Item | Value |
---|---|
geneid | 64927 |
ensemblid | ENSG00000103852.13 |
hgncid | 25730 |
symbol | TTC23 |
name | tetratricopeptide repeat domain 23 |
refseq_nuc | NM_001288615.3 |
refseq_prot | NP_001275544.1 |
ensembl_nuc | ENST00000394132.7 |
ensembl_prot | ENSP00000377690.2 |
mane_status | MANE Select |
chr | chr15 |
start | 99136323 |
end | 99249581 |
strand | - |
ver | v1.2 |
region | chr15:99136323-99249581 |
region5000 | chr15:99131323-99254581 |
regionname0 | TTC23_chr15_99136323_99249581 |
regionname5000 | TTC23_chr15_99131323_99254581 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 447 | 353 | 80 | 65 | 160 | 11 | 35 | 124 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
a0002 | 0/0 | 447 | 6 | 3 | 2 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
a0003 | 0/0 | 447 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
a0004 | 0/0 | 447 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
a0005 | 0/0 | 447 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
a0006 | 0/0 | 447 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
a0007 | 0/0 | 447 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
a0008 | 0/0 | 447 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
a0009 | 0/0 | 447 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | MQESQ others(442): Show |
chr15 | 99131323 | 99254581 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1341 | 242 | 40 | 42 | 129 | 9 | 21 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0001c0002 | 0/0 | 1341 | 44 | 22 | 6 | 10 | 0 | 6 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0001c0003 | 1/0 | 1341 | 40 | 2 | 13 | 15 | 1 | 8 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0001c0004 | 0/0 | 1341 | 12 | 5 | 2 | 4 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0001c0005 | 0/0 | 1341 | 11 | 11 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0001c0007 | 0/0 | 1341 | 2 | 0 | 2 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0001c0009 | 0/0 | 1341 | 2 | 0 | 0 | 2 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0002c0006 | 0/0 | 1341 | 5 | 3 | 1 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0002c0010 | 0/0 | 1341 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0003c0011 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0003c0012 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0004c0008 | 0/0 | 1341 | 2 | 2 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0005c0017 | 0/0 | 1341 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0006c0014 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0007c0015 | 0/0 | 1341 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0008c0016 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 | ||
a0009c0013 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | ATGCA others(1336): Show |
chr15 | 99131323 | 99254581 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3875 | 76 | 11 | 20 | 30 | 4 | 11 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0002 | 0/0 | 3872 | 64 | 3 | 5 | 48 | 3 | 5 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0003 | 0/0 | 3872 | 17 | 1 | 1 | 15 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0004 | 0/0 | 3875 | 24 | 7 | 5 | 9 | 0 | 3 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0006 | 0/0 | 3875 | 14 | 7 | 2 | 5 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0007 | 0/1 | 3875 | 15 | 4 | 6 | 4 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0009 | 0/0 | 3872 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0010 | 0/0 | 3872 | 6 | 2 | 0 | 4 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0011 | 0/0 | 3875 | 4 | 0 | 0 | 1 | 1 | 2 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0012 | 0/0 | 3872 | 4 | 1 | 0 | 3 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0013 | 0/0 | 3872 | 3 | 0 | 0 | 3 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0014 | 0/0 | 3875 | 2 | 0 | 0 | 2 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0015 | 0/0 | 3875 | 2 | 2 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0016 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0017 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0019 | 0/0 | 3872 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0020 | 0/0 | 3872 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0021 | 0/0 | 3872 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0022 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0023 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0024 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0025 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0001t0026 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0002t0001 | 0/0 | 3875 | 2 | 1 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0002t0004 | 0/0 | 3875 | 19 | 17 | 2 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0002t0005 | 0/0 | 3875 | 22 | 4 | 2 | 10 | 0 | 6 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0002t0028 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0003t0002 | 0/0 | 3872 | 4 | 0 | 0 | 4 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0003t0003 | 1/0 | 3872 | 24 | 2 | 8 | 8 | 1 | 4 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0003t0004 | 0/0 | 3875 | 2 | 0 | 0 | 2 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0003t0008 | 0/0 | 3872 | 3 | 0 | 1 | 1 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0003t0009 | 0/0 | 3872 | 7 | 0 | 4 | 0 | 0 | 3 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0004t0003 | 0/0 | 3872 | 5 | 5 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0004t0006 | 0/0 | 3875 | 7 | 0 | 2 | 4 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0005t0003 | 0/0 | 3872 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0005t0008 | 0/0 | 3872 | 9 | 9 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0005t0027 | 0/0 | 3872 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0001c0007t0005 | 0/0 | 3875 | 2 | 0 | 2 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0001c0009t0001 | 0/0 | 3875 | 2 | 0 | 0 | 2 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0002c0006t0003 | 0/0 | 3872 | 5 | 3 | 1 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0002c0010t0004 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0003c0011t0004 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0003c0012t0004 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0004c0008t0011 | 0/0 | 3875 | 2 | 2 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0005c0017t0001 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3870): Show |
chr15 | 99131323 | 99254581 |
a0006c0014t0003 | 0/0 | 3872 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0007c0015t0002 | 0/0 | 3872 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0008c0016t0018 | 0/0 | 3872 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
a0009c0013t0002 | 0/0 | 3872 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | GAGGT others(3867): Show |
chr15 | 99131323 | 99254581 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0010g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0010g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0010g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0010g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0011g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0011g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0011g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0011g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0012g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0012g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0013g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0013g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0014g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0014g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0015g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0015g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0016g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0017g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0019g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0020g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0021g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0022g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0023g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0024g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0025g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0001t0026g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0002t0028g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0008g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0008g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0009g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0009g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0009g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0009g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0003t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0004t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0008g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0005t0027g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0007t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0007t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0009t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0001c0009t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0002c0006t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0002c0006t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0002c0006t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0002c0006t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0002c0006t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0002c0010t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0003c0011t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0003c0012t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0004c0008t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0004c0008t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0005c0017t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0006c0014t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0007c0015t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0008c0016t0018g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
a0009c0013t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | GBR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00099 | hp2 | a0002 | c0006 | t0003 | g0237 | EUR | GBR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00140 | hp2 | a0001 | c0001 | t0011 | g0272 | EUR | GBR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00280 | hp1 | a0001 | c0003 | t0003 | g0223 | EUR | FIN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00280 | hp2 | a0001 | c0001 | t0009 | g0244 | EUR | FIN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00323 | hp1 | a0001 | c0004 | t0006 | g0123 | EUR | FIN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | FIN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00558 | hp1 | a0001 | c0002 | t0005 | g0092 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00621 | hp2 | a0001 | c0001 | t0014 | g0334 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00639 | hp1 | a0002 | c0006 | t0003 | g0229 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0122 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00642 | hp1 | a0005 | c0017 | t0001 | g0270 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00642 | hp2 | a0001 | c0002 | t0005 | g0191 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00733 | hp2 | a0001 | c0002 | t0004 | g0142 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0301 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00735 | hp2 | a0001 | c0003 | t0009 | g0227 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00738 | hp2 | a0001 | c0001 | t0007 | g0170 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0178 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG00741 | hp2 | a0001 | c0003 | t0003 | g0176 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01069 | hp1 | a0001 | c0007 | t0005 | g0143 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01069 | hp2 | a0001 | c0003 | t0009 | g0226 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01071 | hp1 | a0001 | c0007 | t0005 | g0144 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0219 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01081 | hp1 | a0001 | c0003 | t0008 | g0315 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01109 | hp1 | a0001 | c0002 | t0004 | g0136 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01167 | hp1 | a0001 | c0003 | t0003 | g0220 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01243 | hp1 | a0001 | c0001 | t0019 | g0095 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0108 | AMR | PUR | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01255 | hp2 | a0001 | c0001 | t0007 | g0044 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01256 | hp1 | a0001 | c0003 | t0003 | g0207 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01257 | hp1 | a0001 | c0003 | t0003 | g0215 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0356 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01261 | hp1 | a0001 | c0004 | t0006 | g0117 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01346 | hp1 | a0001 | c0003 | t0009 | g0248 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0125 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01361 | hp1 | a0001 | c0003 | t0003 | g0209 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01361 | hp2 | a0001 | c0004 | t0006 | g0124 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01433 | hp2 | a0001 | c0003 | t0003 | g0238 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | IBS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | IBS | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01884 | hp2 | a0001 | c0002 | t0004 | g0027 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01891 | hp1 | a0001 | c0001 | t0024 | g0258 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01891 | hp2 | a0001 | c0004 | t0003 | g0156 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01943 | hp2 | a0001 | c0001 | t0023 | g0172 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01952 | hp1 | a0001 | c0003 | t0003 | g0208 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01975 | hp1 | a0001 | c0001 | t0007 | g0166 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01978 | hp1 | a0001 | c0001 | t0017 | g0177 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01978 | hp2 | a0001 | c0002 | t0028 | g0338 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02004 | hp1 | a0001 | c0001 | t0007 | g0165 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02040 | hp1 | a0001 | c0002 | t0005 | g0014 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02055 | hp1 | a0003 | c0011 | t0004 | g0158 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02055 | hp2 | a0001 | c0004 | t0003 | g0157 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02145 | hp1 | a0001 | c0002 | t0004 | g0135 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0021 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CDX | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CDX | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02257 | hp2 | a0001 | c0004 | t0003 | g0153 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02258 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02273 | hp1 | a0001 | c0001 | t0007 | g0171 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02280 | hp2 | a0001 | c0001 | t0022 | g0179 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02300 | hp2 | a0002 | c0010 | t0004 | g0232 | AMR | PEL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02451 | hp1 | a0001 | c0002 | t0004 | g0160 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02572 | hp1 | a0006 | c0014 | t0003 | g0162 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02572 | hp2 | a0002 | c0006 | t0003 | g0228 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02602 | hp2 | a0001 | c0003 | t0003 | g0212 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02615 | hp1 | a0001 | c0005 | t0008 | g0257 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02647 | hp2 | a0001 | c0005 | t0008 | g0262 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02698 | hp1 | a0001 | c0002 | t0005 | g0173 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02717 | hp2 | a0001 | c0002 | t0004 | g0098 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02735 | hp1 | a0001 | c0001 | t0011 | g0269 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0236 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0365 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02818 | hp1 | a0001 | c0005 | t0003 | g0013 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02818 | hp2 | a0003 | c0012 | t0004 | g0152 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02886 | hp1 | a0001 | c0002 | t0004 | g0146 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02895 | hp1 | a0004 | c0008 | t0011 | g0284 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02895 | hp2 | a0001 | c0005 | t0008 | g0337 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02896 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0326 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02897 | hp1 | a0004 | c0008 | t0011 | g0278 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02922 | hp1 | a0001 | c0004 | t0003 | g0155 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0163 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0020 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02976 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0363 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0180 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03098 | hp2 | a0001 | c0005 | t0008 | g0263 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03130 | hp2 | a0001 | c0002 | t0004 | g0017 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03139 | hp2 | a0001 | c0002 | t0005 | g0133 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03209 | hp2 | a0001 | c0005 | t0008 | g0279 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0187 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03239 | hp1 | a0001 | c0001 | t0011 | g0275 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03453 | hp2 | a0001 | c0002 | t0005 | g0121 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03486 | hp1 | a0001 | c0005 | t0027 | g0360 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0126 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03491 | hp1 | a0001 | c0002 | t0005 | g0168 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03491 | hp2 | a0001 | c0002 | t0005 | g0119 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03492 | hp2 | a0001 | c0002 | t0005 | g0169 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03516 | hp1 | a0001 | c0001 | t0012 | g0138 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03516 | hp2 | a0001 | c0001 | t0010 | g0349 | AFR | ESN | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03540 | hp1 | a0001 | c0001 | t0015 | g0343 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0175 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03669 | hp1 | a0001 | c0003 | t0003 | g0225 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0164 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03831 | hp2 | a0001 | c0002 | t0005 | g0159 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0063 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0364 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0350 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03927 | hp2 | a0001 | c0003 | t0003 | g0214 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0359 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03942 | hp2 | a0001 | c0003 | t0009 | g0230 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG04115 | hp2 | a0001 | c0003 | t0009 | g0246 | SAS | STU | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG04184 | hp1 | a0001 | c0002 | t0005 | g0116 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG04184 | hp2 | a0001 | c0003 | t0009 | g0247 | SAS | BEB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG04204 | hp2 | a0007 | c0015 | t0002 | g0074 | SAS | STU | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | STU | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18522 | hp1 | a0002 | c0006 | t0003 | g0216 | AFR | YRI | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18522 | hp2 | a0001 | c0002 | t0004 | g0134 | AFR | YRI | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | CHB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | CHB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18747 | hp1 | a0001 | c0009 | t0001 | g0361 | EAS | CHB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18939 | hp2 | a0001 | c0003 | t0008 | g0333 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18941 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18945 | hp1 | a0001 | c0003 | t0002 | g0217 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18945 | hp2 | a0001 | c0001 | t0012 | g0141 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18947 | hp2 | a0001 | c0001 | t0013 | g0224 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18948 | hp2 | a0001 | c0003 | t0004 | g0213 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18959 | hp1 | a0001 | c0004 | t0006 | g0130 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18959 | hp2 | a0001 | c0001 | t0021 | g0034 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18961 | hp2 | a0008 | c0016 | t0018 | g0204 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18969 | hp1 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18969 | hp2 | a0001 | c0001 | t0010 | g0271 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18970 | hp2 | a0001 | c0001 | t0025 | g0332 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18971 | hp1 | a0001 | c0003 | t0003 | g0182 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18971 | hp2 | a0001 | c0001 | t0016 | g0127 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18973 | hp1 | a0001 | c0003 | t0004 | g0054 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18973 | hp2 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18977 | hp1 | a0001 | c0002 | t0005 | g0128 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18977 | hp2 | a0001 | c0001 | t0012 | g0140 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18980 | hp1 | a0001 | c0001 | t0020 | g0203 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18980 | hp2 | a0001 | c0002 | t0005 | g0114 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18981 | hp1 | a0001 | c0003 | t0002 | g0240 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18983 | hp1 | a0001 | c0002 | t0005 | g0111 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18984 | hp2 | a0001 | c0004 | t0006 | g0132 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18988 | hp1 | a0001 | c0002 | t0005 | g0115 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18988 | hp2 | a0001 | c0001 | t0010 | g0265 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18990 | hp1 | a0001 | c0003 | t0002 | g0211 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18994 | hp2 | a0001 | c0001 | t0007 | g0184 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18997 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19000 | hp2 | a0001 | c0001 | t0014 | g0358 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19002 | hp1 | a0001 | c0002 | t0005 | g0113 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19004 | hp1 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19005 | hp2 | a0001 | c0003 | t0003 | g0206 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19012 | hp1 | a0001 | c0004 | t0006 | g0118 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19030 | hp2 | a0001 | c0005 | t0008 | g0264 | AFR | LWK | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19043 | hp1 | a0001 | c0005 | t0008 | g0260 | AFR | LWK | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | LWK | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19054 | hp1 | a0001 | c0002 | t0005 | g0112 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19054 | hp2 | a0001 | c0001 | t0010 | g0274 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19055 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19057 | hp2 | a0001 | c0001 | t0011 | g0304 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19058 | hp1 | a0001 | c0002 | t0005 | g0110 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19060 | hp1 | a0001 | c0003 | t0002 | g0218 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19064 | hp2 | a0001 | c0001 | t0013 | g0145 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19065 | hp1 | a0001 | c0001 | t0010 | g0335 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19068 | hp1 | a0001 | c0001 | t0026 | g0288 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19068 | hp2 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19076 | hp2 | a0009 | c0013 | t0002 | g0042 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19077 | hp1 | a0001 | c0003 | t0003 | g0242 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19077 | hp2 | a0001 | c0002 | t0005 | g0131 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19078 | hp1 | a0001 | c0003 | t0003 | g0183 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19082 | hp1 | a0001 | c0009 | t0001 | g0362 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19082 | hp2 | a0001 | c0001 | t0013 | g0147 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19085 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19085 | hp2 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19086 | hp2 | a0001 | c0004 | t0006 | g0109 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19240 | hp1 | a0001 | c0005 | t0008 | g0259 | AFR | YRI | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0028 | AFR | YRI | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ASW | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA20129 | hp2 | a0002 | c0006 | t0003 | g0231 | AFR | ASW | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA20905 | hp1 | a0001 | c0003 | t0003 | g0221 | SAS | GIH | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA20905 | hp2 | a0001 | c0003 | t0008 | g0302 | SAS | GIH | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01123 | hp1 | a0001 | c0003 | t0009 | g0245 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG01123 | hp2 | a0001 | c0002 | t0005 | g0129 | AMR | CLM | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02109 | hp1 | a0001 | c0002 | t0004 | g0099 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02109 | hp2 | a0001 | c0004 | t0003 | g0154 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02559 | hp1 | a0001 | c0002 | t0004 | g0105 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG02559 | hp2 | a0001 | c0002 | t0005 | g0120 | AFR | ACB | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0100 | AFR | MSL | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG06807 | hp1 | a0001 | c0005 | t0008 | g0261 | AFR | USA | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | USA | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA20300 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | USA | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA20300 | hp2 | a0001 | c0003 | t0003 | g0210 | AFR | USA | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | LWK | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
NA21309 | hp2 | a0001 | c0003 | t0003 | g0188 | AFR | LWK | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0167 | REF | REF | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
homoSapiens | grch38p0 | a0001 | c0003 | t0003 | g0222 | REF | REF | TTC23_chr15_99131323_99254581 | TTC23 | chr15 | 99131323 | 99254581 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:99138119 | T | C | 1 | a0006 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1235A>G | p.Lys412Arg | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 2076/3872 | 1235/1344 | 412/447 | chr15 | 99138119 | |||
chr15:99139368 | G | A | 1 | a0004 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1175C>T | p.Pro392Leu | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/14 | 2016/3872 | 1175/1344 | 392/447 | chr15 | 99139368 | |||
chr15:99161772 | A | C | 1 | a0009 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.961T>G | p.Cys321Gly | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/14 | 1802/3872 | 961/1344 | 321/447 | chr15 | 99161772 | |||
chr15:99200071 | T | C | 1 | a0007 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.607A>G | p.Lys203Glu | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/14 | 1448/3872 | 607/1344 | 203/447 | chr15 | 99200071 | |||
chr15:99218652 | A | T | 1 | a0003 | 2 | HG02055.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.517T>A | p.Cys173Ser | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/14 | 1358/3872 | 517/1344 | 173/447 | chr15 | 99218652 | |||
chr15:99218924 | C | T | 1 | a0003 | 2 | HG02055.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.429G>A | p.Met143Ile | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 7/14 | 1270/3872 | 429/1344 | 143/447 | chr15 | 99218924 | |||
chr15:99221762 | G | C | 1 | a0008 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.283C>G | p.Gln95Glu | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/14 | 1124/3872 | 283/1344 | 95/447 | chr15 | 99221762 | |||
chr15:99221765 | C | A | 1 | a0005 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.280G>T | p.Ala94Ser | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/14 | 1121/3872 | 280/1344 | 94/447 | chr15 | 99221765 | |||
chr15:99221836 | C | T | 1 | a0002 | 6 | HG00099.hp2 HG00639.hp1 HG02300.hp2 others(3): Show |
missense_variant | MODERATE | c.209G>A | p.Arg70His | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/14 | 1050/3872 | 209/1344 | 70/447 | chr15 | 99221836 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:99138052 | G | A | 3 | a0001c0002 a0001c0007 a0003c0012 |
47 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(44): Show |
synonymous_variant | LOW | c.1302C>T | p.Asp434Asp | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 2143/3872 | 1302/1344 | 434/447 | chr15 | 99138052 | |||
chr15:99175147 | A | G | 15 | a0001c0001 a0001c0002 a0001c0004 others(12): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
synonymous_variant | LOW | c.768T>C | p.Leu256Leu | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/14 | 1609/3872 | 768/1344 | 256/447 | chr15 | 99175147 | |||
chr15:99199957 | G | A | 1 | a0001c0009 | 2 | NA18747.hp1 NA19082.hp1 |
synonymous_variant | LOW | c.721C>T | p.Leu241Leu | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/14 | 1562/3872 | 721/1344 | 241/447 | chr15 | 99199957 | |||
chr15:99200000 | C | T | 1 | a0001c0005 | 11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
synonymous_variant | LOW | c.678G>A | p.Glu226Glu | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/14 | 1519/3872 | 678/1344 | 226/447 | chr15 | 99200000 | |||
chr15:99221847 | A | G | 2 | a0001c0004 a0001c0007 |
14 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
synonymous_variant | LOW | c.198T>C | p.His66His | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/14 | 1039/3872 | 198/1344 | 66/447 | chr15 | 99221847 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:99136597 | C | G | 1 | a0001c0001t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1413G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 1413 | chr15 | 99136597 | ||||||
chr15:99136684 | G | A | 1 | a0001c0001t0019 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1326C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 1326 | chr15 | 99136684 | ||||||
chr15:99136703 | C | A | 1 | a0001c0001t0021 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1307G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 1307 | chr15 | 99136703 | ||||||
chr15:99136755 | G | GACC | 27 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(24): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1254_*1255insGGT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 1254 | chr15 | 99136755 | ||||||
chr15:99136852 | C | T | 1 | a0001c0001t0025 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1158G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 1158 | chr15 | 99136852 | ||||||
chr15:99136875 | C | A | 2 | a0001c0001t0009 a0001c0003t0009 |
8 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1135G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 1135 | chr15 | 99136875 | ||||||
chr15:99136940 | G | A | 2 | a0001c0001t0012 a0001c0001t0013 |
7 | HG03516.hp1 NA18945.hp2 NA18947.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1070C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 1070 | chr15 | 99136940 | ||||||
chr15:99137105 | C | G | 1 | a0001c0001t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*905G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 905 | chr15 | 99137105 | ||||||
chr15:99137111 | C | A | 9 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(6): Show |
46 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*899G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 899 | chr15 | 99137111 | ||||||
chr15:99137152 | C | T | 5 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0017 others(2): Show |
22 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*858G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 858 | chr15 | 99137152 | ||||||
chr15:99137153 | G | A | 1 | a0001c0001t0020 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*857C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 857 | chr15 | 99137153 | ||||||
chr15:99137209 | A | C | 2 | a0001c0001t0013 a0008c0016t0018 |
4 | NA18947.hp2 NA18961.hp2 NA19064.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*801T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 801 | chr15 | 99137209 | ||||||
chr15:99137215 | A | G | 6 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0017 others(3): Show |
23 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*795T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 795 | chr15 | 99137215 | ||||||
chr15:99137216 | T | C | 1 | a0001c0001t0026 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 794 | chr15 | 99137216 | ||||||
chr15:99137468 | T | C | 4 | a0001c0002t0005 a0001c0002t0028 a0001c0005t0027 others(1): Show |
26 | HG00558.hp1 HG00642.hp2 HG01069.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*542A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 542 | chr15 | 99137468 | ||||||
chr15:99137471 | A | G | 1 | a0001c0001t0024 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*539T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 539 | chr15 | 99137471 | ||||||
chr15:99137502 | G | A | 6 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0021 others(3): Show |
77 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*508C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 508 | chr15 | 99137502 | ||||||
chr15:99137602 | A | G | 2 | a0001c0001t0014 a0001c0001t0016 |
3 | HG00621.hp2 NA18971.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*408T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 408 | chr15 | 99137602 | ||||||
chr15:99137940 | G | A | 8 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(5): Show |
45 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*70C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 14/14 | 70 | chr15 | 99137940 | ||||||
chr15:99249537 | G | C | 16 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(13): Show |
114 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
5_prime_UTR_variant | MODIFIER | c.-797C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/14 | 20825 | chr15 | 99249537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:99138148 | G | A | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227-21C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138148 | |||||||
chr15:99138175 | C | A | 2 | a0001c0001t0003g0010 a0001c0004t0003g0154 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1227-48G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138175 | |||||||
chr15:99138181 | G | T | 1 | a0001c0009t0001g0362 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1227-54C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138181 | |||||||
chr15:99138296 | T | C | 1 | a0001c0001t0004g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1227-169A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138296 | |||||||
chr15:99138398 | C | G | 74 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0002g0011 others(71): Show |
74 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1227-271G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138398 | |||||||
chr15:99138504 | A | G | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1227-377T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138504 | |||||||
chr15:99138564 | C | T | 47 | a0001c0002t0001g0255 a0001c0002t0001g0301 a0001c0002t0004g0017 others(44): Show |
47 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.1227-437G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138564 | |||||||
chr15:99138590 | G | T | 72 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0029 others(69): Show |
72 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1227-463C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138590 | |||||||
chr15:99138615 | T | G | 110 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(107): Show |
110 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1227-488A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138615 | |||||||
chr15:99138672 | A | G | 25 | a0001c0002t0005g0014 a0001c0002t0005g0092 a0001c0002t0005g0110 others(22): Show |
25 | HG00558.hp1 HG00642.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1227-545T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138672 | |||||||
chr15:99138702 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1227-575C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138702 | |||||||
chr15:99138794 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1226+523G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138794 | |||||||
chr15:99138825 | CA | C | 3 | a0001c0003t0003g0219 a0001c0003t0003g0220 a0001c0003t0008g0302 |
3 | HG01074.hp1 HG01167.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1226+491delT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138825 | |||||||
chr15:99138852 | G | A | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1226+465C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138852 | |||||||
chr15:99138874 | C | T | 1 | a0007c0015t0002g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1226+443G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138874 | |||||||
chr15:99138903 | C | A | 1 | a0001c0001t0002g0051 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1226+414G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138903 | |||||||
chr15:99138997 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1226+320C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99138997 | |||||||
chr15:99139189 | T | G | 2 | a0001c0002t0005g0116 a0001c0002t0005g0129 |
2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1226+128A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99139189 | |||||||
chr15:99139284 | GAGAT | G | 92 | a0001c0001t0006g0002 a0001c0001t0006g0037 a0001c0001t0006g0048 others(89): Show |
93 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1226+29_1226+32del others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99139284 | |||||||
chr15:99139316 | C | T | 2 | a0001c0003t0003g0219 a0001c0003t0003g0220 |
2 | HG01074.hp1 HG01167.hp1 |
splice_donor_variant&intron_variant | HIGH | c.1226+1G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 13/13 | chr15 | 99139316 | |||||||
chr15:99139450 | C | A | 45 | a0001c0001t0006g0002 a0001c0001t0006g0037 a0001c0001t0006g0048 others(42): Show |
46 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1144-51G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99139450 | |||||||
chr15:99139617 | T | A | 12 | a0001c0002t0001g0255 a0001c0002t0004g0017 a0001c0002t0004g0018 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1144-218A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99139617 | |||||||
chr15:99139625 | A | G | 96 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(93): Show |
97 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1144-226T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99139625 | |||||||
chr15:99139635 | T | G | 1 | a0001c0005t0027g0360 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1144-236A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99139635 | |||||||
chr15:99139772 | G | T | 9 | a0001c0002t0001g0301 a0001c0002t0004g0098 a0001c0002t0004g0099 others(6): Show |
9 | HG00733.hp2 HG00735.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144-373C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99139772 | |||||||
chr15:99139941 | A | G | 5 | a0001c0002t0001g0301 a0001c0002t0004g0105 a0001c0002t0004g0134 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-542T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99139941 | |||||||
chr15:99140252 | A | G | 2 | a0001c0001t0003g0239 a0001c0001t0019g0095 |
2 | HG01099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1144-853T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99140252 | |||||||
chr15:99140294 | T | G | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1144-895A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99140294 | |||||||
chr15:99140313 | G | T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1144-914C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99140313 | |||||||
chr15:99140751 | CTA | C | 48 | a0001c0001t0004g0139 a0001c0002t0001g0255 a0001c0002t0001g0301 others(45): Show |
48 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.1144-1354_1144-135 others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99140751 | |||||||
chr15:99140786 | T | C | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144-1387A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99140786 | |||||||
chr15:99140835 | C | G | 2 | a0001c0002t0005g0116 a0001c0002t0005g0129 |
2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1144-1436G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99140835 | |||||||
chr15:99140841 | A | G | 3 | a0001c0001t0006g0100 a0001c0001t0015g0343 a0001c0001t0015g0365 |
3 | HG02809.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1144-1442T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99140841 | |||||||
chr15:99140953 | A | G | 3 | a0001c0003t0009g0226 a0001c0003t0009g0227 a0001c0003t0009g0230 |
3 | HG00735.hp2 HG01069.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1144-1554T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99140953 | |||||||
chr15:99141288 | A | G | 25 | a0001c0002t0005g0014 a0001c0002t0005g0092 a0001c0002t0005g0110 others(22): Show |
25 | HG00558.hp1 HG00642.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1144-1889T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99141288 | |||||||
chr15:99141310 | C | T | 45 | a0001c0001t0006g0002 a0001c0001t0006g0037 a0001c0001t0006g0048 others(42): Show |
46 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1144-1911G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99141310 | |||||||
chr15:99141346 | A | G | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144-1947T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99141346 | |||||||
chr15:99141368 | A | G | 1 | a0001c0002t0005g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1144-1969T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99141368 | |||||||
chr15:99141655 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1144-2256G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99141655 | |||||||
chr15:99142022 | G | A | 4 | a0001c0001t0013g0145 a0001c0001t0013g0147 a0001c0001t0013g0224 others(1): Show |
4 | NA18947.hp2 NA18961.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-2623C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142022 | |||||||
chr15:99142047 | A | C | 2 | a0003c0011t0004g0158 a0003c0012t0004g0152 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1144-2648T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142047 | |||||||
chr15:99142085 | T | C | 43 | a0001c0001t0006g0002 a0001c0001t0006g0037 a0001c0001t0006g0048 others(40): Show |
44 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1144-2686A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142085 | |||||||
chr15:99142088 | C | T | 43 | a0001c0001t0006g0002 a0001c0001t0006g0037 a0001c0001t0006g0048 others(40): Show |
44 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1144-2689G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142088 | |||||||
chr15:99142097 | A | G | 196 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(193): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1144-2698T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142097 | |||||||
chr15:99142157 | T | A | 1 | a0001c0002t0004g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1144-2758A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142157 | |||||||
chr15:99142162 | G | C | 195 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(192): Show |
196 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1144-2763C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142162 | |||||||
chr15:99142471 | T | G | 1 | a0001c0001t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1144-3072A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142471 | |||||||
chr15:99142647 | G | A | 45 | a0001c0001t0006g0002 a0001c0001t0006g0037 a0001c0001t0006g0048 others(42): Show |
46 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1144-3248C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142647 | |||||||
chr15:99142786 | A | T | 108 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(105): Show |
108 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1144-3387T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142786 | |||||||
chr15:99142838 | G | A | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-3439C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99142838 | |||||||
chr15:99143046 | A | G | 195 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(192): Show |
196 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1144-3647T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143046 | |||||||
chr15:99143092 | C | A | 1 | a0002c0006t0003g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1144-3693G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143092 | |||||||
chr15:99143360 | C | G | 10 | a0001c0001t0001g0281 a0001c0001t0001g0295 a0001c0001t0001g0307 others(7): Show |
10 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1144-3961G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143360 | |||||||
chr15:99143426 | T | A | 1 | a0001c0003t0008g0333 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1144-4027A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143426 | |||||||
chr15:99143429 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0084 |
3 | NA18940.hp1 NA18954.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1144-4030G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143429 | |||||||
chr15:99143581 | G | A | 94 | a0001c0001t0004g0022 a0001c0001t0006g0002 a0001c0001t0006g0037 others(91): Show |
95 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1144-4182C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143581 | |||||||
chr15:99143652 | C | T | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1144-4253G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143652 | |||||||
chr15:99143723 | C | G | 2 | a0001c0003t0003g0219 a0001c0003t0003g0220 |
2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1144-4324G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143723 | |||||||
chr15:99143900 | T | C | 287 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(284): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1144-4501A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143900 | |||||||
chr15:99143913 | G | A | 6 | a0001c0005t0008g0257 a0001c0005t0008g0260 a0001c0005t0008g0261 others(3): Show |
6 | HG02615.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-4514C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99143913 | |||||||
chr15:99144000 | G | A | 1 | a0001c0001t0007g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1144-4601C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144000 | |||||||
chr15:99144018 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1144-4619C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144018 | |||||||
chr15:99144227 | C | G | 282 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(279): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1144-4828G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144227 | |||||||
chr15:99144381 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1144-4982T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144381 | |||||||
chr15:99144648 | C | G | 1 | a0001c0001t0009g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1144-5249G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144648 | |||||||
chr15:99144726 | C | T | 81 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0029 others(78): Show |
81 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1144-5327G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144726 | |||||||
chr15:99144786 | T | A | 1 | a0001c0002t0028g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1144-5387A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144786 | |||||||
chr15:99144899 | C | G | 1 | a0001c0001t0003g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1144-5500G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144899 | |||||||
chr15:99144944 | G | A | 176 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(173): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1144-5545C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99144944 | |||||||
chr15:99145035 | G | A | 9 | a0001c0002t0001g0301 a0001c0002t0004g0098 a0001c0002t0004g0099 others(6): Show |
9 | HG00733.hp2 HG00735.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144-5636C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99145035 | |||||||
chr15:99145131 | G | C | 7 | a0001c0001t0001g0266 a0001c0001t0001g0282 a0001c0001t0001g0289 others(4): Show |
7 | HG02071.hp2 NA18951.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-5732C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99145131 | |||||||
chr15:99145182 | C | T | 1 | a0001c0002t0004g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1144-5783G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99145182 | |||||||
chr15:99145259 | C | T | 5 | a0001c0003t0002g0211 a0001c0003t0002g0217 a0001c0003t0002g0218 others(2): Show |
5 | HG02055.hp1 NA18945.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-5860G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99145259 | |||||||
chr15:99145396 | A | C | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1144-5997T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99145396 | |||||||
chr15:99145516 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1144-6117G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99145516 | |||||||
chr15:99145700 | T | C | 2 | a0001c0001t0013g0145 a0001c0001t0013g0147 |
2 | NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1144-6301A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99145700 | |||||||
chr15:99146131 | A | G | 72 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0029 others(69): Show |
72 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1144-6732T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146131 | |||||||
chr15:99146152 | T | C | 53 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(50): Show |
53 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1144-6753A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146152 | |||||||
chr15:99146244 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1144-6845G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146244 | |||||||
chr15:99146309 | C | T | 179 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(176): Show |
180 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1144-6910G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146309 | |||||||
chr15:99146429 | G | C | 81 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0029 others(78): Show |
81 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1144-7030C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146429 | |||||||
chr15:99146528 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1144-7129G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146528 | |||||||
chr15:99146616 | A | G | 179 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(176): Show |
180 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1144-7217T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146616 | |||||||
chr15:99146663 | G | T | 49 | a0001c0001t0004g0022 a0001c0002t0001g0255 a0001c0002t0001g0301 others(46): Show |
49 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1144-7264C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146663 | |||||||
chr15:99146671 | G | A | 156 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(153): Show |
157 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1144-7272C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146671 | |||||||
chr15:99146746 | C | T | 71 | a0001c0001t0004g0022 a0001c0001t0006g0002 a0001c0001t0006g0037 others(68): Show |
72 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1144-7347G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146746 | |||||||
chr15:99146748 | AAGGGATA others(10): Show |
A | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1144-7366_1144-735 others(21): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146748 | |||||||
chr15:99146851 | C | A | 9 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-7452G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146851 | |||||||
chr15:99146938 | G | A | 41 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0004g0022 others(38): Show |
41 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1144-7539C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146938 | |||||||
chr15:99146938 | GGAGTCTC others(304): Show |
G | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-7850_1144-754 others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146938 | |||||||
chr15:99146945 | C | T | 1 | a0001c0003t0008g0333 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1144-7546G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146945 | |||||||
chr15:99146953 | T | C | 292 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(289): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1144-7554A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99146953 | |||||||
chr15:99147024 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1144-7625G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147024 | |||||||
chr15:99147064 | G | A | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1144-7665C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147064 | |||||||
chr15:99147099 | G | C | 1 | a0001c0001t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1144-7700C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147099 | |||||||
chr15:99147164 | G | A | 1 | a0001c0003t0008g0333 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1144-7765C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147164 | |||||||
chr15:99147202 | G | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0161 a0001c0001t0010g0326 others(1): Show |
4 | HG01496.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-7803C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147202 | |||||||
chr15:99147206 | T | C | 297 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(294): Show |
299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.1144-7807A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147206 | |||||||
chr15:99147225 | C | A | 1 | a0001c0001t0001g0351 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1144-7826G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147225 | |||||||
chr15:99147225 | C | CT | 6 | a0001c0001t0001g0277 a0001c0001t0001g0316 a0001c0001t0001g0342 others(3): Show |
6 | HG01167.hp2 HG01981.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1144-7827dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147225 | |||||||
chr15:99147225 | CTTT | C | 159 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(156): Show |
160 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1144-7829_1144-782 others(7): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147225 | |||||||
chr15:99147257 | G | A | 79 | a0001c0001t0004g0022 a0001c0001t0004g0122 a0001c0001t0006g0002 others(76): Show |
80 | HG00323.hp1 HG00558.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.1144-7858C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147257 | |||||||
chr15:99147260 | C | G | 67 | a0001c0001t0001g0268 a0001c0001t0002g0012 a0001c0001t0002g0029 others(64): Show |
67 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1144-7861G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147260 | |||||||
chr15:99147265 | A | C | 71 | a0001c0001t0001g0268 a0001c0001t0002g0012 a0001c0001t0002g0029 others(68): Show |
71 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1144-7866T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147265 | |||||||
chr15:99147265 | A | G | 1 | a0001c0001t0021g0034 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1144-7866T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147265 | |||||||
chr15:99147283 | C | T | 272 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(269): Show |
274 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1144-7884G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147283 | |||||||
chr15:99147288 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1144-7889G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147288 | |||||||
chr15:99147295 | A | G | 2 | a0001c0001t0002g0047 a0001c0001t0011g0304 |
2 | NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1144-7896T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147295 | |||||||
chr15:99147299 | C | A | 9 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-7900G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147299 | |||||||
chr15:99147324 | C | G | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-7925G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147324 | |||||||
chr15:99147364 | T | C | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-7965A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147364 | |||||||
chr15:99147370 | C | T | 8 | a0001c0001t0004g0022 a0001c0002t0001g0255 a0001c0002t0004g0017 others(5): Show |
8 | HG02145.hp2 HG02258.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-7971G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147370 | |||||||
chr15:99147375 | G | A | 10 | a0001c0001t0002g0060 a0001c0001t0006g0002 a0001c0001t0006g0100 others(7): Show |
11 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1144-7976C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147375 | |||||||
chr15:99147376 | C | T | 1 | a0001c0003t0003g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1144-7977G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147376 | |||||||
chr15:99147383 | A | G | 7 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(4): Show |
7 | HG01884.hp2 HG02602.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-7984T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147383 | |||||||
chr15:99147429 | G | T | 57 | a0001c0001t0004g0022 a0001c0001t0004g0122 a0001c0001t0012g0005 others(54): Show |
57 | HG00558.hp1 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1144-8030C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147429 | |||||||
chr15:99147460 | C | T | 1 | a0001c0001t0003g0199 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1144-8061G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147460 | |||||||
chr15:99147461 | G | A | 80 | a0001c0001t0001g0252 a0001c0001t0004g0022 a0001c0001t0004g0122 others(77): Show |
81 | HG00323.hp1 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1144-8062C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147461 | |||||||
chr15:99147505 | G | A | 1 | a0001c0001t0002g0089 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1144-8106C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147505 | |||||||
chr15:99147579 | T | C | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1144-8180A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147579 | |||||||
chr15:99147626 | C | T | 22 | a0001c0001t0006g0002 a0001c0001t0006g0037 a0001c0001t0006g0048 others(19): Show |
23 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1144-8227G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147626 | |||||||
chr15:99147745 | G | GTTAGTCA others(1): Show |
9 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-8354_1144-834 others(12): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147745 | |||||||
chr15:99147813 | G | A | 9 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+8335C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147813 | |||||||
chr15:99147814 | C | T | 1 | a0001c0001t0012g0140 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1143+8334G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147814 | |||||||
chr15:99147820 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1143+8328C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147820 | |||||||
chr15:99147837 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1143+8311T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147837 | |||||||
chr15:99147947 | G | A | 1 | a0001c0001t0010g0265 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1143+8201C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147947 | |||||||
chr15:99147989 | G | A | 105 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(102): Show |
106 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1143+8159C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147989 | |||||||
chr15:99147998 | T | C | 3 | a0001c0001t0007g0184 a0001c0001t0007g0185 a0001c0001t0007g0186 |
3 | NA18960.hp2 NA18994.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1143+8150A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99147998 | |||||||
chr15:99148100 | T | C | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1143+8048A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148100 | |||||||
chr15:99148276 | G | A | 166 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(163): Show |
167 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1143+7872C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148276 | |||||||
chr15:99148316 | G | A | 26 | a0001c0001t0004g0122 a0001c0002t0005g0014 a0001c0002t0005g0092 others(23): Show |
26 | HG00558.hp1 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1143+7832C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148316 | |||||||
chr15:99148319 | A | C | 166 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(163): Show |
167 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1143+7829T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148319 | |||||||
chr15:99148360 | C | CAAA | 6 | a0001c0001t0004g0022 a0001c0002t0001g0255 a0001c0002t0004g0018 others(3): Show |
6 | HG02258.hp2 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+7785_1143+778 others(7): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAA | 19 | a0001c0001t0001g0252 a0001c0001t0004g0107 a0001c0001t0006g0002 others(16): Show |
20 | HG00733.hp2 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1143+7784_1143+778 others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAA | 39 | a0001c0001t0001g0268 a0001c0001t0001g0277 a0001c0001t0001g0296 others(36): Show |
39 | HG00323.hp1 HG00733.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.1143+7783_1143+778 others(9): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAA | 65 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0273 others(62): Show |
66 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.1143+7782_1143+778 others(10): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA | 22 | a0001c0001t0001g0253 a0001c0001t0001g0276 a0001c0001t0001g0285 others(19): Show |
22 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.1143+7781_1143+778 others(11): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(1): Show |
29 | a0001c0001t0001g0316 a0001c0001t0001g0318 a0001c0001t0001g0341 others(26): Show |
29 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1143+7780_1143+778 others(12): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(2): Show |
16 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0002g0031 others(13): Show |
16 | HG00544.hp2 HG01081.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.1143+7779_1143+778 others(13): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(3): Show |
21 | a0001c0001t0002g0012 a0001c0001t0002g0039 a0001c0001t0002g0041 others(18): Show |
21 | HG00621.hp1 HG01981.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1143+7778_1143+778 others(14): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(4): Show |
20 | a0001c0001t0001g0256 a0001c0001t0002g0011 a0001c0001t0002g0040 others(17): Show |
20 | HG00423.hp1 HG00597.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1143+7777_1143+778 others(15): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(5): Show |
8 | a0001c0001t0002g0038 a0001c0001t0002g0068 a0001c0001t0002g0250 others(5): Show |
8 | HG02080.hp1 HG02080.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143+7776_1143+778 others(16): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0010g0265 a0001c0001t0024g0258 a0001c0005t0027g0360 |
3 | HG01891.hp1 HG03486.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1143+7775_1143+778 others(17): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0003g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1143+7774_1143+778 others(18): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(8): Show |
8 | a0001c0001t0001g0254 a0001c0001t0003g0243 a0001c0003t0002g0240 others(5): Show |
9 | HG00099.hp2 HG02071.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+7773_1143+778 others(19): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(9): Show |
16 | a0001c0001t0003g0151 a0001c0001t0003g0192 a0001c0001t0003g0198 others(13): Show |
16 | HG00280.hp1 HG00597.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1143+7772_1143+778 others(20): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(10): Show |
10 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG00673.hp1 HG00741.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+7771_1143+778 others(21): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0003g0190 a0001c0003t0008g0333 a0001c0003t0009g0248 |
3 | HG01346.hp1 NA18939.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1143+7770_1143+778 others(22): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(12): Show |
7 | a0001c0001t0009g0244 a0001c0003t0003g0214 a0001c0003t0003g0215 others(4): Show |
7 | HG00280.hp2 HG01123.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+7769_1143+778 others(23): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(13): Show |
2 | a0001c0003t0002g0218 a0001c0003t0008g0315 |
2 | HG01081.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1143+7768_1143+778 others(24): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(14): Show |
4 | a0001c0001t0007g0166 a0001c0001t0007g0178 a0001c0001t0011g0269 others(1): Show |
4 | HG00741.hp1 HG01975.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+7767_1143+778 others(25): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(15): Show |
9 | a0001c0001t0007g0044 a0001c0001t0007g0163 a0001c0001t0011g0272 others(6): Show |
9 | HG00140.hp2 HG00639.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+7766_1143+778 others(26): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0022g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1143+7765_1143+778 others(27): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(17): Show |
2 | a0001c0001t0007g0175 a0001c0003t0003g0183 |
2 | HG03579.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1143+7764_1143+778 others(28): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(19): Show |
2 | a0004c0008t0011g0278 a0004c0008t0011g0284 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1143+7762_1143+778 others(30): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(20): Show |
3 | a0001c0001t0007g0174 a0001c0001t0007g0180 a0001c0001t0007g0184 |
3 | HG03041.hp1 NA18969.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1143+7761_1143+778 others(31): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0007g0186 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1143+7787_1143+778 others(32): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(22): Show |
2 | a0001c0001t0007g0165 a0001c0001t0023g0172 |
2 | HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1143+7787_1143+778 others(33): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0007g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1143+7787_1143+778 others(39): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0017g0177 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1143+7787_1143+778 others(40): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | CAAAAA | C | 27 | a0001c0001t0004g0122 a0001c0002t0005g0014 a0001c0002t0005g0092 others(24): Show |
27 | HG00558.hp1 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1143+7783_1143+778 others(9): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0003g0239 a0001c0003t0003g0207 a0001c0003t0003g0208 others(4): Show |
7 | HG01099.hp1 HG01256.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+7779_1143+778 others(13): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148360 | CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1143+7774_1143+778 others(18): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148360 | |||||||
chr15:99148605 | A | G | 87 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0011 others(84): Show |
87 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1143+7543T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148605 | |||||||
chr15:99148678 | C | T | 1 | a0001c0003t0003g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1143+7470G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148678 | |||||||
chr15:99148802 | C | T | 271 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(268): Show |
273 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1143+7346G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99148802 | |||||||
chr15:99149078 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1143+7070C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149078 | |||||||
chr15:99149255 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0319 a0001c0001t0001g0345 |
3 | HG00323.hp2 HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1143+6893C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149255 | |||||||
chr15:99149279 | A | G | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG00140.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1143+6869T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149279 | |||||||
chr15:99149623 | C | T | 9 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+6525G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149623 | |||||||
chr15:99149657 | G | A | 3 | a0001c0002t0005g0120 a0001c0002t0005g0121 a0001c0002t0005g0126 |
3 | HG02559.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1143+6491C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149657 | |||||||
chr15:99149755 | C | T | 1 | a0003c0011t0004g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1143+6393G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149755 | |||||||
chr15:99149814 | C | T | 5 | a0001c0003t0003g0219 a0001c0003t0003g0220 a0001c0003t0003g0221 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+6334G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149814 | |||||||
chr15:99149815 | G | A | 80 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0012 others(77): Show |
80 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1143+6333C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149815 | |||||||
chr15:99149846 | T | C | 301 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(298): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1143+6302A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149846 | |||||||
chr15:99149857 | A | G | 295 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(292): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1143+6291T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149857 | |||||||
chr15:99149933 | C | T | 80 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0012 others(77): Show |
80 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1143+6215G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99149933 | |||||||
chr15:99150042 | G | C | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1143+6106C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150042 | |||||||
chr15:99150149 | G | A | 2 | a0001c0001t0001g0328 a0001c0001t0001g0356 |
2 | HG01192.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1143+5999C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150149 | |||||||
chr15:99150401 | G | A | 9 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+5747C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150401 | |||||||
chr15:99150545 | C | G | 1 | a0001c0003t0003g0221 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1143+5603G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150545 | |||||||
chr15:99150552 | C | T | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1143+5596G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150552 | |||||||
chr15:99150571 | T | G | 213 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(210): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1143+5577A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150571 | |||||||
chr15:99150692 | A | T | 5 | a0001c0001t0001g0331 a0001c0001t0001g0353 a0001c0001t0001g0357 others(2): Show |
5 | HG00733.hp1 HG01168.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+5456T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150692 | |||||||
chr15:99150723 | G | A | 22 | a0001c0001t0007g0044 a0001c0001t0007g0163 a0001c0001t0007g0165 others(19): Show |
22 | HG00140.hp2 HG00738.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1143+5425C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150723 | |||||||
chr15:99150737 | C | T | 77 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(74): Show |
77 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1143+5411G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150737 | |||||||
chr15:99150775 | G | C | 45 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(42): Show |
45 | HG00558.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1143+5373C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150775 | |||||||
chr15:99150805 | C | T | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+5343G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150805 | |||||||
chr15:99150898 | C | T | 3 | a0001c0001t0007g0044 a0001c0001t0011g0269 a0001c0001t0011g0275 |
3 | HG01255.hp2 HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1143+5250G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150898 | |||||||
chr15:99150918 | T | C | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1143+5230A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150918 | |||||||
chr15:99150930 | G | A | 8 | a0001c0005t0008g0257 a0001c0005t0008g0259 a0001c0005t0008g0260 others(5): Show |
8 | HG02615.hp1 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+5218C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99150930 | |||||||
chr15:99151144 | C | T | 2 | a0001c0001t0003g0239 a0001c0001t0019g0095 |
2 | HG01099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1143+5004G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151144 | |||||||
chr15:99151251 | G | A | 2 | a0001c0002t0005g0116 a0001c0002t0005g0129 |
2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1143+4897C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151251 | |||||||
chr15:99151284 | A | G | 44 | a0001c0001t0006g0002 a0001c0001t0006g0037 a0001c0001t0006g0048 others(41): Show |
45 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1143+4864T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151284 | |||||||
chr15:99151391 | G | GA | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1143+4756dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151391 | |||||||
chr15:99151396 | G | A | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1143+4752C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151396 | |||||||
chr15:99151470 | C | T | 66 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(63): Show |
66 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1143+4678G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151470 | |||||||
chr15:99151575 | G | A | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1143+4573C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151575 | |||||||
chr15:99151623 | T | C | 295 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(292): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1143+4525A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151623 | |||||||
chr15:99151624 | G | A | 116 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(113): Show |
117 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.1143+4524C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151624 | |||||||
chr15:99151681 | C | G | 18 | a0001c0001t0001g0252 a0001c0001t0004g0139 a0001c0001t0012g0005 others(15): Show |
18 | HG00733.hp2 HG00735.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1143+4467G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151681 | |||||||
chr15:99151782 | C | G | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1143+4366G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151782 | |||||||
chr15:99151918 | C | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0024g0258 |
3 | HG01891.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1143+4230G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151918 | |||||||
chr15:99151921 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1143+4227G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99151921 | |||||||
chr15:99152165 | T | C | 9 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0001g0308 others(6): Show |
9 | HG01261.hp2 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+3983A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152165 | |||||||
chr15:99152240 | G | GT | 5 | a0001c0001t0001g0253 a0001c0001t0001g0276 a0001c0001t0004g0015 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+3907dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152240 | |||||||
chr15:99152287 | G | A | 95 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(92): Show |
96 | HG00323.hp1 HG00558.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.1143+3861C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152287 | |||||||
chr15:99152362 | ATTTC | A | 80 | a0001c0001t0001g0252 a0001c0001t0004g0022 a0001c0001t0004g0122 others(77): Show |
81 | HG00323.hp1 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1143+3782_1143+378 others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152362 | |||||||
chr15:99152446 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1143+3702C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152446 | |||||||
chr15:99152524 | T | C | 128 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(125): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1143+3624A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152524 | |||||||
chr15:99152614 | T | A | 1 | a0005c0017t0001g0270 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1143+3534A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152614 | |||||||
chr15:99152766 | A | G | 2 | a0001c0002t0004g0024 a0001c0002t0004g0026 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1143+3382T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152766 | |||||||
chr15:99152790 | C | A | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1143+3358G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152790 | |||||||
chr15:99152971 | G | A | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1143+3177C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99152971 | |||||||
chr15:99153003 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0161 a0001c0001t0010g0326 others(1): Show |
4 | HG01496.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+3145A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153003 | |||||||
chr15:99153006 | C | T | 1 | a0001c0004t0003g0153 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1143+3142G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153006 | |||||||
chr15:99153074 | C | T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1143+3074G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153074 | |||||||
chr15:99153132 | G | A | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1143+3016C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153132 | |||||||
chr15:99153166 | C | T | 2 | a0001c0001t0013g0145 a0001c0001t0013g0147 |
2 | NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1143+2982G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153166 | |||||||
chr15:99153283 | T | G | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+2865A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153283 | |||||||
chr15:99153414 | C | G | 212 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(209): Show |
214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1143+2734G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153414 | |||||||
chr15:99153477 | C | T | 228 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(225): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1143+2671G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153477 | |||||||
chr15:99153595 | A | G | 81 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1143+2553T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153595 | |||||||
chr15:99153861 | A | G | 187 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(184): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1143+2287T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153861 | |||||||
chr15:99153902 | G | A | 118 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(115): Show |
119 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1143+2246C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153902 | |||||||
chr15:99153960 | T | C | 176 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(173): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.1143+2188A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153960 | |||||||
chr15:99153966 | T | C | 185 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(182): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1143+2182A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99153966 | |||||||
chr15:99154075 | T | G | 17 | a0001c0001t0001g0252 a0001c0001t0012g0005 a0001c0001t0012g0138 others(14): Show |
17 | HG00733.hp2 HG00735.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1143+2073A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154075 | |||||||
chr15:99154088 | C | G | 1 | a0001c0001t0001g0280 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1143+2060G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154088 | |||||||
chr15:99154160 | G | A | 102 | a0001c0001t0004g0022 a0001c0001t0004g0122 a0001c0001t0006g0002 others(99): Show |
103 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1143+1988C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154160 | |||||||
chr15:99154184 | T | C | 107 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(104): Show |
108 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1143+1964A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154184 | |||||||
chr15:99154207 | G | A | 118 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(115): Show |
119 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1143+1941C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154207 | |||||||
chr15:99154302 | G | C | 12 | a0001c0001t0002g0161 a0001c0005t0003g0013 a0001c0005t0008g0257 others(9): Show |
12 | HG01496.hp1 HG02615.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1143+1846C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154302 | |||||||
chr15:99154572 | T | C | 302 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(299): Show |
304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1143+1576A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154572 | |||||||
chr15:99154644 | C | A | 2 | a0001c0002t0005g0119 a0001c0002t0005g0169 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1143+1504G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154644 | |||||||
chr15:99154765 | T | G | 1 | a0001c0001t0003g0243 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1143+1383A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154765 | |||||||
chr15:99154961 | T | G | 79 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(76): Show |
79 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1143+1187A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99154961 | |||||||
chr15:99155173 | A | G | 7 | a0001c0001t0012g0005 a0001c0001t0012g0138 a0001c0001t0012g0140 others(4): Show |
7 | HG03516.hp1 NA18945.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+975T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99155173 | |||||||
chr15:99155208 | C | T | 1 | a0001c0003t0004g0054 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1143+940G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99155208 | |||||||
chr15:99155247 | T | C | 108 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(105): Show |
109 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1143+901A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99155247 | |||||||
chr15:99155302 | A | C | 300 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(297): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1143+846T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99155302 | |||||||
chr15:99155468 | G | A | 1 | a0001c0002t0005g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1143+680C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 12/13 | chr15 | 99155468 | |||||||
chr15:99156308 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.994-11T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156308 | |||||||
chr15:99156367 | A | G | 1 | a0001c0002t0005g0113 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.994-70T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156367 | |||||||
chr15:99156397 | G | A | 2 | a0001c0001t0007g0180 a0001c0001t0022g0179 |
2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.994-100C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156397 | |||||||
chr15:99156548 | G | A | 1 | a0001c0001t0001g0347 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.994-251C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156548 | |||||||
chr15:99156565 | G | A | 1 | a0001c0001t0007g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.994-268C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156565 | |||||||
chr15:99156702 | C | T | 2 | a0001c0001t0019g0095 a0001c0002t0004g0146 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.994-405G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156702 | |||||||
chr15:99156758 | G | A | 1 | a0001c0001t0004g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.994-461C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156758 | |||||||
chr15:99156877 | T | C | 2 | a0001c0001t0006g0100 a0001c0001t0015g0365 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.994-580A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156877 | |||||||
chr15:99156961 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.994-664G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99156961 | |||||||
chr15:99157099 | T | A | 1 | a0001c0001t0025g0332 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.994-802A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157099 | |||||||
chr15:99157131 | C | CT | 102 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(99): Show |
104 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.994-835dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157131 | |||||||
chr15:99157131 | CT | C | 24 | a0001c0001t0001g0285 a0001c0001t0001g0310 a0001c0001t0001g0317 others(21): Show |
24 | HG00323.hp2 HG01081.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.994-835delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157131 | |||||||
chr15:99157150 | T | A | 1 | a0001c0003t0004g0054 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.994-853A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157150 | |||||||
chr15:99157211 | G | GT | 77 | a0001c0001t0001g0295 a0001c0001t0001g0348 a0001c0001t0001g0352 others(74): Show |
77 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.994-915dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157211 | |||||||
chr15:99157211 | GT | G | 107 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0280 others(104): Show |
108 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.994-915delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157211 | |||||||
chr15:99157286 | T | C | 290 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(287): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.994-989A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157286 | |||||||
chr15:99157357 | G | A | 1 | a0001c0002t0004g0142 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.994-1060C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157357 | |||||||
chr15:99157433 | A | C | 2 | a0001c0002t0005g0121 a0001c0002t0005g0126 |
2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.994-1136T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157433 | |||||||
chr15:99157629 | A | G | 2 | a0001c0001t0007g0171 a0001c0001t0023g0172 |
2 | HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.994-1332T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157629 | |||||||
chr15:99157753 | A | C | 1 | a0001c0004t0006g0118 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.994-1456T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157753 | |||||||
chr15:99157798 | C | A | 1 | a0001c0001t0002g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.994-1501G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157798 | |||||||
chr15:99157867 | G | A | 1 | a0005c0017t0001g0270 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.994-1570C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157867 | |||||||
chr15:99157971 | A | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.994-1674T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157971 | |||||||
chr15:99157973 | G | A | 98 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(95): Show |
98 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.994-1676C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99157973 | |||||||
chr15:99158058 | C | T | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.994-1761G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158058 | |||||||
chr15:99158116 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.994-1819T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158116 | |||||||
chr15:99158345 | C | T | 57 | a0001c0001t0004g0122 a0001c0001t0006g0002 a0001c0001t0006g0100 others(54): Show |
58 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.994-2048G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158345 | |||||||
chr15:99158361 | C | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.994-2064G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158361 | |||||||
chr15:99158405 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.994-2108G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158405 | |||||||
chr15:99158455 | T | C | 7 | a0001c0001t0004g0022 a0001c0002t0004g0017 a0001c0002t0004g0018 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.994-2158A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158455 | |||||||
chr15:99158532 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.994-2235C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158532 | |||||||
chr15:99158539 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.994-2242G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158539 | |||||||
chr15:99158557 | G | C | 1 | a0001c0001t0009g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.994-2260C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158557 | |||||||
chr15:99158725 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.994-2428T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158725 | |||||||
chr15:99158757 | C | T | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.994-2460G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158757 | |||||||
chr15:99158805 | G | C | 7 | a0001c0001t0004g0022 a0001c0002t0004g0017 a0001c0002t0004g0018 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.994-2508C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158805 | |||||||
chr15:99158828 | T | C | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.994-2531A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158828 | |||||||
chr15:99158852 | C | G | 6 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(3): Show |
7 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-2555G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158852 | |||||||
chr15:99158876 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.994-2579T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158876 | |||||||
chr15:99158895 | A | G | 301 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(298): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.994-2598T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158895 | |||||||
chr15:99158995 | G | A | 18 | a0001c0001t0003g0010 a0001c0001t0004g0022 a0001c0002t0004g0017 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.994-2698C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99158995 | |||||||
chr15:99159052 | T | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2688A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159052 | |||||||
chr15:99159090 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2650T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159090 | |||||||
chr15:99159195 | T | C | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.993+2545A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159195 | |||||||
chr15:99159304 | A | C | 72 | a0001c0001t0002g0161 a0001c0001t0004g0122 a0001c0001t0006g0002 others(69): Show |
73 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.993+2436T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159304 | |||||||
chr15:99159424 | A | C | 3 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0024g0258 |
3 | HG01891.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.993+2316T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159424 | |||||||
chr15:99159465 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2275T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159465 | |||||||
chr15:99159467 | G | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2273C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159467 | |||||||
chr15:99159469 | A | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2271T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159469 | |||||||
chr15:99159470 | G | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2270C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159470 | |||||||
chr15:99159472 | C | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2268G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159472 | |||||||
chr15:99159484 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2256T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159484 | |||||||
chr15:99159717 | C | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+2023G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159717 | |||||||
chr15:99159769 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.993+1971C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159769 | |||||||
chr15:99159787 | A | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1953T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159787 | |||||||
chr15:99159859 | G | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1881C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159859 | |||||||
chr15:99159924 | A | G | 1 | a0002c0006t0003g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.993+1816T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159924 | |||||||
chr15:99159933 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1807T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159933 | |||||||
chr15:99159940 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1800A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159940 | |||||||
chr15:99159958 | C | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1782G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99159958 | |||||||
chr15:99160022 | T | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1718A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160022 | |||||||
chr15:99160023 | C | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1717G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160023 | |||||||
chr15:99160028 | T | G | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.993+1712A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160028 | |||||||
chr15:99160056 | G | C | 1 | a0001c0001t0012g0141 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.993+1684C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160056 | |||||||
chr15:99160091 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1649A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160091 | |||||||
chr15:99160095 | C | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1645G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160095 | |||||||
chr15:99160106 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0010g0326 a0001c0001t0010g0349 |
3 | HG02896.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.993+1634C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160106 | |||||||
chr15:99160113 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1627T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160113 | |||||||
chr15:99160118 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.993+1622G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160118 | |||||||
chr15:99160192 | A | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1548T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160192 | |||||||
chr15:99160205 | C | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1535G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160205 | |||||||
chr15:99160219 | G | A | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.993+1521C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160219 | |||||||
chr15:99160254 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.993+1486C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160254 | |||||||
chr15:99160291 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1449T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160291 | |||||||
chr15:99160307 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1433T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160307 | |||||||
chr15:99160338 | A | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1402T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160338 | |||||||
chr15:99160353 | C | T | 1 | a0001c0001t0002g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.993+1387G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160353 | |||||||
chr15:99160430 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1310T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160430 | |||||||
chr15:99160439 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1301T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160439 | |||||||
chr15:99160551 | A | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1189T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160551 | |||||||
chr15:99160552 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1188A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160552 | |||||||
chr15:99160674 | T | A | 104 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(101): Show |
104 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.993+1066A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160674 | |||||||
chr15:99160693 | T | C | 1 | a0001c0001t0002g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.993+1047A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160693 | |||||||
chr15:99160735 | C | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1005G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160735 | |||||||
chr15:99160736 | CG | C | 14 | a0001c0001t0003g0010 a0001c0001t0004g0022 a0001c0002t0004g0017 others(11): Show |
14 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.993+1003delC | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160736 | |||||||
chr15:99160739 | G | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1001C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160739 | |||||||
chr15:99160740 | C | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+1000G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160740 | |||||||
chr15:99160767 | C | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+973G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160767 | |||||||
chr15:99160786 | G | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+954C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160786 | |||||||
chr15:99160789 | C | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+951G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160789 | |||||||
chr15:99160806 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+934T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160806 | |||||||
chr15:99160856 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+884T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160856 | |||||||
chr15:99160870 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+870A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160870 | |||||||
chr15:99160871 | G | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+869C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160871 | |||||||
chr15:99160883 | G | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+857C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160883 | |||||||
chr15:99160888 | C | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+852G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160888 | |||||||
chr15:99160903 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+837T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160903 | |||||||
chr15:99160926 | T | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+814A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160926 | |||||||
chr15:99160945 | G | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+795C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99160945 | |||||||
chr15:99161012 | C | CA | 60 | a0001c0001t0002g0069 a0001c0001t0002g0079 a0001c0001t0002g0082 others(57): Show |
60 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.993+727dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161012 | |||||||
chr15:99161012 | C | CAA | 10 | a0001c0001t0003g0239 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01099.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.993+726_993+727dup others(2): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161012 | |||||||
chr15:99161038 | G | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+702C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161038 | |||||||
chr15:99161139 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+601A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161139 | |||||||
chr15:99161154 | G | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+586C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161154 | |||||||
chr15:99161155 | T | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+585A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161155 | |||||||
chr15:99161156 | G | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+584C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161156 | |||||||
chr15:99161162 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+578A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161162 | |||||||
chr15:99161164 | G | GTA | 19 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0035 others(16): Show |
19 | HG01496.hp1 HG01891.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.993+574_993+575dup others(2): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161164 | |||||||
chr15:99161164 | G | GTATA | 125 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(122): Show |
126 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.993+572_993+575dup others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161164 | |||||||
chr15:99161164 | G | GTATATA | 8 | a0001c0001t0001g0300 a0001c0001t0011g0275 a0001c0001t0012g0140 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.993+570_993+575dup others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161164 | |||||||
chr15:99161197 | C | T | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.993+543G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161197 | |||||||
chr15:99161360 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+380A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161360 | |||||||
chr15:99161367 | C | T | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.993+373G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161367 | |||||||
chr15:99161379 | C | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+361G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161379 | |||||||
chr15:99161488 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+252A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161488 | |||||||
chr15:99161552 | C | T | 2 | a0001c0001t0007g0163 a0001c0001t0007g0175 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.993+188G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161552 | |||||||
chr15:99161607 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+133A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161607 | |||||||
chr15:99161613 | T | C | 1 | a0001c0002t0004g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.993+127A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161613 | |||||||
chr15:99161629 | G | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+111C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161629 | |||||||
chr15:99161652 | A | G | 134 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(131): Show |
135 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.993+88T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161652 | |||||||
chr15:99161690 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+50A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161690 | |||||||
chr15:99161692 | G | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+48C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161692 | |||||||
chr15:99161695 | T | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+45A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 11/13 | chr15 | 99161695 | |||||||
chr15:99161959 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-92A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99161959 | |||||||
chr15:99161979 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-112T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99161979 | |||||||
chr15:99162163 | G | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-296C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162163 | |||||||
chr15:99162181 | C | T | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.866-314G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162181 | |||||||
chr15:99162227 | C | G | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-360G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162227 | |||||||
chr15:99162228 | T | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-361A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162228 | |||||||
chr15:99162230 | A | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-363T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162230 | |||||||
chr15:99162232 | G | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-365C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162232 | |||||||
chr15:99162266 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-399A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162266 | |||||||
chr15:99162331 | C | T | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.866-464G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162331 | |||||||
chr15:99162382 | T | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-515A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162382 | |||||||
chr15:99162384 | C | A | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-517G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162384 | |||||||
chr15:99162385 | T | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-518A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162385 | |||||||
chr15:99162386 | G | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-519C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162386 | |||||||
chr15:99162518 | G | A | 21 | a0001c0001t0007g0044 a0001c0001t0007g0163 a0001c0001t0007g0165 others(18): Show |
21 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.866-651C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162518 | |||||||
chr15:99162696 | C | T | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-829G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162696 | |||||||
chr15:99162697 | T | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.866-830A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162697 | |||||||
chr15:99162827 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.866-960G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162827 | |||||||
chr15:99162834 | C | T | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-967G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99162834 | |||||||
chr15:99163041 | C | A | 1 | a0001c0005t0027g0360 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.866-1174G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99163041 | |||||||
chr15:99163086 | A | AAAAC | 232 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(229): Show |
233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.866-1223_866-1220d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99163086 | |||||||
chr15:99163303 | C | A | 1 | a0001c0003t0003g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.866-1436G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99163303 | |||||||
chr15:99163395 | T | A | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-1528A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99163395 | |||||||
chr15:99163422 | T | C | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1555A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99163422 | |||||||
chr15:99163567 | C | T | 80 | a0001c0001t0004g0122 a0001c0001t0006g0002 a0001c0001t0006g0037 others(77): Show |
81 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.866-1700G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99163567 | |||||||
chr15:99164187 | T | C | 1 | a0001c0001t0009g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.866-2320A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164187 | |||||||
chr15:99164469 | G | T | 67 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(64): Show |
67 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.866-2602C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164469 | |||||||
chr15:99164499 | T | C | 9 | a0001c0001t0004g0022 a0001c0002t0004g0017 a0001c0002t0004g0018 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.866-2632A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164499 | |||||||
chr15:99164659 | T | C | 1 | a0001c0003t0008g0333 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.866-2792A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164659 | |||||||
chr15:99164749 | A | C | 1 | a0001c0001t0003g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.866-2882T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164749 | |||||||
chr15:99164758 | C | T | 1 | a0001c0001t0007g0174 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.866-2891G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164758 | |||||||
chr15:99164802 | T | G | 205 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(202): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.866-2935A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164802 | |||||||
chr15:99164881 | G | A | 70 | a0001c0001t0004g0122 a0001c0001t0006g0002 a0001c0001t0006g0037 others(67): Show |
71 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.866-3014C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164881 | |||||||
chr15:99164884 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.866-3017A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164884 | |||||||
chr15:99164927 | A | G | 73 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.866-3060T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99164927 | |||||||
chr15:99165053 | T | A | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.866-3186A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165053 | |||||||
chr15:99165130 | G | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0024g0258 |
3 | HG01891.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.866-3263C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165130 | |||||||
chr15:99165158 | TAGC | T | 3 | a0001c0001t0006g0104 a0004c0008t0011g0278 a0004c0008t0011g0284 |
3 | HG02258.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.866-3294_866-3292d others(5): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165158 | |||||||
chr15:99165280 | T | C | 3 | a0001c0005t0008g0260 a0001c0005t0008g0261 a0001c0005t0008g0264 |
3 | HG06807.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.866-3413A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165280 | |||||||
chr15:99165340 | T | C | 1 | a0001c0002t0004g0142 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.866-3473A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165340 | |||||||
chr15:99165431 | C | T | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.866-3564G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165431 | |||||||
chr15:99165477 | G | A | 1 | a0001c0001t0007g0187 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.866-3610C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165477 | |||||||
chr15:99165481 | A | G | 1 | a0001c0001t0004g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.866-3614T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165481 | |||||||
chr15:99165586 | T | A | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.866-3719A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165586 | |||||||
chr15:99165679 | T | C | 1 | a0001c0009t0001g0361 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.866-3812A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165679 | |||||||
chr15:99165734 | G | GA | 301 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(298): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.866-3868_866-3867i others(3): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165734 | |||||||
chr15:99165776 | T | C | 13 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(10): Show |
13 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.866-3909A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165776 | |||||||
chr15:99165854 | A | G | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-3987T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99165854 | |||||||
chr15:99166034 | T | C | 91 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(88): Show |
91 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.866-4167A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166034 | |||||||
chr15:99166069 | C | T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.866-4202G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166069 | |||||||
chr15:99166120 | G | A | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.866-4253C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166120 | |||||||
chr15:99166142 | G | A | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.866-4275C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166142 | |||||||
chr15:99166234 | A | G | 1 | a0001c0002t0005g0131 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.866-4367T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166234 | |||||||
chr15:99166277 | G | T | 1 | a0001c0001t0012g0005 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.866-4410C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166277 | |||||||
chr15:99166428 | C | T | 210 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.866-4561G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166428 | |||||||
chr15:99166461 | C | T | 5 | a0001c0001t0002g0011 a0001c0001t0002g0161 a0001c0001t0010g0326 others(2): Show |
5 | HG01496.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.866-4594G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166461 | |||||||
chr15:99166486 | C | CA | 4 | a0001c0001t0002g0011 a0001c0001t0002g0161 a0001c0001t0010g0326 others(1): Show |
4 | HG01496.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-4620dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166486 | |||||||
chr15:99166515 | C | T | 3 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 |
4 | HG01167.hp2 HG01169.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-4648G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166515 | |||||||
chr15:99166581 | C | T | 1 | a0001c0003t0003g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.866-4714G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166581 | |||||||
chr15:99166628 | G | C | 1 | a0002c0006t0003g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.866-4761C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166628 | |||||||
chr15:99166732 | C | G | 1 | a0001c0001t0001g0291 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.866-4865G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166732 | |||||||
chr15:99166854 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0004g0164 |
2 | HG01517.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.866-4987G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166854 | |||||||
chr15:99166859 | A | G | 198 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(195): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.866-4992T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166859 | |||||||
chr15:99166930 | T | C | 3 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0024g0258 |
3 | HG01891.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.866-5063A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166930 | |||||||
chr15:99166940 | A | G | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-5073T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99166940 | |||||||
chr15:99167092 | A | G | 137 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(134): Show |
138 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.866-5225T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167092 | |||||||
chr15:99167101 | G | T | 1 | a0001c0001t0001g0287 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.866-5234C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167101 | |||||||
chr15:99167137 | GGACA | G | 47 | a0001c0001t0004g0122 a0001c0001t0007g0044 a0001c0001t0007g0163 others(44): Show |
47 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.866-5274_866-5271d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167137 | |||||||
chr15:99167259 | G | A | 3 | a0001c0001t0006g0100 a0001c0001t0015g0343 a0001c0001t0015g0365 |
3 | HG02809.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.866-5392C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167259 | |||||||
chr15:99167449 | C | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0024g0258 |
3 | HG01891.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.866-5582G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167449 | |||||||
chr15:99167600 | A | G | 1 | a0001c0001t0001g0347 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.866-5733T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167600 | |||||||
chr15:99167752 | C | T | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.866-5885G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167752 | |||||||
chr15:99167895 | G | A | 1 | a0001c0001t0009g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.866-6028C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167895 | |||||||
chr15:99167966 | T | C | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-6099A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99167966 | |||||||
chr15:99168029 | G | C | 17 | a0001c0001t0003g0151 a0001c0001t0003g0181 a0001c0001t0003g0190 others(14): Show |
17 | HG00597.hp2 HG00673.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.866-6162C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168029 | |||||||
chr15:99168044 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0085 |
2 | NA18978.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.866-6177T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168044 | |||||||
chr15:99168054 | C | T | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-6187G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168054 | |||||||
chr15:99168115 | G | C | 56 | a0001c0001t0004g0122 a0001c0001t0006g0002 a0001c0001t0006g0100 others(53): Show |
57 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.866-6248C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168115 | |||||||
chr15:99168412 | A | G | 1 | a0001c0001t0004g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.866-6545T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168412 | |||||||
chr15:99168469 | T | C | 129 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(126): Show |
130 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.865+6581A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168469 | |||||||
chr15:99168694 | T | C | 301 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(298): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.865+6356A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168694 | |||||||
chr15:99168813 | C | T | 15 | a0001c0001t0003g0010 a0001c0001t0004g0022 a0001c0002t0004g0017 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.865+6237G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168813 | |||||||
chr15:99168869 | G | T | 1 | a0001c0002t0005g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.865+6181C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168869 | |||||||
chr15:99168900 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.865+6150C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99168900 | |||||||
chr15:99169066 | G | C | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.865+5984C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169066 | |||||||
chr15:99169163 | C | T | 81 | a0001c0001t0004g0122 a0001c0001t0006g0002 a0001c0001t0006g0037 others(78): Show |
82 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.865+5887G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169163 | |||||||
chr15:99169176 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.865+5874A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169176 | |||||||
chr15:99169312 | A | G | 1 | a0001c0003t0008g0333 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.865+5738T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169312 | |||||||
chr15:99169317 | A | G | 300 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(297): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.865+5733T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169317 | |||||||
chr15:99169324 | C | T | 2 | a0001c0001t0006g0100 a0001c0001t0015g0365 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.865+5726G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169324 | |||||||
chr15:99169338 | G | GCTTACTC others(1): Show |
76 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0011 others(73): Show |
76 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.865+5704_865+5711d others(10): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169338 | |||||||
chr15:99169353 | A | T | 76 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0011 others(73): Show |
76 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.865+5697T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169353 | |||||||
chr15:99169583 | G | A | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.865+5467C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169583 | |||||||
chr15:99169590 | G | C | 110 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(107): Show |
111 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.865+5460C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169590 | |||||||
chr15:99169592 | G | A | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.865+5458C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169592 | |||||||
chr15:99169616 | A | G | 3 | a0001c0001t0006g0100 a0001c0001t0015g0343 a0001c0001t0015g0365 |
3 | HG02809.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.865+5434T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169616 | |||||||
chr15:99169748 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.865+5302C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169748 | |||||||
chr15:99169765 | C | T | 1 | a0002c0006t0003g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.865+5285G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169765 | |||||||
chr15:99169776 | G | A | 131 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(128): Show |
132 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.865+5274C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169776 | |||||||
chr15:99169821 | T | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0359 |
2 | HG00738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.865+5229A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169821 | |||||||
chr15:99169848 | A | G | 285 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(282): Show |
287 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.865+5202T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169848 | |||||||
chr15:99169865 | C | A | 1 | a0001c0001t0024g0258 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.865+5185G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99169865 | |||||||
chr15:99170176 | G | C | 105 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(102): Show |
105 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.865+4874C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99170176 | |||||||
chr15:99170401 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.865+4649G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99170401 | |||||||
chr15:99170495 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.865+4555A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99170495 | |||||||
chr15:99170542 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.865+4508G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99170542 | |||||||
chr15:99170590 | T | C | 3 | a0001c0001t0002g0011 a0001c0001t0010g0326 a0001c0001t0010g0349 |
3 | HG02896.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.865+4460A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99170590 | |||||||
chr15:99170635 | G | A | 9 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(6): Show |
9 | NA18959.hp1 NA18970.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.865+4415C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99170635 | |||||||
chr15:99170705 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.865+4345C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99170705 | |||||||
chr15:99170814 | C | T | 1 | a0001c0001t0001g0348 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.865+4236G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99170814 | |||||||
chr15:99171220 | T | G | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.865+3830A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171220 | |||||||
chr15:99171259 | C | G | 1 | a0001c0001t0001g0296 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.865+3791G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171259 | |||||||
chr15:99171309 | C | T | 1 | a0001c0009t0001g0362 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.865+3741G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171309 | |||||||
chr15:99171482 | C | T | 1 | a0001c0002t0001g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.865+3568G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171482 | |||||||
chr15:99171551 | C | T | 37 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0006g0002 others(34): Show |
38 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.865+3499G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171551 | |||||||
chr15:99171559 | C | CT | 194 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(191): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.865+3490dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171559 | |||||||
chr15:99171559 | C | CTT | 32 | a0001c0001t0001g0298 a0001c0001t0001g0324 a0001c0001t0001g0352 others(29): Show |
33 | HG00423.hp2 HG00735.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.865+3489_865+3490d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171559 | |||||||
chr15:99171559 | CT | C | 19 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0006g0002 others(16): Show |
20 | HG01243.hp2 HG01257.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.865+3490delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171559 | |||||||
chr15:99171559 | CTT | C | 12 | a0001c0001t0006g0037 a0001c0001t0006g0048 a0001c0001t0006g0053 others(9): Show |
12 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.865+3489_865+3490d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171559 | |||||||
chr15:99171668 | T | TTCTCATG others(448): Show |
4 | a0001c0002t0001g0301 a0001c0002t0004g0134 a0001c0002t0004g0135 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+2927_865+3381d others(457): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171668 | |||||||
chr15:99171700 | C | T | 1 | a0001c0003t0009g0246 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.865+3350G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171700 | |||||||
chr15:99171822 | G | A | 14 | a0001c0001t0003g0010 a0001c0001t0004g0022 a0001c0002t0004g0017 others(11): Show |
14 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.865+3228C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171822 | |||||||
chr15:99171886 | C | T | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.865+3164G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171886 | |||||||
chr15:99171922 | C | T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.865+3128G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99171922 | |||||||
chr15:99172008 | T | C | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+3042A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172008 | |||||||
chr15:99172014 | T | TCTCACAT others(448): Show |
1 | a0001c0002t0004g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.865+3035_865+3036i others(457): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172014 | |||||||
chr15:99172020 | A | AT | 20 | a0001c0001t0002g0085 a0001c0001t0006g0103 a0001c0003t0003g0182 others(17): Show |
20 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(17): Show |
intron_variant | MODIFIER | c.865+3029dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172020 | |||||||
chr15:99172020 | AT | A | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.865+3029delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172020 | |||||||
chr15:99172193 | T | C | 69 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(66): Show |
69 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.865+2857A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172193 | |||||||
chr15:99172202 | G | C | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.865+2848C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172202 | |||||||
chr15:99172206 | C | T | 2 | a0001c0001t0001g0328 a0001c0001t0001g0356 |
2 | HG01192.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.865+2844G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172206 | |||||||
chr15:99172238 | G | A | 15 | a0001c0001t0012g0005 a0001c0001t0012g0138 a0001c0001t0012g0140 others(12): Show |
15 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.865+2812C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172238 | |||||||
chr15:99172266 | T | C | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.865+2784A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172266 | |||||||
chr15:99172339 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.865+2711G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172339 | |||||||
chr15:99172511 | A | C | 1 | a0001c0001t0001g0320 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.865+2539T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172511 | |||||||
chr15:99172672 | A | C | 119 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(116): Show |
120 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.865+2378T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172672 | |||||||
chr15:99172893 | A | G | 1 | a0007c0015t0002g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.865+2157T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99172893 | |||||||
chr15:99173030 | G | A | 1 | a0001c0001t0011g0272 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.865+2020C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99173030 | |||||||
chr15:99173229 | G | C | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+1821C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99173229 | |||||||
chr15:99173304 | T | C | 9 | a0001c0005t0008g0257 a0001c0005t0008g0259 a0001c0005t0008g0260 others(6): Show |
9 | HG02615.hp1 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.865+1746A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99173304 | |||||||
chr15:99173350 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0348 |
2 | NA18997.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.865+1700C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99173350 | |||||||
chr15:99173479 | C | T | 1 | a0001c0002t0005g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.865+1571G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99173479 | |||||||
chr15:99173610 | A | C | 5 | a0001c0001t0001g0331 a0001c0001t0001g0353 a0001c0001t0001g0357 others(2): Show |
5 | HG00733.hp1 HG01168.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+1440T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99173610 | |||||||
chr15:99173966 | C | T | 8 | a0001c0001t0006g0125 a0001c0004t0006g0109 a0001c0004t0006g0117 others(5): Show |
8 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.865+1084G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99173966 | |||||||
chr15:99174120 | T | C | 318 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(315): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.865+930A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174120 | |||||||
chr15:99174142 | A | G | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.865+908T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174142 | |||||||
chr15:99174462 | C | CA | 148 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(145): Show |
149 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.865+587dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174462 | |||||||
chr15:99174462 | C | CAA | 6 | a0001c0001t0001g0277 a0001c0001t0004g0106 a0001c0001t0004g0107 others(3): Show |
6 | HG02572.hp1 HG02886.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.865+586_865+587dup others(2): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174462 | |||||||
chr15:99174571 | C | T | 317 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(314): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.865+479G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174571 | |||||||
chr15:99174765 | T | TA | 139 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(136): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.865+284dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174765 | |||||||
chr15:99174790 | C | T | 1 | a0001c0001t0002g0249 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.865+260G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174790 | |||||||
chr15:99174883 | C | CA | 8 | a0001c0001t0006g0125 a0001c0004t0006g0109 a0001c0004t0006g0117 others(5): Show |
8 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.865+166dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174883 | |||||||
chr15:99174933 | G | C | 1 | a0001c0005t0008g0279 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.865+117C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174933 | |||||||
chr15:99174987 | G | T | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.865+63C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 10/13 | chr15 | 99174987 | |||||||
chr15:99175165 | CAGAA | C | 4 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-14_760-11delTT others(2): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99175165 | |||||||
chr15:99175297 | A | T | 1 | a0001c0001t0004g0122 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.760-142T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99175297 | |||||||
chr15:99175521 | C | T | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.760-366G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99175521 | |||||||
chr15:99175831 | A | C | 301 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(298): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.760-676T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99175831 | |||||||
chr15:99176221 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.760-1066G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99176221 | |||||||
chr15:99176376 | C | A | 8 | a0001c0001t0006g0125 a0001c0004t0006g0109 a0001c0004t0006g0117 others(5): Show |
8 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.760-1221G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99176376 | |||||||
chr15:99176467 | C | T | 5 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0072 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-1312G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99176467 | |||||||
chr15:99176874 | T | C | 74 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.760-1719A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99176874 | |||||||
chr15:99176916 | G | T | 1 | a0001c0001t0001g0324 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.760-1761C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99176916 | |||||||
chr15:99177079 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.760-1924C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99177079 | |||||||
chr15:99177145 | T | A | 1 | a0001c0001t0010g0335 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.760-1990A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99177145 | |||||||
chr15:99177164 | C | T | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-2009G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99177164 | |||||||
chr15:99177283 | C | G | 1 | a0001c0001t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.760-2128G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99177283 | |||||||
chr15:99177693 | C | G | 74 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.760-2538G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99177693 | |||||||
chr15:99177809 | G | T | 2 | a0001c0001t0003g0239 a0001c0001t0019g0095 |
2 | HG01099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.760-2654C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99177809 | |||||||
chr15:99177904 | G | T | 1 | a0001c0001t0009g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.760-2749C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99177904 | |||||||
chr15:99177935 | C | A | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.760-2780G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99177935 | |||||||
chr15:99178130 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.760-2975G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99178130 | |||||||
chr15:99178267 | A | G | 57 | a0001c0001t0004g0122 a0001c0001t0006g0002 a0001c0001t0006g0100 others(54): Show |
58 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.760-3112T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99178267 | |||||||
chr15:99178370 | T | C | 320 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(317): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.760-3215A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99178370 | |||||||
chr15:99178541 | T | C | 320 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(317): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.760-3386A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99178541 | |||||||
chr15:99178776 | A | G | 1 | a0002c0006t0003g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.760-3621T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99178776 | |||||||
chr15:99178950 | A | C | 21 | a0001c0001t0007g0044 a0001c0001t0007g0163 a0001c0001t0007g0165 others(18): Show |
21 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.760-3795T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99178950 | |||||||
chr15:99178987 | C | G | 74 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.760-3832G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99178987 | |||||||
chr15:99179098 | A | G | 15 | a0001c0001t0003g0010 a0001c0001t0004g0022 a0001c0002t0004g0017 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-3943T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179098 | |||||||
chr15:99179142 | G | C | 8 | a0001c0001t0006g0125 a0001c0004t0006g0109 a0001c0004t0006g0117 others(5): Show |
8 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.760-3987C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179142 | |||||||
chr15:99179555 | T | C | 1 | a0001c0002t0005g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.760-4400A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179555 | |||||||
chr15:99179568 | G | A | 302 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(299): Show |
304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.760-4413C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179568 | |||||||
chr15:99179596 | C | T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.760-4441G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179596 | |||||||
chr15:99179607 | GT | G | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-4453delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179607 | |||||||
chr15:99179609 | A | C | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-4454T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179609 | |||||||
chr15:99179627 | T | C | 8 | a0001c0001t0006g0125 a0001c0004t0006g0109 a0001c0004t0006g0117 others(5): Show |
8 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.760-4472A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179627 | |||||||
chr15:99179628 | G | A | 1 | a0001c0001t0007g0186 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.760-4473C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179628 | |||||||
chr15:99179811 | AG | A | 9 | a0001c0001t0004g0022 a0001c0002t0004g0017 a0001c0002t0004g0018 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-4657delC | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179811 | |||||||
chr15:99179840 | A | G | 109 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(106): Show |
110 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.760-4685T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179840 | |||||||
chr15:99179889 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.760-4734G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99179889 | |||||||
chr15:99180106 | C | A | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.760-4951G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180106 | |||||||
chr15:99180136 | C | T | 24 | a0001c0001t0004g0122 a0001c0002t0005g0014 a0001c0002t0005g0110 others(21): Show |
24 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.760-4981G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180136 | |||||||
chr15:99180229 | T | C | 81 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0011 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.760-5074A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180229 | |||||||
chr15:99180269 | G | C | 1 | a0001c0001t0010g0335 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.760-5114C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180269 | |||||||
chr15:99180276 | T | A | 24 | a0001c0001t0004g0122 a0001c0002t0005g0014 a0001c0002t0005g0110 others(21): Show |
24 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.760-5121A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180276 | |||||||
chr15:99180354 | A | C | 1 | a0001c0001t0004g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.760-5199T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180354 | |||||||
chr15:99180356 | A | C | 2 | a0001c0001t0006g0002 a0001c0001t0006g0102 |
3 | HG02976.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.760-5201T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180356 | |||||||
chr15:99180359 | C | A | 1 | a0001c0001t0004g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.760-5204G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180359 | |||||||
chr15:99180454 | A | G | 133 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0266 others(130): Show |
134 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.760-5299T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180454 | |||||||
chr15:99180565 | G | C | 23 | a0001c0001t0001g0268 a0001c0001t0001g0277 a0001c0001t0001g0283 others(20): Show |
23 | HG00621.hp2 HG00733.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-5410C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180565 | |||||||
chr15:99180619 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.760-5464T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180619 | |||||||
chr15:99180939 | A | G | 1 | a0001c0001t0003g0151 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.760-5784T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180939 | |||||||
chr15:99180995 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0161 a0001c0001t0010g0326 others(1): Show |
4 | HG01496.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-5840A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99180995 | |||||||
chr15:99181026 | TC | T | 17 | a0001c0001t0001g0252 a0001c0001t0012g0005 a0001c0001t0012g0138 others(14): Show |
17 | HG00733.hp2 HG00735.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.760-5872delG | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181026 | |||||||
chr15:99181078 | G | A | 1 | a0001c0001t0004g0196 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.760-5923C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181078 | |||||||
chr15:99181109 | T | C | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-5954A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181109 | |||||||
chr15:99181367 | G | T | 1 | a0001c0002t0004g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-6212C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181367 | |||||||
chr15:99181382 | A | C | 1 | a0001c0003t0003g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.760-6227T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181382 | |||||||
chr15:99181479 | G | C | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.760-6324C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181479 | |||||||
chr15:99181728 | C | A | 225 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(222): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.760-6573G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181728 | |||||||
chr15:99181774 | C | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0024g0258 |
3 | HG01891.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.760-6619G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181774 | |||||||
chr15:99181791 | G | C | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.760-6636C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181791 | |||||||
chr15:99181999 | C | T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.760-6844G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99181999 | |||||||
chr15:99182003 | T | C | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.760-6848A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182003 | |||||||
chr15:99182006 | T | G | 1 | a0001c0001t0001g0277 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.760-6851A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182006 | |||||||
chr15:99182140 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.760-6985G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182140 | |||||||
chr15:99182143 | T | C | 76 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(73): Show |
76 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.760-6988A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182143 | |||||||
chr15:99182206 | C | T | 1 | a0001c0003t0003g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.760-7051G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182206 | |||||||
chr15:99182223 | A | ATC | 19 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0002t0005g0014 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.760-7070_760-7069d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182223 | |||||||
chr15:99182223 | A | ATCTC | 6 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0116 others(3): Show |
6 | HG01123.hp2 HG02572.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-7072_760-7069d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182223 | |||||||
chr15:99182223 | ATC | A | 25 | a0001c0001t0002g0032 a0001c0001t0002g0035 a0001c0001t0002g0036 others(22): Show |
25 | HG00280.hp2 HG01433.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.760-7070_760-7069d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182223 | |||||||
chr15:99182240 | TCTCTCTC others(3): Show |
T | 1 | a0001c0004t0006g0130 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.760-7095_760-7086d others(12): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182240 | |||||||
chr15:99182240 | TCTCTCTC others(5): Show |
T | 6 | a0001c0004t0006g0109 a0001c0004t0006g0117 a0001c0004t0006g0118 others(3): Show |
6 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-7097_760-7086d others(14): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182240 | |||||||
chr15:99182242 | TCTCTCTC others(3): Show |
T | 3 | a0001c0002t0004g0134 a0001c0002t0004g0135 a0001c0002t0004g0136 |
3 | HG01109.hp1 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.760-7097_760-7088d others(12): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182242 | |||||||
chr15:99182242 | TCTCTCTC others(5): Show |
T | 1 | a0001c0001t0007g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.760-7099_760-7088d others(14): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182242 | |||||||
chr15:99182244 | TCTCTCA | T | 14 | a0001c0001t0001g0324 a0001c0001t0001g0352 a0001c0001t0004g0001 others(11): Show |
15 | HG01167.hp2 HG01169.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-7095_760-7090d others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182244 | |||||||
chr15:99182244 | TCTCTCAC others(3): Show |
T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.760-7099_760-7090d others(12): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182244 | |||||||
chr15:99182246 | T | TCA | 29 | a0001c0001t0002g0062 a0001c0001t0003g0151 a0001c0001t0003g0181 others(26): Show |
29 | HG00597.hp2 HG00673.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.760-7092_760-7091i others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182246 | |||||||
chr15:99182246 | T | TCACA | 11 | a0001c0001t0003g0200 a0001c0001t0003g0235 a0001c0003t0003g0182 others(8): Show |
11 | HG00099.hp2 HG03669.hp1 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.760-7092_760-7091i others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182246 | |||||||
chr15:99182246 | T | TCACACA | 3 | a0001c0003t0003g0183 a0001c0003t0003g0202 a0001c0003t0004g0054 |
3 | NA18973.hp1 NA19078.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.760-7092_760-7091i others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182246 | |||||||
chr15:99182246 | TCTCA | T | 10 | a0001c0001t0002g0011 a0001c0001t0002g0060 a0001c0001t0002g0064 others(7): Show |
11 | HG01243.hp2 HG02040.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-7095_760-7092d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182246 | |||||||
chr15:99182246 | TCTCACA | T | 19 | a0001c0001t0002g0234 a0001c0001t0006g0101 a0001c0002t0001g0301 others(16): Show |
19 | HG00099.hp1 HG00735.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.760-7097_760-7092d others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182246 | |||||||
chr15:99182246 | TCTCACAC others(1): Show |
T | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-7099_760-7092d others(10): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182246 | |||||||
chr15:99182246 | TCTCACAC others(5): Show |
T | 2 | a0001c0003t0003g0003 a0001c0003t0003g0206 |
3 | NA18941.hp2 NA19005.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.760-7103_760-7092d others(14): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182246 | |||||||
chr15:99182248 | T | A | 62 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0052 others(59): Show |
62 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.760-7093A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182248 | |||||||
chr15:99182248 | T | TCA | 4 | a0001c0001t0002g0079 a0001c0001t0002g0149 a0001c0001t0002g0150 others(1): Show |
4 | HG01081.hp2 HG02080.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-7095_760-7094d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182248 | |||||||
chr15:99182248 | TCA | T | 33 | a0001c0001t0001g0266 a0001c0001t0001g0286 a0001c0001t0001g0292 others(30): Show |
33 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.760-7095_760-7094d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182248 | |||||||
chr15:99182248 | TCACA | T | 96 | a0001c0001t0001g0253 a0001c0001t0001g0267 a0001c0001t0001g0268 others(93): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.760-7097_760-7094d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182248 | |||||||
chr15:99182248 | TCACACA | T | 4 | a0001c0001t0007g0187 a0001c0001t0022g0179 a0004c0008t0011g0278 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-7099_760-7094d others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182248 | |||||||
chr15:99182248 | TCACACAC others(1): Show |
T | 3 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0007g0185 |
3 | HG02886.hp2 HG03453.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.760-7101_760-7094d others(10): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182248 | |||||||
chr15:99182248 | TCACACAC others(9): Show |
T | 1 | a0001c0001t0001g0328 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.760-7109_760-7094d others(18): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182248 | |||||||
chr15:99182250 | A | T | 26 | a0001c0001t0002g0068 a0001c0001t0002g0249 a0001c0001t0002g0250 others(23): Show |
26 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.760-7095T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182250 | |||||||
chr15:99182252 | A | T | 3 | a0001c0001t0001g0286 a0001c0001t0007g0184 a0001c0002t0005g0159 |
3 | HG03831.hp2 HG04115.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.760-7097T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182252 | |||||||
chr15:99182254 | A | G | 1 | a0001c0001t0004g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.760-7099T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182254 | |||||||
chr15:99182254 | A | T | 14 | a0001c0001t0001g0321 a0001c0001t0001g0340 a0001c0001t0007g0044 others(11): Show |
14 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.760-7099T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182254 | |||||||
chr15:99182258 | A | T | 2 | a0001c0001t0004g0107 a0001c0001t0007g0185 |
2 | HG02886.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.760-7103T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182258 | |||||||
chr15:99182291 | T | C | 1 | a0001c0001t0002g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.760-7136A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182291 | |||||||
chr15:99182314 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.760-7159C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182314 | |||||||
chr15:99182426 | T | C | 7 | a0001c0001t0007g0163 a0001c0001t0007g0175 a0001c0001t0007g0180 others(4): Show |
7 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.760-7271A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182426 | |||||||
chr15:99182457 | G | T | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.760-7302C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182457 | |||||||
chr15:99182809 | A | T | 2 | a0001c0001t0001g0273 a0008c0016t0018g0204 |
2 | HG06807.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.760-7654T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182809 | |||||||
chr15:99182828 | T | TA | 105 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0256 others(102): Show |
105 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.760-7674dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182828 | |||||||
chr15:99182989 | C | A | 1 | a0001c0001t0002g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.760-7834G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99182989 | |||||||
chr15:99183042 | G | A | 1 | a0001c0003t0003g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.760-7887C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183042 | |||||||
chr15:99183092 | A | G | 3 | a0001c0001t0006g0100 a0001c0001t0015g0343 a0001c0001t0015g0365 |
3 | HG02809.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.760-7937T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183092 | |||||||
chr15:99183325 | C | CT | 32 | a0001c0001t0001g0324 a0001c0001t0001g0352 a0001c0001t0003g0239 others(29): Show |
33 | HG00323.hp1 HG00735.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.760-8171dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183325 | |||||||
chr15:99183346 | G | T | 7 | a0001c0001t0001g0324 a0001c0001t0001g0352 a0001c0001t0004g0001 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.760-8191C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183346 | |||||||
chr15:99183385 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.760-8230C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183385 | |||||||
chr15:99183469 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.760-8314C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183469 | |||||||
chr15:99183497 | A | AT | 16 | a0001c0001t0002g0012 a0001c0001t0002g0066 a0001c0001t0002g0067 others(13): Show |
16 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.760-8343dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183497 | |||||||
chr15:99183497 | AT | A | 37 | a0001c0001t0001g0329 a0001c0001t0002g0004 a0001c0001t0002g0011 others(34): Show |
38 | HG01069.hp1 HG01243.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.760-8343delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183497 | |||||||
chr15:99183497 | ATT | A | 111 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0256 others(108): Show |
112 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.760-8344_760-8343d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183497 | |||||||
chr15:99183497 | ATTT | A | 33 | a0001c0001t0001g0252 a0001c0001t0001g0292 a0001c0001t0001g0297 others(30): Show |
33 | HG00323.hp1 HG00423.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.760-8345_760-8343d others(5): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183497 | |||||||
chr15:99183940 | G | A | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-8785C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183940 | |||||||
chr15:99183969 | C | T | 4 | a0001c0003t0002g0211 a0001c0003t0002g0217 a0001c0003t0002g0218 others(1): Show |
4 | NA18945.hp1 NA18981.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-8814G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99183969 | |||||||
chr15:99184052 | T | C | 3 | a0001c0001t0013g0145 a0001c0001t0013g0147 a0001c0001t0013g0224 |
3 | NA18947.hp2 NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.760-8897A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184052 | |||||||
chr15:99184091 | C | T | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-8936G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184091 | |||||||
chr15:99184144 | A | C | 1 | a0001c0001t0003g0194 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.760-8989T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184144 | |||||||
chr15:99184488 | T | A | 1 | a0001c0001t0006g0037 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.760-9333A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184488 | |||||||
chr15:99184489 | A | G | 1 | a0001c0001t0006g0037 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.760-9334T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184489 | |||||||
chr15:99184490 | G | A | 1 | a0001c0001t0006g0037 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.760-9335C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184490 | |||||||
chr15:99184627 | T | G | 1 | a0001c0001t0013g0147 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.760-9472A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184627 | |||||||
chr15:99184630 | C | G | 1 | a0001c0001t0013g0147 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.760-9475G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184630 | |||||||
chr15:99184638 | C | T | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.760-9483G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184638 | |||||||
chr15:99184827 | T | C | 1 | a0001c0001t0006g0037 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.760-9672A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99184827 | |||||||
chr15:99185364 | A | T | 7 | a0001c0004t0006g0109 a0001c0004t0006g0117 a0001c0004t0006g0118 others(4): Show |
7 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-10209T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99185364 | |||||||
chr15:99185659 | G | A | 2 | a0004c0008t0011g0278 a0004c0008t0011g0284 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.760-10504C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99185659 | |||||||
chr15:99185931 | A | C | 1 | a0001c0001t0001g0344 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.760-10776T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99185931 | |||||||
chr15:99185989 | A | G | 228 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(225): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.760-10834T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99185989 | |||||||
chr15:99186042 | C | T | 301 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(298): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.760-10887G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99186042 | |||||||
chr15:99186148 | A | G | 7 | a0001c0004t0006g0109 a0001c0004t0006g0117 a0001c0004t0006g0118 others(4): Show |
7 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-10993T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99186148 | |||||||
chr15:99186231 | G | A | 7 | a0001c0003t0009g0226 a0001c0003t0009g0227 a0001c0003t0009g0230 others(4): Show |
7 | HG00735.hp2 HG01069.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.760-11076C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99186231 | |||||||
chr15:99186290 | C | G | 1 | a0001c0003t0004g0054 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.760-11135G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99186290 | |||||||
chr15:99186407 | T | C | 25 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0002t0005g0014 others(22): Show |
25 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.760-11252A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99186407 | |||||||
chr15:99186536 | C | G | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.760-11381G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99186536 | |||||||
chr15:99186697 | T | C | 243 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.760-11542A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99186697 | |||||||
chr15:99186918 | G | T | 1 | a0001c0001t0002g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.760-11763C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99186918 | |||||||
chr15:99187057 | A | T | 68 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(65): Show |
69 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.760-11902T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187057 | |||||||
chr15:99187214 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.760-12059A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187214 | |||||||
chr15:99187427 | G | T | 301 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(298): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.760-12272C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187427 | |||||||
chr15:99187452 | C | CA | 73 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.760-12298dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAA | 20 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(17): Show |
20 | HG00423.hp1 HG00621.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.760-12299_760-1229 others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAA | 47 | a0001c0001t0002g0031 a0001c0001t0002g0041 a0001c0001t0004g0122 others(44): Show |
47 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.760-12300_760-1229 others(7): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAA | 13 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(10): Show |
14 | HG01109.hp1 HG02258.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.760-12301_760-1229 others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAA | 10 | a0001c0001t0006g0108 a0001c0001t0012g0141 a0001c0001t0013g0145 others(7): Show |
10 | HG00735.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-12302_760-1229 others(9): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAA | 7 | a0001c0001t0004g0196 a0001c0001t0012g0005 a0001c0001t0012g0140 others(4): Show |
7 | HG00733.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-12303_760-1229 others(10): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAAA | 43 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0273 others(40): Show |
43 | HG00323.hp2 HG00558.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.760-12304_760-1229 others(11): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAAA others(1): Show |
27 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0292 others(24): Show |
28 | HG00544.hp1 HG00544.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.760-12305_760-1229 others(12): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0268 a0001c0001t0001g0277 a0001c0001t0001g0298 others(9): Show |
12 | HG00140.hp1 HG00423.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.760-12306_760-1229 others(13): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAAA others(3): Show |
8 | a0001c0001t0001g0253 a0001c0001t0001g0320 a0001c0001t0001g0348 others(5): Show |
8 | HG00621.hp2 HG00673.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.760-12307_760-1229 others(14): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0287 a0001c0001t0004g0164 |
2 | HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.760-12308_760-1229 others(15): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0280 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.760-12309_760-1229 others(16): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0276 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.760-12311_760-1229 others(18): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187452 | C | CAAAAAAA others(9): Show |
1 | a0001c0002t0004g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.760-12313_760-1229 others(20): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187452 | |||||||
chr15:99187462 | A | AAAAAAAG | 16 | a0001c0001t0001g0281 a0001c0001t0001g0295 a0001c0001t0001g0307 others(13): Show |
16 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.760-12308_760-1230 others(11): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187462 | |||||||
chr15:99187464 | A | AAC | 12 | a0001c0001t0003g0010 a0001c0001t0004g0022 a0001c0002t0004g0017 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.760-12310_760-1230 others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187464 | |||||||
chr15:99187469 | C | A | 298 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(295): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.760-12314G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187469 | |||||||
chr15:99187474 | C | A | 132 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(129): Show |
133 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.760-12319G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187474 | |||||||
chr15:99187569 | T | C | 2 | a0001c0001t0004g0196 a0001c0001t0004g0197 |
2 | NA18984.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.759+12350A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187569 | |||||||
chr15:99187609 | C | T | 1 | a0001c0002t0028g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.759+12310G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187609 | |||||||
chr15:99187698 | C | G | 2 | a0003c0011t0004g0158 a0003c0012t0004g0152 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.759+12221G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187698 | |||||||
chr15:99187739 | T | C | 1 | a0001c0001t0003g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.759+12180A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187739 | |||||||
chr15:99187768 | T | G | 2 | a0001c0009t0001g0361 a0001c0009t0001g0362 |
2 | NA18747.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.759+12151A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187768 | |||||||
chr15:99187955 | T | C | 6 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(3): Show |
7 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.759+11964A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187955 | |||||||
chr15:99187974 | A | G | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+11945T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99187974 | |||||||
chr15:99188017 | T | C | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+11902A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99188017 | |||||||
chr15:99188368 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.759+11551A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99188368 | |||||||
chr15:99188391 | G | T | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG00140.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.759+11528C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99188391 | |||||||
chr15:99188482 | A | T | 1 | a0001c0005t0008g0279 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.759+11437T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99188482 | |||||||
chr15:99188717 | T | G | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+11202A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99188717 | |||||||
chr15:99188760 | C | T | 3 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0021g0034 |
3 | NA18942.hp2 NA18959.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.759+11159G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99188760 | |||||||
chr15:99188765 | T | C | 2 | a0001c0002t0004g0098 a0001c0002t0004g0099 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.759+11154A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99188765 | |||||||
chr15:99189043 | AT | A | 55 | a0001c0001t0004g0122 a0001c0001t0006g0002 a0001c0001t0006g0100 others(52): Show |
56 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.759+10875delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189043 | |||||||
chr15:99189048 | T | G | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+10871A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189048 | |||||||
chr15:99189210 | T | C | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.759+10709A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189210 | |||||||
chr15:99189280 | C | T | 2 | a0001c0001t0001g0328 a0001c0001t0001g0356 |
2 | HG01192.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.759+10639G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189280 | |||||||
chr15:99189354 | C | T | 1 | a0001c0002t0001g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.759+10565G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189354 | |||||||
chr15:99189446 | T | C | 2 | a0004c0008t0011g0278 a0004c0008t0011g0284 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.759+10473A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189446 | |||||||
chr15:99189521 | T | G | 1 | a0001c0001t0001g0294 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.759+10398A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189521 | |||||||
chr15:99189584 | A | G | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.759+10335T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189584 | |||||||
chr15:99189660 | A | C | 7 | a0001c0004t0006g0109 a0001c0004t0006g0117 a0001c0004t0006g0118 others(4): Show |
7 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.759+10259T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189660 | |||||||
chr15:99189955 | T | C | 2 | a0001c0002t0001g0301 a0001c0002t0004g0105 |
2 | HG00735.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.759+9964A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99189955 | |||||||
chr15:99190054 | G | A | 115 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(112): Show |
115 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.759+9865C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190054 | |||||||
chr15:99190181 | A | AAAAG | 167 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(164): Show |
168 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.759+9734_759+9737d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190181 | |||||||
chr15:99190187 | A | T | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.759+9732T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190187 | |||||||
chr15:99190257 | G | GT | 111 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(108): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.759+9661dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190257 | |||||||
chr15:99190280 | G | GT | 22 | a0001c0001t0001g0303 a0001c0001t0007g0163 a0001c0001t0007g0165 others(19): Show |
22 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.759+9638dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190280 | |||||||
chr15:99190286 | T | G | 79 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0029 others(76): Show |
79 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.759+9633A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190286 | |||||||
chr15:99190418 | G | A | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.759+9501C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190418 | |||||||
chr15:99190445 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.759+9474A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190445 | |||||||
chr15:99190608 | C | A | 224 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(221): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.759+9311G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190608 | |||||||
chr15:99190663 | C | T | 1 | a0001c0001t0020g0203 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.759+9256G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190663 | |||||||
chr15:99190675 | C | G | 1 | a0001c0002t0004g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.759+9244G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190675 | |||||||
chr15:99190942 | T | C | 9 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.759+8977A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99190942 | |||||||
chr15:99191301 | T | C | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+8618A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99191301 | |||||||
chr15:99191350 | T | C | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+8569A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99191350 | |||||||
chr15:99191410 | C | T | 1 | a0001c0001t0007g0184 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.759+8509G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99191410 | |||||||
chr15:99191415 | G | A | 1 | a0001c0002t0005g0129 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.759+8504C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99191415 | |||||||
chr15:99191579 | T | C | 318 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(315): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.759+8340A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99191579 | |||||||
chr15:99191877 | G | A | 3 | a0001c0002t0005g0120 a0001c0002t0005g0121 a0001c0002t0005g0126 |
3 | HG02559.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.759+8042C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99191877 | |||||||
chr15:99191994 | C | T | 328 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(325): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.759+7925G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99191994 | |||||||
chr15:99192035 | G | A | 4 | a0001c0001t0007g0166 a0001c0001t0007g0170 a0001c0001t0007g0178 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+7884C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192035 | |||||||
chr15:99192048 | C | T | 1 | a0001c0002t0004g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.759+7871G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192048 | |||||||
chr15:99192139 | G | A | 1 | a0001c0001t0001g0356 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.759+7780C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192139 | |||||||
chr15:99192322 | A | G | 312 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(309): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.759+7597T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192322 | |||||||
chr15:99192373 | C | T | 22 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(19): Show |
22 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.759+7546G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192373 | |||||||
chr15:99192374 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.759+7545C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192374 | |||||||
chr15:99192522 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.759+7397T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192522 | |||||||
chr15:99192536 | G | C | 9 | a0001c0001t0004g0022 a0001c0002t0004g0017 a0001c0002t0004g0018 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+7383C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192536 | |||||||
chr15:99192762 | C | T | 1 | a0002c0006t0003g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.759+7157G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192762 | |||||||
chr15:99192800 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.759+7119G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192800 | |||||||
chr15:99192804 | T | C | 321 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(318): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.759+7115A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192804 | |||||||
chr15:99192830 | C | T | 7 | a0001c0004t0006g0109 a0001c0004t0006g0117 a0001c0004t0006g0118 others(4): Show |
7 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.759+7089G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192830 | |||||||
chr15:99192853 | G | C | 6 | a0001c0001t0001g0277 a0001c0001t0004g0045 a0001c0001t0014g0334 others(3): Show |
6 | HG00621.hp2 NA18960.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+7066C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99192853 | |||||||
chr15:99193138 | A | G | 320 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(317): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.759+6781T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99193138 | |||||||
chr15:99193234 | T | C | 9 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.759+6685A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99193234 | |||||||
chr15:99193263 | T | G | 1 | a0001c0001t0006g0053 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.759+6656A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99193263 | |||||||
chr15:99193349 | T | C | 7 | a0001c0001t0007g0163 a0001c0001t0007g0175 a0001c0001t0007g0180 others(4): Show |
7 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.759+6570A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99193349 | |||||||
chr15:99193735 | C | T | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+6184G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99193735 | |||||||
chr15:99194275 | C | T | 9 | a0001c0001t0004g0022 a0001c0002t0004g0017 a0001c0002t0004g0018 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+5644G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194275 | |||||||
chr15:99194358 | A | G | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+5561T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194358 | |||||||
chr15:99194387 | C | T | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.759+5532G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194387 | |||||||
chr15:99194392 | G | A | 2 | a0001c0002t0004g0098 a0001c0002t0004g0099 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.759+5527C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194392 | |||||||
chr15:99194547 | A | G | 1 | a0001c0001t0003g0193 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.759+5372T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194547 | |||||||
chr15:99194552 | C | CA | 29 | a0001c0001t0001g0359 a0001c0001t0002g0011 a0001c0001t0002g0161 others(26): Show |
29 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.759+5366dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194552 | |||||||
chr15:99194552 | CA | C | 13 | a0001c0001t0001g0256 a0001c0001t0001g0305 a0001c0001t0003g0010 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+5366delT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194552 | |||||||
chr15:99194676 | C | T | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.759+5243G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194676 | |||||||
chr15:99194701 | A | C | 320 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(317): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.759+5218T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194701 | |||||||
chr15:99194881 | C | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0319 a0001c0001t0001g0345 others(1): Show |
4 | HG00323.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+5038G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99194881 | |||||||
chr15:99195462 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0161 a0001c0001t0010g0326 others(1): Show |
4 | HG01496.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.759+4457A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99195462 | |||||||
chr15:99195633 | G | A | 9 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0066 others(6): Show |
9 | HG01168.hp2 HG01169.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+4286C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99195633 | |||||||
chr15:99195655 | A | G | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+4264T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99195655 | |||||||
chr15:99195819 | C | T | 6 | a0001c0001t0003g0010 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+4100G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99195819 | |||||||
chr15:99195867 | TA | T | 83 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(80): Show |
83 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.759+4051delT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99195867 | |||||||
chr15:99195867 | TAA | T | 210 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.759+4050_759+4051d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99195867 | |||||||
chr15:99196021 | A | G | 202 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(199): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.759+3898T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196021 | |||||||
chr15:99196151 | C | CA | 8 | a0001c0001t0001g0277 a0001c0001t0001g0300 a0001c0001t0001g0359 others(5): Show |
8 | HG02015.hp1 HG03209.hp1 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.759+3767dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196151 | |||||||
chr15:99196197 | A | T | 1 | a0001c0001t0007g0187 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.759+3722T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196197 | |||||||
chr15:99196329 | A | T | 9 | a0001c0001t0004g0022 a0001c0002t0004g0017 a0001c0002t0004g0018 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+3590T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196329 | |||||||
chr15:99196428 | A | G | 1 | a0003c0011t0004g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.759+3491T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196428 | |||||||
chr15:99196485 | G | A | 184 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(181): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.759+3434C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196485 | |||||||
chr15:99196579 | C | T | 7 | a0001c0001t0001g0320 a0001c0001t0003g0010 a0001c0004t0003g0153 others(4): Show |
7 | HG00673.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.759+3340G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196579 | |||||||
chr15:99196668 | G | C | 2 | a0001c0001t0013g0145 a0001c0001t0013g0147 |
2 | NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.759+3251C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196668 | |||||||
chr15:99196769 | T | C | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.759+3150A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99196769 | |||||||
chr15:99197043 | C | A | 1 | a0001c0001t0001g0318 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.759+2876G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197043 | |||||||
chr15:99197104 | CT | C | 31 | a0001c0001t0006g0125 a0001c0001t0007g0044 a0001c0001t0007g0163 others(28): Show |
31 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.759+2814delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197104 | |||||||
chr15:99197141 | C | T | 1 | a0001c0001t0011g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+2778G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197141 | |||||||
chr15:99197251 | C | T | 12 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(9): Show |
12 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+2668G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197251 | |||||||
chr15:99197257 | C | T | 12 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(9): Show |
12 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+2662G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197257 | |||||||
chr15:99197304 | A | G | 15 | a0001c0001t0001g0308 a0001c0001t0001g0329 a0001c0001t0001g0330 others(12): Show |
15 | HG00558.hp2 HG01496.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.759+2615T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197304 | |||||||
chr15:99197315 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.759+2604C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197315 | |||||||
chr15:99197323 | T | C | 12 | a0001c0001t0002g0148 a0001c0005t0003g0013 a0001c0005t0008g0257 others(9): Show |
12 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.759+2596A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197323 | |||||||
chr15:99197387 | C | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+2532G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197387 | |||||||
chr15:99197397 | C | T | 1 | a0001c0004t0003g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.759+2522G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197397 | |||||||
chr15:99197398 | G | A | 6 | a0001c0003t0003g0182 a0001c0003t0003g0183 a0001c0003t0003g0189 others(3): Show |
6 | NA18948.hp2 NA18971.hp1 NA19068.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+2521C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197398 | |||||||
chr15:99197445 | G | A | 8 | a0001c0001t0006g0125 a0001c0004t0006g0109 a0001c0004t0006g0117 others(5): Show |
8 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.759+2474C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197445 | |||||||
chr15:99197548 | C | A | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+2371G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197548 | |||||||
chr15:99197552 | T | C | 8 | a0001c0001t0006g0125 a0001c0004t0006g0109 a0001c0004t0006g0117 others(5): Show |
8 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.759+2367A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197552 | |||||||
chr15:99197629 | G | T | 1 | a0001c0001t0002g0089 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.759+2290C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197629 | |||||||
chr15:99197992 | T | C | 186 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.759+1927A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99197992 | |||||||
chr15:99198129 | T | C | 1 | a0001c0002t0028g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.759+1790A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198129 | |||||||
chr15:99198396 | C | T | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+1523G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198396 | |||||||
chr15:99198436 | C | T | 3 | a0001c0001t0006g0100 a0001c0001t0015g0343 a0001c0001t0015g0365 |
3 | HG02809.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.759+1483G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198436 | |||||||
chr15:99198470 | A | C | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+1449T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198470 | |||||||
chr15:99198529 | T | C | 1 | a0001c0002t0004g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+1390A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198529 | |||||||
chr15:99198531 | G | T | 1 | a0001c0001t0001g0336 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.759+1388C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198531 | |||||||
chr15:99198535 | G | A | 20 | a0001c0001t0007g0044 a0001c0001t0007g0163 a0001c0001t0007g0165 others(17): Show |
20 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.759+1384C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198535 | |||||||
chr15:99198568 | T | C | 1 | a0001c0001t0011g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+1351A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198568 | |||||||
chr15:99198649 | A | G | 131 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(128): Show |
132 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.759+1270T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198649 | |||||||
chr15:99198712 | A | G | 15 | a0001c0001t0003g0010 a0001c0001t0004g0022 a0001c0002t0004g0017 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.759+1207T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99198712 | |||||||
chr15:99199059 | G | A | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.759+860C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199059 | |||||||
chr15:99199174 | C | T | 221 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.759+745G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199174 | |||||||
chr15:99199230 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.759+689G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199230 | |||||||
chr15:99199322 | G | C | 220 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(217): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.759+597C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199322 | |||||||
chr15:99199404 | C | CA | 32 | a0001c0001t0001g0266 a0001c0001t0001g0273 a0001c0001t0001g0276 others(29): Show |
32 | HG00423.hp2 HG00741.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.759+514dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199404 | |||||||
chr15:99199404 | CA | C | 41 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(38): Show |
41 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(38): Show |
intron_variant | MODIFIER | c.759+514delT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199404 | |||||||
chr15:99199439 | A | G | 1 | a0001c0001t0007g0174 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.759+480T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199439 | |||||||
chr15:99199458 | T | TTG | 78 | a0001c0001t0001g0340 a0001c0001t0002g0031 a0001c0001t0002g0039 others(75): Show |
79 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.759+459_759+460dup others(2): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199458 | |||||||
chr15:99199458 | T | TTGTG | 9 | a0001c0001t0003g0010 a0001c0002t0005g0133 a0001c0004t0003g0153 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+457_759+460dup others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199458 | |||||||
chr15:99199481 | C | T | 1 | a0001c0001t0001g0354 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.759+438G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199481 | |||||||
chr15:99199563 | G | A | 11 | a0001c0005t0003g0013 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG02615.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+356C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199563 | |||||||
chr15:99199587 | C | T | 15 | a0001c0001t0003g0010 a0001c0001t0004g0022 a0001c0002t0004g0017 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.759+332G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199587 | |||||||
chr15:99199600 | CTT | C | 18 | a0001c0001t0004g0122 a0001c0002t0005g0014 a0001c0002t0005g0110 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.759+317_759+318del others(2): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199600 | |||||||
chr15:99199684 | A | C | 94 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(91): Show |
94 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.759+235T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199684 | |||||||
chr15:99199751 | G | A | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.759+168C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 9/13 | chr15 | 99199751 | |||||||
chr15:99200284 | G | C | 123 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
124 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.582-188C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99200284 | |||||||
chr15:99200463 | G | C | 1 | a0001c0004t0006g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.582-367C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99200463 | |||||||
chr15:99200563 | A | G | 1 | a0001c0002t0004g0142 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.582-467T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99200563 | |||||||
chr15:99200610 | A | C | 1 | a0001c0001t0001g0316 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.582-514T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99200610 | |||||||
chr15:99200860 | A | C | 1 | a0001c0001t0002g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.582-764T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99200860 | |||||||
chr15:99200886 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582-790G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99200886 | |||||||
chr15:99201117 | T | A | 1 | a0001c0001t0002g0030 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.582-1021A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201117 | |||||||
chr15:99201193 | TAAGTA | T | 8 | a0001c0001t0003g0010 a0001c0001t0007g0163 a0001c0001t0007g0175 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.582-1102_582-1098d others(7): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201193 | |||||||
chr15:99201237 | A | G | 3 | a0001c0002t0004g0017 a0001c0002t0004g0018 a0001c0002t0004g0028 |
3 | HG02976.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.582-1141T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201237 | |||||||
chr15:99201398 | C | T | 9 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(6): Show |
10 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.582-1302G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201398 | |||||||
chr15:99201587 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.582-1491C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201587 | |||||||
chr15:99201673 | C | G | 32 | a0001c0001t0001g0254 a0001c0001t0001g0306 a0001c0001t0001g0314 others(29): Show |
32 | HG00544.hp1 HG00735.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.582-1577G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201673 | |||||||
chr15:99201721 | A | C | 1 | a0001c0001t0010g0335 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.582-1625T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201721 | |||||||
chr15:99201729 | G | C | 1 | a0001c0001t0001g0363 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.582-1633C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201729 | |||||||
chr15:99201744 | C | G | 1 | a0001c0002t0004g0142 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.582-1648G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201744 | |||||||
chr15:99201894 | A | G | 1 | a0001c0001t0004g0164 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.582-1798T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201894 | |||||||
chr15:99201927 | T | C | 3 | a0001c0002t0004g0134 a0001c0002t0004g0135 a0001c0002t0004g0136 |
3 | HG01109.hp1 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.582-1831A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99201927 | |||||||
chr15:99202005 | T | C | 159 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0289 others(156): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.582-1909A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99202005 | |||||||
chr15:99202178 | G | C | 3 | a0001c0001t0002g0011 a0001c0001t0003g0010 a0001c0001t0003g0239 |
3 | HG01099.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.582-2082C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99202178 | |||||||
chr15:99202291 | T | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0348 |
2 | NA18997.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.582-2195A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99202291 | |||||||
chr15:99202308 | G | A | 92 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(89): Show |
92 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.582-2212C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99202308 | |||||||
chr15:99202358 | T | C | 92 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(89): Show |
93 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.582-2262A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99202358 | |||||||
chr15:99202372 | G | A | 92 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(89): Show |
93 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.582-2276C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99202372 | |||||||
chr15:99202756 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.582-2660T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99202756 | |||||||
chr15:99202913 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.582-2817C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99202913 | |||||||
chr15:99203055 | A | G | 92 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(89): Show |
92 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.582-2959T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203055 | |||||||
chr15:99203178 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.582-3082A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203178 | |||||||
chr15:99203322 | T | A | 20 | a0001c0001t0001g0283 a0001c0001t0004g0063 a0001c0001t0007g0044 others(17): Show |
20 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.582-3226A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203322 | |||||||
chr15:99203323 | A | T | 1 | a0001c0001t0001g0314 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.582-3227T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203323 | |||||||
chr15:99203511 | CA | C | 4 | a0001c0001t0002g0068 a0001c0001t0002g0249 a0001c0001t0002g0250 others(1): Show |
4 | HG02080.hp1 HG02080.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.582-3416delT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203511 | |||||||
chr15:99203715 | A | T | 209 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.582-3619T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203715 | |||||||
chr15:99203909 | T | C | 11 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.582-3813A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203909 | |||||||
chr15:99203921 | G | A | 2 | a0001c0001t0004g0106 a0001c0005t0003g0013 |
2 | HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.582-3825C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203921 | |||||||
chr15:99203983 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.582-3887A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99203983 | |||||||
chr15:99204001 | G | T | 6 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(3): Show |
7 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.582-3905C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204001 | |||||||
chr15:99204012 | G | A | 1 | a0001c0003t0003g0225 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.582-3916C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204012 | |||||||
chr15:99204039 | G | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | NA18947.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.582-3943C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204039 | |||||||
chr15:99204190 | G | T | 77 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0029 others(74): Show |
77 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.582-4094C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204190 | |||||||
chr15:99204319 | C | T | 77 | a0001c0001t0001g0253 a0001c0001t0001g0283 a0001c0001t0004g0015 others(74): Show |
78 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.582-4223G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204319 | |||||||
chr15:99204430 | G | A | 51 | a0001c0001t0001g0283 a0001c0001t0004g0122 a0001c0001t0006g0125 others(48): Show |
51 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.582-4334C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204430 | |||||||
chr15:99204505 | C | T | 5 | a0001c0004t0003g0153 a0001c0004t0003g0154 a0001c0004t0003g0155 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.582-4409G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204505 | |||||||
chr15:99204581 | T | G | 5 | a0001c0004t0003g0153 a0001c0004t0003g0154 a0001c0004t0003g0155 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.582-4485A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204581 | |||||||
chr15:99204632 | G | GT | 63 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(60): Show |
63 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.582-4537dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTT | 17 | a0001c0001t0002g0049 a0001c0001t0002g0052 a0001c0001t0002g0055 others(14): Show |
17 | HG01515.hp2 HG01517.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.582-4538_582-4537d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTT | 16 | a0001c0001t0024g0258 a0001c0004t0006g0109 a0001c0004t0006g0118 others(13): Show |
16 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.582-4540_582-4537d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTT | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0286 others(10): Show |
14 | HG01261.hp1 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.582-4541_582-4537d others(7): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTT | 21 | a0001c0001t0001g0254 a0001c0001t0004g0006 a0001c0001t0004g0007 others(18): Show |
21 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.582-4542_582-4537d others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTG others(6): Show |
3 | a0001c0002t0005g0119 a0001c0002t0005g0168 a0001c0002t0005g0169 |
3 | HG03491.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.582-4537_582-4536i others(15): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT | 45 | a0001c0001t0001g0281 a0001c0001t0001g0287 a0001c0001t0001g0290 others(42): Show |
46 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.582-4543_582-4537d others(9): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT others(1): Show |
44 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0277 others(41): Show |
44 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.582-4544_582-4537d others(10): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT others(2): Show |
31 | a0001c0001t0001g0267 a0001c0001t0001g0273 a0001c0001t0001g0283 others(28): Show |
31 | HG00733.hp1 HG01261.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.582-4545_582-4537d others(11): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT others(3): Show |
8 | a0001c0001t0001g0268 a0001c0001t0001g0308 a0001c0001t0007g0044 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.582-4546_582-4537d others(12): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT others(4): Show |
7 | a0001c0001t0001g0276 a0001c0001t0007g0174 a0001c0001t0022g0179 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.582-4547_582-4537d others(13): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT others(5): Show |
10 | a0001c0001t0007g0166 a0001c0001t0007g0170 a0001c0001t0007g0171 others(7): Show |
10 | HG00140.hp2 HG00738.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.582-4548_582-4537d others(14): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT others(6): Show |
11 | a0001c0001t0006g0125 a0001c0001t0007g0178 a0001c0001t0023g0172 others(8): Show |
11 | HG00741.hp1 HG01123.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.582-4549_582-4537d others(15): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT others(7): Show |
5 | a0001c0001t0004g0122 a0001c0001t0017g0177 a0001c0002t0005g0113 others(2): Show |
5 | HG00639.hp2 HG01978.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.582-4550_582-4537d others(16): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204632 | G | GTTTTTTT others(9): Show |
1 | a0001c0002t0005g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.582-4552_582-4537d others(18): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204632 | |||||||
chr15:99204737 | A | G | 218 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(215): Show |
220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.582-4641T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204737 | |||||||
chr15:99204996 | A | G | 6 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(3): Show |
7 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.582-4900T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99204996 | |||||||
chr15:99205003 | T | C | 2 | a0003c0011t0004g0158 a0003c0012t0004g0152 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.582-4907A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205003 | |||||||
chr15:99205094 | A | T | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.582-4998T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205094 | |||||||
chr15:99205161 | C | G | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.582-5065G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205161 | |||||||
chr15:99205311 | A | AT | 17 | a0001c0001t0001g0285 a0001c0001t0002g0043 a0001c0001t0002g0049 others(14): Show |
17 | HG02015.hp1 HG02027.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.582-5216dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205311 | |||||||
chr15:99205330 | A | G | 1 | a0001c0001t0004g0033 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.582-5234T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205330 | |||||||
chr15:99205381 | T | C | 92 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(89): Show |
93 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.582-5285A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205381 | |||||||
chr15:99205545 | T | C | 10 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.582-5449A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205545 | |||||||
chr15:99205645 | G | GT | 3 | a0001c0001t0002g0161 a0003c0011t0004g0158 a0003c0012t0004g0152 |
3 | HG01496.hp1 HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.582-5550dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205645 | |||||||
chr15:99205721 | T | A | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.582-5625A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205721 | |||||||
chr15:99205738 | T | C | 1 | a0001c0001t0001g0348 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.582-5642A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205738 | |||||||
chr15:99205797 | A | G | 2 | a0001c0001t0004g0106 a0001c0005t0003g0013 |
2 | HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.582-5701T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205797 | |||||||
chr15:99205841 | C | G | 1 | a0001c0001t0002g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.582-5745G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205841 | |||||||
chr15:99205884 | C | G | 3 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | NA18961.hp1 NA19002.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.582-5788G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205884 | |||||||
chr15:99205991 | G | A | 4 | a0001c0004t0003g0153 a0001c0004t0003g0154 a0001c0004t0003g0155 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.582-5895C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99205991 | |||||||
chr15:99206314 | C | T | 6 | a0001c0001t0004g0137 a0001c0004t0003g0153 a0001c0004t0003g0154 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.582-6218G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99206314 | |||||||
chr15:99206516 | C | G | 1 | a0001c0001t0004g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.582-6420G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99206516 | |||||||
chr15:99206568 | T | A | 3 | a0001c0001t0002g0161 a0003c0011t0004g0158 a0003c0012t0004g0152 |
3 | HG01496.hp1 HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.582-6472A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99206568 | |||||||
chr15:99206694 | C | G | 4 | a0001c0004t0006g0109 a0001c0004t0006g0118 a0001c0004t0006g0130 others(1): Show |
4 | NA18959.hp1 NA18984.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.582-6598G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99206694 | |||||||
chr15:99206815 | T | A | 93 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(90): Show |
93 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.582-6719A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99206815 | |||||||
chr15:99206815 | T | G | 28 | a0001c0001t0001g0324 a0001c0001t0001g0352 a0001c0001t0004g0001 others(25): Show |
29 | HG00733.hp2 HG00735.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.582-6719A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99206815 | |||||||
chr15:99206917 | A | G | 2 | a0001c0002t0005g0116 a0001c0002t0005g0129 |
2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.582-6821T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99206917 | |||||||
chr15:99206965 | G | C | 1 | a0001c0001t0002g0250 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.582-6869C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99206965 | |||||||
chr15:99207011 | C | A | 1 | a0001c0001t0002g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.582-6915G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207011 | |||||||
chr15:99207364 | A | G | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.582-7268T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207364 | |||||||
chr15:99207491 | G | C | 1 | a0001c0001t0010g0335 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.582-7395C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207491 | |||||||
chr15:99207525 | C | T | 10 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.582-7429G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207525 | |||||||
chr15:99207574 | C | A | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.582-7478G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207574 | |||||||
chr15:99207575 | G | A | 1 | a0001c0001t0015g0343 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-7479C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207575 | |||||||
chr15:99207617 | C | T | 5 | a0001c0004t0003g0153 a0001c0004t0003g0154 a0001c0004t0003g0155 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.582-7521G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207617 | |||||||
chr15:99207656 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.582-7560C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207656 | |||||||
chr15:99207682 | G | A | 8 | a0001c0005t0008g0257 a0001c0005t0008g0259 a0001c0005t0008g0260 others(5): Show |
8 | HG02615.hp1 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.582-7586C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207682 | |||||||
chr15:99207764 | A | G | 5 | a0001c0001t0013g0224 a0001c0003t0002g0211 a0001c0003t0002g0217 others(2): Show |
5 | NA18945.hp1 NA18947.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.582-7668T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207764 | |||||||
chr15:99207835 | C | T | 1 | a0001c0005t0027g0360 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.582-7739G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207835 | |||||||
chr15:99207841 | A | G | 1 | a0001c0002t0005g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.582-7745T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99207841 | |||||||
chr15:99208045 | G | A | 2 | a0001c0003t0003g0003 a0001c0003t0003g0206 |
3 | NA18941.hp2 NA19005.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.582-7949C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99208045 | |||||||
chr15:99208047 | A | G | 1 | a0001c0001t0004g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.582-7951T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99208047 | |||||||
chr15:99208730 | T | TTATAA | 92 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(89): Show |
93 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.582-8635_582-8634i others(7): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99208730 | |||||||
chr15:99208910 | C | T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.582-8814G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99208910 | |||||||
chr15:99208980 | C | A | 10 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.582-8884G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99208980 | |||||||
chr15:99209144 | T | G | 5 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0198 others(2): Show |
5 | HG00673.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.582-9048A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99209144 | |||||||
chr15:99209159 | C | G | 6 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(3): Show |
7 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.582-9063G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99209159 | |||||||
chr15:99209174 | A | T | 1 | a0001c0001t0004g0045 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.582-9078T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99209174 | |||||||
chr15:99209369 | A | G | 2 | a0001c0002t0001g0301 a0001c0002t0004g0105 |
2 | HG00735.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.581+9219T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99209369 | |||||||
chr15:99209712 | A | G | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.581+8876T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99209712 | |||||||
chr15:99209744 | T | A | 1 | a0001c0001t0011g0304 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.581+8844A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99209744 | |||||||
chr15:99209875 | C | T | 10 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.581+8713G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99209875 | |||||||
chr15:99209939 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.581+8649A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99209939 | |||||||
chr15:99210007 | C | T | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.581+8581G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99210007 | |||||||
chr15:99210072 | T | C | 2 | a0001c0001t0011g0269 a0001c0001t0011g0275 |
2 | HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.581+8516A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99210072 | |||||||
chr15:99210240 | A | G | 73 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(70): Show |
73 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.581+8348T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99210240 | |||||||
chr15:99210251 | G | A | 11 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.581+8337C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99210251 | |||||||
chr15:99210301 | A | G | 128 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(125): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.581+8287T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99210301 | |||||||
chr15:99210521 | C | G | 10 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.581+8067G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99210521 | |||||||
chr15:99210868 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.581+7720A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99210868 | |||||||
chr15:99210978 | C | T | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.581+7610G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99210978 | |||||||
chr15:99211192 | T | G | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.581+7396A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211192 | |||||||
chr15:99211220 | C | CA | 11 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.581+7367dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211220 | |||||||
chr15:99211235 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.581+7353G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211235 | |||||||
chr15:99211248 | A | G | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.581+7340T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211248 | |||||||
chr15:99211383 | C | CAA | 5 | a0001c0004t0003g0153 a0001c0004t0003g0154 a0001c0004t0003g0155 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.581+7203_581+7204d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211383 | |||||||
chr15:99211387 | C | A | 54 | a0001c0001t0001g0283 a0001c0001t0004g0122 a0001c0001t0006g0002 others(51): Show |
55 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.581+7201G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211387 | |||||||
chr15:99211536 | A | T | 1 | a0001c0001t0001g0340 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.581+7052T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211536 | |||||||
chr15:99211630 | A | AG | 168 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(165): Show |
169 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.581+6957_581+6958i others(3): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211630 | |||||||
chr15:99211660 | C | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.581+6928G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211660 | |||||||
chr15:99211704 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.581+6884A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211704 | |||||||
chr15:99211726 | G | A | 1 | a0001c0002t0001g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.581+6862C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211726 | |||||||
chr15:99211813 | T | C | 3 | a0001c0002t0005g0133 a0003c0011t0004g0158 a0003c0012t0004g0152 |
3 | HG02055.hp1 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.581+6775A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211813 | |||||||
chr15:99211932 | C | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.581+6656G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211932 | |||||||
chr15:99211988 | G | A | 58 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(55): Show |
59 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.581+6600C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211988 | |||||||
chr15:99211990 | C | A | 2 | a0001c0002t0004g0017 a0001c0002t0004g0018 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.581+6598G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99211990 | |||||||
chr15:99212048 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.581+6540C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212048 | |||||||
chr15:99212209 | T | C | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.581+6379A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212209 | |||||||
chr15:99212260 | A | ATG | 40 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0306 others(37): Show |
41 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.581+6326_581+6327d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212260 | |||||||
chr15:99212260 | A | ATGTG | 6 | a0001c0001t0001g0328 a0001c0001t0001g0331 a0001c0001t0001g0353 others(3): Show |
6 | HG00733.hp1 HG01168.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.581+6324_581+6327d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212260 | |||||||
chr15:99212260 | ATG | A | 66 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(63): Show |
66 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.581+6326_581+6327d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212260 | |||||||
chr15:99212260 | ATGTG | A | 12 | a0001c0001t0001g0267 a0001c0001t0002g0011 a0001c0001t0002g0161 others(9): Show |
12 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.581+6324_581+6327d others(6): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212260 | |||||||
chr15:99212260 | ATGTGTG | A | 90 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(87): Show |
90 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.581+6322_581+6327d others(8): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212260 | |||||||
chr15:99212405 | C | A | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.581+6183G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212405 | |||||||
chr15:99212500 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.581+6088T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212500 | |||||||
chr15:99212777 | C | T | 22 | a0001c0001t0001g0283 a0001c0001t0007g0044 a0001c0001t0007g0163 others(19): Show |
22 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.581+5811G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212777 | |||||||
chr15:99212984 | C | CA | 130 | a0001c0001t0001g0283 a0001c0001t0002g0012 a0001c0001t0002g0029 others(127): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.581+5603dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212984 | |||||||
chr15:99212984 | C | CAA | 15 | a0001c0001t0002g0065 a0001c0001t0002g0068 a0001c0001t0002g0069 others(12): Show |
15 | HG00741.hp1 HG01496.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.581+5602_581+5603d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99212984 | |||||||
chr15:99213006 | AG | A | 112 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(109): Show |
113 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.581+5581delC | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99213006 | |||||||
chr15:99213006 | AGG | A | 9 | a0001c0001t0004g0007 a0001c0001t0004g0137 a0001c0001t0006g0100 others(6): Show |
9 | HG01169.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.581+5580_581+5581d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99213006 | |||||||
chr15:99213007 | G | A | 237 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.581+5581C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99213007 | |||||||
chr15:99213008 | G | A | 203 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(200): Show |
204 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.581+5580C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99213008 | |||||||
chr15:99213025 | A | G | 59 | a0001c0001t0001g0283 a0001c0001t0004g0122 a0001c0001t0006g0002 others(56): Show |
60 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.581+5563T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99213025 | |||||||
chr15:99213070 | C | T | 2 | a0001c0001t0012g0005 a0001c0001t0012g0140 |
2 | NA18973.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.581+5518G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99213070 | |||||||
chr15:99214030 | C | T | 2 | a0001c0001t0004g0106 a0001c0005t0003g0013 |
2 | HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.581+4558G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214030 | |||||||
chr15:99214149 | T | C | 3 | a0001c0003t0009g0226 a0001c0003t0009g0227 a0001c0003t0009g0230 |
3 | HG00735.hp2 HG01069.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.581+4439A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214149 | |||||||
chr15:99214245 | C | T | 2 | a0003c0011t0004g0158 a0003c0012t0004g0152 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.581+4343G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214245 | |||||||
chr15:99214364 | C | T | 13 | a0001c0001t0001g0282 a0001c0001t0001g0289 a0001c0001t0001g0290 others(10): Show |
13 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.581+4224G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214364 | |||||||
chr15:99214400 | C | T | 1 | a0001c0002t0004g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.581+4188G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214400 | |||||||
chr15:99214504 | T | A | 1 | a0003c0012t0004g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.581+4084A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214504 | |||||||
chr15:99214507 | C | CA | 235 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(232): Show |
236 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.581+4080dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214507 | |||||||
chr15:99214507 | C | CAA | 7 | a0001c0001t0001g0296 a0001c0001t0001g0303 a0001c0001t0002g0030 others(4): Show |
7 | HG02074.hp2 HG02135.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.581+4079_581+4080d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214507 | |||||||
chr15:99214507 | C | CAAA | 54 | a0001c0001t0001g0283 a0001c0001t0002g0161 a0001c0001t0004g0122 others(51): Show |
55 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.581+4078_581+4080d others(5): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214507 | |||||||
chr15:99214566 | T | C | 22 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(19): Show |
22 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.581+4022A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214566 | |||||||
chr15:99214852 | C | CT | 197 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0273 others(194): Show |
198 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.581+3735dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214852 | |||||||
chr15:99214852 | C | CTT | 15 | a0001c0001t0001g0267 a0001c0001t0001g0289 a0001c0001t0001g0313 others(12): Show |
15 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.581+3734_581+3735d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214852 | |||||||
chr15:99214852 | CT | C | 24 | a0001c0001t0001g0253 a0001c0001t0002g0161 a0001c0001t0004g0015 others(21): Show |
24 | HG01496.hp1 HG01891.hp1 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.581+3735delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214852 | |||||||
chr15:99214902 | C | G | 2 | a0001c0007t0005g0143 a0001c0007t0005g0144 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.581+3686G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214902 | |||||||
chr15:99214917 | G | A | 1 | a0001c0009t0001g0362 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.581+3671C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214917 | |||||||
chr15:99214947 | T | C | 221 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.581+3641A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99214947 | |||||||
chr15:99215057 | T | C | 5 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0072 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.581+3531A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215057 | |||||||
chr15:99215103 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.581+3485C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215103 | |||||||
chr15:99215160 | G | C | 1 | a0001c0001t0002g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.581+3428C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215160 | |||||||
chr15:99215178 | T | G | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.581+3410A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215178 | |||||||
chr15:99215386 | T | A | 11 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.581+3202A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215386 | |||||||
chr15:99215415 | T | G | 6 | a0001c0001t0007g0166 a0001c0001t0007g0170 a0001c0001t0007g0171 others(3): Show |
6 | HG00738.hp2 HG00741.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.581+3173A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215415 | |||||||
chr15:99215420 | G | A | 72 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(69): Show |
72 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.581+3168C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215420 | |||||||
chr15:99215485 | C | T | 79 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(76): Show |
80 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.581+3103G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215485 | |||||||
chr15:99215510 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.581+3078G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215510 | |||||||
chr15:99215562 | T | A | 1 | a0001c0002t0001g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.581+3026A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215562 | |||||||
chr15:99215653 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.581+2935T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215653 | |||||||
chr15:99215699 | ACCCCACC others(30): Show |
A | 1 | a0001c0001t0011g0304 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.581+2852_581+2888d others(39): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215699 | |||||||
chr15:99215700 | C | T | 293 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(290): Show |
295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.581+2888G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215700 | |||||||
chr15:99215737 | A | G | 1 | a0001c0001t0011g0304 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.581+2851T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215737 | |||||||
chr15:99215828 | A | T | 1 | a0002c0006t0003g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.581+2760T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215828 | |||||||
chr15:99215829 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.581+2759A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215829 | |||||||
chr15:99215873 | A | T | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.581+2715T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215873 | |||||||
chr15:99215916 | A | G | 128 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(125): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.581+2672T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99215916 | |||||||
chr15:99216111 | G | T | 11 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(8): Show |
11 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.581+2477C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216111 | |||||||
chr15:99216130 | G | C | 6 | a0001c0002t0005g0191 a0001c0003t0003g0207 a0001c0003t0003g0208 others(3): Show |
6 | HG00642.hp2 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.581+2458C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216130 | |||||||
chr15:99216455 | A | C | 12 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(9): Show |
12 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.581+2133T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216455 | |||||||
chr15:99216506 | A | T | 1 | a0001c0001t0006g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.581+2082T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216506 | |||||||
chr15:99216549 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.581+2039A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216549 | |||||||
chr15:99216734 | T | C | 2 | a0001c0002t0005g0116 a0001c0002t0005g0129 |
2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.581+1854A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216734 | |||||||
chr15:99216752 | A | G | 220 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(217): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.581+1836T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216752 | |||||||
chr15:99216762 | T | C | 1 | a0001c0001t0001g0364 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.581+1826A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216762 | |||||||
chr15:99216769 | G | T | 1 | a0001c0001t0001g0344 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.581+1819C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99216769 | |||||||
chr15:99217050 | C | A | 2 | a0001c0001t0001g0300 a0001c0001t0015g0365 |
2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.581+1538G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99217050 | |||||||
chr15:99217163 | C | CT | 128 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(125): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.581+1424dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99217163 | |||||||
chr15:99217989 | A | G | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.581+599T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99217989 | |||||||
chr15:99218107 | G | A | 2 | a0001c0001t0010g0326 a0001c0001t0010g0349 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.581+481C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99218107 | |||||||
chr15:99218158 | A | C | 1 | a0001c0001t0007g0174 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.581+430T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99218158 | |||||||
chr15:99218266 | C | T | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.581+322G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99218266 | |||||||
chr15:99218364 | A | T | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.581+224T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99218364 | |||||||
chr15:99218368 | T | C | 130 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(127): Show |
131 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.581+220A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99218368 | |||||||
chr15:99218491 | C | T | 1 | a0001c0001t0002g0004 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.581+97G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99218491 | |||||||
chr15:99218558 | T | C | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.581+30A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 8/13 | chr15 | 99218558 | |||||||
chr15:99218806 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.455+92G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 7/13 | chr15 | 99218806 | |||||||
chr15:99219079 | C | G | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.305-31G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219079 | |||||||
chr15:99219283 | T | C | 1 | a0001c0001t0026g0288 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.305-235A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219283 | |||||||
chr15:99219377 | A | C | 1 | a0001c0001t0007g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.305-329T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219377 | |||||||
chr15:99219468 | A | C | 57 | a0001c0001t0001g0283 a0001c0001t0004g0122 a0001c0001t0006g0002 others(54): Show |
58 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.305-420T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219468 | |||||||
chr15:99219626 | G | A | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.305-578C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219626 | |||||||
chr15:99219739 | G | C | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG00423.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.305-691C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219739 | |||||||
chr15:99219831 | T | C | 1 | a0001c0001t0007g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.305-783A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219831 | |||||||
chr15:99219863 | A | C | 1 | a0001c0005t0027g0360 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.305-815T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219863 | |||||||
chr15:99219870 | C | G | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.305-822G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219870 | |||||||
chr15:99219876 | A | T | 1 | a0001c0001t0001g0327 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.305-828T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99219876 | |||||||
chr15:99220017 | AG | A | 94 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(91): Show |
94 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.305-970delC | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99220017 | |||||||
chr15:99220050 | A | C | 1 | a0001c0003t0003g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.305-1002T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99220050 | |||||||
chr15:99220118 | A | G | 32 | a0001c0001t0002g0004 a0001c0001t0004g0122 a0001c0001t0006g0125 others(29): Show |
32 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.305-1070T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99220118 | |||||||
chr15:99220664 | G | A | 1 | a0001c0001t0024g0258 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304+1077C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99220664 | |||||||
chr15:99220754 | A | G | 98 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(95): Show |
98 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.304+987T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99220754 | |||||||
chr15:99220956 | C | T | 95 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(92): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.304+785G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99220956 | |||||||
chr15:99221068 | C | G | 1 | a0001c0001t0007g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.304+673G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99221068 | |||||||
chr15:99221205 | A | T | 12 | a0001c0004t0003g0153 a0001c0004t0003g0154 a0001c0004t0003g0155 others(9): Show |
12 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.304+536T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99221205 | |||||||
chr15:99221208 | G | A | 2 | a0001c0001t0006g0100 a0001c0001t0015g0343 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.304+533C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99221208 | |||||||
chr15:99221248 | T | C | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.304+493A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99221248 | |||||||
chr15:99221587 | T | C | 1 | a0009c0013t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.304+154A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99221587 | |||||||
chr15:99221694 | C | T | 2 | a0003c0011t0004g0158 a0003c0012t0004g0152 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.304+47G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99221694 | |||||||
chr15:99221713 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.304+28C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 6/13 | chr15 | 99221713 | |||||||
chr15:99221882 | C | G | 10 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.181-18G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99221882 | |||||||
chr15:99221945 | T | C | 1 | a0001c0004t0003g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.181-81A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99221945 | |||||||
chr15:99222159 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.181-295G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222159 | |||||||
chr15:99222217 | C | T | 12 | a0001c0004t0003g0153 a0001c0004t0003g0154 a0001c0004t0003g0155 others(9): Show |
12 | HG00323.hp1 HG01261.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.181-353G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222217 | |||||||
chr15:99222422 | G | A | 95 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(92): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.181-558C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222422 | |||||||
chr15:99222472 | T | G | 2 | a0001c0001t0002g0094 a0001c0002t0005g0092 |
2 | HG00558.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.181-608A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222472 | |||||||
chr15:99222699 | T | C | 6 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(3): Show |
7 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-835A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222699 | |||||||
chr15:99222721 | G | C | 1 | a0001c0001t0007g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.181-857C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222721 | |||||||
chr15:99222723 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.181-859G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222723 | |||||||
chr15:99222866 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.181-1002C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222866 | |||||||
chr15:99222869 | C | CG | 14 | a0001c0001t0001g0324 a0001c0001t0001g0352 a0001c0001t0004g0001 others(11): Show |
15 | HG01167.hp2 HG01169.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.181-1006dupC | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222869 | |||||||
chr15:99222872 | C | T | 1 | a0001c0001t0004g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.181-1008G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222872 | |||||||
chr15:99222976 | G | C | 11 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.181-1112C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222976 | |||||||
chr15:99222980 | C | T | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.181-1116G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222980 | |||||||
chr15:99222992 | G | A | 113 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(110): Show |
114 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.181-1128C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99222992 | |||||||
chr15:99223118 | C | T | 5 | a0001c0004t0003g0153 a0001c0004t0003g0154 a0001c0004t0003g0155 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-1254G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223118 | |||||||
chr15:99223165 | A | T | 1 | a0001c0001t0003g0151 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.181-1301T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223165 | |||||||
chr15:99223179 | C | T | 2 | a0001c0002t0004g0142 a0001c0002t0004g0146 |
2 | HG00733.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.181-1315G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223179 | |||||||
chr15:99223554 | G | T | 2 | a0001c0001t0004g0106 a0001c0005t0003g0013 |
2 | HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.181-1690C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223554 | |||||||
chr15:99223660 | G | A | 6 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(3): Show |
7 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-1796C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223660 | |||||||
chr15:99223662 | C | G | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-1798G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223662 | |||||||
chr15:99223759 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.181-1895G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223759 | |||||||
chr15:99223855 | G | A | 1 | a0001c0001t0004g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.181-1991C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223855 | |||||||
chr15:99223897 | T | C | 12 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(9): Show |
12 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.181-2033A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223897 | |||||||
chr15:99223913 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.181-2049C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223913 | |||||||
chr15:99223965 | A | C | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.181-2101T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99223965 | |||||||
chr15:99224239 | T | C | 54 | a0001c0001t0001g0283 a0001c0001t0002g0004 a0001c0001t0002g0029 others(51): Show |
54 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.181-2375A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99224239 | |||||||
chr15:99224501 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.181-2637A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99224501 | |||||||
chr15:99224654 | A | G | 200 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(197): Show |
202 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.181-2790T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99224654 | |||||||
chr15:99224656 | A | G | 1 | a0001c0001t0007g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.181-2792T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99224656 | |||||||
chr15:99224735 | C | A | 70 | a0001c0001t0002g0012 a0001c0001t0002g0031 a0001c0001t0002g0032 others(67): Show |
70 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.181-2871G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99224735 | |||||||
chr15:99224878 | T | C | 1 | a0001c0001t0003g0205 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.181-3014A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99224878 | |||||||
chr15:99224948 | C | G | 22 | a0001c0001t0001g0324 a0001c0001t0001g0352 a0001c0001t0004g0001 others(19): Show |
23 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.181-3084G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99224948 | |||||||
chr15:99225119 | G | A | 1 | a0002c0006t0003g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.181-3255C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225119 | |||||||
chr15:99225475 | G | A | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.180+3058C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225475 | |||||||
chr15:99225533 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.180+3000G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225533 | |||||||
chr15:99225544 | G | A | 10 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.180+2989C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225544 | |||||||
chr15:99225605 | C | T | 68 | a0001c0001t0002g0012 a0001c0001t0002g0031 a0001c0001t0002g0032 others(65): Show |
68 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.180+2928G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225605 | |||||||
chr15:99225885 | T | C | 4 | a0001c0002t0005g0116 a0001c0002t0005g0119 a0001c0002t0005g0129 others(1): Show |
4 | HG01123.hp2 HG03491.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+2648A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225885 | |||||||
chr15:99225898 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.180+2635G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225898 | |||||||
chr15:99225930 | A | T | 6 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(3): Show |
7 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+2603T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225930 | |||||||
chr15:99225944 | A | G | 1 | a0001c0001t0001g0340 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.180+2589T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225944 | |||||||
chr15:99225946 | C | T | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.180+2587G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99225946 | |||||||
chr15:99226246 | A | AGTATTAT others(8): Show |
1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.180+2272_180+2286d others(17): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226246 | |||||||
chr15:99226306 | T | C | 134 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(131): Show |
134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.180+2227A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226306 | |||||||
chr15:99226309 | CT | C | 72 | a0001c0001t0002g0012 a0001c0001t0002g0031 a0001c0001t0002g0032 others(69): Show |
72 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.180+2223delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226309 | |||||||
chr15:99226367 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.180+2166T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226367 | |||||||
chr15:99226481 | C | G | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+2052G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226481 | |||||||
chr15:99226565 | G | A | 1 | a0001c0001t0010g0335 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.180+1968C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226565 | |||||||
chr15:99226580 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.180+1953G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226580 | |||||||
chr15:99226591 | C | G | 1 | a0001c0001t0002g0043 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.180+1942G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226591 | |||||||
chr15:99226618 | A | G | 3 | a0001c0001t0001g0300 a0001c0001t0006g0101 a0001c0001t0015g0365 |
3 | HG02717.hp1 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.180+1915T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226618 | |||||||
chr15:99226651 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.180+1882C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226651 | |||||||
chr15:99226657 | G | A | 33 | a0001c0001t0001g0282 a0001c0001t0001g0289 a0001c0001t0001g0290 others(30): Show |
33 | HG00423.hp2 HG00544.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.180+1876C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226657 | |||||||
chr15:99226680 | C | T | 12 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0011 others(9): Show |
12 | HG01243.hp1 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.180+1853G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226680 | |||||||
chr15:99226712 | G | A | 29 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0002g0011 others(26): Show |
29 | HG00423.hp1 HG00621.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.180+1821C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226712 | |||||||
chr15:99226719 | C | T | 17 | a0001c0001t0001g0252 a0001c0001t0001g0299 a0001c0001t0002g0011 others(14): Show |
17 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.180+1814G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226719 | |||||||
chr15:99226776 | C | T | 165 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(162): Show |
166 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.180+1757G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226776 | |||||||
chr15:99226866 | C | T | 247 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(244): Show |
248 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.180+1667G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226866 | |||||||
chr15:99226971 | C | T | 21 | a0001c0001t0003g0151 a0001c0001t0003g0181 a0001c0001t0003g0190 others(18): Show |
21 | HG00597.hp2 HG00673.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.180+1562G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99226971 | |||||||
chr15:99227034 | C | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0100 a0001c0001t0006g0101 others(4): Show |
8 | HG01243.hp2 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+1499G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227034 | |||||||
chr15:99227202 | A | G | 40 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0010g0274 others(37): Show |
40 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.180+1331T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227202 | |||||||
chr15:99227287 | C | T | 17 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0084 others(14): Show |
17 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.180+1246G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227287 | |||||||
chr15:99227326 | T | G | 1 | a0001c0002t0004g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.180+1207A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227326 | |||||||
chr15:99227346 | C | T | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+1187G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227346 | |||||||
chr15:99227714 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.180+819A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227714 | |||||||
chr15:99227790 | G | A | 111 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(108): Show |
111 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.180+743C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227790 | |||||||
chr15:99227843 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.180+690C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227843 | |||||||
chr15:99227854 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.180+679G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227854 | |||||||
chr15:99227938 | C | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0352 |
2 | NA18989.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.180+595G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227938 | |||||||
chr15:99227938 | C | T | 1 | a0002c0006t0003g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.180+595G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99227938 | |||||||
chr15:99228065 | G | C | 1 | a0001c0001t0003g0233 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.180+468C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99228065 | |||||||
chr15:99228069 | C | A | 1 | a0001c0001t0001g0325 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.180+464G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99228069 | |||||||
chr15:99228083 | T | G | 292 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(289): Show |
294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.180+450A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99228083 | |||||||
chr15:99228290 | C | G | 2 | a0001c0001t0004g0008 a0001c0001t0004g0009 |
2 | NA18974.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.180+243G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99228290 | |||||||
chr15:99228319 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.180+214C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99228319 | |||||||
chr15:99228354 | C | T | 1 | a0001c0004t0006g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.180+179G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99228354 | |||||||
chr15:99228437 | G | T | 73 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(70): Show |
73 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.180+96C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99228437 | |||||||
chr15:99228497 | C | T | 1 | a0001c0004t0003g0157 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.180+36G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 5/13 | chr15 | 99228497 | |||||||
chr15:99228816 | T | C | 2 | a0001c0001t0011g0269 a0001c0001t0011g0275 |
2 | HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-20-84A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99228816 | |||||||
chr15:99228981 | A | AACACACA others(26): Show |
118 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(115): Show |
119 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.-20-282_-20-250dup others(33): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99228981 | |||||||
chr15:99229083 | C | CAT | 43 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0030 others(40): Show |
44 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-20-353_-20-352dup others(2): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229083 | |||||||
chr15:99229142 | C | CATAT | 33 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(30): Show |
33 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-20-414_-20-411dup others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229142 | |||||||
chr15:99229228 | C | T | 2 | a0003c0011t0004g0158 a0003c0012t0004g0152 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-20-496G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229228 | |||||||
chr15:99229231 | T | C | 15 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20-499A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229231 | |||||||
chr15:99229242 | G | A | 1 | a0007c0015t0002g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-20-510C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229242 | |||||||
chr15:99229266 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-20-534G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229266 | |||||||
chr15:99229415 | G | A | 1 | a0001c0001t0006g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-20-683C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229415 | |||||||
chr15:99229472 | C | A | 1 | a0001c0002t0004g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-20-740G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229472 | |||||||
chr15:99229526 | G | C | 1 | a0001c0001t0001g0266 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-20-794C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229526 | |||||||
chr15:99229673 | G | T | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-20-941C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229673 | |||||||
chr15:99229794 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-20-1062A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229794 | |||||||
chr15:99229795 | C | A | 2 | a0003c0011t0004g0158 a0003c0012t0004g0152 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-20-1063G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229795 | |||||||
chr15:99229847 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-20-1115G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229847 | |||||||
chr15:99229932 | G | T | 298 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(295): Show |
300 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-20-1200C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229932 | |||||||
chr15:99229948 | G | C | 1 | a0003c0012t0004g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-20-1216C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99229948 | |||||||
chr15:99230020 | C | A | 2 | a0001c0001t0004g0008 a0001c0001t0004g0009 |
2 | NA18974.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-20-1288G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230020 | |||||||
chr15:99230024 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0003g0010 |
2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-20-1292G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230024 | |||||||
chr15:99230094 | T | C | 17 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(14): Show |
17 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-20-1362A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230094 | |||||||
chr15:99230160 | T | C | 10 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0006g0002 others(7): Show |
11 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-1428A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230160 | |||||||
chr15:99230205 | A | G | 118 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(115): Show |
119 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.-20-1473T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230205 | |||||||
chr15:99230324 | T | G | 1 | a0001c0001t0010g0326 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-20-1592A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230324 | |||||||
chr15:99230350 | G | A | 21 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0084 others(18): Show |
21 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-20-1618C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230350 | |||||||
chr15:99230379 | T | G | 1 | a0007c0015t0002g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-20-1647A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230379 | |||||||
chr15:99230384 | G | C | 1 | a0001c0001t0003g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-20-1652C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230384 | |||||||
chr15:99230422 | G | A | 2 | a0001c0002t0004g0142 a0001c0002t0004g0146 |
2 | HG00733.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-20-1690C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230422 | |||||||
chr15:99230519 | G | A | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-20-1787C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230519 | |||||||
chr15:99230674 | T | C | 119 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(116): Show |
120 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.-20-1942A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230674 | |||||||
chr15:99230917 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-20-2185C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230917 | |||||||
chr15:99230927 | T | C | 18 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0277 others(15): Show |
18 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.-20-2195A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99230927 | |||||||
chr15:99231080 | T | G | 1 | a0001c0001t0004g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20-2348A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231080 | |||||||
chr15:99231423 | T | C | 44 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0030 others(41): Show |
45 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.-20-2691A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231423 | |||||||
chr15:99231544 | T | G | 1 | a0001c0001t0001g0345 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-20-2812A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231544 | |||||||
chr15:99231555 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0003g0010 |
2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-20-2823G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231555 | |||||||
chr15:99231556 | G | A | 1 | a0001c0001t0019g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-20-2824C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231556 | |||||||
chr15:99231567 | A | C | 1 | a0001c0001t0003g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-20-2835T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231567 | |||||||
chr15:99231578 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-20-2846G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231578 | |||||||
chr15:99231781 | T | A | 1 | a0001c0001t0007g0174 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-20-3049A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231781 | |||||||
chr15:99231783 | C | T | 71 | a0001c0001t0002g0012 a0001c0001t0002g0031 a0001c0001t0002g0032 others(68): Show |
71 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.-20-3051G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231783 | |||||||
chr15:99231784 | G | A | 3 | a0001c0001t0001g0336 a0001c0002t0004g0098 a0001c0002t0004g0099 |
3 | HG02109.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-20-3052C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231784 | |||||||
chr15:99231858 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-20-3126A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99231858 | |||||||
chr15:99232048 | G | A | 1 | a0001c0001t0011g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-21+2940C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232048 | |||||||
chr15:99232051 | C | T | 1 | a0001c0001t0016g0127 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-21+2937G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232051 | |||||||
chr15:99232097 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-21+2891G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232097 | |||||||
chr15:99232126 | A | G | 1 | a0001c0001t0001g0354 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-21+2862T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232126 | |||||||
chr15:99232164 | C | T | 74 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(71): Show |
74 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-21+2824G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232164 | |||||||
chr15:99232200 | C | A | 1 | a0001c0001t0015g0343 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-21+2788G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232200 | |||||||
chr15:99232254 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0003g0010 |
2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-21+2734G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232254 | |||||||
chr15:99232371 | C | T | 16 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-21+2617G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232371 | |||||||
chr15:99232457 | C | T | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-21+2531G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232457 | |||||||
chr15:99232519 | T | C | 2 | a0001c0002t0005g0116 a0001c0002t0005g0129 |
2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-21+2469A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232519 | |||||||
chr15:99232821 | A | G | 1 | a0001c0001t0002g0035 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-21+2167T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99232821 | |||||||
chr15:99233065 | T | C | 115 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-21+1923A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99233065 | |||||||
chr15:99233121 | C | T | 1 | a0001c0003t0002g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-21+1867G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99233121 | |||||||
chr15:99233176 | T | G | 119 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(116): Show |
120 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.-21+1812A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99233176 | |||||||
chr15:99233449 | C | T | 117 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(114): Show |
118 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.-21+1539G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99233449 | |||||||
chr15:99233574 | T | C | 36 | a0001c0001t0001g0357 a0001c0001t0004g0122 a0001c0001t0006g0125 others(33): Show |
36 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-21+1414A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99233574 | |||||||
chr15:99233701 | C | T | 1 | a0001c0001t0002g0035 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-21+1287G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99233701 | |||||||
chr15:99233771 | T | C | 10 | a0001c0001t0024g0258 a0001c0005t0008g0257 a0001c0005t0008g0259 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21+1217A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99233771 | |||||||
chr15:99233978 | T | C | 10 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0006g0002 others(7): Show |
11 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+1010A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99233978 | |||||||
chr15:99234089 | T | G | 1 | a0001c0001t0002g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-21+899A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234089 | |||||||
chr15:99234176 | T | C | 11 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+812A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234176 | |||||||
chr15:99234222 | T | G | 35 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(32): Show |
35 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-21+766A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234222 | |||||||
chr15:99234337 | A | G | 115 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-21+651T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234337 | |||||||
chr15:99234386 | T | A | 35 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(32): Show |
35 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-21+602A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234386 | |||||||
chr15:99234409 | C | T | 35 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(32): Show |
35 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-21+579G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234409 | |||||||
chr15:99234410 | G | A | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-21+578C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234410 | |||||||
chr15:99234457 | A | G | 284 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(281): Show |
285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-21+531T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234457 | |||||||
chr15:99234505 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-21+483C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234505 | |||||||
chr15:99234537 | A | G | 1 | a0001c0005t0008g0279 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-21+451T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234537 | |||||||
chr15:99234539 | T | C | 1 | a0001c0002t0028g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-21+449A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234539 | |||||||
chr15:99234604 | C | T | 1 | a0001c0002t0005g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-21+384G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234604 | |||||||
chr15:99234681 | C | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | NA18942.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-21+307G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234681 | |||||||
chr15:99234700 | C | A | 18 | a0001c0001t0002g0004 a0001c0001t0004g0001 a0001c0001t0004g0006 others(15): Show |
19 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-21+288G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234700 | |||||||
chr15:99234940 | TA | T | 78 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(75): Show |
78 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.-21+47delT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234940 | |||||||
chr15:99234978 | T | C | 1 | a0001c0001t0004g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-21+10A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 4/13 | chr15 | 99234978 | |||||||
chr15:99235349 | T | C | 74 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(71): Show |
74 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-113-269A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235349 | |||||||
chr15:99235357 | AT | A | 278 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0256 others(275): Show |
280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.-113-278delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235357 | |||||||
chr15:99235480 | C | T | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-113-400G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235480 | |||||||
chr15:99235527 | C | A | 1 | a0001c0002t0005g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-113-447G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235527 | |||||||
chr15:99235630 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-113-550T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235630 | |||||||
chr15:99235665 | C | T | 10 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0006g0002 others(7): Show |
11 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-585G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235665 | |||||||
chr15:99235708 | A | T | 20 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0084 others(17): Show |
20 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-113-628T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235708 | |||||||
chr15:99235806 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | NA18951.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-113-726A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235806 | |||||||
chr15:99235997 | G | T | 74 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(71): Show |
74 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-113-917C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99235997 | |||||||
chr15:99236213 | G | A | 16 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0084 others(13): Show |
16 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-113-1133C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99236213 | |||||||
chr15:99236467 | CT | C | 8 | a0001c0001t0001g0256 a0001c0001t0001g0339 a0001c0001t0001g0340 others(5): Show |
8 | HG01884.hp2 HG02300.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-113-1388delA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99236467 | |||||||
chr15:99236533 | G | A | 10 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0006g0002 others(7): Show |
11 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-1453C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99236533 | |||||||
chr15:99236825 | T | C | 20 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0084 others(17): Show |
20 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-113-1745A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99236825 | |||||||
chr15:99236982 | G | GT | 117 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-113-1903dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99236982 | |||||||
chr15:99236986 | T | A | 1 | a0001c0001t0004g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-113-1906A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99236986 | |||||||
chr15:99237014 | T | C | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-113-1934A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99237014 | |||||||
chr15:99237391 | C | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0030 others(37): Show |
41 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.-113-2311G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99237391 | |||||||
chr15:99237643 | T | A | 11 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0006g0002 others(8): Show |
12 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-113-2563A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99237643 | |||||||
chr15:99237884 | C | T | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-113-2804G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99237884 | |||||||
chr15:99237988 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-113-2908G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99237988 | |||||||
chr15:99238149 | A | C | 22 | a0001c0001t0002g0004 a0001c0001t0004g0001 a0001c0001t0004g0006 others(19): Show |
23 | HG00733.hp2 HG01109.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.-113-3069T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238149 | |||||||
chr15:99238179 | G | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0093 |
2 | NA18955.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-113-3099C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238179 | |||||||
chr15:99238187 | T | G | 1 | a0001c0001t0004g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-113-3107A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238187 | |||||||
chr15:99238324 | T | C | 1 | a0001c0002t0005g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-114+3041A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238324 | |||||||
chr15:99238359 | C | A | 2 | a0001c0002t0004g0098 a0001c0002t0004g0099 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-114+3006G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238359 | |||||||
chr15:99238386 | A | G | 5 | a0001c0001t0009g0244 a0001c0003t0009g0245 a0001c0003t0009g0246 others(2): Show |
5 | HG00280.hp2 HG01123.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-114+2979T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238386 | |||||||
chr15:99238446 | G | A | 10 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0006g0002 others(7): Show |
11 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-114+2919C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238446 | |||||||
chr15:99238660 | T | G | 1 | a0001c0002t0004g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-114+2705A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238660 | |||||||
chr15:99238885 | C | CT | 42 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0030 others(39): Show |
43 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-114+2479dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238885 | |||||||
chr15:99238936 | T | C | 76 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(73): Show |
76 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-114+2429A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238936 | |||||||
chr15:99238999 | G | A | 1 | a0002c0006t0003g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-114+2366C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99238999 | |||||||
chr15:99239221 | C | T | 35 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(32): Show |
35 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-114+2144G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99239221 | |||||||
chr15:99239887 | G | A | 1 | a0001c0001t0015g0343 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+1478C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99239887 | |||||||
chr15:99239922 | C | T | 1 | a0001c0001t0006g0100 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-114+1443G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99239922 | |||||||
chr15:99240159 | C | T | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-114+1206G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99240159 | |||||||
chr15:99240329 | G | T | 1 | a0001c0001t0001g0273 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-114+1036C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99240329 | |||||||
chr15:99240595 | G | A | 1 | a0006c0014t0003g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-114+770C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99240595 | |||||||
chr15:99240710 | C | A | 111 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(108): Show |
111 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-114+655G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99240710 | |||||||
chr15:99240716 | G | C | 1 | a0001c0001t0002g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-114+649C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99240716 | |||||||
chr15:99240806 | G | T | 10 | a0001c0001t0016g0127 a0001c0002t0005g0014 a0001c0002t0005g0110 others(7): Show |
10 | HG02040.hp1 NA18971.hp2 NA18977.hp1 others(7): Show |
intron_variant | MODIFIER | c.-114+559C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99240806 | |||||||
chr15:99240999 | C | T | 129 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-114+366G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99240999 | |||||||
chr15:99241043 | G | A | 1 | a0001c0001t0009g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-114+322C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99241043 | |||||||
chr15:99241114 | C | A | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-114+251G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99241114 | |||||||
chr15:99241115 | G | A | 2 | a0001c0007t0005g0143 a0001c0007t0005g0144 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-114+250C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99241115 | |||||||
chr15:99241263 | C | T | 10 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0006g0002 others(7): Show |
11 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-114+102G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99241263 | |||||||
chr15:99241312 | T | TCAAA | 6 | a0001c0001t0001g0256 a0001c0001t0013g0147 a0001c0004t0003g0153 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-114+49_-114+52dup others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 3/13 | chr15 | 99241312 | |||||||
chr15:99241570 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-308-11C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99241570 | |||||||
chr15:99241622 | C | A | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-308-63G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99241622 | |||||||
chr15:99241636 | C | A | 35 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(32): Show |
35 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-308-77G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99241636 | |||||||
chr15:99241650 | G | C | 1 | a0001c0001t0007g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-308-91C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99241650 | |||||||
chr15:99241759 | C | A | 1 | a0001c0001t0002g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-308-200G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99241759 | |||||||
chr15:99241941 | G | T | 1 | a0001c0001t0010g0271 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-308-382C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99241941 | |||||||
chr15:99241991 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-308-432G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99241991 | |||||||
chr15:99242004 | G | A | 2 | a0001c0001t0001g0344 a0001c0001t0004g0106 |
2 | HG00544.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-308-445C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242004 | |||||||
chr15:99242036 | G | A | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-308-477C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242036 | |||||||
chr15:99242133 | GA | G | 292 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(289): Show |
294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.-308-575delT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242133 | |||||||
chr15:99242182 | T | C | 294 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(291): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-308-623A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242182 | |||||||
chr15:99242241 | C | T | 1 | a0001c0001t0009g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-308-682G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242241 | |||||||
chr15:99242390 | A | G | 120 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
121 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.-308-831T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242390 | |||||||
chr15:99242457 | A | T | 303 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(300): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.-308-898T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242457 | |||||||
chr15:99242778 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-308-1219G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242778 | |||||||
chr15:99242865 | CTTAAA | C | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-308-1311_-308-130 others(9): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242865 | |||||||
chr15:99242873 | T | A | 4 | a0001c0002t0004g0024 a0001c0002t0004g0025 a0001c0002t0004g0026 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-308-1314A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99242873 | |||||||
chr15:99243079 | A | T | 1 | a0001c0005t0008g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-308-1520T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99243079 | |||||||
chr15:99243127 | T | C | 35 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(32): Show |
35 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-308-1568A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99243127 | |||||||
chr15:99243517 | T | C | 1 | a0001c0003t0003g0238 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-309+1872A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99243517 | |||||||
chr15:99243649 | C | T | 1 | a0005c0017t0001g0270 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-309+1740G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99243649 | |||||||
chr15:99243760 | C | A | 112 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.-309+1629G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99243760 | |||||||
chr15:99243834 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-309+1555C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99243834 | |||||||
chr15:99243874 | C | T | 1 | a0001c0001t0011g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-309+1515G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99243874 | |||||||
chr15:99243939 | T | A | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-309+1450A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99243939 | |||||||
chr15:99244005 | A | G | 113 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.-309+1384T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244005 | |||||||
chr15:99244081 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-309+1308G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244081 | |||||||
chr15:99244205 | T | C | 35 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(32): Show |
35 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-309+1184A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244205 | |||||||
chr15:99244235 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-309+1154T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244235 | |||||||
chr15:99244255 | C | T | 1 | a0001c0001t0009g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-309+1134G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244255 | |||||||
chr15:99244277 | T | C | 28 | a0001c0001t0004g0122 a0001c0001t0006g0125 a0001c0001t0016g0127 others(25): Show |
28 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-309+1112A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244277 | |||||||
chr15:99244414 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-309+975G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244414 | |||||||
chr15:99244415 | G | GC | 51 | a0001c0001t0001g0254 a0001c0001t0001g0345 a0001c0001t0001g0346 others(48): Show |
51 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-309+973dupG | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244415 | |||||||
chr15:99244427 | T | C | 1 | a0001c0002t0004g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-309+962A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244427 | |||||||
chr15:99244706 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-309+683T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244706 | |||||||
chr15:99244756 | T | A | 15 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-309+633A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244756 | |||||||
chr15:99244779 | C | A | 1 | a0001c0001t0001g0354 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-309+610G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244779 | |||||||
chr15:99244805 | A | C | 1 | a0001c0001t0010g0265 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-309+584T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244805 | |||||||
chr15:99244833 | C | T | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-309+556G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244833 | |||||||
chr15:99244860 | C | G | 1 | a0001c0002t0005g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-309+529G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99244860 | |||||||
chr15:99245143 | T | G | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-309+246A>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 2/13 | chr15 | 99245143 | |||||||
chr15:99245513 | CA | C | 285 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
splice_region_variant&intron_variant | LOW | c.-430-4delT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99245513 | |||||||
chr15:99245820 | C | CT | 258 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0266 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.-430-311dupA | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99245820 | |||||||
chr15:99245820 | C | CTT | 9 | a0001c0001t0001g0254 a0001c0001t0024g0258 a0001c0005t0008g0257 others(6): Show |
9 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-430-312_-430-311d others(4): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99245820 | |||||||
chr15:99245860 | A | G | 1 | a0001c0004t0006g0109 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-430-350T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99245860 | |||||||
chr15:99246160 | GAAAAA | G | 113 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.-430-655_-430-651d others(7): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246160 | |||||||
chr15:99246398 | G | A | 2 | a0001c0001t0001g0356 a0001c0001t0001g0357 |
2 | HG01192.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.-430-888C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246398 | |||||||
chr15:99246404 | A | G | 10 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0006g0002 others(7): Show |
11 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-430-894T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246404 | |||||||
chr15:99246411 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-430-901G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246411 | |||||||
chr15:99246646 | C | T | 1 | a0001c0003t0003g0182 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-430-1136G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246646 | |||||||
chr15:99246671 | A | G | 11 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-430-1161T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246671 | |||||||
chr15:99246756 | T | C | 1 | a0001c0002t0004g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-430-1246A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246756 | |||||||
chr15:99246764 | C | CA | 5 | a0001c0001t0009g0244 a0001c0003t0009g0245 a0001c0003t0009g0246 others(2): Show |
5 | HG00280.hp2 HG01123.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-430-1255dupT | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246764 | |||||||
chr15:99246787 | G | A | 16 | a0001c0001t0001g0253 a0001c0001t0004g0015 a0001c0001t0004g0016 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-430-1277C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246787 | |||||||
chr15:99246875 | G | A | 1 | a0001c0001t0014g0358 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-430-1365C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246875 | |||||||
chr15:99246912 | A | G | 76 | a0001c0001t0002g0012 a0001c0001t0002g0029 a0001c0001t0002g0030 others(73): Show |
76 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-430-1402T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246912 | |||||||
chr15:99246956 | C | A | 42 | a0001c0001t0002g0004 a0001c0001t0002g0251 a0001c0001t0004g0001 others(39): Show |
43 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-430-1446G>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246956 | |||||||
chr15:99246992 | A | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0256 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-430-1482T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99246992 | |||||||
chr15:99247038 | T | C | 2 | a0001c0001t0007g0180 a0001c0001t0022g0179 |
2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-430-1528A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247038 | |||||||
chr15:99247083 | T | C | 1 | a0001c0001t0001g0359 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-430-1573A>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247083 | |||||||
chr15:99247182 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-430-1672C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247182 | |||||||
chr15:99247223 | G | T | 1 | a0001c0005t0003g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-430-1713C>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247223 | |||||||
chr15:99247262 | A | G | 2 | a0001c0002t0004g0098 a0001c0002t0004g0099 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-430-1752T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247262 | |||||||
chr15:99247325 | AG | A | 79 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0029 others(76): Show |
79 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-430-1816delC | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247325 | |||||||
chr15:99247379 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-431+1792T>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247379 | |||||||
chr15:99247643 | G | A | 1 | a0001c0001t0002g0097 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-431+1528C>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247643 | |||||||
chr15:99247736 | T | TTAGGATG others(21): Show |
168 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0266 others(165): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-431+1407_-431+143 others(32): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247736 | |||||||
chr15:99247736 | T | TTAGGATG others(49): Show |
31 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0002g0161 others(28): Show |
31 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-431+1379_-431+143 others(60): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247736 | |||||||
chr15:99247736 | T | TTAGGATG others(77): Show |
2 | a0001c0001t0007g0180 a0001c0001t0015g0365 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-431+1351_-431+143 others(88): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247736 | |||||||
chr15:99247736 | TTAGGATG others(21): Show |
T | 2 | a0001c0001t0002g0011 a0001c0001t0003g0010 |
2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-431+1407_-431+143 others(32): Show |
TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247736 | |||||||
chr15:99247848 | G | C | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-431+1323C>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247848 | |||||||
chr15:99247910 | A | T | 1 | a0001c0001t0003g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-431+1261T>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99247910 | |||||||
chr15:99248042 | C | T | 277 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.-431+1129G>A | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99248042 | |||||||
chr15:99248261 | C | G | 295 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.-431+910G>C | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99248261 | |||||||
chr15:99248309 | T | A | 3 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0001t0002g0251 |
3 | HG02080.hp2 NA18747.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.-431+862A>T | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99248309 | |||||||
chr15:99249072 | A | C | 7 | a0001c0001t0002g0004 a0001c0001t0004g0001 a0001c0001t0004g0006 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-431+99T>G | TTC23 | ENSG00000103852.13 | transcript | ENST00000394132.7 | protein_coding | 1/13 | chr15 | 99249072 |