Item | Value |
---|---|
geneid | 79809 |
ensemblid | ENSG00000123607.16 |
hgncid | 25660 |
symbol | TTC21B |
name | tetratricopeptide repeat domain 21B |
refseq_nuc | NM_024753.5 |
refseq_prot | NP_079029.3 |
ensembl_nuc | ENST00000243344.8 |
ensembl_prot | ENSP00000243344.7 |
mane_status | MANE Select |
chr | chr2 |
start | 165873362 |
end | 165953776 |
strand | - |
ver | v1.2 |
region | chr2:165873362-165953776 |
region5000 | chr2:165868362-165958776 |
regionname0 | TTC21B_chr2_165873362_165953776 |
regionname5000 | TTC21B_chr2_165868362_165958776 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1316 | 257 | 54 | 43 | 131 | 5 | 24 | 106 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0002 | 0/1 | 1316 | 82 | 14 | 16 | 37 | 3 | 11 | 28 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0003 | 0/0 | 1316 | 30 | 0 | 10 | 20 | 0 | 0 | 17 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0004 | 1/0 | 1316 | 14 | 11 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0005 | 0/0 | 1316 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0006 | 0/0 | 1316 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0007 | 0/0 | 1316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0008 | 0/0 | 1316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0009 | 0/0 | 1316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0010 | 0/0 | 1316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0011 | 0/0 | 1316 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0012 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0013 | 0/0 | 1316 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0014 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0015 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0016 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0017 | 0/0 | 1316 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0018 | 0/0 | 1316 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0019 | 0/0 | 1316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0020 | 0/0 | 1316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
a0021 | 0/0 | 1316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | MDSQE others(1311): Show |
chr2 | 165868362 | 165958776 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3948 | 235 | 37 | 39 | 131 | 4 | 24 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0001c0004 | 0/0 | 3948 | 13 | 13 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0001c0006 | 0/0 | 3948 | 5 | 0 | 4 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0001c0009 | 0/0 | 3948 | 3 | 3 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0001c0024 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0002c0002 | 0/1 | 3948 | 74 | 7 | 16 | 36 | 3 | 11 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0002c0008 | 0/0 | 3948 | 4 | 4 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0002c0014 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0002c0028 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0002c0029 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0003c0003 | 0/0 | 3948 | 30 | 0 | 10 | 20 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0004c0005 | 0/0 | 3948 | 11 | 9 | 2 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0004c0010 | 1/0 | 3948 | 3 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0005c0007 | 0/0 | 3948 | 5 | 4 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0006c0015 | 0/0 | 3948 | 2 | 1 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0007c0012 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0008c0011 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0009c0013 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0010c0019 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0011c0026 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0012c0021 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0013c0027 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0014c0018 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0015c0016 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0016c0030 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0017c0023 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0018c0022 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0019c0020 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0020c0017 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 | ||
a0021c0025 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | ATGGA others(3943): Show |
chr2 | 165868362 | 165958776 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5415 | 140 | 11 | 23 | 91 | 2 | 13 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0002 | 0/0 | 5415 | 46 | 1 | 12 | 22 | 1 | 10 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0003 | 0/0 | 5415 | 23 | 13 | 1 | 8 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0004 | 0/0 | 5415 | 4 | 0 | 0 | 4 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0005 | 0/0 | 5415 | 7 | 7 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0008 | 0/0 | 5415 | 6 | 2 | 3 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0011 | 0/0 | 5415 | 3 | 3 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0012 | 0/0 | 5415 | 2 | 0 | 0 | 2 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0013 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0014 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0019 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0001t0020 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0004t0001 | 0/0 | 5415 | 6 | 6 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0004t0003 | 0/0 | 5415 | 7 | 7 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0006t0001 | 0/0 | 5415 | 5 | 0 | 4 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0009t0001 | 0/0 | 5415 | 3 | 3 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0001c0024t0001 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0002t0001 | 0/0 | 5415 | 38 | 4 | 6 | 18 | 1 | 9 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0002t0004 | 0/1 | 5415 | 19 | 2 | 6 | 7 | 1 | 2 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0002t0007 | 0/0 | 5415 | 8 | 0 | 2 | 6 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0002t0009 | 0/0 | 5415 | 4 | 0 | 0 | 4 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0002t0010 | 0/0 | 5415 | 3 | 1 | 1 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0002t0017 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0002t0021 | 0/0 | 5452 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5447): Show |
chr2 | 165868362 | 165958776 |
a0002c0008t0001 | 0/0 | 5415 | 4 | 4 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0014t0004 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0028t0001 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0002c0029t0001 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0003c0003t0001 | 0/0 | 5415 | 21 | 0 | 10 | 11 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0003c0003t0006 | 0/0 | 5415 | 9 | 0 | 0 | 9 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0004c0005t0001 | 0/0 | 5415 | 11 | 9 | 2 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0004c0010t0001 | 1/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0004c0010t0003 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0004c0010t0018 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0005c0007t0001 | 0/0 | 5415 | 4 | 3 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0005c0007t0015 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0006c0015t0001 | 0/0 | 5415 | 2 | 1 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0007c0012t0001 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0007c0012t0005 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0008c0011t0003 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0009c0013t0001 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0010c0019t0002 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0011c0026t0001 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0012c0021t0005 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0013c0027t0004 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0014c0018t0016 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0015c0016t0001 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0016c0030t0001 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0017c0023t0008 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0018c0022t0001 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0019c0020t0002 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0020c0017t0002 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
a0021c0025t0004 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | GAATT others(5410): Show |
chr2 | 165868362 | 165958776 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0008g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0008g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0008g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0012g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0012g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0013g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0014g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0019g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0001t0020g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0004t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0006t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0006t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0006t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0006t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0006t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0009t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0009t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0009t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0001c0024t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0359 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0007g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0009g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0009g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0009g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0009g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0010g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0010g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0010g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0017g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0002t0021g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0008t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0008t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0008t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0008t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0014t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0028t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0002c0029t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0003c0003t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0005t0001g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0010t0001g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0010t0003g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0004c0010t0018g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0005c0007t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0005c0007t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0005c0007t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0005c0007t0015g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0006c0015t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0006c0015t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0007c0012t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0007c0012t0005g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0008c0011t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0008c0011t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0009c0013t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0009c0013t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0010c0019t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0011c0026t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0012c0021t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0013c0027t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0014c0018t0016g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0015c0016t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0016c0030t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0017c0023t0008g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0018c0022t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0019c0020t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0020c0017t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
a0021c0025t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0008 | g0211 | EUR | GBR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0239 | EUR | GBR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00140 | hp2 | a0002 | c0002 | t0010 | g0092 | EUR | GBR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00323 | hp1 | a0001 | c0006 | t0001 | g0319 | EUR | FIN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00323 | hp2 | a0002 | c0002 | t0004 | g0138 | EUR | FIN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00423 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00438 | hp1 | a0002 | c0002 | t0004 | g0363 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00544 | hp2 | a0002 | c0002 | t0004 | g0361 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00639 | hp2 | a0010 | c0019 | t0002 | g0220 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00673 | hp1 | a0002 | c0002 | t0004 | g0117 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | CHS | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0384 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01069 | hp1 | a0001 | c0006 | t0001 | g0307 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01070 | hp2 | a0001 | c0006 | t0001 | g0317 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01071 | hp1 | a0001 | c0006 | t0001 | g0306 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01074 | hp1 | a0002 | c0002 | t0004 | g0121 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0244 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01106 | hp1 | a0002 | c0002 | t0017 | g0238 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01106 | hp2 | a0004 | c0005 | t0001 | g0368 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0269 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01168 | hp1 | a0002 | c0002 | t0004 | g0270 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01169 | hp2 | a0002 | c0002 | t0004 | g0273 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01175 | hp1 | a0006 | c0015 | t0001 | g0389 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01175 | hp2 | a0001 | c0001 | t0008 | g0226 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01261 | hp1 | a0004 | c0005 | t0001 | g0381 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01346 | hp2 | a0002 | c0002 | t0004 | g0126 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01358 | hp1 | a0002 | c0002 | t0010 | g0011 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0376 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0377 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01496 | hp1 | a0005 | c0007 | t0001 | g0009 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0366 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0122 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01891 | hp1 | a0007 | c0012 | t0001 | g0374 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01891 | hp2 | a0001 | c0009 | t0001 | g0114 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01928 | hp1 | a0002 | c0002 | t0007 | g0130 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01934 | hp1 | a0003 | c0003 | t0001 | g0249 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01952 | hp1 | a0003 | c0003 | t0001 | g0260 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01975 | hp1 | a0003 | c0003 | t0001 | g0241 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01978 | hp2 | a0002 | c0002 | t0004 | g0127 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01993 | hp2 | a0002 | c0002 | t0007 | g0128 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02004 | hp2 | a0003 | c0003 | t0001 | g0246 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02040 | hp2 | a0011 | c0026 | t0001 | g0302 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02055 | hp1 | a0004 | c0005 | t0001 | g0263 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02056 | hp1 | a0003 | c0003 | t0001 | g0077 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02135 | hp1 | a0002 | c0002 | t0004 | g0075 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02148 | hp2 | a0003 | c0003 | t0001 | g0248 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02155 | hp2 | a0002 | c0002 | t0007 | g0149 | EAS | CDX | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02165 | hp1 | a0001 | c0001 | t0014 | g0315 | EAS | CDX | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02165 | hp2 | a0002 | c0002 | t0004 | g0281 | EAS | CDX | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02257 | hp1 | a0004 | c0005 | t0001 | g0391 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02257 | hp2 | a0001 | c0004 | t0003 | g0112 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02258 | hp1 | a0008 | c0011 | t0003 | g0178 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02258 | hp2 | a0012 | c0021 | t0005 | g0026 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02280 | hp2 | a0009 | c0013 | t0001 | g0379 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0247 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02293 | hp2 | a0001 | c0006 | t0001 | g0305 | AMR | PEL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0225 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02523 | hp2 | a0003 | c0003 | t0001 | g0252 | EAS | KHV | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0364 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02602 | hp2 | a0002 | c0002 | t0004 | g0146 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02615 | hp1 | a0004 | c0010 | t0003 | g0387 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02622 | hp1 | a0005 | c0007 | t0001 | g0087 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02622 | hp2 | a0001 | c0004 | t0003 | g0096 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02630 | hp1 | a0004 | c0005 | t0001 | g0385 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02683 | hp2 | a0013 | c0027 | t0004 | g0264 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0237 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02723 | hp1 | a0002 | c0008 | t0001 | g0278 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02818 | hp1 | a0002 | c0002 | t0004 | g0271 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02818 | hp2 | a0001 | c0004 | t0003 | g0098 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0109 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02895 | hp1 | a0002 | c0014 | t0004 | g0005 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02896 | hp1 | a0004 | c0005 | t0001 | g0383 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02896 | hp2 | a0002 | c0008 | t0001 | g0277 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02897 | hp1 | a0002 | c0014 | t0004 | g0005 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02897 | hp2 | a0004 | c0005 | t0001 | g0382 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02922 | hp1 | a0001 | c0001 | t0011 | g0279 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02922 | hp2 | a0001 | c0004 | t0003 | g0102 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02965 | hp1 | a0009 | c0013 | t0001 | g0378 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02965 | hp2 | a0014 | c0018 | t0016 | g0100 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02970 | hp1 | a0015 | c0016 | t0001 | g0084 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02970 | hp2 | a0001 | c0004 | t0003 | g0097 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02976 | hp1 | a0008 | c0011 | t0003 | g0179 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03041 | hp1 | a0016 | c0030 | t0001 | g0274 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0072 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03130 | hp1 | a0001 | c0009 | t0001 | g0113 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03130 | hp2 | a0006 | c0015 | t0001 | g0388 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03195 | hp1 | a0001 | c0004 | t0003 | g0110 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03195 | hp2 | a0004 | c0005 | t0001 | g0367 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03209 | hp1 | a0001 | c0004 | t0003 | g0101 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03225 | hp1 | a0005 | c0007 | t0001 | g0009 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03453 | hp1 | a0005 | c0007 | t0015 | g0086 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03453 | hp2 | a0004 | c0005 | t0001 | g0360 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0224 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03516 | hp1 | a0002 | c0002 | t0004 | g0272 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03516 | hp2 | a0002 | c0028 | t0001 | g0369 | AFR | ESN | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0107 | AFR | GWD | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03579 | hp1 | a0002 | c0008 | t0001 | g0276 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03579 | hp2 | a0001 | c0024 | t0001 | g0108 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0267 | SAS | BEB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03834 | hp2 | a0002 | c0002 | t0004 | g0144 | SAS | BEB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0365 | SAS | BEB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG04199 | hp1 | a0017 | c0023 | t0008 | g0177 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG04204 | hp1 | a0018 | c0022 | t0001 | g0304 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18522 | hp1 | a0002 | c0008 | t0001 | g0275 | AFR | YRI | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | YRI | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18612 | hp1 | a0001 | c0001 | t0013 | g0187 | EAS | CHB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | CHB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | CHB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18939 | hp1 | a0002 | c0029 | t0001 | g0282 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18940 | hp1 | a0003 | c0003 | t0006 | g0262 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18941 | hp1 | a0002 | c0002 | t0007 | g0142 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18942 | hp1 | a0003 | c0003 | t0001 | g0076 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18947 | hp1 | a0002 | c0002 | t0007 | g0145 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18948 | hp2 | a0003 | c0003 | t0006 | g0253 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18952 | hp1 | a0002 | c0002 | t0009 | g0396 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18952 | hp2 | a0003 | c0003 | t0001 | g0250 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18954 | hp1 | a0003 | c0003 | t0006 | g0255 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18956 | hp2 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18969 | hp1 | a0003 | c0003 | t0001 | g0245 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18973 | hp1 | a0001 | c0001 | t0012 | g0300 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18977 | hp1 | a0001 | c0001 | t0012 | g0370 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18978 | hp1 | a0003 | c0003 | t0006 | g0256 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18979 | hp1 | a0003 | c0003 | t0006 | g0254 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18980 | hp2 | a0002 | c0002 | t0007 | g0140 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18981 | hp2 | a0002 | c0002 | t0004 | g0362 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18986 | hp2 | a0003 | c0003 | t0006 | g0242 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18987 | hp1 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18990 | hp2 | a0002 | c0002 | t0009 | g0393 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19003 | hp1 | a0003 | c0003 | t0006 | g0257 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19004 | hp2 | a0019 | c0020 | t0002 | g0184 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19005 | hp1 | a0002 | c0002 | t0009 | g0394 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19006 | hp1 | a0002 | c0002 | t0009 | g0392 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19010 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0105 | AFR | LWK | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19030 | hp2 | a0004 | c0005 | t0001 | g0386 | AFR | LWK | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19043 | hp1 | a0001 | c0004 | t0001 | g0106 | AFR | LWK | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19054 | hp2 | a0002 | c0002 | t0007 | g0129 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19064 | hp2 | a0003 | c0003 | t0006 | g0258 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19065 | hp1 | a0002 | c0002 | t0007 | g0141 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19066 | hp1 | a0002 | c0002 | t0004 | g0125 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19072 | hp2 | a0020 | c0017 | t0002 | g0185 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19078 | hp1 | a0001 | c0001 | t0019 | g0236 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19080 | hp1 | a0003 | c0003 | t0006 | g0243 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19083 | hp1 | a0003 | c0003 | t0001 | g0251 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19083 | hp2 | a0002 | c0002 | t0021 | g0395 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19085 | hp2 | a0001 | c0001 | t0020 | g0014 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19086 | hp1 | a0021 | c0025 | t0004 | g0058 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19091 | hp1 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19240 | hp1 | a0001 | c0009 | t0001 | g0115 | AFR | YRI | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0073 | AFR | YRI | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ASW | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA20129 | hp2 | a0004 | c0005 | t0001 | g0390 | AFR | ASW | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | GIH | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | GIH | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01123 | hp1 | a0001 | c0001 | t0008 | g0227 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG01123 | hp2 | a0002 | c0002 | t0004 | g0139 | AMR | CLM | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02486 | hp1 | a0002 | c0002 | t0010 | g0094 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02486 | hp2 | a0005 | c0007 | t0001 | g0085 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG02559 | hp2 | a0001 | c0004 | t0001 | g0103 | AFR | ACB | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG03471 | hp2 | a0007 | c0012 | t0005 | g0375 | AFR | MSL | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0268 | AFR | USA | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | USA | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA21309 | hp1 | a0004 | c0010 | t0018 | g0380 | AFR | LWK | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | LWK | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
homoSapiens | chm13v2 | a0002 | c0002 | t0004 | g0359 | REF | REF | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
homoSapiens | grch38p0 | a0004 | c0010 | t0001 | g0074 | REF | REF | TTC21B_chr2_165868362_165958776 | TTC21B | chr2 | 165868362 | 165958776 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:165880714 | G | T | 1 | a0012 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.3770C>A | p.Ala1257Glu | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/29 | 3841/5415 | 3770/3951 | 1257/1316 | chr2 | 165880714 | |||
chr2:165901910 | C | T | 1 | a0019 | 1 | NA19004.hp2 | missense_variant&splice_region_variant | MODERATE | c.2569G>A | p.Ala857Thr | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/29 | 2640/5415 | 2569/3951 | 857/1316 | chr2 | 165901910 | |||
chr2:165912578 | G | A | 1 | a0018 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2258C>T | p.Pro753Leu | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/29 | 2329/5415 | 2258/3951 | 753/1316 | chr2 | 165912578 | |||
chr2:165912609 | C | T | 1 | a0016 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2227G>A | p.Val743Ile | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/29 | 2298/5415 | 2227/3951 | 743/1316 | chr2 | 165912609 | |||
chr2:165917286 | T | C | 1 | a0007 | 2 | HG01891.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.1870A>G | p.Ile624Val | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/29 | 1941/5415 | 1870/3951 | 624/1316 | chr2 | 165917286 | |||
chr2:165917310 | G | A | 1 | a0017 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1846C>T | p.Arg616Cys | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/29 | 1917/5415 | 1846/3951 | 616/1316 | chr2 | 165917310 | |||
chr2:165917480 | A | C | 1 | a0008 | 2 | HG02258.hp1 HG02976.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1676T>G | p.Val559Gly | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/29 | 1747/5415 | 1676/3951 | 559/1316 | chr2 | 165917480 | |||
chr2:165919379 | G | C | 1 | a0009 | 2 | HG02280.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.1571C>G | p.Ser524Cys | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/29 | 1642/5415 | 1571/3951 | 524/1316 | chr2 | 165919379 | |||
chr2:165919412 | T | C | 1 | a0021 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.1538A>G | p.Asn513Ser | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/29 | 1609/5415 | 1538/3951 | 513/1316 | chr2 | 165919412 | |||
chr2:165924553 | C | A | 1 | a0011 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1512G>T | p.Leu504Phe | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/29 | 1583/5415 | 1512/3951 | 504/1316 | chr2 | 165924553 | |||
chr2:165924648 | G | A | 1 | a0003 | 30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
missense_variant | MODERATE | c.1417C>T | p.Leu473Phe | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/29 | 1488/5415 | 1417/3951 | 473/1316 | chr2 | 165924648 | |||
chr2:165924678 | G | A | 2 | a0006 a0009 |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1387C>T | p.Pro463Ser | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/29 | 1458/5415 | 1387/3951 | 463/1316 | chr2 | 165924678 | |||
chr2:165929326 | A | G | 1 | a0010 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1195T>C | p.Tyr399His | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/29 | 1266/5415 | 1195/3951 | 399/1316 | chr2 | 165929326 | |||
chr2:165931814 | T | C | 3 | a0005 a0015 a0016 |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
missense_variant | MODERATE | c.838A>G | p.Met280Val | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/29 | 909/5415 | 838/3951 | 280/1316 | chr2 | 165931814 | |||
chr2:165931826 | T | C | 19 | a0001 a0002 a0003 others(16): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
missense_variant | MODERATE | c.826A>G | p.Thr276Ala | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/29 | 897/5415 | 826/3951 | 276/1316 | chr2 | 165931826 | |||
chr2:165933007 | A | G | 1 | a0020 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.761T>C | p.Leu254Pro | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/29 | 832/5415 | 761/3951 | 254/1316 | chr2 | 165933007 | |||
chr2:165933044 | C | T | 1 | a0013 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.724G>A | p.Asp242Asn | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/29 | 795/5415 | 724/3951 | 242/1316 | chr2 | 165933044 | |||
chr2:165941072 | T | A | 3 | a0005 a0015 a0016 |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
missense_variant | MODERATE | c.665A>T | p.Gln222Leu | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/29 | 736/5415 | 665/3951 | 222/1316 | chr2 | 165941072 | |||
chr2:165941136 | C | T | 15 | a0001 a0003 a0006 others(12): Show |
304 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(301): Show |
missense_variant | MODERATE | c.601G>A | p.Val201Met | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/29 | 672/5415 | 601/3951 | 201/1316 | chr2 | 165941136 | |||
chr2:165949457 | G | T | 1 | a0015 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.199C>A | p.Gln67Lys | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/29 | 270/5415 | 199/3951 | 67/1316 | chr2 | 165949457 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:165883959 | A | G | 1 | a0001c0006 | 5 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(2): Show |
synonymous_variant | LOW | c.3519T>C | p.Thr1173Thr | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/29 | 3590/5415 | 3519/3951 | 1173/1316 | chr2 | 165883959 | |||
chr2:165898699 | T | C | 1 | a0002c0014 | 2 | HG02895.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.2937A>G | p.Leu979Leu | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/29 | 3008/5415 | 2937/3951 | 979/1316 | chr2 | 165898699 | |||
chr2:165901737 | G | A | 1 | a0001c0009 | 3 | HG01891.hp2 HG03130.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.2742C>T | p.Cys914Cys | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/29 | 2813/5415 | 2742/3951 | 914/1316 | chr2 | 165901737 | |||
chr2:165911403 | C | G | 1 | a0003c0003 | 30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
synonymous_variant | LOW | c.2385G>C | p.Leu795Leu | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/29 | 2456/5415 | 2385/3951 | 795/1316 | chr2 | 165911403 | |||
chr2:165911454 | G | A | 1 | a0001c0004 | 13 | HG02257.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
synonymous_variant | LOW | c.2334C>T | p.Tyr778Tyr | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/29 | 2405/5415 | 2334/3951 | 778/1316 | chr2 | 165911454 | |||
chr2:165913610 | A | G | 7 | a0001c0024 a0002c0002 a0002c0014 others(4): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
synonymous_variant | LOW | c.2175T>C | p.Phe725Phe | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/29 | 2246/5415 | 2175/3951 | 725/1316 | chr2 | 165913610 | |||
chr2:165915374 | C | T | 1 | a0002c0028 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1965G>A | p.Arg655Arg | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/29 | 2036/5415 | 1965/3951 | 655/1316 | chr2 | 165915374 | |||
chr2:165917461 | G | A | 10 | a0001c0024 a0002c0002 a0002c0014 others(7): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(94): Show |
synonymous_variant | LOW | c.1695C>T | p.Tyr565Tyr | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/29 | 1766/5415 | 1695/3951 | 565/1316 | chr2 | 165917461 | |||
chr2:165931776 | T | C | 1 | a0002c0029 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.876A>G | p.Thr292Thr | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/29 | 947/5415 | 876/3951 | 292/1316 | chr2 | 165931776 | |||
chr2:165949632 | G | C | 1 | a0006c0015 | 2 | HG01175.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.114C>G | p.Val38Val | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 2/29 | 185/5415 | 114/3951 | 38/1316 | chr2 | 165949632 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:165873389 | T | C | 1 | a0005c0007t0015 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1366A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 1366 | chr2 | 165873389 | ||||||
chr2:165873530 | G | A | 1 | a0014c0018t0016 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 1225 | chr2 | 165873530 | ||||||
chr2:165873590 | T | G | 1 | a0002c0002t0017 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1165A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 1165 | chr2 | 165873590 | ||||||
chr2:165873638 | T | C | 1 | a0004c0010t0018 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1117A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 1117 | chr2 | 165873638 | ||||||
chr2:165873650 | C | A | 7 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0013 others(4): Show |
57 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1105G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 1105 | chr2 | 165873650 | ||||||
chr2:165873781 | G | C | 1 | a0002c0002t0010 | 3 | HG00140.hp2 HG01358.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*974C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 974 | chr2 | 165873781 | ||||||
chr2:165873877 | T | C | 8 | a0001c0001t0004 a0002c0002t0004 a0002c0002t0007 others(5): Show |
39 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*878A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 878 | chr2 | 165873877 | ||||||
chr2:165873908 | T | G | 1 | a0001c0001t0013 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 847 | chr2 | 165873908 | ||||||
chr2:165873968 | A | C | 1 | a0001c0001t0014 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*787T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 787 | chr2 | 165873968 | ||||||
chr2:165874099 | C | T | 1 | a0002c0002t0007 | 8 | HG01928.hp1 HG01993.hp2 HG02155.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*656G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 656 | chr2 | 165874099 | ||||||
chr2:165874113 | G | A | 1 | a0001c0001t0019 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 642 | chr2 | 165874113 | ||||||
chr2:165874224 | T | C | 9 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(6): Show |
62 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*531A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 531 | chr2 | 165874224 | ||||||
chr2:165874238 | C | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0013 others(6): Show |
83 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*517G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 517 | chr2 | 165874238 | ||||||
chr2:165874239 | G | A | 1 | a0001c0001t0012 | 2 | NA18973.hp1 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*516C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 516 | chr2 | 165874239 | ||||||
chr2:165874281 | G | C | 1 | a0001c0001t0020 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 474 | chr2 | 165874281 | ||||||
chr2:165874331 | T | C | 1 | a0003c0003t0006 | 9 | NA18940.hp1 NA18948.hp2 NA18954.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*424A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 424 | chr2 | 165874331 | ||||||
chr2:165874650 | C | T | 3 | a0001c0001t0005 a0007c0012t0005 a0012c0021t0005 |
9 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*105G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 105 | chr2 | 165874650 | ||||||
chr2:165874660 | C | CAAAGCAC others(30): Show |
1 | a0002c0002t0021 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*58_*94dupTTCTTCCT others(29): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 29/29 | 94 | chr2 | 165874660 | ||||||
chr2:165953723 | G | A | 2 | a0002c0002t0009 a0002c0002t0021 |
5 | NA18952.hp1 NA18990.hp2 NA19005.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-18C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/29 | 18 | chr2 | 165953723 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:165874985 | G | A | 3 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 |
3 | NA18985.hp2 NA18991.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3874-153C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165874985 | |||||||
chr2:165875037 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0095 a0002c0008t0001g0278 |
3 | HG02055.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3874-205C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875037 | |||||||
chr2:165875041 | A | G | 2 | a0002c0002t0001g0153 a0002c0002t0001g0154 |
2 | NA19072.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.3874-209T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875041 | |||||||
chr2:165875067 | C | CAT | 39 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(36): Show |
39 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.3874-236_3874-235i others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875067 | |||||||
chr2:165875098 | A | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3874-266T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875098 | |||||||
chr2:165875133 | A | G | 5 | a0003c0003t0001g0077 a0003c0003t0001g0078 a0003c0003t0001g0079 others(2): Show |
5 | HG00423.hp1 HG02056.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.3874-301T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875133 | |||||||
chr2:165875209 | C | T | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3874-377G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875209 | |||||||
chr2:165875267 | T | A | 1 | a0002c0002t0001g0137 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3874-435A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875267 | |||||||
chr2:165875269 | C | T | 1 | a0014c0018t0016g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3874-437G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875269 | |||||||
chr2:165875272 | GT | G | 277 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0053 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.3874-441delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875272 | |||||||
chr2:165875272 | GTT | G | 12 | a0001c0001t0003g0091 a0001c0001t0003g0172 a0001c0001t0003g0174 others(9): Show |
12 | HG01255.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3874-442_3874-441d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875272 | |||||||
chr2:165875301 | T | C | 9 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(6): Show |
9 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3874-469A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875301 | |||||||
chr2:165875365 | A | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0095 a0002c0008t0001g0278 |
3 | HG02055.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3874-533T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875365 | |||||||
chr2:165875420 | T | C | 350 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(347): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.3874-588A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875420 | |||||||
chr2:165875625 | T | C | 99 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(96): Show |
101 | HG00140.hp2 HG00544.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.3873+540A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875625 | |||||||
chr2:165875751 | T | C | 1 | a0002c0002t0001g0116 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3873+414A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875751 | |||||||
chr2:165875814 | C | CT | 98 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(95): Show |
100 | HG00544.hp1 HG00639.hp2 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.3873+350dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875814 | |||||||
chr2:165875827 | T | A | 62 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0091 others(59): Show |
63 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.3873+338A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165875827 | |||||||
chr2:165876017 | G | T | 29 | a0002c0002t0001g0008 a0002c0002t0001g0116 a0002c0002t0001g0118 others(26): Show |
30 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.3873+148C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165876017 | |||||||
chr2:165876023 | T | C | 1 | a0001c0001t0001g0312 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3873+142A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 28/28 | chr2 | 165876023 | |||||||
chr2:165876250 | A | G | 1 | a0002c0002t0010g0092 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3806-18T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165876250 | |||||||
chr2:165876281 | A | G | 1 | a0001c0001t0012g0370 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3806-49T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165876281 | |||||||
chr2:165876328 | G | T | 39 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(36): Show |
39 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.3806-96C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165876328 | |||||||
chr2:165876363 | G | A | 9 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(6): Show |
9 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3806-131C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165876363 | |||||||
chr2:165876519 | A | C | 1 | a0014c0018t0016g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3806-287T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165876519 | |||||||
chr2:165876571 | A | T | 1 | a0002c0002t0001g0120 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3806-339T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165876571 | |||||||
chr2:165876654 | T | C | 1 | a0001c0006t0001g0305 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3806-422A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165876654 | |||||||
chr2:165876762 | G | T | 1 | a0001c0001t0002g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3806-530C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165876762 | |||||||
chr2:165877228 | T | C | 59 | a0001c0001t0001g0167 a0001c0001t0001g0316 a0001c0001t0002g0002 others(56): Show |
62 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.3806-996A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877228 | |||||||
chr2:165877408 | C | A | 1 | a0006c0015t0001g0389 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3806-1176G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877408 | |||||||
chr2:165877417 | T | C | 3 | a0001c0001t0002g0007 a0001c0001t0002g0182 a0001c0001t0002g0190 |
4 | HG00639.hp1 HG01099.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.3806-1185A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877417 | |||||||
chr2:165877521 | T | C | 5 | a0001c0001t0004g0033 a0001c0001t0004g0059 a0001c0001t0004g0060 others(2): Show |
5 | NA18980.hp1 NA18982.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.3806-1289A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877521 | |||||||
chr2:165877523 | T | C | 39 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(36): Show |
39 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.3806-1291A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877523 | |||||||
chr2:165877588 | G | A | 1 | a0002c0002t0001g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3806-1356C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877588 | |||||||
chr2:165877646 | C | T | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3806-1414G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877646 | |||||||
chr2:165877667 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.3806-1435G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877667 | |||||||
chr2:165877759 | A | C | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3806-1527T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877759 | |||||||
chr2:165877784 | C | A | 4 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0181 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3806-1552G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877784 | |||||||
chr2:165877830 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0025 |
4 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.3806-1598G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877830 | |||||||
chr2:165877928 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3806-1696A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165877928 | |||||||
chr2:165878056 | G | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0095 a0002c0008t0001g0278 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3806-1824C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878056 | |||||||
chr2:165878114 | T | C | 2 | a0002c0002t0001g0153 a0002c0002t0001g0154 |
2 | NA19072.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.3806-1882A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878114 | |||||||
chr2:165878242 | T | C | 1 | a0007c0012t0001g0374 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3806-2010A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878242 | |||||||
chr2:165878323 | T | C | 11 | a0001c0001t0001g0235 a0001c0001t0003g0159 a0001c0001t0003g0160 others(8): Show |
11 | HG00558.hp2 HG02071.hp1 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.3806-2091A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878323 | |||||||
chr2:165878416 | T | C | 6 | a0001c0001t0001g0171 a0005c0007t0001g0009 a0005c0007t0001g0085 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3806-2184A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878416 | |||||||
chr2:165878423 | T | G | 195 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(192): Show |
200 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.3806-2191A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878423 | |||||||
chr2:165878553 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
57 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3805+2126A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878553 | |||||||
chr2:165878650 | C | T | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3805+2029G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878650 | |||||||
chr2:165878661 | T | C | 29 | a0002c0002t0001g0008 a0002c0002t0001g0116 a0002c0002t0001g0118 others(26): Show |
30 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.3805+2018A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878661 | |||||||
chr2:165878680 | A | AT | 57 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0069 others(54): Show |
57 | HG00423.hp1 HG00642.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3805+1998dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878680 | |||||||
chr2:165878680 | AT | A | 59 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0091 others(56): Show |
59 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3805+1998delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878680 | |||||||
chr2:165878775 | G | A | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3805+1904C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878775 | |||||||
chr2:165878777 | G | C | 20 | a0001c0001t0001g0384 a0001c0004t0001g0103 a0001c0004t0001g0105 others(17): Show |
20 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3805+1902C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878777 | |||||||
chr2:165878874 | G | A | 2 | a0001c0006t0001g0306 a0001c0006t0001g0307 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3805+1805C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878874 | |||||||
chr2:165878960 | G | A | 158 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(155): Show |
163 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.3805+1719C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878960 | |||||||
chr2:165878964 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3805+1715C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878964 | |||||||
chr2:165878971 | T | C | 296 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0053 others(293): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.3805+1708A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165878971 | |||||||
chr2:165879029 | A | T | 1 | a0001c0001t0002g0218 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3805+1650T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879029 | |||||||
chr2:165879077 | C | A | 1 | a0001c0004t0003g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3805+1602G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879077 | |||||||
chr2:165879143 | A | G | 1 | a0002c0002t0007g0141 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3805+1536T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879143 | |||||||
chr2:165879184 | A | G | 2 | a0001c0001t0002g0365 a0001c0001t0002g0366 |
2 | HG01496.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3805+1495T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879184 | |||||||
chr2:165879262 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3805+1417A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879262 | |||||||
chr2:165879347 | T | C | 26 | a0001c0001t0001g0171 a0001c0001t0001g0384 a0001c0004t0001g0103 others(23): Show |
27 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.3805+1332A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879347 | |||||||
chr2:165879425 | T | G | 1 | a0001c0001t0012g0300 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3805+1254A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879425 | |||||||
chr2:165879495 | T | G | 39 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(36): Show |
39 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.3805+1184A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879495 | |||||||
chr2:165879504 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3805+1175A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879504 | |||||||
chr2:165879532 | C | T | 1 | a0002c0002t0001g0364 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3805+1147G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879532 | |||||||
chr2:165879596 | A | C | 31 | a0001c0001t0013g0187 a0003c0003t0001g0076 a0003c0003t0001g0077 others(28): Show |
31 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.3805+1083T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879596 | |||||||
chr2:165879642 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3805+1037G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879642 | |||||||
chr2:165879750 | T | C | 197 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(194): Show |
202 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3805+929A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879750 | |||||||
chr2:165879869 | C | G | 1 | a0002c0002t0007g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3805+810G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879869 | |||||||
chr2:165879899 | T | A | 1 | a0002c0002t0004g0139 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3805+780A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879899 | |||||||
chr2:165879955 | A | C | 2 | a0002c0002t0001g0231 a0002c0002t0001g0232 |
2 | NA18974.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3805+724T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879955 | |||||||
chr2:165879980 | G | A | 5 | a0001c0001t0001g0171 a0005c0007t0001g0009 a0005c0007t0001g0087 others(2): Show |
6 | HG01496.hp1 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3805+699C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165879980 | |||||||
chr2:165880074 | T | C | 1 | a0002c0002t0001g0364 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3805+605A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165880074 | |||||||
chr2:165880114 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3805+565A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165880114 | |||||||
chr2:165880260 | T | C | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3805+419A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 27/28 | chr2 | 165880260 | |||||||
chr2:165880871 | T | C | 11 | a0001c0001t0001g0171 a0002c0002t0010g0011 a0002c0002t0010g0092 others(8): Show |
12 | HG00140.hp2 HG01358.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.3685-72A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165880871 | |||||||
chr2:165880945 | T | C | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3685-146A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165880945 | |||||||
chr2:165881069 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3685-270G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881069 | |||||||
chr2:165881155 | T | G | 240 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(237): Show |
245 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.3685-356A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881155 | |||||||
chr2:165881179 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0024 |
3 | HG02074.hp1 HG02155.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.3685-380A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881179 | |||||||
chr2:165881184 | C | G | 1 | a0001c0001t0003g0181 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3685-385G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881184 | |||||||
chr2:165881196 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3685-397A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881196 | |||||||
chr2:165881245 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3685-446A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881245 | |||||||
chr2:165881249 | T | C | 1 | a0001c0001t0003g0161 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3685-450A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881249 | |||||||
chr2:165881447 | G | A | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3685-648C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881447 | |||||||
chr2:165881746 | T | C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3685-947A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881746 | |||||||
chr2:165881799 | T | C | 1 | a0002c0002t0001g0364 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3685-1000A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881799 | |||||||
chr2:165881807 | T | C | 1 | a0004c0010t0018g0380 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3685-1008A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165881807 | |||||||
chr2:165882029 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3685-1230G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882029 | |||||||
chr2:165882121 | G | A | 240 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(237): Show |
245 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.3685-1322C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882121 | |||||||
chr2:165882251 | T | C | 35 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(32): Show |
35 | HG00544.hp1 HG00642.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.3685-1452A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882251 | |||||||
chr2:165882408 | C | T | 1 | a0001c0001t0001g0335 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3684+1386G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882408 | |||||||
chr2:165882451 | T | C | 2 | a0008c0011t0003g0178 a0008c0011t0003g0179 |
2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3684+1343A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882451 | |||||||
chr2:165882474 | A | G | 2 | a0001c0001t0008g0224 a0001c0001t0008g0225 |
2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3684+1320T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882474 | |||||||
chr2:165882493 | C | T | 1 | a0004c0010t0018g0380 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3684+1301G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882493 | |||||||
chr2:165882865 | TCAG | T | 8 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3684+926_3684+928d others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882865 | |||||||
chr2:165882903 | C | T | 5 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0158 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3684+891G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882903 | |||||||
chr2:165882931 | A | G | 7 | a0001c0001t0001g0171 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3684+863T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165882931 | |||||||
chr2:165883185 | CA | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3684+608delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165883185 | |||||||
chr2:165883187 | A | C | 1 | a0002c0002t0001g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3684+607T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165883187 | |||||||
chr2:165883228 | C | G | 1 | a0001c0001t0005g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3684+566G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165883228 | |||||||
chr2:165883364 | AAATAT | A | 3 | a0005c0007t0001g0085 a0005c0007t0001g0087 a0015c0016t0001g0084 |
3 | HG02486.hp2 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3684+425_3684+429d others(7): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165883364 | |||||||
chr2:165883385 | T | G | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | NA18978.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.3684+409A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165883385 | |||||||
chr2:165883571 | C | T | 1 | a0002c0002t0001g0364 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3684+223G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165883571 | |||||||
chr2:165883592 | A | G | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3684+202T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 26/28 | chr2 | 165883592 | |||||||
chr2:165884068 | C | T | 39 | a0001c0001t0002g0007 a0001c0001t0002g0182 a0001c0001t0002g0186 others(36): Show |
40 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.3460-50G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165884068 | |||||||
chr2:165884153 | A | G | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3460-135T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165884153 | |||||||
chr2:165884634 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3460-616G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165884634 | |||||||
chr2:165884848 | G | A | 184 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(181): Show |
188 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(185): Show |
intron_variant | MODIFIER | c.3460-830C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165884848 | |||||||
chr2:165885105 | G | A | 13 | a0001c0004t0001g0103 a0001c0004t0001g0105 a0001c0004t0001g0106 others(10): Show |
13 | HG02257.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.3460-1087C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165885105 | |||||||
chr2:165885140 | A | G | 25 | a0003c0003t0001g0076 a0003c0003t0001g0241 a0003c0003t0001g0244 others(22): Show |
25 | HG00642.hp1 HG01081.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-1122T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165885140 | |||||||
chr2:165885386 | TC | T | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3460-1369delG | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165885386 | |||||||
chr2:165885587 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3460-1569A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165885587 | |||||||
chr2:165885849 | A | G | 390 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(387): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.3460-1831T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165885849 | |||||||
chr2:165885933 | T | C | 6 | a0001c0001t0001g0095 a0002c0002t0001g0093 a0002c0008t0001g0275 others(3): Show |
6 | HG02055.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3460-1915A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165885933 | |||||||
chr2:165886346 | T | C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3459+1933A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886346 | |||||||
chr2:165886392 | A | G | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3459+1887T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886392 | |||||||
chr2:165886444 | C | T | 14 | a0001c0001t0001g0384 a0001c0024t0001g0108 a0004c0005t0001g0263 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.3459+1835G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886444 | |||||||
chr2:165886639 | C | G | 4 | a0001c0001t0001g0167 a0001c0009t0001g0113 a0001c0009t0001g0114 others(1): Show |
4 | HG01891.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3459+1640G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886639 | |||||||
chr2:165886667 | T | C | 1 | a0002c0008t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3459+1612A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886667 | |||||||
chr2:165886673 | T | G | 2 | a0002c0002t0001g0093 a0002c0002t0010g0094 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3459+1606A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886673 | |||||||
chr2:165886770 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3459+1509A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886770 | |||||||
chr2:165886829 | A | C | 390 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(387): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.3459+1450T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886829 | |||||||
chr2:165886830 | G | A | 127 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0053 others(124): Show |
128 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.3459+1449C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886830 | |||||||
chr2:165886865 | T | C | 1 | a0004c0005t0001g0360 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3459+1414A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886865 | |||||||
chr2:165886960 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3459+1319A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165886960 | |||||||
chr2:165887036 | G | A | 1 | a0016c0030t0001g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3459+1243C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887036 | |||||||
chr2:165887060 | A | T | 14 | a0001c0001t0001g0384 a0001c0024t0001g0108 a0004c0005t0001g0263 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.3459+1219T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887060 | |||||||
chr2:165887078 | C | G | 126 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(123): Show |
127 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.3459+1201G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887078 | |||||||
chr2:165887409 | G | C | 1 | a0001c0001t0001g0323 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3459+870C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887409 | |||||||
chr2:165887465 | G | A | 5 | a0001c0001t0001g0095 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3459+814C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887465 | |||||||
chr2:165887468 | C | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
81 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.3459+811G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887468 | |||||||
chr2:165887595 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
157 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.3459+684C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887595 | |||||||
chr2:165887630 | T | G | 1 | a0001c0001t0001g0325 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3459+649A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887630 | |||||||
chr2:165887665 | C | T | 4 | a0001c0001t0001g0167 a0001c0009t0001g0113 a0001c0009t0001g0114 others(1): Show |
4 | HG01891.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3459+614G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887665 | |||||||
chr2:165887670 | A | G | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3459+609T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887670 | |||||||
chr2:165887805 | T | C | 1 | a0002c0002t0004g0075 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3459+474A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887805 | |||||||
chr2:165887812 | A | G | 1 | a0004c0005t0001g0385 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3459+467T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887812 | |||||||
chr2:165887949 | G | C | 4 | a0001c0004t0003g0097 a0001c0004t0003g0098 a0001c0004t0003g0110 others(1): Show |
4 | HG02257.hp2 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3459+330C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165887949 | |||||||
chr2:165888118 | G | A | 1 | a0002c0002t0004g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3459+161C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165888118 | |||||||
chr2:165888125 | A | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3459+154T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 25/28 | chr2 | 165888125 | |||||||
chr2:165888578 | ACT | A | 10 | a0003c0003t0001g0241 a0003c0003t0001g0244 a0003c0003t0001g0246 others(7): Show |
10 | HG00642.hp1 HG01081.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.3264-106_3264-105d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165888578 | |||||||
chr2:165888607 | C | T | 1 | a0001c0001t0001g0384 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3264-133G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165888607 | |||||||
chr2:165888704 | T | C | 57 | a0001c0001t0001g0167 a0001c0001t0002g0002 a0001c0001t0002g0007 others(54): Show |
60 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3264-230A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165888704 | |||||||
chr2:165888820 | C | G | 1 | a0001c0001t0001g0371 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3264-346G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165888820 | |||||||
chr2:165888920 | GGTAAA | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.3264-451_3264-447d others(7): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165888920 | |||||||
chr2:165889016 | TCAC | T | 5 | a0001c0001t0001g0095 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-545_3264-543d others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889016 | |||||||
chr2:165889166 | A | C | 1 | a0001c0001t0001g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3264-692T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889166 | |||||||
chr2:165889222 | A | C | 14 | a0001c0001t0001g0384 a0001c0024t0001g0108 a0004c0005t0001g0263 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.3264-748T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889222 | |||||||
chr2:165889369 | A | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3264-895T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889369 | |||||||
chr2:165889371 | C | A | 7 | a0001c0001t0001g0171 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3264-897G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889371 | |||||||
chr2:165889503 | T | C | 4 | a0001c0001t0001g0342 a0001c0001t0001g0346 a0001c0001t0001g0350 others(1): Show |
4 | NA18951.hp1 NA18959.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.3263+976A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889503 | |||||||
chr2:165889532 | TGAA | T | 28 | a0001c0001t0001g0173 a0001c0001t0001g0229 a0001c0001t0001g0230 others(25): Show |
28 | HG00558.hp2 HG01074.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.3263+944_3263+946d others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889532 | |||||||
chr2:165889554 | A | G | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3263+925T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889554 | |||||||
chr2:165889783 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3263+696A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889783 | |||||||
chr2:165889944 | G | A | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3263+535C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889944 | |||||||
chr2:165889984 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3263+495G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165889984 | |||||||
chr2:165890162 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.3263+317A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 24/28 | chr2 | 165890162 | |||||||
chr2:165890798 | A | G | 9 | a0003c0003t0006g0242 a0003c0003t0006g0243 a0003c0003t0006g0253 others(6): Show |
9 | NA18940.hp1 NA18948.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.3101+40T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 23/28 | chr2 | 165890798 | |||||||
chr2:165891039 | T | C | 1 | a0003c0003t0001g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2951-51A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891039 | |||||||
chr2:165891179 | T | C | 1 | a0016c0030t0001g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2951-191A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891179 | |||||||
chr2:165891207 | T | C | 14 | a0001c0001t0001g0384 a0001c0024t0001g0108 a0004c0005t0001g0263 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2951-219A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891207 | |||||||
chr2:165891261 | C | T | 5 | a0001c0001t0001g0095 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2951-273G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891261 | |||||||
chr2:165891275 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2951-287T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891275 | |||||||
chr2:165891379 | C | T | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2951-391G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891379 | |||||||
chr2:165891550 | C | A | 5 | a0001c0001t0001g0095 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2951-562G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891550 | |||||||
chr2:165891574 | A | AATTC | 8 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0122 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2951-590_2951-587d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891574 | |||||||
chr2:165891574 | AATTC | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0015 others(170): Show |
178 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.2951-590_2951-587d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891574 | |||||||
chr2:165891574 | AATTCATT others(1): Show |
A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(41): Show |
45 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.2951-594_2951-587d others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891574 | |||||||
chr2:165891574 | AATTCATT others(5): Show |
A | 91 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(88): Show |
92 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.2951-598_2951-587d others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891574 | |||||||
chr2:165891663 | T | A | 90 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(87): Show |
91 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.2951-675A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891663 | |||||||
chr2:165891664 | C | G | 90 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(87): Show |
91 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.2951-676G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891664 | |||||||
chr2:165891680 | G | C | 5 | a0001c0001t0001g0095 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2951-692C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891680 | |||||||
chr2:165891685 | C | G | 1 | a0001c0001t0001g0353 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2951-697G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891685 | |||||||
chr2:165891691 | T | C | 1 | a0001c0009t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2951-703A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891691 | |||||||
chr2:165891779 | A | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(81): Show |
85 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.2951-791T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891779 | |||||||
chr2:165891800 | GA | G | 390 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(387): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.2951-813delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891800 | |||||||
chr2:165891967 | T | G | 1 | a0001c0001t0002g0265 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2951-979A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165891967 | |||||||
chr2:165892394 | C | T | 1 | a0004c0005t0001g0385 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2951-1406G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165892394 | |||||||
chr2:165892403 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2951-1415C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165892403 | |||||||
chr2:165892438 | C | G | 390 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(387): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.2951-1450G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165892438 | |||||||
chr2:165892693 | T | C | 57 | a0001c0001t0001g0167 a0001c0001t0002g0002 a0001c0001t0002g0007 others(54): Show |
60 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.2951-1705A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165892693 | |||||||
chr2:165892902 | T | C | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2951-1914A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165892902 | |||||||
chr2:165892914 | G | A | 390 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(387): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.2951-1926C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165892914 | |||||||
chr2:165893359 | G | A | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2951-2371C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165893359 | |||||||
chr2:165893448 | T | C | 3 | a0001c0001t0002g0209 a0001c0001t0002g0212 a0001c0001t0002g0218 |
3 | NA18991.hp1 NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2951-2460A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165893448 | |||||||
chr2:165893516 | A | G | 3 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0279 |
3 | HG02922.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2951-2528T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165893516 | |||||||
chr2:165893572 | T | C | 7 | a0001c0001t0001g0171 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2951-2584A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165893572 | |||||||
chr2:165894129 | G | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2951-3141C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894129 | |||||||
chr2:165894148 | G | A | 1 | a0002c0008t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2951-3160C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894148 | |||||||
chr2:165894154 | C | T | 1 | a0004c0010t0018g0380 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2951-3166G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894154 | |||||||
chr2:165894155 | T | C | 11 | a0001c0001t0001g0173 a0001c0001t0003g0091 a0001c0001t0003g0161 others(8): Show |
11 | HG01255.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2951-3167A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894155 | |||||||
chr2:165894180 | A | C | 8 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2951-3192T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894180 | |||||||
chr2:165894277 | G | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2951-3289C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894277 | |||||||
chr2:165894341 | T | C | 385 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(382): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.2951-3353A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894341 | |||||||
chr2:165894433 | C | T | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0009c0013t0001g0379 |
3 | HG01074.hp2 HG02280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2951-3445G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894433 | |||||||
chr2:165894462 | C | G | 1 | a0001c0001t0001g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2951-3474G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894462 | |||||||
chr2:165894467 | T | C | 5 | a0001c0001t0001g0095 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2951-3479A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894467 | |||||||
chr2:165894617 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2951-3629C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894617 | |||||||
chr2:165894628 | G | A | 2 | a0002c0002t0001g0093 a0002c0002t0010g0094 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2951-3640C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894628 | |||||||
chr2:165894629 | C | A | 2 | a0002c0002t0001g0093 a0002c0002t0010g0094 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2951-3641G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894629 | |||||||
chr2:165894867 | T | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2950+3819A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894867 | |||||||
chr2:165894889 | A | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2950+3797T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894889 | |||||||
chr2:165894908 | A | G | 1 | a0002c0002t0001g0364 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2950+3778T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894908 | |||||||
chr2:165894998 | G | A | 14 | a0001c0001t0001g0384 a0001c0024t0001g0108 a0004c0005t0001g0263 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2950+3688C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165894998 | |||||||
chr2:165895003 | A | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2950+3683T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895003 | |||||||
chr2:165895096 | TC | T | 5 | a0001c0001t0001g0095 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2950+3589delG | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895096 | |||||||
chr2:165895097 | C | T | 5 | a0001c0001t0002g0194 a0001c0001t0002g0201 a0001c0001t0002g0202 others(2): Show |
5 | HG02027.hp1 NA18948.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2950+3589G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895097 | |||||||
chr2:165895218 | C | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
81 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2950+3468G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895218 | |||||||
chr2:165895246 | T | C | 1 | a0001c0001t0002g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2950+3440A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895246 | |||||||
chr2:165895270 | C | A | 57 | a0001c0001t0001g0167 a0001c0001t0002g0002 a0001c0001t0002g0007 others(54): Show |
60 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.2950+3416G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895270 | |||||||
chr2:165895466 | T | TA | 390 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(387): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.2950+3219dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895466 | |||||||
chr2:165895559 | G | C | 1 | a0001c0001t0002g0191 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2950+3127C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895559 | |||||||
chr2:165895628 | T | C | 6 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0280 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2950+3058A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895628 | |||||||
chr2:165895641 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
168 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.2950+3045C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895641 | |||||||
chr2:165895642 | T | C | 1 | a0002c0014t0004g0005 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2950+3044A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895642 | |||||||
chr2:165895922 | A | G | 57 | a0001c0001t0001g0167 a0001c0001t0002g0002 a0001c0001t0002g0007 others(54): Show |
60 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.2950+2764T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895922 | |||||||
chr2:165895971 | C | T | 7 | a0001c0001t0001g0171 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950+2715G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165895971 | |||||||
chr2:165896125 | G | A | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.2950+2561C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896125 | |||||||
chr2:165896127 | G | C | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.2950+2559C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896127 | |||||||
chr2:165896129 | A | AGG | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.2950+2556_2950+255 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896129 | |||||||
chr2:165896132 | G | GCTCTGA | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.2950+2553_2950+255 others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896132 | |||||||
chr2:165896133 | A | C | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.2950+2553T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896133 | |||||||
chr2:165896176 | A | G | 5 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(2): Show |
5 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2950+2510T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896176 | |||||||
chr2:165896424 | C | T | 2 | a0001c0001t0001g0095 a0002c0008t0001g0278 |
2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2950+2262G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896424 | |||||||
chr2:165896425 | G | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2950+2261C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896425 | |||||||
chr2:165896471 | C | T | 1 | a0002c0008t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2950+2215G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896471 | |||||||
chr2:165896550 | TA | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2950+2135delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896550 | |||||||
chr2:165896569 | A | C | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950+2117T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896569 | |||||||
chr2:165896576 | G | T | 5 | a0001c0001t0001g0095 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2950+2110C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896576 | |||||||
chr2:165896606 | C | T | 1 | a0001c0001t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2950+2080G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896606 | |||||||
chr2:165896667 | T | C | 1 | a0002c0002t0004g0361 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2950+2019A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896667 | |||||||
chr2:165896692 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0054 |
2 | NA18977.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2950+1994C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896692 | |||||||
chr2:165896698 | T | C | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950+1988A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896698 | |||||||
chr2:165896714 | A | T | 7 | a0001c0001t0001g0171 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950+1972T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896714 | |||||||
chr2:165896849 | T | C | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950+1837A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896849 | |||||||
chr2:165896859 | C | T | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2950+1827G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165896859 | |||||||
chr2:165897039 | C | G | 1 | a0001c0001t0001g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2950+1647G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897039 | |||||||
chr2:165897158 | C | T | 230 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0045 others(227): Show |
234 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.2950+1528G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897158 | |||||||
chr2:165897270 | G | A | 3 | a0004c0005t0001g0263 a0004c0005t0001g0368 a0004c0005t0001g0385 |
3 | HG01106.hp2 HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2950+1416C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897270 | |||||||
chr2:165897345 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2950+1341A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897345 | |||||||
chr2:165897440 | T | A | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2950+1246A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897440 | |||||||
chr2:165897518 | C | T | 1 | a0001c0001t0011g0072 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2950+1168G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897518 | |||||||
chr2:165897642 | C | T | 175 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(172): Show |
179 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.2950+1044G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897642 | |||||||
chr2:165897750 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2950+936A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897750 | |||||||
chr2:165897843 | C | G | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2950+843G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897843 | |||||||
chr2:165897937 | C | T | 3 | a0001c0001t0002g0209 a0001c0001t0002g0212 a0001c0001t0002g0218 |
3 | NA18991.hp1 NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2950+749G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897937 | |||||||
chr2:165897951 | TG | T | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950+734delC | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897951 | |||||||
chr2:165897962 | G | A | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2950+724C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165897962 | |||||||
chr2:165898043 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2950+643T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165898043 | |||||||
chr2:165898057 | C | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2950+629G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165898057 | |||||||
chr2:165898101 | G | C | 1 | a0001c0001t0002g0195 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2950+585C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165898101 | |||||||
chr2:165898218 | C | T | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | NA18978.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2950+468G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165898218 | |||||||
chr2:165898269 | C | G | 2 | a0002c0002t0001g0133 a0002c0002t0001g0150 |
2 | HG00558.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2950+417G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165898269 | |||||||
chr2:165898434 | T | C | 1 | a0002c0014t0004g0005 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2950+252A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165898434 | |||||||
chr2:165898670 | A | G | 1 | a0001c0001t0005g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2950+16T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 22/28 | chr2 | 165898670 | |||||||
chr2:165898979 | T | C | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2869-212A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 21/28 | chr2 | 165898979 | |||||||
chr2:165899320 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2868+450G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 21/28 | chr2 | 165899320 | |||||||
chr2:165899630 | G | A | 1 | a0004c0005t0001g0368 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2868+140C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 21/28 | chr2 | 165899630 | |||||||
chr2:165899651 | T | G | 2 | a0006c0015t0001g0388 a0006c0015t0001g0389 |
2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2868+119A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 21/28 | chr2 | 165899651 | |||||||
chr2:165899710 | T | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2868+60A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 21/28 | chr2 | 165899710 | |||||||
chr2:165900008 | C | CA | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
126 | HG00140.hp1 HG00423.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.2758-129dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900008 | |||||||
chr2:165900008 | C | CAA | 9 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0037 others(6): Show |
9 | HG00438.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2758-130_2758-129d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900008 | |||||||
chr2:165900022 | A | C | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2758-142T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900022 | |||||||
chr2:165900053 | C | G | 13 | a0001c0024t0001g0108 a0004c0005t0001g0263 a0004c0005t0001g0360 others(10): Show |
13 | HG01106.hp2 HG01261.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2758-173G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900053 | |||||||
chr2:165900064 | G | GA | 178 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(175): Show |
182 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.2758-185dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900064 | |||||||
chr2:165900438 | CACTT | C | 7 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0279 others(4): Show |
7 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2758-562_2758-559d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900438 | |||||||
chr2:165900541 | G | A | 10 | a0001c0024t0001g0108 a0004c0005t0001g0360 a0004c0005t0001g0367 others(7): Show |
10 | HG01261.hp1 HG02257.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.2758-661C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900541 | |||||||
chr2:165900626 | T | G | 14 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0229 others(11): Show |
14 | HG00558.hp2 HG01074.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2758-746A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900626 | |||||||
chr2:165900635 | T | C | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2758-755A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900635 | |||||||
chr2:165900679 | TA | T | 11 | a0001c0001t0001g0173 a0001c0001t0003g0091 a0001c0001t0003g0161 others(8): Show |
11 | HG01255.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2758-800delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900679 | |||||||
chr2:165900753 | T | TTTA | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2758-874_2758-873i others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900753 | |||||||
chr2:165900882 | T | C | 1 | a0001c0001t0003g0160 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2757+840A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900882 | |||||||
chr2:165900904 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18944.hp1 NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2757+807_2757+817d others(13): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165900904 | |||||||
chr2:165901193 | C | T | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2757+529G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165901193 | |||||||
chr2:165901213 | T | C | 1 | a0001c0009t0001g0113 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2757+509A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165901213 | |||||||
chr2:165901320 | T | A | 1 | a0001c0001t0003g0160 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2757+402A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165901320 | |||||||
chr2:165901349 | C | T | 4 | a0001c0001t0002g0228 a0001c0001t0008g0226 a0001c0001t0008g0227 others(1): Show |
4 | HG01109.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2757+373G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165901349 | |||||||
chr2:165901685 | G | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2757+37C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 20/28 | chr2 | 165901685 | |||||||
chr2:165901914 | G | GA | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2569-5dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165901914 | |||||||
chr2:165901937 | TA | T | 40 | a0001c0001t0001g0053 a0002c0002t0001g0123 a0002c0002t0021g0395 others(37): Show |
41 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.2569-28delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165901937 | |||||||
chr2:165901966 | G | A | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-56C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165901966 | |||||||
chr2:165902037 | C | T | 2 | a0002c0002t0007g0128 a0002c0002t0007g0130 |
2 | HG01928.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2569-127G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165902037 | |||||||
chr2:165902076 | A | G | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-166T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165902076 | |||||||
chr2:165902430 | C | T | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2569-520G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165902430 | |||||||
chr2:165902518 | C | CT | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-609dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165902518 | |||||||
chr2:165902618 | T | C | 1 | a0004c0005t0001g0390 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2569-708A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165902618 | |||||||
chr2:165902748 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2569-838T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165902748 | |||||||
chr2:165902749 | C | T | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2569-839G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165902749 | |||||||
chr2:165902750 | A | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-840T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165902750 | |||||||
chr2:165903178 | T | C | 32 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0173 others(29): Show |
32 | HG00558.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.2569-1268A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903178 | |||||||
chr2:165903203 | C | G | 13 | a0001c0024t0001g0108 a0004c0005t0001g0263 a0004c0005t0001g0360 others(10): Show |
13 | HG01106.hp2 HG01261.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2569-1293G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903203 | |||||||
chr2:165903264 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2569-1354C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903264 | |||||||
chr2:165903286 | A | C | 1 | a0001c0001t0001g0292 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2569-1376T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903286 | |||||||
chr2:165903301 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0052 |
2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2569-1391A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903301 | |||||||
chr2:165903453 | C | G | 1 | a0001c0001t0013g0187 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2569-1543G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903453 | |||||||
chr2:165903587 | T | A | 1 | a0001c0001t0001g0284 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2569-1677A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903587 | |||||||
chr2:165903636 | C | T | 2 | a0001c0001t0001g0013 a0009c0013t0001g0379 |
2 | HG02280.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2569-1726G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903636 | |||||||
chr2:165903694 | T | A | 1 | a0001c0001t0001g0028 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2569-1784A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903694 | |||||||
chr2:165903847 | T | G | 119 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(116): Show |
120 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.2569-1937A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903847 | |||||||
chr2:165903848 | G | C | 119 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(116): Show |
120 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.2569-1938C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165903848 | |||||||
chr2:165904009 | T | C | 3 | a0001c0009t0001g0113 a0001c0009t0001g0114 a0001c0009t0001g0115 |
3 | HG01891.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2569-2099A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904009 | |||||||
chr2:165904193 | C | T | 1 | a0001c0001t0003g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2569-2283G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904193 | |||||||
chr2:165904204 | TAGCTTCT others(4): Show |
T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.2569-2305_2569-229 others(15): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904204 | |||||||
chr2:165904211 | T | C | 1 | a0003c0003t0001g0081 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2569-2301A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904211 | |||||||
chr2:165904218 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.2569-2308A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904218 | |||||||
chr2:165904219 | A | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.2569-2309T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904219 | |||||||
chr2:165904225 | T | G | 11 | a0002c0028t0001g0369 a0005c0007t0001g0009 a0005c0007t0001g0085 others(8): Show |
12 | HG01175.hp1 HG01496.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2569-2315A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904225 | |||||||
chr2:165904330 | A | G | 3 | a0001c0001t0002g0007 a0001c0001t0002g0182 a0001c0001t0002g0190 |
4 | HG00639.hp1 HG01099.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2569-2420T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904330 | |||||||
chr2:165904341 | TTAGA | T | 3 | a0001c0001t0008g0224 a0001c0001t0008g0225 a0017c0023t0008g0177 |
3 | HG02451.hp1 HG03486.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2569-2435_2569-243 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904341 | |||||||
chr2:165904352 | T | G | 1 | a0004c0005t0001g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2569-2442A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904352 | |||||||
chr2:165904458 | C | T | 4 | a0005c0007t0001g0085 a0005c0007t0001g0087 a0005c0007t0015g0086 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2569-2548G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904458 | |||||||
chr2:165904623 | T | A | 1 | a0001c0001t0004g0068 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2569-2713A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904623 | |||||||
chr2:165904680 | G | T | 10 | a0001c0001t0003g0091 a0001c0001t0003g0161 a0001c0001t0003g0166 others(7): Show |
10 | HG01255.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2569-2770C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904680 | |||||||
chr2:165904955 | G | A | 2 | a0001c0001t0011g0072 a0001c0001t0011g0073 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2568+2723C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165904955 | |||||||
chr2:165905064 | T | C | 2 | a0004c0010t0003g0387 a0004c0010t0018g0380 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2568+2614A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905064 | |||||||
chr2:165905155 | A | G | 3 | a0001c0001t0001g0341 a0001c0001t0001g0356 a0001c0001t0001g0372 |
3 | NA18979.hp2 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2568+2523T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905155 | |||||||
chr2:165905156 | T | A | 1 | a0004c0005t0001g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2568+2522A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905156 | |||||||
chr2:165905229 | A | G | 1 | a0001c0009t0001g0113 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2568+2449T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905229 | |||||||
chr2:165905383 | T | G | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(173): Show |
180 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.2568+2295A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905383 | |||||||
chr2:165905513 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2568+2165T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905513 | |||||||
chr2:165905701 | A | G | 1 | a0002c0002t0001g0240 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2568+1977T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905701 | |||||||
chr2:165905722 | T | C | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2568+1956A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905722 | |||||||
chr2:165905766 | A | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2568+1912T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905766 | |||||||
chr2:165905866 | TACAGTAA others(8): Show |
T | 87 | a0001c0024t0001g0108 a0002c0002t0001g0006 a0002c0002t0001g0008 others(84): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2568+1797_2568+181 others(19): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905866 | |||||||
chr2:165905915 | C | T | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2568+1763G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165905915 | |||||||
chr2:165906030 | T | C | 1 | a0003c0003t0006g0262 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2568+1648A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906030 | |||||||
chr2:165906207 | A | G | 1 | a0011c0026t0001g0302 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2568+1471T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906207 | |||||||
chr2:165906254 | T | TA | 79 | a0001c0001t0001g0321 a0001c0001t0001g0333 a0001c0001t0002g0203 others(76): Show |
82 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2568+1423dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906254 | |||||||
chr2:165906254 | T | TAA | 36 | a0001c0001t0001g0053 a0002c0002t0001g0132 a0002c0002t0001g0134 others(33): Show |
37 | HG00423.hp2 HG00642.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.2568+1422_2568+142 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906254 | |||||||
chr2:165906254 | TA | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
76 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2568+1423delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906254 | |||||||
chr2:165906254 | TAA | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0061 others(6): Show |
9 | HG01074.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2568+1422_2568+142 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906254 | |||||||
chr2:165906255 | A | T | 1 | a0002c0002t0007g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2568+1423T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906255 | |||||||
chr2:165906360 | G | C | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2568+1318C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906360 | |||||||
chr2:165906404 | G | A | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2568+1274C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906404 | |||||||
chr2:165906410 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2568+1268A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906410 | |||||||
chr2:165906633 | A | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2568+1045T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906633 | |||||||
chr2:165906696 | G | A | 4 | a0005c0007t0001g0085 a0005c0007t0001g0087 a0005c0007t0015g0086 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2568+982C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906696 | |||||||
chr2:165906697 | C | A | 4 | a0005c0007t0001g0085 a0005c0007t0001g0087 a0005c0007t0015g0086 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2568+981G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906697 | |||||||
chr2:165906911 | T | C | 392 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(389): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.2568+767A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906911 | |||||||
chr2:165906955 | C | CA | 9 | a0001c0001t0001g0287 a0001c0001t0001g0357 a0001c0009t0001g0113 others(6): Show |
9 | HG01891.hp2 HG02723.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2568+722dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906955 | |||||||
chr2:165906955 | CA | C | 81 | a0001c0001t0001g0041 a0001c0001t0001g0067 a0001c0001t0001g0088 others(78): Show |
84 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.2568+722delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906955 | |||||||
chr2:165906955 | CAAAA | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2568+719_2568+722d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906955 | |||||||
chr2:165906973 | A | G | 1 | a0002c0002t0001g0116 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2568+705T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906973 | |||||||
chr2:165906974 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
85 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.2568+704T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165906974 | |||||||
chr2:165907208 | T | C | 2 | a0002c0002t0001g0131 a0002c0002t0001g0147 |
2 | NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2568+470A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165907208 | |||||||
chr2:165907479 | C | T | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2568+199G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165907479 | |||||||
chr2:165907610 | T | C | 3 | a0001c0001t0001g0341 a0001c0001t0001g0356 a0001c0001t0001g0372 |
3 | NA18979.hp2 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2568+68A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 19/28 | chr2 | 165907610 | |||||||
chr2:165907803 | T | G | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2462-19A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165907803 | |||||||
chr2:165907943 | TA | T | 89 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0035 others(86): Show |
90 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.2462-160delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165907943 | |||||||
chr2:165908042 | T | C | 3 | a0002c0002t0001g0008 a0002c0002t0001g0239 a0002c0002t0017g0238 |
4 | HG00099.hp2 HG01106.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.2462-258A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908042 | |||||||
chr2:165908088 | T | C | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(173): Show |
180 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.2462-304A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908088 | |||||||
chr2:165908141 | T | G | 1 | a0001c0024t0001g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2462-357A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908141 | |||||||
chr2:165908170 | T | C | 3 | a0001c0001t0001g0235 a0001c0001t0003g0160 a0001c0001t0019g0236 |
3 | HG00558.hp2 HG02071.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2462-386A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908170 | |||||||
chr2:165908321 | T | C | 1 | a0002c0002t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2462-537A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908321 | |||||||
chr2:165908451 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2462-667A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908451 | |||||||
chr2:165908507 | A | G | 13 | a0001c0024t0001g0108 a0004c0005t0001g0263 a0004c0005t0001g0360 others(10): Show |
13 | HG01106.hp2 HG01261.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2462-723T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908507 | |||||||
chr2:165908688 | G | A | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2462-904C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908688 | |||||||
chr2:165908919 | C | T | 87 | a0001c0024t0001g0108 a0002c0002t0001g0006 a0002c0002t0001g0008 others(84): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2462-1135G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165908919 | |||||||
chr2:165909150 | A | C | 1 | a0001c0001t0002g0057 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2462-1366T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165909150 | |||||||
chr2:165909452 | G | A | 4 | a0001c0001t0002g0228 a0001c0001t0008g0226 a0001c0001t0008g0227 others(1): Show |
4 | HG01109.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2462-1668C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165909452 | |||||||
chr2:165909822 | G | A | 90 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(87): Show |
91 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.2461+1505C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165909822 | |||||||
chr2:165909833 | A | G | 10 | a0001c0001t0003g0091 a0001c0001t0003g0161 a0001c0001t0003g0166 others(7): Show |
10 | HG01255.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2461+1494T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165909833 | |||||||
chr2:165909970 | T | C | 3 | a0001c0001t0001g0294 a0001c0001t0001g0318 a0001c0001t0001g0320 |
3 | HG00738.hp2 HG00741.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2461+1357A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165909970 | |||||||
chr2:165910200 | G | A | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2461+1127C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910200 | |||||||
chr2:165910260 | G | A | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2461+1067C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910260 | |||||||
chr2:165910286 | C | T | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2461+1041G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910286 | |||||||
chr2:165910382 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2461+945T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910382 | |||||||
chr2:165910530 | A | G | 32 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0173 others(29): Show |
32 | HG00558.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.2461+797T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910530 | |||||||
chr2:165910531 | T | G | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2461+796A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910531 | |||||||
chr2:165910562 | T | C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2461+765A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910562 | |||||||
chr2:165910804 | T | C | 3 | a0005c0007t0001g0085 a0005c0007t0001g0087 a0015c0016t0001g0084 |
3 | HG02486.hp2 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2461+523A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910804 | |||||||
chr2:165910808 | G | GA | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(173): Show |
180 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.2461+518dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910808 | |||||||
chr2:165910871 | T | C | 1 | a0002c0002t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2461+456A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165910871 | |||||||
chr2:165911004 | AAAG | A | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2461+320_2461+322d others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165911004 | |||||||
chr2:165911060 | G | A | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461+267C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165911060 | |||||||
chr2:165911204 | C | T | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2461+123G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165911204 | |||||||
chr2:165911263 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2461+64C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 18/28 | chr2 | 165911263 | |||||||
chr2:165911582 | T | C | 13 | a0001c0024t0001g0108 a0004c0005t0001g0263 a0004c0005t0001g0360 others(10): Show |
13 | HG01106.hp2 HG01261.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2323-117A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911582 | |||||||
chr2:165911608 | T | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2323-143A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911608 | |||||||
chr2:165911655 | AAT | A | 4 | a0005c0007t0001g0085 a0005c0007t0001g0087 a0005c0007t0015g0086 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2323-192_2323-191d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911655 | |||||||
chr2:165911665 | TA | T | 3 | a0002c0002t0004g0144 a0005c0007t0001g0009 a0016c0030t0001g0274 |
4 | HG01496.hp1 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2323-201delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911665 | |||||||
chr2:165911666 | A | T | 70 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(67): Show |
73 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2323-201T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911666 | |||||||
chr2:165911668 | A | AT | 18 | a0001c0001t0001g0063 a0001c0001t0001g0284 a0001c0001t0001g0285 others(15): Show |
18 | HG01168.hp2 HG01192.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2323-204dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911668 | |||||||
chr2:165911668 | A | T | 98 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(95): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.2323-203T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911668 | |||||||
chr2:165911669 | T | TA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.2323-205_2323-204i others(3): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911669 | |||||||
chr2:165911670 | T | A | 42 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0173 others(39): Show |
42 | HG00558.hp2 HG00735.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.2323-205A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911670 | |||||||
chr2:165911671 | T | A | 4 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0279 others(1): Show |
4 | HG02922.hp1 HG03041.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2323-206A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911671 | |||||||
chr2:165911672 | T | A | 12 | a0001c0001t0001g0173 a0001c0001t0001g0384 a0001c0001t0003g0091 others(9): Show |
12 | HG00735.hp2 HG01255.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2323-207A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911672 | |||||||
chr2:165911700 | T | C | 1 | a0001c0006t0001g0305 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2323-235A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911700 | |||||||
chr2:165911753 | T | C | 392 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(389): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.2323-288A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911753 | |||||||
chr2:165911846 | G | A | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2323-381C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165911846 | |||||||
chr2:165912015 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18944.hp1 NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2322+499C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165912015 | |||||||
chr2:165912207 | G | C | 2 | a0005c0007t0001g0087 a0015c0016t0001g0084 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2322+307C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165912207 | |||||||
chr2:165912298 | G | A | 5 | a0003c0003t0001g0077 a0003c0003t0001g0078 a0003c0003t0001g0079 others(2): Show |
5 | HG00423.hp1 HG02056.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.2322+216C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165912298 | |||||||
chr2:165912349 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2322+165C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165912349 | |||||||
chr2:165912511 | T | C | 5 | a0003c0003t0001g0077 a0003c0003t0001g0078 a0003c0003t0001g0079 others(2): Show |
5 | HG00423.hp1 HG02056.hp1 NA18956.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2322+3A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 17/28 | chr2 | 165912511 | |||||||
chr2:165912930 | T | C | 3 | a0003c0003t0001g0077 a0003c0003t0001g0078 a0003c0003t0001g0079 |
3 | HG02056.hp1 NA18956.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2212-306A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165912930 | |||||||
chr2:165913044 | A | AT | 93 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0182 others(90): Show |
97 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.2212-421dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913044 | |||||||
chr2:165913185 | G | GGGCTAAT others(206): Show |
1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+388_2211+389i others(215): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913185 | |||||||
chr2:165913206 | T | A | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+368A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913206 | |||||||
chr2:165913226 | A | G | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+348T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913226 | |||||||
chr2:165913231 | G | A | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+343C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913231 | |||||||
chr2:165913238 | C | A | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+336G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913238 | |||||||
chr2:165913245 | T | C | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+329A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913245 | |||||||
chr2:165913248 | A | T | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+326T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913248 | |||||||
chr2:165913252 | T | C | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+322A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913252 | |||||||
chr2:165913256 | T | C | 1 | a0005c0007t0015g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211+318A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913256 | |||||||
chr2:165913315 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2211+259G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913315 | |||||||
chr2:165913439 | A | C | 3 | a0005c0007t0001g0085 a0005c0007t0001g0087 a0015c0016t0001g0084 |
3 | HG02486.hp2 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2211+135T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913439 | |||||||
chr2:165913561 | T | C | 13 | a0001c0024t0001g0108 a0004c0005t0001g0263 a0004c0005t0001g0360 others(10): Show |
13 | HG01106.hp2 HG01261.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2211+13A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 16/28 | chr2 | 165913561 | |||||||
chr2:165913808 | C | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2139-162G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165913808 | |||||||
chr2:165914227 | G | C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2139-581C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914227 | |||||||
chr2:165914236 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2139-590A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914236 | |||||||
chr2:165914324 | T | C | 3 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0279 |
3 | HG02922.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2139-678A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914324 | |||||||
chr2:165914653 | C | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2138+548G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914653 | |||||||
chr2:165914654 | A | AGTGTGTG others(17): Show |
1 | a0002c0002t0001g0132 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2138+546_2138+547i others(26): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914654 | |||||||
chr2:165914655 | A | ATGTGTGT others(3): Show |
1 | a0002c0002t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2138+545_2138+546i others(12): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(5): Show |
3 | a0002c0002t0004g0138 a0002c0002t0004g0270 a0002c0002t0004g0273 |
3 | HG00323.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2138+545_2138+546i others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(7): Show |
3 | a0002c0002t0001g0124 a0002c0002t0001g0143 a0002c0002t0004g0127 |
3 | HG01257.hp1 HG01978.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2138+545_2138+546i others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(9): Show |
9 | a0002c0002t0001g0123 a0002c0002t0001g0137 a0002c0002t0001g0232 others(6): Show |
9 | HG01346.hp2 HG02074.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.2138+545_2138+546i others(18): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(11): Show |
2 | a0002c0002t0001g0364 a0002c0002t0004g0075 |
2 | HG02135.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2138+545_2138+546i others(20): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(13): Show |
12 | a0002c0002t0001g0147 a0002c0002t0001g0150 a0002c0002t0001g0231 others(9): Show |
12 | HG00140.hp2 HG00558.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2138+545_2138+546i others(22): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(15): Show |
19 | a0002c0002t0001g0006 a0002c0002t0001g0116 a0002c0002t0001g0118 others(16): Show |
21 | HG00423.hp2 HG00673.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.2138+545_2138+546i others(24): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(17): Show |
11 | a0002c0002t0001g0131 a0002c0002t0001g0136 a0002c0002t0001g0151 others(8): Show |
11 | HG00438.hp1 HG01106.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.2138+545_2138+546i others(26): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(19): Show |
3 | a0002c0002t0001g0008 a0002c0002t0001g0155 a0002c0002t0009g0392 |
4 | HG03490.hp2 HG03492.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.2138+545_2138+546i others(28): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(21): Show |
2 | a0002c0002t0001g0148 a0002c0002t0004g0362 |
2 | HG01243.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2138+545_2138+546i others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(25): Show |
2 | a0002c0002t0001g0157 a0002c0002t0007g0145 |
2 | NA18947.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2138+545_2138+546i others(34): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(27): Show |
1 | a0002c0002t0001g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2138+545_2138+546i others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | ATGTGTGT others(29): Show |
1 | a0002c0002t0001g0156 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2138+545_2138+546i others(38): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914655 | A | G | 1 | a0002c0002t0001g0132 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2138+546T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914655 | |||||||
chr2:165914657 | C | CTG | 32 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0182 others(29): Show |
35 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.2138+542_2138+543d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTG | 12 | a0001c0001t0002g0188 a0001c0001t0002g0191 a0001c0001t0002g0193 others(9): Show |
12 | HG00609.hp2 HG02040.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2138+540_2138+543d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTG | 3 | a0001c0001t0002g0228 a0001c0001t0008g0227 a0019c0020t0002g0184 |
3 | HG01123.hp1 NA19004.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2138+538_2138+543d others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0347 a0001c0001t0008g0226 a0001c0001t0008g0269 |
3 | HG01109.hp1 HG01175.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.2138+534_2138+543d others(12): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(7): Show |
1 | a0001c0001t0003g0181 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2138+530_2138+543d others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(9): Show |
6 | a0001c0001t0001g0230 a0001c0001t0001g0371 a0001c0001t0003g0160 others(3): Show |
6 | HG00558.hp2 HG02976.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.2138+528_2138+543d others(18): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(11): Show |
6 | a0001c0001t0001g0173 a0001c0001t0001g0229 a0001c0001t0001g0339 others(3): Show |
6 | HG01074.hp2 HG01255.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.2138+526_2138+543d others(20): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(13): Show |
17 | a0001c0001t0001g0012 a0001c0001t0001g0295 a0001c0001t0001g0313 others(14): Show |
17 | HG00741.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.2138+524_2138+543d others(22): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(15): Show |
22 | a0001c0001t0001g0167 a0001c0001t0001g0284 a0001c0001t0001g0297 others(19): Show |
22 | HG00423.hp1 HG01081.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.2138+522_2138+543d others(24): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(17): Show |
31 | a0001c0001t0001g0235 a0001c0001t0001g0285 a0001c0001t0001g0291 others(28): Show |
31 | HG00673.hp2 HG00738.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.2138+520_2138+543d others(26): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(19): Show |
17 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0298 others(14): Show |
17 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2138+518_2138+543d others(28): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(21): Show |
15 | a0001c0001t0001g0171 a0001c0001t0001g0287 a0001c0001t0001g0289 others(12): Show |
15 | HG01255.hp2 HG02280.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.2138+516_2138+543d others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(23): Show |
8 | a0001c0001t0001g0010 a0001c0001t0001g0326 a0001c0001t0001g0332 others(5): Show |
9 | HG01099.hp1 HG01261.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.2138+514_2138+543d others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(25): Show |
13 | a0001c0001t0001g0288 a0001c0001t0001g0316 a0001c0001t0001g0324 others(10): Show |
13 | HG00323.hp1 HG01243.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2138+512_2138+543d others(34): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(27): Show |
6 | a0001c0001t0001g0090 a0001c0001t0001g0286 a0001c0001t0001g0290 others(3): Show |
6 | HG00642.hp2 HG01168.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2138+510_2138+543d others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTGTGTGT others(29): Show |
2 | a0001c0001t0001g0322 a0001c0001t0003g0176 |
2 | HG00544.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.2138+508_2138+543d others(38): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | CTTGTGTG others(20): Show |
1 | a0001c0001t0001g0358 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2138+543_2138+544i others(29): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | C | G | 73 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(70): Show |
76 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.2138+544G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914657 | CTGTGTG | C | 3 | a0001c0001t0002g0209 a0001c0001t0002g0212 a0001c0001t0002g0218 |
3 | NA18991.hp1 NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2138+538_2138+543d others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914657 | |||||||
chr2:165914676 | T | TGTGTGTG others(21): Show |
1 | a0005c0007t0001g0009 | 2 | HG01496.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2138+524_2138+525i others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914676 | |||||||
chr2:165914676 | T | TGTGTGTG others(23): Show |
3 | a0005c0007t0001g0087 a0015c0016t0001g0084 a0016c0030t0001g0274 |
3 | HG02622.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2138+524_2138+525i others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914676 | |||||||
chr2:165914676 | T | TGTGTGTG others(27): Show |
2 | a0005c0007t0001g0085 a0005c0007t0015g0086 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2138+524_2138+525i others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914676 | |||||||
chr2:165914678 | T | TGTGTGTG others(21): Show |
1 | a0001c0001t0001g0384 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2138+522_2138+523i others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914678 | |||||||
chr2:165914678 | T | TGTGTGTG others(23): Show |
1 | a0001c0001t0001g0280 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2138+522_2138+523i others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914678 | |||||||
chr2:165914678 | T | TGTGTGTG others(31): Show |
1 | a0001c0001t0001g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2138+522_2138+523i others(40): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914678 | |||||||
chr2:165914678 | T | TGTGTGTG others(33): Show |
1 | a0001c0001t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2138+522_2138+523i others(42): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914678 | |||||||
chr2:165914680 | T | TGTGTGTG others(21): Show |
1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2138+520_2138+521i others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914680 | T | TGTGTGTG others(21): Show |
2 | a0001c0001t0005g0066 a0001c0004t0001g0268 |
2 | HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2138+520_2138+521i others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914680 | T | TGTGTGTG others(23): Show |
10 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0005g0038 others(7): Show |
10 | HG02647.hp1 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2138+520_2138+521i others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914680 | T | TGTGTGTG others(25): Show |
10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0048 others(7): Show |
10 | HG00609.hp1 HG00741.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2138+520_2138+521i others(34): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914680 | T | TGTGTGTG others(27): Show |
39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(36): Show |
41 | HG00140.hp1 HG00438.hp2 HG02027.hp2 others(38): Show |
intron_variant | MODIFIER | c.2138+520_2138+521i others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914680 | T | TGTGTGTG others(27): Show |
1 | a0021c0025t0004g0058 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2138+520_2138+521i others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914680 | T | TGTGTGTG others(29): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0021 others(14): Show |
19 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.2138+520_2138+521i others(38): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914680 | T | TGTGTGTG others(31): Show |
3 | a0001c0001t0001g0044 a0007c0012t0001g0374 a0007c0012t0005g0375 |
3 | HG01891.hp1 HG03471.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2138+520_2138+521i others(40): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914680 | T | TGTGTGTG others(33): Show |
1 | a0001c0001t0001g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2138+520_2138+521i others(42): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914680 | |||||||
chr2:165914682 | T | TGTGTGTG others(21): Show |
1 | a0001c0001t0011g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2138+518_2138+519i others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914682 | |||||||
chr2:165914682 | T | TGTGTGTG others(25): Show |
1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2138+518_2138+519i others(34): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914682 | |||||||
chr2:165914682 | T | TGTGTGTG others(29): Show |
1 | a0006c0015t0001g0388 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2138+518_2138+519i others(38): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914682 | |||||||
chr2:165914682 | T | TGTGTGTG others(35): Show |
1 | a0006c0015t0001g0389 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2138+518_2138+519i others(44): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914682 | |||||||
chr2:165914682 | T | TGTGTGTG others(31): Show |
1 | a0009c0013t0001g0378 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2138+518_2138+519i others(40): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914682 | |||||||
chr2:165914691 | G | GTGTGTGT others(19): Show |
1 | a0004c0005t0001g0368 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2138+509_2138+510i others(28): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914691 | |||||||
chr2:165914691 | G | GTGTGTGT others(23): Show |
3 | a0001c0024t0001g0108 a0004c0005t0001g0385 a0014c0018t0016g0100 |
3 | HG02630.hp1 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2138+509_2138+510i others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914691 | |||||||
chr2:165914691 | G | GTGTGTGT others(25): Show |
1 | a0004c0005t0001g0367 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2138+509_2138+510i others(34): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914691 | |||||||
chr2:165914691 | G | GTGTGTGT others(27): Show |
4 | a0004c0005t0001g0263 a0004c0005t0001g0360 a0004c0005t0001g0381 others(1): Show |
4 | HG01261.hp1 HG02055.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2138+509_2138+510i others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914691 | |||||||
chr2:165914691 | G | GTGTGTGT others(31): Show |
3 | a0004c0005t0001g0382 a0004c0005t0001g0383 a0004c0005t0001g0390 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2138+509_2138+510i others(40): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914691 | |||||||
chr2:165914691 | G | GTGTGTGT others(41): Show |
1 | a0004c0005t0001g0391 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2138+509_2138+510i others(50): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914691 | |||||||
chr2:165914698 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0001g0340 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2138+502_2138+503i others(15): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914698 | |||||||
chr2:165914698 | T | TGTGTGTG others(20): Show |
1 | a0003c0003t0006g0243 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2138+502_2138+503i others(29): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914698 | |||||||
chr2:165914698 | T | TGTGTGTG others(22): Show |
1 | a0001c0001t0001g0334 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2138+502_2138+503i others(31): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914698 | |||||||
chr2:165914708 | C | T | 2 | a0009c0013t0001g0378 a0009c0013t0001g0379 |
2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2138+493G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914708 | |||||||
chr2:165914791 | A | G | 1 | a0001c0001t0020g0014 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2138+410T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914791 | |||||||
chr2:165914837 | G | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2138+364C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914837 | |||||||
chr2:165914865 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2138+336T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914865 | |||||||
chr2:165914871 | T | C | 392 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(389): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.2138+330A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165914871 | |||||||
chr2:165915092 | C | T | 1 | a0001c0001t0001g0384 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2138+109G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165915092 | |||||||
chr2:165915153 | C | T | 132 | a0001c0024t0001g0108 a0002c0002t0001g0006 a0002c0002t0001g0008 others(129): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.2138+48G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 15/28 | chr2 | 165915153 | |||||||
chr2:165915564 | T | C | 11 | a0001c0001t0001g0173 a0001c0001t0003g0091 a0001c0001t0003g0161 others(8): Show |
11 | HG01255.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1900-125A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165915564 | |||||||
chr2:165915616 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0019g0236 |
2 | HG02071.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1900-177T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165915616 | |||||||
chr2:165915790 | C | A | 1 | a0002c0002t0004g0075 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1900-351G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165915790 | |||||||
chr2:165916070 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1900-631G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916070 | |||||||
chr2:165916075 | T | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1900-636A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916075 | |||||||
chr2:165916075 | T | G | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1900-636A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916075 | |||||||
chr2:165916100 | T | C | 1 | a0002c0002t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1900-661A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916100 | |||||||
chr2:165916230 | G | A | 4 | a0001c0001t0004g0059 a0001c0001t0004g0060 a0001c0001t0004g0068 others(1): Show |
4 | NA18980.hp1 NA18983.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1900-791C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916230 | |||||||
chr2:165916231 | C | T | 2 | a0004c0005t0001g0368 a0004c0005t0001g0385 |
2 | HG01106.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1900-792G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916231 | |||||||
chr2:165916355 | A | T | 1 | a0003c0003t0001g0079 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1899+902T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916355 | |||||||
chr2:165916459 | G | A | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG01257.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1899+798C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916459 | |||||||
chr2:165916539 | G | T | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1899+718C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916539 | |||||||
chr2:165916622 | T | G | 102 | a0001c0024t0001g0108 a0002c0002t0001g0006 a0002c0002t0001g0008 others(99): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1899+635A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916622 | |||||||
chr2:165916730 | C | T | 1 | a0001c0001t0001g0384 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1899+527G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916730 | |||||||
chr2:165916824 | T | C | 2 | a0001c0001t0002g0193 a0001c0001t0002g0195 |
2 | NA18974.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1899+433A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916824 | |||||||
chr2:165916841 | T | C | 1 | a0002c0002t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1899+416A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916841 | |||||||
chr2:165916945 | C | T | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1899+312G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 14/28 | chr2 | 165916945 | |||||||
chr2:165917578 | A | G | 1 | a0002c0002t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1675-97T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165917578 | |||||||
chr2:165917591 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1675-110A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165917591 | |||||||
chr2:165917979 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0035 others(1): Show |
5 | NA18962.hp2 NA18973.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1675-498G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165917979 | |||||||
chr2:165918001 | C | T | 2 | a0001c0001t0003g0082 a0001c0001t0003g0083 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1675-520G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918001 | |||||||
chr2:165918009 | A | G | 1 | a0004c0005t0001g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1675-528T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918009 | |||||||
chr2:165918070 | C | A | 8 | a0002c0002t0001g0006 a0002c0002t0001g0151 a0002c0002t0001g0152 others(5): Show |
9 | NA18975.hp2 NA18988.hp2 NA19007.hp1 others(6): Show |
intron_variant | MODIFIER | c.1675-589G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918070 | |||||||
chr2:165918122 | G | C | 1 | a0002c0008t0001g0278 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1675-641C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918122 | |||||||
chr2:165918150 | C | A | 2 | a0002c0002t0001g0120 a0002c0002t0001g0148 |
2 | HG01243.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1675-669G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918150 | |||||||
chr2:165918171 | G | A | 1 | a0002c0002t0004g0139 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1675-690C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918171 | |||||||
chr2:165918193 | C | T | 1 | a0002c0002t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1675-712G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918193 | |||||||
chr2:165918290 | A | G | 1 | a0001c0001t0011g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1675-809T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918290 | |||||||
chr2:165918464 | T | A | 3 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | NA18942.hp2 NA18987.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1674+812A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918464 | |||||||
chr2:165918485 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1674+791G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918485 | |||||||
chr2:165918627 | A | C | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1674+649T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918627 | |||||||
chr2:165918648 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1674+628T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918648 | |||||||
chr2:165918776 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1674+500A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918776 | |||||||
chr2:165918810 | C | T | 1 | a0001c0004t0003g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1674+466G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918810 | |||||||
chr2:165918900 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1674+376G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918900 | |||||||
chr2:165918994 | C | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674+282G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 13/28 | chr2 | 165918994 | |||||||
chr2:165919503 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1517-70T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165919503 | |||||||
chr2:165919768 | T | C | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-335A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165919768 | |||||||
chr2:165919816 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1517-383A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165919816 | |||||||
chr2:165919841 | G | T | 1 | a0004c0005t0001g0360 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1517-408C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165919841 | |||||||
chr2:165919842 | A | G | 87 | a0001c0024t0001g0108 a0002c0002t0001g0006 a0002c0002t0001g0008 others(84): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1517-409T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165919842 | |||||||
chr2:165919992 | T | C | 2 | a0001c0001t0001g0056 a0004c0010t0018g0380 |
2 | NA19062.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1517-559A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165919992 | |||||||
chr2:165920046 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1517-613A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920046 | |||||||
chr2:165920078 | T | TG | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-646_1517-645i others(3): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920078 | |||||||
chr2:165920146 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1517-713G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920146 | |||||||
chr2:165920216 | T | C | 2 | a0001c0006t0001g0306 a0001c0006t0001g0307 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1517-783A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920216 | |||||||
chr2:165920334 | G | C | 87 | a0001c0024t0001g0108 a0002c0002t0001g0006 a0002c0002t0001g0008 others(84): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1517-901C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920334 | |||||||
chr2:165920374 | A | T | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1517-941T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920374 | |||||||
chr2:165920502 | A | G | 4 | a0002c0002t0007g0140 a0002c0002t0007g0141 a0002c0002t0007g0142 others(1): Show |
4 | NA18941.hp1 NA18947.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517-1069T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920502 | |||||||
chr2:165920565 | T | C | 17 | a0001c0004t0001g0103 a0001c0004t0001g0105 a0001c0004t0001g0106 others(14): Show |
17 | HG01175.hp1 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517-1132A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920565 | |||||||
chr2:165920609 | G | A | 87 | a0001c0024t0001g0108 a0002c0002t0001g0006 a0002c0002t0001g0008 others(84): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1517-1176C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920609 | |||||||
chr2:165920617 | A | G | 1 | a0002c0002t0007g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1517-1184T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920617 | |||||||
chr2:165920622 | A | G | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1517-1189T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920622 | |||||||
chr2:165920631 | A | C | 1 | a0002c0002t0004g0361 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1517-1198T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920631 | |||||||
chr2:165920676 | G | A | 1 | a0009c0013t0001g0378 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1517-1243C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920676 | |||||||
chr2:165920701 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1517-1268A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920701 | |||||||
chr2:165920703 | G | C | 1 | a0001c0001t0001g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1517-1270C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920703 | |||||||
chr2:165920745 | C | CTAAATAT others(21): Show |
119 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(116): Show |
123 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1517-1340_1517-131 others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920745 | |||||||
chr2:165920745 | C | CTAAATAT others(49): Show |
29 | a0001c0001t0001g0173 a0001c0001t0001g0318 a0001c0001t0001g0339 others(26): Show |
29 | HG00673.hp2 HG00738.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1517-1313_1517-131 others(60): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920745 | |||||||
chr2:165920745 | C | CTAAATAT others(77): Show |
23 | a0001c0001t0001g0171 a0001c0001t0001g0229 a0001c0001t0001g0230 others(20): Show |
23 | HG00558.hp2 HG01074.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1517-1313_1517-131 others(88): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920745 | |||||||
chr2:165920745 | C | CTAAATAT others(105): Show |
2 | a0001c0001t0001g0167 a0001c0001t0003g0164 |
2 | HG03139.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1517-1313_1517-131 others(116): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920745 | |||||||
chr2:165920745 | CTAAATAT others(21): Show |
C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1517-1340_1517-131 others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920745 | |||||||
chr2:165920872 | C | A | 1 | a0001c0001t0001g0310 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1517-1439G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165920872 | |||||||
chr2:165921006 | A | C | 1 | a0001c0001t0001g0004 | 2 | NA19007.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1517-1573T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921006 | |||||||
chr2:165921148 | C | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1517-1715G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921148 | |||||||
chr2:165921172 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1517-1739G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921172 | |||||||
chr2:165921216 | G | A | 2 | a0001c0004t0001g0106 a0001c0004t0001g0268 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1517-1783C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921216 | |||||||
chr2:165921229 | T | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1517-1796A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921229 | |||||||
chr2:165921247 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1517-1814G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921247 | |||||||
chr2:165921452 | T | C | 1 | a0001c0001t0001g0384 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1517-2019A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921452 | |||||||
chr2:165921482 | T | C | 5 | a0003c0003t0001g0077 a0003c0003t0001g0078 a0003c0003t0001g0079 others(2): Show |
5 | HG00423.hp1 HG02056.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517-2049A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921482 | |||||||
chr2:165921502 | G | A | 1 | a0001c0001t0003g0172 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1517-2069C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921502 | |||||||
chr2:165921628 | A | T | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-2195T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921628 | |||||||
chr2:165921669 | G | C | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-2236C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921669 | |||||||
chr2:165921788 | C | CT | 20 | a0001c0001t0001g0171 a0001c0004t0001g0103 a0001c0004t0001g0105 others(17): Show |
21 | HG02257.hp2 HG02559.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.1517-2356dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921788 | |||||||
chr2:165921788 | C | CTTT | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1517-2358_1517-235 others(7): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921788 | |||||||
chr2:165921788 | CT | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0303 a0001c0001t0002g0365 others(3): Show |
6 | HG01496.hp2 HG03041.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1517-2356delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921788 | |||||||
chr2:165921826 | T | C | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1517-2393A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921826 | |||||||
chr2:165921864 | G | A | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-2431C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921864 | |||||||
chr2:165921965 | C | A | 1 | a0002c0002t0007g0130 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1517-2532G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165921965 | |||||||
chr2:165922009 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 |
3 | NA19064.hp1 NA19065.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1516+2540A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165922009 | |||||||
chr2:165922023 | C | T | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.1516+2526G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165922023 | |||||||
chr2:165922482 | C | T | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1516+2067G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165922482 | |||||||
chr2:165922566 | C | CA | 206 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0031 others(203): Show |
210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1516+1982dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165922566 | |||||||
chr2:165922566 | C | CAA | 27 | a0001c0001t0001g0061 a0001c0001t0001g0167 a0001c0001t0001g0171 others(24): Show |
27 | HG00558.hp2 HG01074.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1516+1981_1516+198 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165922566 | |||||||
chr2:165922667 | T | C | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1516+1882A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165922667 | |||||||
chr2:165922837 | C | T | 4 | a0001c0001t0002g0200 a0001c0001t0002g0207 a0001c0001t0002g0208 others(1): Show |
4 | NA18747.hp2 NA18950.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+1712G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165922837 | |||||||
chr2:165922913 | G | A | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1516+1636C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165922913 | |||||||
chr2:165923130 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1516+1419C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923130 | |||||||
chr2:165923186 | T | A | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1516+1363A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923186 | |||||||
chr2:165923236 | A | T | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1516+1313T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923236 | |||||||
chr2:165923271 | A | C | 1 | a0001c0001t0001g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1516+1278T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923271 | |||||||
chr2:165923442 | C | CT | 11 | a0001c0001t0002g0201 a0001c0001t0002g0206 a0001c0001t0002g0218 others(8): Show |
11 | HG01070.hp2 HG01891.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+1106dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923442 | |||||||
chr2:165923452 | T | G | 3 | a0001c0001t0011g0072 a0001c0001t0011g0073 a0001c0001t0011g0279 |
3 | HG02922.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1516+1097A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923452 | |||||||
chr2:165923453 | T | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
61 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1516+1096A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923453 | |||||||
chr2:165923457 | T | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
73 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1516+1092A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923457 | |||||||
chr2:165923569 | C | T | 13 | a0001c0024t0001g0108 a0004c0005t0001g0263 a0004c0005t0001g0360 others(10): Show |
13 | HG01106.hp2 HG01261.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1516+980G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923569 | |||||||
chr2:165923580 | G | T | 1 | a0001c0001t0001g0313 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1516+969C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923580 | |||||||
chr2:165923616 | T | TTG | 379 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(376): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1516+931_1516+932d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923616 | |||||||
chr2:165923743 | G | GT | 16 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(13): Show |
16 | HG00423.hp1 HG00544.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1516+805dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923743 | |||||||
chr2:165923743 | G | GTT | 49 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0182 others(46): Show |
52 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1516+804_1516+805d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923743 | |||||||
chr2:165923743 | G | GTTT | 100 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(97): Show |
101 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1516+803_1516+805d others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923743 | |||||||
chr2:165923743 | G | GTTTT | 10 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0290 others(7): Show |
10 | HG02071.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1516+802_1516+805d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923743 | |||||||
chr2:165923743 | GT | G | 16 | a0001c0001t0001g0051 a0002c0002t0001g0156 a0002c0002t0007g0128 others(13): Show |
16 | HG01175.hp1 HG01928.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.1516+805delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923743 | |||||||
chr2:165923743 | GTTTT | G | 13 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(10): Show |
13 | HG01884.hp1 HG02080.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.1516+802_1516+805d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923743 | |||||||
chr2:165923926 | A | AT | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1516+622dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165923926 | |||||||
chr2:165924067 | T | C | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1516+482A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924067 | |||||||
chr2:165924126 | T | C | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1516+423A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924126 | |||||||
chr2:165924138 | G | A | 3 | a0001c0001t0002g0219 a0001c0001t0002g0221 a0010c0019t0002g0220 |
3 | HG00639.hp2 HG02738.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1516+411C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924138 | |||||||
chr2:165924175 | A | G | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+374T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924175 | |||||||
chr2:165924348 | C | A | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1516+201G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924348 | |||||||
chr2:165924351 | A | T | 1 | a0001c0009t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1516+198T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924351 | |||||||
chr2:165924384 | G | C | 2 | a0005c0007t0001g0009 a0016c0030t0001g0274 |
3 | HG01496.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1516+165C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924384 | |||||||
chr2:165924401 | A | G | 89 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(86): Show |
90 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.1516+148T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924401 | |||||||
chr2:165924471 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1516+78G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924471 | |||||||
chr2:165924485 | T | A | 1 | a0001c0001t0001g0289 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1516+64A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 12/28 | chr2 | 165924485 | |||||||
chr2:165924704 | T | C | 1 | a0001c0001t0001g0357 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1387-26A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165924704 | |||||||
chr2:165924711 | A | G | 1 | a0002c0002t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1387-33T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165924711 | |||||||
chr2:165924732 | T | TA | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1387-55dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165924732 | |||||||
chr2:165924940 | C | T | 11 | a0002c0002t0004g0075 a0002c0002t0004g0125 a0002c0002t0004g0281 others(8): Show |
11 | HG00438.hp1 HG00544.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1387-262G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165924940 | |||||||
chr2:165924944 | T | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1387-266A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165924944 | |||||||
chr2:165924954 | AT | A | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1387-277delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165924954 | |||||||
chr2:165925059 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1387-381G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165925059 | |||||||
chr2:165925246 | A | C | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-568T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165925246 | |||||||
chr2:165925434 | C | T | 1 | a0008c0011t0003g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1387-756G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165925434 | |||||||
chr2:165925505 | A | G | 1 | a0002c0002t0004g0117 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1387-827T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165925505 | |||||||
chr2:165925721 | C | T | 56 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0182 others(53): Show |
59 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1387-1043G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165925721 | |||||||
chr2:165925770 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1387-1092G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165925770 | |||||||
chr2:165925886 | G | A | 175 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(172): Show |
179 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.1387-1208C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165925886 | |||||||
chr2:165926063 | T | C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1387-1385A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926063 | |||||||
chr2:165926093 | A | G | 31 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0173 others(28): Show |
31 | HG00558.hp2 HG01074.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1387-1415T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926093 | |||||||
chr2:165926477 | C | T | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1387-1799G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926477 | |||||||
chr2:165926489 | C | T | 1 | a0001c0001t0001g0353 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1387-1811G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926489 | |||||||
chr2:165926577 | A | T | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-1899T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926577 | |||||||
chr2:165926605 | T | C | 2 | a0001c0001t0003g0082 a0001c0001t0003g0083 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1387-1927A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926605 | |||||||
chr2:165926648 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0054 |
2 | NA18977.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1387-1970A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926648 | |||||||
chr2:165926690 | G | A | 3 | a0001c0001t0002g0002 a0001c0001t0002g0198 a0001c0001t0002g0206 |
5 | HG00738.hp1 HG01081.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1387-2012C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926690 | |||||||
chr2:165926873 | G | A | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1387-2195C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926873 | |||||||
chr2:165926905 | A | T | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1387-2227T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926905 | |||||||
chr2:165926981 | T | A | 1 | a0008c0011t0003g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1386+2154A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926981 | |||||||
chr2:165926991 | C | CAT | 77 | a0001c0001t0001g0012 a0001c0001t0001g0088 a0001c0001t0001g0089 others(74): Show |
77 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1386+2142_1386+214 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATAT | 10 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0063 others(7): Show |
11 | HG01099.hp1 HG01109.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+2140_1386+214 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATATAT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(46): Show |
51 | HG00140.hp1 HG00609.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1386+2138_1386+214 others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATATATA others(1): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0027 others(14): Show |
19 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1386+2136_1386+214 others(12): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATATATA others(3): Show |
47 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0049 others(44): Show |
48 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1386+2134_1386+214 others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATATATA others(5): Show |
21 | a0001c0001t0002g0196 a0001c0001t0002g0207 a0001c0001t0002g0208 others(18): Show |
21 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1386+2132_1386+214 others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATATATA others(7): Show |
9 | a0001c0001t0001g0015 a0001c0001t0001g0171 a0001c0001t0002g0002 others(6): Show |
11 | HG00738.hp1 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1386+2130_1386+214 others(18): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATATATA others(9): Show |
18 | a0001c0001t0001g0167 a0001c0001t0002g0200 a0001c0001t0002g0206 others(15): Show |
18 | HG01496.hp2 HG02257.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1386+2128_1386+214 others(20): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATATATA others(11): Show |
6 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0003g0091 others(3): Show |
6 | HG01257.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1386+2126_1386+214 others(22): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | C | CATATATA others(13): Show |
11 | a0001c0001t0001g0173 a0001c0001t0003g0163 a0001c0001t0003g0165 others(8): Show |
11 | HG00423.hp1 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1386+2124_1386+214 others(24): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | CAT | C | 3 | a0004c0005t0001g0263 a0004c0005t0001g0368 a0004c0005t0001g0385 |
3 | HG01106.hp2 HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1386+2142_1386+214 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165926991 | CATATAT | C | 81 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(78): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1386+2138_1386+214 others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165926991 | |||||||
chr2:165927003 | T | C | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1386+2132A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927003 | |||||||
chr2:165927009 | TATATATA others(51): Show |
T | 1 | a0002c0008t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1386+2068_1386+212 others(62): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927009 | |||||||
chr2:165927011 | TATATATC others(49): Show |
T | 1 | a0002c0008t0001g0278 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1386+2068_1386+212 others(60): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927011 | |||||||
chr2:165927014 | ATATCTCC others(7): Show |
A | 4 | a0001c0001t0001g0230 a0001c0001t0003g0164 a0001c0001t0003g0176 others(1): Show |
4 | NA18940.hp2 NA18953.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+2107_1386+212 others(18): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927014 | |||||||
chr2:165927015 | TATCTCCT others(45): Show |
T | 1 | a0002c0008t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1386+2068_1386+211 others(56): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927015 | |||||||
chr2:165927016 | A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0213 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1386+2118_1386+211 others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927016 | |||||||
chr2:165927016 | ATCTCCTA others(5): Show |
A | 10 | a0001c0001t0001g0229 a0001c0001t0002g0204 a0001c0001t0002g0205 others(7): Show |
10 | HG00558.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386+2107_1386+211 others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927016 | |||||||
chr2:165927016 | ATCTCCTA others(41): Show |
A | 1 | a0002c0008t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1386+2071_1386+211 others(52): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927016 | |||||||
chr2:165927017 | TCTCCTAG others(3): Show |
T | 1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1386+2108_1386+211 others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927017 | |||||||
chr2:165927018 | C | A | 8 | a0001c0001t0001g0235 a0001c0001t0003g0161 a0001c0001t0003g0168 others(5): Show |
8 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+2117G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927018 | |||||||
chr2:165927019 | TCCTA | T | 8 | a0001c0001t0001g0235 a0001c0001t0003g0161 a0001c0001t0003g0168 others(5): Show |
8 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+2112_1386+211 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927019 | |||||||
chr2:165927024 | G | A | 9 | a0001c0001t0001g0235 a0001c0001t0003g0083 a0001c0001t0003g0161 others(6): Show |
9 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1386+2111C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927024 | |||||||
chr2:165927027 | G | T | 11 | a0001c0001t0001g0235 a0001c0001t0003g0083 a0001c0001t0003g0161 others(8): Show |
11 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+2108C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927027 | |||||||
chr2:165927028 | T | A | 12 | a0001c0001t0001g0235 a0001c0001t0003g0082 a0001c0001t0003g0083 others(9): Show |
12 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1386+2107A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927028 | |||||||
chr2:165927028 | T | TTA | 3 | a0001c0001t0001g0357 a0007c0012t0001g0374 a0007c0012t0005g0375 |
3 | HG01891.hp1 HG03471.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1386+2105_1386+210 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927028 | |||||||
chr2:165927028 | TTA | T | 4 | a0003c0003t0001g0078 a0003c0003t0001g0079 a0003c0003t0001g0080 others(1): Show |
4 | HG00423.hp1 NA18956.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+2105_1386+210 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927028 | |||||||
chr2:165927042 | A | G | 35 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(32): Show |
37 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1386+2093T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927042 | |||||||
chr2:165927042 | ATGTG | A | 10 | a0001c0001t0001g0229 a0001c0001t0002g0204 a0001c0001t0002g0205 others(7): Show |
10 | HG00558.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386+2089_1386+209 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927042 | |||||||
chr2:165927044 | G | A | 5 | a0001c0001t0001g0230 a0001c0001t0003g0082 a0001c0001t0003g0164 others(2): Show |
5 | HG02647.hp2 NA18940.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+2091C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927044 | |||||||
chr2:165927044 | G | C | 11 | a0001c0001t0001g0235 a0001c0001t0003g0083 a0001c0001t0003g0161 others(8): Show |
11 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+2091C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927044 | |||||||
chr2:165927045 | T | TCCTA | 11 | a0001c0001t0001g0235 a0001c0001t0003g0083 a0001c0001t0003g0161 others(8): Show |
11 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+2089_1386+209 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927045 | |||||||
chr2:165927046 | G | A | 5 | a0001c0001t0001g0230 a0001c0001t0003g0082 a0001c0001t0003g0164 others(2): Show |
5 | HG02647.hp2 NA18940.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+2089C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927046 | |||||||
chr2:165927046 | G | GTA | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+2087_1386+208 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927046 | |||||||
chr2:165927046 | GTATATAT others(19): Show |
G | 8 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(5): Show |
8 | HG01168.hp2 HG01192.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+2063_1386+208 others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927046 | |||||||
chr2:165927048 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1386+2087T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927048 | |||||||
chr2:165927049 | T | G | 11 | a0001c0001t0001g0235 a0001c0001t0003g0083 a0001c0001t0003g0161 others(8): Show |
11 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+2086A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927049 | |||||||
chr2:165927050 | A | T | 11 | a0001c0001t0001g0235 a0001c0001t0003g0083 a0001c0001t0003g0161 others(8): Show |
11 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+2085T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927050 | |||||||
chr2:165927058 | A | C | 15 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0204 others(12): Show |
15 | HG00558.hp2 HG01074.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1386+2077T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927058 | |||||||
chr2:165927058 | ATCCTAG | A | 3 | a0001c0001t0003g0083 a0001c0001t0003g0181 a0001c0001t0003g0183 |
3 | HG02109.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1386+2071_1386+207 others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927058 | |||||||
chr2:165927059 | TCCTA | T | 8 | a0001c0001t0001g0235 a0001c0001t0003g0161 a0001c0001t0003g0168 others(5): Show |
8 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+2072_1386+207 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927059 | |||||||
chr2:165927064 | G | A | 8 | a0001c0001t0001g0235 a0001c0001t0003g0161 a0001c0001t0003g0168 others(5): Show |
8 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+2071C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927064 | |||||||
chr2:165927067 | G | T | 12 | a0001c0001t0001g0235 a0001c0001t0003g0083 a0001c0001t0003g0161 others(9): Show |
12 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1386+2068C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927067 | |||||||
chr2:165927067 | GAT | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
86 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1386+2066_1386+206 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927067 | |||||||
chr2:165927067 | GATAT | G | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+2064_1386+206 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927067 | |||||||
chr2:165927067 | GATATAT | G | 68 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(65): Show |
71 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1386+2062_1386+206 others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927067 | |||||||
chr2:165927067 | GATATATA others(21): Show |
G | 30 | a0001c0001t0001g0063 a0003c0003t0001g0076 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1386+2040_1386+206 others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927067 | |||||||
chr2:165927067 | GATATATA others(25): Show |
G | 1 | a0002c0002t0004g0138 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1386+2036_1386+206 others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927067 | |||||||
chr2:165927068 | A | T | 15 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0204 others(12): Show |
15 | HG00558.hp2 HG01074.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1386+2067T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927068 | |||||||
chr2:165927070 | A | G | 8 | a0001c0001t0001g0235 a0001c0001t0003g0161 a0001c0001t0003g0168 others(5): Show |
8 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+2065T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927070 | |||||||
chr2:165927072 | A | ATATATAT others(7): Show |
13 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0204 others(10): Show |
13 | HG00558.hp2 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1386+2062_1386+206 others(18): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927072 | |||||||
chr2:165927072 | A | ATATATAT others(5): Show |
1 | a0003c0003t0001g0077 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1386+2062_1386+206 others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927072 | |||||||
chr2:165927072 | A | G | 11 | a0001c0001t0001g0235 a0001c0001t0003g0083 a0001c0001t0003g0161 others(8): Show |
11 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+2063T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927072 | |||||||
chr2:165927074 | A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1386+2060_1386+206 others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927074 | |||||||
chr2:165927074 | A | G | 3 | a0001c0001t0003g0083 a0001c0001t0003g0181 a0001c0001t0003g0183 |
3 | HG02109.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1386+2061T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927074 | |||||||
chr2:165927093 | G | GTT | 69 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0093 others(66): Show |
71 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1386+2041_1386+204 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927093 | |||||||
chr2:165927093 | G | GTTAT | 4 | a0002c0002t0001g0008 a0002c0002t0001g0237 a0002c0002t0001g0239 others(1): Show |
5 | HG00099.hp2 HG01106.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+2041_1386+204 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927093 | |||||||
chr2:165927094 | A | T | 12 | a0002c0002t0004g0117 a0002c0008t0001g0275 a0002c0008t0001g0276 others(9): Show |
13 | HG00673.hp1 HG01496.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1386+2041T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927094 | |||||||
chr2:165927095 | TATATATA others(17): Show |
T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
98 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1386+2016_1386+203 others(28): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927095 | |||||||
chr2:165927096 | ATATATAT others(69): Show |
A | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+1963_1386+203 others(80): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927096 | |||||||
chr2:165927097 | TATATATA others(15): Show |
T | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+2016_1386+203 others(26): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927097 | |||||||
chr2:165927098 | ATATATAT others(67): Show |
A | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1386+1963_1386+203 others(78): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927098 | |||||||
chr2:165927099 | TATATATA others(13): Show |
T | 1 | a0001c0004t0001g0103 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1386+2016_1386+203 others(24): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927099 | |||||||
chr2:165927101 | TATATATA others(11): Show |
T | 1 | a0002c0002t0004g0117 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1386+2016_1386+203 others(22): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927101 | |||||||
chr2:165927110 | A | C | 49 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0182 others(46): Show |
52 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1386+2025T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927110 | |||||||
chr2:165927120 | A | T | 217 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0055 others(214): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1386+2015T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927120 | |||||||
chr2:165927122 | ATATATAT others(43): Show |
A | 1 | a0001c0001t0001g0301 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1386+1963_1386+201 others(54): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927122 | |||||||
chr2:165927124 | ATATATAT others(41): Show |
A | 5 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0196 others(2): Show |
5 | HG01433.hp1 HG01496.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+1963_1386+201 others(52): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927124 | |||||||
chr2:165927136 | A | C | 8 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0265 others(5): Show |
8 | HG01109.hp1 HG01123.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+1999T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927136 | |||||||
chr2:165927143 | T | C | 138 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0055 others(135): Show |
142 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.1386+1992A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927143 | |||||||
chr2:165927146 | TTA | T | 238 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(235): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1386+1987_1386+198 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927146 | |||||||
chr2:165927152 | ATATATAT others(13): Show |
A | 2 | a0006c0015t0001g0388 a0006c0015t0001g0389 |
2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1386+1963_1386+198 others(24): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927152 | |||||||
chr2:165927162 | A | C | 73 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(70): Show |
76 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1386+1973T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927162 | |||||||
chr2:165927168 | A | G | 377 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(374): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1386+1967T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927168 | |||||||
chr2:165927169 | C | T | 213 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0055 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1386+1966G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927169 | |||||||
chr2:165927173 | T | TAC | 73 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(70): Show |
76 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1386+1961_1386+196 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927173 | |||||||
chr2:165927186 | A | C | 2 | a0002c0002t0004g0117 a0002c0002t0004g0138 |
2 | HG00323.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1386+1949T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927186 | |||||||
chr2:165927193 | T | C | 15 | a0001c0001t0001g0301 a0001c0001t0002g0188 a0001c0001t0002g0189 others(12): Show |
16 | HG01175.hp1 HG01433.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1386+1942A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927193 | |||||||
chr2:165927196 | T | TTATA | 73 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(70): Show |
76 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1386+1935_1386+193 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927196 | |||||||
chr2:165927198 | ATATATAT others(41): Show |
A | 137 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(134): Show |
141 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1386+1889_1386+193 others(52): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927198 | |||||||
chr2:165927200 | ATATATAT others(39): Show |
A | 1 | a0001c0001t0001g0055 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1386+1889_1386+193 others(50): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927200 | |||||||
chr2:165927220 | T | TTA | 3 | a0001c0001t0001g0069 a0002c0002t0004g0117 a0002c0002t0004g0138 |
3 | HG00323.hp2 HG00673.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1386+1913_1386+191 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927220 | |||||||
chr2:165927220 | TTA | T | 14 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0196 others(11): Show |
15 | HG01175.hp1 HG01433.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1386+1913_1386+191 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927220 | |||||||
chr2:165927222 | ATATATAT others(17): Show |
A | 47 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0054 others(44): Show |
47 | HG00558.hp2 HG01106.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1386+1889_1386+191 others(28): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927222 | |||||||
chr2:165927224 | ATATATAT others(15): Show |
A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
70 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1386+1889_1386+191 others(26): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927224 | |||||||
chr2:165927226 | ATATATAT others(13): Show |
A | 5 | a0001c0001t0004g0068 a0001c0004t0001g0105 a0001c0004t0001g0106 others(2): Show |
5 | HG03540.hp2 HG06807.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+1889_1386+190 others(24): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927226 | |||||||
chr2:165927228 | ATATATAT others(11): Show |
A | 2 | a0001c0004t0001g0103 a0001c0004t0001g0109 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1386+1889_1386+190 others(22): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927228 | |||||||
chr2:165927246 | T | TTA | 10 | a0001c0001t0001g0301 a0001c0001t0002g0188 a0001c0001t0002g0189 others(7): Show |
10 | HG00673.hp1 HG01175.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386+1887_1386+188 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927246 | |||||||
chr2:165927246 | TTA | T | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1386+1887_1386+188 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927246 | |||||||
chr2:165927259 | TATCCTAG others(59): Show |
T | 73 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(70): Show |
76 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1386+1810_1386+187 others(70): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927259 | |||||||
chr2:165927269 | G | GGATATAT others(12): Show |
1 | a0002c0008t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1386+1865_1386+186 others(23): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927269 | |||||||
chr2:165927269 | GTTATATA others(22): Show |
G | 3 | a0002c0008t0001g0276 a0002c0008t0001g0277 a0002c0008t0001g0278 |
3 | HG02723.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1386+1837_1386+186 others(33): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927269 | |||||||
chr2:165927270 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0003g0175 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1386+1839_1386+186 others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927270 | |||||||
chr2:165927271 | T | A | 1 | a0002c0008t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1386+1864A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927271 | |||||||
chr2:165927272 | ATATATAT others(15): Show |
A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1386+1841_1386+186 others(26): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927272 | |||||||
chr2:165927276 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1386+1828_1386+185 others(35): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927276 | |||||||
chr2:165927282 | ATATCCTA others(19): Show |
A | 1 | a0001c0001t0002g0265 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1386+1827_1386+185 others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927282 | |||||||
chr2:165927283 | TATCCTAG others(35): Show |
T | 2 | a0002c0002t0004g0117 a0002c0002t0004g0138 |
2 | HG00323.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1386+1810_1386+185 others(46): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927283 | |||||||
chr2:165927284 | A | T | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+1851T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927284 | |||||||
chr2:165927285 | T | A | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+1850A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927285 | |||||||
chr2:165927286 | C | T | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+1849G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927286 | |||||||
chr2:165927287 | C | A | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+1848G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927287 | |||||||
chr2:165927290 | G | T | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+1845C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927290 | |||||||
chr2:165927292 | A | AT | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+1842_1386+184 others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927292 | |||||||
chr2:165927293 | G | A | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+1842C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927293 | |||||||
chr2:165927295 | T | A | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+1840A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927295 | |||||||
chr2:165927297 | T | C | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1386+1838A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927297 | |||||||
chr2:165927299 | T | G | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+1836A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927299 | |||||||
chr2:165927306 | AT | A | 5 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(2): Show |
5 | HG02723.hp1 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+1828delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927306 | |||||||
chr2:165927307 | T | A | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+1828A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927307 | |||||||
chr2:165927313 | A | AATAT | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | HG01168.hp2 HG01192.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1386+1821_1386+182 others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927313 | |||||||
chr2:165927314 | T | A | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+1821A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927314 | |||||||
chr2:165927320 | AAT | A | 30 | a0001c0001t0001g0053 a0001c0001t0001g0384 a0001c0001t0002g0197 others(27): Show |
30 | HG00642.hp1 HG00735.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1386+1813_1386+181 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927320 | |||||||
chr2:165927321 | A | T | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1386+1814T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927321 | |||||||
chr2:165927330 | T | C | 1 | a0019c0020t0002g0184 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1386+1805A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927330 | |||||||
chr2:165927349 | A | G | 1 | a0004c0010t0018g0380 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1386+1786T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927349 | |||||||
chr2:165927350 | A | T | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1386+1785T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927350 | |||||||
chr2:165927352 | A | T | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1386+1783T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927352 | |||||||
chr2:165927354 | A | T | 2 | a0006c0015t0001g0388 a0006c0015t0001g0389 |
2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1386+1781T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927354 | |||||||
chr2:165927356 | T | A | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1386+1779A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927356 | |||||||
chr2:165927357 | T | A | 3 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0379 |
3 | HG01175.hp1 HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1386+1778A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927357 | |||||||
chr2:165927357 | T | TTA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0167 others(6): Show |
11 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+1776_1386+177 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927357 | |||||||
chr2:165927357 | TTA | T | 31 | a0001c0001t0001g0111 a0003c0003t0001g0076 a0003c0003t0001g0077 others(28): Show |
31 | HG00140.hp1 HG00423.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1386+1776_1386+177 others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927357 | |||||||
chr2:165927362 | T | TA | 4 | a0005c0007t0001g0085 a0005c0007t0001g0087 a0005c0007t0015g0086 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+1772dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927362 | |||||||
chr2:165927363 | AT | A | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1386+1771delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927363 | |||||||
chr2:165927549 | C | T | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1386+1586G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927549 | |||||||
chr2:165927590 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1386+1545G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927590 | |||||||
chr2:165927644 | A | G | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1386+1491T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927644 | |||||||
chr2:165927928 | C | T | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+1207G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165927928 | |||||||
chr2:165928142 | T | C | 1 | a0002c0002t0007g0130 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1386+993A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165928142 | |||||||
chr2:165928306 | A | C | 1 | a0001c0001t0012g0300 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1386+829T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165928306 | |||||||
chr2:165928463 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0034 others(3): Show |
6 | HG02027.hp2 HG02080.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1386+672A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165928463 | |||||||
chr2:165928518 | C | T | 46 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0182 others(43): Show |
49 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1386+617G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165928518 | |||||||
chr2:165928685 | G | A | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+450C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165928685 | |||||||
chr2:165928708 | CT | C | 76 | a0001c0001t0002g0366 a0001c0001t0019g0236 a0002c0002t0001g0006 others(73): Show |
79 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1386+426delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165928708 | |||||||
chr2:165928827 | C | T | 1 | a0001c0004t0003g0098 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1386+308G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 11/28 | chr2 | 165928827 | |||||||
chr2:165929627 | G | C | 3 | a0002c0002t0001g0008 a0002c0002t0001g0239 a0002c0002t0017g0238 |
4 | HG00099.hp2 HG01106.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185+23C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 10/28 | chr2 | 165929627 | |||||||
chr2:165929841 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
87 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1088-94G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 9/28 | chr2 | 165929841 | |||||||
chr2:165929853 | T | C | 1 | a0002c0002t0007g0130 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1088-106A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 9/28 | chr2 | 165929853 | |||||||
chr2:165929861 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1088-114C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 9/28 | chr2 | 165929861 | |||||||
chr2:165929869 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1088-122A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 9/28 | chr2 | 165929869 | |||||||
chr2:165930020 | A | ATTTTAT | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1087+151_1087+152i others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 9/28 | chr2 | 165930020 | |||||||
chr2:165930130 | T | C | 3 | a0003c0003t0001g0077 a0003c0003t0001g0078 a0003c0003t0001g0079 |
3 | HG02056.hp1 NA18956.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1087+42A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 9/28 | chr2 | 165930130 | |||||||
chr2:165930463 | A | C | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.895-99T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930463 | |||||||
chr2:165930617 | C | T | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-253G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930617 | |||||||
chr2:165930697 | G | A | 75 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.895-333C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930697 | |||||||
chr2:165930728 | T | TGGGTGTG others(72): Show |
1 | a0002c0002t0001g0156 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.895-365_895-364ins others(79): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930728 | |||||||
chr2:165930728 | T | TGGGTGTG others(80): Show |
1 | a0002c0002t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.895-365_895-364ins others(87): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930728 | |||||||
chr2:165930728 | TGG | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0005g0032 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.895-366_895-365del others(2): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930728 | |||||||
chr2:165930730 | G | GGTGTGTG others(56): Show |
1 | a0002c0002t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(63): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(62): Show |
1 | a0002c0014t0004g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(69): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(64): Show |
1 | a0002c0014t0004g0005 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(71): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(60): Show |
2 | a0002c0002t0010g0011 a0002c0002t0010g0092 |
2 | HG00140.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.895-367_895-366ins others(67): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(62): Show |
2 | a0002c0002t0004g0138 a0002c0002t0004g0272 |
2 | HG00323.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.895-367_895-366ins others(69): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(64): Show |
1 | a0002c0002t0001g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(71): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(68): Show |
1 | a0002c0002t0009g0393 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(75): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(66): Show |
2 | a0002c0002t0001g0123 a0002c0002t0004g0271 |
2 | HG02818.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.895-367_895-366ins others(73): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(68): Show |
1 | a0002c0002t0007g0145 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(75): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(70): Show |
3 | a0002c0002t0001g0124 a0002c0002t0004g0281 a0002c0002t0007g0141 |
3 | HG01257.hp1 HG02165.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.895-367_895-366ins others(77): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(72): Show |
2 | a0002c0002t0001g0153 a0002c0002t0009g0396 |
2 | NA18952.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.895-367_895-366ins others(79): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(74): Show |
1 | a0002c0002t0001g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(81): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(70): Show |
1 | a0002c0002t0004g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(77): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(72): Show |
2 | a0002c0002t0007g0130 a0002c0002t0007g0149 |
2 | HG01928.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.895-367_895-366ins others(79): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(74): Show |
3 | a0002c0002t0001g0116 a0002c0002t0009g0394 a0002c0002t0021g0395 |
3 | HG02738.hp2 NA19005.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.895-367_895-366ins others(81): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(76): Show |
1 | a0002c0002t0001g0240 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(83): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(70): Show |
1 | a0002c0002t0010g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(77): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(78): Show |
1 | a0002c0002t0001g0147 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(85): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(72): Show |
3 | a0002c0002t0001g0006 a0002c0002t0001g0155 a0002c0002t0001g0157 |
3 | NA18975.hp2 NA19057.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.895-367_895-366ins others(79): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(74): Show |
3 | a0002c0002t0001g0137 a0002c0002t0004g0121 a0002c0002t0007g0140 |
3 | HG01074.hp1 HG02074.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.895-367_895-366ins others(81): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(76): Show |
4 | a0001c0001t0019g0236 a0002c0002t0001g0154 a0002c0002t0001g0237 others(1): Show |
4 | HG01346.hp2 HG02698.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-367_895-366ins others(83): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(74): Show |
5 | a0002c0002t0001g0006 a0002c0002t0001g0148 a0002c0002t0001g0152 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-367_895-366ins others(81): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(78): Show |
2 | a0002c0002t0001g0239 a0002c0002t0009g0392 |
2 | HG00099.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.895-367_895-366ins others(85): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(72): Show |
1 | a0002c0002t0004g0125 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(79): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(80): Show |
4 | a0002c0002t0001g0150 a0002c0002t0001g0364 a0002c0002t0004g0362 others(1): Show |
4 | HG00558.hp1 HG01106.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-367_895-366ins others(87): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(82): Show |
1 | a0002c0002t0001g0118 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(89): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(78): Show |
2 | a0002c0002t0001g0120 a0002c0002t0001g0151 |
2 | HG01361.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.895-367_895-366ins others(85): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(80): Show |
1 | a0002c0029t0001g0282 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(87): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(82): Show |
2 | a0002c0002t0001g0122 a0002c0002t0001g0134 |
2 | HG00423.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.895-367_895-366ins others(89): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(84): Show |
1 | a0002c0002t0004g0363 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(91): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(82): Show |
1 | a0002c0002t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(89): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(84): Show |
1 | a0002c0002t0001g0008 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(91): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(86): Show |
1 | a0002c0002t0001g0132 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(93): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(88): Show |
1 | a0002c0002t0001g0143 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(95): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(84): Show |
1 | a0002c0002t0007g0129 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(91): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(86): Show |
1 | a0002c0002t0001g0008 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(93): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(90): Show |
1 | a0002c0002t0004g0075 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(97): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GGTGTGTG others(88): Show |
1 | a0002c0002t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(95): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GTGTGTGT others(63): Show |
1 | a0002c0002t0007g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(70): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GTGTGTGT others(75): Show |
1 | a0002c0002t0007g0142 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(82): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GTGTGTGT others(77): Show |
1 | a0002c0002t0004g0361 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(84): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GTGTGTGT others(83): Show |
1 | a0002c0002t0001g0119 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.895-367_895-366ins others(90): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | G | GTGTGTGT others(85): Show |
1 | a0002c0002t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.895-367_895-366ins others(92): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | GGGGT | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
79 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.895-370_895-367del others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | GGGGTGT | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0316 a0001c0001t0002g0192 others(5): Show |
9 | HG01099.hp1 HG01175.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.895-372_895-367del others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930730 | GGGGTGTG others(3): Show |
G | 1 | a0001c0001t0001g0024 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.895-376_895-367del others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930730 | |||||||
chr2:165930732 | G | GGTGTGTG others(68): Show |
1 | a0013c0027t0004g0264 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.895-369_895-368ins others(75): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | G | GGTGTGTG others(72): Show |
1 | a0002c0002t0004g0117 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.895-369_895-368ins others(79): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | G | GGTGTGTG others(74): Show |
1 | a0002c0002t0004g0139 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.895-369_895-368ins others(81): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | G | GGTGTGTG others(74): Show |
1 | a0002c0002t0001g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.895-369_895-368ins others(81): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | G | GGTGTGTG others(76): Show |
1 | a0002c0002t0004g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.895-369_895-368ins others(83): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | G | GGTGTGTG others(86): Show |
1 | a0002c0002t0004g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.895-369_895-368ins others(93): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | G | GTGTGTGT others(79): Show |
1 | a0002c0002t0001g0232 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.895-369_895-368ins others(86): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | G | T | 69 | a0001c0001t0001g0037 a0001c0001t0019g0236 a0002c0002t0001g0006 others(66): Show |
72 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.895-368C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | GGT | G | 9 | a0004c0005t0001g0263 a0004c0005t0001g0360 a0004c0005t0001g0381 others(6): Show |
9 | HG01261.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-370_895-369del others(2): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | GGTGT | G | 45 | a0001c0001t0001g0167 a0001c0001t0001g0384 a0001c0001t0002g0194 others(42): Show |
46 | HG00423.hp1 HG00642.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.895-372_895-369del others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | GGTGTGT | G | 161 | a0001c0001t0001g0012 a0001c0001t0001g0088 a0001c0001t0001g0089 others(158): Show |
164 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.895-374_895-369del others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930732 | GGTGTGTG others(7): Show |
G | 2 | a0004c0005t0001g0368 a0004c0005t0001g0385 |
2 | HG01106.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.895-382_895-369del others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930732 | |||||||
chr2:165930740 | T | G | 1 | a0001c0009t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.895-376A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930740 | |||||||
chr2:165930809 | C | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
89 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.895-445G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930809 | |||||||
chr2:165930878 | G | C | 1 | a0002c0008t0001g0278 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.895-514C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165930878 | |||||||
chr2:165931162 | T | C | 1 | a0012c0021t0005g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.894+596A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165931162 | |||||||
chr2:165931231 | T | C | 1 | a0001c0001t0001g0352 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.894+527A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165931231 | |||||||
chr2:165931282 | C | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+476G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165931282 | |||||||
chr2:165931310 | C | T | 1 | a0001c0001t0003g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.894+448G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165931310 | |||||||
chr2:165931549 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.894+209A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165931549 | |||||||
chr2:165931640 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.894+118A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165931640 | |||||||
chr2:165931650 | C | T | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+108G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 8/28 | chr2 | 165931650 | |||||||
chr2:165932101 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.796-245A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932101 | |||||||
chr2:165932228 | C | A | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.796-372G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932228 | |||||||
chr2:165932234 | C | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.796-378G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932234 | |||||||
chr2:165932333 | A | G | 80 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(77): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.796-477T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932333 | |||||||
chr2:165932418 | A | G | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+555T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932418 | |||||||
chr2:165932455 | C | T | 174 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(171): Show |
178 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.795+518G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932455 | |||||||
chr2:165932523 | T | A | 7 | a0002c0028t0001g0369 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+450A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932523 | |||||||
chr2:165932631 | C | T | 25 | a0003c0003t0001g0076 a0003c0003t0001g0241 a0003c0003t0001g0244 others(22): Show |
25 | HG00642.hp1 HG01081.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.795+342G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932631 | |||||||
chr2:165932660 | G | A | 76 | a0001c0001t0019g0236 a0002c0002t0001g0006 a0002c0002t0001g0008 others(73): Show |
79 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.795+313C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932660 | |||||||
chr2:165932663 | T | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | NA18944.hp1 NA18962.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.795+310A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932663 | |||||||
chr2:165932929 | A | G | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.795+44T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 7/28 | chr2 | 165932929 | |||||||
chr2:165933174 | A | G | 2 | a0006c0015t0001g0388 a0006c0015t0001g0389 |
2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.711-117T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165933174 | |||||||
chr2:165933195 | T | C | 1 | a0001c0001t0001g0312 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.711-138A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165933195 | |||||||
chr2:165933304 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.711-247C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165933304 | |||||||
chr2:165933625 | C | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0316 |
3 | HG01099.hp1 HG01243.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.711-568G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165933625 | |||||||
chr2:165933740 | A | G | 8 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-683T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165933740 | |||||||
chr2:165933993 | A | C | 3 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 |
3 | HG02896.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.711-936T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165933993 | |||||||
chr2:165934118 | G | A | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-1061C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934118 | |||||||
chr2:165934337 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.711-1280G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934337 | |||||||
chr2:165934363 | G | A | 12 | a0004c0005t0001g0263 a0004c0005t0001g0360 a0004c0005t0001g0367 others(9): Show |
12 | HG01106.hp2 HG01261.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.711-1306C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934363 | |||||||
chr2:165934367 | T | C | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.711-1310A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934367 | |||||||
chr2:165934488 | G | A | 295 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(292): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.711-1431C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934488 | |||||||
chr2:165934500 | C | CA | 19 | a0001c0001t0001g0298 a0001c0001t0001g0338 a0001c0001t0001g0339 others(16): Show |
19 | HG01106.hp2 HG01261.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.711-1444dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934500 | |||||||
chr2:165934500 | C | CAAA | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
78 | HG00140.hp1 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.711-1446_711-1444d others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934500 | |||||||
chr2:165934500 | C | CAAAA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0049 others(4): Show |
7 | HG00438.hp2 HG02071.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.711-1447_711-1444d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934500 | |||||||
chr2:165934500 | CA | C | 34 | a0001c0001t0001g0088 a0001c0001t0001g0344 a0001c0001t0001g0348 others(31): Show |
34 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.711-1444delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934500 | |||||||
chr2:165934515 | A | G | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.711-1458T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934515 | |||||||
chr2:165934517 | A | AG | 72 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(69): Show |
75 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.711-1461_711-1460i others(3): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934517 | |||||||
chr2:165934517 | A | G | 3 | a0002c0002t0001g0157 a0002c0028t0001g0369 a0002c0029t0001g0282 |
3 | HG03516.hp2 NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.711-1460T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934517 | |||||||
chr2:165934593 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
89 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.711-1536A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934593 | |||||||
chr2:165934603 | TA | T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(341): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.711-1547delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934603 | |||||||
chr2:165934603 | TAA | T | 34 | a0001c0001t0004g0033 a0002c0002t0004g0075 a0002c0002t0004g0117 others(31): Show |
34 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.711-1548_711-1547d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934603 | |||||||
chr2:165934661 | T | C | 1 | a0008c0011t0003g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.711-1604A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934661 | |||||||
chr2:165934741 | G | GAA | 25 | a0003c0003t0001g0076 a0003c0003t0001g0241 a0003c0003t0001g0244 others(22): Show |
25 | HG00642.hp1 HG01081.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.711-1686_711-1685d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934741 | |||||||
chr2:165934848 | G | A | 25 | a0003c0003t0001g0076 a0003c0003t0001g0241 a0003c0003t0001g0244 others(22): Show |
25 | HG00642.hp1 HG01081.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.711-1791C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934848 | |||||||
chr2:165934954 | C | T | 1 | a0009c0013t0001g0378 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.711-1897G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165934954 | |||||||
chr2:165935106 | A | T | 7 | a0002c0028t0001g0369 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-2049T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935106 | |||||||
chr2:165935157 | G | A | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-2100C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935157 | |||||||
chr2:165935237 | A | T | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.711-2180T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935237 | |||||||
chr2:165935338 | T | C | 1 | a0009c0013t0001g0378 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.711-2281A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935338 | |||||||
chr2:165935385 | A | G | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.711-2328T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935385 | |||||||
chr2:165935389 | C | A | 7 | a0002c0028t0001g0369 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-2332G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935389 | |||||||
chr2:165935391 | C | CAGTGTG | 7 | a0002c0028t0001g0369 a0005c0007t0001g0009 a0005c0007t0001g0085 others(4): Show |
8 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-2335_711-2334i others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935391 | |||||||
chr2:165935436 | A | G | 78 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.711-2379T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935436 | |||||||
chr2:165935439 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
89 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.711-2382G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935439 | |||||||
chr2:165935475 | A | G | 392 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(389): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.711-2418T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935475 | |||||||
chr2:165935489 | A | C | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(173): Show |
180 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.711-2432T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935489 | |||||||
chr2:165935565 | A | G | 1 | a0001c0001t0012g0370 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.711-2508T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935565 | |||||||
chr2:165935600 | A | T | 2 | a0005c0007t0001g0009 a0016c0030t0001g0274 |
3 | HG01496.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.711-2543T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935600 | |||||||
chr2:165935616 | T | C | 1 | a0002c0002t0001g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.711-2559A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935616 | |||||||
chr2:165935662 | A | C | 1 | a0002c0002t0001g0137 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.711-2605T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935662 | |||||||
chr2:165935721 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.711-2664G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935721 | |||||||
chr2:165935744 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
89 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.711-2687G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935744 | |||||||
chr2:165935793 | A | T | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(173): Show |
180 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.711-2736T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935793 | |||||||
chr2:165935806 | A | C | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-2749T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935806 | |||||||
chr2:165935892 | G | C | 4 | a0002c0002t0004g0139 a0002c0002t0004g0144 a0002c0002t0004g0146 others(1): Show |
4 | HG01123.hp2 HG02602.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-2835C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935892 | |||||||
chr2:165935956 | CAA | C | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.711-2901_711-2900d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165935956 | |||||||
chr2:165936096 | TGTG | T | 49 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0182 others(46): Show |
52 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.711-3042_711-3040d others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165936096 | |||||||
chr2:165936199 | A | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.711-3142T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165936199 | |||||||
chr2:165936660 | T | C | 2 | a0004c0010t0003g0387 a0004c0010t0018g0380 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.711-3603A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165936660 | |||||||
chr2:165936685 | T | C | 1 | a0003c0003t0001g0080 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.711-3628A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165936685 | |||||||
chr2:165936718 | G | A | 1 | a0003c0003t0001g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.711-3661C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165936718 | |||||||
chr2:165936738 | C | G | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.711-3681G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165936738 | |||||||
chr2:165936751 | C | T | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-3694G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165936751 | |||||||
chr2:165936899 | A | G | 11 | a0001c0001t0001g0173 a0001c0001t0003g0091 a0001c0001t0003g0161 others(8): Show |
11 | HG01255.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.711-3842T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165936899 | |||||||
chr2:165937306 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.710+3721A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937306 | |||||||
chr2:165937364 | G | A | 1 | a0001c0001t0003g0176 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.710+3663C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937364 | |||||||
chr2:165937437 | C | T | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+3590G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937437 | |||||||
chr2:165937448 | C | T | 2 | a0006c0015t0001g0388 a0006c0015t0001g0389 |
2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.710+3579G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937448 | |||||||
chr2:165937518 | C | A | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.710+3509G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937518 | |||||||
chr2:165937706 | T | G | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+3321A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937706 | |||||||
chr2:165937736 | C | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.710+3291G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937736 | |||||||
chr2:165937738 | C | CA | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.710+3288dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937738 | |||||||
chr2:165937770 | A | C | 1 | a0001c0001t0002g0190 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.710+3257T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937770 | |||||||
chr2:165937771 | C | A | 1 | a0001c0001t0002g0190 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.710+3256G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | C | CCA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(45): Show |
52 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.710+3254_710+3255d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | C | CCACA | 28 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0024 others(25): Show |
28 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.710+3252_710+3255d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | C | CCACACA | 7 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0054 others(4): Show |
7 | HG01109.hp2 HG01952.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.710+3250_710+3255d others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | C | CCACACAC others(1): Show |
3 | a0001c0001t0001g0045 a0001c0001t0005g0039 a0001c0004t0001g0109 |
3 | HG02647.hp1 HG02683.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.710+3248_710+3255d others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | C | CCACACAC others(3): Show |
5 | a0001c0004t0001g0103 a0001c0004t0001g0105 a0001c0004t0001g0106 others(2): Show |
5 | HG02559.hp2 HG06807.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.710+3246_710+3255d others(12): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | C | CCACACAC others(5): Show |
1 | a0006c0015t0001g0389 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.710+3244_710+3255d others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | C | CCACACAC others(7): Show |
1 | a0001c0004t0001g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.710+3242_710+3255d others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | C | CCACACAC others(4): Show |
1 | a0007c0012t0001g0374 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.710+3255_710+3256i others(13): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCA | C | 36 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0028 others(33): Show |
36 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.710+3254_710+3255d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACA | C | 58 | a0001c0001t0001g0004 a0001c0001t0002g0002 a0001c0001t0002g0007 others(55): Show |
62 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.710+3252_710+3255d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACA | C | 32 | a0001c0001t0001g0173 a0001c0001t0001g0229 a0001c0001t0001g0230 others(29): Show |
33 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.710+3250_710+3255d others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACAC others(1): Show |
C | 30 | a0001c0001t0001g0167 a0001c0001t0001g0233 a0001c0001t0001g0234 others(27): Show |
31 | HG00423.hp1 HG01243.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.710+3248_710+3255d others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACAC others(3): Show |
C | 41 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(38): Show |
41 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.710+3246_710+3255d others(12): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACAC others(5): Show |
C | 56 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0286 others(53): Show |
58 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.710+3244_710+3255d others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACAC others(7): Show |
C | 1 | a0011c0026t0001g0302 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.710+3242_710+3255d others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACAC others(9): Show |
C | 8 | a0001c0001t0001g0289 a0001c0001t0003g0082 a0001c0001t0003g0083 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+3240_710+3255d others(18): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACAC others(11): Show |
C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710+3238_710+3255d others(20): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACAC others(13): Show |
C | 1 | a0001c0009t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.710+3236_710+3255d others(22): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937771 | CCACACAC others(21): Show |
C | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+3228_710+3255d others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937771 | |||||||
chr2:165937878 | T | A | 78 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(75): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.710+3149A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937878 | |||||||
chr2:165937901 | T | C | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(173): Show |
180 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.710+3126A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165937901 | |||||||
chr2:165938120 | CTCA | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(311): Show |
323 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.710+2904_710+2906d others(5): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938120 | |||||||
chr2:165938203 | AT | A | 33 | a0001c0001t0001g0056 a0002c0002t0001g0147 a0003c0003t0001g0076 others(30): Show |
33 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.710+2823delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938203 | |||||||
chr2:165938244 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.710+2783G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938244 | |||||||
chr2:165938295 | G | A | 1 | a0002c0008t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.710+2732C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938295 | |||||||
chr2:165938357 | C | T | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.710+2670G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938357 | |||||||
chr2:165938363 | C | T | 45 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(42): Show |
46 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.710+2664G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938363 | |||||||
chr2:165938408 | A | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.710+2619T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938408 | |||||||
chr2:165938410 | G | T | 56 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0182 others(53): Show |
59 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.710+2617C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938410 | |||||||
chr2:165938477 | A | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0021 others(10): Show |
13 | HG00609.hp1 HG02027.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.710+2550T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938477 | |||||||
chr2:165938517 | AT | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.710+2509delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938517 | |||||||
chr2:165938519 | G | T | 10 | a0001c0001t0003g0091 a0001c0001t0003g0161 a0001c0001t0003g0166 others(7): Show |
10 | HG01255.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.710+2508C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938519 | |||||||
chr2:165938560 | G | A | 69 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0116 others(66): Show |
72 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.710+2467C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938560 | |||||||
chr2:165938582 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710+2445G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938582 | |||||||
chr2:165938688 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.710+2339C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938688 | |||||||
chr2:165938689 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.710+2338T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938689 | |||||||
chr2:165938692 | A | C | 1 | a0001c0001t0003g0164 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.710+2335T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938692 | |||||||
chr2:165938801 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.710+2226G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938801 | |||||||
chr2:165938805 | G | C | 16 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0229 others(13): Show |
16 | HG00558.hp2 HG01074.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.710+2222C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938805 | |||||||
chr2:165938917 | T | A | 85 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(82): Show |
89 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.710+2110A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938917 | |||||||
chr2:165938945 | A | G | 1 | a0002c0002t0001g0152 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.710+2082T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165938945 | |||||||
chr2:165939126 | C | T | 34 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(31): Show |
34 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.710+1901G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165939126 | |||||||
chr2:165939217 | T | C | 1 | a0003c0003t0001g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.710+1810A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165939217 | |||||||
chr2:165939222 | G | A | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.710+1805C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165939222 | |||||||
chr2:165939331 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.710+1696G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165939331 | |||||||
chr2:165939879 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.710+1148T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165939879 | |||||||
chr2:165940042 | T | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
304 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.710+985A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940042 | |||||||
chr2:165940081 | G | T | 1 | a0001c0001t0011g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.710+946C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940081 | |||||||
chr2:165940176 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.710+851T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940176 | |||||||
chr2:165940237 | T | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.710+790A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940237 | |||||||
chr2:165940275 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
94 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.710+752C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940275 | |||||||
chr2:165940393 | T | C | 1 | a0002c0008t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.710+634A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940393 | |||||||
chr2:165940620 | C | T | 1 | a0004c0005t0001g0367 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.710+407G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940620 | |||||||
chr2:165940934 | T | A | 86 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(83): Show |
87 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+93A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940934 | |||||||
chr2:165940940 | C | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
304 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.710+87G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940940 | |||||||
chr2:165940969 | T | C | 1 | a0002c0002t0001g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.710+58A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 6/28 | chr2 | 165940969 | |||||||
chr2:165941250 | G | C | 4 | a0006c0015t0001g0388 a0006c0015t0001g0389 a0009c0013t0001g0378 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-66C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165941250 | |||||||
chr2:165941445 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.553-261C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165941445 | |||||||
chr2:165941446 | G | C | 2 | a0005c0007t0001g0009 a0016c0030t0001g0274 |
3 | HG01496.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.553-262C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165941446 | |||||||
chr2:165941478 | C | CAGG | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
311 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.553-295_553-294ins others(3): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165941478 | |||||||
chr2:165941511 | GA | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
304 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.553-328delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165941511 | |||||||
chr2:165941665 | G | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
94 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.553-481C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165941665 | |||||||
chr2:165941695 | C | A | 1 | a0002c0002t0004g0075 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.553-511G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165941695 | |||||||
chr2:165941828 | T | C | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-644A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165941828 | |||||||
chr2:165942082 | T | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.553-898A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942082 | |||||||
chr2:165942108 | T | C | 9 | a0003c0003t0006g0242 a0003c0003t0006g0243 a0003c0003t0006g0253 others(6): Show |
9 | NA18940.hp1 NA18948.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-924A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942108 | |||||||
chr2:165942319 | A | C | 2 | a0001c0001t0008g0224 a0001c0001t0008g0225 |
2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.552+900T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942319 | |||||||
chr2:165942486 | A | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
311 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.552+733T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942486 | |||||||
chr2:165942510 | C | T | 5 | a0003c0003t0001g0077 a0003c0003t0001g0078 a0003c0003t0001g0079 others(2): Show |
5 | HG00423.hp1 HG02056.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+709G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942510 | |||||||
chr2:165942551 | A | G | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+668T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942551 | |||||||
chr2:165942682 | T | C | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+537A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942682 | |||||||
chr2:165942717 | T | C | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.552+502A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942717 | |||||||
chr2:165942795 | T | C | 1 | a0003c0003t0001g0079 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.552+424A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942795 | |||||||
chr2:165942797 | A | T | 1 | a0001c0001t0019g0236 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.552+422T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942797 | |||||||
chr2:165942980 | AAAC | A | 3 | a0003c0003t0001g0077 a0003c0003t0001g0078 a0003c0003t0001g0079 |
3 | HG02056.hp1 NA18956.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.552+236_552+238del others(3): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165942980 | |||||||
chr2:165943080 | C | T | 4 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0280 others(1): Show |
4 | HG00735.hp2 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+139G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165943080 | |||||||
chr2:165943086 | T | C | 381 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(378): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.552+133A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 5/28 | chr2 | 165943086 | |||||||
chr2:165943599 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.430-258T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165943599 | |||||||
chr2:165943687 | G | T | 76 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(73): Show |
79 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.430-346C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165943687 | |||||||
chr2:165943715 | G | A | 1 | a0003c0003t0001g0259 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.430-374C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165943715 | |||||||
chr2:165943749 | C | G | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.430-408G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165943749 | |||||||
chr2:165943788 | A | C | 10 | a0001c0001t0003g0091 a0001c0001t0003g0161 a0001c0001t0003g0166 others(7): Show |
10 | HG01255.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-447T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165943788 | |||||||
chr2:165943865 | G | A | 1 | a0003c0003t0001g0260 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.430-524C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165943865 | |||||||
chr2:165943903 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.430-562G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165943903 | |||||||
chr2:165944046 | G | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.430-705C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165944046 | |||||||
chr2:165944362 | C | T | 2 | a0001c0001t0012g0300 a0001c0001t0012g0370 |
2 | NA18973.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.430-1021G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165944362 | |||||||
chr2:165944364 | T | C | 1 | a0001c0001t0001g0004 | 2 | NA19007.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.430-1023A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165944364 | |||||||
chr2:165944367 | G | A | 392 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(389): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.430-1026C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165944367 | |||||||
chr2:165944576 | T | C | 1 | a0002c0002t0007g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.429+948A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165944576 | |||||||
chr2:165944593 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.429+931A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165944593 | |||||||
chr2:165944750 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0182 a0001c0001t0002g0190 others(1): Show |
5 | HG00639.hp1 HG01099.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+774G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165944750 | |||||||
chr2:165944953 | C | T | 1 | a0016c0030t0001g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429+571G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165944953 | |||||||
chr2:165945015 | G | C | 2 | a0006c0015t0001g0388 a0006c0015t0001g0389 |
2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.429+509C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165945015 | |||||||
chr2:165945140 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0025 |
4 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+384A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165945140 | |||||||
chr2:165945262 | AAAAG | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.429+258_429+261del others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165945262 | |||||||
chr2:165945372 | T | G | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.429+152A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165945372 | |||||||
chr2:165945414 | C | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
302 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.429+110G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165945414 | |||||||
chr2:165945417 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.429+107C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 4/28 | chr2 | 165945417 | |||||||
chr2:165945779 | CTT | C | 4 | a0002c0002t0001g0093 a0002c0002t0010g0011 a0002c0002t0010g0092 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-91_263-90delAA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165945779 | |||||||
chr2:165945796 | ACTGT | A | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.263-110_263-107del others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165945796 | |||||||
chr2:165945834 | C | CT | 5 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0196 others(2): Show |
5 | HG01433.hp1 HG01496.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-145dupA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165945834 | |||||||
chr2:165945850 | A | G | 1 | a0001c0001t0003g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.263-160T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165945850 | |||||||
chr2:165945912 | T | A | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-222A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165945912 | |||||||
chr2:165946035 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.263-345G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946035 | |||||||
chr2:165946055 | G | A | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263-365C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946055 | |||||||
chr2:165946141 | C | T | 3 | a0003c0003t0006g0242 a0003c0003t0006g0243 a0003c0003t0006g0262 |
3 | NA18940.hp1 NA18986.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.263-451G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946141 | |||||||
chr2:165946169 | CA | C | 167 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(164): Show |
171 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.263-480delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946169 | |||||||
chr2:165946169 | CAA | C | 110 | a0001c0001t0001g0235 a0001c0001t0001g0295 a0001c0001t0003g0160 others(107): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.263-481_263-480del others(2): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946169 | |||||||
chr2:165946199 | C | T | 3 | a0001c0001t0004g0059 a0001c0001t0004g0060 a0021c0025t0004g0058 |
3 | NA18980.hp1 NA18989.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.263-509G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946199 | |||||||
chr2:165946295 | C | T | 10 | a0001c0001t0001g0173 a0002c0028t0001g0369 a0005c0007t0001g0009 others(7): Show |
11 | HG01175.hp1 HG01496.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.263-605G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946295 | |||||||
chr2:165946297 | C | T | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263-607G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946297 | |||||||
chr2:165946320 | T | C | 32 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0173 others(29): Show |
32 | HG00558.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.263-630A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946320 | |||||||
chr2:165946371 | A | G | 1 | a0017c0023t0008g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.263-681T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946371 | |||||||
chr2:165946393 | A | T | 1 | a0001c0001t0013g0187 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.263-703T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946393 | |||||||
chr2:165946433 | T | C | 4 | a0002c0008t0001g0275 a0002c0008t0001g0276 a0002c0008t0001g0277 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-743A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946433 | |||||||
chr2:165946582 | G | A | 83 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(80): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.263-892C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946582 | |||||||
chr2:165946658 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.263-968G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946658 | |||||||
chr2:165946742 | C | G | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.263-1052G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946742 | |||||||
chr2:165946860 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
90 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.263-1170A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946860 | |||||||
chr2:165946877 | T | C | 4 | a0004c0005t0001g0381 a0004c0005t0001g0386 a0004c0005t0001g0390 others(1): Show |
4 | HG01261.hp1 HG02257.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1187A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946877 | |||||||
chr2:165946889 | T | C | 7 | a0001c0001t0005g0032 a0001c0001t0005g0038 a0001c0001t0005g0039 others(4): Show |
7 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-1199A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946889 | |||||||
chr2:165946899 | G | A | 74 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0093 others(71): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.263-1209C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165946899 | |||||||
chr2:165947143 | ACT | A | 5 | a0001c0001t0004g0033 a0001c0001t0004g0059 a0001c0001t0004g0060 others(2): Show |
5 | NA18980.hp1 NA18982.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1455_263-1454d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947143 | |||||||
chr2:165947143 | ACTCT | A | 88 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(85): Show |
89 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.263-1457_263-1454d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947143 | |||||||
chr2:165947169 | C | CAT | 33 | a0001c0001t0001g0337 a0001c0001t0008g0224 a0001c0001t0008g0225 others(30): Show |
33 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.263-1481_263-1480d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATAT | 9 | a0001c0001t0001g0111 a0001c0001t0003g0223 a0004c0010t0018g0380 others(6): Show |
10 | HG00140.hp1 HG01496.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.263-1483_263-1480d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATAT | 31 | a0001c0001t0002g0002 a0001c0001t0002g0196 a0001c0001t0002g0197 others(28): Show |
33 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.263-1485_263-1480d others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(1): Show |
22 | a0001c0001t0001g0067 a0001c0001t0001g0384 a0001c0001t0002g0007 others(19): Show |
23 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.263-1487_263-1480d others(10): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(3): Show |
4 | a0001c0001t0001g0336 a0001c0001t0002g0186 a0004c0005t0001g0381 others(1): Show |
4 | HG01261.hp1 HG02148.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1489_263-1480d others(12): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(5): Show |
3 | a0001c0004t0003g0110 a0002c0028t0001g0369 a0019c0020t0002g0184 |
3 | HG03195.hp1 HG03516.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.263-1491_263-1480d others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(7): Show |
9 | a0001c0001t0001g0065 a0001c0001t0001g0235 a0001c0001t0003g0183 others(6): Show |
9 | HG02071.hp1 HG02723.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-1493_263-1480d others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(9): Show |
3 | a0001c0001t0002g0182 a0002c0002t0001g0093 a0002c0008t0001g0276 |
3 | HG02615.hp2 HG03579.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.263-1495_263-1480d others(18): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(11): Show |
3 | a0001c0001t0003g0181 a0002c0002t0010g0011 a0002c0008t0001g0275 |
3 | HG01358.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.263-1497_263-1480d others(20): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(13): Show |
26 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0063 others(23): Show |
27 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.263-1499_263-1480d others(22): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(15): Show |
11 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0290 others(8): Show |
11 | HG01934.hp2 HG02109.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.263-1501_263-1480d others(24): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(17): Show |
16 | a0001c0001t0001g0288 a0001c0001t0001g0308 a0001c0001t0001g0309 others(13): Show |
16 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.263-1503_263-1480d others(26): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(19): Show |
13 | a0001c0001t0001g0056 a0001c0001t0001g0090 a0001c0001t0001g0095 others(10): Show |
13 | HG01884.hp1 HG02040.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(28): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(21): Show |
15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG01168.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(30): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(23): Show |
13 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
13 | HG01891.hp1 HG02735.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(32): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(25): Show |
21 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
22 | HG00438.hp2 HG00741.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(34): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(27): Show |
9 | a0001c0001t0001g0373 a0001c0001t0003g0091 a0001c0001t0003g0176 others(6): Show |
9 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(29): Show |
13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG00609.hp1 HG01255.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(38): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(31): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
17 | HG00140.hp2 HG00735.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(40): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(33): Show |
16 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0028 others(13): Show |
16 | HG02071.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(42): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(35): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(9): Show |
13 | HG01109.hp2 HG02155.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(44): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(37): Show |
9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG00558.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.263-1480_263-1479i others(46): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(39): Show |
1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.263-1480_263-1479i others(48): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(41): Show |
1 | a0001c0009t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.263-1480_263-1479i others(50): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(45): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02523.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.263-1480_263-1479i others(54): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(51): Show |
1 | a0001c0001t0001g0358 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.263-1480_263-1479i others(60): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | C | CATATATA others(27): Show |
2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.263-1480_263-1479i others(36): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | CAT | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0002c0002t0001g0151 others(1): Show |
4 | HG00673.hp1 NA18972.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1481_263-1480d others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | CATAT | C | 68 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0116 others(65): Show |
71 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.263-1483_263-1480d others(6): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947169 | CATATATA others(5): Show |
C | 4 | a0001c0001t0002g0228 a0001c0001t0008g0226 a0001c0001t0008g0227 others(1): Show |
4 | HG01109.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1491_263-1480d others(14): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947169 | |||||||
chr2:165947193 | T | TATATATA others(30): Show |
1 | a0001c0004t0003g0112 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.263-1504_263-1503i others(39): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947193 | |||||||
chr2:165947193 | T | TATATATA others(42): Show |
1 | a0001c0001t0001g0071 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.263-1504_263-1503i others(51): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947193 | |||||||
chr2:165947276 | GAAGAAAT others(2): Show |
G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.263-1595_263-1587d others(11): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947276 | |||||||
chr2:165947594 | T | C | 1 | a0009c0013t0001g0378 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.262+1800A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947594 | |||||||
chr2:165947617 | C | G | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.262+1777G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947617 | |||||||
chr2:165947783 | T | C | 1 | a0002c0002t0001g0157 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.262+1611A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947783 | |||||||
chr2:165947846 | C | G | 1 | a0001c0001t0001g0290 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.262+1548G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947846 | |||||||
chr2:165947891 | C | T | 1 | a0004c0005t0001g0381 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.262+1503G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947891 | |||||||
chr2:165947992 | T | A | 1 | a0009c0013t0001g0379 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.262+1402A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165947992 | |||||||
chr2:165948028 | G | A | 1 | a0002c0002t0001g0364 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.262+1366C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948028 | |||||||
chr2:165948058 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0020g0014 |
2 | NA19009.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.262+1336G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948058 | |||||||
chr2:165948060 | G | A | 1 | a0001c0001t0001g0357 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.262+1334C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948060 | |||||||
chr2:165948117 | C | T | 175 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(172): Show |
179 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.262+1277G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948117 | |||||||
chr2:165948236 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.262+1158A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948236 | |||||||
chr2:165948262 | A | ATT | 249 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(246): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.262+1131_262+1132i others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948262 | |||||||
chr2:165948274 | G | A | 89 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(86): Show |
90 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.262+1120C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948274 | |||||||
chr2:165948440 | T | C | 1 | a0002c0002t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.262+954A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948440 | |||||||
chr2:165948546 | T | C | 1 | a0002c0002t0001g0364 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.262+848A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948546 | |||||||
chr2:165948616 | T | C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.262+778A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948616 | |||||||
chr2:165948757 | G | T | 175 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(172): Show |
179 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.262+637C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165948757 | |||||||
chr2:165949083 | C | T | 1 | a0003c0003t0001g0241 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.262+311G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 3/28 | chr2 | 165949083 | |||||||
chr2:165949883 | A | T | 1 | a0001c0001t0002g0265 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.22-159T>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165949883 | |||||||
chr2:165950070 | T | TA | 236 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(233): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.22-347dupT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950070 | |||||||
chr2:165950070 | T | TAA | 9 | a0001c0001t0001g0338 a0002c0002t0001g0006 a0002c0002t0001g0151 others(6): Show |
10 | NA18972.hp2 NA18975.hp2 NA18988.hp2 others(7): Show |
intron_variant | MODIFIER | c.22-348_22-347dupTT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950070 | |||||||
chr2:165950096 | G | T | 68 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0116 others(65): Show |
71 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.22-372C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950096 | |||||||
chr2:165950124 | TA | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
115 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.22-401delT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950124 | |||||||
chr2:165950124 | TAA | T | 281 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(278): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.22-402_22-401delTT | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950124 | |||||||
chr2:165950242 | C | T | 1 | a0002c0008t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.22-518G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950242 | |||||||
chr2:165950294 | G | A | 1 | a0002c0002t0009g0396 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.22-570C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950294 | |||||||
chr2:165950399 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.22-675T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950399 | |||||||
chr2:165950423 | G | T | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG01168.hp2 HG01192.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-699C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950423 | |||||||
chr2:165950549 | G | C | 89 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(86): Show |
90 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.22-825C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950549 | |||||||
chr2:165950776 | T | A | 21 | a0001c0001t0001g0339 a0001c0001t0001g0340 a0001c0001t0001g0341 others(18): Show |
21 | HG00673.hp2 HG01884.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.22-1052A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950776 | |||||||
chr2:165950949 | T | C | 1 | a0007c0012t0005g0375 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.22-1225A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165950949 | |||||||
chr2:165951020 | T | C | 5 | a0002c0002t0001g0008 a0002c0002t0001g0237 a0002c0002t0001g0239 others(2): Show |
6 | HG00099.hp2 HG01106.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.22-1296A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951020 | |||||||
chr2:165951090 | C | T | 249 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0088 others(246): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.22-1366G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951090 | |||||||
chr2:165951253 | G | A | 30 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.22-1529C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951253 | |||||||
chr2:165951259 | T | C | 1 | a0002c0028t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.22-1535A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951259 | |||||||
chr2:165951269 | G | A | 380 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(377): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.22-1545C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951269 | |||||||
chr2:165951284 | A | G | 1 | a0002c0014t0004g0005 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.22-1560T>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951284 | |||||||
chr2:165951549 | T | A | 12 | a0001c0001t0001g0384 a0004c0005t0001g0263 a0004c0005t0001g0360 others(9): Show |
12 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.22-1825A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951549 | |||||||
chr2:165951576 | C | A | 1 | a0004c0010t0003g0387 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.22-1852G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951576 | |||||||
chr2:165951754 | G | A | 1 | a0001c0001t0001g0358 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.21+1931C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951754 | |||||||
chr2:165951770 | T | C | 1 | a0013c0027t0004g0264 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.21+1915A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951770 | |||||||
chr2:165951877 | T | A | 2 | a0001c0001t0011g0072 a0001c0001t0011g0073 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.21+1808A>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951877 | |||||||
chr2:165951922 | A | C | 5 | a0001c0001t0011g0279 a0002c0008t0001g0275 a0002c0008t0001g0276 others(2): Show |
5 | HG02723.hp1 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.21+1763T>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951922 | |||||||
chr2:165951994 | C | T | 6 | a0005c0007t0001g0009 a0005c0007t0001g0085 a0005c0007t0001g0087 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.21+1691G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165951994 | |||||||
chr2:165952006 | T | G | 2 | a0001c0001t0011g0072 a0001c0001t0011g0073 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.21+1679A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952006 | |||||||
chr2:165952072 | G | C | 2 | a0001c0001t0001g0358 a0001c0001t0002g0265 |
2 | HG02698.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.21+1613C>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952072 | |||||||
chr2:165952128 | G | A | 2 | a0002c0002t0001g0266 a0002c0002t0001g0267 |
2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.21+1557C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952128 | |||||||
chr2:165952257 | AT | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
90 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.21+1427delA | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952257 | |||||||
chr2:165952291 | T | G | 2 | a0003c0003t0001g0080 a0003c0003t0001g0081 |
2 | HG00423.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.21+1394A>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952291 | |||||||
chr2:165952366 | A | ATG | 376 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(373): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.21+1318_21+1319ins others(2): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952366 | |||||||
chr2:165952425 | C | T | 1 | a0001c0009t0001g0113 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.21+1260G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952425 | |||||||
chr2:165952620 | G | T | 1 | a0004c0005t0001g0360 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.21+1065C>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952620 | |||||||
chr2:165952750 | T | C | 391 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(388): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.21+935A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165952750 | |||||||
chr2:165953054 | C | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
98 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.21+631G>C | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953054 | |||||||
chr2:165953241 | T | C | 2 | a0001c0001t0003g0082 a0001c0001t0003g0083 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.21+444A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953241 | |||||||
chr2:165953263 | T | C | 1 | a0001c0001t0008g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.21+422A>G | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953263 | |||||||
chr2:165953388 | C | A | 4 | a0002c0002t0004g0270 a0002c0002t0004g0271 a0002c0002t0004g0272 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.21+297G>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953388 | |||||||
chr2:165953508 | G | A | 8 | a0001c0001t0011g0279 a0002c0008t0001g0275 a0002c0008t0001g0276 others(5): Show |
9 | HG01496.hp1 HG02723.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.21+177C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953508 | |||||||
chr2:165953520 | G | A | 5 | a0001c0001t0001g0280 a0005c0007t0001g0085 a0005c0007t0001g0087 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.21+165C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953520 | |||||||
chr2:165953556 | G | A | 2 | a0006c0015t0001g0388 a0006c0015t0001g0389 |
2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.21+129C>T | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953556 | |||||||
chr2:165953603 | C | T | 2 | a0007c0012t0001g0374 a0007c0012t0005g0375 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.21+82G>A | TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953603 | |||||||
chr2:165953651 | G | GCCCGCCC others(5): Show |
79 | a0001c0001t0001g0010 a0001c0001t0001g0284 a0001c0001t0001g0285 others(76): Show |
80 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.21+33_21+34insTGAG others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953651 | |||||||
chr2:165953651 | G | GCCCGCCC others(13): Show |
4 | a0001c0001t0001g0371 a0001c0001t0001g0372 a0001c0001t0001g0373 others(1): Show |
4 | NA18977.hp1 NA19006.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+33_21+34insTGAG others(16): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953651 | |||||||
chr2:165953651 | G | GCCCGCCC others(5): Show |
3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18944.hp1 NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.21+33_21+34insTGAG others(8): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953651 | |||||||
chr2:165953651 | G | GCCCGCTC others(1): Show |
196 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0111 others(193): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.21+26_21+33dupTGAG others(4): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953651 | |||||||
chr2:165953651 | G | GCCCGCTC others(9): Show |
15 | a0001c0001t0002g0365 a0001c0001t0002g0366 a0002c0002t0001g0364 others(12): Show |
15 | HG00438.hp1 HG00544.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.21+18_21+33dupTGAG others(12): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953651 | |||||||
chr2:165953651 | G | GCCCGCTC others(17): Show |
16 | a0001c0001t0001g0384 a0003c0003t0001g0376 a0003c0003t0001g0377 others(13): Show |
16 | HG00735.hp2 HG01175.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.21+10_21+33dupTGAG others(20): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953651 | |||||||
chr2:165953651 | G | GCCCGCTC others(25): Show |
2 | a0004c0005t0001g0390 a0004c0005t0001g0391 |
2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.21+2_21+33dupTGAGC others(27): Show |
TTC21B | ENSG00000123607.16 | transcript | ENST00000243344.8 | protein_coding | 1/28 | chr2 | 165953651 |