Item | Value |
---|---|
geneid | 6905 |
ensemblid | ENSG00000284770.2 |
hgncid | 11582 |
symbol | TBCE |
name | tubulin folding cofactor E |
refseq_nuc | NM_003193.5 |
refseq_prot | NP_003184.1 |
ensembl_nuc | ENST00000642610.2 |
ensembl_prot | ENSP00000494796.1 |
mane_status | MANE Select |
chr | chr1 |
start | 235367427 |
end | 235452443 |
strand | + |
ver | v1.2 |
region | chr1:235367427-235452443 |
region5000 | chr1:235362427-235457443 |
regionname0 | TBCE_chr1_235367427_235452443 |
regionname5000 | TBCE_chr1_235362427_235457443 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 527 | 261 | 70 | 60 | 85 | 8 | 36 | 67 | TBCE_chr1_235362427_235457443 | TBCE | MSDTL others(522): Show |
chr1 | 235362427 | 235457443 |
a0002 | 0/0 | 527 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | MSDTL others(522): Show |
chr1 | 235362427 | 235457443 |
a0003 | 0/0 | 527 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | MSDTL others(522): Show |
chr1 | 235362427 | 235457443 |
a0004 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | MSDTL others(522): Show |
chr1 | 235362427 | 235457443 |
a0005 | 0/0 | 527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | MSDTL others(522): Show |
chr1 | 235362427 | 235457443 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1581 | 254 | 66 | 57 | 85 | 8 | 36 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 | ||
a0001c0003 | 0/0 | 1581 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 | ||
a0001c0005 | 0/0 | 1581 | 2 | 1 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 | ||
a0001c0007 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 | ||
a0001c0009 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 | ||
a0002c0002 | 0/0 | 1581 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 | ||
a0003c0004 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 | ||
a0004c0006 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 | ||
a0005c0008 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | ATGAG others(1576): Show |
chr1 | 235362427 | 235457443 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5373 | 65 | 7 | 21 | 24 | 1 | 11 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0002 | 1/0 | 5374 | 60 | 2 | 14 | 32 | 1 | 10 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0003 | 0/0 | 5372 | 32 | 5 | 9 | 11 | 5 | 2 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5367): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0004 | 0/0 | 5378 | 27 | 14 | 4 | 3 | 0 | 6 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5373): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0005 | 0/0 | 5371 | 14 | 10 | 3 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5366): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0006 | 0/0 | 5374 | 9 | 2 | 0 | 7 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0007 | 0/0 | 5374 | 6 | 4 | 0 | 2 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0008 | 0/0 | 5371 | 5 | 5 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5366): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0009 | 0/0 | 5378 | 3 | 2 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5373): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0011 | 0/0 | 5375 | 3 | 0 | 0 | 1 | 0 | 2 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5370): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0012 | 0/0 | 5372 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5367): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0013 | 0/0 | 5373 | 3 | 1 | 2 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0014 | 0/0 | 5372 | 2 | 2 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5367): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0015 | 0/0 | 5373 | 2 | 0 | 0 | 1 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0016 | 0/0 | 5370 | 2 | 1 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5365): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0017 | 0/0 | 5378 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5373): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0018 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5366): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0019 | 0/0 | 5378 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5373): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0020 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0021 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0022 | 0/0 | 5374 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0023 | 0/0 | 5374 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0024 | 0/0 | 5374 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0025 | 0/0 | 5374 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0026 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5356): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0027 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5356): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0028 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0029 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0030 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0032 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5367): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0033 | 0/0 | 5372 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5367): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0034 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0001t0036 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0003t0001 | 0/0 | 5373 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0005t0035 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0005t0038 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0007t0001 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0001c0009t0007 | 0/0 | 5374 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0002c0002t0010 | 0/0 | 5378 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5373): Show |
chr1 | 235362427 | 235457443 |
a0003c0004t0031 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0003c0004t0037 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
a0004c0006t0002 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5369): Show |
chr1 | 235362427 | 235457443 |
a0005c0008t0001 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | GCCAG others(5368): Show |
chr1 | 235362427 | 235457443 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0009g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0011g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0011g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0013g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0013g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0014g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0015g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0015g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0016g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0017g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0018g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0019g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0020g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0021g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0022g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0023g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0024g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0025g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0026g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0027g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0028g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0029g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0030g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0032g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0033g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0034g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0001t0036g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0005t0035g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0005t0038g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0007t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0001c0009t0007g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0002c0002t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0002c0002t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0002c0002t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0003c0004t0031g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0003c0004t0037g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0004c0006t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
a0005c0008t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0069 | EUR | GBR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0015 | EUR | GBR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | GBR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0066 | EUR | FIN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0212 | EUR | FIN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00642 | hp2 | a0001 | c0001 | t0032 | g0064 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00733 | hp1 | a0001 | c0001 | t0020 | g0001 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01070 | hp2 | a0001 | c0005 | t0038 | g0155 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01099 | hp2 | a0001 | c0007 | t0001 | g0060 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0020 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01109 | hp2 | a0001 | c0001 | t0016 | g0183 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01168 | hp1 | a0001 | c0001 | t0013 | g0130 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01169 | hp2 | a0001 | c0001 | t0013 | g0131 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01243 | hp1 | a0001 | c0009 | t0007 | g0264 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0162 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0169 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01891 | hp1 | a0002 | c0002 | t0010 | g0023 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02027 | hp1 | a0001 | c0001 | t0019 | g0157 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0073 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02071 | hp1 | a0001 | c0001 | t0025 | g0091 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0265 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | CDX | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0186 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02258 | hp1 | a0001 | c0001 | t0016 | g0185 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02280 | hp2 | a0001 | c0001 | t0018 | g0009 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02572 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02622 | hp1 | a0001 | c0001 | t0014 | g0189 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0177 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02738 | hp1 | a0001 | c0001 | t0021 | g0199 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0173 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0013 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02922 | hp1 | a0002 | c0002 | t0010 | g0017 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02976 | hp2 | a0004 | c0006 | t0002 | g0123 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03017 | hp2 | a0001 | c0001 | t0022 | g0206 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03098 | hp1 | a0001 | c0001 | t0034 | g0031 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03130 | hp1 | a0001 | c0001 | t0033 | g0261 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03130 | hp2 | a0001 | c0001 | t0036 | g0175 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0168 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0203 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03491 | hp1 | a0001 | c0001 | t0011 | g0232 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03516 | hp2 | a0001 | c0001 | t0030 | g0154 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03540 | hp2 | a0001 | c0001 | t0027 | g0128 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03579 | hp2 | a0001 | c0001 | t0012 | g0141 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03654 | hp2 | a0001 | c0001 | t0015 | g0254 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03669 | hp2 | a0001 | c0001 | t0023 | g0230 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03704 | hp2 | a0001 | c0001 | t0011 | g0247 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0197 | SAS | BEB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0184 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0159 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18522 | hp2 | a0003 | c0004 | t0031 | g0016 | AFR | YRI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | YRI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18906 | hp2 | a0001 | c0001 | t0026 | g0129 | AFR | YRI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18951 | hp2 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18956 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19011 | hp1 | a0001 | c0001 | t0028 | g0071 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19011 | hp2 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19012 | hp1 | a0005 | c0008 | t0001 | g0242 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19012 | hp2 | a0001 | c0001 | t0011 | g0223 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19057 | hp1 | a0001 | c0001 | t0015 | g0239 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19082 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19085 | hp2 | a0001 | c0001 | t0029 | g0082 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA20129 | hp1 | a0001 | c0001 | t0017 | g0021 | AFR | ASW | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | ASW | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA20805 | hp1 | a0001 | c0001 | t0024 | g0211 | EUR | TSI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0067 | EUR | TSI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | GIH | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02559 | hp1 | a0001 | c0001 | t0013 | g0152 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03471 | hp1 | a0001 | c0005 | t0035 | g0260 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG06807 | hp1 | a0002 | c0002 | t0010 | g0019 | AFR | USA | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | USA | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA20300 | hp1 | a0003 | c0004 | t0037 | g0172 | AFR | USA | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | USA | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0070 | REF | REF | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0213 | REF | REF | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:235430758 | T | C | 1 | a0003 | 2 | NA18522.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.614T>C | p.Val205Ala | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/17 | 723/5374 | 614/1584 | 205/527 | chr1 | 235430758 | |||
chr1:235434210 | C | T | 1 | a0005 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.667C>T | p.Arg223Trp | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/17 | 776/5374 | 667/1584 | 223/527 | chr1 | 235434210 | |||
chr1:235436560 | G | C | 1 | a0004 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.915G>C | p.Met305Ile | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/17 | 1024/5374 | 915/1584 | 305/527 | chr1 | 235436560 | |||
chr1:235437356 | G | C | 1 | a0002 | 3 | HG01891.hp1 HG02922.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.998G>C | p.Ser333Thr | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/17 | 1107/5374 | 998/1584 | 333/527 | chr1 | 235437356 | |||
chr1:235438878 | A | G | 1 | a0003 | 2 | NA18522.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.1226A>G | p.Glu409Gly | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/17 | 1335/5374 | 1226/1584 | 409/527 | chr1 | 235438878 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:235430729 | C | T | 1 | a0001c0009 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.585C>T | p.Ser195Ser | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/17 | 694/5374 | 585/1584 | 195/527 | chr1 | 235430729 | |||
chr1:235436395 | A | G | 1 | a0001c0007 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.843A>G | p.Gln281Gln | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 10/17 | 952/5374 | 843/1584 | 281/527 | chr1 | 235436395 | |||
chr1:235437408 | A | G | 1 | a0001c0003 | 3 | HG02809.hp2 HG03195.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.1050A>G | p.Glu350Glu | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/17 | 1159/5374 | 1050/1584 | 350/527 | chr1 | 235437408 | |||
chr1:235437426 | A | G | 2 | a0001c0005 a0003c0004 |
4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.1068A>G | p.Leu356Leu | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/17 | 1177/5374 | 1068/1584 | 356/527 | chr1 | 235437426 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:235367443 | T | A | 3 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0018 |
5 | HG01109.hp1 HG02280.hp2 HG03195.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-93T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/17 | 12607 | chr1 | 235367443 | ||||||
chr1:235367487 | T | C | 6 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0014 others(3): Show |
15 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-49T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/17 | 12563 | chr1 | 235367487 | ||||||
chr1:235448811 | T | C | 1 | a0001c0001t0017 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 49 | chr1 | 235448811 | ||||||
chr1:235448904 | T | A | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(2): Show |
35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*142T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 142 | chr1 | 235448904 | ||||||
chr1:235448913 | G | A | 1 | a0001c0001t0020 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 151 | chr1 | 235448913 | ||||||
chr1:235448991 | A | G | 1 | a0001c0005t0038 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*229A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 229 | chr1 | 235448991 | ||||||
chr1:235449005 | C | T | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(31): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 243 | chr1 | 235449005 | ||||||
chr1:235449079 | C | CAGTT | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(2): Show |
35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*322dupGTTA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 323 | INFO_REALIGN_3_PRIME | chr1 | 235449079 | |||||
chr1:235449138 | AAAGGGTT others(5): Show |
A | 2 | a0001c0001t0026 a0001c0001t0027 |
2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379_*390delGGGTTA others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 379 | INFO_REALIGN_3_PRIME | chr1 | 235449138 | |||||
chr1:235449314 | ATCT | A | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0016 others(1): Show |
22 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*559_*561delTCT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 559 | INFO_REALIGN_3_PRIME | chr1 | 235449314 | |||||
chr1:235449341 | T | C | 1 | a0001c0001t0021 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 579 | chr1 | 235449341 | ||||||
chr1:235449512 | T | C | 2 | a0001c0001t0026 a0001c0001t0027 |
2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*750T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 750 | chr1 | 235449512 | ||||||
chr1:235449704 | T | C | 1 | a0001c0001t0028 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*942T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 942 | chr1 | 235449704 | ||||||
chr1:235449933 | G | T | 1 | a0001c0001t0025 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1171G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1171 | chr1 | 235449933 | ||||||
chr1:235449983 | C | T | 1 | a0003c0004t0037 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1221 | chr1 | 235449983 | ||||||
chr1:235450009 | T | G | 2 | a0001c0001t0026 a0001c0001t0027 |
2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1247T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1247 | chr1 | 235450009 | ||||||
chr1:235450103 | G | C | 1 | a0001c0001t0022 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1341G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1341 | chr1 | 235450103 | ||||||
chr1:235450114 | C | T | 1 | a0001c0001t0036 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1352C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1352 | chr1 | 235450114 | ||||||
chr1:235450264 | G | A | 1 | a0001c0001t0019 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1502G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1502 | chr1 | 235450264 | ||||||
chr1:235450412 | A | G | 2 | a0001c0005t0035 a0001c0005t0038 |
2 | HG01070.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1650A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1650 | chr1 | 235450412 | ||||||
chr1:235450599 | C | T | 1 | a0001c0001t0034 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1837C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1837 | chr1 | 235450599 | ||||||
chr1:235450708 | G | A | 2 | a0001c0001t0026 a0001c0001t0027 |
2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1946 | chr1 | 235450708 | ||||||
chr1:235450794 | T | C | 2 | a0001c0001t0029 a0001c0001t0036 |
2 | HG03130.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2032T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2032 | chr1 | 235450794 | ||||||
chr1:235450814 | T | TA | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(2): Show |
35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2058dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2059 | INFO_REALIGN_3_PRIME | chr1 | 235450814 | |||||
chr1:235450926 | A | G | 1 | a0001c0001t0027 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2164A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2164 | chr1 | 235450926 | ||||||
chr1:235451063 | A | G | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(29): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*2301A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2301 | chr1 | 235451063 | ||||||
chr1:235451090 | G | A | 1 | a0001c0001t0012 | 3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2328G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2328 | chr1 | 235451090 | ||||||
chr1:235451350 | G | T | 1 | a0001c0005t0035 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2588G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2588 | chr1 | 235451350 | ||||||
chr1:235451472 | C | CA | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(3): Show |
33 | HG00733.hp2 HG01255.hp1 HG01261.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2730dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2731 | INFO_REALIGN_3_PRIME | chr1 | 235451472 | |||||
chr1:235451472 | CA | C | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0014 others(4): Show |
42 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2730delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2730 | INFO_REALIGN_3_PRIME | chr1 | 235451472 | |||||
chr1:235451630 | C | T | 1 | a0001c0001t0033 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2868C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2868 | chr1 | 235451630 | ||||||
chr1:235451690 | T | C | 2 | a0001c0001t0026 a0001c0001t0027 |
2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2928T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2928 | chr1 | 235451690 | ||||||
chr1:235452019 | GT | G | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(29): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*3268delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3268 | INFO_REALIGN_3_PRIME | chr1 | 235452019 | |||||
chr1:235452103 | C | A | 1 | a0001c0001t0013 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3341C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3341 | chr1 | 235452103 | ||||||
chr1:235452158 | G | A | 1 | a0001c0001t0023 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3396G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3396 | chr1 | 235452158 | ||||||
chr1:235452260 | C | T | 1 | a0001c0001t0036 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3498 | chr1 | 235452260 | ||||||
chr1:235452265 | C | T | 1 | a0001c0001t0024 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3503C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3503 | chr1 | 235452265 | ||||||
chr1:235452345 | G | C | 1 | a0001c0001t0032 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3583G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3583 | chr1 | 235452345 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:235367549 | G | C | 1 | a0001c0001t0006g0002 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-32+45G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235367549 | |||||||
chr1:235367550 | C | G | 1 | a0001c0001t0006g0002 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-32+46C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235367550 | |||||||
chr1:235367740 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-32+236T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235367740 | |||||||
chr1:235368053 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-32+549G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368053 | |||||||
chr1:235368071 | A | G | 8 | a0001c0001t0001g0262 a0001c0001t0001g0267 a0001c0001t0004g0263 others(5): Show |
8 | HG01243.hp1 HG01981.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32+567A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368071 | |||||||
chr1:235368136 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-32+632T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368136 | |||||||
chr1:235368142 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-32+638A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368142 | |||||||
chr1:235368262 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-32+758G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368262 | |||||||
chr1:235368290 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-32+786C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368290 | |||||||
chr1:235368414 | C | T | 5 | a0001c0001t0002g0195 a0001c0001t0004g0194 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+910C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368414 | |||||||
chr1:235368442 | C | CA | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+941dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368442 | ||||||
chr1:235368552 | C | CT | 22 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0258 others(19): Show |
22 | HG00140.hp1 HG01069.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32+1071dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | ||||||
chr1:235368552 | C | CTT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0025 others(107): Show |
110 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-32+1070_-32+1071d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | ||||||
chr1:235368552 | C | CTTT | 22 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(19): Show |
22 | HG00099.hp2 HG00621.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32+1069_-32+1071d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | ||||||
chr1:235368552 | C | CTTTT | 6 | a0001c0001t0002g0195 a0001c0001t0003g0153 a0001c0001t0004g0194 others(3): Show |
6 | HG01070.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+1068_-32+1071d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | ||||||
chr1:235368552 | C | CTTTTTT | 21 | a0001c0001t0001g0171 a0001c0001t0004g0156 a0001c0001t0004g0158 others(18): Show |
21 | HG00733.hp2 HG01255.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-32+1066_-32+1071d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | ||||||
chr1:235368552 | C | CTTTTTTT | 15 | a0001c0001t0002g0179 a0001c0001t0002g0190 a0001c0001t0003g0188 others(12): Show |
15 | HG00642.hp1 HG01109.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-32+1065_-32+1071d others(9): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | ||||||
chr1:235368596 | C | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32+1092C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368596 | |||||||
chr1:235368599 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1095C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368599 | |||||||
chr1:235368643 | C | T | 10 | a0001c0001t0008g0024 a0001c0001t0009g0008 a0001c0001t0009g0020 others(7): Show |
10 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32+1139C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368643 | |||||||
chr1:235368663 | A | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1159A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368663 | |||||||
chr1:235368791 | C | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1287C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368791 | |||||||
chr1:235368815 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1311T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368815 | |||||||
chr1:235368837 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1333G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368837 | |||||||
chr1:235368923 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1419T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368923 | |||||||
chr1:235368924 | A | T | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1420A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368924 | |||||||
chr1:235368925 | T | A | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1421T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368925 | |||||||
chr1:235368930 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1426C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368930 | |||||||
chr1:235368936 | G | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1432G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368936 | |||||||
chr1:235368948 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1444T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368948 | |||||||
chr1:235368951 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1447C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368951 | |||||||
chr1:235368960 | T | TCCTAATC others(30): Show |
1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1456_-32+1457i others(39): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368960 | |||||||
chr1:235368962 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1458A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368962 | |||||||
chr1:235368984 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1480A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368984 | |||||||
chr1:235368993 | G | T | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1489G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368993 | |||||||
chr1:235369040 | C | G | 44 | a0001c0001t0001g0171 a0001c0001t0002g0179 a0001c0001t0002g0190 others(41): Show |
44 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-32+1536C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369040 | |||||||
chr1:235369062 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1558G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369062 | |||||||
chr1:235369069 | C | T | 5 | a0001c0001t0001g0262 a0001c0001t0001g0267 a0001c0001t0004g0263 others(2): Show |
5 | HG01981.hp2 HG02109.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+1565C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369069 | |||||||
chr1:235369161 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+1657T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369161 | |||||||
chr1:235369202 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1698T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369202 | |||||||
chr1:235369208 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-32+1704T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369208 | |||||||
chr1:235369266 | T | G | 1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-32+1762T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369266 | |||||||
chr1:235369335 | C | T | 25 | a0001c0001t0001g0262 a0001c0001t0001g0267 a0001c0001t0002g0195 others(22): Show |
25 | HG01070.hp2 HG01109.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.-32+1831C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369335 | |||||||
chr1:235369437 | A | G | 1 | a0001c0001t0002g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-32+1933A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369437 | |||||||
chr1:235369461 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-32+1957C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369461 | |||||||
chr1:235369543 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-32+2039T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369543 | |||||||
chr1:235369604 | C | T | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-32+2100C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369604 | |||||||
chr1:235369659 | TA | T | 46 | a0001c0001t0001g0171 a0001c0001t0002g0179 a0001c0001t0002g0190 others(43): Show |
46 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.-32+2164delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235369659 | ||||||
chr1:235369659 | TAA | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.-32+2163_-32+2164d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235369659 | ||||||
chr1:235369790 | C | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32+2286C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369790 | |||||||
chr1:235369828 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-32+2324G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369828 | |||||||
chr1:235369832 | C | CA | 27 | a0001c0001t0001g0028 a0001c0001t0002g0179 a0001c0001t0002g0198 others(24): Show |
27 | HG00621.hp1 HG00642.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-32+2343dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235369832 | ||||||
chr1:235369832 | CA | C | 32 | a0001c0001t0001g0171 a0001c0001t0002g0190 a0001c0001t0003g0188 others(29): Show |
32 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-32+2343delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235369832 | ||||||
chr1:235369859 | C | T | 11 | a0001c0001t0002g0179 a0001c0001t0004g0007 a0001c0001t0004g0156 others(8): Show |
11 | HG00642.hp1 HG01361.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32+2355C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369859 | |||||||
chr1:235369867 | A | T | 10 | a0001c0001t0008g0024 a0001c0001t0009g0008 a0001c0001t0009g0020 others(7): Show |
10 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32+2363A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369867 | |||||||
chr1:235369909 | G | T | 5 | a0001c0001t0001g0262 a0001c0001t0001g0267 a0001c0001t0004g0263 others(2): Show |
5 | HG01981.hp2 HG02109.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+2405G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369909 | |||||||
chr1:235370088 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-32+2584G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370088 | |||||||
chr1:235370121 | G | A | 26 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0267 others(23): Show |
26 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.-32+2617G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370121 | |||||||
chr1:235370154 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-32+2650A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370154 | |||||||
chr1:235370252 | C | CT | 6 | a0001c0001t0002g0122 a0001c0001t0002g0249 a0001c0001t0002g0250 others(3): Show |
6 | HG02027.hp1 HG02300.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+2765dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370252 | ||||||
chr1:235370252 | C | CTT | 37 | a0001c0001t0001g0171 a0001c0001t0001g0262 a0001c0001t0001g0267 others(34): Show |
37 | HG00733.hp2 HG01070.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-32+2764_-32+2765d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370252 | ||||||
chr1:235370252 | CT | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0002g0034 others(4): Show |
7 | HG01069.hp1 HG01069.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32+2765delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370252 | ||||||
chr1:235370269 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-32+2765T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370269 | |||||||
chr1:235370276 | C | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32+2772C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370276 | |||||||
chr1:235370320 | C | T | 3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-32+2816C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370320 | |||||||
chr1:235370339 | T | C | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-32+2835T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370339 | |||||||
chr1:235370465 | T | C | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-32+2961T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370465 | |||||||
chr1:235370530 | C | T | 36 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0105 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32+3026C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370530 | |||||||
chr1:235370534 | A | G | 3 | a0001c0001t0008g0024 a0001c0001t0012g0013 a0001c0001t0012g0014 |
3 | HG02895.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-32+3030A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370534 | |||||||
chr1:235370540 | T | C | 3 | a0001c0001t0001g0037 a0001c0005t0035g0260 a0001c0005t0038g0155 |
3 | HG01070.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-32+3036T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370540 | |||||||
chr1:235370542 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-32+3038C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370542 | |||||||
chr1:235370543 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0121 a0001c0001t0002g0244 others(1): Show |
4 | HG02015.hp1 HG02257.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32+3039A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370543 | |||||||
chr1:235370546 | C | T | 28 | a0001c0001t0001g0171 a0001c0001t0003g0188 a0001c0001t0005g0124 others(25): Show |
28 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-32+3042C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370546 | |||||||
chr1:235370548 | G | GC | 3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-32+3045dupC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370548 | ||||||
chr1:235370550 | A | AT | 10 | a0001c0001t0001g0037 a0001c0001t0001g0145 a0001c0001t0001g0146 others(7): Show |
10 | HG01981.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32+3062dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370550 | ||||||
chr1:235370550 | A | T | 3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-32+3046A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370550 | |||||||
chr1:235370550 | AT | A | 60 | a0001c0001t0001g0171 a0001c0001t0002g0179 a0001c0001t0003g0188 others(57): Show |
60 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-32+3062delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370550 | ||||||
chr1:235370681 | A | G | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-32+3177A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370681 | |||||||
chr1:235370734 | C | CCTTT | 37 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(34): Show |
37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.-32+3233_-32+3234i others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370734 | ||||||
chr1:235370734 | CCTTGT | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.-32+3234_-32+3238d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370734 | ||||||
chr1:235370743 | T | G | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32+3239T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370743 | |||||||
chr1:235370745 | C | CT | 66 | a0001c0001t0001g0171 a0001c0001t0002g0179 a0001c0001t0002g0256 others(63): Show |
66 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.-32+3255dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370745 | ||||||
chr1:235370808 | G | C | 19 | a0001c0001t0001g0171 a0001c0001t0005g0124 a0001c0001t0005g0160 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-32+3304G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370808 | |||||||
chr1:235370810 | C | T | 11 | a0001c0001t0004g0011 a0001c0001t0004g0027 a0001c0001t0004g0038 others(8): Show |
11 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+3306C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370810 | |||||||
chr1:235370835 | G | T | 1 | a0001c0001t0002g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-32+3331G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370835 | |||||||
chr1:235370861 | T | C | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-32+3357T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370861 | |||||||
chr1:235371038 | C | CT | 29 | a0001c0001t0001g0032 a0001c0001t0001g0258 a0001c0001t0002g0047 others(26): Show |
29 | HG00140.hp2 HG01361.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32+3568dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | C | CTT | 16 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0121 others(13): Show |
16 | HG00621.hp1 HG02148.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-32+3567_-32+3568d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | C | CTTT | 31 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
31 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.-32+3566_-32+3568d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | C | CTTTT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(52): Show |
55 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.-32+3565_-32+3568d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | C | CTTTTT | 29 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0037 others(26): Show |
29 | HG00544.hp1 HG00544.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32+3564_-32+3568d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32+3556_-32+3568d others(15): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | CTTTTT | C | 22 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0041 others(19): Show |
22 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32+3564_-32+3568d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | CTTTTTT | C | 24 | a0001c0001t0002g0179 a0001c0001t0004g0011 a0001c0001t0004g0027 others(21): Show |
24 | HG00642.hp1 HG01261.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32+3563_-32+3568d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | CTTTTTTT | C | 13 | a0001c0001t0005g0124 a0001c0001t0005g0162 a0001c0001t0005g0163 others(10): Show |
13 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-32+3562_-32+3568d others(9): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0005g0160 a0001c0001t0022g0206 |
2 | HG02897.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-32+3557_-32+3568d others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | CTTTTTTT others(8): Show |
C | 3 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0135 |
3 | HG02809.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-32+3554_-32+3568d others(17): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | CTTTTTTT others(11): Show |
C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+3551_-32+3568d others(20): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371038 | CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-32+3548_-32+3568d others(23): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | ||||||
chr1:235371107 | A | C | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-32+3603A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371107 | |||||||
chr1:235371169 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+3665A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371169 | |||||||
chr1:235371197 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+3693C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371197 | |||||||
chr1:235371205 | C | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32+3701C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371205 | |||||||
chr1:235371435 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-32+3931A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371435 | |||||||
chr1:235371527 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-32+4023A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371527 | |||||||
chr1:235371564 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+4060T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371564 | |||||||
chr1:235371830 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+4326A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371830 | |||||||
chr1:235371838 | A | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+4334A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371838 | |||||||
chr1:235371963 | T | C | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+4459T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371963 | |||||||
chr1:235372002 | A | T | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+4498A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372002 | |||||||
chr1:235372067 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+4563G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372067 | |||||||
chr1:235372194 | A | G | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-32+4690A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372194 | |||||||
chr1:235372198 | C | T | 1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-32+4694C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372198 | |||||||
chr1:235372214 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-32+4710C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372214 | |||||||
chr1:235372250 | A | G | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+4746A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372250 | |||||||
chr1:235372347 | C | T | 1 | a0001c0001t0003g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-32+4843C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372347 | |||||||
chr1:235372461 | T | C | 1 | a0001c0001t0013g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-32+4957T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372461 | |||||||
chr1:235372552 | C | T | 1 | a0001c0001t0007g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-32+5048C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372552 | |||||||
chr1:235372562 | T | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5058T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372562 | |||||||
chr1:235372589 | C | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-32+5085C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372589 | |||||||
chr1:235372664 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5160T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372664 | |||||||
chr1:235372720 | C | T | 3 | a0001c0001t0002g0195 a0001c0001t0004g0194 a0001c0005t0035g0260 |
3 | HG02559.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-32+5216C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372720 | |||||||
chr1:235372750 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5246A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372750 | |||||||
chr1:235372781 | G | A | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+5277G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372781 | |||||||
chr1:235372785 | G | A | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+5281G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372785 | |||||||
chr1:235372872 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5368T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372872 | |||||||
chr1:235372881 | A | G | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32+5377A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372881 | |||||||
chr1:235372882 | C | T | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32+5378C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372882 | |||||||
chr1:235372922 | T | TA | 47 | a0001c0001t0001g0094 a0001c0001t0001g0125 a0001c0001t0001g0192 others(44): Show |
47 | HG00544.hp2 HG00642.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.-32+5441dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235372922 | ||||||
chr1:235372922 | TA | T | 8 | a0001c0001t0001g0032 a0001c0001t0002g0046 a0001c0001t0002g0222 others(5): Show |
8 | HG00099.hp1 HG01256.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32+5441delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235372922 | ||||||
chr1:235372948 | G | A | 1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-32+5444G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372948 | |||||||
chr1:235373071 | A | G | 3 | a0001c0001t0026g0129 a0001c0001t0027g0128 a0003c0004t0031g0016 |
3 | HG03540.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-32+5567A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373071 | |||||||
chr1:235373303 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5799A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373303 | |||||||
chr1:235373358 | G | A | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+5854G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373358 | |||||||
chr1:235373523 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+6019A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373523 | |||||||
chr1:235373570 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+6066A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373570 | |||||||
chr1:235373604 | C | T | 17 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.-32+6100C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373604 | |||||||
chr1:235373620 | TTTTATTT others(3): Show |
T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+6130_-32+6139d others(12): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235373620 | ||||||
chr1:235373630 | ATTTATT | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.-32+6141_-32+6146d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235373630 | ||||||
chr1:235373671 | C | T | 1 | a0001c0001t0011g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-32+6167C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373671 | |||||||
chr1:235373750 | GCCATTCT others(1265): Show |
G | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-31-6228_-31-4957d others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235373750 | ||||||
chr1:235373773 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-6246C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373773 | |||||||
chr1:235373791 | A | G | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6228A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373791 | |||||||
chr1:235373794 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-31-6225G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373794 | |||||||
chr1:235373795 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-31-6224C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373795 | |||||||
chr1:235373797 | C | T | 1 | a0001c0001t0034g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31-6222C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373797 | |||||||
chr1:235373803 | C | T | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6216C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373803 | |||||||
chr1:235373809 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.-31-6210T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373809 | |||||||
chr1:235373842 | T | G | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6177T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373842 | |||||||
chr1:235373843 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-6176G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373843 | |||||||
chr1:235373853 | G | T | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6166G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373853 | |||||||
chr1:235373860 | A | G | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6159A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373860 | |||||||
chr1:235373892 | T | G | 2 | a0001c0001t0008g0174 a0001c0005t0035g0260 |
2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-31-6127T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373892 | |||||||
chr1:235373929 | G | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-31-6090G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373929 | |||||||
chr1:235374097 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5922C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374097 | |||||||
chr1:235374103 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5916C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374103 | |||||||
chr1:235374155 | C | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31-5864C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374155 | |||||||
chr1:235374165 | A | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31-5854A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374165 | |||||||
chr1:235374207 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-31-5812C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374207 | |||||||
chr1:235374344 | G | T | 40 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0113 others(37): Show |
40 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.-31-5675G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374344 | |||||||
chr1:235374550 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5469A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374550 | |||||||
chr1:235374557 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5462G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374557 | |||||||
chr1:235374583 | C | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31-5436C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374583 | |||||||
chr1:235374584 | T | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-31-5435T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374584 | |||||||
chr1:235374680 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-31-5339T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374680 | |||||||
chr1:235374690 | G | A | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31-5329G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374690 | |||||||
chr1:235374790 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5229T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374790 | |||||||
chr1:235374920 | C | CT | 6 | a0001c0001t0001g0094 a0001c0001t0002g0198 a0001c0001t0005g0160 others(3): Show |
6 | HG00544.hp2 HG00621.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-5081dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235374920 | ||||||
chr1:235374920 | CT | C | 14 | a0001c0001t0001g0058 a0001c0001t0002g0144 a0001c0001t0002g0202 others(11): Show |
14 | HG01069.hp1 HG01099.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31-5081delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235374920 | ||||||
chr1:235374924 | T | C | 3 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0141 |
3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-31-5095T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374924 | |||||||
chr1:235375001 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.-31-5018A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375001 | |||||||
chr1:235375110 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-4909T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375110 | |||||||
chr1:235375118 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-4901T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375118 | |||||||
chr1:235375143 | A | G | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-31-4876A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375143 | |||||||
chr1:235375152 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG00099.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.-31-4867C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375152 | |||||||
chr1:235375253 | T | TAAC | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.-31-4763_-31-4761d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235375253 | ||||||
chr1:235375257 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-31-4762A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375257 | |||||||
chr1:235375705 | A | G | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-31-4314A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375705 | |||||||
chr1:235375768 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-4251C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375768 | |||||||
chr1:235375893 | A | G | 3 | a0001c0001t0026g0129 a0001c0001t0027g0128 a0003c0004t0031g0016 |
3 | HG03540.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-31-4126A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375893 | |||||||
chr1:235375904 | C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31-4115C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375904 | |||||||
chr1:235375986 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-4033T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375986 | |||||||
chr1:235376040 | T | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-31-3979T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376040 | |||||||
chr1:235376100 | T | C | 2 | a0001c0001t0002g0195 a0001c0001t0004g0194 |
2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-31-3919T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376100 | |||||||
chr1:235376129 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3890C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376129 | |||||||
chr1:235376173 | T | A | 1 | a0001c0001t0002g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-31-3846T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376173 | |||||||
chr1:235376225 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3794C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376225 | |||||||
chr1:235376276 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3743C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376276 | |||||||
chr1:235376411 | A | AG | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-3607dupG | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235376411 | ||||||
chr1:235376548 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-31-3471C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376548 | |||||||
chr1:235376842 | C | T | 35 | a0001c0001t0002g0179 a0001c0001t0002g0216 a0001c0001t0004g0006 others(32): Show |
35 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-31-3177C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376842 | |||||||
chr1:235376873 | G | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3146G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376873 | |||||||
chr1:235376967 | T | TAAAAAAA others(303): Show |
1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-31-3040_-31-3039i others(312): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235376967 | ||||||
chr1:235377094 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-31-2925G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377094 | |||||||
chr1:235377350 | T | A | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31-2669T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377350 | |||||||
chr1:235377389 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-2630T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377389 | |||||||
chr1:235377400 | C | T | 1 | a0001c0001t0007g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-31-2619C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377400 | |||||||
chr1:235377478 | C | G | 1 | a0001c0001t0013g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-31-2541C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377478 | |||||||
chr1:235377478 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-31-2541C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377478 | |||||||
chr1:235377501 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(51): Show |
54 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31-2518T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377501 | |||||||
chr1:235377656 | C | CT | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-31-2350dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235377656 | ||||||
chr1:235377744 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-31-2275C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377744 | |||||||
chr1:235377773 | T | A | 1 | a0001c0001t0003g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-31-2246T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377773 | |||||||
chr1:235377802 | G | A | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-31-2217G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377802 | |||||||
chr1:235377841 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-31-2178C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377841 | |||||||
chr1:235377925 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-2094A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377925 | |||||||
chr1:235377957 | C | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0100 others(1): Show |
4 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-2062C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377957 | |||||||
chr1:235378110 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-31-1909A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378110 | |||||||
chr1:235378189 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-31-1830G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378189 | |||||||
chr1:235378366 | G | A | 2 | a0001c0001t0022g0206 a0003c0004t0031g0016 |
2 | HG03017.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-31-1653G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378366 | |||||||
chr1:235378395 | AT | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-31-1615delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235378395 | ||||||
chr1:235378524 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0062 a0001c0001t0001g0087 |
3 | HG03710.hp1 NA18999.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-31-1495A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378524 | |||||||
chr1:235378572 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-1447C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378572 | |||||||
chr1:235378619 | A | G | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.-31-1400A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378619 | |||||||
chr1:235378708 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-31-1311A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378708 | |||||||
chr1:235378735 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-31-1284C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378735 | |||||||
chr1:235378848 | G | A | 1 | a0001c0001t0022g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-31-1171G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378848 | |||||||
chr1:235379088 | C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-31-931C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379088 | |||||||
chr1:235379249 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-31-770C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379249 | |||||||
chr1:235379253 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-31-766C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379253 | |||||||
chr1:235379275 | C | T | 6 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0054 others(3): Show |
6 | NA18956.hp1 NA18990.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31-744C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379275 | |||||||
chr1:235379345 | T | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-31-674T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379345 | |||||||
chr1:235379566 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-31-453C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379566 | |||||||
chr1:235379739 | A | G | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-31-280A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379739 | |||||||
chr1:235379818 | G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-201G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379818 | |||||||
chr1:235379834 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-185G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379834 | |||||||
chr1:235379947 | C | CA | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-31-55dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235379947 | ||||||
chr1:235379947 | C | CAA | 14 | a0001c0001t0001g0097 a0001c0001t0001g0125 a0001c0001t0001g0243 others(11): Show |
14 | HG01361.hp1 HG02109.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31-56_-31-55dupAA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235379947 | ||||||
chr1:235380155 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.100+6C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380155 | |||||||
chr1:235380161 | T | TTG | 2 | a0001c0001t0002g0224 a0001c0001t0002g0234 |
2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.100+64_100+65dupGT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTG | T | 27 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(24): Show |
27 | HG00621.hp1 HG01074.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.100+64_100+65delGT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTG | T | 19 | a0001c0001t0002g0106 a0001c0001t0002g0144 a0001c0001t0002g0195 others(16): Show |
19 | HG00639.hp2 HG01168.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.100+62_100+65delGT others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTG | T | 11 | a0001c0001t0002g0047 a0001c0001t0002g0122 a0001c0001t0002g0200 others(8): Show |
11 | HG00558.hp2 HG01256.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+60_100+65delGT others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(1): Show |
T | 15 | a0001c0001t0002g0088 a0001c0001t0002g0209 a0001c0001t0002g0225 others(12): Show |
15 | HG00544.hp1 HG00733.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+58_100+65delGT others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(3): Show |
T | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100+56_100+65delGT others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(5): Show |
T | 5 | a0001c0001t0001g0117 a0001c0001t0003g0067 a0001c0001t0007g0265 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+54_100+65delGT others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(7): Show |
T | 34 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0113 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.100+52_100+65delGT others(12): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(9): Show |
T | 18 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0061 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+50_100+65delGT others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(11): Show |
T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
63 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.100+48_100+65delGT others(16): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(13): Show |
T | 16 | a0001c0001t0001g0072 a0001c0001t0001g0136 a0001c0001t0002g0179 others(13): Show |
16 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+46_100+65delGT others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(15): Show |
T | 28 | a0001c0001t0002g0048 a0001c0001t0004g0007 a0001c0001t0004g0011 others(25): Show |
28 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.100+44_100+65delGT others(20): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380161 | TTGTGTGT others(17): Show |
T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+42_100+65delGT others(22): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | ||||||
chr1:235380202 | T | C | 1 | a0001c0001t0004g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.100+53T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380202 | |||||||
chr1:235380255 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+106T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380255 | |||||||
chr1:235380400 | A | G | 4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+251A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380400 | |||||||
chr1:235380496 | G | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+347G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380496 | |||||||
chr1:235380680 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+531A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380680 | |||||||
chr1:235380807 | C | T | 1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100+658C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380807 | |||||||
chr1:235380808 | A | G | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100+659A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380808 | |||||||
chr1:235380825 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+676A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380825 | |||||||
chr1:235380838 | T | G | 1 | a0001c0001t0004g0134 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100+689T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380838 | |||||||
chr1:235381003 | TCGAA | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+856_100+859del others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381003 | ||||||
chr1:235381022 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+873T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381022 | |||||||
chr1:235381150 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+1001A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381150 | |||||||
chr1:235381407 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+1258G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381407 | |||||||
chr1:235381430 | T | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+1281T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381430 | |||||||
chr1:235381542 | G | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+1393G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381542 | |||||||
chr1:235381557 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+1408A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381557 | |||||||
chr1:235381624 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+1475G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381624 | |||||||
chr1:235381664 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+1515G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381664 | |||||||
chr1:235381672 | G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.100+1523G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381672 | |||||||
chr1:235381685 | C | CA | 21 | a0001c0001t0001g0087 a0001c0001t0002g0046 a0001c0001t0002g0047 others(18): Show |
21 | HG00280.hp2 HG00558.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+1563dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381685 | ||||||
chr1:235381685 | CA | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.100+1563delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381685 | ||||||
chr1:235381685 | CAA | C | 31 | a0001c0001t0002g0179 a0001c0001t0003g0066 a0001c0001t0004g0011 others(28): Show |
31 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.100+1562_100+1563d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381685 | ||||||
chr1:235381733 | A | G | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100+1584A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381733 | |||||||
chr1:235381750 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+1601T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381750 | |||||||
chr1:235381779 | CT | C | 6 | a0001c0001t0002g0253 a0001c0001t0002g0259 a0001c0001t0007g0045 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+1638delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381779 | ||||||
chr1:235381959 | C | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100+1810C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381959 | |||||||
chr1:235381965 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100+1816T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381965 | |||||||
chr1:235382109 | C | T | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+1960C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382109 | |||||||
chr1:235382220 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2071G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382220 | |||||||
chr1:235382264 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2115A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382264 | |||||||
chr1:235382285 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2136G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382285 | |||||||
chr1:235382308 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2159G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382308 | |||||||
chr1:235382354 | G | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.100+2205G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382354 | |||||||
chr1:235382384 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2235C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382384 | |||||||
chr1:235382431 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.100+2282A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382431 | |||||||
chr1:235382454 | C | T | 1 | a0005c0008t0001g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.100+2305C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382454 | |||||||
chr1:235382641 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2492C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382641 | |||||||
chr1:235382740 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.100+2591G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382740 | |||||||
chr1:235382776 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.100+2627T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382776 | |||||||
chr1:235382890 | C | T | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+2741C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382890 | |||||||
chr1:235382897 | A | G | 25 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(22): Show |
25 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.100+2748A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382897 | |||||||
chr1:235382983 | A | C | 7 | a0001c0001t0001g0065 a0001c0001t0001g0117 a0001c0001t0001g0120 others(4): Show |
7 | HG00558.hp1 NA18975.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+2834A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382983 | |||||||
chr1:235383011 | T | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.100+2862T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383011 | |||||||
chr1:235383153 | C | T | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100+3004C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383153 | |||||||
chr1:235383189 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+3040A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383189 | |||||||
chr1:235383291 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0057 others(4): Show |
7 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+3142C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383291 | |||||||
chr1:235383296 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.100+3147C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383296 | |||||||
chr1:235383443 | C | T | 2 | a0001c0001t0003g0188 a0001c0001t0014g0018 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.100+3294C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383443 | |||||||
chr1:235383582 | T | C | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+3433T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383582 | |||||||
chr1:235383725 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+3576G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383725 | |||||||
chr1:235383735 | C | G | 1 | a0001c0001t0003g0068 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100+3586C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383735 | |||||||
chr1:235383843 | C | G | 1 | a0001c0001t0002g0215 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.100+3694C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383843 | |||||||
chr1:235383878 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
53 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.100+3729C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383878 | |||||||
chr1:235384076 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+3927T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384076 | |||||||
chr1:235384119 | T | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+3970T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384119 | |||||||
chr1:235384301 | G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4152G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384301 | |||||||
chr1:235384336 | G | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+4187G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384336 | |||||||
chr1:235384363 | A | G | 2 | a0001c0001t0001g0084 a0004c0006t0002g0123 |
2 | HG02976.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.100+4214A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384363 | |||||||
chr1:235384424 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4275C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384424 | |||||||
chr1:235384467 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4318G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384467 | |||||||
chr1:235384637 | G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4488G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384637 | |||||||
chr1:235384731 | G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.100+4582G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384731 | |||||||
chr1:235384822 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4673C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384822 | |||||||
chr1:235384971 | C | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4822C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384971 | |||||||
chr1:235385178 | G | A | 1 | a0001c0001t0005g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100+5029G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385178 | |||||||
chr1:235385202 | T | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.100+5053T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385202 | |||||||
chr1:235385330 | C | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5181C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385330 | |||||||
chr1:235385365 | C | G | 2 | a0001c0005t0035g0260 a0001c0005t0038g0155 |
2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100+5216C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385365 | |||||||
chr1:235385373 | G | A | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+5224G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385373 | |||||||
chr1:235385384 | G | C | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+5235G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385384 | |||||||
chr1:235385388 | C | T | 2 | a0001c0001t0004g0208 a0001c0001t0022g0206 |
2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.100+5239C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385388 | |||||||
chr1:235385395 | C | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+5246C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385395 | |||||||
chr1:235385436 | C | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+5287C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385436 | |||||||
chr1:235385438 | T | A | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+5289T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385438 | |||||||
chr1:235385518 | A | G | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+5369A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385518 | |||||||
chr1:235385561 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5412T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385561 | |||||||
chr1:235385669 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5520G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385669 | |||||||
chr1:235385687 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5538T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385687 | |||||||
chr1:235385809 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.100+5660C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385809 | |||||||
chr1:235385838 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5689G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385838 | |||||||
chr1:235385960 | G | C | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+5811G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385960 | |||||||
chr1:235386185 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+6036C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386185 | |||||||
chr1:235386197 | G | C | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+6048G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386197 | |||||||
chr1:235386255 | G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6106G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386255 | |||||||
chr1:235386286 | C | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.100+6137C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386286 | |||||||
chr1:235386387 | A | G | 1 | a0001c0001t0003g0081 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.100+6238A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386387 | |||||||
chr1:235386469 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+6320C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386469 | |||||||
chr1:235386551 | A | C | 1 | a0001c0001t0011g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.100+6402A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386551 | |||||||
chr1:235386558 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.100+6409A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386558 | |||||||
chr1:235386566 | T | C | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.100+6417T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386566 | |||||||
chr1:235386592 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6443A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386592 | |||||||
chr1:235386760 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+6611C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386760 | |||||||
chr1:235386796 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6647A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386796 | |||||||
chr1:235386799 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6650T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386799 | |||||||
chr1:235386815 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6666T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386815 | |||||||
chr1:235386838 | G | A | 1 | a0001c0001t0005g0163 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.100+6689G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386838 | |||||||
chr1:235386845 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6696G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386845 | |||||||
chr1:235386872 | G | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+6723G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386872 | |||||||
chr1:235386887 | G | A | 21 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(18): Show |
21 | HG00544.hp1 HG00738.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.100+6738G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386887 | |||||||
chr1:235386936 | A | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0033 others(7): Show |
10 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+6787A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386936 | |||||||
chr1:235386988 | C | A | 17 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.100+6839C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386988 | |||||||
chr1:235387094 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6945A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387094 | |||||||
chr1:235387102 | C | T | 2 | a0001c0001t0002g0198 a0001c0001t0015g0239 |
2 | HG00621.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.100+6953C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387102 | |||||||
chr1:235387111 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0004g0007 |
2 | HG00642.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.100+6962G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387111 | |||||||
chr1:235387197 | G | T | 6 | a0001c0001t0003g0143 a0001c0001t0003g0149 a0001c0001t0012g0013 others(3): Show |
6 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+7048G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387197 | |||||||
chr1:235387236 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7087A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387236 | |||||||
chr1:235387287 | A | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.100+7138A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387287 | |||||||
chr1:235387299 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7150A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387299 | |||||||
chr1:235387338 | G | A | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100+7189G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387338 | |||||||
chr1:235387436 | A | C | 1 | a0001c0001t0002g0255 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.100+7287A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387436 | |||||||
chr1:235387489 | A | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7340A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387489 | |||||||
chr1:235387524 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7375G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387524 | |||||||
chr1:235387531 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7382T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387531 | |||||||
chr1:235387583 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+7434A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387583 | |||||||
chr1:235387605 | G | T | 1 | a0001c0001t0002g0231 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.100+7456G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387605 | |||||||
chr1:235387635 | T | G | 1 | a0001c0001t0002g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.100+7486T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387635 | |||||||
chr1:235387644 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7495T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387644 | |||||||
chr1:235387680 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7531C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387680 | |||||||
chr1:235387738 | C | A | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.100+7589C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387738 | |||||||
chr1:235387806 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7657G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387806 | |||||||
chr1:235387818 | C | T | 5 | a0001c0001t0005g0165 a0001c0001t0005g0166 a0001c0001t0005g0167 others(2): Show |
5 | HG02622.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+7669C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387818 | |||||||
chr1:235387841 | A | C | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+7692A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387841 | |||||||
chr1:235388210 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8061T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388210 | |||||||
chr1:235388271 | T | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8122T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388271 | |||||||
chr1:235388283 | C | CT | 13 | a0001c0001t0001g0097 a0001c0001t0001g0145 a0001c0001t0002g0179 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+8156dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235388283 | ||||||
chr1:235388283 | CT | C | 29 | a0001c0001t0001g0108 a0001c0001t0002g0122 a0001c0001t0002g0127 others(26): Show |
29 | HG00733.hp2 HG01099.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.100+8156delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235388283 | ||||||
chr1:235388607 | G | A | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100+8458G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388607 | |||||||
chr1:235388645 | A | G | 1 | a0001c0001t0003g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.100+8496A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388645 | |||||||
chr1:235388649 | T | A | 1 | a0001c0001t0008g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+8500T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388649 | |||||||
chr1:235388658 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8509C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388658 | |||||||
chr1:235388664 | A | G | 4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+8515A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388664 | |||||||
chr1:235388665 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8516G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388665 | |||||||
chr1:235388847 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8698T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388847 | |||||||
chr1:235388970 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8821A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388970 | |||||||
chr1:235389004 | T | C | 5 | a0001c0001t0006g0044 a0001c0001t0007g0045 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+8855T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389004 | |||||||
chr1:235389045 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+8896C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389045 | |||||||
chr1:235389242 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100+9093C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389242 | |||||||
chr1:235389396 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9247C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389396 | |||||||
chr1:235389505 | G | GT | 6 | a0001c0001t0001g0074 a0001c0001t0001g0125 a0001c0001t0002g0233 others(3): Show |
6 | HG01361.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+9363dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235389505 | ||||||
chr1:235389521 | C | T | 17 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.100+9372C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389521 | |||||||
chr1:235389638 | A | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9489A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389638 | |||||||
chr1:235389920 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9771T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389920 | |||||||
chr1:235389983 | G | A | 24 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(21): Show |
24 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+9834G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389983 | |||||||
chr1:235390050 | C | T | 3 | a0001c0001t0002g0209 a0001c0001t0002g0225 a0001c0001t0002g0251 |
3 | NA19005.hp2 NA19056.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.100+9901C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390050 | |||||||
chr1:235390058 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9909A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390058 | |||||||
chr1:235390123 | C | CA | 11 | a0001c0001t0002g0195 a0001c0001t0004g0194 a0001c0001t0006g0029 others(8): Show |
11 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+9985dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235390123 | ||||||
chr1:235390135 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9986G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390135 | |||||||
chr1:235390155 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100+10006A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390155 | |||||||
chr1:235390214 | C | T | 1 | a0001c0001t0011g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.100+10065C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390214 | |||||||
chr1:235390376 | A | G | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.100+10227A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390376 | |||||||
chr1:235390578 | C | A | 1 | a0001c0001t0002g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.100+10429C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390578 | |||||||
chr1:235390638 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+10489A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390638 | |||||||
chr1:235390754 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+10605G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390754 | |||||||
chr1:235390758 | C | CA | 27 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0003g0107 others(24): Show |
27 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.100+10629dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235390758 | ||||||
chr1:235390758 | CA | C | 45 | a0001c0001t0001g0136 a0001c0001t0001g0171 a0001c0001t0001g0193 others(42): Show |
45 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.100+10629delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235390758 | ||||||
chr1:235390863 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.101-10640G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390863 | |||||||
chr1:235391009 | G | T | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-10494G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391009 | |||||||
chr1:235391057 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.101-10446G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391057 | |||||||
chr1:235391102 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-10401T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391102 | |||||||
chr1:235391280 | G | A | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-10223G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391280 | |||||||
chr1:235391302 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.101-10201C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391302 | |||||||
chr1:235391434 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.101-10069G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391434 | |||||||
chr1:235391480 | C | CA | 6 | a0001c0001t0001g0063 a0001c0001t0002g0195 a0001c0001t0002g0251 others(3): Show |
6 | HG00140.hp1 HG01257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-10011dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391480 | ||||||
chr1:235391546 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9957T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391546 | |||||||
chr1:235391600 | C | CT | 36 | a0001c0001t0002g0049 a0001c0001t0002g0089 a0001c0001t0002g0179 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.101-9879dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | ||||||
chr1:235391600 | C | CTT | 7 | a0001c0001t0004g0041 a0001c0001t0004g0050 a0001c0001t0004g0159 others(4): Show |
7 | HG01243.hp2 HG02027.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-9880_101-9879d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | ||||||
chr1:235391600 | CT | C | 27 | a0001c0001t0001g0217 a0001c0001t0002g0201 a0001c0001t0005g0124 others(24): Show |
27 | HG00733.hp2 HG01255.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-9879delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | ||||||
chr1:235391600 | CTTTTT | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0096 others(12): Show |
15 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.101-9883_101-9879d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | ||||||
chr1:235391600 | CTTTTTT | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.101-9884_101-9879d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | ||||||
chr1:235391803 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9700T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391803 | |||||||
chr1:235391806 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9697C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391806 | |||||||
chr1:235391830 | C | A | 1 | a0001c0001t0003g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.101-9673C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391830 | |||||||
chr1:235391848 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.101-9655C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391848 | |||||||
chr1:235391902 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-9601C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391902 | |||||||
chr1:235392045 | G | C | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-9458G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392045 | |||||||
chr1:235392171 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9332A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392171 | |||||||
chr1:235392219 | G | A | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.101-9284G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392219 | |||||||
chr1:235392277 | C | G | 5 | a0001c0001t0003g0036 a0001c0001t0003g0102 a0001c0001t0003g0103 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-9226C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392277 | |||||||
chr1:235392408 | T | TTC | 5 | a0001c0001t0001g0079 a0001c0001t0001g0125 a0001c0001t0003g0067 others(2): Show |
5 | HG02055.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-9094_101-9093i others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235392408 | ||||||
chr1:235392409 | T | TC | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.101-9094_101-9093i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392409 | |||||||
chr1:235392410 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0003g0068 a0001c0001t0008g0024 |
3 | HG00639.hp1 NA19062.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-9093T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392410 | |||||||
chr1:235392433 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9070A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392433 | |||||||
chr1:235392505 | G | T | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.101-8998G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392505 | |||||||
chr1:235392591 | G | A | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8912G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392591 | |||||||
chr1:235392701 | A | T | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8802A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392701 | |||||||
chr1:235392702 | C | T | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8801C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392702 | |||||||
chr1:235392757 | T | G | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8746T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392757 | |||||||
chr1:235392780 | T | C | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8723T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392780 | |||||||
chr1:235392802 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-8701A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392802 | |||||||
chr1:235392804 | T | C | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8699T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392804 | |||||||
chr1:235393015 | A | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.101-8488A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393015 | |||||||
chr1:235393021 | A | T | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-8482A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393021 | |||||||
chr1:235393168 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(7): Show |
10 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-8335T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393168 | |||||||
chr1:235393260 | C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.101-8243C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393260 | |||||||
chr1:235393274 | C | T | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-8229C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393274 | |||||||
chr1:235393355 | G | A | 1 | a0001c0009t0007g0264 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.101-8148G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393355 | |||||||
chr1:235393408 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-8095C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393408 | |||||||
chr1:235393479 | G | A | 4 | a0001c0001t0034g0031 a0001c0003t0001g0051 a0001c0003t0001g0052 others(1): Show |
4 | HG02809.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-8024G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393479 | |||||||
chr1:235393608 | GT | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.101-7886delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235393608 | ||||||
chr1:235393794 | T | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.101-7709T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393794 | |||||||
chr1:235394105 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.101-7398C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394105 | |||||||
chr1:235394165 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-7338G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394165 | |||||||
chr1:235394176 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-7327G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394176 | |||||||
chr1:235394343 | G | C | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-7160G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394343 | |||||||
chr1:235394353 | C | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG02015.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.101-7150C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394353 | |||||||
chr1:235394418 | C | CT | 20 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0078 others(17): Show |
20 | HG01168.hp1 HG01256.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.101-7060dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | ||||||
chr1:235394418 | C | CTT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.101-7061_101-7060d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | ||||||
chr1:235394418 | C | CTTT | 28 | a0001c0001t0001g0080 a0001c0001t0001g0125 a0001c0001t0001g0126 others(25): Show |
28 | HG00733.hp2 HG01255.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.101-7062_101-7060d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | ||||||
chr1:235394418 | CT | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0226 a0001c0001t0002g0229 others(3): Show |
6 | HG02055.hp2 HG03704.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-7060delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | ||||||
chr1:235394418 | CTT | C | 31 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(28): Show |
31 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.101-7061_101-7060d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | ||||||
chr1:235394418 | CTTTT | C | 6 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0187 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-7063_101-7060d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | ||||||
chr1:235394418 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-7070_101-7060d others(13): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | ||||||
chr1:235394429 | T | C | 1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-7074T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394429 | |||||||
chr1:235394620 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101-6883G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394620 | |||||||
chr1:235394910 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-6593G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394910 | |||||||
chr1:235394910 | G | C | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.101-6593G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394910 | |||||||
chr1:235394963 | C | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-6540C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394963 | |||||||
chr1:235395191 | A | T | 34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-6312A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395191 | |||||||
chr1:235395344 | G | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-6159G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395344 | |||||||
chr1:235395391 | C | T | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-6112C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395391 | |||||||
chr1:235395489 | C | G | 26 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0113 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.101-6014C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395489 | |||||||
chr1:235395548 | C | CT | 27 | a0001c0001t0002g0207 a0001c0001t0002g0214 a0001c0001t0004g0006 others(24): Show |
27 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-5941dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235395548 | ||||||
chr1:235395548 | CT | C | 5 | a0001c0001t0002g0055 a0001c0001t0002g0144 a0001c0001t0002g0202 others(2): Show |
5 | HG01069.hp1 HG02451.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-5941delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235395548 | ||||||
chr1:235395575 | C | T | 4 | a0001c0001t0034g0031 a0001c0003t0001g0051 a0001c0003t0001g0052 others(1): Show |
4 | HG02809.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-5928C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395575 | |||||||
chr1:235395905 | A | G | 1 | a0001c0001t0011g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.101-5598A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395905 | |||||||
chr1:235395955 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5548C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395955 | |||||||
chr1:235396203 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-5300T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235396203 | |||||||
chr1:235396275 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-5228G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235396275 | |||||||
chr1:235396349 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.101-5154T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235396349 | |||||||
chr1:235396473 | A | G | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-5030A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235396473 | |||||||
chr1:235396954 | G | GTTTA | 108 | a0001c0001t0001g0065 a0001c0001t0001g0117 a0001c0001t0001g0120 others(105): Show |
108 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.101-4521_101-4518d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | ||||||
chr1:235396954 | G | GTTTATTT others(1): Show |
15 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(12): Show |
15 | HG00642.hp1 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.101-4525_101-4518d others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | ||||||
chr1:235396954 | G | GTTTATTT others(5): Show |
4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-4529_101-4518d others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | ||||||
chr1:235396954 | G | GTTTGTTT others(5): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-4546_101-4545i others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | ||||||
chr1:235396954 | GTTTA | G | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.101-4521_101-4518d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | ||||||
chr1:235397035 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.101-4468C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397035 | |||||||
chr1:235397071 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-4432C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397071 | |||||||
chr1:235397123 | C | T | 1 | a0001c0001t0027g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.101-4380C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397123 | |||||||
chr1:235397196 | A | G | 1 | a0001c0001t0003g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.101-4307A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397196 | |||||||
chr1:235397200 | CT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.101-4284delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235397200 | ||||||
chr1:235397200 | CTT | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0003g0137 others(4): Show |
7 | HG02451.hp1 HG02922.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-4285_101-4284d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235397200 | ||||||
chr1:235397343 | G | C | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.101-4160G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397343 | |||||||
chr1:235397410 | C | T | 1 | a0005c0008t0001g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.101-4093C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397410 | |||||||
chr1:235397491 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-4012G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397491 | |||||||
chr1:235397512 | A | G | 2 | a0001c0001t0002g0198 a0001c0001t0015g0239 |
2 | HG00621.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.101-3991A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397512 | |||||||
chr1:235397649 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-3854A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397649 | |||||||
chr1:235397741 | C | T | 36 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-3762C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397741 | |||||||
chr1:235397917 | G | A | 3 | a0001c0001t0004g0158 a0001c0001t0004g0180 a0001c0001t0004g0181 |
3 | NA18943.hp2 NA18954.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.101-3586G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397917 | |||||||
chr1:235398142 | CT | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.101-3346delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235398142 | ||||||
chr1:235398311 | A | G | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-3192A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398311 | |||||||
chr1:235398442 | G | A | 6 | a0001c0001t0003g0030 a0001c0001t0003g0066 a0001c0001t0003g0067 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-3061G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398442 | |||||||
chr1:235398680 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2823A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398680 | |||||||
chr1:235398734 | C | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-2769C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398734 | |||||||
chr1:235398753 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2750C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398753 | |||||||
chr1:235398754 | T | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2749T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398754 | |||||||
chr1:235398755 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2748A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398755 | |||||||
chr1:235398796 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2707G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398796 | |||||||
chr1:235398905 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.101-2598A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398905 | |||||||
chr1:235398935 | G | A | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.101-2568G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398935 | |||||||
chr1:235399387 | G | C | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.101-2116G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399387 | |||||||
chr1:235399497 | C | T | 1 | a0001c0001t0007g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.101-2006C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399497 | |||||||
chr1:235399723 | C | T | 1 | a0001c0001t0004g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.101-1780C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399723 | |||||||
chr1:235399869 | A | C | 1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.101-1634A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399869 | |||||||
chr1:235399902 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1601A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399902 | |||||||
chr1:235399903 | A | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1600A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399903 | |||||||
chr1:235399904 | A | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1599A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399904 | |||||||
chr1:235399905 | A | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1598A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399905 | |||||||
chr1:235399906 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1597C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399906 | |||||||
chr1:235399944 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.101-1559C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399944 | |||||||
chr1:235399977 | A | G | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.101-1526A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399977 | |||||||
chr1:235400153 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-1350G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400153 | |||||||
chr1:235400226 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.101-1277C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400226 | |||||||
chr1:235400408 | C | CTTTTTTT others(1): Show |
34 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(31): Show |
34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-1092_101-1085d others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | ||||||
chr1:235400408 | C | CTTTTTTT others(6): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-1085_101-1084i others(15): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | ||||||
chr1:235400408 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0002g0195 a0004c0006t0002g0123 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.101-1085_101-1084i others(16): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | ||||||
chr1:235400408 | C | CTTTTTTT others(8): Show |
33 | a0001c0001t0001g0032 a0001c0001t0001g0076 a0001c0001t0003g0036 others(30): Show |
33 | HG00733.hp2 HG01070.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.101-1085_101-1084i others(17): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | ||||||
chr1:235400408 | C | CTTTTTTT others(9): Show |
98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.101-1085_101-1084i others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | ||||||
chr1:235400408 | C | CTTTTTTT others(10): Show |
23 | a0001c0001t0001g0037 a0001c0001t0001g0053 a0001c0001t0001g0061 others(20): Show |
23 | HG00621.hp2 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.101-1085_101-1084i others(19): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | ||||||
chr1:235400432 | G | A | 17 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-1071G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400432 | |||||||
chr1:235400493 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-1010C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400493 | |||||||
chr1:235400525 | G | A | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-978G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400525 | |||||||
chr1:235400624 | A | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-879A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400624 | |||||||
chr1:235400658 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-845T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400658 | |||||||
chr1:235400660 | A | G | 2 | a0001c0001t0002g0207 a0001c0001t0002g0214 |
2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.101-843A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400660 | |||||||
chr1:235400671 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101-832G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400671 | |||||||
chr1:235400679 | C | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG02015.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.101-824C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400679 | |||||||
chr1:235400787 | C | T | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.101-716C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400787 | |||||||
chr1:235400905 | GCCAGTCT others(3): Show |
G | 25 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(22): Show |
25 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.101-587_101-578del others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400905 | ||||||
chr1:235400939 | G | A | 39 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0113 others(36): Show |
39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.101-564G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400939 | |||||||
chr1:235400983 | C | T | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-520C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400983 | |||||||
chr1:235401065 | C | T | 4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-438C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401065 | |||||||
chr1:235401075 | A | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.101-428A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401075 | |||||||
chr1:235401097 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.101-406G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401097 | |||||||
chr1:235401416 | C | T | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.101-87C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401416 | |||||||
chr1:235401448 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-55G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401448 | |||||||
chr1:235401498 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.101-5G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401498 | |||||||
chr1:235401609 | G | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0003g0119 |
3 | HG01123.hp1 HG02300.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.185+22G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235401609 | |||||||
chr1:235401806 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+219A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235401806 | |||||||
chr1:235401811 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+224G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235401811 | |||||||
chr1:235401826 | C | CT | 10 | a0001c0001t0002g0048 a0001c0001t0002g0195 a0001c0001t0002g0245 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+262dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235401826 | ||||||
chr1:235401826 | C | CTTT | 31 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(28): Show |
31 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.185+260_185+262dup others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235401826 | ||||||
chr1:235401826 | CT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.185+262delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235401826 | ||||||
chr1:235401826 | CTT | C | 9 | a0001c0001t0001g0033 a0001c0001t0001g0076 a0001c0001t0001g0100 others(6): Show |
9 | HG01070.hp1 HG01167.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+261_185+262del others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235401826 | ||||||
chr1:235402000 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.185+413T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402000 | |||||||
chr1:235402065 | C | CT | 7 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0002g0207 others(4): Show |
7 | HG00738.hp2 HG01074.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+495dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235402065 | ||||||
chr1:235402156 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+569T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402156 | |||||||
chr1:235402171 | C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.185+584C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402171 | |||||||
chr1:235402282 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+695C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402282 | |||||||
chr1:235402357 | C | T | 6 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0110 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+770C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402357 | |||||||
chr1:235402394 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+807C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402394 | |||||||
chr1:235402511 | G | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+924G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402511 | |||||||
chr1:235402587 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+1000G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402587 | |||||||
chr1:235402589 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.185+1002G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402589 | |||||||
chr1:235402597 | C | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.185+1010C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402597 | |||||||
chr1:235402624 | T | G | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.185+1037T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402624 | |||||||
chr1:235402770 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+1183G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402770 | |||||||
chr1:235402808 | T | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+1221T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402808 | |||||||
chr1:235402888 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+1301C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402888 | |||||||
chr1:235402948 | A | G | 1 | a0001c0001t0002g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.185+1361A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402948 | |||||||
chr1:235402976 | C | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.185+1389C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402976 | |||||||
chr1:235403542 | T | G | 1 | a0001c0001t0002g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.185+1955T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235403542 | |||||||
chr1:235403637 | C | T | 4 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0110 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+2050C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235403637 | |||||||
chr1:235403690 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.185+2103C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235403690 | |||||||
chr1:235403786 | G | C | 1 | a0001c0001t0023g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.185+2199G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235403786 | |||||||
chr1:235404001 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+2414G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404001 | |||||||
chr1:235404071 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.185+2484G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404071 | |||||||
chr1:235404131 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.185+2544G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404131 | |||||||
chr1:235404231 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.185+2644C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404231 | |||||||
chr1:235404247 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.185+2660A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404247 | |||||||
chr1:235404254 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+2667G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404254 | |||||||
chr1:235404271 | C | T | 2 | a0001c0001t0001g0097 a0001c0005t0035g0260 |
2 | HG03471.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.185+2684C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404271 | |||||||
chr1:235404289 | AAATT | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.185+2705_185+2708d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235404289 | ||||||
chr1:235404319 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+2732T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404319 | |||||||
chr1:235404385 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+2798C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404385 | |||||||
chr1:235404853 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3266G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404853 | |||||||
chr1:235404877 | G | C | 1 | a0001c0001t0002g0090 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.185+3290G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404877 | |||||||
chr1:235404939 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3352C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404939 | |||||||
chr1:235404958 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3371T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404958 | |||||||
chr1:235404960 | C | CT | 6 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0002g0195 others(3): Show |
6 | HG00621.hp2 HG01106.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+3392dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235404960 | ||||||
chr1:235404960 | CT | C | 38 | a0001c0001t0002g0179 a0001c0001t0003g0153 a0001c0001t0004g0006 others(35): Show |
38 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.185+3392delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235404960 | ||||||
chr1:235405107 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3520C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405107 | |||||||
chr1:235405205 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3618T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405205 | |||||||
chr1:235405207 | C | T | 8 | a0001c0001t0002g0179 a0001c0001t0004g0007 a0001c0001t0004g0158 others(5): Show |
8 | HG00642.hp1 HG01361.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+3620C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405207 | |||||||
chr1:235405212 | C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.185+3625C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405212 | |||||||
chr1:235405266 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3679G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405266 | |||||||
chr1:235405320 | CT | C | 18 | a0001c0001t0001g0117 a0001c0001t0001g0145 a0001c0001t0002g0201 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG02976.hp2 others(15): Show |
intron_variant | MODIFIER | c.185+3752delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235405320 | ||||||
chr1:235405320 | CTT | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.185+3751_185+3752d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235405320 | ||||||
chr1:235405320 | CTTT | C | 8 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0087 others(5): Show |
8 | HG01167.hp1 HG01496.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+3750_185+3752d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235405320 | ||||||
chr1:235405336 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+3749T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405336 | |||||||
chr1:235405446 | G | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3859G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405446 | |||||||
chr1:235405457 | T | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3870T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405457 | |||||||
chr1:235405498 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3911T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405498 | |||||||
chr1:235405831 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0171 a0003c0004t0037g0172 |
3 | HG01106.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.185+4244G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405831 | |||||||
chr1:235405918 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4331C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405918 | |||||||
chr1:235406072 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4485C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406072 | |||||||
chr1:235406124 | A | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4537A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406124 | |||||||
chr1:235406487 | C | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4900C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406487 | |||||||
chr1:235406543 | A | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4956A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406543 | |||||||
chr1:235406556 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4969G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406556 | |||||||
chr1:235406559 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4972T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406559 | |||||||
chr1:235406571 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.185+4984G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406571 | |||||||
chr1:235406645 | C | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+5058C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406645 | |||||||
chr1:235406676 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.185+5089C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406676 | |||||||
chr1:235406762 | A | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+5175A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406762 | |||||||
chr1:235406829 | C | CT | 13 | a0001c0001t0001g0145 a0001c0001t0002g0144 a0001c0001t0002g0229 others(10): Show |
13 | HG00733.hp2 HG01361.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+5264dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235406829 | ||||||
chr1:235406829 | CT | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.185+5264delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235406829 | ||||||
chr1:235406829 | CTT | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0072 a0001c0001t0001g0171 others(4): Show |
7 | HG00738.hp1 HG01081.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+5263_185+5264d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235406829 | ||||||
chr1:235406857 | G | A | 2 | a0001c0001t0002g0229 a0001c0001t0002g0240 |
2 | NA19082.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.185+5270G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406857 | |||||||
chr1:235406975 | T | C | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.185+5388T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406975 | |||||||
chr1:235407118 | T | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.185+5531T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407118 | |||||||
chr1:235407118 | T | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+5531T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407118 | |||||||
chr1:235407131 | C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.185+5544C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407131 | |||||||
chr1:235407134 | C | CT | 31 | a0001c0001t0001g0125 a0001c0001t0001g0145 a0001c0001t0001g0147 others(28): Show |
31 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.185+5563dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235407134 | ||||||
chr1:235407155 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.185+5568G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407155 | |||||||
chr1:235407188 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.185+5601C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407188 | |||||||
chr1:235407208 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.185+5621G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407208 | |||||||
chr1:235407319 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.185+5732T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407319 | |||||||
chr1:235407636 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.185+6049G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407636 | |||||||
chr1:235407819 | T | A | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.185+6232T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407819 | |||||||
chr1:235407878 | G | GT | 39 | a0001c0001t0002g0179 a0001c0001t0002g0198 a0001c0001t0004g0006 others(36): Show |
39 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.185+6301dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235407878 | ||||||
chr1:235408028 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.186-6405C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408028 | |||||||
chr1:235408087 | T | A | 37 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(34): Show |
37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-6346T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408087 | |||||||
chr1:235408097 | C | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-6336C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408097 | |||||||
chr1:235408098 | C | G | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.186-6335C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408098 | |||||||
chr1:235408113 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.186-6320G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408113 | |||||||
chr1:235408251 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.186-6182T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408251 | |||||||
chr1:235408264 | A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-6169A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408264 | |||||||
chr1:235408347 | A | T | 37 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(34): Show |
37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-6086A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408347 | |||||||
chr1:235408432 | A | AT | 38 | a0001c0001t0001g0072 a0001c0001t0001g0145 a0001c0001t0002g0179 others(35): Show |
38 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.186-5986dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235408432 | ||||||
chr1:235408432 | AT | A | 8 | a0001c0001t0001g0117 a0001c0001t0002g0048 a0001c0001t0002g0055 others(5): Show |
8 | HG02559.hp2 HG02895.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-5986delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235408432 | ||||||
chr1:235408502 | T | TTAC | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-5931_186-5930i others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408502 | |||||||
chr1:235408719 | G | A | 37 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(34): Show |
37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-5714G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408719 | |||||||
chr1:235408722 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
55 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.186-5711C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408722 | |||||||
chr1:235408767 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.186-5666C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408767 | |||||||
chr1:235409009 | CT | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.186-5406delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409009 | ||||||
chr1:235409009 | CTT | C | 33 | a0001c0001t0002g0179 a0001c0001t0003g0098 a0001c0001t0004g0007 others(30): Show |
33 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.186-5407_186-5406d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409009 | ||||||
chr1:235409031 | A | G | 32 | a0001c0001t0002g0179 a0001c0001t0004g0007 a0001c0001t0004g0011 others(29): Show |
32 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.186-5402A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409031 | |||||||
chr1:235409079 | T | C | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-5354T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409079 | |||||||
chr1:235409354 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.186-5079T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409354 | |||||||
chr1:235409440 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4993C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409440 | |||||||
chr1:235409499 | G | A | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-4934G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409499 | |||||||
chr1:235409803 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.186-4630C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409803 | |||||||
chr1:235409824 | T | TTCGAGAC others(3814): Show |
1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3823): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3815): Show |
1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3824): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3828): Show |
1 | a0001c0001t0003g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3837): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3831): Show |
1 | a0005c0008t0001g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3829): Show |
1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3839): Show |
1 | a0001c0001t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3848): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3829): Show |
2 | a0001c0001t0003g0188 a0001c0001t0014g0018 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3828): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0100 |
2 | HG01070.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3837): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3829): Show |
40 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3830): Show |
40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0037 others(37): Show |
40 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3831): Show |
12 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0074 others(9): Show |
12 | HG00544.hp2 HG01099.hp2 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3831): Show |
3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
16 | a0001c0001t0005g0124 a0001c0001t0005g0165 a0001c0001t0005g0166 others(13): Show |
16 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3833): Show |
1 | a0001c0001t0005g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3842): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0160 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3833): Show |
1 | a0001c0001t0005g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3842): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0163 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3833): Show |
1 | a0001c0001t0006g0002 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3842): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3830): Show |
1 | a0001c0001t0001g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3830): Show |
1 | a0001c0001t0003g0015 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3829): Show |
5 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0003g0104 others(2): Show |
5 | HG01081.hp1 HG01123.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3830): Show |
1 | a0001c0001t0003g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3833): Show |
1 | a0001c0001t0003g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3842): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3817): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3826): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3843): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3852): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3821): Show |
3 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 |
3 | HG02145.hp1 HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3830): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3822): Show |
1 | a0001c0009t0007g0264 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3831): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3822): Show |
1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3831): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3830): Show |
2 | a0001c0001t0003g0110 a0001c0001t0003g0111 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTCGAGAC others(3831): Show |
2 | a0001c0001t0003g0102 a0001c0001t0003g0103 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3838): Show |
1 | a0001c0001t0004g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3847): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3831): Show |
4 | a0001c0001t0009g0008 a0001c0001t0009g0020 a0001c0001t0009g0022 others(1): Show |
4 | HG01109.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-4608_186-4607i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3815): Show |
2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4608_186-4607i others(3824): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3830): Show |
22 | a0001c0001t0004g0011 a0001c0001t0004g0027 a0001c0001t0004g0038 others(19): Show |
22 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-4608_186-4607i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3831): Show |
1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3829): Show |
1 | a0001c0001t0004g0158 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3830): Show |
2 | a0001c0001t0004g0180 a0001c0001t0019g0157 |
2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.186-4608_186-4607i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3830): Show |
1 | a0001c0001t0004g0181 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3831): Show |
1 | a0001c0001t0004g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3830): Show |
1 | a0001c0001t0004g0007 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409824 | T | TTGGAGAC others(3826): Show |
1 | a0001c0001t0002g0179 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3835): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | ||||||
chr1:235409838 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.186-4595A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409838 | |||||||
chr1:235409875 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4558A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409875 | |||||||
chr1:235409891 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-4542G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409891 | |||||||
chr1:235409978 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4455C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409978 | |||||||
chr1:235410029 | CAAACAAA others(5): Show |
C | 1 | a0001c0001t0027g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.186-4394_186-4383d others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235410029 | ||||||
chr1:235410074 | G | C | 1 | a0001c0001t0003g0103 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.186-4359G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410074 | |||||||
chr1:235410075 | C | G | 1 | a0001c0001t0003g0103 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.186-4358C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410075 | |||||||
chr1:235410080 | T | G | 1 | a0001c0001t0013g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.186-4353T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410080 | |||||||
chr1:235410139 | CGGGAGGC others(25): Show |
C | 3 | a0001c0001t0026g0129 a0001c0001t0027g0128 a0003c0004t0031g0016 |
3 | HG03540.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4281_186-4250d others(34): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235410139 | ||||||
chr1:235410163 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.186-4270C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410163 | |||||||
chr1:235410171 | A | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.186-4262A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410171 | |||||||
chr1:235410312 | CTGGGTGC others(46): Show |
C | 1 | a0001c0001t0006g0054 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.186-4119_186-4067d others(55): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235410312 | ||||||
chr1:235410361 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.186-4072G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410361 | |||||||
chr1:235410434 | G | T | 1 | a0001c0001t0003g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.186-3999G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410434 | |||||||
chr1:235410460 | G | C | 4 | a0001c0001t0004g0197 a0001c0001t0004g0203 a0001c0001t0004g0204 others(1): Show |
4 | HG02735.hp1 HG03490.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-3973G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410460 | |||||||
chr1:235410648 | T | C | 3 | a0001c0001t0003g0109 a0001c0001t0003g0151 a0001c0001t0003g0191 |
3 | HG00741.hp2 HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.186-3785T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410648 | |||||||
chr1:235410711 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.186-3722T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410711 | |||||||
chr1:235410782 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-3651A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410782 | |||||||
chr1:235411082 | T | G | 3 | a0001c0001t0026g0129 a0001c0001t0027g0128 a0003c0004t0031g0016 |
3 | HG03540.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-3351T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411082 | |||||||
chr1:235411162 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0267 |
2 | HG01981.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.186-3271C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411162 | |||||||
chr1:235411188 | G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-3245G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411188 | |||||||
chr1:235411292 | C | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-3141C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411292 | |||||||
chr1:235411330 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-3103A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411330 | |||||||
chr1:235411404 | A | T | 1 | a0001c0001t0016g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186-3029A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411404 | |||||||
chr1:235411436 | G | C | 1 | a0001c0001t0005g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.186-2997G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411436 | |||||||
chr1:235411603 | G | GAATAATA others(6): Show |
1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186-2829_186-2817d others(15): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235411603 | ||||||
chr1:235411659 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.186-2774C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411659 | |||||||
chr1:235411809 | A | G | 3 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0135 |
3 | HG02809.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.186-2624A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411809 | |||||||
chr1:235411814 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.186-2619A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411814 | |||||||
chr1:235411866 | C | T | 5 | a0001c0001t0002g0055 a0001c0001t0004g0197 a0001c0001t0004g0203 others(2): Show |
5 | HG02735.hp1 HG03490.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-2567C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411866 | |||||||
chr1:235411891 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.186-2542C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411891 | |||||||
chr1:235411902 | C | G | 1 | a0001c0001t0003g0015 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.186-2531C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411902 | |||||||
chr1:235411960 | C | T | 1 | a0001c0001t0008g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.186-2473C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411960 | |||||||
chr1:235412006 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.186-2427C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412006 | |||||||
chr1:235412092 | G | GTTTCCCT others(9): Show |
2 | a0001c0001t0002g0240 a0001c0001t0006g0044 |
2 | HG06807.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.186-2315_186-2300d others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | ||||||
chr1:235412092 | G | GTTTCCCT others(25): Show |
106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.186-2331_186-2300d others(34): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | ||||||
chr1:235412092 | G | GTTTCCCT others(41): Show |
6 | a0001c0001t0001g0065 a0001c0001t0001g0117 a0001c0001t0003g0115 others(3): Show |
6 | HG00558.hp1 NA18975.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-2300_186-2299i others(50): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | ||||||
chr1:235412092 | G | GTTTCCCT others(57): Show |
3 | a0001c0001t0005g0162 a0001c0001t0006g0161 a0001c0001t0016g0183 |
3 | HG01109.hp2 HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.186-2300_186-2299i others(66): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | ||||||
chr1:235412092 | G | GTTTCCCT others(89): Show |
1 | a0001c0001t0003g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186-2300_186-2299i others(98): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | ||||||
chr1:235412101 | C | CCCATCCC others(24): Show |
1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-2330_186-2300d others(33): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412101 | ||||||
chr1:235412112 | C | CCTTCCCA others(23): Show |
1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-2320_186-2319i others(32): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412112 | ||||||
chr1:235412115 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-2318T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412115 | |||||||
chr1:235412117 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-2316C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412117 | |||||||
chr1:235412118 | C | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-2315C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412118 | |||||||
chr1:235412120 | A | C | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-2313A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412120 | |||||||
chr1:235412122 | CCCTTT | C | 20 | a0001c0001t0002g0179 a0001c0001t0004g0011 a0001c0001t0004g0027 others(17): Show |
20 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.186-2308_186-2304d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412122 | ||||||
chr1:235412125 | T | C | 15 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0041 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-2308T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412125 | |||||||
chr1:235412131 | T | C | 15 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0041 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-2302T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412131 | |||||||
chr1:235412134 | T | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0074 others(72): Show |
75 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.186-2299T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412134 | |||||||
chr1:235412135 | C | CATCCCTT others(301): Show |
1 | a0001c0001t0016g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186-2298_186-2297i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | |||||||
chr1:235412135 | C | CATCCCTT others(318): Show |
2 | a0001c0001t0008g0024 a0001c0001t0018g0009 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.186-2298_186-2297i others(327): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | |||||||
chr1:235412135 | C | CATCCCTT others(298): Show |
12 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0163 others(9): Show |
12 | HG00733.hp2 HG01261.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.186-2298_186-2297i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | |||||||
chr1:235412135 | C | CATCCCTT others(282): Show |
4 | a0001c0001t0005g0187 a0001c0001t0008g0173 a0001c0001t0008g0176 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-2298_186-2297i others(291): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | |||||||
chr1:235412135 | C | CATCCCTT others(287): Show |
1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.186-2298_186-2297i others(296): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | |||||||
chr1:235412135 | C | CATCCCTT others(381): Show |
1 | a0001c0001t0015g0239 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.186-2298_186-2297i others(390): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | |||||||
chr1:235412135 | C | CATCCCTT others(379): Show |
1 | a0001c0001t0002g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.186-2298_186-2297i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | |||||||
chr1:235412136 | C | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0074 others(15): Show |
18 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-2297C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412136 | |||||||
chr1:235412137 | T | C | 22 | a0001c0001t0002g0198 a0001c0001t0005g0124 a0001c0001t0005g0160 others(19): Show |
22 | HG00621.hp1 HG00733.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-2296T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412137 | |||||||
chr1:235412141 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0074 others(15): Show |
18 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-2292C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412141 | |||||||
chr1:235412141 | CT | C | 25 | a0001c0001t0002g0179 a0001c0001t0004g0011 a0001c0001t0004g0027 others(22): Show |
25 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.186-2290delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412141 | ||||||
chr1:235412142 | T | G | 22 | a0001c0001t0002g0198 a0001c0001t0005g0124 a0001c0001t0005g0160 others(19): Show |
22 | HG00621.hp1 HG00733.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-2291T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | |||||||
chr1:235412142 | T | TCCCC | 3 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0203 |
3 | HG01361.hp1 HG02572.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.186-2291_186-2290i others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | |||||||
chr1:235412142 | T | TCCCCTCC others(2): Show |
4 | a0001c0001t0009g0008 a0001c0001t0009g0020 a0001c0001t0009g0022 others(1): Show |
4 | HG01109.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2291_186-2290i others(11): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | |||||||
chr1:235412142 | T | TCCCCTCC others(5): Show |
1 | a0001c0001t0004g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186-2291_186-2290i others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | |||||||
chr1:235412142 | T | TCCCCTCC others(10): Show |
1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186-2291_186-2290i others(19): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | |||||||
chr1:235412142 | T | TCCCCTCC others(36): Show |
1 | a0001c0001t0004g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.186-2291_186-2290i others(45): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | |||||||
chr1:235412143 | T | C | 1 | a0001c0001t0004g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186-2290T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412143 | |||||||
chr1:235412143 | T | TCCCTTCC others(355): Show |
1 | a0001c0001t0001g0074 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.186-2287_186-2286i others(364): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412143 | ||||||
chr1:235412143 | T | TCCCTTCC others(343): Show |
1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.186-2287_186-2286i others(352): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412143 | ||||||
chr1:235412146 | C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-2287C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412146 | |||||||
chr1:235412147 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0074 |
2 | HG03017.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.186-2286C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412147 | |||||||
chr1:235412147 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(13): Show |
16 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-2286C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412147 | |||||||
chr1:235412148 | T | C | 4 | a0001c0001t0009g0008 a0001c0001t0009g0020 a0001c0001t0009g0022 others(1): Show |
4 | HG01109.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2285T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412148 | |||||||
chr1:235412151 | C | T | 22 | a0001c0001t0002g0198 a0001c0001t0005g0124 a0001c0001t0005g0160 others(19): Show |
22 | HG00621.hp1 HG00733.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-2282C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412151 | |||||||
chr1:235412152 | C | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(13): Show |
16 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-2281C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412152 | |||||||
chr1:235412156 | C | CG | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.186-2277_186-2276i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412156 | |||||||
chr1:235412156 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0074 |
2 | HG03017.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.186-2277C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412156 | |||||||
chr1:235412157 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(12): Show |
15 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.186-2276C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412157 | |||||||
chr1:235412157 | CT | C | 4 | a0001c0001t0004g0050 a0001c0001t0004g0133 a0001c0001t0004g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2275delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412157 | |||||||
chr1:235412158 | T | C | 1 | a0001c0001t0004g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.186-2275T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412158 | |||||||
chr1:235412158 | T | TC | 23 | a0001c0001t0002g0198 a0001c0001t0005g0124 a0001c0001t0005g0160 others(20): Show |
23 | HG00621.hp1 HG00733.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-2271dupC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412158 | ||||||
chr1:235412159 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(13): Show |
16 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-2274C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412159 | |||||||
chr1:235412161 | C | T | 1 | a0001c0001t0004g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.186-2272C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412161 | |||||||
chr1:235412163 | T | C | 45 | a0001c0001t0001g0097 a0001c0001t0002g0179 a0001c0001t0002g0198 others(42): Show |
45 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.186-2270T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TCCCCCTC others(270): Show |
1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-2270_186-2269i others(279): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TCCCCCTC others(292): Show |
1 | a0001c0001t0001g0053 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.186-2270_186-2269i others(301): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TCCCCCTC others(292): Show |
1 | a0001c0001t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.186-2270_186-2269i others(301): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TCCCCCTC others(309): Show |
1 | a0001c0001t0006g0085 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.186-2270_186-2269i others(318): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TCCCCCTC others(251): Show |
2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.186-2270_186-2269i others(260): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TCCCCCTC others(289): Show |
1 | a0001c0001t0001g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.186-2270_186-2269i others(298): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TCCCCCTC others(308): Show |
1 | a0001c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.186-2270_186-2269i others(317): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TCCCCCTC others(307): Show |
1 | a0001c0001t0001g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.186-2270_186-2269i others(316): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | T | TTCCCCTC others(375): Show |
1 | a0001c0001t0002g0246 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(384): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412163 | ||||||
chr1:235412163 | TTC | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.186-2269_186-2268d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412163 | TTCC | T | 4 | a0001c0001t0004g0050 a0001c0001t0004g0133 a0001c0001t0004g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2269_186-2267d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | |||||||
chr1:235412164 | T | C | 37 | a0001c0001t0001g0012 a0001c0001t0001g0074 a0001c0001t0001g0145 others(34): Show |
37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-2269T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412164 | |||||||
chr1:235412165 | C | CTCCT | 14 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(11): Show |
14 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-2268_186-2267i others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412165 | |||||||
chr1:235412166 | C | CCATCACC others(382): Show |
1 | a0001c0001t0006g0054 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.186-2266_186-2265i others(391): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCATCCCT others(343): Show |
1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186-2266_186-2265i others(352): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCCCTCC others(3): Show |
3 | a0001c0001t0002g0198 a0001c0001t0002g0246 a0001c0001t0015g0239 |
3 | HG00621.hp1 NA18983.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.186-2257_186-2248d others(12): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCT | 9 | a0001c0001t0002g0190 a0001c0001t0002g0227 a0001c0001t0002g0228 others(6): Show |
9 | HG01243.hp2 HG02071.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-2265_186-2264i others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(376): Show |
1 | a0001c0001t0002g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(385): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(374): Show |
1 | a0001c0001t0002g0055 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(383): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(374): Show |
1 | a0001c0001t0002g0233 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(383): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(364): Show |
1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(373): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(411): Show |
1 | a0001c0001t0011g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(420): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(397): Show |
1 | a0001c0001t0002g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(406): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(384): Show |
1 | a0001c0001t0002g0226 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(393): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(417): Show |
1 | a0001c0001t0002g0210 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(426): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(384): Show |
1 | a0001c0001t0002g0244 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(393): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(380): Show |
1 | a0001c0001t0002g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(420): Show |
1 | a0001c0001t0011g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(429): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(436): Show |
1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(445): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(393): Show |
1 | a0001c0001t0001g0258 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(402): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(375): Show |
1 | a0001c0001t0002g0106 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(384): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(367): Show |
5 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(2): Show |
5 | HG01346.hp1 HG02523.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-2265_186-2264i others(376): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(379): Show |
1 | a0001c0001t0002g0245 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(380): Show |
1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(380): Show |
1 | a0001c0001t0021g0199 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(374): Show |
2 | a0001c0001t0002g0090 a0001c0001t0002g0216 |
2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.186-2265_186-2264i others(383): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(380): Show |
1 | a0001c0001t0002g0236 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(379): Show |
25 | a0001c0001t0002g0046 a0001c0001t0002g0088 a0001c0001t0002g0092 others(22): Show |
25 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(384): Show |
1 | a0001c0001t0002g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(393): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(372): Show |
1 | a0001c0001t0002g0209 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(381): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(379): Show |
1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(378): Show |
1 | a0001c0001t0002g0220 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(387): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(378): Show |
1 | a0001c0001t0002g0202 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(387): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(379): Show |
2 | a0001c0001t0002g0255 a0001c0001t0002g0256 |
2 | HG01496.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(367): Show |
1 | a0001c0001t0002g0222 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(376): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(301): Show |
1 | a0001c0001t0002g0231 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(380): Show |
1 | a0001c0001t0002g0201 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(379): Show |
2 | a0001c0001t0002g0034 a0001c0001t0002g0093 |
2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCCTCCCC others(294): Show |
1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(303): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCTCCTCC others(69): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2266_186-2265i others(78): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCTCCTCC others(52): Show |
2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-2266_186-2265i others(61): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | CCTCCTCC others(35): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-2266_186-2265i others(44): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | ||||||
chr1:235412166 | C | T | 21 | a0001c0001t0002g0179 a0001c0001t0004g0011 a0001c0001t0004g0027 others(18): Show |
21 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.186-2267C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412166 | |||||||
chr1:235412169 | C | CCTCCCCT others(23): Show |
2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.186-2253_186-2252i others(32): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412169 | ||||||
chr1:235412169 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0006g0054 |
2 | NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.186-2264C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412169 | |||||||
chr1:235412170 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0136 others(12): Show |
15 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.186-2263C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412170 | |||||||
chr1:235412171 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.186-2262T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412171 | |||||||
chr1:235412172 | C | CCCGCTCC others(401): Show |
1 | a0001c0001t0002g0228 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.186-2259_186-2258i others(410): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412172 | ||||||
chr1:235412174 | C | CG | 5 | a0001c0001t0002g0190 a0001c0001t0002g0227 a0001c0001t0002g0249 others(2): Show |
5 | HG02071.hp1 HG02300.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-2259_186-2258i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412174 | |||||||
chr1:235412174 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186-2259C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412174 | |||||||
chr1:235412176 | T | TCCCCATC others(302): Show |
1 | a0001c0001t0014g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-2253_186-2252i others(311): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412176 | ||||||
chr1:235412181 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0006g0054 a0003c0004t0031g0016 |
3 | NA18522.hp2 NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.186-2252T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412181 | |||||||
chr1:235412181 | TC | T | 20 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0163 others(17): Show |
20 | HG00733.hp2 HG01261.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.186-2247delC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412181 | ||||||
chr1:235412182 | C | CCCCATCC others(309): Show |
1 | a0001c0001t0003g0103 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(318): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(358): Show |
1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(367): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(316): Show |
1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(325): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(301): Show |
1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(301): Show |
1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
1 | a0001c0001t0003g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(302): Show |
1 | a0001c0001t0003g0015 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(311): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(296): Show |
1 | a0001c0001t0001g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(305): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(300): Show |
1 | a0001c0001t0003g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(301): Show |
1 | a0001c0001t0003g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(301): Show |
1 | a0001c0001t0003g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(300): Show |
2 | a0001c0001t0001g0061 a0001c0001t0003g0035 |
2 | HG04199.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(300): Show |
1 | a0001c0001t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(300): Show |
1 | a0001c0001t0001g0079 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
1 | a0001c0001t0003g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
1 | a0001c0001t0001g0032 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(300): Show |
1 | a0001c0001t0028g0071 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(300): Show |
1 | a0001c0001t0001g0221 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
53 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0037 others(50): Show |
53 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(300): Show |
1 | a0001c0001t0001g0192 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
1 | a0001c0001t0001g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(298): Show |
1 | a0001c0001t0003g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(270): Show |
1 | a0001c0001t0013g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(279): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(320): Show |
1 | a0001c0001t0003g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(329): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(298): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0105 a0001c0001t0007g0142 |
3 | HG02300.hp1 NA18950.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(302): Show |
1 | a0001c0001t0032g0064 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(311): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(298): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0114 |
3 | HG01070.hp1 HG01071.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(297): Show |
1 | a0001c0001t0003g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(306): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(296): Show |
1 | a0001c0001t0001g0148 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(305): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(298): Show |
1 | a0001c0001t0001g0028 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(297): Show |
1 | a0001c0001t0001g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(306): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
1 | a0001c0001t0003g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(298): Show |
1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(245): Show |
1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(254): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(298): Show |
1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCATCC others(299): Show |
1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCTCCC others(105): Show |
4 | a0001c0001t0004g0006 a0001c0001t0009g0008 a0001c0001t0009g0020 others(1): Show |
4 | HG01109.hp1 HG02572.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-2248_186-2247i others(114): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | CCCCTCCC others(115): Show |
1 | a0001c0001t0017g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(124): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | ||||||
chr1:235412182 | C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-2251C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412182 | |||||||
chr1:235412185 | C | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(11): Show |
14 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-2248C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412185 | |||||||
chr1:235412186 | C | A | 10 | a0001c0001t0001g0121 a0001c0001t0005g0162 a0001c0001t0006g0161 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-2247C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412186 | |||||||
chr1:235412192 | T | C | 1 | a0001c0001t0011g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.186-2241T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412192 | |||||||
chr1:235412192 | T | TCCCTTCC others(283): Show |
1 | a0001c0001t0034g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.186-2238_186-2237i others(292): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412192 | ||||||
chr1:235412192 | T | TCCCTTCC others(282): Show |
1 | a0001c0001t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.186-2238_186-2237i others(291): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412192 | ||||||
chr1:235412192 | T | TCCCTTCC others(212): Show |
1 | a0001c0001t0006g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-2238_186-2237i others(221): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412192 | ||||||
chr1:235412192 | TC | T | 5 | a0001c0001t0004g0006 a0001c0001t0009g0008 a0001c0001t0009g0020 others(2): Show |
5 | HG01109.hp1 HG02572.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-2236delC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412192 | ||||||
chr1:235412193 | C | CCCCCTCC others(106): Show |
1 | a0001c0001t0004g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(115): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(351): Show |
1 | a0001c0001t0002g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(360): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(358): Show |
1 | a0001c0001t0002g0227 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(367): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(343): Show |
1 | a0001c0001t0002g0249 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.186-2237_186-2236i others(352): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(348): Show |
1 | a0001c0001t0011g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(357): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(357): Show |
1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(366): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(33): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(42): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(38): Show |
2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-2237_186-2236i others(47): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(126): Show |
2 | a0001c0001t0004g0197 a0001c0001t0004g0204 |
2 | HG02735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.186-2237_186-2236i others(135): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(105): Show |
1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(114): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(110): Show |
11 | a0001c0001t0002g0179 a0001c0001t0004g0039 a0001c0001t0004g0040 others(8): Show |
11 | HG00642.hp1 HG01891.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.186-2237_186-2236i others(119): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(126): Show |
1 | a0001c0001t0004g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(135): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(110): Show |
1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(119): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(115): Show |
2 | a0001c0001t0004g0043 a0001c0001t0004g0134 |
2 | HG01106.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.186-2237_186-2236i others(124): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(120): Show |
2 | a0001c0001t0004g0027 a0001c0001t0004g0194 |
2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.186-2237_186-2236i others(129): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(166): Show |
1 | a0001c0001t0004g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.186-2237_186-2236i others(175): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(125): Show |
1 | a0001c0001t0004g0042 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(134): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(145): Show |
1 | a0001c0001t0004g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.186-2237_186-2236i others(154): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(115): Show |
1 | a0001c0001t0004g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186-2237_186-2236i others(124): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(74): Show |
1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(83): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCCTCCC others(79): Show |
1 | a0001c0001t0004g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(88): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCTTCCC others(215): Show |
1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-2238_186-2237i others(224): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCTTCCC others(208): Show |
4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2238_186-2237i others(217): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCTTCCC others(231): Show |
1 | a0001c0001t0016g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.186-2238_186-2237i others(240): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412193 | C | CCCTTCCC others(219): Show |
1 | a0001c0001t0005g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.186-2238_186-2237i others(228): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | ||||||
chr1:235412197 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0006g0044 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.186-2236C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412197 | |||||||
chr1:235412198 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0006g0044 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.186-2235T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412198 | |||||||
chr1:235412198 | T | TCCCCTC | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.186-2231_186-2226d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCCCTCC others(322): Show |
1 | a0001c0001t0012g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(331): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCCCTCC others(322): Show |
1 | a0001c0001t0003g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(331): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCCCTCC others(327): Show |
1 | a0005c0008t0001g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.186-2221_186-2220i others(336): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCCCTCC others(319): Show |
1 | a0001c0001t0007g0059 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(328): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCCCTCC others(319): Show |
1 | a0001c0001t0012g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(328): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCCCTCC others(318): Show |
1 | a0001c0001t0001g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.186-2221_186-2220i others(327): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCCCTCC others(323): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0001g0140 others(4): Show |
7 | HG01891.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-2221_186-2220i others(332): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCCCTCC others(316): Show |
1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(325): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412198 | T | TCCTCCCC others(3): Show |
1 | a0001c0001t0014g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-2233_186-2232i others(12): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | ||||||
chr1:235412203 | T | C | 1 | a0001c0001t0016g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186-2230T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412203 | |||||||
chr1:235412204 | C | CCCCTCCC others(19): Show |
1 | a0001c0001t0011g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.186-2210_186-2209i others(28): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412204 | ||||||
chr1:235412208 | T | TCCCTCCC others(4): Show |
1 | a0001c0001t0014g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-2222_186-2221i others(13): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412208 | ||||||
chr1:235412213 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.186-2220C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412213 | |||||||
chr1:235412214 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.186-2219T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412214 | |||||||
chr1:235412214 | T | TCCCCTCC others(21): Show |
1 | a0001c0001t0002g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.186-2210_186-2209i others(30): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412214 | ||||||
chr1:235412219 | T | C | 1 | a0001c0001t0014g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-2214T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412219 | |||||||
chr1:235412223 | C | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-2210C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412223 | |||||||
chr1:235412224 | T | TCCCCCTC others(10): Show |
1 | a0001c0001t0002g0227 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.186-2198_186-2197i others(19): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412224 | ||||||
chr1:235412224 | TCCCCC | T | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0013g0130 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-2208_186-2204d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412224 | |||||||
chr1:235412225 | C | CCCCTCCC others(15): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2205_186-2204i others(24): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412225 | ||||||
chr1:235412225 | C | CCCCTCCC others(123): Show |
1 | a0001c0001t0004g0203 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.186-2205_186-2204i others(132): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412225 | ||||||
chr1:235412228 | C | CTCCCCTC others(118): Show |
1 | a0001c0001t0004g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.186-2205_186-2204i others(127): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412228 | |||||||
chr1:235412229 | C | CTCCCCTC others(4): Show |
26 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0121 others(23): Show |
26 | HG01106.hp1 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.186-2198_186-2197i others(13): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412229 | ||||||
chr1:235412229 | C | CTCCCCTC others(19): Show |
1 | a0001c0001t0006g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-2198_186-2197i others(28): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412229 | ||||||
chr1:235412229 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.186-2204C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412229 | |||||||
chr1:235412230 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.186-2203T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412230 | |||||||
chr1:235412230 | T | TCCCCCCT others(11): Show |
32 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0011 others(29): Show |
32 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.186-2199_186-2198i others(20): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412230 | ||||||
chr1:235412230 | T | TCCCCTCC others(32): Show |
2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-2198_186-2197i others(41): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412230 | ||||||
chr1:235412230 | T | TCCCCTCC others(32): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-2198_186-2197i others(41): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412230 | ||||||
chr1:235412230 | T | TCCCCTGC others(105): Show |
1 | a0001c0001t0004g0007 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.186-2198_186-2197i others(114): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412230 | ||||||
chr1:235412234 | C | CTCCCCTC others(9): Show |
1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186-2198_186-2197i others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412234 | ||||||
chr1:235412236 | T | A | 4 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | HG02523.hp1 NA18943.hp1 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-2197T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412236 | |||||||
chr1:235412236 | T | C | 1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186-2197T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412236 | |||||||
chr1:235412237 | C | A | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.186-2196C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412237 | |||||||
chr1:235412269 | C | T | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-2164C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412269 | |||||||
chr1:235412270 | G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.186-2163G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412270 | |||||||
chr1:235412506 | A | C | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.186-1927A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412506 | |||||||
chr1:235412519 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.186-1914C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412519 | |||||||
chr1:235412558 | C | T | 4 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0122 others(1): Show |
4 | HG02523.hp1 HG02809.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-1875C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412558 | |||||||
chr1:235412567 | C | T | 3 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0135 |
3 | HG02809.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.186-1866C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412567 | |||||||
chr1:235412633 | T | C | 1 | a0001c0001t0011g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.186-1800T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412633 | |||||||
chr1:235412745 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-1688C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412745 | |||||||
chr1:235412797 | AATTATT | A | 39 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(36): Show |
39 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.186-1623_186-1618d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412797 | ||||||
chr1:235412857 | G | A | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-1576G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412857 | |||||||
chr1:235413007 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-1426T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413007 | |||||||
chr1:235413172 | G | A | 39 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(36): Show |
39 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.186-1261G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413172 | |||||||
chr1:235413335 | G | A | 1 | a0001c0001t0027g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.186-1098G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413335 | |||||||
chr1:235413363 | T | TA | 24 | a0001c0001t0001g0079 a0001c0001t0001g0136 a0001c0001t0001g0146 others(21): Show |
24 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.186-1052dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413363 | ||||||
chr1:235413363 | TA | T | 16 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0075 others(13): Show |
16 | HG01070.hp2 HG01168.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-1052delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413363 | ||||||
chr1:235413499 | TA | T | 3 | a0001c0001t0001g0028 a0001c0001t0003g0103 a0001c0001t0006g0161 |
3 | HG01169.hp1 HG02451.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.186-929delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413499 | ||||||
chr1:235413569 | A | G | 17 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.186-864A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413569 | |||||||
chr1:235413634 | G | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.186-799G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413634 | |||||||
chr1:235413662 | C | CA | 43 | a0001c0001t0001g0074 a0001c0001t0002g0179 a0001c0001t0002g0200 others(40): Show |
43 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.186-759dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413662 | ||||||
chr1:235413676 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.186-757A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413676 | |||||||
chr1:235413752 | CT | C | 38 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(35): Show |
38 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.186-672delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413752 | ||||||
chr1:235413846 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-587C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413846 | |||||||
chr1:235413848 | A | AT | 11 | a0001c0001t0002g0106 a0001c0001t0002g0179 a0001c0001t0002g0190 others(8): Show |
11 | HG00642.hp1 HG01106.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.186-560dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413848 | ||||||
chr1:235413848 | AT | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.186-560delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413848 | ||||||
chr1:235413848 | ATT | A | 18 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0072 others(15): Show |
18 | HG01070.hp1 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-561_186-560del others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413848 | ||||||
chr1:235413893 | C | T | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.186-540C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413893 | |||||||
chr1:235414327 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.186-106T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235414327 | |||||||
chr1:235414953 | T | C | 6 | a0001c0001t0008g0024 a0001c0001t0008g0173 a0001c0001t0008g0174 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+335T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235414953 | |||||||
chr1:235415140 | T | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.371+522T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415140 | |||||||
chr1:235415448 | CTGGCCAG others(4): Show |
C | 2 | a0001c0001t0002g0202 a0001c0001t0002g0233 |
2 | HG01069.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.371+833_371+843del others(11): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235415448 | ||||||
chr1:235415491 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.371+873C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415491 | |||||||
chr1:235415548 | T | C | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.371+930T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415548 | |||||||
chr1:235415879 | G | A | 35 | a0001c0001t0002g0179 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.371+1261G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415879 | |||||||
chr1:235415926 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+1308T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415926 | |||||||
chr1:235416104 | C | T | 2 | a0001c0001t0001g0057 a0001c0005t0038g0155 |
2 | HG01070.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.371+1486C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416104 | |||||||
chr1:235416168 | C | CA | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.371+1568dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416168 | ||||||
chr1:235416168 | C | CAA | 27 | a0001c0001t0001g0026 a0001c0001t0001g0074 a0001c0001t0001g0079 others(24): Show |
27 | HG00558.hp1 HG00621.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.371+1567_371+1568d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416168 | ||||||
chr1:235416168 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.371+1558_371+1568d others(13): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416168 | ||||||
chr1:235416168 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.371+1555_371+1568d others(16): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416168 | ||||||
chr1:235416412 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.371+1794A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416412 | |||||||
chr1:235416523 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.371+1905C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416523 | |||||||
chr1:235416541 | CA | C | 15 | a0001c0001t0001g0053 a0001c0001t0001g0074 a0001c0001t0001g0095 others(12): Show |
15 | HG01106.hp2 HG01168.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.371+1935delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416541 | ||||||
chr1:235416541 | CAA | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.371+1934_371+1935d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416541 | ||||||
chr1:235416554 | C | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.371+1936C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416554 | |||||||
chr1:235416597 | T | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.371+1979T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416597 | |||||||
chr1:235416876 | G | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.371+2258G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416876 | |||||||
chr1:235417067 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.372-2406A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417067 | |||||||
chr1:235417284 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.372-2189C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417284 | |||||||
chr1:235417331 | G | C | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.372-2142G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417331 | |||||||
chr1:235417356 | T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.372-2117T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417356 | |||||||
chr1:235417412 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.372-2061A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417412 | |||||||
chr1:235417462 | A | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.372-2011A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417462 | |||||||
chr1:235417506 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.372-1967A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417506 | |||||||
chr1:235417514 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.372-1959C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417514 | |||||||
chr1:235417613 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.372-1860G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417613 | |||||||
chr1:235417760 | C | CT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.372-1705dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235417760 | ||||||
chr1:235417845 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.372-1628C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417845 | |||||||
chr1:235417951 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.372-1522T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417951 | |||||||
chr1:235418096 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.372-1377C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418096 | |||||||
chr1:235418168 | C | T | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.372-1305C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418168 | |||||||
chr1:235418186 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.372-1287C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418186 | |||||||
chr1:235418207 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.372-1266T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418207 | |||||||
chr1:235418222 | G | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.372-1251G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418222 | |||||||
chr1:235418487 | TTAACAAA others(15): Show |
T | 1 | a0001c0001t0002g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.372-984_372-963del others(22): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235418487 | ||||||
chr1:235418558 | G | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | NA18954.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.372-915G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418558 | |||||||
chr1:235418643 | G | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.372-830G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418643 | |||||||
chr1:235418957 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.372-516A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418957 | |||||||
chr1:235419073 | A | G | 2 | a0001c0005t0035g0260 a0001c0005t0038g0155 |
2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.372-400A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235419073 | |||||||
chr1:235419131 | T | C | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.372-342T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235419131 | |||||||
chr1:235419145 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.372-328T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235419145 | |||||||
chr1:235419228 | C | T | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.372-245C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235419228 | |||||||
chr1:235419609 | T | G | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+48T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419609 | |||||||
chr1:235419761 | C | G | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+200C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419761 | |||||||
chr1:235419818 | T | G | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+257T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419818 | |||||||
chr1:235419869 | C | T | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+308C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419869 | |||||||
chr1:235419888 | A | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.460+327A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419888 | |||||||
chr1:235420039 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.460+478C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420039 | |||||||
chr1:235420079 | T | C | 3 | a0001c0001t0001g0113 a0001c0001t0003g0077 a0001c0001t0003g0081 |
3 | HG02155.hp1 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.460+518T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420079 | |||||||
chr1:235420109 | T | G | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+548T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420109 | |||||||
chr1:235420169 | C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.460+608C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420169 | |||||||
chr1:235420274 | T | C | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+713T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420274 | |||||||
chr1:235420296 | T | C | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.460+735T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420296 | |||||||
chr1:235420318 | C | CT | 39 | a0001c0001t0001g0171 a0001c0001t0002g0246 a0001c0001t0002g0257 others(36): Show |
39 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.460+771dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235420318 | ||||||
chr1:235420375 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.460+814C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420375 | |||||||
chr1:235420400 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
83 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.460+839C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420400 | |||||||
chr1:235420458 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.460+897G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420458 | |||||||
chr1:235420463 | C | T | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.460+902C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420463 | |||||||
chr1:235420464 | G | A | 31 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(28): Show |
31 | HG00733.hp2 HG01070.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.460+903G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420464 | |||||||
chr1:235420481 | A | AT | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.460+940dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235420481 | ||||||
chr1:235420481 | A | ATT | 15 | a0001c0001t0001g0061 a0001c0001t0001g0074 a0001c0001t0001g0117 others(12): Show |
15 | HG01109.hp1 HG02027.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.460+939_460+940dup others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235420481 | ||||||
chr1:235420617 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.460+1056G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420617 | |||||||
chr1:235420619 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.460+1058G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420619 | |||||||
chr1:235420735 | C | A | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1174C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420735 | |||||||
chr1:235420740 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+1179C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420740 | |||||||
chr1:235420878 | G | A | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.460+1317G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420878 | |||||||
chr1:235421043 | G | T | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1482G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421043 | |||||||
chr1:235421078 | T | C | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.460+1517T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421078 | |||||||
chr1:235421085 | T | C | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1524T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421085 | |||||||
chr1:235421108 | G | A | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1547G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421108 | |||||||
chr1:235421228 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.460+1667C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421228 | |||||||
chr1:235421233 | C | CTTG | 2 | a0001c0001t0002g0202 a0001c0001t0002g0233 |
2 | HG01069.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.460+1674_460+1676d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235421233 | ||||||
chr1:235421245 | A | C | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.460+1684A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421245 | |||||||
chr1:235421399 | C | T | 3 | a0001c0001t0006g0044 a0001c0001t0026g0129 a0001c0001t0027g0128 |
3 | HG03540.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+1838C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421399 | |||||||
chr1:235421460 | T | C | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1899T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421460 | |||||||
chr1:235421524 | C | A | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1963C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421524 | |||||||
chr1:235421640 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+2079C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421640 | |||||||
chr1:235421642 | G | A | 1 | a0001c0001t0005g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.460+2081G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421642 | |||||||
chr1:235421772 | C | T | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+2211C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421772 | |||||||
chr1:235421802 | C | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+2241C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421802 | |||||||
chr1:235422093 | A | G | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+2532A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422093 | |||||||
chr1:235422123 | A | G | 4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.460+2562A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422123 | |||||||
chr1:235422299 | G | C | 2 | a0001c0005t0035g0260 a0001c0005t0038g0155 |
2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.460+2738G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422299 | |||||||
chr1:235422328 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.460+2767A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422328 | |||||||
chr1:235422409 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.460+2848A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422409 | |||||||
chr1:235422543 | G | A | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+2982G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422543 | |||||||
chr1:235422783 | C | T | 1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.460+3222C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422783 | |||||||
chr1:235422831 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.460+3270A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422831 | |||||||
chr1:235423015 | T | A | 2 | a0001c0005t0035g0260 a0001c0005t0038g0155 |
2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.460+3454T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423015 | |||||||
chr1:235423016 | T | A | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+3455T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423016 | |||||||
chr1:235423061 | C | T | 31 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(28): Show |
31 | HG00733.hp2 HG01070.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.460+3500C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423061 | |||||||
chr1:235423116 | T | G | 31 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(28): Show |
31 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.460+3555T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423116 | |||||||
chr1:235423195 | G | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+3634G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423195 | |||||||
chr1:235423229 | C | T | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+3668C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423229 | |||||||
chr1:235423298 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.460+3737C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423298 | |||||||
chr1:235423428 | G | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.461-3712G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423428 | |||||||
chr1:235423482 | T | A | 1 | a0001c0001t0002g0255 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.461-3658T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423482 | |||||||
chr1:235423578 | T | C | 29 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(26): Show |
29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.461-3562T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423578 | |||||||
chr1:235423626 | C | G | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.461-3514C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423626 | |||||||
chr1:235423659 | A | G | 26 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(23): Show |
26 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.461-3481A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423659 | |||||||
chr1:235423757 | C | T | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.461-3383C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423757 | |||||||
chr1:235423797 | A | G | 6 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-3343A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423797 | |||||||
chr1:235423833 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.461-3307G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423833 | |||||||
chr1:235423858 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.461-3282A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423858 | |||||||
chr1:235423946 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.461-3194G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423946 | |||||||
chr1:235423955 | C | G | 6 | a0001c0001t0003g0036 a0001c0001t0003g0102 a0001c0001t0003g0103 others(3): Show |
6 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-3185C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423955 | |||||||
chr1:235424094 | G | T | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-3046G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424094 | |||||||
chr1:235424193 | G | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-2947G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424193 | |||||||
chr1:235424202 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.461-2938G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424202 | |||||||
chr1:235424230 | T | G | 3 | a0001c0001t0005g0187 a0003c0004t0031g0016 a0003c0004t0037g0172 |
3 | HG02109.hp1 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-2910T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424230 | |||||||
chr1:235424322 | C | CT | 7 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0002g0227 others(4): Show |
7 | NA18949.hp1 NA18951.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.461-2798dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235424322 | ||||||
chr1:235424322 | CT | C | 8 | a0001c0001t0001g0262 a0001c0001t0003g0077 a0001c0001t0003g0102 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.461-2798delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235424322 | ||||||
chr1:235424388 | G | A | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-2752G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424388 | |||||||
chr1:235424427 | G | GC | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.461-2713_461-2712i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424427 | |||||||
chr1:235424502 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.461-2638G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424502 | |||||||
chr1:235425094 | C | A | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.461-2046C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425094 | |||||||
chr1:235425096 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.461-2044C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425096 | |||||||
chr1:235425200 | C | T | 2 | a0001c0001t0004g0043 a0001c0001t0004g0134 |
2 | HG01106.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.461-1940C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425200 | |||||||
chr1:235425485 | G | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.461-1655G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425485 | |||||||
chr1:235425616 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.461-1524C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425616 | |||||||
chr1:235425617 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.461-1523G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425617 | |||||||
chr1:235425650 | C | T | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.461-1490C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425650 | |||||||
chr1:235425799 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.461-1341G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425799 | |||||||
chr1:235425987 | T | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-1153T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425987 | |||||||
chr1:235426088 | C | A | 3 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0141 |
3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.461-1052C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426088 | |||||||
chr1:235426133 | G | A | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-1007G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426133 | |||||||
chr1:235426166 | G | C | 4 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0110 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-974G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426166 | |||||||
chr1:235426464 | A | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-676A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426464 | |||||||
chr1:235426533 | C | T | 1 | a0001c0001t0028g0071 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.461-607C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426533 | |||||||
chr1:235426793 | G | A | 1 | a0001c0007t0001g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.461-347G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426793 | |||||||
chr1:235426919 | T | C | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-221T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426919 | |||||||
chr1:235426936 | G | A | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-204G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426936 | |||||||
chr1:235426950 | A | T | 1 | a0001c0001t0004g0007 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.461-190A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426950 | |||||||
chr1:235426963 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.461-177G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426963 | |||||||
chr1:235427244 | G | A | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
splice_region_variant&intron_variant | LOW | c.560+5G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427244 | |||||||
chr1:235427447 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.560+208A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427447 | |||||||
chr1:235427470 | G | A | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+231G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427470 | |||||||
chr1:235427471 | C | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+232C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427471 | |||||||
chr1:235427504 | A | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+265A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427504 | |||||||
chr1:235427530 | A | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+291A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427530 | |||||||
chr1:235427622 | A | T | 58 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(55): Show |
58 | HG00733.hp2 HG00741.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.560+383A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427622 | |||||||
chr1:235427645 | A | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+406A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427645 | |||||||
chr1:235427740 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560+501G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427740 | |||||||
chr1:235427828 | T | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+589T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427828 | |||||||
chr1:235427945 | G | T | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.560+706G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427945 | |||||||
chr1:235428024 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0114 |
2 | HG01123.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.560+785C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428024 | |||||||
chr1:235428025 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.560+786G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428025 | |||||||
chr1:235428047 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.560+808A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428047 | |||||||
chr1:235428050 | C | T | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+811C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428050 | |||||||
chr1:235428095 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.560+856C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428095 | |||||||
chr1:235428184 | C | T | 1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.560+945C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428184 | |||||||
chr1:235428197 | A | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+958A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428197 | |||||||
chr1:235428217 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0114 |
2 | HG01123.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.560+978G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428217 | |||||||
chr1:235428310 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.560+1071C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428310 | |||||||
chr1:235428370 | C | T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0259 |
2 | NA18951.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.560+1131C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428370 | |||||||
chr1:235428380 | C | T | 2 | a0001c0001t0002g0198 a0001c0001t0015g0239 |
2 | HG00621.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.560+1141C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428380 | |||||||
chr1:235428488 | T | A | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.560+1249T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428488 | |||||||
chr1:235428586 | T | A | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+1347T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428586 | |||||||
chr1:235428595 | C | A | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+1356C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428595 | |||||||
chr1:235428631 | C | CTTTA | 25 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0163 others(22): Show |
25 | HG00733.hp2 HG01109.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.560+1420_560+1423d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | ||||||
chr1:235428631 | C | CTTTATTT others(1): Show |
99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.560+1416_560+1423d others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | ||||||
chr1:235428631 | C | CTTTATTT others(5): Show |
20 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0037 others(17): Show |
20 | HG01167.hp1 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.560+1412_560+1423d others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | ||||||
chr1:235428631 | C | CTTTATTT others(9): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0063 others(1): Show |
4 | HG00738.hp1 HG01099.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+1408_560+1423d others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | ||||||
chr1:235428631 | C | CTTTATTT others(13): Show |
5 | a0001c0001t0001g0057 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+1404_560+1423d others(22): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | ||||||
chr1:235428631 | C | CTTTATTT others(17): Show |
1 | a0001c0003t0001g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.560+1400_560+1423d others(26): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | ||||||
chr1:235428631 | CTTTATTT others(1): Show |
C | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.560+1416_560+1423d others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | ||||||
chr1:235428800 | C | T | 2 | a0001c0005t0035g0260 a0001c0005t0038g0155 |
2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.560+1561C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428800 | |||||||
chr1:235428830 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.560+1591G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428830 | |||||||
chr1:235428844 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.560+1605A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428844 | |||||||
chr1:235428873 | A | T | 1 | a0001c0001t0003g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.560+1634A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428873 | |||||||
chr1:235428969 | G | GTATATA | 4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-1724_561-1719d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428969 | ||||||
chr1:235428969 | G | GTGTGTGT others(25): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560+1731_560+1732i others(34): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428969 | ||||||
chr1:235428969 | G | GTGTGTGT others(27): Show |
1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.560+1731_560+1732i others(36): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428969 | ||||||
chr1:235428971 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.560+1732A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428971 | |||||||
chr1:235428983 | A | AT | 17 | a0001c0001t0004g0006 a0001c0001t0004g0027 a0001c0001t0004g0038 others(14): Show |
17 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.561-1721dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428983 | ||||||
chr1:235428983 | ATAT | A | 14 | a0001c0001t0005g0124 a0001c0001t0005g0162 a0001c0001t0005g0163 others(11): Show |
14 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.561-1720_561-1718d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428983 | ||||||
chr1:235428985 | A | AT | 12 | a0001c0001t0002g0198 a0001c0001t0002g0227 a0001c0001t0004g0007 others(9): Show |
12 | HG00621.hp1 HG01361.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-1700dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428985 | ||||||
chr1:235428985 | A | T | 24 | a0001c0001t0002g0195 a0001c0001t0002g0207 a0001c0001t0002g0214 others(21): Show |
24 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.561-1720A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428985 | |||||||
chr1:235428985 | AT | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.561-1700delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428985 | ||||||
chr1:235428985 | ATTT | A | 8 | a0001c0001t0005g0160 a0001c0001t0005g0184 a0001c0001t0008g0024 others(5): Show |
8 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-1702_561-1700d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428985 | ||||||
chr1:235428986 | T | TA | 4 | a0001c0001t0002g0046 a0001c0001t0004g0158 a0001c0001t0004g0180 others(1): Show |
4 | HG02976.hp2 HG04228.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-1719_561-1718i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428986 | |||||||
chr1:235428986 | T | TATA | 4 | a0001c0001t0006g0044 a0001c0001t0026g0129 a0001c0001t0027g0128 others(1): Show |
4 | HG01070.hp2 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-1719_561-1718i others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428986 | |||||||
chr1:235428987 | T | A | 50 | a0001c0001t0001g0105 a0001c0001t0001g0113 a0001c0001t0001g0117 others(47): Show |
50 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.561-1718T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428987 | |||||||
chr1:235428988 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.561-1717T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428988 | |||||||
chr1:235428989 | T | A | 36 | a0001c0001t0001g0105 a0001c0001t0001g0113 a0001c0001t0001g0117 others(33): Show |
36 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.561-1716T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428989 | |||||||
chr1:235428990 | T | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0032 others(28): Show |
31 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.561-1715T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428990 | |||||||
chr1:235428991 | T | A | 3 | a0001c0001t0003g0112 a0001c0001t0003g0151 a0001c0005t0035g0260 |
3 | HG01433.hp1 HG03471.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.561-1714T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428991 | |||||||
chr1:235428992 | T | A | 2 | a0001c0001t0001g0012 a0001c0001t0003g0137 |
2 | HG03017.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.561-1713T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428992 | |||||||
chr1:235429004 | T | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1701T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429004 | |||||||
chr1:235429135 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.561-1570C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429135 | |||||||
chr1:235429180 | G | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.561-1525G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429180 | |||||||
chr1:235429488 | A | G | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-1217A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429488 | |||||||
chr1:235429545 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1160G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429545 | |||||||
chr1:235429580 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1125A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429580 | |||||||
chr1:235429722 | A | AT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.561-970dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235429722 | ||||||
chr1:235429790 | T | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-915T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429790 | |||||||
chr1:235429803 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.561-902C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429803 | |||||||
chr1:235429997 | C | T | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-708C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429997 | |||||||
chr1:235430007 | C | T | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-698C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430007 | |||||||
chr1:235430058 | ATGTGAG | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.561-643_561-638del others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235430058 | ||||||
chr1:235430122 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0032g0064 |
2 | HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.561-583G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430122 | |||||||
chr1:235430163 | G | A | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-542G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430163 | |||||||
chr1:235430201 | C | T | 5 | a0001c0001t0005g0165 a0001c0001t0005g0166 a0001c0001t0005g0167 others(2): Show |
5 | HG02622.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-504C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430201 | |||||||
chr1:235430210 | T | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-495T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430210 | |||||||
chr1:235430383 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.561-322A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430383 | |||||||
chr1:235430443 | A | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-262A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430443 | |||||||
chr1:235430457 | G | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-248G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430457 | |||||||
chr1:235430867 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.660+63A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235430867 | |||||||
chr1:235430935 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.660+131A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235430935 | |||||||
chr1:235431101 | A | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+297A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431101 | |||||||
chr1:235431176 | G | C | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.660+372G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431176 | |||||||
chr1:235431213 | C | T | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.660+409C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431213 | |||||||
chr1:235431214 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.660+410G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431214 | |||||||
chr1:235431301 | T | G | 1 | a0001c0001t0032g0064 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.660+497T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431301 | |||||||
chr1:235431321 | T | C | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.660+517T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431321 | |||||||
chr1:235431363 | CT | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0072 others(6): Show |
9 | HG01069.hp2 HG01168.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+574delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr1 | 235431363 | ||||||
chr1:235431515 | T | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+711T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431515 | |||||||
chr1:235431521 | C | T | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+717C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431521 | |||||||
chr1:235431572 | G | A | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.660+768G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431572 | |||||||
chr1:235431580 | C | T | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.660+776C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431580 | |||||||
chr1:235431636 | G | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.660+832G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431636 | |||||||
chr1:235431650 | C | T | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+846C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431650 | |||||||
chr1:235431719 | G | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+915G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431719 | |||||||
chr1:235431828 | A | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1024A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431828 | |||||||
chr1:235431903 | T | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1099T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431903 | |||||||
chr1:235431961 | C | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.660+1157C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431961 | |||||||
chr1:235431962 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.660+1158G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431962 | |||||||
chr1:235432014 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.660+1210C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432014 | |||||||
chr1:235432068 | C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.660+1264C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432068 | |||||||
chr1:235432107 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0138 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+1303C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432107 | |||||||
chr1:235432108 | A | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1304A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432108 | |||||||
chr1:235432128 | C | T | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1324C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432128 | |||||||
chr1:235432223 | A | C | 58 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(55): Show |
58 | HG00733.hp2 HG00741.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.660+1419A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432223 | |||||||
chr1:235432275 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.660+1471T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432275 | |||||||
chr1:235432298 | T | G | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1494T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432298 | |||||||
chr1:235432390 | C | T | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1586C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432390 | |||||||
chr1:235432391 | C | T | 1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+1587C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432391 | |||||||
chr1:235432505 | C | T | 4 | a0001c0001t0004g0197 a0001c0001t0004g0203 a0001c0001t0004g0204 others(1): Show |
4 | HG02735.hp1 HG03490.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1699C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432505 | |||||||
chr1:235432680 | G | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-1524G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432680 | |||||||
chr1:235432738 | C | T | 1 | a0001c0001t0003g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.661-1466C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432738 | |||||||
chr1:235432739 | T | C | 1 | a0001c0001t0003g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.661-1465T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432739 | |||||||
chr1:235432755 | C | T | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.661-1449C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432755 | |||||||
chr1:235432916 | AT | A | 6 | a0001c0001t0001g0138 a0001c0001t0007g0045 a0001c0001t0007g0132 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-1277delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr1 | 235432916 | ||||||
chr1:235433008 | C | T | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-1196C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433008 | |||||||
chr1:235433081 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.661-1123C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433081 | |||||||
chr1:235433089 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.661-1115C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433089 | |||||||
chr1:235433312 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.661-892C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433312 | |||||||
chr1:235433366 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.661-838G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433366 | |||||||
chr1:235433466 | T | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-738T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433466 | |||||||
chr1:235433508 | A | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-696A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433508 | |||||||
chr1:235433567 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.661-637C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433567 | |||||||
chr1:235433652 | G | A | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.661-552G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433652 | |||||||
chr1:235433883 | T | C | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-321T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433883 | |||||||
chr1:235433937 | T | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.661-267T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433937 | |||||||
chr1:235434008 | T | G | 1 | a0001c0001t0007g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.661-196T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235434008 | |||||||
chr1:235434085 | G | A | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-119G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235434085 | |||||||
chr1:235434520 | T | C | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.737+240T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235434520 | |||||||
chr1:235434549 | C | CTTTCTT | 5 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0164 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+272_737+273ins others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235434549 | ||||||
chr1:235434549 | C | CTTTTT | 7 | a0001c0001t0001g0117 a0001c0001t0005g0167 a0001c0001t0007g0045 others(4): Show |
7 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.737+272_737+276dup others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235434549 | ||||||
chr1:235434549 | C | CTTTTTT | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.737+271_737+276dup others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235434549 | ||||||
chr1:235434578 | G | A | 3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.737+298G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235434578 | |||||||
chr1:235434604 | T | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.737+324T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235434604 | |||||||
chr1:235434777 | C | T | 1 | a0001c0001t0005g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.737+497C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235434777 | |||||||
chr1:235435075 | C | T | 3 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0141 |
3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.738-670C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435075 | |||||||
chr1:235435107 | G | GT | 36 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(33): Show |
36 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.738-628dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235435107 | ||||||
chr1:235435107 | G | T | 2 | a0001c0001t0004g0180 a0001c0001t0004g0181 |
2 | NA18943.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.738-638G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435107 | |||||||
chr1:235435122 | T | TAGAGTTT others(9): Show |
1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-608_738-607ins others(16): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235435122 | ||||||
chr1:235435290 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-455G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435290 | |||||||
chr1:235435310 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-435C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435310 | |||||||
chr1:235435311 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-434G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435311 | |||||||
chr1:235435348 | G | A | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.738-397G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435348 | |||||||
chr1:235435406 | G | A | 3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.738-339G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435406 | |||||||
chr1:235435437 | TAATC | T | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.738-306_738-303del others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235435437 | ||||||
chr1:235435438 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.738-307A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435438 | |||||||
chr1:235435529 | A | G | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.738-216A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435529 | |||||||
chr1:235435556 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.738-189G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435556 | |||||||
chr1:235435571 | C | T | 17 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.738-174C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435571 | |||||||
chr1:235435572 | G | A | 2 | a0003c0004t0031g0016 a0003c0004t0037g0172 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.738-173G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435572 | |||||||
chr1:235435585 | G | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.738-160G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435585 | |||||||
chr1:235435656 | A | G | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.738-89A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435656 | |||||||
chr1:235435658 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.738-87C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435658 | |||||||
chr1:235435990 | G | C | 1 | a0001c0001t0023g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.833+150G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235435990 | |||||||
chr1:235435993 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.833+153T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235435993 | |||||||
chr1:235436113 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.833+273C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436113 | |||||||
chr1:235436177 | C | G | 1 | a0001c0001t0005g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.834-209C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436177 | |||||||
chr1:235436180 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.834-206G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436180 | |||||||
chr1:235436309 | T | G | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.834-77T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436309 | |||||||
chr1:235436316 | C | T | 6 | a0001c0001t0008g0024 a0001c0001t0008g0173 a0001c0001t0008g0174 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.834-70C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436316 | |||||||
chr1:235436507 | T | A | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.899-37T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 10/16 | chr1 | 235436507 | |||||||
chr1:235436734 | A | C | 4 | a0001c0005t0035g0260 a0001c0005t0038g0155 a0003c0004t0031g0016 others(1): Show |
4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+126A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436734 | |||||||
chr1:235436738 | A | AC | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
65 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.963+130_963+131ins others(1): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436738 | |||||||
chr1:235436741 | C | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0139 others(2): Show |
5 | HG00621.hp2 HG02027.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+133C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436741 | |||||||
chr1:235436814 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.963+206T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436814 | |||||||
chr1:235436841 | G | A | 3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.963+233G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436841 | |||||||
chr1:235436893 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.963+285C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436893 | |||||||
chr1:235436916 | C | G | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.963+308C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436916 | |||||||
chr1:235436951 | T | TCTA | 5 | a0001c0001t0008g0024 a0001c0001t0008g0174 a0001c0001t0008g0176 others(2): Show |
5 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+347_963+349dup others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr1 | 235436951 | ||||||
chr1:235436956 | T | TA | 14 | a0001c0001t0001g0097 a0001c0001t0001g0136 a0001c0001t0001g0145 others(11): Show |
14 | HG00621.hp1 HG01106.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.964-351dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr1 | 235436956 | ||||||
chr1:235436990 | G | A | 2 | a0001c0001t0005g0168 a0001c0001t0005g0170 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-332G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436990 | |||||||
chr1:235437086 | G | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.964-236G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235437086 | |||||||
chr1:235437129 | AAAAAC | A | 3 | a0001c0001t0006g0044 a0003c0004t0031g0016 a0003c0004t0037g0172 |
3 | HG06807.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.964-173_964-169del others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr1 | 235437129 | ||||||
chr1:235437275 | G | A | 4 | a0001c0005t0035g0260 a0001c0005t0038g0155 a0003c0004t0031g0016 others(1): Show |
4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-47G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235437275 | |||||||
chr1:235437290 | C | T | 2 | a0001c0001t0003g0151 a0001c0001t0003g0191 |
2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.964-32C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235437290 | |||||||
chr1:235437496 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1116+22A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437496 | |||||||
chr1:235437498 | A | C | 4 | a0001c0005t0035g0260 a0001c0005t0038g0155 a0003c0004t0031g0016 others(1): Show |
4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+24A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437498 | |||||||
chr1:235437538 | G | A | 2 | a0001c0001t0004g0180 a0001c0001t0004g0181 |
2 | NA18943.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1116+64G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437538 | |||||||
chr1:235437596 | C | G | 4 | a0001c0005t0035g0260 a0001c0005t0038g0155 a0003c0004t0031g0016 others(1): Show |
4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+122C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437596 | |||||||
chr1:235437601 | C | A | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1116+127C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437601 | |||||||
chr1:235437654 | A | C | 1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1116+180A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437654 | |||||||
chr1:235437781 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1116+307C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437781 | |||||||
chr1:235437847 | A | G | 2 | a0001c0001t0002g0236 a0001c0001t0002g0241 |
2 | NA18975.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1116+373A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437847 | |||||||
chr1:235437899 | G | T | 1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1116+425G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437899 | |||||||
chr1:235437987 | T | C | 3 | a0001c0001t0004g0038 a0001c0001t0004g0042 a0001c0001t0004g0133 |
3 | HG00741.hp1 HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1116+513T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437987 | |||||||
chr1:235438025 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1116+551A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438025 | |||||||
chr1:235438181 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1117-588G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438181 | |||||||
chr1:235438237 | C | T | 8 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0164 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-532C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438237 | |||||||
chr1:235438366 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1117-403C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438366 | |||||||
chr1:235438518 | A | C | 7 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(4): Show |
7 | HG01070.hp2 HG01243.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-251A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438518 | |||||||
chr1:235438552 | T | TAAA | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1117-208_1117-206d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr1 | 235438552 | ||||||
chr1:235438564 | G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1117-205G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438564 | |||||||
chr1:235438643 | G | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1117-126G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438643 | |||||||
chr1:235438646 | C | G | 2 | a0001c0001t0012g0013 a0001c0001t0012g0014 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1117-123C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438646 | |||||||
chr1:235438989 | G | A | 27 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(24): Show |
27 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1270+67G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235438989 | |||||||
chr1:235439085 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1270+163G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439085 | |||||||
chr1:235439089 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1270+167G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439089 | |||||||
chr1:235439214 | G | A | 3 | a0001c0001t0001g0140 a0003c0004t0031g0016 a0003c0004t0037g0172 |
3 | HG03471.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1270+292G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439214 | |||||||
chr1:235439229 | G | C | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+307G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439229 | |||||||
chr1:235439235 | T | A | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1270+313T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439235 | |||||||
chr1:235439238 | T | C | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1270+316T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439238 | |||||||
chr1:235439246 | T | C | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+324T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439246 | |||||||
chr1:235439257 | T | C | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+335T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439257 | |||||||
chr1:235439258 | G | A | 23 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1270+336G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439258 | |||||||
chr1:235439266 | T | C | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+344T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439266 | |||||||
chr1:235439267 | G | T | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1270+345G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439267 | |||||||
chr1:235439277 | G | C | 22 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0163 others(19): Show |
22 | HG00733.hp2 HG01109.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1270+355G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439277 | |||||||
chr1:235439299 | A | G | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+377A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439299 | |||||||
chr1:235439315 | C | G | 7 | a0001c0001t0008g0024 a0001c0001t0008g0173 a0001c0001t0008g0174 others(4): Show |
7 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1270+393C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439315 | |||||||
chr1:235439322 | C | T | 7 | a0001c0001t0008g0024 a0001c0001t0008g0173 a0001c0001t0008g0174 others(4): Show |
7 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1270+400C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439322 | |||||||
chr1:235439335 | C | CA | 6 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(3): Show |
6 | HG01243.hp1 HG02071.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270+424dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 235439335 | ||||||
chr1:235439335 | C | CAA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.1270+423_1270+424d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 235439335 | ||||||
chr1:235439335 | CAAAAA | C | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+420_1270+424d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 235439335 | ||||||
chr1:235439348 | G | T | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+426G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439348 | |||||||
chr1:235439352 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1270+430C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439352 | |||||||
chr1:235439357 | G | A | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+435G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439357 | |||||||
chr1:235439359 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0003g0116 a0001c0001t0003g0118 others(1): Show |
4 | NA18975.hp1 NA19005.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+437G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439359 | |||||||
chr1:235439369 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0003g0116 a0001c0001t0003g0118 others(1): Show |
4 | NA18975.hp1 NA19005.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+447A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439369 | |||||||
chr1:235439424 | G | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1270+502G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439424 | |||||||
chr1:235439569 | C | T | 1 | a0001c0001t0005g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1270+647C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439569 | |||||||
chr1:235439616 | TAG | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1270+695_1270+696d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439616 | |||||||
chr1:235439636 | C | T | 1 | a0001c0001t0002g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1270+714C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439636 | |||||||
chr1:235439710 | A | G | 4 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | HG02523.hp1 NA18943.hp1 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+788A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439710 | |||||||
chr1:235439739 | C | T | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1270+817C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439739 | |||||||
chr1:235439805 | C | A | 8 | a0001c0001t0002g0034 a0001c0001t0002g0088 a0001c0001t0002g0089 others(5): Show |
8 | HG00544.hp1 HG01081.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1270+883C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439805 | |||||||
chr1:235439846 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1270+924G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439846 | |||||||
chr1:235439903 | G | A | 4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1270+981G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439903 | |||||||
chr1:235440009 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1270+1087C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440009 | |||||||
chr1:235440026 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1270+1104A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440026 | |||||||
chr1:235440080 | C | T | 3 | a0001c0001t0004g0158 a0001c0001t0004g0180 a0001c0001t0004g0181 |
3 | NA18943.hp2 NA18954.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1270+1158C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440080 | |||||||
chr1:235440100 | G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1270+1178G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440100 | |||||||
chr1:235440108 | C | T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0259 |
2 | NA18951.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1270+1186C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440108 | |||||||
chr1:235440120 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1270+1198A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440120 | |||||||
chr1:235440172 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1270+1250G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440172 | |||||||
chr1:235440217 | A | G | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+1295A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440217 | |||||||
chr1:235440231 | G | A | 2 | a0001c0001t0008g0173 a0001c0001t0008g0177 |
2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1270+1309G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440231 | |||||||
chr1:235440262 | G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1270+1340G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440262 | |||||||
chr1:235440266 | A | G | 6 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270+1344A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440266 | |||||||
chr1:235440377 | G | C | 38 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0027 others(35): Show |
38 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1271-1437G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440377 | |||||||
chr1:235440380 | T | C | 38 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0027 others(35): Show |
38 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1271-1434T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440380 | |||||||
chr1:235440390 | G | GTA | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-1412_1271-141 others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 235440390 | ||||||
chr1:235440402 | A | T | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1271-1412A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440402 | |||||||
chr1:235440417 | T | A | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1271-1397T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440417 | |||||||
chr1:235440483 | C | G | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-1331C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440483 | |||||||
chr1:235440636 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1271-1178C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440636 | |||||||
chr1:235440784 | G | GTGTAGTT others(8): Show |
1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1271-1030_1271-102 others(19): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440784 | |||||||
chr1:235440785 | G | A | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1271-1029G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440785 | |||||||
chr1:235440959 | A | G | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-855A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440959 | |||||||
chr1:235441028 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1271-786A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441028 | |||||||
chr1:235441065 | A | G | 4 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1271-749A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441065 | |||||||
chr1:235441238 | G | T | 1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1271-576G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441238 | |||||||
chr1:235441405 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1271-409C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441405 | |||||||
chr1:235441520 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1271-294C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441520 | |||||||
chr1:235441573 | C | T | 4 | a0001c0001t0026g0129 a0001c0001t0027g0128 a0001c0001t0030g0154 others(1): Show |
4 | HG03516.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1271-241C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441573 | |||||||
chr1:235441680 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1271-134A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441680 | |||||||
chr1:235442008 | A | T | 26 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(23): Show |
26 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1339+126A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442008 | |||||||
chr1:235442008 | AT | A | 6 | a0001c0001t0001g0097 a0001c0001t0001g0117 a0001c0001t0002g0089 others(3): Show |
6 | HG01070.hp2 HG02897.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339+143delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr1 | 235442008 | ||||||
chr1:235442009 | T | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0063 a0001c0001t0003g0107 |
3 | HG01257.hp2 HG02135.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1339+127T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442009 | |||||||
chr1:235442146 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1339+264C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442146 | |||||||
chr1:235442169 | C | T | 1 | a0001c0001t0004g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1339+287C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442169 | |||||||
chr1:235442248 | G | A | 3 | a0001c0005t0035g0260 a0001c0005t0038g0155 a0003c0004t0037g0172 |
3 | HG01070.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1339+366G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442248 | |||||||
chr1:235442280 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1339+398C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442280 | |||||||
chr1:235442416 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1340-436C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442416 | |||||||
chr1:235442446 | C | T | 1 | a0001c0001t0012g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1340-406C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442446 | |||||||
chr1:235442480 | A | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1340-372A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442480 | |||||||
chr1:235442604 | G | A | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1340-248G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442604 | |||||||
chr1:235442663 | A | G | 4 | a0001c0001t0026g0129 a0001c0001t0027g0128 a0001c0001t0030g0154 others(1): Show |
4 | HG03516.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1340-189A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442663 | |||||||
chr1:235442666 | G | A | 4 | a0001c0001t0026g0129 a0001c0001t0027g0128 a0001c0001t0030g0154 others(1): Show |
4 | HG03516.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1340-186G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442666 | |||||||
chr1:235443087 | G | GC | 7 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(4): Show |
7 | HG01070.hp2 HG01243.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399+181dupC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443087 | ||||||
chr1:235443110 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1399+199C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443110 | |||||||
chr1:235443177 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1399+266C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443177 | |||||||
chr1:235443183 | C | CAT | 7 | a0001c0001t0008g0024 a0001c0001t0008g0173 a0001c0001t0008g0174 others(4): Show |
7 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399+273_1399+274i others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443183 | ||||||
chr1:235443183 | C | CATAT | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1399+273_1399+274i others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443183 | ||||||
chr1:235443185 | C | CATAT | 16 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(13): Show |
16 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.1399+282_1399+285d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443185 | ||||||
chr1:235443185 | C | T | 41 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(38): Show |
41 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1399+274C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443185 | |||||||
chr1:235443185 | CAT | C | 4 | a0001c0001t0007g0045 a0001c0001t0007g0265 a0001c0001t0007g0266 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1399+284_1399+285d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443185 | ||||||
chr1:235443195 | T | TAC | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1399+298_1399+299d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443195 | ||||||
chr1:235443398 | C | T | 5 | a0001c0001t0007g0045 a0001c0001t0007g0132 a0001c0001t0007g0265 others(2): Show |
5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399+487C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443398 | |||||||
chr1:235443450 | G | A | 4 | a0001c0001t0026g0129 a0001c0001t0027g0128 a0001c0001t0030g0154 others(1): Show |
4 | HG03516.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399+539G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443450 | |||||||
chr1:235443579 | GCTGTTTC others(8): Show |
G | 3 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0001t0013g0152 |
3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1399+673_1399+687d others(17): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443579 | ||||||
chr1:235443915 | A | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1399+1004A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443915 | |||||||
chr1:235444218 | A | C | 3 | a0001c0001t0002g0210 a0001c0001t0002g0228 a0001c0001t0011g0223 |
3 | NA18956.hp2 NA18962.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1399+1307A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444218 | |||||||
chr1:235444241 | A | C | 3 | a0001c0005t0035g0260 a0001c0005t0038g0155 a0003c0004t0037g0172 |
3 | HG01070.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1399+1330A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444241 | |||||||
chr1:235444304 | G | A | 1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1399+1393G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444304 | |||||||
chr1:235444437 | C | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1399+1526C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444437 | |||||||
chr1:235444704 | A | G | 58 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(55): Show |
58 | HG00733.hp2 HG00741.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.1399+1793A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444704 | |||||||
chr1:235444707 | C | T | 3 | a0001c0001t0004g0011 a0001c0001t0004g0043 a0001c0001t0004g0134 |
3 | HG01106.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1399+1796C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444707 | |||||||
chr1:235444844 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1399+1933T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444844 | |||||||
chr1:235445002 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1399+2091A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445002 | |||||||
chr1:235445128 | A | G | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1399+2217A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445128 | |||||||
chr1:235445297 | G | T | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1399+2386G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445297 | |||||||
chr1:235445410 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG00099.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.1399+2499C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445410 | |||||||
chr1:235445434 | G | A | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1399+2523G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445434 | |||||||
chr1:235445503 | G | A | 17 | a0001c0001t0002g0034 a0001c0001t0002g0088 a0001c0001t0002g0089 others(14): Show |
17 | HG00544.hp1 HG01081.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1399+2592G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445503 | |||||||
chr1:235445560 | T | C | 2 | a0001c0001t0026g0129 a0001c0001t0027g0128 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1399+2649T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445560 | |||||||
chr1:235445602 | A | G | 24 | a0001c0001t0005g0124 a0001c0001t0005g0160 a0001c0001t0005g0162 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1399+2691A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445602 | |||||||
chr1:235445967 | A | G | 1 | a0002c0002t0010g0023 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1400-2382A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445967 | |||||||
chr1:235446183 | C | CT | 35 | a0001c0001t0002g0127 a0001c0001t0004g0006 a0001c0001t0004g0007 others(32): Show |
35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1400-2156dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235446183 | ||||||
chr1:235446326 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0120 |
2 | NA18982.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1400-2023G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235446326 | |||||||
chr1:235446420 | G | A | 1 | a0001c0001t0006g0054 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1400-1929G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235446420 | |||||||
chr1:235446429 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1400-1920G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235446429 | |||||||
chr1:235446695 | G | GT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
61 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1400-1638dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235446695 | ||||||
chr1:235446695 | G | GTT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0074 a0001c0001t0001g0218 others(2): Show |
5 | HG00738.hp2 HG01074.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1400-1639_1400-163 others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235446695 | ||||||
chr1:235446829 | C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1400-1520C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235446829 | |||||||
chr1:235447253 | G | T | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1400-1096G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447253 | |||||||
chr1:235447333 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1400-1016C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447333 | |||||||
chr1:235447629 | A | G | 2 | a0001c0001t0030g0154 a0003c0004t0031g0016 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1400-720A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447629 | |||||||
chr1:235447778 | A | G | 35 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(32): Show |
35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1400-571A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447778 | |||||||
chr1:235447893 | T | TACTTGGG others(21): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1400-431_1400-430i others(30): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235447893 | ||||||
chr1:235447951 | T | C | 1 | a0001c0001t0002g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1400-398T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447951 | |||||||
chr1:235447970 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1400-379G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447970 | |||||||
chr1:235447978 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1400-371G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447978 | |||||||
chr1:235448014 | G | T | 4 | a0001c0001t0004g0158 a0001c0001t0004g0180 a0001c0001t0004g0181 others(1): Show |
4 | HG02027.hp1 NA18943.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1400-335G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448014 | |||||||
chr1:235448018 | G | A | 13 | a0001c0001t0004g0027 a0001c0001t0004g0039 a0001c0001t0004g0040 others(10): Show |
13 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1400-331G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448018 | |||||||
chr1:235448019 | G | T | 1 | a0001c0001t0003g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1400-330G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448019 | |||||||
chr1:235448085 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0003g0119 |
2 | HG02300.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1400-264A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448085 | |||||||
chr1:235448125 | G | A | 2 | a0001c0001t0007g0132 a0001c0005t0038g0155 |
2 | HG01070.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1400-224G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448125 | |||||||
chr1:235448206 | A | C | 3 | a0001c0001t0001g0140 a0001c0005t0035g0260 a0001c0005t0038g0155 |
3 | HG01070.hp2 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1400-143A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448206 | |||||||
chr1:235448210 | A | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0072 others(6): Show |
9 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1400-139A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448210 | |||||||
chr1:235448220 | C | CA | 11 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0074 others(8): Show |
11 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1400-109dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | ||||||
chr1:235448220 | C | CAA | 8 | a0001c0001t0002g0195 a0001c0001t0002g0241 a0001c0001t0004g0038 others(5): Show |
8 | HG01070.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1400-110_1400-109d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | ||||||
chr1:235448220 | C | CAAA | 25 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(22): Show |
25 | HG00741.hp1 HG01243.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.1400-111_1400-109d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | ||||||
chr1:235448220 | C | CAAAA | 6 | a0001c0001t0004g0043 a0001c0001t0004g0050 a0001c0001t0004g0133 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1400-112_1400-109d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | ||||||
chr1:235448220 | CA | C | 13 | a0001c0001t0001g0193 a0001c0001t0002g0179 a0001c0001t0002g0222 others(10): Show |
13 | HG00099.hp1 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1400-109delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | ||||||
chr1:235448322 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1400-27G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448322 | |||||||
chr1:235448588 | C | T | 1 | a0001c0001t0005g0163 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1492-82C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 16/16 | chr1 | 235448588 | |||||||
chr1:235448612 | G | A | 1 | a0001c0001t0002g0048 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1492-58G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 16/16 | chr1 | 235448612 |