Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1352 |
|---|---|
| ensemblid | ENSG00000006695.12 |
| hgncid | 2260 |
| symbol | COX10 |
| name | cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 |
| refseq_nuc | NM_001303.4 |
| refseq_prot | NP_001294.2 |
| ensembl_nuc | ENST00000261643.8 |
| ensembl_prot | ENSP00000261643.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 14069504 |
| end | 14208677 |
| strand | + |
| ver | v1.2 |
| region | chr17:14069504-14208677 |
| region5000 | chr17:14064504-14213677 |
| regionname0 | COX10_chr17_14069504_14208677 |
| regionname5000 | COX10_chr17_14064504_14213677 |
| 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 | 1/0 | 443 | 144 | 39 | 30 | 53 | 4 | 17 | 34 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002 | 0/0 | 443 | 118 | 30 | 24 | 49 | 7 | 8 | 35 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003 | 0/1 | 443 | 40 | 1 | 10 | 23 | 1 | 4 | 20 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004 | 0/0 | 443 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0005 | 0/0 | 443 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0006 | 0/0 | 443 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0007 | 0/0 | 443 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0008 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0009 | 0/0 | 443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0010 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0011 | 0/0 | 443 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0012 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| 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 | 0/0 | 1332 | 49 | 9 | 8 | 25 | 2 | 5 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0002 | 0/0 | 1332 | 40 | 13 | 7 | 14 | 2 | 4 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0003 | 0/0 | 1332 | 38 | 9 | 9 | 16 | 1 | 3 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0004 | 1/0 | 1332 | 32 | 11 | 7 | 9 | 1 | 3 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0005 | 0/0 | 1332 | 30 | 2 | 6 | 19 | 1 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0006 | 0/0 | 1332 | 25 | 2 | 10 | 8 | 3 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0007 | 0/0 | 1332 | 20 | 6 | 5 | 3 | 0 | 6 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0008 | 0/0 | 1332 | 18 | 8 | 1 | 8 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0009 | 0/0 | 1332 | 13 | 1 | 9 | 3 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0010 | 0/0 | 1332 | 12 | 0 | 0 | 12 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0011 | 0/0 | 1332 | 6 | 0 | 1 | 2 | 1 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0012 | 0/0 | 1332 | 4 | 3 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0013 | 0/0 | 1332 | 4 | 0 | 0 | 4 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0014 | 0/0 | 1332 | 4 | 0 | 0 | 4 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0015 | 0/0 | 1332 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0016 | 0/0 | 1332 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0017 | 0/0 | 1332 | 3 | 0 | 0 | 2 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0018 | 0/0 | 1332 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0019 | 0/0 | 1332 | 3 | 2 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0020 | 0/0 | 1332 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0021 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0022 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0023 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0024 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0025 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0026 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0027 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0028 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0029 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| c0030 | 0/1 | 1332 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| 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 | 1/0 | 1567 | 83 | 47 | 8 | 22 | 2 | 3 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0002 | 0/0 | 1567 | 62 | 6 | 13 | 27 | 5 | 11 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0003 | 0/1 | 1563 | 61 | 5 | 7 | 38 | 1 | 9 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0004 | 0/0 | 1567 | 52 | 2 | 15 | 25 | 4 | 6 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0005 | 0/0 | 1566 | 12 | 7 | 2 | 3 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0006 | 0/0 | 1567 | 12 | 0 | 0 | 12 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0007 | 0/0 | 1567 | 10 | 1 | 9 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0008 | 0/0 | 1563 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0009 | 0/0 | 1566 | 3 | 0 | 2 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0010 | 0/0 | 1567 | 3 | 2 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0011 | 0/0 | 1567 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0012 | 0/0 | 1567 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0013 | 0/0 | 1564 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0014 | 0/0 | 1567 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0015 | 0/0 | 1567 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0016 | 0/0 | 1567 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0017 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0018 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0019 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0020 | 0/0 | 1567 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0021 | 0/0 | 1567 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0022 | 0/0 | 1567 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0023 | 0/0 | 1567 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0024 | 0/0 | 1567 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| t0025 | 0/0 | 1567 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| 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 | 0/0 | 1332 | 49 | 9 | 8 | 25 | 2 | 5 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0003 | 0/0 | 1332 | 38 | 9 | 9 | 16 | 1 | 3 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0004 | 1/0 | 1332 | 32 | 11 | 7 | 9 | 1 | 3 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0007 | 0/0 | 1332 | 20 | 6 | 5 | 3 | 0 | 6 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0012 | 0/0 | 1332 | 4 | 3 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0023 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0002 | 0/0 | 1332 | 40 | 13 | 7 | 14 | 2 | 4 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0005 | 0/0 | 1332 | 30 | 2 | 6 | 19 | 1 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0006 | 0/0 | 1332 | 25 | 2 | 10 | 8 | 3 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0008 | 0/0 | 1332 | 18 | 8 | 1 | 8 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0015 | 0/0 | 1332 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0020 | 0/0 | 1332 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0009 | 0/0 | 1332 | 13 | 1 | 9 | 3 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0010 | 0/0 | 1332 | 12 | 0 | 0 | 12 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0011 | 0/0 | 1332 | 6 | 0 | 1 | 2 | 1 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0014 | 0/0 | 1332 | 4 | 0 | 0 | 4 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0017 | 0/0 | 1332 | 3 | 0 | 0 | 2 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0029 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0030 | 0/1 | 1332 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004c0018 | 0/0 | 1332 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004c0019 | 0/0 | 1332 | 3 | 2 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004c0025 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0005c0013 | 0/0 | 1332 | 4 | 0 | 0 | 4 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0006c0016 | 0/0 | 1332 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0007c0027 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0008c0026 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0009c0028 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0010c0021 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0011c0022 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0012c0024 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2898 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0001t0003 | 0/0 | 2894 | 33 | 0 | 5 | 23 | 1 | 4 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0001t0004 | 0/0 | 2898 | 5 | 1 | 1 | 1 | 1 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0001t0005 | 0/0 | 2897 | 5 | 4 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0001t0011 | 0/0 | 2898 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0001t0019 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0003t0001 | 0/0 | 2898 | 7 | 3 | 0 | 3 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0003t0002 | 0/0 | 2898 | 25 | 6 | 6 | 10 | 1 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0003t0005 | 0/0 | 2897 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0003t0006 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0003t0015 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0003t0020 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0004t0001 | 1/0 | 2898 | 10 | 9 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0004t0002 | 0/0 | 2898 | 17 | 0 | 4 | 9 | 1 | 3 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0004t0003 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0004t0014 | 0/0 | 2898 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0004t0025 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0007t0001 | 0/0 | 2898 | 3 | 1 | 0 | 0 | 0 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0007t0003 | 0/0 | 2894 | 4 | 0 | 0 | 2 | 0 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0007t0004 | 0/0 | 2898 | 6 | 1 | 2 | 1 | 0 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0007t0005 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0007t0008 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0007t0010 | 0/0 | 2898 | 3 | 2 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0007t0013 | 0/0 | 2895 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0012t0001 | 0/0 | 2898 | 4 | 3 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0001c0023t0001 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0002t0001 | 0/0 | 2898 | 22 | 13 | 2 | 7 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0002t0002 | 0/0 | 2898 | 15 | 0 | 3 | 6 | 2 | 4 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0002t0003 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0002t0005 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0002t0022 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0005t0001 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0005t0003 | 0/0 | 2894 | 7 | 0 | 0 | 5 | 0 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0005t0004 | 0/0 | 2898 | 19 | 0 | 5 | 13 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0005t0005 | 0/0 | 2897 | 2 | 1 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0005t0008 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0006t0001 | 0/0 | 2898 | 3 | 0 | 2 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0006t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0006t0004 | 0/0 | 2898 | 18 | 0 | 7 | 7 | 2 | 2 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0006t0005 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0006t0008 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0006t0009 | 0/0 | 2897 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0008t0001 | 0/0 | 2898 | 12 | 6 | 0 | 6 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0008t0002 | 0/0 | 2898 | 2 | 0 | 0 | 1 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0008t0003 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0008t0023 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0008t0024 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0015t0001 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0015t0021 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0002c0020t0001 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0009t0001 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0009t0006 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0009t0007 | 0/0 | 2898 | 10 | 1 | 9 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0010t0001 | 0/0 | 2898 | 4 | 0 | 0 | 4 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0010t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0010t0006 | 0/0 | 2898 | 6 | 0 | 0 | 6 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0010t0018 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0011t0001 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0011t0003 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0011t0004 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0011t0009 | 0/0 | 2897 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0011t0017 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0014t0001 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0014t0002 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0014t0006 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0017t0003 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0017t0004 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0029t0002 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0003c0030t0003 | 0/1 | 2894 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004c0018t0001 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004c0018t0003 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004c0019t0001 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004c0019t0003 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0004c0025t0001 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0005c0013t0003 | 0/0 | 2894 | 3 | 0 | 0 | 3 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0005c0013t0004 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0006c0016t0012 | 0/0 | 2898 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0007c0027t0009 | 0/0 | 2897 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0008c0026t0001 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0009c0028t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0010c0021t0001 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0011c0022t0002 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| a0012c0024t0016 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | copy fasta | chr17 | 14064504 | 14213677 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0011g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0011g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0001t0019g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0015g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0003t0020g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0014g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0014g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0004t0025g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0010g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0010g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0010g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0013g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0007t0013g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0012t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0012t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0012t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0012t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0001c0023t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0002t0022g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0005t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0006t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0023g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0008t0024g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0015t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0015t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0015t0021g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0020t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0002c0020t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0009t0007g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0010t0018g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0011t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0011t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0011t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0011t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0011t0009g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0011t0017g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0014t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0014t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0014t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0014t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0017t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0017t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0017t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0029t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0003c0030t0003g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0004c0018t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0004c0018t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0004c0018t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0004c0019t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0004c0019t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0004c0019t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0004c0025t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0005c0013t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0005c0013t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0005c0013t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0005c0013t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0006c0016t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0006c0016t0012g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0007c0027t0009g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0008c0026t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0009c0028t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0010c0021t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0011c0022t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| a0012c0024t0016g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0131 | EUR | GBR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00099 | hp2 | a0002 | c0006 | t0004 | g0176 | EUR | GBR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00280 | hp1 | a0002 | c0005 | t0004 | g0207 | EUR | FIN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00280 | hp2 | a0003 | c0011 | t0001 | g0039 | EUR | FIN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0153 | EUR | FIN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00323 | hp2 | a0002 | c0008 | t0002 | g0255 | EUR | FIN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00408 | hp1 | a0002 | c0005 | t0004 | g0215 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0026 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00438 | hp2 | a0002 | c0008 | t0001 | g0219 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00544 | hp1 | a0002 | c0005 | t0004 | g0237 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00597 | hp1 | a0002 | c0006 | t0004 | g0205 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0071 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0065 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00621 | hp2 | a0002 | c0006 | t0003 | g0217 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00639 | hp1 | a0002 | c0005 | t0004 | g0230 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00639 | hp2 | a0001 | c0004 | t0002 | g0027 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00673 | hp1 | a0002 | c0006 | t0004 | g0204 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00673 | hp2 | a0001 | c0007 | t0003 | g0124 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00733 | hp1 | a0004 | c0019 | t0003 | g0057 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00733 | hp2 | a0001 | c0004 | t0002 | g0160 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0110 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00738 | hp1 | a0002 | c0006 | t0001 | g0307 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00738 | hp2 | a0002 | c0006 | t0004 | g0180 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0118 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG00741 | hp2 | a0002 | c0005 | t0004 | g0228 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01070 | hp1 | a0001 | c0004 | t0014 | g0126 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01071 | hp2 | a0001 | c0004 | t0014 | g0149 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01074 | hp1 | a0002 | c0006 | t0004 | g0266 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0240 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01081 | hp1 | a0003 | c0009 | t0007 | g0051 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01081 | hp2 | a0002 | c0006 | t0009 | g0259 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01106 | hp1 | a0003 | c0009 | t0007 | g0034 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01106 | hp2 | a0002 | c0006 | t0004 | g0192 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01109 | hp1 | a0001 | c0004 | t0025 | g0301 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0023 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01167 | hp1 | a0001 | c0007 | t0013 | g0130 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01167 | hp2 | a0002 | c0002 | t0003 | g0211 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0304 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01168 | hp2 | a0001 | c0003 | t0005 | g0123 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01169 | hp1 | a0001 | c0003 | t0005 | g0122 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01169 | hp2 | a0001 | c0007 | t0013 | g0129 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0008 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01243 | hp2 | a0002 | c0006 | t0004 | g0241 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01255 | hp1 | a0001 | c0004 | t0002 | g0077 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01255 | hp2 | a0001 | c0003 | t0002 | g0100 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01257 | hp1 | a0002 | c0006 | t0004 | g0258 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01258 | hp1 | a0001 | c0007 | t0004 | g0220 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01261 | hp2 | a0001 | c0007 | t0004 | g0024 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01346 | hp1 | a0002 | c0008 | t0024 | g0306 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01346 | hp2 | a0002 | c0006 | t0004 | g0225 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01358 | hp1 | a0001 | c0003 | t0015 | g0113 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01358 | hp2 | a0003 | c0009 | t0007 | g0048 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01433 | hp1 | a0001 | c0012 | t0001 | g0295 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01433 | hp2 | a0002 | c0006 | t0001 | g0309 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0101 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01516 | hp1 | a0002 | c0006 | t0004 | g0226 | EUR | IBS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0253 | EUR | IBS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01884 | hp1 | a0001 | c0012 | t0001 | g0292 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0312 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01934 | hp1 | a0001 | c0004 | t0002 | g0103 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01934 | hp2 | a0001 | c0007 | t0010 | g0318 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01943 | hp1 | a0002 | c0005 | t0004 | g0280 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01943 | hp2 | a0003 | c0009 | t0007 | g0049 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01952 | hp1 | a0003 | c0009 | t0007 | g0035 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01952 | hp2 | a0002 | c0005 | t0001 | g0305 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01978 | hp1 | a0003 | c0009 | t0007 | g0053 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01978 | hp2 | a0002 | c0005 | t0004 | g0261 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01981 | hp1 | a0002 | c0005 | t0004 | g0229 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01981 | hp2 | a0003 | c0009 | t0007 | g0052 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02004 | hp1 | a0007 | c0027 | t0009 | g0209 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02004 | hp2 | a0003 | c0009 | t0007 | g0055 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02015 | hp1 | a0002 | c0005 | t0003 | g0201 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02015 | hp2 | a0001 | c0004 | t0002 | g0281 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02027 | hp2 | a0001 | c0003 | t0006 | g0102 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02056 | hp1 | a0002 | c0006 | t0004 | g0193 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0015 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02071 | hp2 | a0002 | c0005 | t0004 | g0239 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02080 | hp1 | a0003 | c0011 | t0003 | g0033 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02080 | hp2 | a0001 | c0004 | t0002 | g0109 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02083 | hp2 | a0001 | c0004 | t0002 | g0070 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02132 | hp2 | a0002 | c0005 | t0004 | g0244 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02135 | hp2 | a0002 | c0006 | t0004 | g0188 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02145 | hp1 | a0001 | c0004 | t0003 | g0105 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0300 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02155 | hp1 | a0002 | c0006 | t0004 | g0232 | EAS | CDX | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02155 | hp2 | a0001 | c0004 | t0002 | g0133 | EAS | CDX | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02165 | hp1 | a0001 | c0003 | t0002 | g0072 | EAS | CDX | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | CDX | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02257 | hp2 | a0002 | c0015 | t0001 | g0298 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02258 | hp1 | a0002 | c0020 | t0001 | g0319 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02258 | hp2 | a0001 | c0007 | t0010 | g0316 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02280 | hp1 | a0001 | c0007 | t0004 | g0074 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02280 | hp2 | a0002 | c0008 | t0001 | g0212 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02293 | hp1 | a0003 | c0009 | t0007 | g0050 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02293 | hp2 | a0002 | c0002 | t0022 | g0234 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02523 | hp1 | a0003 | c0011 | t0003 | g0042 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02523 | hp2 | a0002 | c0008 | t0001 | g0221 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02615 | hp1 | a0002 | c0008 | t0001 | g0196 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02615 | hp2 | a0002 | c0005 | t0005 | g0198 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02622 | hp1 | a0002 | c0008 | t0003 | g0242 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02622 | hp2 | a0002 | c0008 | t0001 | g0273 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02647 | hp2 | a0001 | c0012 | t0001 | g0294 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02683 | hp1 | a0001 | c0007 | t0004 | g0162 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02683 | hp2 | a0001 | c0007 | t0001 | g0016 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02698 | hp1 | a0002 | c0006 | t0004 | g0254 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0168 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02717 | hp2 | a0001 | c0007 | t0008 | g0114 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0288 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0289 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02818 | hp1 | a0001 | c0012 | t0001 | g0296 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02818 | hp2 | a0004 | c0018 | t0003 | g0063 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02886 | hp1 | a0004 | c0019 | t0001 | g0062 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02895 | hp1 | a0002 | c0020 | t0001 | g0310 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0283 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02896 | hp1 | a0006 | c0016 | t0012 | g0003 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0284 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0285 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02897 | hp2 | a0006 | c0016 | t0012 | g0003 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02922 | hp1 | a0001 | c0023 | t0001 | g0163 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0269 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0290 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0315 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02976 | hp1 | a0006 | c0016 | t0012 | g0202 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03017 | hp1 | a0003 | c0029 | t0002 | g0047 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03017 | hp2 | a0003 | c0011 | t0004 | g0040 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0276 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03098 | hp2 | a0002 | c0008 | t0003 | g0302 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03130 | hp1 | a0002 | c0008 | t0001 | g0272 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03130 | hp2 | a0001 | c0007 | t0005 | g0128 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03139 | hp1 | a0001 | c0004 | t0003 | g0167 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0291 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03195 | hp1 | a0001 | c0001 | t0019 | g0277 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0287 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0286 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03225 | hp1 | a0012 | c0024 | t0016 | g0297 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03225 | hp2 | a0004 | c0019 | t0001 | g0058 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03486 | hp1 | a0002 | c0015 | t0021 | g0311 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0022 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0257 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0007 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03540 | hp1 | a0004 | c0018 | t0001 | g0059 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03579 | hp1 | a0004 | c0018 | t0001 | g0060 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03654 | hp1 | a0001 | c0007 | t0003 | g0014 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03654 | hp2 | a0001 | c0007 | t0004 | g0121 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0032 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0166 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03710 | hp2 | a0001 | c0007 | t0001 | g0293 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0178 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03834 | hp1 | a0003 | c0011 | t0009 | g0043 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0216 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03927 | hp1 | a0001 | c0004 | t0002 | g0164 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0256 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG04115 | hp1 | a0002 | c0005 | t0003 | g0187 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG04115 | hp2 | a0011 | c0022 | t0002 | g0004 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG04184 | hp1 | a0001 | c0007 | t0003 | g0107 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG04184 | hp2 | a0001 | c0003 | t0002 | g0021 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG04204 | hp1 | a0003 | c0017 | t0003 | g0036 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0117 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG04228 | hp1 | a0002 | c0005 | t0003 | g0208 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG04228 | hp2 | a0001 | c0004 | t0002 | g0012 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | CHB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18612 | hp2 | a0003 | c0010 | t0006 | g0089 | EAS | CHB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18906 | hp1 | a0010 | c0021 | t0001 | g0185 | AFR | YRI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18906 | hp2 | a0002 | c0006 | t0005 | g0303 | AFR | YRI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18939 | hp1 | a0001 | c0004 | t0002 | g0020 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18939 | hp2 | a0002 | c0005 | t0004 | g0182 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18944 | hp1 | a0003 | c0010 | t0006 | g0083 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18944 | hp2 | a0002 | c0008 | t0001 | g0278 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18946 | hp2 | a0002 | c0005 | t0004 | g0235 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18948 | hp1 | a0003 | c0010 | t0018 | g0093 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18950 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18957 | hp1 | a0003 | c0010 | t0001 | g0091 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18959 | hp1 | a0002 | c0008 | t0002 | g0233 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18959 | hp2 | a0003 | c0014 | t0001 | g0046 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18962 | hp1 | a0003 | c0017 | t0004 | g0084 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18962 | hp2 | a0003 | c0014 | t0002 | g0045 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18963 | hp1 | a0001 | c0003 | t0020 | g0005 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0076 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18965 | hp1 | a0001 | c0003 | t0002 | g0069 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18967 | hp2 | a0002 | c0005 | t0003 | g0248 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18968 | hp1 | a0005 | c0013 | t0004 | g0139 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18968 | hp2 | a0002 | c0005 | t0004 | g0206 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18969 | hp2 | a0003 | c0010 | t0006 | g0088 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18970 | hp1 | a0002 | c0008 | t0001 | g0263 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18971 | hp2 | a0001 | c0004 | t0002 | g0282 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18972 | hp1 | a0001 | c0004 | t0002 | g0161 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18974 | hp1 | a0001 | c0007 | t0003 | g0144 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18974 | hp2 | a0003 | c0014 | t0006 | g0037 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18983 | hp1 | a0002 | c0008 | t0001 | g0181 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18985 | hp1 | a0002 | c0005 | t0003 | g0264 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18994 | hp2 | a0003 | c0014 | t0006 | g0044 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18995 | hp1 | a0003 | c0017 | t0004 | g0085 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19000 | hp2 | a0002 | c0005 | t0004 | g0194 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19001 | hp1 | a0003 | c0010 | t0003 | g0095 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19002 | hp1 | a0003 | c0010 | t0006 | g0087 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19002 | hp2 | a0001 | c0004 | t0002 | g0017 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19004 | hp1 | a0002 | c0006 | t0004 | g0227 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19005 | hp2 | a0002 | c0005 | t0003 | g0197 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19007 | hp1 | a0003 | c0010 | t0001 | g0096 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0067 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19011 | hp1 | a0001 | c0004 | t0002 | g0066 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19011 | hp2 | a0005 | c0013 | t0003 | g0141 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19012 | hp1 | a0002 | c0005 | t0005 | g0252 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19012 | hp2 | a0001 | c0007 | t0004 | g0075 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19030 | hp1 | a0001 | c0007 | t0010 | g0317 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0159 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19056 | hp1 | a0002 | c0005 | t0004 | g0238 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19058 | hp1 | a0003 | c0009 | t0001 | g0094 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19058 | hp2 | a0002 | c0008 | t0023 | g0249 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19060 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19060 | hp2 | a0002 | c0005 | t0004 | g0236 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19063 | hp1 | a0005 | c0013 | t0003 | g0116 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19065 | hp1 | a0009 | c0028 | t0003 | g0041 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19065 | hp2 | a0002 | c0005 | t0004 | g0186 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19066 | hp1 | a0001 | c0003 | t0006 | g0112 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19066 | hp2 | a0002 | c0002 | t0005 | g0265 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19068 | hp1 | a0002 | c0005 | t0004 | g0231 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19068 | hp2 | a0005 | c0013 | t0003 | g0140 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19070 | hp1 | a0002 | c0005 | t0004 | g0191 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19075 | hp1 | a0002 | c0006 | t0004 | g0223 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19075 | hp2 | a0003 | c0010 | t0001 | g0082 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19078 | hp1 | a0003 | c0010 | t0001 | g0098 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19078 | hp2 | a0002 | c0008 | t0001 | g0184 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19079 | hp2 | a0003 | c0010 | t0006 | g0086 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19080 | hp1 | a0002 | c0005 | t0003 | g0247 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19080 | hp2 | a0003 | c0009 | t0006 | g0090 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19085 | hp1 | a0003 | c0009 | t0006 | g0097 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19086 | hp1 | a0003 | c0010 | t0006 | g0092 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | YRI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0169 | AFR | YRI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA20129 | hp1 | a0003 | c0009 | t0007 | g0054 | AFR | ASW | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0314 | AFR | ASW | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0210 | EUR | TSI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA20752 | hp2 | a0001 | c0004 | t0002 | g0011 | EUR | TSI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0111 | EUR | TSI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA20805 | hp2 | a0002 | c0006 | t0001 | g0308 | EUR | TSI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA20905 | hp1 | a0002 | c0006 | t0004 | g0224 | SAS | GIH | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA20905 | hp2 | a0001 | c0004 | t0002 | g0073 | SAS | GIH | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01123 | hp1 | a0002 | c0006 | t0004 | g0175 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG01123 | hp2 | a0003 | c0011 | t0017 | g0081 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0267 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0010 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02486 | hp2 | a0002 | c0008 | t0001 | g0243 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02559 | hp1 | a0004 | c0025 | t0001 | g0061 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG02559 | hp2 | a0002 | c0015 | t0001 | g0279 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0313 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG06807 | hp1 | a0002 | c0008 | t0001 | g0271 | AFR | USA | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| HG06807 | hp2 | a0008 | c0026 | t0001 | g0056 | AFR | USA | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA21309 | hp1 | a0002 | c0005 | t0008 | g0246 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| NA21309 | hp2 | a0002 | c0006 | t0008 | g0274 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0030 | t0003 | g0038 | REF | REF | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0299 | REF | REF | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:14069646
|
C | T | 1 | a0007 | 1 | HG02004.hp1 | missense_variant&splice_region_variant | MODERATE | c.41C>T | p.Thr14Ile | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/7 | 143/2898 | 41/1332 | 14/443 | chr17 | 14069646 | ||
| chr17:14074362
|
C | T | 2 | a0004a0008 | 8 | HG00733.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
missense_variant | MODERATE | c.83C>T | p.Thr28Ile | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/7 | 185/2898 | 83/1332 | 28/443 | chr17 | 14074362 | ||
| chr17:14076741
|
A | T | 2 | a0003a0009 | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
missense_variant | MODERATE | c.184A>T | p.Thr62Ser | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/7 | 286/2898 | 184/1332 | 62/443 | chr17 | 14076741 | ||
| chr17:14076817
|
C | T | 1 | a0005 | 4 | NA18968.hp1 NA19011.hp2 NA19063.hp1 others(1): Show |
missense_variant | MODERATE | c.260C>T | p.Thr87Ile | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/7 | 362/2898 | 260/1332 | 87/443 | chr17 | 14076817 | ||
| chr17:14076847
|
A | G | 2 | a0004a0008 | 8 | HG00733.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
missense_variant | MODERATE | c.290A>G | p.Tyr97Cys | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/7 | 392/2898 | 290/1332 | 97/443 | chr17 | 14076847 | ||
| chr17:14077033
|
G | A | 4 | a0002a0006a0007others(1): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
missense_variant | MODERATE | c.476G>A | p.Arg159Gln | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/7 | 578/2898 | 476/1332 | 159/443 | chr17 | 14077033 | ||
| chr17:14102181
|
G | A | 1 | a0009 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.563G>A | p.Cys188Tyr | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/7 | 665/2898 | 563/1332 | 188/443 | chr17 | 14102181 | ||
| chr17:14159934
|
C | T | 1 | a0006 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.682C>T | p.Arg228Cys | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/7 | 784/2898 | 682/1332 | 228/443 | chr17 | 14159934 | ||
| chr17:14206957
|
G | A | 1 | a0011 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1076G>A | p.Arg359His | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1178/2898 | 1076/1332 | 359/443 | chr17 | 14206957 | ||
| chr17:14206977
|
G | T | 3 | a0008a0010a0012 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.1096G>T | p.Val366Leu | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1198/2898 | 1096/1332 | 366/443 | chr17 | 14206977 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:14069638
|
C | T | 5 | a0003c0011a0003c0014a0003c0029others(2): Show | 13 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(10): Show |
synonymous_variant | LOW | c.33C>T | p.Arg11Arg | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/7 | 135/2898 | 33/1332 | 11/443 | chr17 | 14069638 | ||
| chr17:14102122
|
G | A | 15 | a0001c0003a0001c0007a0001c0023others(12): Show | 161 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
synonymous_variant | LOW | c.504G>A | p.Leu168Leu | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/7 | 606/2898 | 504/1332 | 168/443 | chr17 | 14102122 | ||
| chr17:14191992
|
A | G | 19 | a0001c0001a0001c0007a0001c0012others(16): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
synonymous_variant | LOW | c.699A>G | p.Pro233Pro | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/7 | 801/2898 | 699/1332 | 233/443 | chr17 | 14191992 | ||
| chr17:14206919
|
G | A | 4 | a0001c0012a0001c0023a0002c0015others(1): Show | 10 | HG01433.hp1 HG01884.hp1 HG02257.hp2 others(7): Show |
synonymous_variant | LOW | c.1038G>A | p.Ser346Ser | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1140/2898 | 1038/1332 | 346/443 | chr17 | 14206919 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:14069543
|
C | T | 1 | a0001c0004t0014 | 2 | HG01070.hp1 HG01071.hp2 |
5_prime_UTR_variant | MODIFIER | c.-63C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/7 | 63 | chr17 | 14069543 | |||||
| chr17:14069559
|
G | A | 1 | a0001c0003t0015 | 1 | HG01358.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/7 | 47 | chr17 | 14069559 | |||||
| chr17:14069560
|
A | G | 1 | a0001c0003t0015 | 1 | HG01358.hp1 | 5_prime_UTR_variant | MODIFIER | c.-46A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/7 | 46 | chr17 | 14069560 | |||||
| chr17:14207257
|
G | A | 1 | a0012c0024t0016 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 44 | chr17 | 14207257 | |||||
| chr17:14207351
|
GT | G | 12 | a0001c0001t0005a0001c0001t0019a0001c0003t0005others(9): Show | 19 | HG01081.hp2 HG01167.hp1 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*152delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 152 | INFO_REALIGN_3_PRIME | chr17 | 14207351 | ||||
| chr17:14207351
|
GTT | G | 19 | a0001c0001t0003a0001c0004t0003a0001c0007t0003others(16): Show | 65 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*151_*152delTT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 151 | INFO_REALIGN_3_PRIME | chr17 | 14207351 | ||||
| chr17:14207510
|
G | A | 7 | a0001c0001t0004a0001c0007t0004a0002c0005t0004others(4): Show | 52 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*297G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 297 | chr17 | 14207510 | |||||
| chr17:14207511
|
G | T | 1 | a0001c0004t0025 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 298 | chr17 | 14207511 | |||||
| chr17:14207518
|
A | G | 1 | a0002c0008t0024 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 305 | chr17 | 14207518 | |||||
| chr17:14207535
|
T | C | 20 | a0001c0001t0003a0001c0004t0003a0001c0007t0003others(17): Show | 67 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*322T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 322 | chr17 | 14207535 | |||||
| chr17:14207584
|
A | G | 23 | a0001c0001t0003a0001c0001t0011a0001c0001t0019others(20): Show | 74 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*371A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 371 | chr17 | 14207584 | |||||
| chr17:14207651
|
G | C | 9 | a0001c0003t0006a0002c0006t0009a0003c0009t0006others(6): Show | 26 | HG01081.hp1 HG01081.hp2 HG01106.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*438G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 438 | chr17 | 14207651 | |||||
| chr17:14207859
|
C | A | 20 | a0001c0001t0003a0001c0004t0003a0001c0007t0003others(17): Show | 67 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*646C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 646 | chr17 | 14207859 | |||||
| chr17:14207859
|
C | G | 3 | a0002c0006t0009a0003c0011t0009a0007c0027t0009 | 3 | HG01081.hp2 HG02004.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*646C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 646 | chr17 | 14207859 | |||||
| chr17:14207865
|
C | T | 1 | a0002c0008t0023 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*652C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 652 | chr17 | 14207865 | |||||
| chr17:14207970
|
T | C | 20 | a0001c0001t0003a0001c0004t0003a0001c0007t0003others(17): Show | 67 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*757T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 757 | chr17 | 14207970 | |||||
| chr17:14208043
|
CCT | C | 20 | a0001c0001t0003a0001c0004t0003a0001c0007t0003others(17): Show | 67 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*833_*834delCT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 833 | INFO_REALIGN_3_PRIME | chr17 | 14208043 | ||||
| chr17:14208117
|
C | G | 1 | a0001c0001t0019 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 904 | chr17 | 14208117 | |||||
| chr17:14208148
|
G | T | 1 | a0002c0002t0022 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*935G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 935 | chr17 | 14208148 | |||||
| chr17:14208187
|
C | A | 9 | a0001c0003t0006a0002c0006t0009a0003c0009t0006others(6): Show | 26 | HG01081.hp1 HG01081.hp2 HG01106.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*974C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 974 | chr17 | 14208187 | |||||
| chr17:14208289
|
T | C | 22 | a0001c0001t0003a0001c0001t0011a0001c0001t0019others(19): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1076T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1076 | chr17 | 14208289 | |||||
| chr17:14208291
|
C | T | 7 | a0001c0001t0004a0001c0007t0004a0002c0005t0004others(4): Show | 52 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1078C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1078 | chr17 | 14208291 | |||||
| chr17:14208292
|
G | A | 1 | a0001c0007t0010 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1079G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1079 | chr17 | 14208292 | |||||
| chr17:14208314
|
C | T | 2 | a0001c0001t0011a0001c0001t0019 | 4 | HG01884.hp2 HG03195.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1101C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1101 | chr17 | 14208314 | |||||
| chr17:14208358
|
C | T | 1 | a0002c0015t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1145 | chr17 | 14208358 | |||||
| chr17:14208401
|
C | A | 1 | a0002c0015t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1188C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1188 | chr17 | 14208401 | |||||
| chr17:14208413
|
G | A | 1 | a0001c0003t0020 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1200G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1200 | chr17 | 14208413 | |||||
| chr17:14208480
|
A | G | 1 | a0003c0011t0017 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1267A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1267 | chr17 | 14208480 | |||||
| chr17:14208537
|
C | T | 5 | a0001c0003t0006a0003c0009t0006a0003c0010t0006others(2): Show | 13 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1324C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1324 | chr17 | 14208537 | |||||
| chr17:14208596
|
G | A | 3 | a0001c0007t0008a0002c0005t0008a0002c0006t0008 | 3 | HG02717.hp2 NA21309.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1383G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1383 | chr17 | 14208596 | |||||
| chr17:14208598
|
C | T | 12 | a0001c0003t0002a0001c0003t0015a0001c0003t0020others(9): Show | 67 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1385C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 7/7 | 1385 | chr17 | 14208598 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:14069814
|
T | C | 95 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(92): Show | 95 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.43+166T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14069814 | ||||||
| chr17:14069832
|
G | T | 17 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(14): Show | 17 | NA18612.hp2 NA18944.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.43+184G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14069832 | ||||||
| chr17:14070066
|
T | C | 29 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(26): Show | 29 | HG00438.hp1 HG00639.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.43+418T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14070066 | ||||||
| chr17:14070116
|
T | G | 73 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0099others(70): Show | 74 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.43+468T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14070116 | ||||||
| chr17:14070208
|
A | G | 1 | a0002c0020t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43+560A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14070208 | ||||||
| chr17:14070340
|
A | T | 1 | a0003c0011t0017g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.43+692A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14070340 | ||||||
| chr17:14070418
|
T | C | 3 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0173 | 3 | HG02109.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.43+770T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14070418 | ||||||
| chr17:14070968
|
G | A | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.43+1320G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14070968 | ||||||
| chr17:14070978
|
T | C | 1 | a0002c0002t0002g0174 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.43+1330T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14070978 | ||||||
| chr17:14070991
|
G | A | 8 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0018t0003g0063others(5): Show | 8 | HG00733.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+1343G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14070991 | ||||||
| chr17:14071061
|
A | C | 1 | a0003c0011t0017g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.43+1413A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071061 | ||||||
| chr17:14071106
|
A | G | 1 | a0001c0001t0003g0170 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.43+1458A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071106 | ||||||
| chr17:14071160
|
A | G | 4 | a0001c0003t0002g0315a0001c0007t0010g0316a0001c0007t0010g0317others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+1512A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071160 | ||||||
| chr17:14071198
|
T | G | 2 | a0002c0006t0004g0175a0002c0006t0004g0176 | 2 | HG00099.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.43+1550T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071198 | ||||||
| chr17:14071225
|
C | T | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.43+1577C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071225 | ||||||
| chr17:14071231
|
A | C | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.43+1583A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071231 | ||||||
| chr17:14071370
|
C | T | 10 | a0002c0002t0002g0304a0002c0005t0001g0305a0002c0006t0001g0307others(7): Show | 10 | HG00738.hp1 HG01168.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+1722C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071370 | ||||||
| chr17:14071453
|
A | G | 1 | a0001c0003t0001g0032 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.43+1805A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071453 | ||||||
| chr17:14071491
|
A | C | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0031 | 3 | HG01257.hp2 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.43+1843A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071491 | ||||||
| chr17:14071730
|
C | CA | 141 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(138): Show | 142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.43+2102dupA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 14071730 | |||||
| chr17:14071730
|
C | CAA | 161 | a0001c0001t0003g0068a0001c0001t0003g0099a0001c0001t0003g0104others(158): Show | 163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.43+2101_43+2102dup others(2): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 14071730 | |||||
| chr17:14071730
|
C | CAAA | 13 | a0001c0001t0005g0064a0002c0002t0001g0177a0002c0002t0001g0183others(10): Show | 13 | HG00738.hp2 HG01106.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+2100_43+2102dup others(3): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 14071730 | |||||
| chr17:14071798
|
G | T | 138 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(135): Show | 139 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.43+2150G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071798 | ||||||
| chr17:14071822
|
T | C | 314 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.43+2174T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14071822 | ||||||
| chr17:14072114
|
C | A | 82 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0099others(79): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.44-2209C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072114 | ||||||
| chr17:14072365
|
C | T | 9 | a0002c0002t0002g0304a0002c0005t0001g0305a0002c0006t0001g0307others(6): Show | 9 | HG00738.hp1 HG01168.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-1958C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072365 | ||||||
| chr17:14072474
|
G | T | 10 | a0002c0002t0002g0304a0002c0005t0001g0305a0002c0006t0001g0307others(7): Show | 10 | HG00738.hp1 HG01168.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.44-1849G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072474 | ||||||
| chr17:14072480
|
C | A | 30 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(27): Show | 30 | HG00438.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.44-1843C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072480 | ||||||
| chr17:14072574
|
C | T | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-1749C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072574 | ||||||
| chr17:14072736
|
A | G | 8 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0018t0003g0063others(5): Show | 8 | HG00733.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-1587A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072736 | ||||||
| chr17:14072750
|
G | A | 1 | a0002c0005t0004g0186 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.44-1573G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072750 | ||||||
| chr17:14072793
|
T | C | 5 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-1530T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072793 | ||||||
| chr17:14072830
|
C | T | 1 | a0001c0007t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44-1493C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072830 | ||||||
| chr17:14072846
|
T | C | 7 | a0002c0002t0002g0304a0002c0005t0001g0305a0002c0006t0001g0307others(4): Show | 7 | HG00738.hp1 HG01168.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-1477T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14072846 | ||||||
| chr17:14073057
|
G | A | 1 | a0001c0001t0011g0312 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.44-1266G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073057 | ||||||
| chr17:14073081
|
G | A | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.44-1242G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073081 | ||||||
| chr17:14073243
|
T | A | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.44-1080T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073243 | ||||||
| chr17:14073282
|
G | C | 6 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(3): Show | 6 | HG01192.hp1 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-1041G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073282 | ||||||
| chr17:14073343
|
G | A | 4 | a0001c0003t0002g0315a0001c0007t0010g0316a0001c0007t0010g0317others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-980G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073343 | ||||||
| chr17:14073350
|
GGATGTTC others(12): Show |
G | 16 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(13): Show | 16 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.44-955_44-937delCA others(17): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 14073350 | |||||
| chr17:14073401
|
T | G | 47 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(44): Show | 47 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.44-922T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073401 | ||||||
| chr17:14073402
|
G | T | 1 | a0003c0029t0002g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.44-921G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073402 | ||||||
| chr17:14073592
|
G | A | 1 | a0002c0005t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.44-731G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073592 | ||||||
| chr17:14073627
|
A | G | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.44-696A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073627 | ||||||
| chr17:14073638
|
T | G | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.44-685T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073638 | ||||||
| chr17:14073965
|
T | A | 1 | a0001c0007t0003g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.44-358T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073965 | ||||||
| chr17:14073975
|
T | C | 1 | a0002c0006t0004g0188 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.44-348T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14073975 | ||||||
| chr17:14074014
|
G | A | 2 | a0001c0004t0002g0281a0001c0004t0002g0282 | 2 | HG02015.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.44-309G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14074014 | ||||||
| chr17:14074014
|
G | C | 1 | a0001c0001t0005g0289 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.44-309G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14074014 | ||||||
| chr17:14074036
|
G | A | 8 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0018t0003g0063others(5): Show | 8 | HG00733.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-287G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14074036 | ||||||
| chr17:14074042
|
A | G | 2 | a0001c0004t0001g0168a0001c0004t0001g0169 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.44-281A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14074042 | ||||||
| chr17:14074048
|
C | T | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.44-275C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14074048 | ||||||
| chr17:14074059
|
C | T | 1 | a0006c0016t0012g0003 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.44-264C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14074059 | ||||||
| chr17:14074145
|
G | A | 138 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(135): Show | 139 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.44-178G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14074145 | ||||||
| chr17:14074261
|
G | A | 3 | a0001c0001t0003g0099a0001c0003t0002g0100a0001c0003t0002g0101 | 3 | HG01255.hp2 HG01496.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.44-62G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 1/6 | chr17 | 14074261 | ||||||
| chr17:14074473
|
A | G | 1 | a0002c0002t0001g0275 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.177+17A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14074473 | ||||||
| chr17:14074479
|
A | C | 1 | a0003c0014t0001g0046 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.177+23A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14074479 | ||||||
| chr17:14074496
|
C | CTTTA | 314 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.177+43_177+44insAT others(2): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 14074496 | |||||
| chr17:14074623
|
C | T | 9 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(6): Show | 9 | HG02109.hp1 HG02622.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.177+167C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14074623 | ||||||
| chr17:14074847
|
A | G | 10 | a0002c0002t0002g0304a0002c0005t0001g0305a0002c0006t0001g0307others(7): Show | 10 | HG00738.hp1 HG01168.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.177+391A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14074847 | ||||||
| chr17:14074963
|
C | G | 17 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(14): Show | 17 | NA18612.hp2 NA18944.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+507C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14074963 | ||||||
| chr17:14075038
|
G | A | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.177+582G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075038 | ||||||
| chr17:14075388
|
G | T | 1 | a0002c0006t0004g0266 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.177+932G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075388 | ||||||
| chr17:14075400
|
G | A | 1 | a0001c0001t0003g0108 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.177+944G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075400 | ||||||
| chr17:14075417
|
C | T | 139 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(136): Show | 140 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.177+961C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075417 | ||||||
| chr17:14075444
|
G | A | 9 | a0001c0001t0005g0289a0001c0001t0005g0290a0001c0004t0001g0291others(6): Show | 9 | HG01433.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.177+988G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075444 | ||||||
| chr17:14075460
|
A | G | 129 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(126): Show | 130 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.177+1004A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075460 | ||||||
| chr17:14075530
|
A | G | 2 | a0001c0004t0002g0281a0001c0004t0002g0282 | 2 | HG02015.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.177+1074A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075530 | ||||||
| chr17:14075570
|
A | G | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.177+1114A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075570 | ||||||
| chr17:14075717
|
G | A | 1 | a0001c0004t0002g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.178-1018G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075717 | ||||||
| chr17:14075812
|
A | G | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.178-923A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075812 | ||||||
| chr17:14075833
|
T | TA | 5 | a0001c0003t0002g0315a0001c0007t0010g0316a0001c0007t0010g0317others(2): Show | 5 | HG01934.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-893dupA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 14075833 | |||||
| chr17:14075860
|
C | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.178-875C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14075860 | ||||||
| chr17:14075991
|
CA | C | 256 | a0001c0001t0001g0018a0001c0001t0003g0001a0001c0001t0003g0019others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.178-723delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 14075991 | |||||
| chr17:14076111
|
C | CT | 186 | a0001c0001t0003g0001a0001c0001t0003g0029a0001c0001t0003g0099others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.178-604dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 14076111 | |||||
| chr17:14076111
|
C | CTT | 91 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0030others(88): Show | 92 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.178-605_178-604dup others(2): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 14076111 | |||||
| chr17:14076111
|
C | CTTT | 12 | a0001c0001t0001g0120a0001c0001t0003g0028a0001c0001t0003g0031others(9): Show | 12 | HG01099.hp2 HG01192.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-606_178-604dup others(3): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 14076111 | |||||
| chr17:14076173
|
C | T | 6 | a0002c0002t0002g0304a0002c0005t0001g0305a0002c0006t0001g0307others(3): Show | 6 | HG00738.hp1 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-562C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14076173 | ||||||
| chr17:14076270
|
T | A | 1 | a0003c0009t0007g0048 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.178-465T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14076270 | ||||||
| chr17:14076339
|
T | C | 1 | a0002c0002t0001g0200 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.178-396T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14076339 | ||||||
| chr17:14076450
|
A | AT | 122 | a0001c0007t0004g0220a0002c0002t0001g0002a0002c0002t0001g0171others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.178-284dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 14076450 | |||||
| chr17:14076481
|
A | G | 1 | a0002c0005t0003g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.178-254A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14076481 | ||||||
| chr17:14076483
|
A | G | 8 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0018t0003g0063others(5): Show | 8 | HG00733.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-252A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 2/6 | chr17 | 14076483 | ||||||
| chr17:14077197
|
G | A | 1 | a0001c0007t0003g0124 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.499+141G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14077197 | ||||||
| chr17:14077333
|
T | G | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.499+277T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14077333 | ||||||
| chr17:14077375
|
G | C | 305 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(302): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.499+319G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14077375 | ||||||
| chr17:14077375
|
G | T | 9 | a0001c0001t0005g0289a0001c0001t0005g0290a0001c0004t0001g0291others(6): Show | 9 | HG01433.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+319G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14077375 | ||||||
| chr17:14077584
|
C | T | 14 | a0001c0001t0003g0068a0001c0001t0005g0064a0001c0003t0002g0065others(11): Show | 14 | HG00597.hp2 HG00621.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.499+528C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14077584 | ||||||
| chr17:14077922
|
ATT | A | 7 | a0001c0001t0003g0104a0001c0001t0019g0277a0001c0003t0002g0076others(4): Show | 7 | HG02015.hp2 HG03195.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.499+886_499+887del others(2): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14077922 | |||||
| chr17:14077922
|
ATTT | A | 296 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(293): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.499+885_499+887del others(3): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14077922 | |||||
| chr17:14077922
|
ATTTT | A | 9 | a0001c0001t0003g0029a0001c0001t0003g0125a0001c0001t0005g0290others(6): Show | 9 | HG01070.hp1 HG01168.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+884_499+887del others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14077922 | |||||
| chr17:14078058
|
G | A | 4 | a0002c0002t0001g0203a0002c0006t0004g0204a0006c0016t0012g0003others(1): Show | 5 | HG00673.hp1 HG01243.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+1002G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078058 | ||||||
| chr17:14078094
|
A | G | 2 | a0001c0001t0004g0157a0001c0001t0004g0158 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.499+1038A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078094 | ||||||
| chr17:14078183
|
G | A | 5 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0058others(2): Show | 5 | HG00733.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+1127G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078183 | ||||||
| chr17:14078478
|
C | G | 1 | a0001c0007t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.499+1422C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078478 | ||||||
| chr17:14078498
|
C | T | 17 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(14): Show | 17 | NA18612.hp2 NA18944.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.499+1442C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078498 | ||||||
| chr17:14078527
|
C | T | 1 | a0003c0009t0006g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.499+1471C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078527 | ||||||
| chr17:14078655
|
C | A | 2 | a0001c0003t0002g0065a0001c0003t0002g0067 | 2 | HG00621.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.499+1599C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078655 | ||||||
| chr17:14078676
|
G | T | 2 | a0001c0003t0002g0065a0001c0003t0002g0067 | 2 | HG00621.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.499+1620G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078676 | ||||||
| chr17:14078738
|
G | C | 1 | a0002c0005t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.499+1682G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078738 | ||||||
| chr17:14078755
|
C | T | 1 | a0002c0006t0009g0259 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.499+1699C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078755 | ||||||
| chr17:14078913
|
A | G | 1 | a0002c0006t0004g0258 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.499+1857A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14078913 | ||||||
| chr17:14079159
|
G | A | 9 | a0002c0002t0002g0304a0002c0005t0001g0305a0002c0006t0001g0307others(6): Show | 9 | HG00738.hp1 HG01168.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.499+2103G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14079159 | ||||||
| chr17:14079318
|
A | T | 2 | a0001c0004t0002g0281a0001c0004t0002g0282 | 2 | HG02015.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.499+2262A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14079318 | ||||||
| chr17:14079426
|
C | A | 1 | a0001c0001t0004g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.499+2370C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14079426 | ||||||
| chr17:14079848
|
A | G | 4 | a0001c0003t0002g0315a0001c0007t0010g0316a0001c0007t0010g0317others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+2792A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14079848 | ||||||
| chr17:14079856
|
ATATG | A | 261 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0099others(258): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.499+2820_499+2823d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14079856 | |||||
| chr17:14079856
|
ATATGTAT others(5): Show |
A | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.499+2812_499+2823d others(14): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14079856 | |||||
| chr17:14079858
|
ATG | A | 51 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(48): Show | 51 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.499+2804_499+2805d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14079858 | |||||
| chr17:14079860
|
G | GTATGTAT others(19146): Show |
1 | a0002c0020t0001g0310 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.499+2819_499+2820i others(19155): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14079860 | |||||
| chr17:14079955
|
T | C | 1 | a0001c0007t0005g0128 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.499+2899T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14079955 | ||||||
| chr17:14080219
|
C | CT | 18 | a0001c0001t0003g0119a0001c0003t0002g0315a0001c0003t0015g0113others(15): Show | 18 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.499+3185dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14080219 | |||||
| chr17:14080219
|
C | CTT | 13 | a0003c0011t0001g0039a0003c0011t0003g0033a0003c0011t0003g0042others(10): Show | 13 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.499+3184_499+3185d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14080219 | |||||
| chr17:14080219
|
C | CTTT | 26 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(23): Show | 26 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.499+3183_499+3185d others(5): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14080219 | |||||
| chr17:14080219
|
CT | C | 51 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(48): Show | 51 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.499+3185delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14080219 | |||||
| chr17:14080219
|
CTTTTTTT others(4): Show |
C | 3 | a0002c0002t0002g0174a0002c0002t0005g0265a0002c0006t0004g0205 | 3 | HG00597.hp1 NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.499+3175_499+3185d others(13): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14080219 | |||||
| chr17:14080316
|
C | T | 3 | a0002c0005t0004g0207a0002c0006t0004g0254a0002c0008t0002g0255 | 3 | HG00280.hp1 HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.499+3260C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14080316 | ||||||
| chr17:14080577
|
G | A | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.499+3521G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14080577 | ||||||
| chr17:14080606
|
A | G | 314 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.499+3550A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14080606 | ||||||
| chr17:14080667
|
G | C | 1 | a0004c0025t0001g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.499+3611G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14080667 | ||||||
| chr17:14080857
|
G | A | 1 | a0001c0007t0008g0114 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.499+3801G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14080857 | ||||||
| chr17:14081073
|
G | C | 3 | a0003c0009t0007g0048a0003c0009t0007g0051a0003c0009t0007g0052 | 3 | HG01081.hp1 HG01358.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.499+4017G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081073 | ||||||
| chr17:14081143
|
T | C | 10 | a0001c0001t0005g0289a0001c0001t0005g0290a0001c0004t0001g0291others(7): Show | 10 | HG01433.hp1 HG01884.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.499+4087T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081143 | ||||||
| chr17:14081162
|
C | T | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.499+4106C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081162 | ||||||
| chr17:14081246
|
C | G | 50 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(47): Show | 50 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.499+4190C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081246 | ||||||
| chr17:14081276
|
T | C | 14 | a0001c0001t0003g0068a0001c0001t0005g0064a0001c0003t0002g0065others(11): Show | 14 | HG00597.hp2 HG00621.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.499+4220T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081276 | ||||||
| chr17:14081291
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.499+4235C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081291 | ||||||
| chr17:14081445
|
G | A | 82 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0099others(79): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.499+4389G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081445 | ||||||
| chr17:14081476
|
G | A | 4 | a0001c0003t0002g0315a0001c0007t0010g0316a0001c0007t0010g0317others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+4420G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081476 | ||||||
| chr17:14081936
|
G | T | 1 | a0002c0002t0002g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.499+4880G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081936 | ||||||
| chr17:14081987
|
G | A | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.499+4931G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14081987 | ||||||
| chr17:14082102
|
A | G | 1 | a0001c0001t0003g0155 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.499+5046A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14082102 | ||||||
| chr17:14082117
|
A | C | 1 | a0002c0005t0005g0252 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.499+5061A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14082117 | ||||||
| chr17:14082235
|
C | T | 4 | a0002c0002t0002g0199a0002c0002t0002g0250a0002c0002t0002g0251others(1): Show | 4 | NA18977.hp1 NA19005.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+5179C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14082235 | ||||||
| chr17:14082277
|
T | C | 1 | a0001c0001t0011g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.499+5221T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14082277 | ||||||
| chr17:14082519
|
T | G | 17 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(14): Show | 17 | NA18612.hp2 NA18944.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.499+5463T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14082519 | ||||||
| chr17:14082528
|
A | G | 28 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(25): Show | 28 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.499+5472A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14082528 | ||||||
| chr17:14082601
|
G | GCTTA | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.499+5546_499+5549d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14082601 | |||||
| chr17:14082632
|
C | T | 1 | a0003c0011t0009g0043 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.499+5576C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14082632 | ||||||
| chr17:14083075
|
A | C | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.499+6019A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14083075 | ||||||
| chr17:14083165
|
C | T | 1 | a0012c0024t0016g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.499+6109C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14083165 | ||||||
| chr17:14083190
|
G | A | 1 | a0002c0006t0004g0193 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.499+6134G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14083190 | ||||||
| chr17:14083601
|
G | A | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.499+6545G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14083601 | ||||||
| chr17:14083667
|
A | G | 3 | a0002c0002t0001g0203a0006c0016t0012g0003a0006c0016t0012g0202 | 4 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+6611A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14083667 | ||||||
| chr17:14083726
|
A | G | 1 | a0001c0001t0003g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.499+6670A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14083726 | ||||||
| chr17:14084099
|
G | A | 112 | a0001c0007t0004g0220a0002c0002t0001g0002a0002c0002t0001g0171others(109): Show | 114 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.499+7043G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14084099 | ||||||
| chr17:14084109
|
C | G | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.499+7053C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14084109 | ||||||
| chr17:14084124
|
A | G | 316 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.499+7068A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14084124 | ||||||
| chr17:14084319
|
A | G | 316 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.499+7263A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14084319 | ||||||
| chr17:14084684
|
A | G | 9 | a0001c0001t0005g0289a0001c0001t0005g0290a0001c0004t0001g0291others(6): Show | 9 | HG01433.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+7628A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14084684 | ||||||
| chr17:14084712
|
G | A | 3 | a0001c0001t0003g0131a0001c0007t0013g0129a0001c0007t0013g0130 | 3 | HG00099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.499+7656G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14084712 | ||||||
| chr17:14084788
|
G | A | 17 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(14): Show | 17 | NA18612.hp2 NA18944.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.499+7732G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14084788 | ||||||
| chr17:14085191
|
G | A | 79 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0099others(76): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.499+8135G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14085191 | ||||||
| chr17:14085258
|
C | T | 2 | a0002c0005t0003g0247a0002c0005t0003g0248 | 2 | NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.499+8202C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14085258 | ||||||
| chr17:14085352
|
T | A | 1 | a0002c0005t0005g0252 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.499+8296T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14085352 | ||||||
| chr17:14085505
|
G | T | 1 | a0002c0002t0002g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.499+8449G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14085505 | ||||||
| chr17:14085565
|
T | G | 47 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(44): Show | 47 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.499+8509T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14085565 | ||||||
| chr17:14086216
|
A | G | 2 | a0002c0005t0005g0198a0002c0005t0008g0246 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.499+9160A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14086216 | ||||||
| chr17:14086449
|
A | G | 1 | a0003c0010t0001g0096 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.499+9393A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14086449 | ||||||
| chr17:14086546
|
C | T | 4 | a0001c0003t0002g0315a0001c0007t0010g0316a0001c0007t0010g0317others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+9490C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14086546 | ||||||
| chr17:14086591
|
A | G | 1 | a0001c0004t0003g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.499+9535A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14086591 | ||||||
| chr17:14086723
|
G | A | 1 | a0002c0006t0008g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.499+9667G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14086723 | ||||||
| chr17:14086791
|
C | T | 122 | a0001c0007t0004g0220a0002c0002t0001g0002a0002c0002t0001g0171others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.499+9735C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14086791 | ||||||
| chr17:14086821
|
G | C | 9 | a0001c0001t0005g0289a0001c0001t0005g0290a0001c0004t0001g0291others(6): Show | 9 | HG01433.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+9765G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14086821 | ||||||
| chr17:14087074
|
A | T | 1 | a0001c0004t0002g0027 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.499+10018A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087074 | ||||||
| chr17:14087152
|
A | T | 1 | a0002c0002t0001g0177 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.499+10096A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087152 | ||||||
| chr17:14087296
|
C | T | 79 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0099others(76): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.499+10240C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087296 | ||||||
| chr17:14087564
|
T | A | 1 | a0002c0005t0003g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.499+10508T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087564 | ||||||
| chr17:14087725
|
G | T | 1 | a0001c0003t0002g0166 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.499+10669G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087725 | ||||||
| chr17:14087748
|
C | A | 1 | a0001c0003t0002g0166 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.499+10692C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087748 | ||||||
| chr17:14087750
|
G | T | 1 | a0001c0003t0002g0166 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.499+10694G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087750 | ||||||
| chr17:14087969
|
C | T | 122 | a0001c0007t0004g0220a0002c0002t0001g0002a0002c0002t0001g0171others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.499+10913C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087969 | ||||||
| chr17:14087970
|
G | A | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.499+10914G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14087970 | ||||||
| chr17:14088038
|
A | C | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.499+10982A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14088038 | ||||||
| chr17:14088220
|
A | T | 47 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(44): Show | 47 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.499+11164A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14088220 | ||||||
| chr17:14088279
|
T | C | 9 | a0001c0001t0005g0289a0001c0001t0005g0290a0001c0004t0001g0291others(6): Show | 9 | HG01433.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+11223T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14088279 | ||||||
| chr17:14088325
|
C | T | 7 | a0003c0011t0003g0033a0003c0011t0003g0042a0003c0014t0001g0046others(4): Show | 7 | HG02080.hp1 HG02523.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.499+11269C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14088325 | ||||||
| chr17:14088408
|
A | G | 1 | a0001c0003t0002g0153 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.499+11352A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14088408 | ||||||
| chr17:14088428
|
T | A | 4 | a0001c0003t0002g0315a0001c0007t0010g0316a0001c0007t0010g0317others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+11372T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14088428 | ||||||
| chr17:14088441
|
GA | G | 50 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(47): Show | 50 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.499+11396delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14088441 | |||||
| chr17:14088764
|
A | G | 1 | a0001c0003t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.499+11708A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14088764 | ||||||
| chr17:14089172
|
C | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.499+12116C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14089172 | ||||||
| chr17:14089195
|
T | C | 1 | a0002c0006t0004g0193 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.499+12139T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14089195 | ||||||
| chr17:14089350
|
G | C | 17 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(14): Show | 17 | NA18612.hp2 NA18944.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.499+12294G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14089350 | ||||||
| chr17:14089566
|
T | C | 2 | a0002c0015t0001g0279a0002c0015t0001g0298 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.499+12510T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14089566 | ||||||
| chr17:14089702
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.500-12416C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14089702 | ||||||
| chr17:14089883
|
G | A | 50 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(47): Show | 50 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.500-12235G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14089883 | ||||||
| chr17:14090052
|
G | A | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.500-12066G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14090052 | ||||||
| chr17:14090171
|
G | A | 3 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269 | 3 | HG02109.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.500-11947G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14090171 | ||||||
| chr17:14090596
|
A | G | 1 | a0002c0002t0001g0275 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.500-11522A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14090596 | ||||||
| chr17:14090606
|
G | A | 13 | a0003c0011t0001g0039a0003c0011t0003g0033a0003c0011t0003g0042others(10): Show | 13 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.500-11512G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14090606 | ||||||
| chr17:14090825
|
C | G | 51 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(48): Show | 51 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.500-11293C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14090825 | ||||||
| chr17:14090854
|
G | A | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.500-11264G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14090854 | ||||||
| chr17:14091059
|
T | C | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.500-11059T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091059 | ||||||
| chr17:14091298
|
T | C | 50 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(47): Show | 50 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.500-10820T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091298 | ||||||
| chr17:14091299
|
G | A | 1 | a0001c0003t0001g0078 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.500-10819G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091299 | ||||||
| chr17:14091388
|
A | T | 1 | a0002c0002t0001g0245 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.500-10730A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091388 | ||||||
| chr17:14091539
|
A | G | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.500-10579A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091539 | ||||||
| chr17:14091552
|
A | G | 2 | a0001c0003t0002g0015a0001c0003t0002g0026 | 2 | HG00438.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.500-10566A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091552 | ||||||
| chr17:14091664
|
C | T | 47 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(44): Show | 47 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-10454C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091664 | ||||||
| chr17:14091816
|
G | T | 2 | a0001c0004t0003g0105a0001c0004t0003g0167 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.500-10302G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091816 | ||||||
| chr17:14091848
|
A | G | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.500-10270A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091848 | ||||||
| chr17:14091859
|
A | G | 1 | a0002c0015t0021g0311 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.500-10259A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14091859 | ||||||
| chr17:14091896
|
A | AT | 88 | a0001c0007t0004g0220a0002c0002t0001g0177a0002c0002t0001g0183others(85): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.500-10215dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14091896 | |||||
| chr17:14092119
|
A | G | 5 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0058others(2): Show | 5 | HG00733.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-9999A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14092119 | ||||||
| chr17:14092428
|
A | G | 2 | a0002c0005t0004g0244a0002c0006t0004g0193 | 2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.500-9690A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14092428 | ||||||
| chr17:14092648
|
C | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.500-9470C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14092648 | ||||||
| chr17:14092772
|
C | T | 41 | a0003c0009t0001g0094a0003c0009t0006g0090a0003c0009t0006g0097others(38): Show | 41 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.500-9346C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14092772 | ||||||
| chr17:14092789
|
G | A | 1 | a0001c0003t0002g0008 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.500-9329G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14092789 | ||||||
| chr17:14092872
|
A | G | 13 | a0003c0011t0001g0039a0003c0011t0003g0033a0003c0011t0003g0042others(10): Show | 13 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.500-9246A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14092872 | ||||||
| chr17:14093080
|
A | G | 46 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(43): Show | 46 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.500-9038A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093080 | ||||||
| chr17:14093105
|
A | C | 1 | a0002c0020t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.500-9013A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093105 | ||||||
| chr17:14093189
|
G | A | 89 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0028others(86): Show | 89 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.500-8929G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093189 | ||||||
| chr17:14093258
|
T | C | 1 | a0002c0005t0004g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.500-8860T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093258 | ||||||
| chr17:14093735
|
G | A | 1 | a0002c0015t0021g0311 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.500-8383G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093735 | ||||||
| chr17:14093736
|
C | G | 1 | a0002c0015t0021g0311 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.500-8382C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093736 | ||||||
| chr17:14093737
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0058 | 3 | HG03225.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.500-8381G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093737 | ||||||
| chr17:14093845
|
A | C | 4 | a0001c0003t0002g0315a0001c0007t0010g0316a0001c0007t0010g0317others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-8273A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093845 | ||||||
| chr17:14093950
|
A | C | 5 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0058others(2): Show | 5 | HG00733.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-8168A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093950 | ||||||
| chr17:14093968
|
G | A | 2 | a0001c0003t0001g0079a0001c0003t0001g0080 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.500-8150G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14093968 | ||||||
| chr17:14094005
|
G | T | 1 | a0001c0003t0002g0076 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.500-8113G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14094005 | ||||||
| chr17:14094101
|
T | G | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.500-8017T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14094101 | ||||||
| chr17:14094145
|
A | T | 85 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(82): Show | 85 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.500-7973A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14094145 | ||||||
| chr17:14094273
|
T | TA | 9 | a0001c0001t0005g0289a0001c0001t0005g0290a0001c0004t0001g0291others(6): Show | 9 | HG01433.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.500-7844dupA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14094273 | |||||
| chr17:14094553
|
GT | G | 87 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(84): Show | 87 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.500-7561delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14094553 | |||||
| chr17:14094590
|
A | G | 3 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296 | 3 | HG01433.hp1 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.500-7528A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14094590 | ||||||
| chr17:14094605
|
T | A | 2 | a0002c0015t0001g0279a0002c0015t0001g0298 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.500-7513T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14094605 | ||||||
| chr17:14095111
|
C | A | 1 | a0002c0008t0023g0249 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.500-7007C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14095111 | ||||||
| chr17:14095129
|
A | G | 1 | a0001c0003t0006g0112 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.500-6989A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14095129 | ||||||
| chr17:14095186
|
A | C | 1 | a0001c0001t0003g0152 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.500-6932A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14095186 | ||||||
| chr17:14095418
|
G | A | 1 | a0001c0007t0001g0293 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.500-6700G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14095418 | ||||||
| chr17:14095461
|
C | T | 3 | a0002c0006t0001g0307a0002c0006t0001g0308a0002c0006t0001g0309 | 3 | HG00738.hp1 HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.500-6657C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14095461 | ||||||
| chr17:14095884
|
T | C | 1 | a0002c0002t0002g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.500-6234T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14095884 | ||||||
| chr17:14096053
|
G | A | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.500-6065G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096053 | ||||||
| chr17:14096169
|
A | G | 14 | a0001c0001t0003g0154a0001c0001t0004g0111a0001c0003t0002g0100others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.500-5949A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096169 | ||||||
| chr17:14096211
|
A | C | 294 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(291): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.500-5907A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096211 | ||||||
| chr17:14096261
|
T | C | 104 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0028others(101): Show | 107 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.500-5857T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096261 | ||||||
| chr17:14096335
|
A | G | 1 | a0001c0001t0003g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.500-5783A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096335 | ||||||
| chr17:14096375
|
TTTC | T | 11 | a0002c0008t0001g0278a0003c0011t0001g0039a0003c0011t0003g0033others(8): Show | 11 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.500-5740_500-5738d others(5): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14096375 | |||||
| chr17:14096377
|
TC | T | 3 | a0001c0003t0001g0151a0001c0007t0001g0276a0002c0008t0001g0184 | 3 | HG03098.hp1 NA18967.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.500-5740delC | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096377 | ||||||
| chr17:14096378
|
C | T | 1 | a0002c0008t0003g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.500-5740C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096378 | ||||||
| chr17:14096378
|
CT | C | 83 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0154others(80): Show | 85 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.500-5724delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14096378 | |||||
| chr17:14096378
|
CTT | C | 217 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0028others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.500-5725_500-5724d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14096378 | |||||
| chr17:14096380
|
T | C | 14 | a0001c0003t0001g0151a0001c0007t0001g0276a0002c0008t0001g0184others(11): Show | 14 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.500-5738T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096380 | ||||||
| chr17:14096411
|
G | A | 14 | a0001c0001t0003g0154a0001c0001t0004g0111a0001c0003t0002g0100others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.500-5707G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096411 | ||||||
| chr17:14096508
|
A | G | 6 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(3): Show | 6 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-5610A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096508 | ||||||
| chr17:14096520
|
A | T | 5 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-5598A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096520 | ||||||
| chr17:14096675
|
A | T | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.500-5443A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096675 | ||||||
| chr17:14096713
|
G | T | 5 | a0002c0002t0002g0240a0002c0006t0004g0175a0002c0006t0004g0176others(2): Show | 5 | HG00099.hp2 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-5405G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096713 | ||||||
| chr17:14096800
|
C | T | 18 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0001g0094others(15): Show | 18 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.500-5318C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096800 | ||||||
| chr17:14096819
|
T | C | 1 | a0003c0017t0003g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.500-5299T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096819 | ||||||
| chr17:14096908
|
C | T | 1 | a0001c0007t0001g0293 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.500-5210C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096908 | ||||||
| chr17:14097001
|
A | G | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.500-5117A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097001 | ||||||
| chr17:14097045
|
C | A | 1 | a0001c0001t0003g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.500-5073C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097045 | ||||||
| chr17:14097144
|
T | G | 3 | a0002c0002t0002g0240a0002c0006t0004g0192a0002c0006t0004g0241 | 3 | HG01074.hp2 HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.500-4974T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097144 | ||||||
| chr17:14097176
|
A | G | 1 | a0002c0005t0004g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.500-4942A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097176 | ||||||
| chr17:14097291
|
A | G | 2 | a0001c0003t0002g0015a0001c0003t0002g0026 | 2 | HG00438.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.500-4827A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097291 | ||||||
| chr17:14097311
|
CTTTTGGG others(5): Show |
C | 1 | a0002c0005t0003g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.500-4802_500-4791d others(14): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14097311 | |||||
| chr17:14097318
|
GT | G | 82 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.500-4789delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14097318 | |||||
| chr17:14097407
|
A | G | 82 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.500-4711A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097407 | ||||||
| chr17:14097488
|
G | T | 293 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.500-4630G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097488 | ||||||
| chr17:14097677
|
A | G | 16 | a0001c0001t0003g0154a0001c0001t0004g0111a0001c0003t0002g0100others(13): Show | 16 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.500-4441A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097677 | ||||||
| chr17:14097758
|
G | T | 81 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(78): Show | 81 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.500-4360G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097758 | ||||||
| chr17:14097844
|
G | A | 3 | a0001c0003t0001g0148a0001c0003t0001g0151a0003c0017t0003g0036 | 3 | HG04204.hp1 NA18967.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.500-4274G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097844 | ||||||
| chr17:14097940
|
G | A | 38 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(35): Show | 38 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.500-4178G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14097940 | ||||||
| chr17:14098082
|
C | T | 5 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0058others(2): Show | 5 | HG00733.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-4036C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14098082 | ||||||
| chr17:14098096
|
C | A | 38 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(35): Show | 38 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.500-4022C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14098096 | ||||||
| chr17:14098118
|
C | T | 2 | a0001c0004t0003g0105a0001c0004t0003g0167 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.500-4000C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14098118 | ||||||
| chr17:14098165
|
A | G | 3 | a0002c0002t0002g0174a0002c0002t0005g0265a0002c0006t0004g0205 | 3 | HG00597.hp1 NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.500-3953A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14098165 | ||||||
| chr17:14098472
|
G | A | 296 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(293): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.500-3646G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14098472 | ||||||
| chr17:14098693
|
A | G | 6 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(3): Show | 6 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-3425A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14098693 | ||||||
| chr17:14098831
|
C | T | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.500-3287C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14098831 | ||||||
| chr17:14099094
|
C | T | 1 | a0002c0005t0003g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.500-3024C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14099094 | ||||||
| chr17:14099098
|
A | G | 98 | a0001c0001t0004g0117a0001c0003t0001g0032a0001c0003t0001g0148others(95): Show | 98 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.500-3020A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14099098 | ||||||
| chr17:14099497
|
C | T | 1 | a0002c0006t0001g0309 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.500-2621C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14099497 | ||||||
| chr17:14099558
|
C | G | 3 | a0004c0018t0003g0063a0004c0019t0001g0062a0004c0025t0001g0061 | 3 | HG02559.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.500-2560C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14099558 | ||||||
| chr17:14099648
|
A | G | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.500-2470A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14099648 | ||||||
| chr17:14099822
|
T | C | 5 | a0001c0007t0001g0016a0001c0007t0001g0293a0002c0006t0001g0307others(2): Show | 5 | HG00738.hp1 HG01433.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-2296T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14099822 | ||||||
| chr17:14099893
|
C | T | 1 | a0002c0020t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.500-2225C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14099893 | ||||||
| chr17:14099969
|
A | C | 7 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(4): Show | 7 | HG01192.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.500-2149A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14099969 | ||||||
| chr17:14100004
|
A | G | 1 | a0002c0002t0002g0174 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.500-2114A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14100004 | ||||||
| chr17:14100134
|
C | T | 1 | a0003c0009t0007g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.500-1984C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14100134 | ||||||
| chr17:14100613
|
A | G | 15 | a0001c0001t0003g0154a0001c0001t0004g0111a0001c0003t0002g0100others(12): Show | 15 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.500-1505A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14100613 | ||||||
| chr17:14100624
|
C | T | 1 | a0001c0004t0002g0161 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.500-1494C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14100624 | ||||||
| chr17:14100777
|
A | C | 2 | a0001c0001t0003g0099a0001c0001t0003g0145 | 2 | HG01261.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.500-1341A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14100777 | ||||||
| chr17:14100780
|
C | G | 33 | a0001c0003t0005g0122a0001c0003t0005g0123a0001c0004t0014g0126others(30): Show | 35 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.500-1338C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14100780 | ||||||
| chr17:14100832
|
A | AT | 211 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0028others(208): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.500-1285dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 14100832 | |||||
| chr17:14100979
|
G | A | 1 | a0001c0004t0025g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.500-1139G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14100979 | ||||||
| chr17:14100995
|
T | A | 7 | a0001c0001t0001g0120a0001c0001t0005g0159a0002c0005t0001g0305others(4): Show | 7 | HG01192.hp2 HG01952.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.500-1123T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14100995 | ||||||
| chr17:14101100
|
G | T | 1 | a0001c0004t0025g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.500-1018G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101100 | ||||||
| chr17:14101258
|
C | T | 2 | a0001c0004t0002g0073a0001c0004t0002g0077 | 2 | HG01255.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.500-860C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101258 | ||||||
| chr17:14101278
|
T | G | 38 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(35): Show | 38 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.500-840T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101278 | ||||||
| chr17:14101319
|
T | C | 69 | a0001c0001t0001g0120a0001c0001t0003g0001a0001c0001t0003g0028others(66): Show | 70 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.500-799T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101319 | ||||||
| chr17:14101407
|
G | A | 15 | a0001c0001t0003g0154a0001c0001t0004g0111a0001c0003t0002g0100others(12): Show | 15 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.500-711G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101407 | ||||||
| chr17:14101429
|
G | C | 2 | a0003c0017t0004g0084a0003c0017t0004g0085 | 2 | NA18962.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.500-689G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101429 | ||||||
| chr17:14101430
|
C | T | 16 | a0001c0001t0003g0154a0001c0001t0004g0111a0001c0003t0002g0100others(13): Show | 16 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.500-688C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101430 | ||||||
| chr17:14101575
|
C | T | 82 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.500-543C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101575 | ||||||
| chr17:14101607
|
C | T | 3 | a0002c0002t0001g0195a0002c0008t0001g0243a0002c0008t0003g0242 | 3 | HG02486.hp2 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.500-511C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101607 | ||||||
| chr17:14101738
|
G | T | 14 | a0001c0001t0003g0154a0001c0001t0004g0111a0001c0003t0002g0100others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.500-380G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101738 | ||||||
| chr17:14101755
|
G | T | 37 | a0001c0001t0001g0018a0001c0001t0003g0019a0001c0001t0003g0068others(34): Show | 37 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.500-363G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101755 | ||||||
| chr17:14101789
|
T | A | 2 | a0001c0003t0001g0079a0001c0003t0001g0080 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.500-329T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101789 | ||||||
| chr17:14101950
|
A | G | 19 | a0001c0001t0003g0068a0001c0003t0002g0069a0001c0003t0002g0071others(16): Show | 19 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.500-168A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101950 | ||||||
| chr17:14101963
|
T | C | 7 | a0001c0001t0003g0115a0001c0001t0003g0119a0001c0001t0003g0132others(4): Show | 7 | HG02015.hp1 HG02165.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.500-155T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101963 | ||||||
| chr17:14101988
|
C | T | 2 | a0002c0015t0001g0279a0002c0015t0001g0298 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.500-130C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14101988 | ||||||
| chr17:14102056
|
C | T | 307 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.500-62C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14102056 | ||||||
| chr17:14102069
|
T | C | 240 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(237): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.500-49T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14102069 | ||||||
| chr17:14102078
|
C | T | 15 | a0002c0002t0022g0234a0003c0009t0007g0034a0003c0009t0007g0035others(12): Show | 15 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.500-40C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14102078 | ||||||
| chr17:14102330
|
C | CAT | 198 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(195): Show | 200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.624+93_624+94dupAT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14102330 | |||||
| chr17:14102381
|
T | C | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+139T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14102381 | ||||||
| chr17:14102389
|
A | G | 39 | a0001c0001t0019g0277a0001c0003t0001g0078a0001c0003t0002g0007others(36): Show | 39 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+147A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14102389 | ||||||
| chr17:14102409
|
T | G | 22 | a0001c0004t0001g0286a0002c0002t0001g0002a0002c0002t0001g0171others(19): Show | 23 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.624+167T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14102409 | ||||||
| chr17:14102632
|
G | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.624+390G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14102632 | ||||||
| chr17:14102678
|
T | C | 1 | a0002c0008t0003g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.624+436T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14102678 | ||||||
| chr17:14102818
|
C | T | 166 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0157others(163): Show | 168 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.624+576C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14102818 | ||||||
| chr17:14102825
|
C | T | 151 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(148): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.624+583C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14102825 | ||||||
| chr17:14102835
|
G | A | 28 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(25): Show | 28 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.624+593G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14102835 | ||||||
| chr17:14103035
|
A | G | 1 | a0002c0005t0004g0280 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.624+793A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14103035 | ||||||
| chr17:14103108
|
G | T | 120 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0157others(117): Show | 121 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.624+866G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14103108 | ||||||
| chr17:14103309
|
G | A | 1 | a0001c0001t0004g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.624+1067G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14103309 | ||||||
| chr17:14103699
|
T | A | 1 | a0003c0011t0009g0043 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.624+1457T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14103699 | ||||||
| chr17:14103728
|
A | G | 2 | a0001c0003t0002g0015a0001c0003t0002g0026 | 2 | HG00438.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.624+1486A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14103728 | ||||||
| chr17:14103828
|
T | C | 28 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(25): Show | 28 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.624+1586T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14103828 | ||||||
| chr17:14104106
|
C | A | 1 | a0001c0001t0003g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.624+1864C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14104106 | ||||||
| chr17:14104543
|
C | T | 166 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0157others(163): Show | 168 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.624+2301C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14104543 | ||||||
| chr17:14104585
|
A | G | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+2343A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14104585 | ||||||
| chr17:14104610
|
C | T | 2 | a0001c0007t0003g0124a0001c0007t0003g0144 | 2 | HG00673.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.624+2368C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14104610 | ||||||
| chr17:14104894
|
C | T | 310 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(307): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.624+2652C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14104894 | ||||||
| chr17:14104909
|
T | C | 1 | a0003c0011t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.624+2667T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14104909 | ||||||
| chr17:14105098
|
A | G | 2 | a0001c0003t0005g0122a0001c0003t0005g0123 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.624+2856A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105098 | ||||||
| chr17:14105367
|
A | T | 5 | a0001c0004t0001g0168a0001c0004t0001g0169a0001c0007t0001g0276others(2): Show | 5 | HG02559.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+3125A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105367 | ||||||
| chr17:14105472
|
A | G | 1 | a0001c0001t0004g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.624+3230A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105472 | ||||||
| chr17:14105545
|
G | A | 1 | a0002c0008t0001g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.624+3303G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105545 | ||||||
| chr17:14105550
|
T | A | 34 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(31): Show | 34 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.624+3308T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105550 | ||||||
| chr17:14105619
|
A | G | 4 | a0001c0007t0001g0016a0002c0006t0001g0307a0002c0006t0001g0308others(1): Show | 4 | HG00738.hp1 HG01433.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+3377A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105619 | ||||||
| chr17:14105677
|
A | G | 7 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(4): Show | 7 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+3435A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105677 | ||||||
| chr17:14105780
|
G | T | 2 | a0001c0004t0002g0073a0001c0004t0002g0077 | 2 | HG01255.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.624+3538G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105780 | ||||||
| chr17:14105859
|
A | T | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+3617A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105859 | ||||||
| chr17:14105892
|
CAT | C | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.624+3653_624+3654d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14105892 | |||||
| chr17:14105996
|
T | C | 1 | a0001c0001t0003g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.624+3754T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14105996 | ||||||
| chr17:14106019
|
TTG | T | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+3779_624+3780d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14106019 | |||||
| chr17:14106021
|
GT | G | 303 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.624+3788delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14106021 | |||||
| chr17:14106152
|
T | G | 151 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(148): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.624+3910T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14106152 | ||||||
| chr17:14106206
|
G | C | 2 | a0001c0001t0003g0099a0001c0001t0003g0145 | 2 | HG01261.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.624+3964G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14106206 | ||||||
| chr17:14106549
|
A | G | 25 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0110others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.624+4307A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14106549 | ||||||
| chr17:14106655
|
G | C | 1 | a0003c0009t0006g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.624+4413G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14106655 | ||||||
| chr17:14106897
|
C | A | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+4655C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14106897 | ||||||
| chr17:14107078
|
C | A | 1 | a0002c0008t0001g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.624+4836C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107078 | ||||||
| chr17:14107145
|
T | A | 2 | a0001c0004t0003g0105a0001c0004t0003g0167 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.624+4903T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107145 | ||||||
| chr17:14107146
|
T | C | 2 | a0001c0004t0003g0105a0001c0004t0003g0167 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.624+4904T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107146 | ||||||
| chr17:14107163
|
G | T | 1 | a0002c0006t0004g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.624+4921G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107163 | ||||||
| chr17:14107223
|
A | AT | 160 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0157others(157): Show | 161 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.624+4991dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14107223 | |||||
| chr17:14107239
|
A | T | 1 | a0004c0019t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.624+4997A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107239 | ||||||
| chr17:14107283
|
G | A | 1 | a0002c0006t0004g0193 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.624+5041G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107283 | ||||||
| chr17:14107289
|
C | G | 3 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0173 | 3 | HG02109.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.624+5047C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107289 | ||||||
| chr17:14107414
|
A | T | 1 | a0001c0001t0003g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.624+5172A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107414 | ||||||
| chr17:14107431
|
GCTATT | G | 7 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(4): Show | 7 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+5191_624+5195d others(7): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14107431 | |||||
| chr17:14107492
|
T | G | 1 | a0002c0005t0004g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.624+5250T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107492 | ||||||
| chr17:14107670
|
T | TAC | 25 | a0001c0001t0005g0013a0001c0003t0006g0102a0001c0003t0006g0112others(22): Show | 25 | HG00438.hp2 HG02027.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.624+5451_624+5452d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14107670 | |||||
| chr17:14107670
|
TAC | T | 93 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(90): Show | 95 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.624+5451_624+5452d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14107670 | |||||
| chr17:14107724
|
C | T | 1 | a0001c0001t0004g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.624+5482C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14107724 | ||||||
| chr17:14107939
|
AGTTCTGC others(31109): Show |
A | 1 | a0002c0005t0003g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.624+5701_625-20819 others(3): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14107939 | |||||
| chr17:14108013
|
C | A | 3 | a0001c0003t0002g0069a0001c0003t0002g0071a0001c0004t0002g0070 | 3 | HG00597.hp2 HG02083.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.624+5771C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14108013 | ||||||
| chr17:14108195
|
G | A | 1 | a0004c0019t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.624+5953G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14108195 | ||||||
| chr17:14108306
|
A | G | 18 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(15): Show | 18 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.624+6064A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14108306 | ||||||
| chr17:14108620
|
CAT | C | 18 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(15): Show | 18 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.624+6379_624+6380d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14108620 | ||||||
| chr17:14108676
|
TA | T | 316 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.624+6441delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14108676 | |||||
| chr17:14108849
|
G | A | 1 | a0002c0005t0004g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.624+6607G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14108849 | ||||||
| chr17:14109200
|
T | C | 34 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(31): Show | 34 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.624+6958T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14109200 | ||||||
| chr17:14109371
|
C | A | 3 | a0006c0016t0012g0003a0006c0016t0012g0202a0008c0026t0001g0056 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+7129C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14109371 | ||||||
| chr17:14109436
|
A | C | 2 | a0002c0002t0002g0210a0002c0002t0003g0211 | 2 | HG01167.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.624+7194A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14109436 | ||||||
| chr17:14109456
|
T | A | 2 | a0001c0004t0014g0126a0001c0004t0014g0149 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.624+7214T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14109456 | ||||||
| chr17:14109705
|
G | C | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.624+7463G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14109705 | ||||||
| chr17:14110004
|
G | C | 1 | a0002c0005t0005g0252 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.624+7762G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14110004 | ||||||
| chr17:14110027
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(6): Show | 9 | HG00735.hp1 HG01192.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.624+7785G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14110027 | ||||||
| chr17:14110095
|
T | C | 2 | a0001c0003t0002g0006a0001c0004t0002g0017 | 2 | NA18950.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.624+7853T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14110095 | ||||||
| chr17:14110481
|
A | G | 2 | a0002c0008t0003g0242a0002c0008t0003g0302 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.624+8239A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14110481 | ||||||
| chr17:14110780
|
G | A | 1 | a0001c0003t0002g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.624+8538G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14110780 | ||||||
| chr17:14110817
|
T | C | 162 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0157others(159): Show | 163 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.624+8575T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14110817 | ||||||
| chr17:14110836
|
ACT | A | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.624+8599_624+8600d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14110836 | |||||
| chr17:14110877
|
T | C | 35 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(32): Show | 35 | HG00438.hp1 HG00597.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.624+8635T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14110877 | ||||||
| chr17:14111194
|
C | G | 79 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(76): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.624+8952C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14111194 | ||||||
| chr17:14111295
|
T | G | 18 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(15): Show | 18 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.624+9053T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14111295 | ||||||
| chr17:14111703
|
T | C | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+9461T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14111703 | ||||||
| chr17:14111744
|
G | A | 20 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0001t0011g0312others(17): Show | 20 | HG00738.hp1 HG01433.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.624+9502G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14111744 | ||||||
| chr17:14112161
|
C | T | 9 | a0001c0007t0001g0016a0001c0007t0001g0293a0001c0012t0001g0294others(6): Show | 9 | HG00738.hp1 HG01433.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.624+9919C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14112161 | ||||||
| chr17:14112348
|
C | T | 1 | a0001c0007t0003g0144 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.624+10106C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14112348 | ||||||
| chr17:14112488
|
T | G | 20 | a0001c0004t0001g0286a0002c0002t0001g0002a0002c0002t0001g0171others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.624+10246T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14112488 | ||||||
| chr17:14112625
|
A | T | 316 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.624+10383A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14112625 | ||||||
| chr17:14112760
|
C | A | 1 | a0003c0010t0006g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.624+10518C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14112760 | ||||||
| chr17:14112943
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+10701G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14112943 | ||||||
| chr17:14112996
|
A | G | 1 | a0002c0005t0004g0230 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.624+10754A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14112996 | ||||||
| chr17:14113018
|
C | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.624+10776C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113018 | ||||||
| chr17:14113193
|
C | T | 25 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0110others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.624+10951C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113193 | ||||||
| chr17:14113204
|
A | G | 1 | a0010c0021t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+10962A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113204 | ||||||
| chr17:14113224
|
A | G | 1 | a0001c0003t0002g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.624+10982A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113224 | ||||||
| chr17:14113376
|
T | A | 1 | a0002c0002t0001g0183 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.624+11134T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113376 | ||||||
| chr17:14113383
|
C | T | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.624+11141C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113383 | ||||||
| chr17:14113517
|
C | G | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.624+11275C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113517 | ||||||
| chr17:14113685
|
G | A | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+11443G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113685 | ||||||
| chr17:14113720
|
A | G | 1 | a0001c0001t0003g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.624+11478A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14113720 | ||||||
| chr17:14114529
|
T | A | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.624+12287T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14114529 | ||||||
| chr17:14114728
|
C | T | 3 | a0001c0003t0001g0032a0002c0005t0003g0187a0002c0005t0003g0208 | 3 | HG03669.hp2 HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.624+12486C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14114728 | ||||||
| chr17:14114943
|
A | G | 2 | a0001c0003t0002g0288a0001c0003t0002g0315 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.624+12701A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14114943 | ||||||
| chr17:14114974
|
C | T | 1 | a0001c0003t0001g0079 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.624+12732C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14114974 | ||||||
| chr17:14115228
|
A | G | 3 | a0002c0008t0001g0271a0002c0008t0001g0272a0002c0008t0001g0273 | 3 | HG02622.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.624+12986A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14115228 | ||||||
| chr17:14115236
|
C | T | 1 | a0001c0003t0001g0079 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.624+12994C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14115236 | ||||||
| chr17:14115606
|
G | A | 13 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0028others(10): Show | 13 | HG00735.hp1 HG01099.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.624+13364G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14115606 | ||||||
| chr17:14115634
|
G | A | 1 | a0002c0006t0004g0258 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.624+13392G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14115634 | ||||||
| chr17:14115659
|
G | A | 1 | a0001c0004t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.624+13417G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14115659 | ||||||
| chr17:14115775
|
A | G | 1 | a0003c0010t0018g0093 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.624+13533A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14115775 | ||||||
| chr17:14115951
|
C | T | 7 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(4): Show | 7 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+13709C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14115951 | ||||||
| chr17:14115966
|
G | A | 1 | a0002c0006t0004g0254 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.624+13724G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14115966 | ||||||
| chr17:14116004
|
C | T | 10 | a0001c0007t0001g0016a0001c0007t0001g0293a0001c0012t0001g0294others(7): Show | 10 | HG00738.hp1 HG01433.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+13762C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116004 | ||||||
| chr17:14116071
|
A | G | 36 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0110others(33): Show | 36 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.624+13829A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116071 | ||||||
| chr17:14116097
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+13855G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116097 | ||||||
| chr17:14116260
|
A | C | 152 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0157others(149): Show | 153 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.624+14018A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116260 | ||||||
| chr17:14116262
|
C | T | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.624+14020C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116262 | ||||||
| chr17:14116272
|
A | C | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.624+14030A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116272 | ||||||
| chr17:14116601
|
T | C | 1 | a0001c0001t0003g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.624+14359T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116601 | ||||||
| chr17:14116654
|
T | C | 2 | a0001c0003t0001g0150a0001c0003t0002g0006 | 2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.624+14412T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116654 | ||||||
| chr17:14116654
|
T | TAC | 110 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0157others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.624+14433_624+1443 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14116654 | |||||
| chr17:14116654
|
T | TACAC | 64 | a0001c0001t0003g0019a0001c0001t0003g0028a0001c0001t0003g0029others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.624+14431_624+1443 others(8): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14116654 | |||||
| chr17:14116654
|
TACAC | T | 36 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(33): Show | 36 | HG00438.hp1 HG00597.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.624+14431_624+1443 others(8): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14116654 | |||||
| chr17:14116749
|
T | G | 65 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(62): Show | 66 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.624+14507T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116749 | ||||||
| chr17:14116845
|
A | G | 1 | a0001c0007t0004g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.624+14603A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116845 | ||||||
| chr17:14117280
|
A | G | 3 | a0006c0016t0012g0003a0006c0016t0012g0202a0008c0026t0001g0056 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+15038A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117280 | ||||||
| chr17:14117441
|
T | G | 6 | a0003c0011t0001g0039a0003c0011t0003g0033a0003c0011t0003g0042others(3): Show | 6 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+15199T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117441 | ||||||
| chr17:14117607
|
G | A | 1 | a0002c0006t0004g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.624+15365G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117607 | ||||||
| chr17:14117800
|
A | G | 1 | a0006c0016t0012g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.624+15558A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117800 | ||||||
| chr17:14117827
|
G | A | 1 | a0001c0003t0002g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.624+15585G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117827 | ||||||
| chr17:14117941
|
G | C | 1 | a0001c0003t0020g0005 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.624+15699G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117941 | ||||||
| chr17:14117963
|
C | T | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.624+15721C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117963 | ||||||
| chr17:14117964
|
G | A | 7 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(4): Show | 7 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+15722G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117964 | ||||||
| chr17:14117972
|
G | C | 105 | a0001c0001t0003g0125a0001c0001t0004g0111a0001c0001t0004g0117others(102): Show | 106 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.624+15730G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14117972 | ||||||
| chr17:14118099
|
T | C | 38 | a0001c0003t0002g0065a0001c0003t0002g0067a0001c0003t0002g0100others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.624+15857T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14118099 | ||||||
| chr17:14118259
|
G | A | 3 | a0002c0005t0004g0191a0002c0005t0004g0235a0002c0005t0004g0236 | 3 | NA18946.hp2 NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.624+16017G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14118259 | ||||||
| chr17:14118420
|
G | T | 1 | a0002c0002t0001g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.624+16178G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14118420 | ||||||
| chr17:14118489
|
A | G | 1 | a0002c0008t0001g0263 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.624+16247A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14118489 | ||||||
| chr17:14118543
|
G | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(8): Show | 12 | HG00735.hp1 HG01192.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+16301G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14118543 | ||||||
| chr17:14118695
|
C | G | 3 | a0001c0003t0001g0079a0002c0002t0001g0171a0002c0002t0001g0172 | 3 | HG02109.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.624+16453C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14118695 | ||||||
| chr17:14119084
|
T | C | 45 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(42): Show | 46 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.624+16842T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119084 | ||||||
| chr17:14119125
|
G | A | 3 | a0001c0004t0001g0286a0002c0002t0001g0213a0002c0002t0001g0214 | 3 | HG02572.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.624+16883G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119125 | ||||||
| chr17:14119335
|
C | A | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.624+17093C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119335 | ||||||
| chr17:14119391
|
A | C | 1 | a0002c0002t0001g0002 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.624+17149A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119391 | ||||||
| chr17:14119391
|
A | G | 2 | a0001c0003t0002g0065a0001c0003t0002g0067 | 2 | HG00621.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.624+17149A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119391 | ||||||
| chr17:14119456
|
G | T | 3 | a0001c0004t0003g0105a0001c0004t0003g0167a0010c0021t0001g0185 | 3 | HG02145.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624+17214G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119456 | ||||||
| chr17:14119696
|
T | G | 5 | a0002c0005t0005g0198a0002c0005t0008g0246a0004c0018t0001g0059others(2): Show | 5 | HG02615.hp2 HG02886.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+17454T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119696 | ||||||
| chr17:14119699
|
G | A | 2 | a0001c0004t0014g0126a0001c0004t0014g0149 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.624+17457G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119699 | ||||||
| chr17:14119745
|
C | T | 16 | a0001c0001t0003g0001a0001c0001t0003g0115a0001c0001t0003g0119others(13): Show | 17 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.624+17503C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119745 | ||||||
| chr17:14119798
|
C | A | 153 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(150): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.624+17556C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119798 | ||||||
| chr17:14119956
|
A | G | 1 | a0004c0019t0001g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.624+17714A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14119956 | ||||||
| chr17:14120031
|
G | C | 3 | a0003c0011t0003g0033a0003c0011t0003g0042a0009c0028t0003g0041 | 3 | HG02080.hp1 HG02523.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.624+17789G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120031 | ||||||
| chr17:14120041
|
A | C | 1 | a0001c0001t0003g0146 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.624+17799A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120041 | ||||||
| chr17:14120464
|
C | T | 2 | a0001c0004t0002g0020a0002c0002t0001g0183 | 2 | NA18939.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.624+18222C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120464 | ||||||
| chr17:14120523
|
A | G | 5 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(2): Show | 5 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.624+18281A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120523 | ||||||
| chr17:14120749
|
T | A | 311 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(308): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.624+18507T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120749 | ||||||
| chr17:14120845
|
A | G | 1 | a0001c0007t0008g0114 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.624+18603A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120845 | ||||||
| chr17:14120911
|
G | A | 157 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(154): Show | 158 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.624+18669G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120911 | ||||||
| chr17:14120962
|
T | C | 5 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.624+18720T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120962 | ||||||
| chr17:14120966
|
C | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.624+18724C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14120966 | ||||||
| chr17:14121162
|
T | A | 153 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(150): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.624+18920T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121162 | ||||||
| chr17:14121217
|
T | A | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.624+18975T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121217 | ||||||
| chr17:14121304
|
G | C | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.624+19062G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121304 | ||||||
| chr17:14121392
|
C | T | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+19150C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121392 | ||||||
| chr17:14121406
|
C | G | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+19164C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121406 | ||||||
| chr17:14121487
|
A | G | 159 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(156): Show | 160 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.624+19245A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121487 | ||||||
| chr17:14121504
|
G | A | 157 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(154): Show | 158 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.624+19262G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121504 | ||||||
| chr17:14121572
|
T | G | 2 | a0001c0001t0003g0099a0001c0001t0003g0145 | 2 | HG01261.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.624+19330T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121572 | ||||||
| chr17:14121573
|
C | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.624+19331C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121573 | ||||||
| chr17:14121669
|
C | T | 9 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(6): Show | 9 | HG01109.hp2 HG01192.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+19427C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121669 | ||||||
| chr17:14121900
|
C | T | 61 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.624+19658C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14121900 | ||||||
| chr17:14122129
|
G | A | 1 | a0002c0008t0001g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.624+19887G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14122129 | ||||||
| chr17:14122136
|
C | T | 3 | a0002c0002t0002g0210a0002c0002t0002g0253a0002c0002t0003g0211 | 3 | HG01167.hp2 HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.624+19894C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14122136 | ||||||
| chr17:14122418
|
T | G | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.624+20176T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14122418 | ||||||
| chr17:14122490
|
C | T | 26 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.624+20248C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14122490 | ||||||
| chr17:14122505
|
T | C | 159 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(156): Show | 160 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.624+20263T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14122505 | ||||||
| chr17:14122506
|
A | G | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.624+20264A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14122506 | ||||||
| chr17:14123319
|
C | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.624+21077C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14123319 | ||||||
| chr17:14123331
|
C | T | 28 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(25): Show | 28 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.624+21089C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14123331 | ||||||
| chr17:14123498
|
C | T | 193 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(190): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.624+21256C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14123498 | ||||||
| chr17:14123615
|
T | C | 1 | a0001c0003t0002g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.624+21373T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14123615 | ||||||
| chr17:14123674
|
G | A | 1 | a0003c0009t0006g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.624+21432G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14123674 | ||||||
| chr17:14123698
|
G | A | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.624+21456G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14123698 | ||||||
| chr17:14123826
|
G | A | 1 | a0004c0018t0001g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.624+21584G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14123826 | ||||||
| chr17:14123933
|
AT | A | 37 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(34): Show | 37 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.624+21700delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14123933 | |||||
| chr17:14124057
|
A | G | 1 | a0002c0005t0004g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.624+21815A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14124057 | ||||||
| chr17:14124077
|
G | A | 3 | a0001c0007t0004g0024a0001c0007t0004g0220a0002c0006t0004g0254 | 3 | HG01258.hp1 HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.624+21835G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14124077 | ||||||
| chr17:14124188
|
G | C | 1 | a0001c0003t0002g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.624+21946G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14124188 | ||||||
| chr17:14124602
|
T | A | 1 | a0001c0007t0004g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.624+22360T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14124602 | ||||||
| chr17:14124752
|
A | G | 1 | a0002c0002t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.624+22510A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14124752 | ||||||
| chr17:14124934
|
A | G | 1 | a0004c0018t0003g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.624+22692A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14124934 | ||||||
| chr17:14124983
|
T | C | 1 | a0002c0002t0001g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.624+22741T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14124983 | ||||||
| chr17:14125009
|
C | A | 6 | a0002c0006t0009g0259a0003c0011t0001g0039a0003c0011t0003g0033others(3): Show | 6 | HG00280.hp2 HG01081.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+22767C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14125009 | ||||||
| chr17:14125047
|
G | A | 1 | a0003c0017t0003g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.624+22805G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14125047 | ||||||
| chr17:14125241
|
C | T | 3 | a0002c0005t0004g0191a0002c0005t0004g0235a0002c0005t0004g0236 | 3 | NA18946.hp2 NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.624+22999C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14125241 | ||||||
| chr17:14125350
|
T | C | 262 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(259): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.624+23108T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14125350 | ||||||
| chr17:14125351
|
G | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+23109G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14125351 | ||||||
| chr17:14125428
|
T | A | 1 | a0003c0010t0006g0083 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.624+23186T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14125428 | ||||||
| chr17:14125625
|
G | A | 1 | a0001c0004t0025g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.624+23383G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14125625 | ||||||
| chr17:14125986
|
G | A | 2 | a0002c0015t0001g0279a0002c0015t0001g0298 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.624+23744G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14125986 | ||||||
| chr17:14126009
|
C | T | 3 | a0002c0002t0001g0262a0002c0008t0001g0184a0003c0010t0001g0082 | 3 | NA18969.hp1 NA19075.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.624+23767C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126009 | ||||||
| chr17:14126057
|
C | A | 1 | a0002c0008t0001g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.624+23815C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126057 | ||||||
| chr17:14126300
|
A | G | 1 | a0001c0004t0002g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.624+24058A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126300 | ||||||
| chr17:14126321
|
G | A | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.624+24079G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126321 | ||||||
| chr17:14126411
|
A | G | 1 | a0001c0001t0003g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.624+24169A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126411 | ||||||
| chr17:14126418
|
A | T | 1 | a0001c0007t0008g0114 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.624+24176A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126418 | ||||||
| chr17:14126665
|
C | T | 19 | a0001c0004t0001g0286a0002c0002t0001g0002a0002c0002t0001g0173others(16): Show | 20 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.624+24423C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126665 | ||||||
| chr17:14126900
|
T | G | 2 | a0002c0005t0004g0231a0002c0006t0004g0232 | 2 | HG02155.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.624+24658T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126900 | ||||||
| chr17:14126965
|
A | ATAGT | 298 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(295): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.624+24724_624+2472 others(8): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14126965 | |||||
| chr17:14126965
|
A | T | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.624+24723A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14126965 | ||||||
| chr17:14127099
|
G | A | 17 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(14): Show | 17 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(14): Show |
intron_variant | MODIFIER | c.624+24857G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127099 | ||||||
| chr17:14127158
|
C | T | 301 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.624+24916C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127158 | ||||||
| chr17:14127225
|
T | G | 9 | a0003c0010t0003g0095a0003c0010t0006g0083a0003c0010t0006g0086others(6): Show | 9 | NA18612.hp2 NA18944.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+24983T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127225 | ||||||
| chr17:14127278
|
T | C | 1 | a0002c0008t0001g0221 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.624+25036T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127278 | ||||||
| chr17:14127335
|
T | A | 153 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(150): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.624+25093T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127335 | ||||||
| chr17:14127356
|
T | C | 1 | a0001c0007t0003g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.624+25114T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127356 | ||||||
| chr17:14127563
|
A | G | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+25321A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127563 | ||||||
| chr17:14127714
|
T | C | 1 | a0004c0025t0001g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.624+25472T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127714 | ||||||
| chr17:14127865
|
G | A | 1 | a0002c0005t0004g0182 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.624+25623G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127865 | ||||||
| chr17:14127898
|
T | C | 1 | a0002c0002t0022g0234 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.624+25656T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14127898 | ||||||
| chr17:14127927
|
A | ATG | 12 | a0001c0001t0003g0147a0001c0003t0001g0078a0001c0003t0002g0008others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+25722_624+2572 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14127927 | |||||
| chr17:14127927
|
A | ATGTG | 29 | a0001c0001t0005g0013a0001c0003t0002g0007a0001c0003t0002g0009others(26): Show | 29 | HG01109.hp2 HG01934.hp1 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.624+25720_624+2572 others(8): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14127927 | |||||
| chr17:14127927
|
A | ATGTGTG | 3 | a0001c0003t0002g0288a0002c0006t0008g0274a0002c0008t0002g0255 | 3 | HG00323.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.624+25718_624+2572 others(10): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14127927 | |||||
| chr17:14127927
|
ATG | A | 145 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.624+25722_624+2572 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14127927 | |||||
| chr17:14127927
|
ATGTG | A | 37 | a0001c0001t0004g0111a0001c0003t0006g0102a0001c0003t0006g0112others(34): Show | 37 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.624+25720_624+2572 others(8): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14127927 | |||||
| chr17:14127927
|
ATGTGTG | A | 34 | a0001c0001t0004g0157a0001c0003t0002g0015a0001c0003t0002g0026others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.624+25718_624+2572 others(10): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14127927 | |||||
| chr17:14127927
|
ATGTGTGT others(1): Show |
A | 7 | a0001c0004t0003g0105a0001c0004t0003g0167a0001c0007t0004g0162others(4): Show | 7 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+25716_624+2572 others(12): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14127927 | |||||
| chr17:14128073
|
G | A | 33 | a0001c0003t0006g0102a0001c0003t0006g0112a0002c0006t0009g0259others(30): Show | 33 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.624+25831G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128073 | ||||||
| chr17:14128182
|
C | G | 1 | a0002c0002t0002g0179 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.624+25940C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128182 | ||||||
| chr17:14128308
|
A | G | 1 | a0002c0002t0002g0179 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.624+26066A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128308 | ||||||
| chr17:14128506
|
T | C | 2 | a0001c0001t0003g0104a0001c0001t0003g0125 | 2 | NA18964.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.624+26264T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128506 | ||||||
| chr17:14128784
|
C | T | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+26542C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128784 | ||||||
| chr17:14128808
|
C | A | 3 | a0001c0003t0002g0069a0001c0003t0002g0071a0001c0004t0002g0070 | 3 | HG00597.hp2 HG02083.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.624+26566C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128808 | ||||||
| chr17:14128827
|
A | G | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+26585A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128827 | ||||||
| chr17:14128876
|
G | T | 6 | a0002c0006t0009g0259a0003c0011t0001g0039a0003c0011t0003g0033others(3): Show | 6 | HG00280.hp2 HG01081.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+26634G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128876 | ||||||
| chr17:14128884
|
G | A | 1 | a0004c0019t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.624+26642G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128884 | ||||||
| chr17:14128893
|
C | T | 2 | a0001c0003t0005g0122a0001c0003t0005g0123 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.624+26651C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128893 | ||||||
| chr17:14128898
|
G | A | 4 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(1): Show | 4 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+26656G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128898 | ||||||
| chr17:14128909
|
C | T | 1 | a0001c0023t0001g0163 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.624+26667C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128909 | ||||||
| chr17:14128994
|
C | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.624+26752C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14128994 | ||||||
| chr17:14129147
|
A | AT | 12 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(9): Show | 12 | HG00733.hp2 HG00735.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+26922dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14129147 | |||||
| chr17:14129147
|
AT | A | 46 | a0001c0001t0003g0135a0001c0001t0003g0146a0001c0003t0002g0015others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.624+26922delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14129147 | |||||
| chr17:14129425
|
T | G | 5 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(2): Show | 5 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.624+27183T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14129425 | ||||||
| chr17:14129594
|
A | G | 2 | a0001c0003t0005g0122a0001c0003t0005g0123 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.624+27352A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14129594 | ||||||
| chr17:14129617
|
C | G | 2 | a0001c0004t0002g0160a0003c0029t0002g0047 | 2 | HG00733.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.624+27375C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14129617 | ||||||
| chr17:14129758
|
A | T | 1 | a0002c0005t0005g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.624+27516A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14129758 | ||||||
| chr17:14129919
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.624+27677G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14129919 | ||||||
| chr17:14129930
|
T | C | 1 | a0001c0001t0003g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.624+27688T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14129930 | ||||||
| chr17:14130099
|
C | T | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.624+27857C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130099 | ||||||
| chr17:14130532
|
T | TC | 314 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.624+28290_624+2829 others(5): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130532 | ||||||
| chr17:14130647
|
C | T | 48 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.624+28405C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130647 | ||||||
| chr17:14130722
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.624+28480G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130722 | ||||||
| chr17:14130813
|
T | C | 6 | a0002c0006t0009g0259a0003c0011t0001g0039a0003c0011t0003g0033others(3): Show | 6 | HG00280.hp2 HG01081.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+28571T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130813 | ||||||
| chr17:14130846
|
C | T | 33 | a0001c0003t0006g0102a0001c0003t0006g0112a0002c0006t0009g0259others(30): Show | 33 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.624+28604C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130846 | ||||||
| chr17:14130847
|
G | A | 33 | a0001c0003t0006g0102a0001c0003t0006g0112a0002c0006t0009g0259others(30): Show | 33 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.624+28605G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130847 | ||||||
| chr17:14130889
|
G | A | 104 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(101): Show | 105 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.624+28647G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130889 | ||||||
| chr17:14130904
|
C | T | 1 | a0002c0002t0002g0216 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.624+28662C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14130904 | ||||||
| chr17:14131184
|
T | A | 314 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.625-28693T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14131184 | ||||||
| chr17:14131357
|
A | T | 1 | a0004c0018t0003g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.625-28520A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14131357 | ||||||
| chr17:14131873
|
A | G | 28 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(25): Show | 28 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.625-28004A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14131873 | ||||||
| chr17:14131919
|
A | G | 1 | a0002c0002t0002g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.625-27958A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14131919 | ||||||
| chr17:14131997
|
C | T | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-27880C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14131997 | ||||||
| chr17:14131998
|
A | G | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.625-27879A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14131998 | ||||||
| chr17:14132103
|
C | G | 33 | a0001c0003t0006g0102a0001c0003t0006g0112a0002c0006t0009g0259others(30): Show | 33 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.625-27774C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132103 | ||||||
| chr17:14132153
|
G | A | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-27724G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132153 | ||||||
| chr17:14132190
|
T | G | 1 | a0002c0005t0004g0244 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.625-27687T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132190 | ||||||
| chr17:14132199
|
A | G | 2 | a0002c0015t0001g0279a0002c0015t0001g0298 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.625-27678A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132199 | ||||||
| chr17:14132247
|
C | G | 1 | a0002c0006t0005g0303 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.625-27630C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132247 | ||||||
| chr17:14132287
|
A | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-27590A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132287 | ||||||
| chr17:14132410
|
G | A | 26 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.625-27467G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132410 | ||||||
| chr17:14132417
|
T | A | 56 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(53): Show | 57 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.625-27460T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132417 | ||||||
| chr17:14132434
|
A | G | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-27443A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132434 | ||||||
| chr17:14132466
|
C | T | 1 | a0011c0022t0002g0004 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.625-27411C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132466 | ||||||
| chr17:14132485
|
C | G | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-27392C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132485 | ||||||
| chr17:14132508
|
G | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-27369G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132508 | ||||||
| chr17:14132533
|
T | C | 1 | a0001c0007t0004g0220 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.625-27344T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132533 | ||||||
| chr17:14132803
|
T | C | 5 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(2): Show | 5 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-27074T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132803 | ||||||
| chr17:14132919
|
T | A | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-26958T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132919 | ||||||
| chr17:14132984
|
A | G | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-26893A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14132984 | ||||||
| chr17:14133396
|
T | C | 2 | a0001c0004t0002g0020a0002c0002t0001g0183 | 2 | NA18939.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.625-26481T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14133396 | ||||||
| chr17:14133509
|
T | A | 14 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0001t0019g0277others(11): Show | 14 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-26368T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14133509 | ||||||
| chr17:14133665
|
G | A | 1 | a0003c0009t0007g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.625-26212G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14133665 | ||||||
| chr17:14133829
|
A | T | 1 | a0001c0007t0005g0128 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.625-26048A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14133829 | ||||||
| chr17:14133880
|
A | C | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.625-25997A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14133880 | ||||||
| chr17:14133925
|
T | A | 2 | a0002c0006t0009g0259a0003c0011t0001g0039 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.625-25952T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14133925 | ||||||
| chr17:14133991
|
G | A | 58 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(55): Show | 59 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.625-25886G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14133991 | ||||||
| chr17:14134154
|
G | A | 60 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.625-25723G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134154 | ||||||
| chr17:14134225
|
T | G | 14 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0001t0019g0277others(11): Show | 14 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-25652T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134225 | ||||||
| chr17:14134351
|
G | A | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-25526G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134351 | ||||||
| chr17:14134438
|
C | A | 1 | a0001c0001t0003g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.625-25439C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134438 | ||||||
| chr17:14134481
|
C | T | 1 | a0002c0008t0001g0181 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.625-25396C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134481 | ||||||
| chr17:14134593
|
A | G | 14 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0001t0019g0277others(11): Show | 14 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-25284A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134593 | ||||||
| chr17:14134736
|
A | G | 1 | a0002c0005t0004g0186 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.625-25141A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134736 | ||||||
| chr17:14134765
|
T | A | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.625-25112T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134765 | ||||||
| chr17:14134776
|
G | GT | 6 | a0001c0001t0003g0170a0002c0005t0004g0244a0002c0006t0003g0217others(3): Show | 6 | HG00408.hp2 HG00621.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.625-25088dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14134776 | |||||
| chr17:14134780
|
T | G | 1 | a0004c0019t0001g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.625-25097T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134780 | ||||||
| chr17:14134922
|
C | A | 13 | a0001c0001t0005g0290a0001c0001t0019g0277a0001c0007t0001g0016others(10): Show | 13 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.625-24955C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134922 | ||||||
| chr17:14134982
|
G | A | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-24895G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14134982 | ||||||
| chr17:14135033
|
G | A | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-24844G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135033 | ||||||
| chr17:14135294
|
T | C | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-24583T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135294 | ||||||
| chr17:14135422
|
G | A | 17 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(14): Show | 17 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(14): Show |
intron_variant | MODIFIER | c.625-24455G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135422 | ||||||
| chr17:14135596
|
G | A | 9 | a0001c0001t0005g0290a0001c0007t0001g0016a0001c0007t0001g0276others(6): Show | 9 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.625-24281G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135596 | ||||||
| chr17:14135599
|
G | T | 39 | a0001c0003t0006g0102a0001c0003t0006g0112a0001c0004t0003g0105others(36): Show | 39 | HG00280.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.625-24278G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135599 | ||||||
| chr17:14135688
|
A | T | 1 | a0001c0001t0003g0146 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.625-24189A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135688 | ||||||
| chr17:14135762
|
A | G | 33 | a0001c0003t0006g0102a0001c0003t0006g0112a0002c0006t0009g0259others(30): Show | 33 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.625-24115A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135762 | ||||||
| chr17:14135768
|
C | T | 2 | a0002c0002t0002g0256a0002c0002t0002g0257 | 2 | HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.625-24109C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135768 | ||||||
| chr17:14135821
|
A | G | 2 | a0001c0003t0002g0100a0001c0003t0002g0101 | 2 | HG01255.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.625-24056A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14135821 | ||||||
| chr17:14136055
|
A | G | 2 | a0002c0008t0001g0196a0002c0008t0001g0212 | 2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.625-23822A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14136055 | ||||||
| chr17:14136196
|
C | T | 1 | a0001c0003t0002g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.625-23681C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14136196 | ||||||
| chr17:14136229
|
G | C | 1 | a0002c0008t0003g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.625-23648G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14136229 | ||||||
| chr17:14136544
|
C | T | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-23333C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14136544 | ||||||
| chr17:14136576
|
T | G | 26 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.625-23301T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14136576 | ||||||
| chr17:14136846
|
A | G | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-23031A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14136846 | ||||||
| chr17:14136929
|
A | G | 49 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.625-22948A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14136929 | ||||||
| chr17:14137021
|
T | G | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-22856T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137021 | ||||||
| chr17:14137044
|
G | A | 1 | a0001c0003t0001g0032 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.625-22833G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137044 | ||||||
| chr17:14137209
|
C | T | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-22668C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137209 | ||||||
| chr17:14137379
|
A | G | 60 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.625-22498A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137379 | ||||||
| chr17:14137469
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.625-22408T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137469 | ||||||
| chr17:14137539
|
C | T | 49 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.625-22338C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137539 | ||||||
| chr17:14137672
|
C | T | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-22205C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137672 | ||||||
| chr17:14137677
|
CAT | C | 33 | a0001c0003t0006g0102a0001c0003t0006g0112a0002c0006t0009g0259others(30): Show | 33 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.625-22194_625-2219 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14137677 | |||||
| chr17:14137869
|
TAGGTCAT others(2): Show |
T | 4 | a0001c0001t0003g0106a0001c0001t0003g0108a0001c0001t0003g0137others(1): Show | 4 | HG02132.hp1 NA18963.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-22007_625-2199 others(13): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137869 | ||||||
| chr17:14137950
|
G | GT | 57 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.625-21906dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14137950 | |||||
| chr17:14137950
|
GT | G | 85 | a0001c0001t0003g0135a0001c0003t0001g0032a0001c0003t0001g0079others(82): Show | 86 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.625-21906delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14137950 | |||||
| chr17:14137950
|
GTT | G | 76 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(73): Show | 76 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.625-21907_625-2190 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14137950 | |||||
| chr17:14137950
|
GTTT | G | 47 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.625-21908_625-2190 others(7): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14137950 | |||||
| chr17:14137957
|
T | G | 31 | a0001c0003t0006g0102a0001c0003t0006g0112a0002c0006t0009g0259others(28): Show | 31 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-21920T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137957 | ||||||
| chr17:14137961
|
T | G | 13 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(10): Show | 13 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.625-21916T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14137961 | ||||||
| chr17:14138142
|
T | A | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.625-21735T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14138142 | ||||||
| chr17:14138378
|
A | T | 3 | a0001c0003t0001g0078a0001c0004t0001g0291a0001c0012t0001g0292 | 3 | HG01884.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.625-21499A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14138378 | ||||||
| chr17:14138725
|
T | C | 1 | a0002c0006t0004g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.625-21152T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14138725 | ||||||
| chr17:14138891
|
C | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-20986C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14138891 | ||||||
| chr17:14138983
|
A | G | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-20894A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14138983 | ||||||
| chr17:14139240
|
G | C | 1 | a0004c0025t0001g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625-20637G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14139240 | ||||||
| chr17:14139327
|
T | C | 1 | a0003c0010t0018g0093 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.625-20550T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14139327 | ||||||
| chr17:14139626
|
T | C | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-20251T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14139626 | ||||||
| chr17:14139697
|
A | G | 1 | a0003c0009t0007g0055 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.625-20180A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14139697 | ||||||
| chr17:14139990
|
G | T | 16 | a0001c0003t0001g0148a0001c0003t0001g0151a0002c0002t0001g0177others(13): Show | 16 | HG00438.hp2 HG02027.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.625-19887G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14139990 | ||||||
| chr17:14140389
|
G | A | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-19488G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14140389 | ||||||
| chr17:14140542
|
A | T | 8 | a0001c0003t0002g0110a0001c0003t0002g0118a0001c0003t0002g0166others(5): Show | 8 | HG00735.hp2 HG00741.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.625-19335A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14140542 | ||||||
| chr17:14140578
|
T | C | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-19299T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14140578 | ||||||
| chr17:14140705
|
C | T | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.625-19172C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14140705 | ||||||
| chr17:14140900
|
G | A | 45 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(42): Show | 45 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.625-18977G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14140900 | ||||||
| chr17:14141034
|
C | T | 1 | a0001c0007t0004g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.625-18843C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141034 | ||||||
| chr17:14141054
|
C | T | 17 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(14): Show | 17 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(14): Show |
intron_variant | MODIFIER | c.625-18823C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141054 | ||||||
| chr17:14141128
|
A | C | 2 | a0003c0010t0001g0091a0003c0010t0006g0092 | 2 | NA18957.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.625-18749A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141128 | ||||||
| chr17:14141128
|
A | G | 1 | a0002c0002t0001g0171 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.625-18749A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141128 | ||||||
| chr17:14141521
|
C | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-18356C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141521 | ||||||
| chr17:14141529
|
C | CA | 38 | a0001c0001t0003g0119a0001c0001t0005g0013a0001c0003t0002g0008others(35): Show | 38 | HG00597.hp2 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.625-18323dupA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14141529 | |||||
| chr17:14141529
|
C | CAA | 51 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(48): Show | 52 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.625-18324_625-1832 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14141529 | |||||
| chr17:14141529
|
CA | C | 135 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(132): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.625-18323delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14141529 | |||||
| chr17:14141529
|
CAA | C | 14 | a0001c0003t0005g0122a0001c0003t0005g0123a0002c0002t0001g0270others(11): Show | 14 | HG00544.hp1 HG00597.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-18324_625-1832 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14141529 | |||||
| chr17:14141529
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0007t0003g0014 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.625-18333_625-1832 others(15): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14141529 | |||||
| chr17:14141529
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0004t0002g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.625-18334_625-1832 others(16): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14141529 | |||||
| chr17:14141573
|
G | C | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-18304G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141573 | ||||||
| chr17:14141641
|
A | G | 56 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(53): Show | 57 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.625-18236A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141641 | ||||||
| chr17:14141755
|
A | G | 1 | a0004c0019t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.625-18122A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141755 | ||||||
| chr17:14141847
|
G | A | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-18030G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14141847 | ||||||
| chr17:14142146
|
T | C | 1 | a0002c0005t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.625-17731T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14142146 | ||||||
| chr17:14142357
|
C | T | 12 | a0001c0001t0005g0159a0001c0001t0005g0289a0001c0001t0005g0290others(9): Show | 12 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.625-17520C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14142357 | ||||||
| chr17:14142537
|
T | C | 56 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(53): Show | 57 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.625-17340T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14142537 | ||||||
| chr17:14142733
|
G | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-17144G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14142733 | ||||||
| chr17:14142846
|
T | G | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.625-17031T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14142846 | ||||||
| chr17:14142924
|
G | A | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.625-16953G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14142924 | ||||||
| chr17:14143063
|
A | G | 1 | a0001c0001t0005g0289 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.625-16814A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143063 | ||||||
| chr17:14143215
|
A | G | 26 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.625-16662A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143215 | ||||||
| chr17:14143377
|
A | G | 1 | a0001c0003t0001g0079 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.625-16500A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143377 | ||||||
| chr17:14143485
|
A | G | 1 | a0001c0003t0006g0112 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.625-16392A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143485 | ||||||
| chr17:14143574
|
A | G | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-16303A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143574 | ||||||
| chr17:14143655
|
G | C | 13 | a0001c0001t0005g0013a0001c0001t0005g0159a0001c0001t0005g0289others(10): Show | 13 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.625-16222G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143655 | ||||||
| chr17:14143727
|
A | G | 1 | a0002c0005t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.625-16150A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143727 | ||||||
| chr17:14143864
|
T | A | 9 | a0002c0006t0009g0259a0003c0011t0001g0039a0003c0011t0003g0033others(6): Show | 9 | HG00280.hp2 HG01081.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.625-16013T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143864 | ||||||
| chr17:14143895
|
T | C | 51 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(48): Show | 52 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.625-15982T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143895 | ||||||
| chr17:14143985
|
T | C | 38 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0131others(35): Show | 38 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.625-15892T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14143985 | ||||||
| chr17:14144150
|
T | G | 38 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(35): Show | 38 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.625-15727T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144150 | ||||||
| chr17:14144160
|
G | A | 44 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(41): Show | 44 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.625-15717G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144160 | ||||||
| chr17:14144300
|
G | A | 50 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(47): Show | 50 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.625-15577G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144300 | ||||||
| chr17:14144341
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-15536G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144341 | ||||||
| chr17:14144531
|
T | G | 2 | a0001c0001t0004g0117a0001c0007t0004g0162 | 2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.625-15346T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144531 | ||||||
| chr17:14144679
|
G | T | 1 | a0002c0002t0002g0257 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.625-15198G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144679 | ||||||
| chr17:14144774
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.625-15103C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144774 | ||||||
| chr17:14144838
|
C | T | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.625-15039C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144838 | ||||||
| chr17:14144965
|
C | T | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-14912C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144965 | ||||||
| chr17:14144991
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.625-14886T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14144991 | ||||||
| chr17:14145097
|
A | G | 1 | a0001c0004t0002g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.625-14780A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145097 | ||||||
| chr17:14145301
|
G | A | 2 | a0001c0007t0013g0129a0001c0007t0013g0130 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.625-14576G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145301 | ||||||
| chr17:14145450
|
G | A | 125 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(122): Show | 126 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.625-14427G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145450 | ||||||
| chr17:14145516
|
G | A | 116 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.625-14361G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145516 | ||||||
| chr17:14145526
|
C | G | 17 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(14): Show | 17 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(14): Show |
intron_variant | MODIFIER | c.625-14351C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145526 | ||||||
| chr17:14145598
|
C | G | 1 | a0002c0002t0002g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.625-14279C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145598 | ||||||
| chr17:14145627
|
C | T | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-14250C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145627 | ||||||
| chr17:14145654
|
T | C | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-14223T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145654 | ||||||
| chr17:14145776
|
G | A | 1 | a0003c0009t0007g0049 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.625-14101G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145776 | ||||||
| chr17:14145907
|
C | T | 313 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.625-13970C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14145907 | ||||||
| chr17:14146077
|
A | G | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.625-13800A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146077 | ||||||
| chr17:14146154
|
G | A | 131 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(128): Show | 132 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.625-13723G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146154 | ||||||
| chr17:14146178
|
A | T | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.625-13699A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146178 | ||||||
| chr17:14146203
|
C | T | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.625-13674C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146203 | ||||||
| chr17:14146221
|
C | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-13656C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146221 | ||||||
| chr17:14146404
|
A | C | 4 | a0001c0007t0008g0114a0002c0005t0005g0198a0002c0005t0008g0246others(1): Show | 4 | HG02615.hp2 HG02717.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-13473A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146404 | ||||||
| chr17:14146404
|
A | G | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-13473A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146404 | ||||||
| chr17:14146432
|
C | A | 3 | a0002c0005t0004g0186a0002c0005t0004g0194a0005c0013t0004g0139 | 3 | NA18968.hp1 NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.625-13445C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146432 | ||||||
| chr17:14146460
|
C | A | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-13417C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14146460 | ||||||
| chr17:14147003
|
G | T | 4 | a0002c0005t0004g0191a0002c0005t0004g0235a0002c0005t0004g0236others(1): Show | 4 | NA18946.hp2 NA19056.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-12874G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147003 | ||||||
| chr17:14147031
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.625-12846G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147031 | ||||||
| chr17:14147056
|
T | G | 1 | a0001c0003t0002g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.625-12821T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147056 | ||||||
| chr17:14147072
|
A | G | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.625-12805A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147072 | ||||||
| chr17:14147133
|
C | G | 7 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(4): Show | 7 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-12744C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147133 | ||||||
| chr17:14147200
|
T | C | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-12677T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147200 | ||||||
| chr17:14147408
|
A | G | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-12469A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147408 | ||||||
| chr17:14147429
|
G | A | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.625-12448G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147429 | ||||||
| chr17:14147463
|
T | C | 1 | a0002c0002t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.625-12414T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147463 | ||||||
| chr17:14147485
|
G | T | 125 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(122): Show | 126 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.625-12392G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147485 | ||||||
| chr17:14147503
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0120a0002c0005t0001g0305 | 3 | HG00735.hp1 HG01192.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.625-12374A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147503 | ||||||
| chr17:14147579
|
C | T | 1 | a0002c0008t0001g0272 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.625-12298C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147579 | ||||||
| chr17:14147662
|
AGATAAGT others(507): Show |
A | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-12214_625-1170 others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147662 | ||||||
| chr17:14147714
|
A | G | 1 | a0001c0003t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.625-12163A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147714 | ||||||
| chr17:14147780
|
A | G | 6 | a0001c0001t0003g0019a0001c0001t0003g0099a0001c0001t0003g0145others(3): Show | 6 | HG00673.hp2 HG01261.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.625-12097A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147780 | ||||||
| chr17:14147797
|
T | A | 8 | a0001c0004t0003g0105a0001c0004t0003g0167a0001c0007t0008g0114others(5): Show | 8 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.625-12080T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147797 | ||||||
| chr17:14147817
|
CT | C | 150 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(147): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.625-12057delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14147817 | |||||
| chr17:14147952
|
T | C | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.625-11925T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14147952 | ||||||
| chr17:14148119
|
C | A | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.625-11758C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148119 | ||||||
| chr17:14148120
|
C | G | 27 | a0001c0001t0005g0064a0001c0003t0006g0102a0001c0003t0006g0112others(24): Show | 27 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.625-11757C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148120 | ||||||
| chr17:14148164
|
G | A | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.625-11713G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148164 | ||||||
| chr17:14148178
|
C | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-11699C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148178 | ||||||
| chr17:14148179
|
C | G | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-11698C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148179 | ||||||
| chr17:14148218
|
G | A | 19 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(16): Show | 19 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.625-11659G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148218 | ||||||
| chr17:14148278
|
T | G | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.625-11599T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148278 | ||||||
| chr17:14148324
|
A | T | 1 | a0002c0002t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.625-11553A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148324 | ||||||
| chr17:14148380
|
G | T | 1 | a0001c0001t0005g0290 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.625-11497G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148380 | ||||||
| chr17:14148394
|
G | T | 1 | a0001c0007t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.625-11483G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148394 | ||||||
| chr17:14148609
|
G | A | 2 | a0002c0005t0005g0198a0002c0005t0008g0246 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.625-11268G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148609 | ||||||
| chr17:14148718
|
G | A | 2 | a0001c0001t0003g0099a0001c0001t0003g0145 | 2 | HG01261.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.625-11159G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148718 | ||||||
| chr17:14148771
|
A | G | 2 | a0002c0006t0004g0266a0003c0011t0004g0040 | 2 | HG01074.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.625-11106A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148771 | ||||||
| chr17:14148984
|
A | G | 2 | a0002c0002t0002g0210a0002c0002t0003g0211 | 2 | HG01167.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.625-10893A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14148984 | ||||||
| chr17:14149044
|
C | T | 1 | a0002c0015t0021g0311 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.625-10833C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149044 | ||||||
| chr17:14149071
|
G | A | 313 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.625-10806G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149071 | ||||||
| chr17:14149081
|
C | T | 3 | a0002c0005t0004g0191a0002c0005t0004g0235a0002c0005t0004g0236 | 3 | NA18946.hp2 NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.625-10796C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149081 | ||||||
| chr17:14149106
|
T | C | 2 | a0002c0005t0004g0244a0002c0006t0004g0193 | 2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.625-10771T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149106 | ||||||
| chr17:14149317
|
A | T | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.625-10560A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149317 | ||||||
| chr17:14149472
|
T | C | 27 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(24): Show | 27 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.625-10405T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149472 | ||||||
| chr17:14149480
|
G | A | 45 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(42): Show | 45 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.625-10397G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149480 | ||||||
| chr17:14149643
|
C | T | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.625-10234C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149643 | ||||||
| chr17:14149786
|
A | G | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-10091A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149786 | ||||||
| chr17:14149899
|
C | G | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-9978C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149899 | ||||||
| chr17:14149992
|
C | T | 1 | a0001c0003t0002g0153 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.625-9885C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14149992 | ||||||
| chr17:14150027
|
C | G | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.625-9850C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150027 | ||||||
| chr17:14150042
|
C | T | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.625-9835C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150042 | ||||||
| chr17:14150222
|
G | A | 1 | a0002c0008t0003g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.625-9655G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150222 | ||||||
| chr17:14150226
|
T | G | 27 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(24): Show | 27 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.625-9651T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150226 | ||||||
| chr17:14150430
|
A | G | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-9447A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150430 | ||||||
| chr17:14150524
|
A | G | 158 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(155): Show | 159 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.625-9353A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150524 | ||||||
| chr17:14150687
|
T | C | 4 | a0001c0007t0008g0114a0002c0005t0005g0198a0002c0005t0008g0246others(1): Show | 4 | HG02615.hp2 HG02717.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-9190T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150687 | ||||||
| chr17:14150754
|
A | G | 2 | a0001c0003t0002g0006a0001c0004t0002g0017 | 2 | NA18950.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.625-9123A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150754 | ||||||
| chr17:14150936
|
G | A | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.625-8941G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14150936 | ||||||
| chr17:14151067
|
GA | G | 163 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(160): Show | 164 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.625-8800delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151067 | |||||
| chr17:14151271
|
C | T | 1 | a0004c0019t0001g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.625-8606C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151271 | ||||||
| chr17:14151526
|
AAC | A | 25 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.625-8304_625-8303d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151526
|
AACAC | A | 14 | a0001c0001t0019g0277a0001c0003t0002g0008a0001c0004t0002g0164others(11): Show | 15 | HG01192.hp1 HG01433.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.625-8306_625-8303d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151526
|
AACACAC | A | 36 | a0001c0001t0003g0019a0001c0001t0003g0106a0001c0001t0005g0013others(33): Show | 36 | HG00323.hp2 HG01109.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.625-8308_625-8303d others(8): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151526
|
AACACACA others(1): Show |
A | 68 | a0001c0001t0003g0028a0001c0001t0003g0108a0001c0001t0003g0135others(65): Show | 68 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.625-8310_625-8303d others(10): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151526
|
AACACACA others(3): Show |
A | 124 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0029others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.625-8312_625-8303d others(12): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151526
|
AACACACA others(5): Show |
A | 38 | a0001c0001t0003g0145a0001c0001t0003g0170a0001c0001t0005g0159others(35): Show | 38 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.625-8314_625-8303d others(14): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151526
|
AACACACA others(7): Show |
A | 5 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(2): Show | 5 | HG01884.hp2 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-8316_625-8303d others(16): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151526
|
AACACACA others(9): Show |
A | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.625-8318_625-8303d others(18): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151526
|
AACACACA others(15): Show |
A | 3 | a0001c0001t0003g0001a0001c0001t0003g0142a0001c0001t0003g0165 | 4 | HG02056.hp2 NA18957.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-8324_625-8303d others(24): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14151526 | |||||
| chr17:14151546
|
C | T | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.625-8331C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151546 | ||||||
| chr17:14151574
|
C | T | 1 | a0002c0002t0001g0183 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.625-8303C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151574 | ||||||
| chr17:14151666
|
A | G | 1 | a0002c0002t0002g0218 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.625-8211A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151666 | ||||||
| chr17:14151822
|
A | G | 17 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(14): Show | 17 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(14): Show |
intron_variant | MODIFIER | c.625-8055A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151822 | ||||||
| chr17:14151837
|
T | G | 3 | a0001c0003t0002g0008a0001c0003t0002g0010a0001c0003t0002g0023 | 3 | HG01109.hp2 HG01192.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.625-8040T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151837 | ||||||
| chr17:14151861
|
C | T | 3 | a0001c0003t0002g0021a0001c0004t0002g0073a0001c0004t0002g0077 | 3 | HG01255.hp1 HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.625-8016C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151861 | ||||||
| chr17:14151897
|
G | T | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.625-7980G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151897 | ||||||
| chr17:14151910
|
G | A | 11 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0005g0122others(8): Show | 11 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-7967G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151910 | ||||||
| chr17:14151988
|
G | C | 1 | a0002c0002t0001g0183 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.625-7889G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14151988 | ||||||
| chr17:14152398
|
A | T | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-7479A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14152398 | ||||||
| chr17:14152441
|
C | T | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.625-7436C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14152441 | ||||||
| chr17:14152450
|
C | A | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-7427C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14152450 | ||||||
| chr17:14152545
|
G | A | 53 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.625-7332G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14152545 | ||||||
| chr17:14152716
|
G | A | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-7161G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14152716 | ||||||
| chr17:14152842
|
A | G | 11 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(8): Show | 11 | HG00738.hp1 HG01433.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.625-7035A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14152842 | ||||||
| chr17:14153036
|
C | T | 158 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(155): Show | 159 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.625-6841C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153036 | ||||||
| chr17:14153040
|
A | G | 160 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(157): Show | 161 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.625-6837A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153040 | ||||||
| chr17:14153285
|
G | C | 5 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-6592G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153285 | ||||||
| chr17:14153469
|
A | G | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-6408A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153469 | ||||||
| chr17:14153542
|
T | C | 1 | a0002c0005t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.625-6335T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153542 | ||||||
| chr17:14153666
|
G | A | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.625-6211G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153666 | ||||||
| chr17:14153811
|
T | C | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.625-6066T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153811 | ||||||
| chr17:14153838
|
A | G | 2 | a0001c0003t0002g0006a0001c0004t0002g0017 | 2 | NA18950.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.625-6039A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153838 | ||||||
| chr17:14153944
|
G | A | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.625-5933G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153944 | ||||||
| chr17:14153947
|
A | G | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.625-5930A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14153947 | ||||||
| chr17:14154002
|
A | T | 1 | a0001c0004t0002g0012 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.625-5875A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154002 | ||||||
| chr17:14154006
|
G | A | 1 | a0002c0005t0004g0237 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.625-5871G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154006 | ||||||
| chr17:14154027
|
A | G | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-5850A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154027 | ||||||
| chr17:14154129
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-5748G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154129 | ||||||
| chr17:14154134
|
A | G | 4 | a0001c0003t0005g0122a0001c0003t0005g0123a0001c0004t0014g0126others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-5743A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154134 | ||||||
| chr17:14154262
|
T | C | 1 | a0004c0025t0001g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625-5615T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154262 | ||||||
| chr17:14154296
|
G | A | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.625-5581G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154296 | ||||||
| chr17:14154378
|
G | A | 1 | a0002c0002t0001g0267 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.625-5499G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154378 | ||||||
| chr17:14154526
|
G | A | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-5351G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154526 | ||||||
| chr17:14154550
|
T | G | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.625-5327T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154550 | ||||||
| chr17:14154703
|
C | T | 1 | a0002c0002t0022g0234 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.625-5174C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154703 | ||||||
| chr17:14154771
|
C | T | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.625-5106C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154771 | ||||||
| chr17:14154868
|
CTG | C | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.625-5007_625-5006d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14154868 | |||||
| chr17:14155184
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-4693G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155184 | ||||||
| chr17:14155269
|
G | A | 45 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(42): Show | 45 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.625-4608G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155269 | ||||||
| chr17:14155329
|
TA | T | 122 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0064others(119): Show | 124 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.625-4531delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14155329 | |||||
| chr17:14155329
|
TAA | T | 183 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(180): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.625-4532_625-4531d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14155329 | |||||
| chr17:14155331
|
A | G | 13 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0064others(10): Show | 14 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-4546A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155331 | ||||||
| chr17:14155332
|
A | G | 140 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.625-4545A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155332 | ||||||
| chr17:14155333
|
A | G | 1 | a0002c0020t0001g0310 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.625-4544A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155333 | ||||||
| chr17:14155334
|
A | G | 1 | a0002c0015t0021g0311 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.625-4543A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155334 | ||||||
| chr17:14155405
|
A | G | 1 | a0001c0007t0004g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.625-4472A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155405 | ||||||
| chr17:14155421
|
G | A | 1 | a0001c0004t0002g0020 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.625-4456G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155421 | ||||||
| chr17:14155455
|
C | T | 3 | a0001c0003t0001g0079a0002c0002t0001g0171a0002c0002t0001g0172 | 3 | HG02109.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.625-4422C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155455 | ||||||
| chr17:14155490
|
T | A | 45 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(42): Show | 45 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.625-4387T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155490 | ||||||
| chr17:14155532
|
G | A | 1 | a0001c0007t0004g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.625-4345G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155532 | ||||||
| chr17:14155607
|
T | C | 184 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.625-4270T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155607 | ||||||
| chr17:14155716
|
AAAAAAAA others(3): Show |
A | 13 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(10): Show | 13 | HG00733.hp2 HG00735.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-4146_625-4137d others(12): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14155716 | |||||
| chr17:14155750
|
G | A | 55 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.625-4127G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155750 | ||||||
| chr17:14155779
|
C | T | 1 | a0002c0006t0004g0193 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.625-4098C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155779 | ||||||
| chr17:14155805
|
G | C | 1 | a0001c0012t0001g0294 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.625-4072G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155805 | ||||||
| chr17:14155911
|
C | T | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.625-3966C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14155911 | ||||||
| chr17:14156061
|
T | C | 4 | a0001c0007t0008g0114a0002c0005t0005g0198a0002c0005t0008g0246others(1): Show | 4 | HG02615.hp2 HG02717.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-3816T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156061 | ||||||
| chr17:14156236
|
T | A | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.625-3641T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156236 | ||||||
| chr17:14156318
|
C | T | 61 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.625-3559C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156318 | ||||||
| chr17:14156390
|
C | T | 2 | a0001c0003t0002g0021a0003c0009t0001g0094 | 2 | HG04184.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.625-3487C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156390 | ||||||
| chr17:14156464
|
G | A | 1 | a0002c0005t0004g0261 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.625-3413G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156464 | ||||||
| chr17:14156471
|
G | A | 7 | a0001c0007t0001g0016a0001c0007t0001g0293a0002c0006t0001g0307others(4): Show | 8 | HG00738.hp1 HG01433.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.625-3406G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156471 | ||||||
| chr17:14156497
|
G | A | 1 | a0001c0003t0002g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.625-3380G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156497 | ||||||
| chr17:14156518
|
G | A | 5 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-3359G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156518 | ||||||
| chr17:14156602
|
G | A | 154 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.625-3275G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156602 | ||||||
| chr17:14156617
|
A | T | 1 | a0002c0006t0003g0217 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.625-3260A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156617 | ||||||
| chr17:14156710
|
C | T | 53 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.625-3167C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156710 | ||||||
| chr17:14156797
|
C | T | 5 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-3080C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156797 | ||||||
| chr17:14156866
|
G | A | 156 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.625-3011G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156866 | ||||||
| chr17:14156901
|
G | T | 1 | a0010c0021t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.625-2976G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156901 | ||||||
| chr17:14156918
|
C | T | 156 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.625-2959C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156918 | ||||||
| chr17:14156991
|
C | T | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-2886C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156991 | ||||||
| chr17:14157010
|
G | A | 128 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.625-2867G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157010 | ||||||
| chr17:14157185
|
G | A | 1 | a0010c0021t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.625-2692G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157185 | ||||||
| chr17:14157241
|
A | G | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.625-2636A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157241 | ||||||
| chr17:14157264
|
G | T | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.625-2613G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157264 | ||||||
| chr17:14157322
|
G | A | 1 | a0001c0004t0002g0020 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.625-2555G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157322 | ||||||
| chr17:14157468
|
C | T | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.625-2409C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157468 | ||||||
| chr17:14157476
|
T | C | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-2401T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157476 | ||||||
| chr17:14157481
|
A | G | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-2396A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157481 | ||||||
| chr17:14157504
|
G | A | 4 | a0002c0006t0009g0259a0003c0011t0009g0043a0006c0016t0012g0003others(1): Show | 5 | HG01081.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-2373G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157504 | ||||||
| chr17:14157625
|
G | T | 1 | a0001c0001t0004g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.625-2252G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157625 | ||||||
| chr17:14157773
|
T | A | 4 | a0001c0007t0008g0114a0002c0005t0005g0198a0002c0005t0008g0246others(1): Show | 4 | HG02615.hp2 HG02717.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-2104T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157773 | ||||||
| chr17:14157832
|
G | T | 1 | a0002c0002t0001g0177 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.625-2045G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157832 | ||||||
| chr17:14157857
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-2020G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157857 | ||||||
| chr17:14157925
|
G | A | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-1952G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157925 | ||||||
| chr17:14157955
|
G | A | 1 | a0001c0004t0002g0282 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.625-1922G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14157955 | ||||||
| chr17:14158200
|
A | T | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.625-1677A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14158200 | ||||||
| chr17:14158234
|
T | TA | 10 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(7): Show | 10 | HG00597.hp2 HG01884.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-1633dupA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14158234 | |||||
| chr17:14158255
|
G | A | 156 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.625-1622G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14158255 | ||||||
| chr17:14158317
|
G | A | 1 | a0004c0019t0001g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.625-1560G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14158317 | ||||||
| chr17:14158318
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.625-1559G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14158318 | ||||||
| chr17:14158692
|
A | C | 6 | a0001c0001t0019g0277a0001c0012t0001g0294a0001c0012t0001g0295others(3): Show | 6 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.625-1185A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14158692 | ||||||
| chr17:14158851
|
G | A | 55 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.625-1026G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14158851 | ||||||
| chr17:14159109
|
G | A | 1 | a0002c0005t0004g0206 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.625-768G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159109 | ||||||
| chr17:14159300
|
T | C | 1 | a0002c0006t0008g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.625-577T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159300 | ||||||
| chr17:14159360
|
C | T | 157 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(154): Show | 158 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.625-517C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159360 | ||||||
| chr17:14159407
|
T | C | 158 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.625-470T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159407 | ||||||
| chr17:14159650
|
G | T | 55 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.625-227G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159650 | ||||||
| chr17:14159657
|
G | A | 156 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.625-220G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159657 | ||||||
| chr17:14159682
|
AATT | A | 156 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.625-191_625-189del others(3): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 14159682 | |||||
| chr17:14159830
|
A | C | 1 | a0001c0007t0004g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.625-47A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159830 | ||||||
| chr17:14159975
|
A | G | 16 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0001t0019g0277others(13): Show | 16 | HG00738.hp1 HG01433.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.695+28A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14159975 | ||||||
| chr17:14160072
|
G | T | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.695+125G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160072 | ||||||
| chr17:14160077
|
A | C | 58 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(55): Show | 59 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.695+130A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160077 | ||||||
| chr17:14160088
|
A | G | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.695+141A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160088 | ||||||
| chr17:14160151
|
G | GT | 6 | a0001c0001t0003g0068a0001c0001t0003g0115a0001c0003t0020g0005others(3): Show | 6 | HG01261.hp2 HG01981.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+213dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14160151 | |||||
| chr17:14160179
|
A | T | 1 | a0003c0011t0004g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.695+232A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160179 | ||||||
| chr17:14160191
|
T | A | 3 | a0003c0011t0003g0033a0003c0011t0003g0042a0009c0028t0003g0041 | 3 | HG02080.hp1 HG02523.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.695+244T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160191 | ||||||
| chr17:14160270
|
C | T | 1 | a0001c0007t0004g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.695+323C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160270 | ||||||
| chr17:14160368
|
T | A | 1 | a0002c0005t0003g0201 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.695+421T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160368 | ||||||
| chr17:14160430
|
C | T | 1 | a0002c0006t0009g0259 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.695+483C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160430 | ||||||
| chr17:14160481
|
C | A | 53 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.695+534C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160481 | ||||||
| chr17:14160495
|
CT | C | 5 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318others(2): Show | 6 | HG01934.hp2 HG02258.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+557delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14160495 | |||||
| chr17:14160506
|
A | G | 126 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(123): Show | 127 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.695+559A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160506 | ||||||
| chr17:14160537
|
A | C | 1 | a0003c0010t0006g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.695+590A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160537 | ||||||
| chr17:14160660
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0170 | 2 | HG00408.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.695+713A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160660 | ||||||
| chr17:14160721
|
A | G | 27 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(24): Show | 27 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.695+774A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160721 | ||||||
| chr17:14160812
|
A | G | 1 | a0001c0004t0002g0017 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.695+865A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160812 | ||||||
| chr17:14160903
|
G | A | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695+956G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160903 | ||||||
| chr17:14160993
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.695+1046A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14160993 | ||||||
| chr17:14161222
|
C | G | 1 | a0002c0002t0001g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695+1275C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14161222 | ||||||
| chr17:14161330
|
G | T | 157 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(154): Show | 158 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.695+1383G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14161330 | ||||||
| chr17:14161542
|
G | A | 1 | a0002c0006t0004g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.695+1595G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14161542 | ||||||
| chr17:14161854
|
G | A | 1 | a0002c0008t0001g0273 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.695+1907G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14161854 | ||||||
| chr17:14161873
|
A | G | 159 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(156): Show | 160 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.695+1926A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14161873 | ||||||
| chr17:14162031
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.695+2084G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14162031 | ||||||
| chr17:14162044
|
A | G | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.695+2097A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14162044 | ||||||
| chr17:14162070
|
T | C | 27 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(24): Show | 27 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.695+2123T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14162070 | ||||||
| chr17:14162231
|
T | C | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.695+2284T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14162231 | ||||||
| chr17:14162576
|
C | T | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.695+2629C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14162576 | ||||||
| chr17:14162622
|
CT | C | 299 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.695+2690delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14162622 | |||||
| chr17:14162622
|
CTT | C | 9 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0005t0004g0239others(6): Show | 10 | HG00733.hp1 HG02071.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.695+2689_695+2690d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14162622 | |||||
| chr17:14162739
|
T | C | 1 | a0002c0006t0004g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.695+2792T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14162739 | ||||||
| chr17:14163065
|
A | T | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.695+3118A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14163065 | ||||||
| chr17:14163090
|
T | C | 1 | a0001c0001t0003g0104 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.695+3143T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14163090 | ||||||
| chr17:14163092
|
C | G | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.695+3145C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14163092 | ||||||
| chr17:14163236
|
A | AATTT | 107 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(104): Show | 108 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.695+3323_695+3326d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14163236 | |||||
| chr17:14163236
|
A | AATTTATT others(1): Show |
72 | a0001c0001t0003g0106a0001c0001t0003g0108a0001c0001t0003g0132others(69): Show | 73 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.695+3319_695+3326d others(10): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14163236 | |||||
| chr17:14163236
|
A | AATTTATT others(5): Show |
26 | a0001c0003t0001g0078a0001c0003t0002g0023a0001c0003t0002g0065others(23): Show | 26 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.695+3315_695+3326d others(14): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14163236 | |||||
| chr17:14163236
|
A | AATTTATT others(9): Show |
6 | a0002c0002t0002g0210a0003c0010t0006g0088a0003c0010t0006g0092others(3): Show | 6 | NA18962.hp1 NA18969.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+3311_695+3326d others(18): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14163236 | |||||
| chr17:14163236
|
A | AATTTATT others(13): Show |
7 | a0001c0003t0006g0112a0002c0002t0002g0240a0002c0002t0003g0211others(4): Show | 7 | HG01074.hp2 HG01167.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+3307_695+3326d others(22): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14163236 | |||||
| chr17:14163236
|
A | AATTTATT others(17): Show |
1 | a0003c0009t0006g0090 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.695+3303_695+3326d others(26): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14163236 | |||||
| chr17:14163236
|
AATTT | A | 73 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(70): Show | 74 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.695+3323_695+3326d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14163236 | |||||
| chr17:14163247
|
T | G | 53 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.695+3300T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14163247 | ||||||
| chr17:14163965
|
G | T | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.695+4018G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14163965 | ||||||
| chr17:14164046
|
T | C | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695+4099T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164046 | ||||||
| chr17:14164050
|
C | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.695+4103C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164050 | ||||||
| chr17:14164062
|
A | G | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.695+4115A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164062 | ||||||
| chr17:14164336
|
TCTAA | T | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.695+4392_695+4395d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14164336 | |||||
| chr17:14164443
|
A | G | 156 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.695+4496A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164443 | ||||||
| chr17:14164453
|
A | G | 5 | a0002c0005t0004g0228a0002c0005t0004g0229a0002c0005t0004g0230others(2): Show | 5 | HG00639.hp1 HG00741.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+4506A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164453 | ||||||
| chr17:14164520
|
A | T | 6 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(3): Show | 6 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+4573A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164520 | ||||||
| chr17:14164673
|
A | G | 4 | a0001c0007t0001g0016a0002c0006t0001g0307a0002c0006t0001g0308others(1): Show | 4 | HG00738.hp1 HG01433.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+4726A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164673 | ||||||
| chr17:14164772
|
C | G | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.695+4825C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164772 | ||||||
| chr17:14164924
|
T | A | 185 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.695+4977T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164924 | ||||||
| chr17:14164928
|
G | A | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.695+4981G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164928 | ||||||
| chr17:14164945
|
G | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.695+4998G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164945 | ||||||
| chr17:14165046
|
G | A | 3 | a0003c0011t0003g0033a0003c0011t0003g0042a0009c0028t0003g0041 | 3 | HG02080.hp1 HG02523.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.695+5099G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14165046 | ||||||
| chr17:14165313
|
G | C | 156 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.695+5366G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14165313 | ||||||
| chr17:14165384
|
A | G | 8 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+5437A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14165384 | ||||||
| chr17:14165514
|
C | T | 1 | a0002c0008t0001g0181 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.695+5567C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14165514 | ||||||
| chr17:14165706
|
G | A | 156 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.695+5759G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14165706 | ||||||
| chr17:14165737
|
C | T | 6 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(3): Show | 6 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+5790C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14165737 | ||||||
| chr17:14165900
|
T | A | 1 | a0003c0009t0007g0053 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.695+5953T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14165900 | ||||||
| chr17:14165914
|
GCCTAATC others(11): Show |
G | 1 | a0002c0005t0004g0231 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.695+5973_695+5990d others(20): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14165914 | |||||
| chr17:14166015
|
A | G | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.695+6068A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166015 | ||||||
| chr17:14166084
|
A | G | 1 | a0003c0009t0001g0094 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.695+6137A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166084 | ||||||
| chr17:14166141
|
C | T | 124 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(121): Show | 125 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.695+6194C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166141 | ||||||
| chr17:14166168
|
C | T | 1 | a0001c0012t0001g0295 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.695+6221C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166168 | ||||||
| chr17:14166207
|
T | A | 313 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.695+6260T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166207 | ||||||
| chr17:14166612
|
C | CT | 14 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0064others(11): Show | 14 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.695+6686dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166612 | |||||
| chr17:14166612
|
CT | C | 199 | a0001c0001t0003g0019a0001c0001t0003g0028a0001c0001t0003g0029others(196): Show | 200 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.695+6686delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166612 | |||||
| chr17:14166612
|
CTT | C | 7 | a0001c0004t0001g0284a0001c0004t0001g0285a0001c0004t0014g0126others(4): Show | 7 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+6685_695+6686d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166612 | |||||
| chr17:14166654
|
C | CAGGCTGG others(1): Show |
128 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.695+6708_695+6715d others(10): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166654 | |||||
| chr17:14166666
|
C | T | 17 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(14): Show | 17 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(14): Show |
intron_variant | MODIFIER | c.695+6719C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166666 | ||||||
| chr17:14166686
|
A | G | 1 | a0001c0004t0002g0160 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.695+6739A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166686 | ||||||
| chr17:14166768
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.695+6821C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166768 | ||||||
| chr17:14166777
|
ATTTC | A | 7 | a0002c0002t0001g0200a0002c0002t0002g0179a0002c0002t0002g0199others(4): Show | 7 | NA18962.hp2 NA18977.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+6838_695+6841d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166777 | |||||
| chr17:14166785
|
C | CT | 33 | a0001c0003t0001g0032a0001c0003t0001g0148a0001c0003t0001g0151others(30): Show | 33 | HG00438.hp2 HG00738.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.695+6860dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166785 | |||||
| chr17:14166785
|
C | CTTT | 16 | a0001c0003t0006g0112a0003c0009t0006g0090a0003c0009t0006g0097others(13): Show | 16 | HG03225.hp2 NA18612.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.695+6858_695+6860d others(5): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166785 | |||||
| chr17:14166785
|
C | CTTTT | 12 | a0001c0003t0006g0102a0003c0009t0007g0034a0003c0009t0007g0035others(9): Show | 12 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.695+6857_695+6860d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166785 | |||||
| chr17:14166785
|
CT | C | 124 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.695+6860delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14166785 | |||||
| chr17:14166790
|
T | C | 2 | a0001c0001t0005g0064a0002c0005t0005g0252 | 2 | NA18999.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.695+6843T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166790 | ||||||
| chr17:14166855
|
C | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.695+6908C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166855 | ||||||
| chr17:14166952
|
G | T | 4 | a0001c0003t0005g0122a0001c0003t0005g0123a0001c0004t0014g0126others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+7005G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14166952 | ||||||
| chr17:14167172
|
G | T | 1 | a0002c0006t0004g0254 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.695+7225G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167172 | ||||||
| chr17:14167293
|
T | C | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.695+7346T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167293 | ||||||
| chr17:14167298
|
G | C | 1 | a0001c0004t0002g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.695+7351G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167298 | ||||||
| chr17:14167311
|
T | G | 2 | a0002c0005t0005g0198a0002c0005t0008g0246 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.695+7364T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167311 | ||||||
| chr17:14167325
|
G | A | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.695+7378G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167325 | ||||||
| chr17:14167357
|
T | C | 2 | a0001c0003t0001g0078a0001c0004t0001g0291 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.695+7410T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167357 | ||||||
| chr17:14167395
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.695+7448C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167395 | ||||||
| chr17:14167533
|
C | T | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.695+7586C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167533 | ||||||
| chr17:14167575
|
A | G | 10 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(7): Show | 10 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.695+7628A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14167575 | ||||||
| chr17:14168008
|
A | G | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.695+8061A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14168008 | ||||||
| chr17:14168180
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.695+8233A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14168180 | ||||||
| chr17:14168220
|
C | A | 7 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(4): Show | 7 | HG00738.hp1 HG01433.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+8273C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14168220 | ||||||
| chr17:14168295
|
C | A | 1 | a0001c0001t0004g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.695+8348C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14168295 | ||||||
| chr17:14168519
|
C | T | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+8572C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14168519 | ||||||
| chr17:14168589
|
C | T | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+8642C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14168589 | ||||||
| chr17:14168925
|
A | T | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695+8978A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14168925 | ||||||
| chr17:14169285
|
A | G | 1 | a0001c0004t0002g0160 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.695+9338A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14169285 | ||||||
| chr17:14169338
|
A | G | 1 | a0002c0005t0004g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.695+9391A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14169338 | ||||||
| chr17:14169646
|
C | T | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.695+9699C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14169646 | ||||||
| chr17:14169770
|
A | C | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.695+9823A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14169770 | ||||||
| chr17:14169841
|
G | T | 1 | a0003c0009t0007g0050 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.695+9894G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14169841 | ||||||
| chr17:14169859
|
G | A | 126 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(123): Show | 127 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.695+9912G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14169859 | ||||||
| chr17:14170014
|
A | G | 3 | a0003c0011t0003g0033a0003c0011t0003g0042a0009c0028t0003g0041 | 3 | HG02080.hp1 HG02523.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.695+10067A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170014 | ||||||
| chr17:14170193
|
C | T | 1 | a0002c0008t0001g0273 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.695+10246C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170193 | ||||||
| chr17:14170224
|
G | A | 1 | a0001c0004t0001g0287 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.695+10277G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170224 | ||||||
| chr17:14170257
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.695+10310C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170257 | ||||||
| chr17:14170366
|
A | C | 56 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(53): Show | 57 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.695+10419A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170366 | ||||||
| chr17:14170438
|
GTTAC | G | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+10495_695+1049 others(8): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14170438 | |||||
| chr17:14170537
|
C | T | 55 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.695+10590C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170537 | ||||||
| chr17:14170538
|
A | G | 126 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.695+10591A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170538 | ||||||
| chr17:14170554
|
C | T | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.695+10607C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170554 | ||||||
| chr17:14170555
|
C | G | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+10608C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170555 | ||||||
| chr17:14170559
|
A | G | 128 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(125): Show | 129 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.695+10612A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170559 | ||||||
| chr17:14170569
|
A | G | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.695+10622A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170569 | ||||||
| chr17:14170599
|
G | A | 1 | a0002c0005t0005g0252 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.695+10652G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170599 | ||||||
| chr17:14170601
|
G | A | 1 | a0002c0005t0004g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.695+10654G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170601 | ||||||
| chr17:14170653
|
G | A | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+10706G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170653 | ||||||
| chr17:14170685
|
G | A | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.695+10738G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170685 | ||||||
| chr17:14170759
|
G | A | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.695+10812G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170759 | ||||||
| chr17:14170840
|
G | A | 1 | a0002c0006t0004g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.695+10893G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170840 | ||||||
| chr17:14170896
|
T | G | 1 | a0002c0002t0001g0200 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.695+10949T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170896 | ||||||
| chr17:14170930
|
G | A | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+10983G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170930 | ||||||
| chr17:14170961
|
G | A | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+11014G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170961 | ||||||
| chr17:14171155
|
G | C | 1 | a0002c0006t0004g0225 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.695+11208G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171155 | ||||||
| chr17:14171188
|
C | T | 1 | a0002c0002t0001g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.695+11241C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171188 | ||||||
| chr17:14171189
|
G | A | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.695+11242G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171189 | ||||||
| chr17:14171230
|
T | C | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.695+11283T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171230 | ||||||
| chr17:14171261
|
A | G | 11 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0005g0122others(8): Show | 11 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.695+11314A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171261 | ||||||
| chr17:14171327
|
G | A | 43 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(40): Show | 43 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.695+11380G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171327 | ||||||
| chr17:14171601
|
A | G | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+11654A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171601 | ||||||
| chr17:14171753
|
A | C | 1 | a0002c0006t0004g0254 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.695+11806A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171753 | ||||||
| chr17:14171823
|
T | G | 1 | a0003c0009t0007g0035 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.695+11876T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171823 | ||||||
| chr17:14171920
|
A | G | 2 | a0002c0002t0001g0171a0002c0002t0001g0172 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.695+11973A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14171920 | ||||||
| chr17:14172100
|
C | A | 8 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+12153C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172100 | ||||||
| chr17:14172107
|
TCTGTCTT others(8): Show |
T | 1 | a0002c0008t0002g0233 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.695+12164_695+1217 others(19): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14172107 | |||||
| chr17:14172144
|
A | G | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.695+12197A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172144 | ||||||
| chr17:14172265
|
G | A | 1 | a0001c0004t0002g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.695+12318G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172265 | ||||||
| chr17:14172266
|
G | A | 8 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+12319G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172266 | ||||||
| chr17:14172271
|
TACTC | T | 19 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(16): Show | 19 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.695+12326_695+1232 others(8): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14172271 | |||||
| chr17:14172291
|
A | G | 153 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.695+12344A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172291 | ||||||
| chr17:14172424
|
C | T | 1 | a0001c0003t0002g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.695+12477C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172424 | ||||||
| chr17:14172512
|
AT | A | 4 | a0002c0002t0002g0250a0002c0002t0002g0251a0002c0008t0023g0249others(1): Show | 4 | NA18962.hp2 NA18977.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+12567delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14172512 | |||||
| chr17:14172533
|
C | T | 153 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.695+12586C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172533 | ||||||
| chr17:14172536
|
G | A | 4 | a0001c0001t0003g0156a0001c0007t0010g0316a0001c0007t0010g0317others(1): Show | 4 | HG01934.hp2 HG02135.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+12589G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172536 | ||||||
| chr17:14172543
|
T | A | 1 | a0002c0005t0004g0206 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.695+12596T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172543 | ||||||
| chr17:14172543
|
T | G | 152 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+12596T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172543 | ||||||
| chr17:14172572
|
CT | C | 5 | a0001c0003t0001g0150a0001c0003t0005g0123a0002c0002t0002g0253others(2): Show | 5 | HG01168.hp2 HG01516.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+12630delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14172572 | |||||
| chr17:14172577
|
T | C | 122 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(119): Show | 123 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.695+12630T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172577 | ||||||
| chr17:14172578
|
C | CT | 14 | a0001c0003t0002g0021a0001c0004t0001g0283a0001c0004t0001g0284others(11): Show | 14 | HG00438.hp2 HG01109.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.695+12651dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14172578 | |||||
| chr17:14172578
|
CT | C | 16 | a0001c0001t0003g0068a0001c0001t0003g0145a0001c0001t0003g0147others(13): Show | 17 | HG01261.hp1 HG01884.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.695+12651delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14172578 | |||||
| chr17:14172578
|
CTT | C | 135 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.695+12650_695+1265 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14172578 | |||||
| chr17:14172579
|
T | C | 5 | a0001c0003t0001g0150a0001c0003t0005g0123a0002c0002t0002g0253others(2): Show | 5 | HG01168.hp2 HG01516.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+12632T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172579 | ||||||
| chr17:14172647
|
A | G | 1 | a0002c0005t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.695+12700A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172647 | ||||||
| chr17:14172729
|
C | T | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+12782C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172729 | ||||||
| chr17:14172989
|
G | A | 1 | a0004c0019t0001g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.695+13042G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14172989 | ||||||
| chr17:14173114
|
G | A | 153 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.695+13167G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173114 | ||||||
| chr17:14173151
|
C | T | 2 | a0002c0008t0003g0242a0002c0008t0003g0302 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.695+13204C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173151 | ||||||
| chr17:14173176
|
C | A | 5 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+13229C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173176 | ||||||
| chr17:14173185
|
G | A | 5 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+13238G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173185 | ||||||
| chr17:14173219
|
G | T | 1 | a0001c0003t0001g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.695+13272G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173219 | ||||||
| chr17:14173775
|
A | G | 5 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(2): Show | 5 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+13828A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173775 | ||||||
| chr17:14173780
|
CATT | C | 4 | a0002c0006t0009g0259a0003c0011t0009g0043a0006c0016t0012g0003others(1): Show | 5 | HG01081.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+13834_695+1383 others(7): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173780 | ||||||
| chr17:14173944
|
C | T | 26 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(23): Show | 26 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.695+13997C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173944 | ||||||
| chr17:14173945
|
G | A | 1 | a0002c0005t0004g0235 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.695+13998G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14173945 | ||||||
| chr17:14174005
|
A | G | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.695+14058A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174005 | ||||||
| chr17:14174125
|
T | C | 1 | a0003c0010t0006g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.695+14178T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174125 | ||||||
| chr17:14174155
|
G | C | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.695+14208G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174155 | ||||||
| chr17:14174197
|
G | C | 6 | a0001c0007t0001g0016a0001c0007t0001g0293a0002c0006t0001g0307others(3): Show | 6 | HG00738.hp1 HG01433.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+14250G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174197 | ||||||
| chr17:14174307
|
T | A | 135 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0019others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.695+14360T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174307 | ||||||
| chr17:14174324
|
T | C | 4 | a0001c0004t0002g0103a0002c0002t0001g0195a0002c0002t0002g0178others(1): Show | 4 | HG01934.hp1 HG02486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+14377T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174324 | ||||||
| chr17:14174325
|
G | A | 2 | a0001c0004t0002g0103a0002c0002t0002g0178 | 2 | HG01934.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.695+14378G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174325 | ||||||
| chr17:14174335
|
T | C | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.695+14388T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174335 | ||||||
| chr17:14174404
|
A | C | 2 | a0002c0015t0001g0279a0002c0015t0001g0298 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.695+14457A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174404 | ||||||
| chr17:14174413
|
G | C | 2 | a0001c0004t0002g0103a0002c0002t0002g0178 | 2 | HG01934.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.695+14466G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174413 | ||||||
| chr17:14174456
|
C | CA | 11 | a0001c0001t0003g0029a0001c0001t0004g0158a0001c0001t0011g0312others(8): Show | 11 | HG00438.hp2 HG00738.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.695+14528dupA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14174456 | |||||
| chr17:14174456
|
C | CAA | 54 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.695+14527_695+1452 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14174456 | |||||
| chr17:14174456
|
CA | C | 41 | a0001c0001t0019g0277a0001c0003t0006g0102a0001c0003t0006g0112others(38): Show | 41 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.695+14528delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14174456 | |||||
| chr17:14174480
|
G | A | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.695+14533G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174480 | ||||||
| chr17:14174499
|
C | T | 154 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.695+14552C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174499 | ||||||
| chr17:14174892
|
T | G | 1 | a0001c0003t0002g0065 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.695+14945T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174892 | ||||||
| chr17:14174921
|
A | C | 1 | a0003c0011t0004g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.695+14974A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174921 | ||||||
| chr17:14174967
|
C | T | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.695+15020C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174967 | ||||||
| chr17:14174997
|
CA | C | 153 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.695+15051delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174997 | ||||||
| chr17:14175045
|
T | C | 1 | a0001c0007t0004g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.695+15098T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175045 | ||||||
| chr17:14175080
|
T | C | 94 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.695+15133T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175080 | ||||||
| chr17:14175081
|
A | G | 94 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.695+15134A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175081 | ||||||
| chr17:14175083
|
C | CGGGGGGG others(3): Show |
3 | a0001c0003t0002g0008a0001c0003t0002g0010a0001c0003t0002g0022 | 3 | HG01192.hp1 HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.695+15141_695+1515 others(14): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175083 | |||||
| chr17:14175083
|
C | CGGGGGGG others(4): Show |
5 | a0001c0003t0002g0007a0001c0003t0002g0009a0001c0003t0002g0023others(2): Show | 5 | HG01109.hp2 HG03516.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+15140_695+1515 others(15): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175083 | |||||
| chr17:14175083
|
C | CGGGGGGG others(5): Show |
2 | a0001c0004t0002g0011a0011c0022t0002g0004 | 2 | HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.695+15139_695+1515 others(16): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175083 | |||||
| chr17:14175083
|
C | CGGGGGGG others(15): Show |
1 | a0002c0008t0002g0233 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.695+15150_695+1515 others(26): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175083 | |||||
| chr17:14175083
|
CG | C | 25 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(22): Show | 25 | HG00735.hp2 HG01071.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.695+15150delG | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175083 | |||||
| chr17:14175083
|
CGG | C | 36 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(33): Show | 37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.695+15149_695+1515 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175083 | |||||
| chr17:14175084
|
G | GGT | 29 | a0001c0001t0004g0117a0001c0001t0004g0157a0001c0001t0004g0158others(26): Show | 29 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.695+15138_695+1513 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175084 | |||||
| chr17:14175085
|
G | GT | 21 | a0001c0001t0004g0111a0001c0001t0004g0127a0001c0001t0005g0064others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.695+15138_695+1513 others(5): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175085 | ||||||
| chr17:14175086
|
G | C | 2 | a0002c0002t0001g0190a0003c0010t0001g0096 | 2 | NA18948.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.695+15139G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175086 | ||||||
| chr17:14175086
|
G | T | 38 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0013others(35): Show | 38 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.695+15139G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175086 | ||||||
| chr17:14175090
|
G | T | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+15143G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175090 | ||||||
| chr17:14175091
|
G | C | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.695+15144G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175091 | ||||||
| chr17:14175092
|
G | C | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.695+15145G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175092 | ||||||
| chr17:14175092
|
G | GA | 35 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0029others(32): Show | 36 | HG00099.hp1 HG00408.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.695+15145_695+1514 others(5): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175092 | ||||||
| chr17:14175092
|
G | GGA | 20 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0031others(17): Show | 20 | HG00544.hp2 HG01099.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.695+15146_695+1514 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175092 | |||||
| chr17:14175093
|
G | A | 37 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0013others(34): Show | 37 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.695+15146G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175093 | ||||||
| chr17:14175094
|
G | C | 1 | a0002c0006t0004g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.695+15147G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175094 | ||||||
| chr17:14175094
|
G | T | 1 | a0001c0007t0010g0318 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.695+15147G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175094 | ||||||
| chr17:14175095
|
G | A | 1 | a0002c0006t0003g0217 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.695+15148G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175095 | ||||||
| chr17:14175095
|
G | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.695+15148G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175095 | ||||||
| chr17:14175098
|
T | TGCGGG | 94 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.695+15152_695+1515 others(9): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175098 | |||||
| chr17:14175102
|
T | C | 94 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.695+15155T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175102 | ||||||
| chr17:14175119
|
T | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0013others(47): Show | 50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.695+15172T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175119 | ||||||
| chr17:14175128
|
G | A | 159 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.695+15181G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175128 | ||||||
| chr17:14175158
|
A | G | 11 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(8): Show | 11 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.695+15211A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175158 | ||||||
| chr17:14175164
|
T | C | 12 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0003t0002g0006others(9): Show | 12 | HG00738.hp1 HG01433.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.695+15217T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175164 | ||||||
| chr17:14175201
|
C | CT | 48 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(45): Show | 48 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.695+15267dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175201 | |||||
| chr17:14175201
|
CT | C | 68 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.695+15267delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175201 | |||||
| chr17:14175201
|
CTT | C | 90 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(87): Show | 92 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.695+15266_695+1526 others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14175201 | |||||
| chr17:14175232
|
A | T | 1 | a0001c0007t0001g0293 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.695+15285A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175232 | ||||||
| chr17:14175269
|
G | A | 1 | a0003c0011t0004g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.695+15322G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175269 | ||||||
| chr17:14175270
|
T | G | 1 | a0003c0011t0004g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.695+15323T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175270 | ||||||
| chr17:14175353
|
C | T | 1 | a0001c0001t0005g0064 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.695+15406C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175353 | ||||||
| chr17:14175380
|
T | C | 3 | a0001c0003t0002g0069a0001c0003t0002g0071a0001c0004t0002g0070 | 3 | HG00597.hp2 HG02083.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.695+15433T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175380 | ||||||
| chr17:14175393
|
T | A | 168 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.695+15446T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175393 | ||||||
| chr17:14175394
|
T | A | 1 | a0004c0019t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.695+15447T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175394 | ||||||
| chr17:14175399
|
G | C | 6 | a0001c0003t0002g0069a0001c0003t0002g0071a0001c0004t0002g0070others(3): Show | 6 | HG00280.hp1 HG00597.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+15452G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175399 | ||||||
| chr17:14175492
|
C | T | 1 | a0001c0001t0003g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.695+15545C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175492 | ||||||
| chr17:14175510
|
T | C | 157 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.695+15563T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175510 | ||||||
| chr17:14175642
|
A | C | 5 | a0001c0007t0008g0114a0002c0005t0005g0198a0002c0005t0005g0252others(2): Show | 5 | HG02615.hp2 HG02717.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+15695A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175642 | ||||||
| chr17:14175652
|
A | G | 5 | a0001c0007t0008g0114a0002c0005t0005g0198a0002c0005t0005g0252others(2): Show | 5 | HG02615.hp2 HG02717.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+15705A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175652 | ||||||
| chr17:14175720
|
C | T | 1 | a0002c0005t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.695+15773C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175720 | ||||||
| chr17:14175846
|
G | A | 28 | a0001c0003t0001g0032a0001c0003t0001g0148a0001c0003t0001g0150others(25): Show | 28 | HG00438.hp2 HG01109.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.695+15899G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175846 | ||||||
| chr17:14175863
|
G | C | 1 | a0002c0002t0001g0002 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.695+15916G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175863 | ||||||
| chr17:14175914
|
G | A | 1 | a0002c0005t0004g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.695+15967G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14175914 | ||||||
| chr17:14176151
|
G | T | 1 | a0002c0006t0004g0188 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.696-15838G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176151 | ||||||
| chr17:14176206
|
T | C | 158 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.696-15783T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176206 | ||||||
| chr17:14176307
|
TAGAACGT others(8): Show |
T | 1 | a0002c0002t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.696-15677_696-1566 others(19): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14176307 | |||||
| chr17:14176313
|
G | A | 55 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.696-15676G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176313 | ||||||
| chr17:14176438
|
G | T | 1 | a0001c0007t0003g0014 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.696-15551G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176438 | ||||||
| chr17:14176490
|
C | T | 8 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-15499C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176490 | ||||||
| chr17:14176651
|
G | A | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-15338G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176651 | ||||||
| chr17:14176737
|
C | T | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-15252C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176737 | ||||||
| chr17:14176798
|
T | A | 1 | a0001c0003t0002g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.696-15191T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176798 | ||||||
| chr17:14176962
|
A | AT | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-15017dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14176962 | |||||
| chr17:14177128
|
C | G | 5 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(2): Show | 5 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-14861C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177128 | ||||||
| chr17:14177615
|
T | C | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.696-14374T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177615 | ||||||
| chr17:14177792
|
A | G | 1 | a0001c0004t0002g0012 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.696-14197A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177792 | ||||||
| chr17:14177812
|
A | G | 1 | a0001c0004t0002g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.696-14177A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177812 | ||||||
| chr17:14177821
|
G | C | 1 | a0005c0013t0004g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.696-14168G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177821 | ||||||
| chr17:14177834
|
C | T | 157 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.696-14155C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177834 | ||||||
| chr17:14177915
|
C | T | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.696-14074C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177915 | ||||||
| chr17:14177942
|
T | C | 157 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.696-14047T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177942 | ||||||
| chr17:14177965
|
A | G | 1 | a0002c0005t0004g0244 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.696-14024A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14177965 | ||||||
| chr17:14178002
|
G | A | 1 | a0001c0007t0004g0075 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.696-13987G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178002 | ||||||
| chr17:14178350
|
A | G | 157 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.696-13639A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178350 | ||||||
| chr17:14178374
|
G | A | 157 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.696-13615G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178374 | ||||||
| chr17:14178389
|
G | A | 153 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.696-13600G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178389 | ||||||
| chr17:14178411
|
G | A | 157 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.696-13578G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178411 | ||||||
| chr17:14178496
|
A | C | 2 | a0010c0021t0001g0185a0012c0024t0016g0297 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.696-13493A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178496 | ||||||
| chr17:14178533
|
A | G | 1 | a0001c0003t0002g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.696-13456A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178533 | ||||||
| chr17:14178573
|
G | A | 157 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.696-13416G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178573 | ||||||
| chr17:14178770
|
C | G | 1 | a0002c0002t0001g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.696-13219C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178770 | ||||||
| chr17:14179126
|
G | C | 1 | a0002c0002t0001g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.696-12863G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14179126 | ||||||
| chr17:14179296
|
T | TA | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-12693_696-1269 others(5): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14179296 | ||||||
| chr17:14179683
|
A | G | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.696-12306A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14179683 | ||||||
| chr17:14179721
|
T | G | 56 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.696-12268T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14179721 | ||||||
| chr17:14179739
|
A | G | 182 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.696-12250A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14179739 | ||||||
| chr17:14179741
|
C | T | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.696-12248C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14179741 | ||||||
| chr17:14179886
|
A | G | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-12103A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14179886 | ||||||
| chr17:14180018
|
C | G | 2 | a0001c0003t0002g0006a0001c0004t0002g0017 | 2 | NA18950.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.696-11971C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180018 | ||||||
| chr17:14180031
|
G | A | 1 | a0002c0006t0004g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.696-11958G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180031 | ||||||
| chr17:14180046
|
C | T | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.696-11943C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180046 | ||||||
| chr17:14180123
|
G | A | 1 | a0002c0008t0003g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.696-11866G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180123 | ||||||
| chr17:14180277
|
A | T | 10 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(7): Show | 10 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.696-11712A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180277 | ||||||
| chr17:14180303
|
T | C | 1 | a0002c0002t0001g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.696-11686T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180303 | ||||||
| chr17:14180322
|
A | G | 9 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(6): Show | 9 | HG01109.hp2 HG01192.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-11667A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180322 | ||||||
| chr17:14180552
|
G | A | 43 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(40): Show | 43 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.696-11437G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180552 | ||||||
| chr17:14180633
|
T | C | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.696-11356T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180633 | ||||||
| chr17:14180643
|
A | G | 55 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.696-11346A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180643 | ||||||
| chr17:14180709
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.696-11280C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180709 | ||||||
| chr17:14180798
|
G | A | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.696-11191G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180798 | ||||||
| chr17:14180893
|
TG | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.696-11095delG | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14180893 | ||||||
| chr17:14181097
|
G | A | 24 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.696-10892G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181097 | ||||||
| chr17:14181120
|
G | A | 24 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(21): Show | 24 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.696-10869G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181120 | ||||||
| chr17:14181210
|
T | C | 5 | a0001c0001t0004g0117a0001c0003t0005g0122a0001c0003t0005g0123others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-10779T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181210 | ||||||
| chr17:14181213
|
A | G | 1 | a0002c0002t0001g0195 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.696-10776A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181213 | ||||||
| chr17:14181215
|
T | C | 1 | a0002c0002t0001g0195 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.696-10774T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181215 | ||||||
| chr17:14181264
|
T | C | 3 | a0001c0001t0003g0142a0002c0002t0002g0218a0002c0008t0001g0278 | 3 | HG01071.hp1 NA18944.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.696-10725T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181264 | ||||||
| chr17:14181416
|
G | A | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.696-10573G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181416 | ||||||
| chr17:14181491
|
G | T | 1 | a0001c0001t0003g0068 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.696-10498G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181491 | ||||||
| chr17:14181532
|
T | G | 1 | a0001c0003t0001g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.696-10457T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181532 | ||||||
| chr17:14181545
|
C | T | 179 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(176): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.696-10444C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181545 | ||||||
| chr17:14181685
|
A | G | 3 | a0001c0007t0001g0276a0001c0007t0005g0128a0004c0025t0001g0061 | 3 | HG02559.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.696-10304A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181685 | ||||||
| chr17:14181875
|
G | T | 1 | a0001c0004t0002g0160 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.696-10114G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181875 | ||||||
| chr17:14181940
|
C | G | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.696-10049C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14181940 | ||||||
| chr17:14182004
|
C | CT | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-9973dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14182004 | |||||
| chr17:14182016
|
T | A | 4 | a0001c0003t0002g0110a0001c0003t0002g0166a0002c0002t0002g0304others(1): Show | 4 | HG00735.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-9973T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182016 | ||||||
| chr17:14182075
|
G | A | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-9914G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182075 | ||||||
| chr17:14182079
|
T | G | 60 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(57): Show | 61 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.696-9910T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182079 | ||||||
| chr17:14182150
|
C | T | 2 | a0002c0006t0009g0259a0003c0011t0009g0043 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.696-9839C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182150 | ||||||
| chr17:14182158
|
A | G | 1 | a0002c0006t0004g0193 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.696-9831A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182158 | ||||||
| chr17:14182176
|
C | T | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.696-9813C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182176 | ||||||
| chr17:14182259
|
A | AAAAT | 30 | a0001c0001t0003g0135a0001c0003t0002g0076a0001c0004t0001g0286others(27): Show | 30 | HG00323.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.696-9686_696-9683d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14182259 | |||||
| chr17:14182259
|
A | AAAATAAA others(1): Show |
4 | a0001c0003t0002g0072a0002c0002t0001g0002a0002c0002t0002g0189others(1): Show | 5 | HG01081.hp2 HG02165.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-9690_696-9683d others(10): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14182259 | |||||
| chr17:14182259
|
AAAAT | A | 68 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(65): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-9686_696-9683d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14182259 | |||||
| chr17:14182259
|
AAAATAAA others(1): Show |
A | 15 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(12): Show | 15 | HG01109.hp2 HG01192.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.696-9690_696-9683d others(10): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14182259 | |||||
| chr17:14182259
|
AAAATAAA others(5): Show |
A | 101 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0136others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.696-9694_696-9683d others(14): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14182259 | |||||
| chr17:14182259
|
AAAATAAA others(9): Show |
A | 44 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(41): Show | 44 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.696-9698_696-9683d others(18): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14182259 | |||||
| chr17:14182259
|
AAAATAAA others(17): Show |
A | 1 | a0001c0003t0002g0315 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.696-9706_696-9683d others(26): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14182259 | |||||
| chr17:14182333
|
G | A | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-9656G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182333 | ||||||
| chr17:14182387
|
G | T | 1 | a0001c0001t0003g0028 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.696-9602G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182387 | ||||||
| chr17:14182591
|
C | G | 3 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.696-9398C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182591 | ||||||
| chr17:14182633
|
C | T | 1 | a0003c0011t0017g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.696-9356C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182633 | ||||||
| chr17:14182859
|
A | G | 157 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.696-9130A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182859 | ||||||
| chr17:14182890
|
T | C | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.696-9099T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14182890 | ||||||
| chr17:14183090
|
C | T | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.696-8899C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14183090 | ||||||
| chr17:14183113
|
C | G | 1 | a0002c0006t0001g0309 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.696-8876C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14183113 | ||||||
| chr17:14183689
|
G | A | 2 | a0001c0003t0005g0122a0001c0003t0005g0123 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.696-8300G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14183689 | ||||||
| chr17:14183697
|
A | G | 56 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.696-8292A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14183697 | ||||||
| chr17:14183838
|
C | T | 1 | a0006c0016t0012g0003 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.696-8151C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14183838 | ||||||
| chr17:14183921
|
C | G | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.696-8068C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14183921 | ||||||
| chr17:14184132
|
G | A | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.696-7857G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184132 | ||||||
| chr17:14184151
|
A | G | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-7838A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184151 | ||||||
| chr17:14184290
|
A | G | 2 | a0001c0001t0005g0013a0001c0001t0005g0290 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.696-7699A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184290 | ||||||
| chr17:14184573
|
A | G | 1 | a0002c0006t0004g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.696-7416A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184573 | ||||||
| chr17:14184622
|
A | C | 1 | a0001c0007t0003g0014 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.696-7367A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184622 | ||||||
| chr17:14184794
|
T | C | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.696-7195T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184794 | ||||||
| chr17:14184806
|
G | A | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-7183G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184806 | ||||||
| chr17:14184954
|
G | A | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.696-7035G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184954 | ||||||
| chr17:14184997
|
G | A | 1 | a0002c0015t0001g0279 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.696-6992G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14184997 | ||||||
| chr17:14185228
|
C | T | 36 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0064others(33): Show | 36 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.696-6761C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14185228 | ||||||
| chr17:14185229
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.696-6760G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14185229 | ||||||
| chr17:14185253
|
A | G | 19 | a0001c0004t0001g0286a0002c0002t0001g0002a0002c0002t0001g0173others(16): Show | 20 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.696-6736A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14185253 | ||||||
| chr17:14185282
|
T | TGGTTTTT others(306): Show |
2 | a0001c0001t0011g0312a0001c0001t0011g0314 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.696-6692_696-6691i others(315): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14185282 | |||||
| chr17:14185282
|
T | TGGTTTTT others(307): Show |
1 | a0001c0001t0011g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.696-6692_696-6691i others(316): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14185282 | |||||
| chr17:14185747
|
C | T | 1 | a0001c0007t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.696-6242C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14185747 | ||||||
| chr17:14185749
|
CTTTA | C | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-6235_696-6232d others(6): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14185749 | |||||
| chr17:14185891
|
A | C | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.696-6098A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14185891 | ||||||
| chr17:14185928
|
T | C | 3 | a0002c0002t0002g0210a0002c0002t0002g0253a0002c0002t0003g0211 | 3 | HG01167.hp2 HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.696-6061T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14185928 | ||||||
| chr17:14185979
|
G | A | 2 | a0001c0004t0002g0160a0004c0019t0001g0058 | 2 | HG00733.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.696-6010G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14185979 | ||||||
| chr17:14186097
|
G | A | 3 | a0001c0004t0003g0105a0001c0004t0003g0167a0004c0019t0003g0057 | 3 | HG00733.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.696-5892G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186097 | ||||||
| chr17:14186176
|
C | G | 3 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.696-5813C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186176 | ||||||
| chr17:14186190
|
TA | T | 13 | a0002c0002t0002g0304a0002c0008t0001g0181a0003c0009t0007g0034others(10): Show | 13 | HG01081.hp1 HG01106.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.696-5793delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14186190 | |||||
| chr17:14186208
|
C | G | 1 | a0002c0005t0003g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.696-5781C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186208 | ||||||
| chr17:14186382
|
A | T | 27 | a0001c0003t0002g0065a0001c0003t0002g0067a0001c0003t0002g0100others(24): Show | 27 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.696-5607A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186382 | ||||||
| chr17:14186384
|
A | G | 41 | a0001c0001t0019g0277a0001c0003t0001g0079a0001c0003t0001g0080others(38): Show | 41 | HG01070.hp2 HG01081.hp2 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.696-5605A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186384 | ||||||
| chr17:14186459
|
C | A | 118 | a0001c0001t0003g0165a0001c0001t0004g0111a0001c0001t0004g0117others(115): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.696-5530C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186459 | ||||||
| chr17:14186533
|
G | A | 1 | a0003c0011t0009g0043 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.696-5456G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186533 | ||||||
| chr17:14186652
|
C | T | 8 | a0001c0001t0003g0131a0001c0007t0013g0129a0001c0007t0013g0130others(5): Show | 8 | HG00099.hp1 HG00621.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-5337C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186652 | ||||||
| chr17:14186654
|
A | G | 8 | a0001c0001t0003g0131a0001c0007t0013g0129a0001c0007t0013g0130others(5): Show | 8 | HG00099.hp1 HG00621.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-5335A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186654 | ||||||
| chr17:14186668
|
A | G | 8 | a0001c0001t0003g0115a0001c0001t0003g0131a0001c0007t0013g0129others(5): Show | 8 | HG00099.hp1 HG00621.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-5321A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186668 | ||||||
| chr17:14186735
|
G | C | 1 | a0001c0001t0003g0170 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.696-5254G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186735 | ||||||
| chr17:14186761
|
C | T | 146 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.696-5228C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186761 | ||||||
| chr17:14186799
|
G | A | 9 | a0002c0002t0001g0203a0002c0002t0002g0210a0002c0002t0002g0253others(6): Show | 9 | HG00621.hp2 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-5190G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186799 | ||||||
| chr17:14186834
|
A | G | 7 | a0002c0002t0002g0210a0002c0002t0002g0253a0002c0002t0003g0211others(4): Show | 7 | HG00621.hp2 HG00733.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.696-5155A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186834 | ||||||
| chr17:14186954
|
C | T | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-5035C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186954 | ||||||
| chr17:14186985
|
GT | G | 154 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.696-4992delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14186985 | |||||
| chr17:14187102
|
T | C | 8 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-4887T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14187102 | ||||||
| chr17:14187168
|
G | A | 10 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(7): Show | 10 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.696-4821G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14187168 | ||||||
| chr17:14187193
|
T | G | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.696-4796T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14187193 | ||||||
| chr17:14187572
|
C | T | 3 | a0001c0007t0008g0114a0002c0005t0008g0246a0002c0006t0008g0274 | 3 | HG02717.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.696-4417C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14187572 | ||||||
| chr17:14187702
|
A | G | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.696-4287A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14187702 | ||||||
| chr17:14187710
|
T | A | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-4279T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14187710 | ||||||
| chr17:14188012
|
C | T | 126 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(123): Show | 127 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.696-3977C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188012 | ||||||
| chr17:14188032
|
G | A | 3 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269 | 3 | HG02109.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.696-3957G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188032 | ||||||
| chr17:14188102
|
C | CT | 231 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(228): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.696-3868dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14188102 | |||||
| chr17:14188102
|
C | CTT | 23 | a0001c0001t0003g0119a0001c0001t0004g0117a0001c0001t0019g0277others(20): Show | 23 | HG00280.hp2 HG00738.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.696-3869_696-3868d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14188102 | |||||
| chr17:14188102
|
CT | C | 22 | a0001c0003t0002g0026a0001c0003t0002g0065a0001c0003t0002g0067others(19): Show | 22 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.696-3868delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14188102 | |||||
| chr17:14188104
|
T | TC | 3 | a0001c0001t0003g0099a0001c0001t0003g0145a0002c0008t0001g0243 | 3 | HG01261.hp1 HG02486.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.696-3885_696-3884i others(3): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188104 | ||||||
| chr17:14188213
|
G | GAA | 142 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.696-3766_696-3765d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14188213 | |||||
| chr17:14188213
|
GA | G | 43 | a0001c0003t0002g0006a0001c0003t0002g0007a0001c0003t0002g0008others(40): Show | 43 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.696-3765delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14188213 | |||||
| chr17:14188217
|
A | AAG | 8 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-3771_696-3770i others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14188217 | |||||
| chr17:14188285
|
C | G | 2 | a0002c0015t0001g0279a0002c0015t0001g0298 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.696-3704C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188285 | ||||||
| chr17:14188349
|
C | A | 1 | a0002c0002t0001g0222 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.696-3640C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188349 | ||||||
| chr17:14188421
|
T | C | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.696-3568T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188421 | ||||||
| chr17:14188449
|
GA | G | 53 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.696-3534delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14188449 | |||||
| chr17:14188477
|
A | T | 1 | a0002c0006t0004g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.696-3512A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188477 | ||||||
| chr17:14188488
|
A | AC | 5 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-3500dupC | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14188488 | |||||
| chr17:14188488
|
A | C | 306 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(303): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.696-3501A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188488 | ||||||
| chr17:14188532
|
A | G | 5 | a0001c0007t0001g0016a0001c0007t0001g0293a0002c0006t0001g0307others(2): Show | 5 | HG00738.hp1 HG01433.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-3457A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188532 | ||||||
| chr17:14188753
|
C | T | 1 | a0012c0024t0016g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.696-3236C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188753 | ||||||
| chr17:14188962
|
A | G | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.696-3027A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188962 | ||||||
| chr17:14189079
|
C | CT | 124 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(121): Show | 126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.696-2893dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14189079 | |||||
| chr17:14189079
|
C | CTT | 8 | a0001c0004t0001g0283a0001c0004t0001g0284a0001c0004t0001g0285others(5): Show | 8 | HG01109.hp1 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-2894_696-2893d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14189079 | |||||
| chr17:14189079
|
CT | C | 64 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.696-2893delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 14189079 | |||||
| chr17:14189131
|
T | G | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.696-2858T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189131 | ||||||
| chr17:14189184
|
G | A | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-2805G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189184 | ||||||
| chr17:14189486
|
A | G | 3 | a0001c0007t0008g0114a0002c0005t0008g0246a0002c0006t0008g0274 | 3 | HG02717.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.696-2503A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189486 | ||||||
| chr17:14189501
|
T | C | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.696-2488T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189501 | ||||||
| chr17:14189603
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.696-2386C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189603 | ||||||
| chr17:14189611
|
A | G | 1 | a0001c0003t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.696-2378A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189611 | ||||||
| chr17:14189651
|
T | G | 53 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.696-2338T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189651 | ||||||
| chr17:14189829
|
G | T | 53 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.696-2160G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189829 | ||||||
| chr17:14189841
|
G | A | 154 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.696-2148G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189841 | ||||||
| chr17:14189904
|
G | A | 2 | a0001c0001t0004g0117a0001c0007t0004g0162 | 2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.696-2085G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189904 | ||||||
| chr17:14189980
|
G | T | 1 | a0003c0009t0007g0050 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.696-2009G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14189980 | ||||||
| chr17:14190061
|
A | G | 1 | a0002c0015t0001g0279 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.696-1928A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190061 | ||||||
| chr17:14190173
|
T | C | 10 | a0003c0009t0007g0034a0003c0009t0007g0035a0003c0009t0007g0048others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.696-1816T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190173 | ||||||
| chr17:14190194
|
A | G | 1 | a0002c0002t0002g0304 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.696-1795A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190194 | ||||||
| chr17:14190247
|
G | A | 3 | a0001c0001t0003g0131a0001c0007t0013g0129a0001c0007t0013g0130 | 3 | HG00099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.696-1742G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190247 | ||||||
| chr17:14190455
|
G | T | 5 | a0002c0006t0009g0259a0003c0011t0009g0043a0006c0016t0012g0003others(2): Show | 6 | HG01081.hp2 HG02004.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1534G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190455 | ||||||
| chr17:14190520
|
C | T | 1 | a0002c0020t0001g0310 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.696-1469C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190520 | ||||||
| chr17:14190704
|
C | A | 154 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.696-1285C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190704 | ||||||
| chr17:14190726
|
G | C | 3 | a0002c0006t0009g0259a0003c0011t0009g0043a0007c0027t0009g0209 | 3 | HG01081.hp2 HG02004.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.696-1263G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190726 | ||||||
| chr17:14190761
|
C | T | 1 | a0003c0009t0007g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.696-1228C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190761 | ||||||
| chr17:14190921
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.696-1068T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14190921 | ||||||
| chr17:14191185
|
T | C | 3 | a0001c0001t0003g0106a0001c0001t0003g0108a0001c0001t0003g0137 | 3 | NA18963.hp2 NA18977.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.696-804T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191185 | ||||||
| chr17:14191207
|
G | T | 4 | a0001c0003t0001g0079a0002c0002t0001g0171a0002c0002t0001g0172others(1): Show | 4 | HG01070.hp2 HG02109.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-782G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191207 | ||||||
| chr17:14191280
|
A | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.696-709A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191280 | ||||||
| chr17:14191320
|
G | C | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.696-669G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191320 | ||||||
| chr17:14191355
|
A | G | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-634A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191355 | ||||||
| chr17:14191362
|
C | T | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-627C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191362 | ||||||
| chr17:14191445
|
T | A | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.696-544T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191445 | ||||||
| chr17:14191540
|
C | G | 1 | a0001c0007t0003g0144 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.696-449C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191540 | ||||||
| chr17:14191857
|
C | A | 5 | a0002c0006t0009g0259a0003c0011t0009g0043a0006c0016t0012g0003others(2): Show | 6 | HG01081.hp2 HG02004.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-132C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191857 | ||||||
| chr17:14192233
|
G | A | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.928+12G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14192233 | ||||||
| chr17:14192249
|
T | C | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.928+28T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14192249 | ||||||
| chr17:14192322
|
A | G | 3 | a0002c0006t0009g0259a0003c0011t0009g0043a0007c0027t0009g0209 | 3 | HG01081.hp2 HG02004.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.928+101A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14192322 | ||||||
| chr17:14192365
|
T | C | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.928+144T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14192365 | ||||||
| chr17:14192391
|
G | A | 4 | a0001c0007t0010g0316a0008c0026t0001g0056a0010c0021t0001g0185others(1): Show | 4 | HG02258.hp2 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.928+170G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14192391 | ||||||
| chr17:14192584
|
G | A | 1 | a0001c0007t0004g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.928+363G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14192584 | ||||||
| chr17:14192745
|
AT | A | 8 | a0001c0012t0001g0292a0001c0012t0001g0294a0001c0012t0001g0295others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.928+531delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14192745 | |||||
| chr17:14192805
|
G | C | 2 | a0001c0007t0010g0317a0001c0007t0010g0318 | 2 | HG01934.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.928+584G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14192805 | ||||||
| chr17:14193164
|
T | C | 3 | a0001c0023t0001g0163a0002c0006t0004g0226a0008c0026t0001g0056 | 3 | HG01516.hp1 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.928+943T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193164 | ||||||
| chr17:14193187
|
C | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0064others(6): Show | 9 | HG00280.hp2 HG00735.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.928+966C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193187 | ||||||
| chr17:14193210
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0120a0002c0005t0001g0305 | 3 | HG00735.hp1 HG01192.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.928+989G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193210 | ||||||
| chr17:14193222
|
A | C | 2 | a0002c0015t0001g0279a0002c0015t0001g0298 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.928+1001A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193222 | ||||||
| chr17:14193263
|
C | T | 1 | a0002c0002t0001g0245 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.928+1042C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193263 | ||||||
| chr17:14193266
|
A | G | 5 | a0001c0001t0003g0019a0001c0001t0003g0131a0001c0007t0013g0129others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+1045A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193266 | ||||||
| chr17:14193273
|
C | T | 2 | a0001c0001t0003g0019a0003c0011t0001g0039 | 2 | HG00280.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.928+1052C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193273 | ||||||
| chr17:14193291
|
C | T | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.928+1070C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193291 | ||||||
| chr17:14193300
|
C | T | 4 | a0001c0007t0010g0316a0008c0026t0001g0056a0010c0021t0001g0185others(1): Show | 4 | HG02258.hp2 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.928+1079C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193300 | ||||||
| chr17:14193329
|
C | T | 1 | a0001c0007t0001g0293 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.928+1108C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193329 | ||||||
| chr17:14193358
|
C | T | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.928+1137C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193358 | ||||||
| chr17:14193359
|
A | G | 54 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(51): Show | 54 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.928+1138A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193359 | ||||||
| chr17:14193400
|
A | G | 25 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.928+1179A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193400 | ||||||
| chr17:14193457
|
G | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(57): Show | 61 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.928+1236G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193457 | ||||||
| chr17:14193507
|
C | T | 18 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0005g0064others(15): Show | 19 | HG00735.hp1 HG01192.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.928+1286C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193507 | ||||||
| chr17:14193527
|
G | C | 1 | a0001c0012t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928+1306G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193527 | ||||||
| chr17:14193549
|
C | T | 140 | a0001c0001t0005g0064a0001c0003t0001g0032a0001c0003t0001g0078others(137): Show | 140 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.928+1328C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193549 | ||||||
| chr17:14193587
|
G | T | 139 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0156others(136): Show | 140 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.928+1366G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193587 | ||||||
| chr17:14193707
|
A | G | 54 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(51): Show | 54 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.928+1486A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193707 | ||||||
| chr17:14193736
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.928+1515G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193736 | ||||||
| chr17:14193753
|
C | T | 3 | a0001c0007t0008g0114a0002c0005t0008g0246a0002c0006t0008g0274 | 3 | HG02717.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928+1532C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193753 | ||||||
| chr17:14193794
|
C | A | 6 | a0001c0004t0003g0105a0001c0004t0003g0167a0002c0008t0003g0242others(3): Show | 6 | HG00733.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+1573C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193794 | ||||||
| chr17:14193794
|
C | G | 2 | a0001c0003t0005g0122a0001c0003t0005g0123 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.928+1573C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193794 | ||||||
| chr17:14193794
|
C | T | 26 | a0001c0001t0003g0068a0001c0003t0002g0015a0001c0003t0002g0026others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.928+1573C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193794 | ||||||
| chr17:14193801
|
G | A | 26 | a0001c0001t0003g0068a0001c0003t0002g0015a0001c0003t0002g0026others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.928+1580G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193801 | ||||||
| chr17:14193991
|
C | T | 2 | a0001c0003t0001g0078a0001c0004t0001g0291 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.928+1770C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14193991 | ||||||
| chr17:14194197
|
G | A | 25 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(22): Show | 25 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.928+1976G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194197 | ||||||
| chr17:14194253
|
G | A | 25 | a0001c0003t0002g0015a0001c0003t0002g0026a0001c0003t0002g0065others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.928+2032G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194253 | ||||||
| chr17:14194343
|
A | C | 5 | a0001c0001t0005g0289a0002c0006t0005g0303a0008c0026t0001g0056others(2): Show | 5 | HG02809.hp2 HG03225.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+2122A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194343 | ||||||
| chr17:14194419
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0120a0002c0005t0001g0305 | 3 | HG00735.hp1 HG01192.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.928+2198A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194419 | ||||||
| chr17:14194457
|
C | G | 54 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.928+2236C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194457 | ||||||
| chr17:14194466
|
G | A | 1 | a0002c0006t0004g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.928+2245G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194466 | ||||||
| chr17:14194527
|
A | G | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.928+2306A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194527 | ||||||
| chr17:14194529
|
C | T | 1 | a0002c0005t0004g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.928+2308C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194529 | ||||||
| chr17:14194667
|
C | T | 2 | a0001c0003t0001g0078a0001c0004t0001g0291 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.928+2446C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194667 | ||||||
| chr17:14194720
|
T | C | 25 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(22): Show | 25 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.928+2499T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194720 | ||||||
| chr17:14194889
|
C | T | 1 | a0001c0004t0001g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.928+2668C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194889 | ||||||
| chr17:14194960
|
T | G | 12 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(9): Show | 12 | HG00738.hp1 HG01433.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.928+2739T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194960 | ||||||
| chr17:14194983
|
A | G | 1 | a0002c0002t0001g0195 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.928+2762A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194983 | ||||||
| chr17:14194986
|
G | T | 1 | a0001c0004t0001g0287 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.928+2765G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14194986 | ||||||
| chr17:14195376
|
G | A | 2 | a0001c0001t0003g0134a0001c0001t0003g0143 | 2 | NA18612.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.928+3155G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14195376 | ||||||
| chr17:14195468
|
C | T | 1 | a0001c0001t0003g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.928+3247C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14195468 | ||||||
| chr17:14195560
|
C | A | 1 | a0006c0016t0012g0003 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.928+3339C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14195560 | ||||||
| chr17:14195735
|
C | G | 2 | a0001c0003t0006g0102a0001c0003t0006g0112 | 2 | HG02027.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.928+3514C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14195735 | ||||||
| chr17:14195779
|
A | G | 140 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.928+3558A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14195779 | ||||||
| chr17:14195782
|
A | G | 3 | a0001c0007t0008g0114a0002c0005t0008g0246a0002c0006t0008g0274 | 3 | HG02717.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928+3561A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14195782 | ||||||
| chr17:14195800
|
T | C | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.928+3579T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14195800 | ||||||
| chr17:14196250
|
C | G | 9 | a0001c0003t0002g0076a0002c0002t0001g0200a0002c0002t0002g0179others(6): Show | 9 | NA18959.hp1 NA18962.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+4029C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196250 | ||||||
| chr17:14196425
|
T | G | 54 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(51): Show | 54 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.928+4204T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196425 | ||||||
| chr17:14196442
|
T | C | 6 | a0002c0002t0001g0222a0002c0008t0001g0219a0002c0008t0001g0221others(3): Show | 6 | HG00438.hp2 HG02523.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.928+4221T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196442 | ||||||
| chr17:14196530
|
G | A | 1 | a0001c0001t0005g0289 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.928+4309G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196530 | ||||||
| chr17:14196733
|
C | T | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.928+4512C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196733 | ||||||
| chr17:14196749
|
C | A | 1 | a0004c0019t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.928+4528C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196749 | ||||||
| chr17:14196751
|
C | T | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.928+4530C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196751 | ||||||
| chr17:14196873
|
C | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.928+4652C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196873 | ||||||
| chr17:14197071
|
C | G | 1 | a0002c0002t0001g0195 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.928+4850C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197071 | ||||||
| chr17:14197125
|
C | T | 1 | a0003c0017t0003g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.928+4904C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197125 | ||||||
| chr17:14197131
|
T | C | 2 | a0002c0015t0021g0311a0002c0020t0001g0310 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.928+4910T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197131 | ||||||
| chr17:14197170
|
ATTGGTAG others(20): Show |
A | 1 | a0002c0002t0002g0240 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.928+4953_928+4979d others(29): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14197170 | |||||
| chr17:14197223
|
C | A | 2 | a0001c0004t0003g0105a0001c0004t0003g0167 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.928+5002C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197223 | ||||||
| chr17:14197341
|
T | C | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.928+5120T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197341 | ||||||
| chr17:14197605
|
C | A | 1 | a0002c0002t0002g0240 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.928+5384C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197605 | ||||||
| chr17:14197712
|
G | A | 155 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.928+5491G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197712 | ||||||
| chr17:14197726
|
G | A | 179 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(176): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.928+5505G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197726 | ||||||
| chr17:14197732
|
CA | C | 55 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(52): Show | 56 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.928+5512delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197732 | ||||||
| chr17:14197772
|
A | G | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.928+5551A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197772 | ||||||
| chr17:14197825
|
A | G | 3 | a0002c0006t0009g0259a0003c0011t0009g0043a0007c0027t0009g0209 | 3 | HG01081.hp2 HG02004.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.928+5604A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197825 | ||||||
| chr17:14197842
|
C | T | 3 | a0008c0026t0001g0056a0010c0021t0001g0185a0012c0024t0016g0297 | 3 | HG03225.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.928+5621C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197842 | ||||||
| chr17:14197921
|
G | A | 34 | a0001c0003t0001g0078a0001c0003t0002g0007a0001c0003t0002g0008others(31): Show | 34 | HG00323.hp2 HG01109.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.928+5700G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197921 | ||||||
| chr17:14197964
|
C | A | 24 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(21): Show | 24 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.928+5743C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197964 | ||||||
| chr17:14197978
|
T | G | 2 | a0006c0016t0012g0003a0006c0016t0012g0202 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.928+5757T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197978 | ||||||
| chr17:14198625
|
G | A | 1 | a0002c0005t0003g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.928+6404G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14198625 | ||||||
| chr17:14198639
|
C | T | 1 | a0002c0005t0004g0182 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.928+6418C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14198639 | ||||||
| chr17:14199099
|
G | A | 23 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(20): Show | 23 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.928+6878G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14199099 | ||||||
| chr17:14199146
|
G | A | 1 | a0002c0015t0001g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.928+6925G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14199146 | ||||||
| chr17:14199219
|
G | C | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.928+6998G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14199219 | ||||||
| chr17:14199550
|
C | T | 5 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(2): Show | 5 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.929-7260C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14199550 | ||||||
| chr17:14199648
|
A | C | 3 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314 | 3 | HG01884.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.929-7162A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14199648 | ||||||
| chr17:14200041
|
G | A | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.929-6769G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14200041 | ||||||
| chr17:14200143
|
G | A | 1 | a0001c0003t0006g0102 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.929-6667G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14200143 | ||||||
| chr17:14200358
|
T | C | 5 | a0001c0012t0001g0294a0001c0012t0001g0295a0001c0012t0001g0296others(2): Show | 5 | HG01433.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.929-6452T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14200358 | ||||||
| chr17:14200375
|
G | A | 2 | a0001c0004t0014g0126a0001c0004t0014g0149 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.929-6435G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14200375 | ||||||
| chr17:14200407
|
G | A | 1 | a0001c0001t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.929-6403G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14200407 | ||||||
| chr17:14200607
|
G | A | 1 | a0001c0003t0001g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.929-6203G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14200607 | ||||||
| chr17:14200754
|
A | G | 1 | a0002c0008t0002g0255 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.929-6056A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14200754 | ||||||
| chr17:14200917
|
C | A | 2 | a0001c0007t0008g0114a0002c0006t0008g0274 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.929-5893C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14200917 | ||||||
| chr17:14201305
|
A | G | 1 | a0002c0008t0001g0243 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.929-5505A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14201305 | ||||||
| chr17:14201405
|
C | T | 2 | a0002c0008t0001g0196a0002c0008t0001g0212 | 2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.929-5405C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14201405 | ||||||
| chr17:14201627
|
A | G | 225 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(222): Show | 226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.929-5183A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14201627 | ||||||
| chr17:14201758
|
C | T | 1 | a0001c0001t0005g0159 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.929-5052C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14201758 | ||||||
| chr17:14201791
|
G | A | 1 | a0002c0005t0004g0236 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.929-5019G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14201791 | ||||||
| chr17:14201900
|
A | G | 25 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(22): Show | 25 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.929-4910A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14201900 | ||||||
| chr17:14201940
|
T | C | 200 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(197): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.929-4870T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14201940 | ||||||
| chr17:14202039
|
C | G | 1 | a0001c0007t0004g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.929-4771C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202039 | ||||||
| chr17:14202062
|
G | T | 1 | a0004c0019t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.929-4748G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202062 | ||||||
| chr17:14202084
|
A | ATC | 120 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(117): Show | 121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.929-4718_929-4717d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14202084 | |||||
| chr17:14202092
|
CTT | C | 65 | a0001c0003t0002g0006a0001c0003t0002g0007a0001c0003t0002g0008others(62): Show | 65 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.929-4706_929-4705d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14202092 | |||||
| chr17:14202093
|
T | TC | 11 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(8): Show | 11 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.929-4717_929-4716i others(3): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202093 | ||||||
| chr17:14202094
|
T | C | 1 | a0002c0002t0002g0304 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.929-4716T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202094 | ||||||
| chr17:14202203
|
T | G | 312 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.929-4607T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202203 | ||||||
| chr17:14202223
|
C | CT | 181 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(178): Show | 182 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.929-4570dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14202223 | |||||
| chr17:14202223
|
C | CTT | 6 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318others(3): Show | 6 | HG01934.hp2 HG02258.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.929-4571_929-4570d others(4): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14202223 | |||||
| chr17:14202223
|
CT | C | 9 | a0001c0001t0003g0031a0001c0012t0001g0292a0002c0002t0003g0211others(6): Show | 9 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.929-4570delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14202223 | |||||
| chr17:14202329
|
ATCCTCCC others(3): Show |
A | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.929-4478_929-4469d others(12): Show |
COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14202329 | |||||
| chr17:14202557
|
C | T | 52 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0080others(49): Show | 53 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.929-4253C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202557 | ||||||
| chr17:14202661
|
G | A | 2 | a0002c0002t0005g0265a0002c0005t0005g0252 | 2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.929-4149G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202661 | ||||||
| chr17:14202690
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.929-4120G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202690 | ||||||
| chr17:14202746
|
C | T | 1 | a0011c0022t0002g0004 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.929-4064C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202746 | ||||||
| chr17:14202760
|
T | C | 1 | a0001c0003t0002g0315 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.929-4050T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202760 | ||||||
| chr17:14203016
|
A | G | 11 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(8): Show | 11 | HG00738.hp1 HG01433.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.929-3794A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203016 | ||||||
| chr17:14203236
|
A | C | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.929-3574A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203236 | ||||||
| chr17:14203240
|
T | A | 1 | a0001c0001t0003g0125 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.929-3570T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203240 | ||||||
| chr17:14203442
|
C | G | 1 | a0001c0001t0003g0170 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.929-3368C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203442 | ||||||
| chr17:14203444
|
G | C | 3 | a0001c0004t0001g0286a0002c0002t0001g0213a0002c0002t0001g0214 | 3 | HG02572.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.929-3366G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203444 | ||||||
| chr17:14203475
|
A | G | 1 | a0004c0025t0001g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-3335A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203475 | ||||||
| chr17:14203484
|
G | A | 10 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(7): Show | 10 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.929-3326G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203484 | ||||||
| chr17:14203572
|
A | G | 57 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.929-3238A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203572 | ||||||
| chr17:14203575
|
G | T | 3 | a0002c0005t0004g0186a0002c0005t0004g0194a0005c0013t0004g0139 | 3 | NA18968.hp1 NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.929-3235G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203575 | ||||||
| chr17:14203583
|
C | G | 1 | a0001c0001t0003g0146 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.929-3227C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203583 | ||||||
| chr17:14203602
|
T | A | 14 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(11): Show | 14 | HG00738.hp1 HG01081.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-3208T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203602 | ||||||
| chr17:14203914
|
C | G | 1 | a0008c0026t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.929-2896C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203914 | ||||||
| chr17:14203917
|
A | T | 194 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(191): Show | 195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.929-2893A>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14203917 | ||||||
| chr17:14204262
|
C | T | 191 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(188): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.929-2548C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204262 | ||||||
| chr17:14204377
|
C | T | 3 | a0001c0007t0010g0316a0001c0007t0010g0317a0001c0007t0010g0318 | 3 | HG01934.hp2 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.929-2433C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204377 | ||||||
| chr17:14204447
|
A | C | 2 | a0004c0018t0001g0059a0004c0018t0001g0060 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.929-2363A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204447 | ||||||
| chr17:14204492
|
C | T | 8 | a0001c0001t0005g0013a0001c0001t0005g0290a0001c0007t0001g0016others(5): Show | 8 | HG00738.hp1 HG01433.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.929-2318C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204492 | ||||||
| chr17:14204630
|
T | G | 191 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(188): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.929-2180T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204630 | ||||||
| chr17:14204697
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.929-2113C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204697 | ||||||
| chr17:14204769
|
T | C | 1 | a0001c0001t0003g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.929-2041T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204769 | ||||||
| chr17:14204781
|
C | CT | 191 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(188): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.929-2028dupT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14204781 | |||||
| chr17:14204789
|
C | T | 1 | a0001c0001t0003g0108 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.929-2021C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204789 | ||||||
| chr17:14204872
|
C | A | 23 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(20): Show | 23 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.929-1938C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204872 | ||||||
| chr17:14204979
|
C | T | 191 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(188): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.929-1831C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14204979 | ||||||
| chr17:14205061
|
T | C | 215 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(212): Show | 216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.929-1749T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205061 | ||||||
| chr17:14205143
|
CT | C | 192 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(189): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.929-1658delT | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14205143 | |||||
| chr17:14205230
|
C | T | 52 | a0001c0001t0004g0111a0001c0001t0004g0117a0001c0001t0004g0127others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.929-1580C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205230 | ||||||
| chr17:14205246
|
C | T | 57 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.929-1564C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205246 | ||||||
| chr17:14205328
|
G | C | 67 | a0001c0003t0002g0006a0001c0003t0002g0007a0001c0003t0002g0008others(64): Show | 67 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.929-1482G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205328 | ||||||
| chr17:14205332
|
C | T | 2 | a0002c0002t0001g0195a0002c0008t0001g0243 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.929-1478C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205332 | ||||||
| chr17:14205336
|
C | T | 67 | a0001c0003t0002g0006a0001c0003t0002g0007a0001c0003t0002g0008others(64): Show | 67 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.929-1474C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205336 | ||||||
| chr17:14205341
|
C | T | 1 | a0001c0003t0002g0315 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.929-1469C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205341 | ||||||
| chr17:14205408
|
C | T | 124 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(121): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.929-1402C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205408 | ||||||
| chr17:14205433
|
G | A | 3 | a0002c0006t0009g0259a0003c0011t0009g0043a0007c0027t0009g0209 | 3 | HG01081.hp2 HG02004.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.929-1377G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205433 | ||||||
| chr17:14205472
|
C | G | 191 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(188): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.929-1338C>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205472 | ||||||
| chr17:14205478
|
G | A | 23 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(20): Show | 23 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.929-1332G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205478 | ||||||
| chr17:14205577
|
C | A | 1 | a0004c0019t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.929-1233C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205577 | ||||||
| chr17:14205594
|
C | T | 2 | a0002c0002t0005g0265a0002c0005t0005g0252 | 2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.929-1216C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205594 | ||||||
| chr17:14205595
|
G | A | 3 | a0001c0001t0003g0131a0001c0007t0013g0129a0001c0007t0013g0130 | 3 | HG00099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.929-1215G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205595 | ||||||
| chr17:14205596
|
C | A | 56 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(53): Show | 57 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.929-1214C>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205596 | ||||||
| chr17:14205732
|
T | C | 124 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0004g0111others(121): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.929-1078T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205732 | ||||||
| chr17:14205825
|
A | G | 1 | a0002c0006t0004g0227 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.929-985A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205825 | ||||||
| chr17:14205928
|
G | A | 1 | a0001c0004t0002g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.929-882G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14205928 | ||||||
| chr17:14206018
|
C | T | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.929-792C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206018 | ||||||
| chr17:14206043
|
T | G | 23 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(20): Show | 23 | HG01081.hp1 HG01106.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.929-767T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206043 | ||||||
| chr17:14206191
|
G | A | 271 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.929-619G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206191 | ||||||
| chr17:14206233
|
A | G | 315 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0003g0001others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.929-577A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206233 | ||||||
| chr17:14206291
|
A | G | 57 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.929-519A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206291 | ||||||
| chr17:14206366
|
A | G | 13 | a0001c0003t0006g0102a0001c0003t0006g0112a0003c0009t0006g0090others(10): Show | 13 | HG02027.hp2 NA18612.hp2 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.929-444A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206366 | ||||||
| chr17:14206424
|
C | T | 55 | a0001c0003t0001g0032a0001c0003t0001g0078a0001c0003t0001g0079others(52): Show | 56 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.929-386C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206424 | ||||||
| chr17:14206495
|
G | A | 1 | a0001c0004t0002g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-315G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206495 | ||||||
| chr17:14206618
|
C | T | 3 | a0002c0005t0004g0186a0002c0005t0004g0194a0005c0013t0004g0139 | 3 | NA18968.hp1 NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.929-192C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206618 | ||||||
| chr17:14206683
|
G | A | 1 | a0002c0005t0004g0206 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.929-127G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206683 | ||||||
| chr17:14206724
|
G | A | 75 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0028others(72): Show | 77 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.929-86G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206724 | ||||||
| chr17:14206752
|
T | C | 3 | a0004c0018t0001g0059a0004c0018t0001g0060a0004c0019t0001g0062 | 3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.929-58T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206752 | ||||||
| chr17:14206798
|
A | ACCC | 28 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(25): Show | 28 | HG00323.hp2 HG01109.hp2 HG01192.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.929-9_929-7dupCCC | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 14206798 |