Item | Value |
---|---|
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 | 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 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0002 | 0/0 | 443 | 118 | 30 | 24 | 49 | 7 | 8 | 35 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0003 | 0/1 | 443 | 40 | 1 | 10 | 23 | 1 | 4 | 20 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0004 | 0/0 | 443 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0005 | 0/0 | 443 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0006 | 0/0 | 443 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0007 | 0/0 | 443 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0008 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0009 | 0/0 | 443 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0010 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0011 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
a0012 | 0/0 | 443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | MAASP others(438): Show |
chr17 | 14064504 | 14213677 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1329 | 49 | 9 | 8 | 25 | 2 | 5 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0001c0003 | 0/0 | 1329 | 38 | 9 | 9 | 16 | 1 | 3 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0001c0004 | 1/0 | 1329 | 32 | 11 | 7 | 9 | 1 | 3 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0001c0007 | 0/0 | 1329 | 20 | 6 | 5 | 3 | 0 | 6 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0001c0012 | 0/0 | 1329 | 4 | 3 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0001c0023 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0002c0002 | 0/0 | 1329 | 40 | 13 | 7 | 14 | 2 | 4 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0002c0005 | 0/0 | 1329 | 30 | 2 | 6 | 19 | 1 | 2 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0002c0006 | 0/0 | 1329 | 25 | 2 | 10 | 8 | 3 | 2 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0002c0008 | 0/0 | 1329 | 18 | 8 | 1 | 8 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0002c0015 | 0/0 | 1329 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0002c0020 | 0/0 | 1329 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0003c0009 | 0/0 | 1329 | 13 | 1 | 9 | 3 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0003c0010 | 0/0 | 1329 | 12 | 0 | 0 | 12 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0003c0011 | 0/0 | 1329 | 6 | 0 | 1 | 2 | 1 | 2 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0003c0014 | 0/0 | 1329 | 4 | 0 | 0 | 4 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0003c0017 | 0/0 | 1329 | 3 | 0 | 0 | 2 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0003c0029 | 0/0 | 1329 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0003c0030 | 0/1 | 1329 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0004c0018 | 0/0 | 1329 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0004c0019 | 0/0 | 1329 | 3 | 2 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0004c0025 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0005c0013 | 0/0 | 1329 | 4 | 0 | 0 | 4 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0006c0016 | 0/0 | 1329 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0007c0027 | 0/0 | 1329 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0008c0024 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0009c0022 | 0/0 | 1329 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0010c0026 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0011c0021 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
chr17 | 14064504 | 14213677 | ||
a0012c0028 | 0/0 | 1329 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ATGGC others(1324): Show |
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 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0001t0003 | 0/0 | 2894 | 33 | 0 | 5 | 23 | 1 | 4 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0001c0001t0004 | 0/0 | 2898 | 5 | 1 | 1 | 1 | 1 | 1 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0001t0005 | 0/0 | 2897 | 5 | 4 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0001c0001t0011 | 0/0 | 2898 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0001t0019 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0001c0003t0001 | 0/0 | 2898 | 7 | 3 | 0 | 3 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0003t0002 | 0/0 | 2898 | 25 | 6 | 6 | 10 | 1 | 2 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0003t0005 | 0/0 | 2897 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0001c0003t0006 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0003t0015 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0003t0020 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0004t0001 | 1/0 | 2898 | 10 | 9 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0004t0002 | 0/0 | 2898 | 17 | 0 | 4 | 9 | 1 | 3 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0004t0003 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0001c0004t0014 | 0/0 | 2898 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0004t0025 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0007t0001 | 0/0 | 2898 | 3 | 1 | 0 | 0 | 0 | 2 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0007t0003 | 0/0 | 2894 | 4 | 0 | 0 | 2 | 0 | 2 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0001c0007t0004 | 0/0 | 2898 | 6 | 1 | 2 | 1 | 0 | 2 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0007t0005 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0001c0007t0008 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0001c0007t0010 | 0/0 | 2898 | 3 | 2 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0007t0013 | 0/0 | 2895 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2890): Show |
chr17 | 14064504 | 14213677 |
a0001c0012t0001 | 0/0 | 2898 | 4 | 3 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0001c0023t0001 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0002t0001 | 0/0 | 2898 | 22 | 13 | 2 | 7 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0002t0002 | 0/0 | 2898 | 15 | 0 | 3 | 6 | 2 | 4 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0002t0003 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0002c0002t0005 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0002c0002t0022 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0005t0001 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0005t0003 | 0/0 | 2894 | 7 | 0 | 0 | 5 | 0 | 2 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0002c0005t0004 | 0/0 | 2898 | 19 | 0 | 5 | 13 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0005t0005 | 0/0 | 2897 | 2 | 1 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0002c0005t0008 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0002c0006t0001 | 0/0 | 2898 | 3 | 0 | 2 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0006t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0002c0006t0004 | 0/0 | 2898 | 18 | 0 | 7 | 7 | 2 | 2 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0006t0005 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0002c0006t0008 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0002c0006t0009 | 0/0 | 2897 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0002c0008t0001 | 0/0 | 2898 | 12 | 6 | 0 | 6 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0008t0002 | 0/0 | 2898 | 2 | 0 | 0 | 1 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0008t0003 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0002c0008t0023 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0008t0024 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0015t0001 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0015t0021 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0002c0020t0001 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0009t0001 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0009t0006 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0009t0007 | 0/0 | 2898 | 10 | 1 | 9 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0010t0001 | 0/0 | 2898 | 4 | 0 | 0 | 4 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0010t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0003c0010t0006 | 0/0 | 2898 | 6 | 0 | 0 | 6 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0010t0018 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0003c0011t0001 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0011t0003 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0003c0011t0004 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0011t0009 | 0/0 | 2897 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0003c0011t0017 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0003c0014t0001 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0014t0002 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0014t0006 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0017t0003 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0003c0017t0004 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0029t0002 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0003c0030t0003 | 0/1 | 2894 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0004c0018t0001 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0004c0018t0003 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0004c0019t0001 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0004c0019t0003 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0004c0025t0001 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0005c0013t0003 | 0/0 | 2894 | 3 | 0 | 0 | 3 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
a0005c0013t0004 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0006c0016t0012 | 0/0 | 2898 | 3 | 3 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0007c0027t0009 | 0/0 | 2897 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2892): Show |
chr17 | 14064504 | 14213677 |
a0008c0024t0016 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0009c0022t0002 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0010c0026t0001 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0011c0021t0001 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2893): Show |
chr17 | 14064504 | 14213677 |
a0012c0028t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | ACTAC others(2889): Show |
chr17 | 14064504 | 14213677 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0001g0121 | 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 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0126 | 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 |
a0001c0001t0003g0133 | 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 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0141 | 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 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0001t0005g0288 | 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 |
a0001c0001t0011g0311 | 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 |
a0001c0001t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0001g0149 | 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 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0009 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0003t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0003t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0068 | 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 |
a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0003t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0015g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0003t0020g0006 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0001g0282 | 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 |
a0001c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0001g0298 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0078 | 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 |
a0001c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0004t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0014g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0014g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0004t0025g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0010g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0010g0316 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0007t0013g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0007t0013g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0012t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0012t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0012t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0001c0012t0001g0295 | 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 |
a0002c0002t0001g0003 | 0/0 | 2 | 2 | 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 |
a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0185 | 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 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 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 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0002t0022g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0002c0005t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0187 | 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 |
a0002c0005t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0234 | 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 |
a0002c0005t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0005t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0194 | 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 |
a0002c0006t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0002c0006t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0008g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0006t0009g0258 | 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 |
a0002c0008t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0002c0008t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0023g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0008t0024g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0015t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0015t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0002c0015t0021g0309 | 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 |
a0002c0020t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0009t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0009t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0009t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0003c0009t0007g0036 | 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 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0009t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0009t0007g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0010t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0010t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0010t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0010t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0010t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0010t0006g0084 | 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 |
a0003c0010t0006g0090 | 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 |
a0003c0010t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0010t0018g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0011t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0011t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0011t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0011t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0011t0009g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0011t0017g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0014t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0014t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0014t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0014t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0017t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0003c0017t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0029t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0003c0030t0003g0039 | 0/1 | 1 | 0 | 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 |
a0004c0018t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0004c0018t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0004c0019t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0004c0019t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0004c0019t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0004c0025t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0005c0013t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0005c0013t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0005c0013t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0005c0013t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0006c0016t0012g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0006c0016t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0007c0027t0009g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0008c0024t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0009c0022t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0010c0026t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0011c0021t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
a0012c0028t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0177 | EUR | GBR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00280 | hp1 | a0002 | c0005 | t0004 | g0208 | EUR | FIN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00280 | hp2 | a0003 | c0011 | t0001 | g0040 | EUR | FIN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00323 | hp1 | a0001 | c0003 | t0002 | g0154 | EUR | FIN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00323 | hp2 | a0002 | c0008 | t0002 | g0254 | EUR | FIN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00408 | hp1 | a0002 | c0005 | t0004 | g0216 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00438 | hp1 | a0001 | c0003 | t0002 | g0027 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00438 | hp2 | a0002 | c0008 | t0001 | g0220 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00544 | hp1 | a0002 | c0005 | t0004 | g0234 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00597 | hp1 | a0002 | c0006 | t0004 | g0206 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00597 | hp2 | a0001 | c0003 | t0002 | g0075 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00621 | hp1 | a0001 | c0003 | t0002 | g0066 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00621 | hp2 | a0002 | c0006 | t0003 | g0218 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00639 | hp1 | a0002 | c0005 | t0004 | g0002 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00639 | hp2 | a0001 | c0004 | t0002 | g0028 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00673 | hp1 | a0002 | c0006 | t0004 | g0205 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00673 | hp2 | a0001 | c0007 | t0003 | g0125 | EAS | CHS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00733 | hp1 | a0004 | c0019 | t0003 | g0058 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00733 | hp2 | a0001 | c0004 | t0002 | g0161 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00735 | hp2 | a0001 | c0003 | t0002 | g0111 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00738 | hp1 | a0002 | c0006 | t0001 | g0306 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00738 | hp2 | a0002 | c0006 | t0004 | g0182 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0119 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG00741 | hp2 | a0002 | c0005 | t0004 | g0002 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01070 | hp1 | a0001 | c0004 | t0014 | g0127 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01071 | hp2 | a0001 | c0004 | t0014 | g0151 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01074 | hp1 | a0002 | c0006 | t0004 | g0265 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0239 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01081 | hp1 | a0003 | c0009 | t0007 | g0052 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01081 | hp2 | a0002 | c0006 | t0009 | g0258 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01106 | hp1 | a0003 | c0009 | t0007 | g0035 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01106 | hp2 | a0002 | c0006 | t0004 | g0193 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01109 | hp1 | a0001 | c0004 | t0025 | g0300 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0021 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01167 | hp1 | a0001 | c0007 | t0013 | g0132 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01167 | hp2 | a0002 | c0002 | t0003 | g0212 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0303 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01168 | hp2 | a0001 | c0003 | t0005 | g0124 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01169 | hp1 | a0001 | c0003 | t0005 | g0123 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01169 | hp2 | a0001 | c0007 | t0013 | g0130 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01192 | hp1 | a0001 | c0003 | t0002 | g0009 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01243 | hp2 | a0002 | c0006 | t0004 | g0240 | AMR | PUR | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01255 | hp1 | a0001 | c0004 | t0002 | g0078 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01255 | hp2 | a0001 | c0003 | t0002 | g0101 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01257 | hp1 | a0002 | c0006 | t0004 | g0257 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01258 | hp1 | a0001 | c0007 | t0004 | g0224 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01261 | hp2 | a0001 | c0007 | t0004 | g0025 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01346 | hp1 | a0002 | c0008 | t0024 | g0305 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01346 | hp2 | a0002 | c0006 | t0004 | g0223 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01358 | hp1 | a0001 | c0003 | t0015 | g0114 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01358 | hp2 | a0003 | c0009 | t0007 | g0049 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01433 | hp1 | a0001 | c0012 | t0001 | g0294 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01433 | hp2 | a0002 | c0006 | t0001 | g0308 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01496 | hp1 | a0001 | c0003 | t0002 | g0102 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0032 | 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 | g0252 | EUR | IBS | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01884 | hp1 | a0001 | c0012 | t0001 | g0291 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0311 | 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 | g0316 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01943 | hp1 | a0002 | c0005 | t0004 | g0279 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01943 | hp2 | a0003 | c0009 | t0007 | g0050 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01952 | hp1 | a0003 | c0009 | t0007 | g0036 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01952 | hp2 | a0002 | c0005 | t0001 | g0304 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01978 | hp1 | a0003 | c0009 | t0007 | g0054 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01978 | hp2 | a0002 | c0005 | t0004 | g0260 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01981 | hp1 | a0002 | c0005 | t0004 | g0227 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01981 | hp2 | a0003 | c0009 | t0007 | g0053 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02004 | hp1 | a0007 | c0027 | t0009 | g0210 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02004 | hp2 | a0003 | c0009 | t0007 | g0056 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02015 | hp1 | a0002 | c0005 | t0003 | g0202 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02015 | hp2 | a0001 | c0004 | t0002 | g0280 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02027 | hp2 | a0001 | c0003 | t0006 | g0104 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02056 | hp1 | a0002 | c0006 | t0004 | g0194 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02071 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02071 | hp2 | a0002 | c0005 | t0004 | g0238 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02080 | hp1 | a0003 | c0011 | t0003 | g0034 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02080 | hp2 | a0001 | c0004 | t0002 | g0110 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02083 | hp2 | a0001 | c0004 | t0002 | g0073 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02132 | hp2 | a0002 | c0005 | t0004 | g0243 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02135 | hp2 | a0002 | c0006 | t0004 | g0189 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02145 | hp1 | a0001 | c0004 | t0003 | g0106 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02145 | hp2 | a0001 | c0004 | t0001 | g0299 | 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 | g0134 | EAS | CDX | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02165 | hp1 | a0001 | c0003 | t0002 | g0074 | EAS | CDX | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0133 | 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 | g0297 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02258 | hp1 | a0002 | c0020 | t0001 | g0318 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02258 | hp2 | a0001 | c0007 | t0010 | g0317 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02280 | hp1 | a0001 | c0007 | t0004 | g0069 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02280 | hp2 | a0002 | c0008 | t0001 | g0213 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02293 | hp1 | a0003 | c0009 | t0007 | g0051 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02293 | hp2 | a0002 | c0002 | t0022 | g0233 | AMR | PEL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02523 | hp1 | a0003 | c0011 | t0003 | g0043 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02523 | hp2 | a0002 | c0008 | t0001 | g0229 | EAS | KHV | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02615 | hp1 | a0002 | c0008 | t0001 | g0197 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02615 | hp2 | a0002 | c0005 | t0005 | g0199 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02622 | hp1 | a0002 | c0008 | t0003 | g0241 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02622 | hp2 | a0002 | c0008 | t0001 | g0272 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0080 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02647 | hp2 | a0001 | c0012 | t0001 | g0293 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02683 | hp1 | a0001 | c0007 | t0004 | g0164 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02683 | hp2 | a0001 | c0007 | t0001 | g0017 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02698 | hp1 | a0002 | c0006 | t0004 | g0253 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02717 | hp1 | a0001 | c0004 | t0001 | g0169 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02717 | hp2 | a0001 | c0007 | t0008 | g0115 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02809 | hp1 | a0001 | c0003 | t0002 | g0287 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02818 | hp1 | a0001 | c0012 | t0001 | g0295 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02818 | hp2 | a0004 | c0018 | t0003 | g0064 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02886 | hp1 | a0004 | c0019 | t0001 | g0063 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0079 | 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 | g0282 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02896 | hp1 | a0006 | c0016 | t0012 | g0004 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0283 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0284 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02897 | hp2 | a0006 | c0016 | t0012 | g0004 | 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 | g0268 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0314 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02976 | hp1 | a0006 | c0016 | t0012 | g0203 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0081 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03017 | hp1 | a0003 | c0029 | t0002 | g0048 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03017 | hp2 | a0003 | c0011 | t0004 | g0041 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03098 | hp1 | a0001 | c0007 | t0001 | g0275 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03098 | hp2 | a0002 | c0008 | t0003 | g0301 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03130 | hp1 | a0002 | c0008 | t0001 | g0271 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03130 | hp2 | a0001 | c0007 | t0005 | g0129 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03139 | hp1 | a0001 | c0004 | t0003 | g0168 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0290 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03195 | hp1 | a0001 | c0001 | t0019 | g0276 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0286 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0285 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03225 | hp1 | a0008 | c0024 | t0016 | g0296 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03225 | hp2 | a0004 | c0019 | t0001 | g0059 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03486 | hp1 | a0002 | c0015 | t0021 | g0309 | 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 | g0256 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03516 | hp1 | a0001 | c0003 | t0002 | g0008 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ESN | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03540 | hp1 | a0004 | c0018 | t0001 | g0060 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03579 | hp1 | a0004 | c0018 | t0001 | g0061 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03654 | hp1 | a0001 | c0007 | t0003 | g0015 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03654 | hp2 | a0001 | c0007 | t0004 | g0122 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0033 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0167 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03710 | hp2 | a0001 | c0007 | t0001 | g0292 | SAS | PJL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0179 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03834 | hp1 | a0003 | c0011 | t0009 | g0044 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0217 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03927 | hp1 | a0001 | c0004 | t0002 | g0165 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0255 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG04115 | hp1 | a0002 | c0005 | t0003 | g0188 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG04115 | hp2 | a0009 | c0022 | t0002 | g0005 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG04184 | hp1 | a0001 | c0007 | t0003 | g0108 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG04184 | hp2 | a0001 | c0003 | t0002 | g0024 | SAS | BEB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG04204 | hp1 | a0003 | c0017 | t0003 | g0037 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0118 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG04228 | hp1 | a0002 | c0005 | t0003 | g0209 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG04228 | hp2 | a0001 | c0004 | t0002 | g0013 | SAS | STU | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | CHB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18612 | hp2 | a0003 | c0010 | t0006 | g0090 | EAS | CHB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18906 | hp1 | a0011 | c0021 | t0001 | g0186 | AFR | YRI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18906 | hp2 | a0002 | c0006 | t0005 | g0302 | AFR | YRI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18939 | hp1 | a0001 | c0004 | t0002 | g0023 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18939 | hp2 | a0002 | c0005 | t0004 | g0184 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18944 | hp1 | a0003 | c0010 | t0006 | g0084 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18944 | hp2 | a0002 | c0008 | t0001 | g0277 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18946 | hp2 | a0002 | c0005 | t0004 | g0236 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18948 | hp1 | a0003 | c0010 | t0018 | g0087 | 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 | g0007 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18957 | hp1 | a0003 | c0010 | t0001 | g0093 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18959 | hp1 | a0002 | c0008 | t0002 | g0231 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18959 | hp2 | a0003 | c0014 | t0001 | g0047 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18962 | hp1 | a0003 | c0017 | t0004 | g0085 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18962 | hp2 | a0003 | c0014 | t0002 | g0046 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18963 | hp1 | a0001 | c0003 | t0020 | g0006 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18964 | hp1 | a0001 | c0003 | t0002 | g0077 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18965 | hp1 | a0001 | c0003 | t0002 | g0072 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18967 | hp2 | a0002 | c0005 | t0003 | g0247 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18968 | hp1 | a0005 | c0013 | t0004 | g0135 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18968 | hp2 | a0002 | c0005 | t0004 | g0207 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18969 | hp2 | a0003 | c0010 | t0006 | g0089 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18970 | hp1 | a0002 | c0008 | t0001 | g0262 | 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 | g0281 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18972 | hp1 | a0001 | c0004 | t0002 | g0162 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18974 | hp1 | a0001 | c0007 | t0003 | g0146 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18974 | hp2 | a0003 | c0014 | t0006 | g0038 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18983 | hp1 | a0002 | c0008 | t0001 | g0183 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18985 | hp1 | a0002 | c0005 | t0003 | g0263 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18994 | hp2 | a0003 | c0014 | t0006 | g0045 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18995 | hp1 | a0003 | c0017 | t0004 | g0086 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19000 | hp2 | a0002 | c0005 | t0004 | g0195 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19001 | hp1 | a0003 | c0010 | t0003 | g0096 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19002 | hp1 | a0003 | c0010 | t0006 | g0088 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19002 | hp2 | a0001 | c0004 | t0002 | g0018 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19004 | hp1 | a0002 | c0006 | t0004 | g0225 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19005 | hp2 | a0002 | c0005 | t0003 | g0198 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19007 | hp1 | a0003 | c0010 | t0001 | g0097 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0068 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19011 | hp1 | a0001 | c0004 | t0002 | g0067 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19011 | hp2 | a0005 | c0013 | t0003 | g0137 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19012 | hp1 | a0002 | c0005 | t0005 | g0251 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19012 | hp2 | a0001 | c0007 | t0004 | g0070 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19030 | hp1 | a0001 | c0007 | t0010 | g0315 | 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 | g0269 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19056 | hp1 | a0002 | c0005 | t0004 | g0235 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19058 | hp1 | a0003 | c0009 | t0001 | g0095 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19058 | hp2 | a0002 | c0008 | t0023 | g0248 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19060 | hp1 | a0001 | c0003 | t0002 | g0026 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19060 | hp2 | a0002 | c0005 | t0004 | g0237 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19063 | hp1 | a0005 | c0013 | t0003 | g0117 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19065 | hp1 | a0012 | c0028 | t0003 | g0042 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19065 | hp2 | a0002 | c0005 | t0004 | g0187 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19066 | hp1 | a0001 | c0003 | t0006 | g0113 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19066 | hp2 | a0002 | c0002 | t0005 | g0264 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19068 | hp1 | a0002 | c0005 | t0004 | g0230 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19068 | hp2 | a0005 | c0013 | t0003 | g0136 | 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 | g0150 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19075 | hp1 | a0002 | c0006 | t0004 | g0221 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19075 | hp2 | a0003 | c0010 | t0001 | g0083 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19078 | hp1 | a0003 | c0010 | t0001 | g0099 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19078 | hp2 | a0002 | c0008 | t0001 | g0181 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19079 | hp2 | a0003 | c0010 | t0006 | g0092 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19080 | hp1 | a0002 | c0005 | t0003 | g0246 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19080 | hp2 | a0003 | c0009 | t0006 | g0091 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19085 | hp1 | a0003 | c0009 | t0006 | g0098 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19086 | hp1 | a0003 | c0010 | t0006 | g0094 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19240 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | YRI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0170 | AFR | YRI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA20129 | hp1 | a0003 | c0009 | t0007 | g0055 | AFR | ASW | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0313 | AFR | ASW | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0211 | EUR | TSI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA20752 | hp2 | a0001 | c0004 | t0002 | g0012 | EUR | TSI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0112 | EUR | TSI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA20805 | hp2 | a0002 | c0006 | t0001 | g0307 | EUR | TSI | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA20905 | hp1 | a0002 | c0006 | t0004 | g0222 | SAS | GIH | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA20905 | hp2 | a0001 | c0004 | t0002 | g0076 | SAS | GIH | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01123 | hp1 | a0002 | c0006 | t0004 | g0176 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG01123 | hp2 | a0003 | c0011 | t0017 | g0082 | AMR | CLM | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0266 | 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 | g0242 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02559 | hp1 | a0004 | c0025 | t0001 | g0062 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG02559 | hp2 | a0002 | c0015 | t0001 | g0278 | AFR | ACB | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0312 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG06807 | hp1 | a0002 | c0008 | t0001 | g0270 | AFR | USA | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
HG06807 | hp2 | a0010 | c0026 | t0001 | g0057 | AFR | USA | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA21309 | hp1 | a0002 | c0005 | t0008 | g0245 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
NA21309 | hp2 | a0002 | c0006 | t0008 | g0273 | AFR | LWK | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
homoSapiens | chm13v2 | a0003 | c0030 | t0003 | g0039 | REF | REF | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0298 | REF | REF | COX10_chr17_14064504_14213677 | COX10 | chr17 | 14064504 | 14213677 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0004 a0010 |
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 | a0003 a0012 |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0004 a0010 |
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 | a0002 a0006 a0007 others(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 | a0012 | 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 | a0009 | 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 | a0008 a0010 a0011 |
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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:14069638 | C | T | 4 | a0003c0011 a0003c0014 a0003c0029 others(1): Show |
12 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(9): 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 | a0001c0003 a0001c0007 a0001c0023 others(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 | 18 | a0001c0001 a0001c0007 a0001c0012 others(15): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0012 a0001c0023 a0002c0015 others(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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0008c0024t0016 | 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 | a0001c0001t0005 a0001c0001t0019 a0001c0003t0005 others(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 | 18 | a0001c0001t0003 a0001c0004t0003 a0001c0007t0003 others(15): Show |
64 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(61): 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 | a0001c0001t0004 a0001c0007t0004 a0002c0005t0004 others(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 | 19 | a0001c0001t0003 a0001c0004t0003 a0001c0007t0003 others(16): Show |
66 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(63): 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 | 22 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0019 others(19): Show |
73 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(70): 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 | a0001c0003t0006 a0002c0006t0009 a0003c0009t0006 others(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 | 19 | a0001c0001t0003 a0001c0004t0003 a0001c0007t0003 others(16): Show |
66 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(63): 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 | a0002c0006t0009 a0003c0011t0009 a0007c0027t0009 |
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 | 19 | a0001c0001t0003 a0001c0004t0003 a0001c0007t0003 others(16): Show |
66 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(63): 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 | 19 | a0001c0001t0003 a0001c0004t0003 a0001c0007t0003 others(16): Show |
66 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(63): 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 | a0001c0003t0006 a0002c0006t0009 a0003c0009t0006 others(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 | 21 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0019 others(18): Show |
70 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(67): 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 | a0001c0001t0004 a0001c0007t0004 a0002c0005t0004 others(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 | a0001c0001t0011 a0001c0001t0019 |
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 | a0001c0003t0006 a0003c0009t0006 a0003c0010t0006 others(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 | a0001c0007t0008 a0002c0005t0008 a0002c0006t0008 |
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 | a0001c0003t0002 a0001c0003t0015 a0001c0003t0020 others(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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:14069814 | T | C | 94 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(91): Show |
94 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(91): 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 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0100 others(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 | a0002c0020t0001g0318 | 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 | a0003c0011t0017g0082 | 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 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 |
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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0002c0002t0002g0175 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0018t0003g0064 others(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 | a0003c0011t0017g0082 | 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 | a0001c0001t0003g0171 | 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 | a0001c0003t0002g0314 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | a0002c0006t0004g0176 a0002c0006t0004g0177 |
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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0002c0002t0002g0303 a0002c0005t0001g0304 a0002c0006t0001g0306 others(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 | a0001c0003t0001g0033 | 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 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0032 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(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 | 159 | a0001c0001t0003g0071 a0001c0001t0003g0100 a0001c0001t0003g0105 others(156): Show |
162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): 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 | a0001c0001t0005g0065 a0002c0002t0001g0178 a0002c0002t0001g0185 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(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 | 312 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(309): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): 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 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0100 others(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 | a0002c0002t0002g0303 a0002c0005t0001g0304 a0002c0006t0001g0306 others(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 | a0002c0002t0002g0303 a0002c0005t0001g0304 a0002c0006t0001g0306 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0018t0003g0064 others(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 | a0002c0005t0004g0187 | 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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | a0001c0007t0001g0275 | 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 | a0002c0002t0002g0303 a0002c0005t0001g0304 a0002c0006t0001g0306 others(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 | a0001c0001t0011g0311 | 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 | a0010c0026t0001g0057 | 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 | a0001c0001t0019g0276 | 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 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(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 | a0001c0003t0002g0314 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0003c0029t0002g0048 | 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 | a0002c0005t0003g0188 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0001c0007t0003g0108 | 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 | a0002c0006t0004g0189 | 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 | a0001c0004t0002g0280 a0001c0004t0002g0281 |
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 | a0001c0001t0005g0288 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0018t0003g0064 others(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 | a0001c0004t0001g0169 a0001c0004t0001g0170 |
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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0006c0016t0012g0004 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(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 | a0001c0001t0003g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
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 | a0002c0002t0001g0274 | 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 | a0003c0014t0001g0047 | 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 | 312 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(309): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): 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 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0268 others(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 | a0002c0002t0002g0303 a0002c0005t0001g0304 a0002c0006t0001g0306 others(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 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0002c0006t0004g0265 | 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 | a0001c0001t0003g0109 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(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 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0004t0001g0290 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(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 | a0001c0004t0002g0280 a0001c0004t0002g0281 |
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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0001c0004t0002g0280 | 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 | a0001c0001t0019g0276 | 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 | a0001c0003t0002g0314 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | a0001c0001t0019g0276 | 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 | 254 | a0001c0001t0001g0019 a0001c0001t0003g0001 a0001c0001t0003g0020 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): 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 | 185 | a0001c0001t0003g0001 a0001c0001t0003g0030 a0001c0001t0003g0100 others(182): 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0031 others(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 | a0001c0001t0001g0121 a0001c0001t0003g0029 a0001c0001t0003g0032 others(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 | a0002c0002t0002g0303 a0002c0005t0001g0304 a0002c0006t0001g0306 others(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 | a0003c0009t0007g0049 | 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 | a0002c0002t0001g0201 | 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 | 121 | a0001c0007t0004g0224 a0002c0002t0001g0003 a0002c0002t0001g0172 others(118): 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 | a0002c0005t0003g0263 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0018t0003g0064 others(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 | a0001c0007t0003g0125 | 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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.499+277T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14077333 | |||||||
chr17:14077375 | G | C | 303 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): 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 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0004t0001g0290 others(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 | a0001c0001t0003g0071 a0001c0001t0005g0065 a0001c0003t0002g0066 others(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 | a0001c0001t0003g0105 a0001c0001t0019g0276 a0001c0003t0002g0077 others(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 | 294 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(291): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): 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 | a0001c0001t0003g0030 a0001c0001t0003g0126 a0001c0001t0005g0289 others(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 | a0002c0002t0001g0204 a0002c0006t0004g0205 a0006c0016t0012g0004 others(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 | a0001c0001t0004g0158 a0001c0001t0004g0159 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0059 others(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 | a0001c0007t0001g0275 | 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 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | a0003c0009t0006g0098 | 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 | a0001c0003t0002g0066 a0001c0003t0002g0068 |
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 | a0001c0003t0002g0066 a0001c0003t0002g0068 |
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 | a0002c0005t0001g0304 | 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 | a0002c0006t0009g0258 | 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 | a0002c0006t0004g0257 | 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 | a0002c0002t0002g0303 a0002c0005t0001g0304 a0002c0006t0001g0306 others(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 | a0001c0004t0002g0280 a0001c0004t0002g0281 |
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 | a0001c0001t0004g0128 | 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 | a0001c0003t0002g0314 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | 259 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0100 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0007t0005g0129 | 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 | a0001c0001t0003g0120 a0001c0003t0002g0314 a0001c0003t0015g0114 others(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 | 12 | a0003c0011t0001g0040 a0003c0011t0003g0034 a0003c0011t0003g0043 others(9): Show |
12 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(9): 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 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0002c0002t0002g0175 a0002c0002t0005g0264 a0002c0006t0004g0206 |
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 | a0002c0005t0004g0208 a0002c0006t0004g0253 a0002c0008t0002g0254 |
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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.499+3521G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14080577 | |||||||
chr17:14080606 | A | G | 312 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(309): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): 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 | a0004c0025t0001g0062 | 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 | a0001c0007t0008g0115 | 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 | a0003c0009t0007g0049 a0003c0009t0007g0052 a0003c0009t0007g0053 |
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 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0004t0001g0290 others(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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0001t0003g0071 a0001c0001t0005g0065 a0001c0003t0002g0066 others(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 | a0001c0001t0003g0157 | 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 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0100 others(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 | a0001c0003t0002g0314 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | a0002c0002t0002g0252 | 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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0001c0001t0003g0156 | 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 | a0002c0005t0005g0251 | 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 | a0002c0002t0002g0200 a0002c0002t0002g0249 a0002c0002t0002g0250 others(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 | a0001c0001t0011g0312 | 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 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0003c0011t0009g0044 | 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 | a0001c0001t0019g0276 | 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 | a0008c0024t0016g0296 | 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 | a0002c0006t0004g0194 | 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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0002c0002t0001g0204 a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0001t0003g0155 | 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 | 111 | a0001c0007t0004g0224 a0002c0002t0001g0003 a0002c0002t0001g0172 others(108): 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 | a0001c0001t0019g0276 | 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 | 314 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(311): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.499+7068A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14084124 | |||||||
chr17:14084319 | A | G | 314 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(311): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): 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 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0004t0001g0290 others(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 | a0001c0001t0003g0131 a0001c0007t0013g0130 a0001c0007t0013g0132 |
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 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0100 others(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 | a0002c0005t0003g0246 a0002c0005t0003g0247 |
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 | a0002c0005t0005g0251 | 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 | a0002c0002t0002g0179 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0002c0005t0005g0199 a0002c0005t0008g0245 |
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 | a0003c0010t0001g0097 | 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 | a0001c0003t0002g0314 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | a0001c0004t0003g0168 | 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 | a0002c0006t0008g0273 | 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 | 121 | a0001c0007t0004g0224 a0002c0002t0001g0003 a0002c0002t0001g0172 others(118): 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 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0004t0001g0290 others(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 | a0001c0004t0002g0028 | 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 | a0002c0002t0001g0178 | 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 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0100 others(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 | a0002c0005t0003g0209 | 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 | a0001c0003t0002g0167 | 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 | a0001c0003t0002g0167 | 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 | a0001c0003t0002g0167 | 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 | 121 | a0001c0007t0004g0224 a0002c0002t0001g0003 a0002c0002t0001g0172 others(118): 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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0004t0001g0290 others(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 | a0003c0011t0003g0034 a0003c0011t0003g0043 a0003c0014t0001g0047 others(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 | a0001c0003t0002g0154 | 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 | a0001c0003t0002g0314 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0003t0001g0081 | 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 | a0001c0001t0019g0276 | 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 | a0002c0006t0004g0194 | 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 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | a0002c0015t0001g0278 a0002c0015t0001g0297 |
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 | a0001c0001t0003g0166 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0001t0019g0276 | 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 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0268 |
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 | a0002c0002t0001g0274 | 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 | 12 | a0003c0011t0001g0040 a0003c0011t0003g0034 a0003c0011t0003g0043 others(9): Show |
12 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(9): 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0003t0001g0079 | 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 | a0002c0002t0001g0244 | 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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0004t0003g0106 a0001c0004t0003g0168 |
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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0002c0015t0021g0309 | 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 | 87 | a0001c0007t0004g0224 a0002c0002t0001g0178 a0002c0002t0001g0185 others(84): 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0059 others(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 | a0002c0005t0004g0243 a0002c0006t0004g0194 |
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 | a0001c0001t0019g0276 | 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 | 40 | a0003c0009t0001g0095 a0003c0009t0006g0091 a0003c0009t0006g0098 others(37): Show |
40 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(37): 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 | a0001c0003t0002g0009 | 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 | 12 | a0003c0011t0001g0040 a0003c0011t0003g0034 a0003c0011t0003g0043 others(9): Show |
12 | HG00280.hp2 HG01123.hp2 HG02080.hp1 others(9): 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0002c0020t0001g0318 | 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 | 88 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0029 others(85): Show |
88 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(85): 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 | a0002c0005t0004g0216 | 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 | a0002c0015t0021g0309 | 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 | a0002c0015t0021g0309 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0059 |
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 | a0001c0003t0002g0314 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0059 others(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 | a0001c0003t0001g0080 a0001c0003t0001g0081 |
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 | a0001c0003t0002g0077 | 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 | a0001c0001t0019g0276 | 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 | 84 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(81): Show |
84 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(81): 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 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0004t0001g0290 others(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 | 86 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(83): Show |
86 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(83): 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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 |
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 | a0002c0015t0001g0278 a0002c0015t0001g0297 |
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 | a0002c0008t0023g0248 | 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 | a0001c0003t0006g0113 | 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 | a0001c0001t0003g0153 | 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 | a0001c0007t0001g0292 | 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 | a0002c0006t0001g0306 a0002c0006t0001g0307 a0002c0006t0001g0308 |
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 | a0002c0002t0002g0252 | 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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0001c0001t0003g0155 a0001c0001t0004g0112 a0001c0003t0002g0101 others(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 | 292 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(289): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.500-5907A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14096211 | |||||||
chr17:14096261 | T | C | 103 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0029 others(100): Show |
106 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(103): 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 | a0001c0001t0003g0148 | 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 | a0002c0008t0001g0277 a0003c0011t0001g0040 a0003c0011t0003g0034 others(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 | a0001c0003t0001g0149 a0001c0007t0001g0275 a0002c0008t0001g0181 |
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 | a0002c0008t0003g0301 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0155 others(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 | 215 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0029 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): 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 | a0001c0003t0001g0149 a0001c0007t0001g0275 a0002c0008t0001g0181 others(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 | a0001c0001t0003g0155 a0001c0001t0004g0112 a0001c0003t0002g0101 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 others(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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): 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 | a0002c0002t0002g0239 a0002c0006t0004g0176 a0002c0006t0004g0177 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0001g0095 others(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 | a0003c0017t0003g0037 | 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 | a0001c0007t0001g0292 | 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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0001t0003g0155 | 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 | a0002c0002t0002g0239 a0002c0006t0004g0193 a0002c0006t0004g0240 |
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 | a0002c0005t0004g0238 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 |
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 | a0002c0005t0003g0263 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(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 | 291 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(288): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): 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 | a0001c0001t0003g0155 a0001c0001t0004g0112 a0001c0003t0002g0101 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(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 | a0001c0003t0001g0149 a0001c0003t0001g0150 a0003c0017t0003g0037 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0059 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(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 | a0001c0004t0003g0106 a0001c0004t0003g0168 |
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 | a0002c0002t0002g0175 a0002c0002t0005g0264 a0002c0006t0004g0206 |
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 | 294 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(291): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 others(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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0002c0005t0003g0263 | 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 | 97 | a0001c0001t0004g0118 a0001c0003t0001g0033 a0001c0003t0001g0149 others(94): 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 | a0002c0006t0001g0308 | 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 | a0004c0018t0003g0064 a0004c0019t0001g0063 a0004c0025t0001g0062 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0001c0007t0001g0017 a0001c0007t0001g0292 a0002c0006t0001g0306 others(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 | a0002c0020t0001g0318 | 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 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(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 | a0002c0002t0002g0175 | 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 | a0003c0009t0007g0053 | 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 | a0001c0001t0003g0155 a0001c0001t0004g0112 a0001c0003t0002g0101 others(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 | a0001c0004t0002g0162 | 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 | a0001c0001t0003g0100 a0001c0001t0003g0147 |
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 | a0001c0003t0005g0123 a0001c0003t0005g0124 a0001c0004t0014g0127 others(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 | 209 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0029 others(206): Show |
213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): 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 | a0001c0004t0025g0300 | 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 | a0001c0001t0001g0121 a0001c0001t0005g0160 a0002c0005t0001g0304 others(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 | a0001c0004t0025g0300 | 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 | a0001c0004t0002g0076 a0001c0004t0002g0078 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(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 | 68 | a0001c0001t0001g0121 a0001c0001t0003g0001 a0001c0001t0003g0029 others(65): Show |
69 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(66): 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 | a0001c0001t0003g0155 a0001c0001t0004g0112 a0001c0003t0002g0101 others(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 | a0003c0017t0004g0085 a0003c0017t0004g0086 |
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 | a0001c0001t0003g0155 a0001c0001t0004g0112 a0001c0003t0002g0101 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(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 | a0002c0002t0001g0196 a0002c0008t0001g0242 a0002c0008t0003g0241 |
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 | a0001c0001t0003g0155 a0001c0001t0004g0112 a0001c0003t0002g0101 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0071 others(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 | a0001c0003t0001g0080 a0001c0003t0001g0081 |
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 | a0001c0001t0003g0071 a0001c0003t0002g0072 a0001c0003t0002g0074 others(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 | a0001c0001t0003g0116 a0001c0001t0003g0120 a0001c0001t0003g0133 others(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 | a0002c0015t0001g0278 a0002c0015t0001g0297 |
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 | 305 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(302): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.500-62C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 3/6 | chr17 | 14102056 | |||||||
chr17:14102069 | T | C | 238 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0002c0002t0022g0233 a0003c0009t0007g0035 a0003c0009t0007g0036 others(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 | 197 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(194): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0001t0019g0276 a0001c0003t0001g0079 a0001c0003t0002g0008 others(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 | a0001c0004t0001g0285 a0002c0002t0001g0003 a0002c0002t0001g0172 others(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 | 53 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(50): Show |
54 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(51): 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 | a0002c0008t0003g0301 | 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 | 165 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0158 others(162): 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 | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0002c0005t0004g0279 | 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 | 119 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0158 others(116): 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 | a0001c0001t0004g0112 | 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 | a0003c0011t0009g0044 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 |
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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0001t0003g0155 | 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 | 165 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0158 others(162): 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0007t0003g0125 a0001c0007t0003g0146 |
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 | 308 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): 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 | a0003c0011t0001g0040 | 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 | a0001c0003t0005g0123 a0001c0003t0005g0124 |
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 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0007t0001g0275 others(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 | a0001c0001t0004g0112 | 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 | a0002c0008t0001g0270 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0007t0001g0017 a0002c0006t0001g0306 a0002c0006t0001g0307 others(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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0004t0002g0076 a0001c0004t0002g0078 |
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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0001t0003g0155 | 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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | 301 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): 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 | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): 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 | a0001c0001t0003g0100 a0001c0001t0003g0147 |
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 | a0001c0003t0002g0101 a0001c0003t0002g0102 a0001c0003t0002g0111 others(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 | a0003c0009t0006g0098 | 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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0002c0008t0001g0181 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 |
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 | a0002c0006t0004g0177 | 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 | 159 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0158 others(156): 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 | a0004c0019t0001g0063 | 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 | a0002c0006t0004g0194 | 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 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 |
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 | a0001c0001t0003g0155 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0002c0005t0004g0216 | 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 | a0001c0001t0005g0014 a0001c0003t0006g0104 a0001c0003t0006g0113 others(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 | 92 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(89): Show |
94 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(91): 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 | a0001c0001t0004g0112 | 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 | a0002c0005t0003g0263 | 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 | a0001c0003t0002g0072 a0001c0003t0002g0075 a0001c0004t0002g0073 |
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 | a0004c0019t0001g0063 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | 314 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(311): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): 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 | a0002c0005t0004g0238 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0006c0016t0012g0004 a0006c0016t0012g0203 a0010c0026t0001g0057 |
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 | a0002c0002t0002g0211 a0002c0002t0003g0212 |
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 | a0001c0004t0014g0127 a0001c0004t0014g0151 |
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 | 151 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(148): Show |
152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): 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 | a0002c0005t0005g0251 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0001c0003t0002g0007 a0001c0004t0002g0018 |
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 | a0002c0008t0003g0241 a0002c0008t0003g0301 |
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 | a0001c0003t0002g0008 | 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 | 161 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0158 others(158): 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | 78 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(75): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0001t0011g0311 others(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 | a0001c0007t0001g0017 a0001c0007t0001g0292 a0001c0012t0001g0293 others(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 | a0001c0007t0003g0146 | 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 | a0001c0004t0001g0285 a0002c0002t0001g0003 a0002c0002t0001g0172 others(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 | 314 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(311): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): 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 | a0003c0010t0006g0092 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0002c0005t0004g0002 | 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 | 53 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(50): Show |
54 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(51): 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 | a0001c0003t0002g0101 a0001c0003t0002g0102 a0001c0003t0002g0111 others(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 | a0011c0021t0001g0186 | 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 | a0001c0003t0002g0021 | 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 | a0002c0002t0001g0185 | 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0001c0001t0003g0140 | 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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): 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 | a0001c0003t0001g0033 a0002c0005t0003g0188 a0002c0005t0003g0209 |
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 | a0001c0003t0002g0287 a0001c0003t0002g0314 |
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 | a0001c0003t0001g0080 | 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 | a0002c0008t0001g0270 a0002c0008t0001g0271 a0002c0008t0001g0272 |
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 | a0001c0003t0001g0080 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0029 others(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 | a0002c0006t0004g0257 | 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 | a0001c0004t0002g0076 | 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 | a0003c0010t0018g0087 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0002c0006t0004g0253 | 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 | a0001c0007t0001g0017 a0001c0007t0001g0292 a0001c0012t0001g0293 others(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 | a0001c0003t0002g0101 a0001c0003t0002g0102 a0001c0003t0002g0111 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | 151 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0158 others(148): 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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.624+14020C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14116262 | |||||||
chr17:14116272 | A | C | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): 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 | a0001c0001t0003g0141 | 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 | a0001c0003t0001g0152 a0001c0003t0002g0007 |
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 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0158 others(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 | 63 | a0001c0001t0003g0020 a0001c0001t0003g0029 a0001c0001t0003g0030 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(60): 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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | 64 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(61): Show |
65 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(62): 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 | a0001c0007t0004g0025 | 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 a0010c0026t0001g0057 |
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 | a0003c0011t0001g0040 a0003c0011t0003g0034 a0003c0011t0003g0043 others(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 | a0002c0006t0004g0182 | 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 | a0006c0016t0012g0203 | 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 | a0001c0003t0002g0011 | 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 | a0001c0003t0020g0006 | 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | 104 | a0001c0001t0003g0126 a0001c0001t0004g0112 a0001c0001t0004g0118 others(101): 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 | a0001c0003t0002g0066 a0001c0003t0002g0068 a0001c0003t0002g0101 others(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 | a0002c0005t0004g0191 a0002c0005t0004g0236 a0002c0005t0004g0237 |
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 | a0002c0002t0001g0259 | 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 | a0002c0008t0001g0262 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0001c0003t0001g0080 a0002c0002t0001g0172 a0002c0002t0001g0174 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0001c0004t0001g0285 a0002c0002t0001g0214 a0002c0002t0001g0215 |
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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0002c0002t0001g0003 | 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 | a0001c0003t0002g0066 a0001c0003t0002g0068 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0011c0021t0001g0186 |
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 | a0002c0005t0005g0199 a0002c0005t0008g0245 a0004c0018t0001g0060 others(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 | a0001c0004t0014g0127 a0001c0004t0014g0151 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0116 a0001c0001t0003g0120 others(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 | 152 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(149): 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 | a0004c0019t0001g0059 | 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 | a0003c0011t0003g0034 a0003c0011t0003g0043 a0012c0028t0003g0042 |
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 | a0001c0001t0003g0144 | 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 | a0001c0004t0002g0023 a0002c0002t0001g0185 |
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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | 309 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(306): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): 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 | a0001c0007t0008g0115 | 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 | 156 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(153): 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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | a0001c0001t0019g0276 | 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 | 152 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(149): 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | 158 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(155): 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 | 156 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(153): 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 | a0001c0001t0003g0100 a0001c0001t0003g0147 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(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 | 60 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(58): 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 | a0002c0008t0001g0197 | 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 | a0002c0002t0002g0211 a0002c0002t0002g0252 a0002c0002t0003g0212 |
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 | a0001c0001t0019g0276 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | 158 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(155): 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 | a0001c0012t0001g0291 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | 192 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(189): 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 | a0001c0003t0002g0102 | 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 | a0003c0009t0006g0098 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0004c0018t0001g0060 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0002c0005t0004g0238 | 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 | a0001c0007t0004g0025 a0001c0007t0004g0224 a0002c0006t0004g0253 |
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 | a0001c0003t0002g0011 | 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 | a0001c0007t0004g0025 | 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 | a0002c0002t0001g0215 | 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 | a0004c0018t0003g0064 | 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 | a0002c0002t0001g0269 | 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 | a0002c0006t0009g0258 a0003c0011t0001g0040 a0003c0011t0003g0034 others(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 | a0003c0017t0003g0037 | 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 | a0002c0005t0004g0191 a0002c0005t0004g0236 a0002c0005t0004g0237 |
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 | 260 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0003c0010t0006g0084 | 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 | a0001c0004t0025g0300 | 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 | a0002c0015t0001g0278 a0002c0015t0001g0297 |
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 | a0002c0002t0001g0261 a0002c0008t0001g0181 a0003c0010t0001g0083 |
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 | a0002c0008t0001g0213 | 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 | a0001c0004t0002g0078 | 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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0001c0007t0008g0115 | 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 | a0001c0004t0001g0285 a0002c0002t0001g0003 a0002c0002t0001g0173 others(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 | a0002c0005t0004g0230 a0002c0006t0004g0232 |
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 | 296 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(293): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): 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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | 299 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(296): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): 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 | a0003c0010t0003g0096 a0003c0010t0006g0084 a0003c0010t0006g0088 others(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 | a0002c0008t0001g0229 | 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 | 152 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(149): 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 | a0001c0007t0003g0108 | 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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0004c0025t0001g0062 | 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 | a0002c0005t0004g0184 | 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 | a0002c0002t0022g0233 | 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 | a0001c0001t0003g0148 a0001c0003t0001g0079 a0001c0003t0002g0009 others(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 | a0001c0001t0005g0014 a0001c0003t0002g0008 a0001c0003t0002g0011 others(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 | a0001c0003t0002g0287 a0002c0006t0008g0273 a0002c0008t0002g0254 |
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 | 143 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(140): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): 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 | a0001c0001t0004g0112 a0001c0003t0006g0104 a0001c0003t0006g0113 others(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 | a0001c0001t0004g0159 a0001c0003t0002g0016 a0001c0003t0002g0027 others(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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0001c0007t0004g0164 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0002c0006t0009g0258 others(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 | a0002c0002t0002g0180 | 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 | a0002c0002t0002g0180 | 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 | a0001c0001t0003g0105 a0001c0001t0003g0126 |
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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0003t0002g0072 a0001c0003t0002g0075 a0001c0004t0002g0073 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0002c0006t0009g0258 a0003c0011t0001g0040 a0003c0011t0003g0034 others(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 | a0004c0019t0001g0063 | 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 | a0001c0003t0005g0123 a0001c0003t0005g0124 |
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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0001c0001t0003g0139 a0001c0001t0003g0144 a0001c0003t0002g0016 others(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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | a0001c0003t0005g0123 a0001c0003t0005g0124 |
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 | a0001c0004t0002g0161 a0003c0029t0002g0048 |
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 | a0002c0005t0005g0199 | 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 | a0001c0001t0003g0032 | 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 | a0001c0001t0003g0155 | 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | 312 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(309): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): 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 | 47 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(44): 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0002c0006t0009g0258 a0003c0011t0001g0040 a0003c0011t0003g0034 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0002c0006t0009g0258 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0002c0006t0009g0258 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0002c0002t0002g0217 | 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 | 312 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(309): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): 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 | a0004c0018t0003g0064 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0002c0002t0002g0252 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0010c0026t0001g0057 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0002c0006t0009g0258 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0002c0005t0004g0243 | 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 | a0002c0015t0001g0278 a0002c0015t0001g0297 |
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 | a0002c0006t0005g0302 | 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 | a0001c0001t0019g0276 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0009c0022t0002g0005 | 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 | a0001c0001t0019g0276 | 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 | a0001c0001t0019g0276 | 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 | a0001c0007t0004g0224 | 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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0004t0002g0023 a0002c0002t0001g0185 |
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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0001t0019g0276 others(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 | a0003c0009t0007g0053 | 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 | a0001c0007t0005g0129 | 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0002c0006t0009g0258 a0003c0011t0001g0040 |
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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | 59 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(56): 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0001t0019g0276 others(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 | a0001c0001t0019g0276 | 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 | a0001c0001t0003g0133 | 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 | a0002c0008t0001g0183 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0001t0019g0276 others(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 | a0002c0005t0004g0187 | 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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): 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 | a0001c0001t0003g0171 a0002c0005t0004g0243 a0002c0006t0003g0218 others(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 | a0004c0019t0001g0059 | 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 | a0001c0001t0005g0289 a0001c0001t0019g0276 a0001c0007t0001g0017 others(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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0001t0019g0276 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0001t0005g0289 a0001c0007t0001g0017 a0001c0007t0001g0275 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0001c0004t0003g0106 others(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 | a0001c0001t0003g0144 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0002c0006t0009g0258 others(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 | a0002c0002t0002g0255 a0002c0002t0002g0256 |
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 | a0001c0003t0002g0101 a0001c0003t0002g0102 |
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 | a0002c0008t0001g0197 a0002c0008t0001g0213 |
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 | a0001c0003t0002g0102 | 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 | a0002c0008t0003g0241 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | 48 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(45): 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0003t0001g0033 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | 59 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(56): 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 | a0002c0002t0001g0204 | 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 | 48 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(45): 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0002c0006t0009g0258 others(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 | a0001c0001t0003g0107 a0001c0001t0003g0109 a0001c0001t0003g0138 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0001t0003g0139 a0001c0003t0001g0033 a0001c0003t0001g0080 others(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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | 46 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(43): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0002c0006t0009g0258 others(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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0001c0003t0001g0079 a0001c0004t0001g0290 a0001c0012t0001g0291 |
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 | a0001c0001t0019g0276 | 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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0004c0025t0001g0062 | 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 | a0003c0010t0018g0087 | 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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0003c0009t0007g0056 | 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 | a0001c0003t0001g0149 a0001c0003t0001g0150 a0002c0002t0001g0178 others(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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0001c0003t0002g0111 a0001c0003t0002g0119 a0001c0003t0002g0167 others(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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0007t0004g0025 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0003c0010t0001g0093 a0003c0010t0006g0094 |
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 | a0002c0002t0001g0174 | 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 | a0001c0001t0019g0276 | 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 | a0001c0001t0003g0120 a0001c0001t0005g0014 a0001c0003t0002g0009 others(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 | 50 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(47): Show |
51 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(48): 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 | 134 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(131): 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 | a0001c0003t0005g0123 a0001c0003t0005g0124 a0002c0002t0001g0269 others(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 | a0001c0007t0003g0015 | 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 | a0001c0004t0002g0280 | 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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | 55 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(52): Show |
56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): 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 | a0004c0019t0001g0063 | 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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0002c0005t0003g0188 | 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 | a0001c0001t0005g0160 a0001c0001t0005g0288 a0001c0001t0005g0289 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0010c0026t0001g0057 | 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0001t0005g0288 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0003t0001g0080 | 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 | a0001c0003t0006g0113 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0001t0005g0014 a0001c0001t0005g0160 a0001c0001t0005g0288 others(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 | a0002c0005t0003g0188 | 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 | a0002c0006t0009g0258 a0003c0011t0001g0040 a0003c0011t0003g0034 others(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 | 50 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(47): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0131 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0001t0004g0118 a0001c0007t0004g0164 |
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 | a0002c0002t0002g0256 | 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 | a0001c0001t0003g0155 | 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0001t0003g0020 | 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 | a0001c0004t0002g0110 | 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 | a0001c0007t0013g0130 a0001c0007t0013g0132 |
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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | 114 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(111): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0002c0002t0002g0192 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0003c0009t0007g0050 | 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 | 311 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(308): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0001t0019g0276 | 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 | a0001c0007t0008g0115 a0002c0005t0005g0199 a0002c0005t0008g0245 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0002c0005t0004g0187 a0002c0005t0004g0195 a0005c0013t0004g0135 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0002c0005t0004g0191 a0002c0005t0004g0235 a0002c0005t0004g0236 others(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 | a0002c0002t0001g0259 | 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0002c0005t0001g0304 |
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 | a0002c0008t0001g0271 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0003t0001g0081 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0100 a0001c0001t0003g0147 others(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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0001c0007t0008g0115 others(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 | 148 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(145): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): 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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0001c0001t0005g0065 a0001c0003t0006g0104 a0001c0003t0006g0113 others(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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0002c0002t0001g0215 | 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 | a0001c0001t0005g0289 | 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 | a0001c0007t0001g0275 | 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 | a0002c0005t0005g0199 a0002c0005t0008g0245 |
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 | a0001c0001t0003g0100 a0001c0001t0003g0147 |
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 | a0002c0006t0004g0265 a0003c0011t0004g0041 |
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 | a0002c0002t0002g0211 a0002c0002t0003g0212 |
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 | a0002c0015t0021g0309 | 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 | 311 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(308): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): 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 | a0002c0005t0004g0191 a0002c0005t0004g0236 a0002c0005t0004g0237 |
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 | a0002c0005t0004g0243 a0002c0006t0004g0194 |
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 | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0012t0001g0291 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0003t0002g0154 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0002c0008t0003g0301 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0001c0007t0008g0115 a0002c0005t0005g0199 a0002c0005t0008g0245 others(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 | a0001c0003t0002g0007 a0001c0004t0002g0018 |
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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 others(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 | a0004c0019t0001g0059 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0001t0019g0276 a0001c0003t0002g0009 a0001c0004t0002g0165 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0107 a0001c0001t0005g0014 others(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 | a0001c0001t0003g0029 a0001c0001t0003g0109 a0001c0001t0003g0138 others(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 | 122 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0030 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): 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 | a0001c0001t0003g0147 a0001c0001t0003g0171 a0001c0001t0005g0160 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 others(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 | a0010c0026t0001g0057 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0145 a0001c0001t0003g0166 |
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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0002c0002t0001g0185 | 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 | a0002c0002t0002g0219 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0003t0002g0009 a0001c0003t0002g0010 a0001c0003t0002g0021 |
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 | a0001c0003t0002g0024 a0001c0004t0002g0076 a0001c0004t0002g0078 |
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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0003t0001g0080 a0001c0003t0001g0081 a0001c0003t0005g0123 others(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 | a0002c0002t0001g0185 | 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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | 52 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(49): 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0002c0005t0001g0304 | 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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0003t0002g0007 a0001c0004t0002g0018 |
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 | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0004t0002g0013 | 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 | a0002c0005t0004g0234 | 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 | a0001c0001t0019g0276 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0003t0005g0123 a0001c0003t0005g0124 a0001c0004t0014g0127 others(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 | a0004c0025t0001g0062 | 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 | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0002c0002t0001g0266 | 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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0002c0002t0022g0233 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.625-5106C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14154771 | |||||||
chr17:14154868 | CTG | C | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0065 others(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 | 181 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(178): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0065 others(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 | 138 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): 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 | a0002c0015t0021g0309 | 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 | a0001c0007t0004g0122 | 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 | a0001c0004t0002g0023 | 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 | a0001c0003t0001g0080 a0002c0002t0001g0172 a0002c0002t0001g0174 |
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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0007t0004g0025 | 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 | 182 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | 54 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): 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 | a0002c0006t0004g0194 | 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 | a0001c0012t0001g0293 | 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0001c0007t0008g0115 a0002c0005t0005g0199 a0002c0005t0008g0245 others(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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.625-3641T>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14156236 | |||||||
chr17:14156318 | C | T | 60 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(58): 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 | a0001c0003t0002g0024 a0003c0009t0001g0095 |
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 | a0002c0005t0004g0260 | 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 | a0001c0007t0001g0017 a0001c0007t0001g0292 a0002c0006t0001g0306 others(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 | a0001c0003t0002g0011 | 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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | 152 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(149): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): 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 | a0002c0006t0003g0218 | 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 | 52 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(49): 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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | 154 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): 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 | a0011c0021t0001g0186 | 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 | 154 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | 126 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): 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 | a0011c0021t0001g0186 | 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0001c0004t0002g0023 | 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0001t0019g0276 | 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 a0006c0016t0012g0004 others(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 | a0001c0001t0004g0128 | 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 | a0001c0007t0008g0115 a0002c0005t0005g0199 a0002c0005t0008g0245 others(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 | a0002c0002t0001g0178 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0004t0002g0281 | 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 | a0001c0012t0001g0291 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 others(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 | 154 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): 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 | a0004c0019t0001g0059 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0001c0001t0019g0276 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | 54 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): 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 | a0002c0005t0004g0207 | 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 | a0002c0006t0008g0273 | 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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | 156 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.625-470T>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159407 | |||||||
chr17:14159650 | G | T | 54 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.625-227G>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159650 | |||||||
chr17:14159657 | G | A | 154 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.625-220G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 4/6 | chr17 | 14159657 | |||||||
chr17:14159682 | AATT | A | 154 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): 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 | a0001c0007t0004g0164 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0001t0019g0276 others(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 | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0001c0001t0003g0071 a0001c0001t0003g0116 a0001c0003t0020g0006 others(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 | a0003c0011t0004g0041 | 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 | a0003c0011t0003g0034 a0003c0011t0003g0043 a0012c0028t0003g0042 |
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 | a0001c0007t0004g0025 | 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 | a0002c0005t0003g0202 | 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 | a0002c0006t0009g0258 | 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 | 52 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(49): 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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0003c0010t0006g0092 | 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 | a0001c0001t0003g0139 a0001c0001t0003g0171 |
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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0004t0002g0018 | 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 | a0001c0012t0001g0291 | 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 | a0001c0001t0003g0166 | 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 | a0002c0002t0001g0269 | 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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0002c0006t0004g0205 | 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 | a0002c0008t0001g0272 | 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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | 297 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0005t0004g0238 others(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 | a0002c0006t0004g0222 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0001t0003g0105 | 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(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 | a0001c0001t0003g0107 a0001c0001t0003g0109 a0001c0001t0003g0133 others(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 | a0001c0003t0001g0079 a0001c0003t0002g0021 a0001c0003t0002g0066 others(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 | a0002c0002t0002g0211 a0003c0010t0006g0089 a0003c0010t0006g0094 others(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 | a0001c0003t0006g0113 a0002c0002t0002g0239 a0002c0002t0003g0212 others(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 | a0003c0009t0006g0091 | 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 | 72 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(69): 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 | 52 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(49): 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0012t0001g0291 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0010c0026t0001g0057 | 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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | 154 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.695+4496A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14164443 | |||||||
chr17:14164453 | A | G | 4 | a0002c0005t0004g0002 a0002c0005t0004g0227 a0002c0005t0004g0260 others(1): 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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | a0001c0007t0001g0017 a0002c0006t0001g0306 a0002c0006t0001g0307 others(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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | 183 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): 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 | a0001c0001t0019g0276 | 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 | a0001c0001t0019g0276 | 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 | a0003c0011t0003g0034 a0003c0011t0003g0043 a0012c0028t0003g0042 |
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 | 154 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): 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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | a0002c0008t0001g0183 | 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 | 154 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): 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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | a0003c0009t0007g0054 | 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 | a0002c0005t0004g0230 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0003c0009t0001g0095 | 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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0001c0012t0001g0294 | 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 | 311 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(308): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0065 others(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 | 198 | a0001c0001t0003g0020 a0001c0001t0003g0029 a0001c0001t0003g0030 others(195): Show |
199 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(196): 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 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0014g0127 others(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 |
126 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0004t0002g0161 | 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 | a0001c0001t0003g0100 | 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 | a0002c0002t0001g0201 a0002c0002t0002g0180 a0002c0002t0002g0200 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0149 a0001c0003t0001g0150 others(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 | a0001c0003t0006g0113 a0003c0009t0006g0091 a0003c0009t0006g0098 others(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 | a0001c0003t0006g0104 a0003c0009t0007g0035 a0003c0009t0007g0036 others(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 | 122 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): 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 | a0001c0001t0005g0065 a0002c0005t0005g0251 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0003t0005g0123 a0001c0003t0005g0124 a0001c0004t0014g0127 others(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 | a0002c0006t0004g0253 | 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0004t0002g0134 | 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 | a0002c0005t0005g0199 a0002c0005t0008g0245 |
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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0001c0003t0001g0079 a0001c0004t0001g0290 |
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 | a0002c0002t0001g0204 | 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 | a0010c0026t0001g0057 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0001c0001t0003g0157 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0001c0001t0004g0128 | 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 | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.695+8572C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14168519 | |||||||
chr17:14168589 | C | T | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): 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 | a0001c0012t0001g0291 | 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 | a0001c0004t0002g0161 | 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 | a0002c0005t0004g0238 | 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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0003c0009t0007g0051 | 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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0003c0011t0003g0034 a0003c0011t0003g0043 a0012c0028t0003g0042 |
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 | a0002c0008t0001g0272 | 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 | a0001c0004t0001g0286 | 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 | a0001c0001t0003g0155 | 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 | 55 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(52): Show |
56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.695+10419A>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170366 | |||||||
chr17:14170438 | GTTAC | G | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): 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 | 54 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.695+10590C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170537 | |||||||
chr17:14170538 | A | G | 124 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): 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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0010c0026t0001g0057 | 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 | a0002c0005t0005g0251 | 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 | a0002c0005t0004g0216 | 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 | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0002c0006t0004g0205 | 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 | a0002c0002t0001g0201 | 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 | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.695+10983G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14170930 | |||||||
chr17:14170961 | G | A | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): 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 | a0002c0006t0004g0223 | 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 | a0002c0002t0001g0214 | 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0001c0003t0001g0080 a0001c0003t0001g0081 a0001c0003t0005g0123 others(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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0002c0006t0004g0253 | 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 | a0003c0009t0007g0036 | 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 | a0002c0002t0001g0172 a0002c0002t0001g0174 |
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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | a0002c0008t0002g0231 | 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0001c0004t0002g0078 | 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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | 151 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(148): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): 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 | a0001c0003t0002g0102 | 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 | a0002c0002t0002g0249 a0002c0002t0002g0250 a0002c0008t0023g0248 others(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 | 151 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(148): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): 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 | a0001c0001t0003g0157 a0001c0007t0010g0315 a0001c0007t0010g0316 others(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 | a0002c0005t0004g0207 | 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 | 150 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): 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 | a0001c0003t0001g0152 a0001c0003t0005g0124 a0002c0002t0002g0252 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0001c0003t0002g0024 a0001c0004t0001g0282 a0001c0004t0001g0283 others(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 | a0001c0001t0003g0071 a0001c0001t0003g0147 a0001c0001t0003g0148 others(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 | 133 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): 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 | a0001c0003t0001g0152 a0001c0003t0005g0124 a0002c0002t0002g0252 others(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 | a0002c0005t0001g0304 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0004c0019t0001g0059 | 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 | 151 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(148): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): 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 | a0002c0008t0003g0241 a0002c0008t0003g0301 |
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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | a0001c0003t0001g0152 | 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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | a0002c0006t0009g0258 a0003c0011t0009g0044 a0006c0016t0012g0004 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0002c0005t0004g0236 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0003c0010t0006g0090 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0007t0001g0017 a0001c0007t0001g0292 a0002c0006t0001g0306 others(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 | 133 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0020 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): 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 | a0001c0004t0002g0103 a0002c0002t0001g0196 a0002c0002t0002g0179 others(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 | a0001c0004t0002g0103 a0002c0002t0002g0179 |
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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0002c0015t0001g0278 a0002c0015t0001g0297 |
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 | a0001c0004t0002g0103 a0002c0002t0002g0179 |
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 | a0001c0001t0003g0030 a0001c0001t0004g0158 a0001c0001t0011g0311 others(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 | 53 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(50): Show |
54 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(51): 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 | a0001c0001t0019g0276 a0001c0003t0006g0104 a0001c0003t0006g0113 others(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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | 152 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(149): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): 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 | a0001c0003t0002g0066 | 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 | a0003c0011t0004g0041 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.695+15020C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174967 | |||||||
chr17:14174997 | CA | C | 151 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(148): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.695+15051delA | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14174997 | |||||||
chr17:14175045 | T | C | 1 | a0001c0007t0004g0025 | 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 | 93 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(90): 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 | 93 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(90): 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 | a0001c0003t0002g0009 a0001c0003t0002g0010 a0001c0003t0002g0022 |
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 | a0001c0003t0002g0008 a0001c0003t0002g0011 a0001c0003t0002g0021 others(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 | a0001c0004t0002g0012 a0009c0022t0002g0005 |
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 | a0002c0008t0002g0231 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0158 a0001c0001t0004g0159 others(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 | a0001c0001t0004g0112 a0001c0001t0004g0128 a0001c0001t0005g0065 others(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 | a0002c0002t0001g0190 a0003c0010t0001g0097 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0014 others(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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0001t0019g0276 | 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 | 34 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0030 others(31): Show |
35 | HG00099.hp1 HG00408.hp2 HG00621.hp2 others(32): 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 | a0001c0001t0003g0029 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0014 others(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 | a0002c0006t0004g0222 | 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 | a0001c0007t0010g0316 | 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 | a0002c0006t0003g0218 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | 93 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(90): 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 | 93 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(90): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0014 others(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 | 157 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(154): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0003t0002g0007 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | 67 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(64): 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 | 89 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(86): Show |
91 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(88): 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 | a0001c0007t0001g0292 | 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 | a0003c0011t0004g0041 | 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 | a0003c0011t0004g0041 | 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 | a0001c0001t0005g0065 | 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 | a0001c0003t0002g0072 a0001c0003t0002g0075 a0001c0004t0002g0073 |
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 | 166 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(163): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): 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 | a0004c0019t0001g0063 | 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 | a0001c0003t0002g0072 a0001c0003t0002g0075 a0001c0004t0002g0073 others(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 | a0001c0001t0003g0133 | 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 | 155 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): 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 | a0001c0007t0008g0115 a0002c0005t0005g0199 a0002c0005t0005g0251 others(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 | a0001c0007t0008g0115 a0002c0005t0005g0199 a0002c0005t0005g0251 others(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 | a0002c0005t0003g0188 | 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 | a0001c0003t0001g0033 a0001c0003t0001g0149 a0001c0003t0001g0150 others(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 | a0002c0002t0001g0003 | 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 | a0002c0005t0004g0216 | 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 | a0002c0006t0004g0189 | 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 | 156 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): 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 | a0002c0002t0001g0215 | 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 | 54 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): 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 | a0001c0007t0003g0015 | 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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.696-15338G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14176651 | |||||||
chr17:14176737 | C | T | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0004t0002g0013 | 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 | a0001c0004t0002g0110 | 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 | a0005c0013t0004g0135 | 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 | 155 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): 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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | 155 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): 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 | a0002c0005t0004g0243 | 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 | a0001c0007t0004g0070 | 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 | 155 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.696-13639A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178350 | |||||||
chr17:14178374 | G | A | 155 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.696-13615G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178374 | |||||||
chr17:14178389 | G | A | 151 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.696-13600G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14178389 | |||||||
chr17:14178411 | G | A | 155 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): 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 | a0008c0024t0016g0296 a0011c0021t0001g0186 |
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 | a0001c0003t0002g0287 | 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 | 155 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): 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 | a0002c0002t0001g0204 | 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 | a0002c0002t0001g0204 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | 55 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(52): 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 | 180 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(177): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): 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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0003t0002g0007 a0001c0004t0002g0018 |
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 | a0002c0006t0004g0222 | 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 | a0001c0012t0001g0291 | 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 | a0002c0008t0003g0241 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0002c0002t0001g0215 | 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 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | 54 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): 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 | a0002c0002t0001g0204 | 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 | a0001c0012t0001g0291 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0160 others(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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0001t0004g0118 a0001c0003t0005g0123 a0001c0003t0005g0124 others(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 | a0002c0002t0001g0196 | 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 | a0002c0002t0001g0196 | 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 | a0001c0001t0003g0145 a0002c0002t0002g0219 a0002c0008t0001g0277 |
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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0001t0003g0071 | 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 | a0001c0003t0001g0152 | 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 | 177 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): 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 | a0001c0007t0001g0275 a0001c0007t0005g0129 a0004c0025t0001g0062 |
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 | a0001c0004t0002g0161 | 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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0003t0002g0111 a0001c0003t0002g0167 a0002c0002t0002g0303 others(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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | a0002c0006t0009g0258 a0003c0011t0009g0044 |
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 | a0002c0006t0004g0194 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0001c0001t0003g0139 a0001c0003t0002g0077 a0001c0004t0001g0285 others(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 | a0001c0003t0002g0074 a0002c0002t0001g0003 a0002c0002t0002g0192 others(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 | 67 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(64): Show |
68 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(65): 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 others(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 | 100 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0142 others(97): 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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | a0001c0003t0002g0314 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0001t0003g0029 | 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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 |
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 | a0003c0011t0017g0082 | 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 | 155 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0002c0006t0001g0308 | 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 | a0001c0003t0005g0123 a0001c0003t0005g0124 |
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 | 55 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(52): 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 | a0006c0016t0012g0004 | 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 |
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 | a0002c0006t0004g0205 | 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 | a0001c0007t0003g0015 | 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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0002c0015t0001g0278 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0065 others(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 | a0002c0002t0001g0178 | 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 | a0001c0004t0001g0285 a0002c0002t0001g0003 a0002c0002t0001g0173 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0313 |
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 | a0001c0001t0011g0312 | 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 | a0001c0007t0001g0275 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): 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 | a0002c0002t0002g0211 a0002c0002t0002g0252 a0002c0002t0003g0212 |
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 | a0001c0004t0002g0161 a0004c0019t0001g0059 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0004c0019t0003g0058 |
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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 |
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 | a0002c0002t0002g0303 a0002c0008t0001g0183 a0003c0009t0007g0035 others(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 | a0002c0005t0003g0263 | 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 | 26 | a0001c0003t0002g0066 a0001c0003t0002g0068 a0001c0003t0002g0101 others(23): 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 | a0001c0001t0019g0276 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | 117 | a0001c0001t0003g0166 a0001c0001t0004g0112 a0001c0001t0004g0118 others(114): 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 | a0003c0011t0009g0044 | 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 | a0001c0001t0003g0131 a0001c0007t0013g0130 a0001c0007t0013g0132 others(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 | a0001c0001t0003g0131 a0001c0007t0013g0130 a0001c0007t0013g0132 others(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 | a0001c0001t0003g0116 a0001c0001t0003g0131 a0001c0007t0013g0130 others(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 | a0001c0001t0003g0171 | 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 | 144 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): 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 | a0002c0002t0001g0204 a0002c0002t0002g0211 a0002c0002t0002g0252 others(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 | a0002c0002t0002g0211 a0002c0002t0002g0252 a0002c0002t0003g0212 others(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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.696-5035C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14186954 | |||||||
chr17:14186985 | GT | G | 152 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(149): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): 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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): 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 | a0001c0007t0008g0115 a0002c0005t0008g0245 a0002c0006t0008g0273 |
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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0268 |
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 | 229 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): 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 | a0001c0001t0003g0120 a0001c0001t0004g0118 a0001c0001t0019g0276 others(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 | a0001c0003t0002g0027 a0001c0003t0002g0066 a0001c0003t0002g0068 others(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 | a0001c0001t0003g0100 a0001c0001t0003g0147 a0002c0008t0001g0242 |
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 | 140 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(137): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): 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 | a0001c0003t0002g0007 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | a0002c0015t0001g0278 a0002c0015t0001g0297 |
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 | a0002c0002t0001g0228 | 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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | 52 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(49): 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 | a0002c0006t0004g0205 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | 304 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): 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 | a0001c0007t0001g0017 a0001c0007t0001g0292 a0002c0006t0001g0306 others(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 | a0008c0024t0016g0296 | 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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.696-3027A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14188962 | |||||||
chr17:14189079 | C | CT | 123 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(120): Show |
125 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(122): 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 | a0001c0004t0001g0282 a0001c0004t0001g0283 a0001c0004t0001g0284 others(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 | 63 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(60): 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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0007t0008g0115 a0002c0005t0008g0245 a0002c0006t0008g0273 |
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 | a0001c0001t0019g0276 | 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 | a0001c0001t0001g0121 | 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 | a0001c0003t0001g0081 | 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 | 52 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(49): 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 | 52 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(49): 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 | 152 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(149): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): 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 | a0001c0001t0004g0118 a0001c0007t0004g0164 |
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 | a0003c0009t0007g0051 | 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 | a0002c0015t0001g0278 | 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 | a0003c0009t0007g0035 a0003c0009t0007g0036 a0003c0009t0007g0049 others(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 | a0002c0002t0002g0303 | 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 | a0001c0001t0003g0131 a0001c0007t0013g0130 a0001c0007t0013g0132 |
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 | a0002c0006t0009g0258 a0003c0011t0009g0044 a0006c0016t0012g0004 others(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 | 152 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(149): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 a0007c0027t0009g0210 |
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 | a0003c0009t0007g0053 | 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 | a0001c0004t0002g0165 | 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 | a0001c0001t0003g0107 a0001c0001t0003g0109 a0001c0001t0003g0138 |
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 | a0001c0003t0001g0080 a0002c0002t0001g0172 a0002c0002t0001g0174 others(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 | a0001c0001t0019g0276 | 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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.696-669G>C | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191320 | |||||||
chr17:14191355 | A | G | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.696-634A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191355 | |||||||
chr17:14191362 | C | T | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.696-627C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 5/6 | chr17 | 14191362 | |||||||
chr17:14191445 | T | A | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0007t0003g0146 | 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 a0006c0016t0012g0004 others(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 | a0001c0001t0019g0276 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 a0007c0027t0009g0210 |
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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0007t0010g0317 a0008c0024t0016g0296 a0010c0026t0001g0057 others(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 | a0001c0007t0004g0164 | 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 | a0001c0012t0001g0291 a0001c0012t0001g0293 a0001c0012t0001g0294 others(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 | a0001c0007t0010g0315 a0001c0007t0010g0316 |
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 | a0001c0023t0001g0163 a0002c0006t0004g0226 a0010c0026t0001g0057 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0065 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0002c0005t0001g0304 |
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 | a0002c0015t0001g0278 a0002c0015t0001g0297 |
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 | a0002c0002t0001g0244 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0131 a0001c0007t0013g0130 others(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 | a0001c0001t0003g0020 a0003c0011t0001g0040 |
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 | a0010c0026t0001g0057 | 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 | a0001c0007t0010g0317 a0008c0024t0016g0296 a0010c0026t0001g0057 others(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 | a0001c0007t0001g0292 | 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 | a0001c0001t0019g0276 | 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 | 53 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(50): 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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | 59 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(56): Show |
60 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(57): 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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0005g0065 others(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 | a0001c0012t0001g0291 | 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 | a0001c0001t0005g0065 a0001c0003t0001g0033 a0001c0003t0001g0079 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0157 others(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 | 53 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(50): 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 | a0001c0001t0003g0071 | 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 | a0001c0007t0008g0115 a0002c0005t0008g0245 a0002c0006t0008g0273 |
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 | a0001c0004t0003g0106 a0001c0004t0003g0168 a0002c0008t0003g0241 others(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 | a0001c0003t0005g0123 a0001c0003t0005g0124 |
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 | a0001c0001t0003g0071 a0001c0003t0002g0016 a0001c0003t0002g0027 others(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 | a0001c0001t0003g0071 a0001c0003t0002g0016 a0001c0003t0002g0027 others(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 | a0001c0003t0001g0079 a0001c0004t0001g0290 |
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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0003t0002g0016 a0001c0003t0002g0027 a0001c0003t0002g0066 others(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 | a0001c0001t0005g0288 a0002c0006t0005g0302 a0008c0024t0016g0296 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0002c0005t0001g0304 |
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 | 53 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(50): Show |
54 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(51): 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 | a0002c0006t0004g0177 | 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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0002c0005t0004g0238 | 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 | a0001c0003t0001g0079 a0001c0004t0001g0290 |
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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0004t0001g0299 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0002c0002t0001g0196 | 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 | a0001c0004t0001g0286 | 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 | a0001c0001t0003g0140 a0001c0001t0003g0141 |
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 | a0001c0001t0003g0140 | 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 | a0006c0016t0012g0004 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 |
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 | 138 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): 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 | a0001c0007t0008g0115 a0002c0005t0008g0245 a0002c0006t0008g0273 |
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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0001c0003t0002g0077 a0002c0002t0001g0201 a0002c0002t0002g0180 others(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 | 53 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(50): 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 | a0002c0002t0001g0228 a0002c0008t0001g0220 a0002c0008t0001g0229 others(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 | a0001c0001t0005g0288 | 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 | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0004c0019t0001g0063 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.928+4530C>T | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14196751 | |||||||
chr17:14196873 | C | T | 53 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(50): Show |
54 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(51): 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 | a0002c0002t0001g0196 | 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 | a0003c0017t0003g0037 | 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 | a0002c0015t0021g0309 a0002c0020t0001g0310 |
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 | a0002c0002t0002g0239 | 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 | a0001c0004t0003g0106 a0001c0004t0003g0168 |
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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0002c0002t0002g0239 | 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 | 153 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.928+5491G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14197712 | |||||||
chr17:14197726 | G | A | 177 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): 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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 a0007c0027t0009g0210 |
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 | a0008c0024t0016g0296 a0010c0026t0001g0057 a0011c0021t0001g0186 |
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 | a0001c0003t0001g0079 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0006c0016t0012g0004 a0006c0016t0012g0203 |
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 | a0002c0005t0003g0209 | 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 | a0002c0005t0004g0184 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0002c0015t0001g0297 | 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | a0001c0001t0011g0311 a0001c0001t0011g0312 a0001c0001t0011g0313 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0001c0003t0006g0104 | 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 | a0001c0012t0001g0293 a0001c0012t0001g0294 a0001c0012t0001g0295 others(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 | a0001c0004t0014g0127 a0001c0004t0014g0151 |
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 | a0001c0001t0019g0276 | 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 | a0001c0003t0001g0152 | 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 | a0002c0008t0002g0254 | 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 | a0001c0007t0008g0115 a0002c0006t0008g0273 |
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 | a0002c0008t0001g0242 | 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 | a0002c0008t0001g0197 a0002c0008t0001g0213 |
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 | 224 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(221): 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 | a0001c0001t0005g0160 | 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 | a0002c0005t0004g0237 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | 199 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(196): 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 | a0001c0007t0004g0069 | 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 | a0004c0019t0001g0063 | 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 | 119 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(116): 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 | a0001c0003t0002g0007 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0002c0002t0002g0303 | 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 | 310 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(307): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.929-4607T>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14202203 | |||||||
chr17:14202223 | C | CT | 180 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(177): 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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 others(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 | a0001c0001t0003g0032 a0001c0012t0001g0291 a0002c0002t0003g0212 others(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 | a0010c0026t0001g0057 | 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 | a0001c0003t0001g0033 a0001c0003t0001g0080 a0001c0003t0001g0081 others(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 | a0002c0002t0005g0264 a0002c0005t0005g0251 |
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 | a0002c0002t0001g0259 | 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 | a0009c0022t0002g0005 | 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 | a0001c0003t0002g0314 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0001c0001t0003g0126 | 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 | a0001c0001t0003g0171 | 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 | a0001c0004t0001g0285 a0002c0002t0001g0214 a0002c0002t0001g0215 |
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 | a0004c0025t0001g0062 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | 56 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(53): Show |
57 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(54): 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 | a0002c0005t0004g0187 a0002c0005t0004g0195 a0005c0013t0004g0135 |
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 | a0001c0001t0003g0144 | 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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | a0010c0026t0001g0057 | 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 | 193 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(190): 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 | 190 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(187): 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 | a0001c0007t0010g0315 a0001c0007t0010g0316 a0001c0007t0010g0317 |
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 | a0004c0018t0001g0060 a0004c0018t0001g0061 |
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 | a0001c0001t0005g0014 a0001c0001t0005g0289 a0001c0007t0001g0017 others(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 | 190 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(187): 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 | a0002c0002t0001g0196 | 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 | a0001c0001t0003g0100 | 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 | 190 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(187): 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 | a0001c0001t0003g0109 | 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | 190 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(187): 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 | 214 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(211): 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 | 191 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(188): 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 | 51 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0128 others(48): 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 | 56 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(53): Show |
57 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(54): 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 | a0001c0003t0002g0007 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0002c0002t0001g0196 a0002c0008t0001g0242 |
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 | a0001c0003t0002g0007 a0001c0003t0002g0008 a0001c0003t0002g0009 others(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 | a0001c0003t0002g0314 | 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 | 123 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(120): 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 | a0002c0006t0009g0258 a0003c0011t0009g0044 a0007c0027t0009g0210 |
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 | 190 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(187): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0004c0019t0001g0063 | 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 | a0002c0002t0005g0264 a0002c0005t0005g0251 |
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 | a0001c0001t0003g0131 a0001c0007t0013g0130 a0001c0007t0013g0132 |
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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | 123 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0004g0112 others(120): 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 | a0002c0006t0004g0225 | 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 | a0001c0004t0002g0165 | 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 | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | 269 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.929-619G>A | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206191 | |||||||
chr17:14206233 | A | G | 313 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0003g0001 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.929-577A>G | COX10 | ENSG00000006695.12 | transcript | ENST00000261643.8 | protein_coding | 6/6 | chr17 | 14206233 | |||||||
chr17:14206291 | A | G | 56 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(53): Show |
57 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(54): 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 | a0001c0003t0006g0104 a0001c0003t0006g0113 a0003c0009t0006g0091 others(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 | a0001c0003t0001g0033 a0001c0003t0001g0079 a0001c0003t0001g0080 others(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 | a0001c0004t0002g0280 | 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 | a0002c0005t0004g0187 a0002c0005t0004g0195 a0005c0013t0004g0135 |
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 | a0002c0005t0004g0207 | 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 | 74 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0029 others(71): Show |
76 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(73): 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 | a0004c0018t0001g0060 a0004c0018t0001g0061 a0004c0019t0001g0063 |
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 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(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 |