG01109.hp2 HG01891.hp2 HG01981.hp2 others(26): Show |
intron_variant | MODIFIER | c.2301+837delT | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758452 | |||||
| chr1:236758480
|
G | A | 2 | a0001c0002t0002g0017a0001c0002t0002g0302 | 2 | HG00140.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.2301+848G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758480 | ||||||
| chr1:236758485
|
T | C | 2 | a0001c0003t0002g0170a0001c0028t0026g0106 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2301+853T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758485 | ||||||
| chr1:236758487
|
C | T | 78 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0002t0002g0016others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2301+855C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758487 | ||||||
| chr1:236758541
|
G | A | 2 | a0001c0003t0002g0170a0001c0028t0026g0106 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2301+909G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758541 | ||||||
| chr1:236758596
|
T | TTTTTG | 110 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0005g0055others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.2301+992_2301+996d others(7): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758596 | |||||
| chr1:236758596
|
T | TTTTTGTT others(3): Show |
20 | a0001c0001t0004g0075a0001c0001t0004g0200a0001c0001t0005g0151others(17): Show | 20 | HG01891.hp2 HG01981.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2301+987_2301+996d others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758596 | |||||
| chr1:236758596
|
T | TTTTTGTT others(8): Show |
5 | a0001c0001t0009g0073a0001c0001t0009g0091a0001c0001t0009g0152others(2): Show | 5 | HG01109.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2301+982_2301+996d others(17): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758596 | |||||
| chr1:236758596
|
TTTTTG | T | 5 | a0001c0001t0001g0158a0001c0001t0003g0153a0001c0001t0003g0155others(2): Show | 5 | HG00438.hp1 NA18969.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.2301+992_2301+996d others(7): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758596 | |||||
| chr1:236758624
|
T | TTGTTC | 17 | a0001c0001t0011g0067a0001c0001t0011g0090a0002c0005t0004g0008others(14): Show | 17 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2301+997_2301+1001 others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | 236758624 | |||||
| chr1:236758722
|
C | T | 1 | a0001c0004t0005g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2302-1002C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758722 | ||||||
| chr1:236758780
|
T | C | 1 | a0001c0001t0004g0204 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2302-944T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758780 | ||||||
| chr1:236758868
|
G | T | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2302-856G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758868 | ||||||
| chr1:236758901
|
G | A | 1 | a0001c0002t0002g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2302-823G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758901 | ||||||
| chr1:236758912
|
C | T | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2302-812C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758912 | ||||||
| chr1:236758954
|
G | A | 84 | a0001c0001t0001g0184a0001c0001t0002g0156a0001c0001t0017g0097others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2302-770G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758954 | ||||||
| chr1:236758983
|
T | C | 2 | a0001c0003t0002g0170a0001c0028t0026g0106 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2302-741T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758983 | ||||||
| chr1:236758999
|
A | G | 22 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0009g0073others(19): Show | 22 | HG01109.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.2302-725A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236758999 | ||||||
| chr1:236759023
|
G | T | 3 | a0001c0001t0004g0075a0001c0001t0004g0200a0001c0004t0002g0240 | 3 | HG02145.hp1 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2302-701G>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759023 | ||||||
| chr1:236759050
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2302-674C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759050 | ||||||
| chr1:236759185
|
G | A | 1 | a0001c0006t0002g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2302-539G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759185 | ||||||
| chr1:236759581
|
T | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-143T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759581 | ||||||
| chr1:236759582
|
C | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-142C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759582 | ||||||
| chr1:236759583
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-141C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759583 | ||||||
| chr1:236759584
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-140T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759584 | ||||||
| chr1:236759585
|
T | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-139T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759585 | ||||||
| chr1:236759586
|
C | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-138C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759586 | ||||||
| chr1:236759588
|
C | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-136C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759588 | ||||||
| chr1:236759590
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-134C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759590 | ||||||
| chr1:236759591
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0307 | 2 | HG00609.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2302-133A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759591 | ||||||
| chr1:236759659
|
T | A | 1 | a0001c0003t0005g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2302-65T>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | 236759659 | ||||||
| chr1:236759897
|
C | T | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2367+108C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236759897 | ||||||
| chr1:236759898
|
G | A | 2 | a0001c0002t0002g0072a0001c0002t0002g0179 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2367+109G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236759898 | ||||||
| chr1:236759999
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2367+210A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236759999 | ||||||
| chr1:236760090
|
C | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2367+301C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760090 | ||||||
| chr1:236760177
|
C | T | 1 | a0001c0007t0004g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2367+388C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760177 | ||||||
| chr1:236760205
|
C | T | 1 | a0002c0019t0004g0002 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2367+416C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760205 | ||||||
| chr1:236760377
|
C | T | 21 | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2367+588C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760377 | ||||||
| chr1:236760434
|
A | G | 5 | a0001c0001t0005g0055a0001c0001t0005g0080a0001c0031t0005g0053others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2368-581A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760434 | ||||||
| chr1:236760587
|
T | C | 15 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(12): Show | 15 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2368-428T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760587 | ||||||
| chr1:236760705
|
C | T | 2 | a0001c0002t0002g0072a0001c0002t0002g0179 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2368-310C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760705 | ||||||
| chr1:236760738
|
G | A | 1 | a0001c0002t0002g0313 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2368-277G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760738 | ||||||
| chr1:236760743
|
C | T | 3 | a0001c0001t0010g0044a0001c0001t0010g0045a0001c0001t0010g0046 | 3 | HG03490.hp1 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2368-272C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760743 | ||||||
| chr1:236760846
|
C | A | 2 | a0001c0001t0018g0088a0001c0001t0018g0303 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2368-169C>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760846 | ||||||
| chr1:236760939
|
C | G | 1 | a0001c0004t0002g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2368-76C>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760939 | ||||||
| chr1:236760980
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2368-35G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760980 | ||||||
| chr1:236760990
|
A | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0090 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2368-25A>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760990 | ||||||
| chr1:236760998
|
T | C | 15 | a0002c0005t0004g0008a0002c0005t0004g0009a0002c0005t0004g0035others(12): Show | 15 | HG02015.hp1 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2368-17T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236760998 | ||||||
| chr1:236761006
|
T | C | 1 | a0001c0001t0003g0202 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2368-9T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 19/20 | chr1 | 236761006 | ||||||
| chr1:236761206
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2526+33A>G | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761206 | ||||||
| chr1:236761272
|
G | A | 2 | a0001c0001t0003g0202a0001c0001t0003g0284 | 2 | NA18955.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2526+99G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761272 | ||||||
| chr1:236761432
|
C | CAT | 4 | a0001c0001t0004g0102a0001c0001t0004g0119a0001c0003t0022g0093others(1): Show | 4 | HG01243.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2526+259_2526+260i others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761432 | ||||||
| chr1:236761432
|
C | CGT | 26 | a0001c0001t0003g0147a0001c0001t0012g0019a0001c0001t0012g0109others(23): Show | 26 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.2526+284_2526+285d others(4): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr1 | 236761432 | |||||
| chr1:236761432
|
C | CGTGT | 96 | a0001c0001t0002g0156a0001c0001t0004g0075a0001c0001t0004g0200others(93): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2526+282_2526+285d others(6): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr1 | 236761432 | |||||
| chr1:236761432
|
C | CGTGTGT | 12 | a0001c0001t0001g0184a0001c0001t0011g0036a0001c0002t0002g0072others(9): Show | 12 | HG00099.hp2 HG01106.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2526+280_2526+285d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr1 | 236761432 | |||||
| chr1:236761432
|
C | CGTGTGTG others(1): Show |
20 | a0001c0001t0005g0151a0001c0001t0005g0181a0001c0001t0009g0073others(17): Show | 20 | HG01109.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.2526+278_2526+285d others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr1 | 236761432 | |||||
| chr1:236761432
|
CGTGTGT | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2526+280_2526+285d others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr1 | 236761432 | |||||
| chr1:236761434
|
T | C | 1 | a0001c0001t0003g0024 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2526+261T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761434 | ||||||
| chr1:236761440
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2526+267T>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761440 | ||||||
| chr1:236761464
|
C | T | 1 | a0001c0001t0009g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2526+291C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761464 | ||||||
| chr1:236761466
|
C | T | 1 | a0001c0003t0002g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2526+293C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761466 | ||||||
| chr1:236761776
|
C | T | 1 | a0001c0001t0011g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2526+603C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761776 | ||||||
| chr1:236761845
|
G | A | 2 | a0001c0003t0001g0129a0001c0003t0001g0133 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.2527-616G>A | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236761845 | ||||||
| chr1:236762166
|
A | C | 1 | a0001c0001t0003g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2527-295A>C | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236762166 | ||||||
| chr1:236762191
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2527-270C>T | ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 20/20 | chr1 | 236762191 |