Item | Value |
---|---|
geneid | 10941 |
ensemblid | ENSG00000173610.13 |
hgncid | 12542 |
symbol | UGT2A1 |
name | UDP glucuronosyltransferase family 2 member A1 complex locus |
refseq_nuc | NM_001252275.3 |
refseq_prot | NP_001239204.2 |
ensembl_nuc | ENST00000286604.9 |
ensembl_prot | ENSP00000286604.4 |
mane_status | MANE Select |
chr | chr4 |
start | 69588417 |
end | 69653247 |
strand | - |
ver | v1.2 |
region | chr4:69588417-69653247 |
region5000 | chr4:69583417-69658247 |
regionname0 | UGT2A1_chr4_69588417_69653247 |
regionname5000 | UGT2A1_chr4_69583417_69658247 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 527 | 289 | 47 | 48 | 156 | 9 | 27 | 119 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0002 | 0/0 | 527 | 33 | 23 | 4 | 4 | 1 | 1 | 4 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0003 | 0/0 | 527 | 21 | 2 | 7 | 5 | 1 | 6 | 4 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0004 | 0/0 | 527 | 18 | 1 | 10 | 0 | 3 | 4 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0005 | 0/0 | 527 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0006 | 0/0 | 191 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(186): Show |
chr4 | 69583417 | 69658247 |
a0007 | 0/0 | 527 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0008 | 0/0 | 527 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0009 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0010 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0011 | 0/0 | 527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
a0012 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | MLNNL others(522): Show |
chr4 | 69583417 | 69658247 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1581 | 285 | 47 | 48 | 155 | 9 | 24 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0001c0007 | 0/0 | 1581 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0001c0011 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0001c0017 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0002c0002 | 0/0 | 1581 | 33 | 23 | 4 | 4 | 1 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0003c0003 | 0/0 | 1581 | 19 | 2 | 7 | 4 | 1 | 5 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0003c0009 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0003c0010 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0004c0004 | 0/0 | 1581 | 18 | 1 | 10 | 0 | 3 | 4 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0005c0005 | 0/0 | 1581 | 6 | 6 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0006c0006 | 0/0 | 1581 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0006c0008 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0007c0014 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0008c0018 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0009c0013 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0010c0012 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0011c0015 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 | ||
a0012c0016 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ATGTT others(1576): Show |
chr4 | 69583417 | 69658247 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2653 | 194 | 29 | 36 | 107 | 5 | 17 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0001c0001t0002 | 1/1 | 2653 | 80 | 9 | 11 | 47 | 4 | 7 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0001c0001t0003 | 0/0 | 2653 | 7 | 7 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0001c0001t0006 | 0/0 | 2653 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0001c0001t0009 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0001c0001t0010 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0001c0007t0001 | 0/0 | 2653 | 2 | 0 | 0 | 0 | 0 | 2 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0001c0011t0001 | 0/0 | 2653 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0001c0017t0001 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0002c0002t0001 | 0/0 | 2653 | 22 | 14 | 3 | 3 | 1 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0002c0002t0003 | 0/0 | 2653 | 8 | 8 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0002c0002t0008 | 0/0 | 2653 | 2 | 1 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0002c0002t0012 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0003c0003t0002 | 0/0 | 2653 | 16 | 2 | 7 | 1 | 1 | 5 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0003c0003t0004 | 0/0 | 2653 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0003c0009t0002 | 0/0 | 2653 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0003c0010t0002 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0004c0004t0001 | 0/0 | 2653 | 16 | 1 | 9 | 0 | 3 | 3 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0004c0004t0002 | 0/0 | 2653 | 2 | 0 | 1 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0005c0005t0002 | 0/0 | 2653 | 4 | 4 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0005c0005t0005 | 0/0 | 2653 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0006c0006t0002 | 0/0 | 2653 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0006c0008t0001 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0007c0014t0002 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0008c0018t0001 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0009c0013t0007 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0010c0012t0007 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0011c0015t0001 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
a0012c0016t0011 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | ACATT others(2648): Show |
chr4 | 69583417 | 69658247 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0009g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0001t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0007t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0011t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0001c0017t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0008g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0002c0002t0012g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0003t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0009t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0003c0010t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0004c0004t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0005c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0005c0005t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0005c0005t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0005c0005t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0005c0005t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0005c0005t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0006c0006t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0006c0006t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0006c0008t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0007c0014t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0008c0018t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0009c0013t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0010c0012t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0011c0015t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
a0012c0016t0011g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0004 | t0001 | g0300 | EUR | GBR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | GBR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | GBR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0100 | EUR | FIN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00280 | hp2 | a0004 | c0004 | t0001 | g0039 | EUR | FIN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0314 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00733 | hp2 | a0004 | c0004 | t0001 | g0193 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00735 | hp1 | a0006 | c0008 | t0001 | g0064 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00738 | hp2 | a0004 | c0004 | t0001 | g0181 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG00741 | hp2 | a0004 | c0004 | t0001 | g0074 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01070 | hp2 | a0004 | c0004 | t0001 | g0316 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01071 | hp2 | a0007 | c0014 | t0002 | g0086 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01081 | hp2 | a0004 | c0004 | t0001 | g0309 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01109 | hp1 | a0004 | c0004 | t0001 | g0311 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01109 | hp2 | a0002 | c0002 | t0008 | g0348 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01168 | hp2 | a0004 | c0004 | t0002 | g0315 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01175 | hp1 | a0006 | c0006 | t0002 | g0080 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01192 | hp1 | a0001 | c0001 | t0009 | g0020 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01243 | hp1 | a0008 | c0018 | t0001 | g0273 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01261 | hp2 | a0004 | c0004 | t0001 | g0219 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01346 | hp2 | a0003 | c0003 | t0002 | g0148 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01358 | hp1 | a0003 | c0003 | t0002 | g0296 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01496 | hp1 | a0004 | c0004 | t0001 | g0061 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0195 | EUR | IBS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01517 | hp2 | a0003 | c0003 | t0002 | g0318 | EUR | IBS | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01884 | hp1 | a0009 | c0013 | t0007 | g0345 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0122 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01928 | hp1 | a0003 | c0003 | t0002 | g0149 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01943 | hp2 | a0004 | c0004 | t0001 | g0063 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01952 | hp2 | a0003 | c0003 | t0002 | g0280 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01981 | hp1 | a0003 | c0003 | t0002 | g0338 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01993 | hp2 | a0003 | c0003 | t0002 | g0340 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02165 | hp1 | a0003 | c0010 | t0002 | g0145 | EAS | CDX | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02258 | hp1 | a0002 | c0002 | t0003 | g0194 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02280 | hp2 | a0002 | c0002 | t0003 | g0067 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02300 | hp2 | a0003 | c0003 | t0002 | g0186 | AMR | PEL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02451 | hp1 | a0003 | c0003 | t0002 | g0334 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02602 | hp1 | a0001 | c0011 | t0001 | g0131 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02602 | hp2 | a0003 | c0009 | t0002 | g0212 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02615 | hp2 | a0003 | c0003 | t0002 | g0216 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02622 | hp2 | a0002 | c0002 | t0003 | g0312 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02630 | hp2 | a0010 | c0012 | t0007 | g0202 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02698 | hp1 | a0003 | c0003 | t0002 | g0239 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02717 | hp1 | a0005 | c0005 | t0002 | g0206 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02738 | hp2 | a0003 | c0003 | t0002 | g0132 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02809 | hp1 | a0005 | c0005 | t0002 | g0291 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02965 | hp1 | a0002 | c0002 | t0003 | g0076 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02965 | hp2 | a0005 | c0005 | t0002 | g0294 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03130 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0324 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03195 | hp1 | a0002 | c0002 | t0003 | g0068 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0323 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03239 | hp2 | a0003 | c0003 | t0002 | g0336 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03453 | hp1 | a0005 | c0005 | t0002 | g0271 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0346 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0325 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0292 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03540 | hp2 | a0005 | c0005 | t0005 | g0284 | AFR | GWD | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03579 | hp2 | a0005 | c0005 | t0005 | g0124 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03654 | hp1 | a0004 | c0004 | t0002 | g0310 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03654 | hp2 | a0003 | c0003 | t0002 | g0218 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03688 | hp1 | a0004 | c0004 | t0001 | g0062 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03704 | hp1 | a0004 | c0004 | t0001 | g0285 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03704 | hp2 | a0004 | c0004 | t0001 | g0313 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03834 | hp1 | a0001 | c0007 | t0001 | g0211 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03942 | hp2 | a0003 | c0003 | t0002 | g0337 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG04204 | hp2 | a0001 | c0007 | t0001 | g0106 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0198 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0288 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0331 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18942 | hp1 | a0003 | c0003 | t0002 | g0240 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18965 | hp2 | a0001 | c0017 | t0001 | g0274 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18970 | hp2 | a0003 | c0003 | t0004 | g0011 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18981 | hp2 | a0011 | c0015 | t0001 | g0166 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18997 | hp1 | a0003 | c0003 | t0004 | g0142 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19000 | hp1 | a0001 | c0001 | t0010 | g0107 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19011 | hp2 | a0002 | c0002 | t0012 | g0351 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0347 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19057 | hp2 | a0003 | c0003 | t0004 | g0011 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20129 | hp1 | a0012 | c0016 | t0011 | g0225 | AFR | ASW | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ASW | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | TSI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20752 | hp2 | a0004 | c0004 | t0001 | g0307 | EUR | TSI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | TSI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0301 | EUR | TSI | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | GIH | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | GIH | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01123 | hp1 | a0006 | c0006 | t0002 | g0081 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03471 | hp1 | a0002 | c0002 | t0008 | g0289 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | USA | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | USA | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | USA | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA20300 | hp2 | a0004 | c0004 | t0001 | g0308 | AFR | USA | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0269 | REF | REF | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0224 | REF | REF | UGT2A1_chr4_69583417_69658247 | UGT2A1 | chr4 | 69583417 | 69658247 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:69589433 | T | C | 1 | a0011 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1523A>G | p.Gln508Arg | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1637/2653 | 1523/1584 | 508/527 | chr4 | 69589433 | |||
chr4:69589530 | C | T | 1 | a0007 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.1426G>A | p.Val476Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1540/2653 | 1426/1584 | 476/527 | chr4 | 69589530 | |||
chr4:69589581 | C | T | 1 | a0008 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1375G>A | p.Val459Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1489/2653 | 1375/1584 | 459/527 | chr4 | 69589581 | |||
chr4:69589642 | C | A | 1 | a0009 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1314G>T | p.Glu438Asp | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1428/2653 | 1314/1584 | 438/527 | chr4 | 69589642 | |||
chr4:69594602 | C | T | 2 | a0009 a0010 |
2 | HG01884.hp1 HG02630.hp2 |
missense_variant | MODERATE | c.1179G>A | p.Met393Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/7 | 1293/2653 | 1179/1584 | 393/527 | chr4 | 69594602 | |||
chr4:69594610 | C | T | 4 | a0003 a0005 a0009 others(1): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
missense_variant | MODERATE | c.1171G>A | p.Val391Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/7 | 1285/2653 | 1171/1584 | 391/527 | chr4 | 69594610 | |||
chr4:69595221 | G | C | 1 | a0012 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.1025C>G | p.Pro342Arg | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 5/7 | 1139/2653 | 1025/1584 | 342/527 | chr4 | 69595221 | |||
chr4:69599287 | C | A | 1 | a0012 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.955G>T | p.Val319Phe | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/7 | 1069/2653 | 955/1584 | 319/527 | chr4 | 69599287 | |||
chr4:69635733 | G | A | 3 | a0002 a0004 a0005 |
57 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(54): Show |
missense_variant | MODERATE | c.805C>T | p.Arg269Cys | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/7 | 919/2653 | 805/1584 | 269/527 | chr4 | 69635733 | |||
chr4:69647055 | A | G | 1 | a0004 | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(15): Show |
missense_variant | MODERATE | c.590T>C | p.Leu197Ser | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 704/2653 | 590/1584 | 197/527 | chr4 | 69647055 | |||
chr4:69647069 | A | T | 1 | a0006 | 3 | HG00735.hp1 HG01123.hp1 HG01175.hp1 |
stop_gained | HIGH | c.576T>A | p.Tyr192* | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 690/2653 | 576/1584 | 192/527 | chr4 | 69647069 | |||
chr4:69647083 | A | G | 1 | a0004 | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(15): Show |
missense_variant | MODERATE | c.562T>C | p.Tyr188His | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 676/2653 | 562/1584 | 188/527 | chr4 | 69647083 | |||
chr4:69653188 | C | T | 1 | a0001 | 1 | HG01192.hp1 | splice_region_variant | LOW | c.-55G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/7 | chr4 | 69653188 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:69589513 | G | A | 1 | a0006c0006 | 2 | HG01123.hp1 HG01175.hp1 |
synonymous_variant | LOW | c.1443C>T | p.Leu481Leu | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 1557/2653 | 1443/1584 | 481/527 | chr4 | 69589513 | |||
chr4:69599342 | G | A | 1 | a0001c0017 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.900C>T | p.Ile300Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/7 | 1014/2653 | 900/1584 | 300/527 | chr4 | 69599342 | |||
chr4:69599381 | C | T | 1 | a0001c0011 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.861G>A | p.Thr287Thr | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/7 | 975/2653 | 861/1584 | 287/527 | chr4 | 69599381 | |||
chr4:69635782 | C | T | 1 | a0003c0010 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.756G>A | p.Ala252Ala | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/7 | 870/2653 | 756/1584 | 252/527 | chr4 | 69635782 | |||
chr4:69647003 | G | T | 2 | a0001c0007 a0003c0009 |
3 | HG02602.hp2 HG03834.hp1 HG04204.hp2 |
synonymous_variant | LOW | c.642C>A | p.Ile214Ile | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 756/2653 | 642/1584 | 214/527 | chr4 | 69647003 | |||
chr4:69647375 | G | A | 1 | a0008c0018 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.270C>T | p.Phe90Phe | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/7 | 384/2653 | 270/1584 | 90/527 | chr4 | 69647375 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:69588503 | G | T | 1 | a0001c0001t0006 | 2 | HG02572.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*869C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 869 | chr4 | 69588503 | ||||||
chr4:69588571 | A | G | 13 | a0001c0001t0001 a0001c0001t0006 a0001c0007t0001 others(10): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*801T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 801 | chr4 | 69588571 | ||||||
chr4:69588588 | G | T | 2 | a0001c0001t0003 a0002c0002t0003 |
15 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*784C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 784 | chr4 | 69588588 | ||||||
chr4:69588620 | C | A | 2 | a0009c0013t0007 a0010c0012t0007 |
2 | HG01884.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*752G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 752 | chr4 | 69588620 | ||||||
chr4:69588682 | T | C | 2 | a0009c0013t0007 a0010c0012t0007 |
2 | HG01884.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 690 | chr4 | 69588682 | ||||||
chr4:69588811 | C | T | 1 | a0012c0016t0011 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 561 | chr4 | 69588811 | ||||||
chr4:69588935 | C | T | 1 | a0005c0005t0005 | 2 | HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 437 | chr4 | 69588935 | ||||||
chr4:69589006 | T | C | 1 | a0002c0002t0008 | 2 | HG01109.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*366A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 366 | chr4 | 69589006 | ||||||
chr4:69589273 | C | T | 1 | a0003c0003t0004 | 3 | NA18970.hp2 NA18997.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*99G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 99 | chr4 | 69589273 | ||||||
chr4:69589280 | T | C | 1 | a0001c0001t0010 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 92 | chr4 | 69589280 | ||||||
chr4:69589340 | T | G | 1 | a0012c0016t0011 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 7/7 | 32 | chr4 | 69589340 | ||||||
chr4:69653201 | G | C | 1 | a0002c0002t0012 | 1 | NA19011.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/7 | chr4 | 69653201 | |||||||
chr4:69653205 | A | T | 1 | a0001c0001t0009 | 1 | HG01192.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/7 | 5561 | chr4 | 69653205 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:69589760 | G | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(259): Show |
274 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1305-109C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589760 | |||||||
chr4:69589857 | T | C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1305-206A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589857 | |||||||
chr4:69589861 | C | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1305-210G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589861 | |||||||
chr4:69589881 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1305-230A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589881 | |||||||
chr4:69589932 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1305-281T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589932 | |||||||
chr4:69589946 | G | C | 3 | a0001c0001t0001g0319 a0008c0018t0001g0273 a0012c0016t0011g0225 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1305-295C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69589946 | |||||||
chr4:69590001 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1305-350A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590001 | |||||||
chr4:69590166 | C | T | 82 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(79): Show |
87 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1305-515G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590166 | |||||||
chr4:69590468 | G | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(231): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1305-817C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590468 | |||||||
chr4:69590526 | G | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1305-875C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590526 | |||||||
chr4:69590559 | G | A | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1305-908C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590559 | |||||||
chr4:69590597 | G | A | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1305-946C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590597 | |||||||
chr4:69590638 | A | AGT | 30 | a0001c0001t0001g0025 a0001c0001t0001g0127 a0001c0001t0001g0184 others(27): Show |
30 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1305-989_1305-988d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590638 | |||||||
chr4:69590638 | A | AGTGT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(107): Show |
116 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.1305-991_1305-988d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590638 | |||||||
chr4:69590638 | AGT | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
89 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1305-989_1305-988d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590638 | |||||||
chr4:69590677 | C | A | 3 | a0001c0001t0001g0319 a0008c0018t0001g0273 a0012c0016t0011g0225 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1305-1026G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590677 | |||||||
chr4:69590710 | A | T | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1305-1059T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590710 | |||||||
chr4:69590771 | G | T | 3 | a0001c0001t0001g0319 a0008c0018t0001g0273 a0012c0016t0011g0225 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1305-1120C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590771 | |||||||
chr4:69590777 | G | T | 1 | a0001c0001t0002g0088 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1305-1126C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590777 | |||||||
chr4:69590778 | A | G | 1 | a0008c0018t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1305-1127T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590778 | |||||||
chr4:69590793 | A | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0028 a0001c0001t0002g0082 |
5 | NA18952.hp1 NA18984.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305-1142T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590793 | |||||||
chr4:69590856 | A | G | 1 | a0012c0016t0011g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1305-1205T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590856 | |||||||
chr4:69590997 | T | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0335 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1305-1346A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69590997 | |||||||
chr4:69591195 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1305-1544G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591195 | |||||||
chr4:69591303 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(259): Show |
274 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1305-1652A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591303 | |||||||
chr4:69591319 | T | G | 1 | a0001c0001t0002g0267 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1305-1668A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591319 | |||||||
chr4:69591607 | C | G | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1305-1956G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591607 | |||||||
chr4:69591749 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1305-2098A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591749 | |||||||
chr4:69591838 | T | C | 86 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(83): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.1305-2187A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591838 | |||||||
chr4:69591838 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1305-2187A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591838 | |||||||
chr4:69591954 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1305-2303A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591954 | |||||||
chr4:69591972 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(148): Show |
157 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1305-2321G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69591972 | |||||||
chr4:69592159 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(231): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1304+2318C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592159 | |||||||
chr4:69592214 | A | G | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1304+2263T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592214 | |||||||
chr4:69592345 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1304+2132G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592345 | |||||||
chr4:69592422 | G | T | 1 | a0001c0001t0002g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1304+2055C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592422 | |||||||
chr4:69592464 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1304+2013G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592464 | |||||||
chr4:69592524 | G | C | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1304+1953C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592524 | |||||||
chr4:69592924 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1304+1553G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592924 | |||||||
chr4:69592930 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(231): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1304+1547G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592930 | |||||||
chr4:69592931 | T | C | 78 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(75): Show |
83 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1304+1546A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592931 | |||||||
chr4:69592941 | A | C | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1304+1536T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69592941 | |||||||
chr4:69593231 | C | A | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1304+1246G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593231 | |||||||
chr4:69593261 | T | C | 4 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0008c0018t0001g0273 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+1216A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593261 | |||||||
chr4:69593265 | A | G | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1304+1212T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593265 | |||||||
chr4:69593309 | G | A | 1 | a0012c0016t0011g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1304+1168C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593309 | |||||||
chr4:69593313 | GA | G | 82 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(79): Show |
87 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1304+1163delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593313 | |||||||
chr4:69593347 | T | A | 1 | a0001c0001t0001g0247 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1304+1130A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593347 | |||||||
chr4:69593434 | T | C | 3 | a0001c0001t0001g0319 a0008c0018t0001g0273 a0012c0016t0011g0225 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1304+1043A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593434 | |||||||
chr4:69593559 | CTT | C | 7 | a0001c0001t0001g0053 a0001c0001t0002g0088 a0002c0002t0001g0017 others(4): Show |
8 | HG00733.hp1 HG01516.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1304+916_1304+917d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593559 | |||||||
chr4:69593649 | T | A | 1 | a0001c0001t0006g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1304+828A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593649 | |||||||
chr4:69593675 | A | T | 36 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(33): Show |
38 | HG00438.hp2 HG00609.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1304+802T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593675 | |||||||
chr4:69593742 | T | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1304+735A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593742 | |||||||
chr4:69593753 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1304+724C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593753 | |||||||
chr4:69593811 | G | A | 1 | a0002c0002t0001g0325 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1304+666C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593811 | |||||||
chr4:69593861 | A | G | 78 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(75): Show |
83 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1304+616T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593861 | |||||||
chr4:69593915 | A | C | 2 | a0005c0005t0005g0124 a0005c0005t0005g0284 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1304+562T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593915 | |||||||
chr4:69593915 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1304+562T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593915 | |||||||
chr4:69593964 | AGT | A | 4 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0008c0018t0001g0273 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+511_1304+512d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593964 | |||||||
chr4:69593973 | T | G | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1304+504A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593973 | |||||||
chr4:69593975 | TTG | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0001g0072 others(5): Show |
8 | HG01167.hp2 HG01891.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1304+500_1304+501d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593975 | |||||||
chr4:69593976 | TG | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(183): Show |
195 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1304+500delC | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593976 | |||||||
chr4:69593977 | G | T | 42 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0051 others(39): Show |
43 | HG00099.hp1 HG00609.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1304+500C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593977 | |||||||
chr4:69593981 | G | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(231): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1304+496C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593981 | |||||||
chr4:69593985 | T | G | 32 | a0001c0001t0002g0100 a0001c0001t0003g0217 a0001c0001t0003g0322 others(29): Show |
33 | HG00280.hp1 HG01346.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.1304+492A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69593985 | |||||||
chr4:69594067 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1304+410G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69594067 | |||||||
chr4:69594119 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0191 |
2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1304+358G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69594119 | |||||||
chr4:69594458 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1304+19A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 6/6 | chr4 | 69594458 | |||||||
chr4:69594981 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0168 |
2 | NA18984.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1084+181C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 5/6 | chr4 | 69594981 | |||||||
chr4:69595095 | G | T | 1 | a0001c0001t0002g0085 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1084+67C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 5/6 | chr4 | 69595095 | |||||||
chr4:69595096 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1084+66G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 5/6 | chr4 | 69595096 | |||||||
chr4:69595328 | A | G | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.997-79T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595328 | |||||||
chr4:69595345 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.997-96C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595345 | |||||||
chr4:69595443 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(237): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.997-194G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595443 | |||||||
chr4:69595466 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.997-217T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595466 | |||||||
chr4:69595634 | G | A | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.997-385C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595634 | |||||||
chr4:69595727 | A | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0191 |
2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.997-478T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595727 | |||||||
chr4:69595846 | G | C | 2 | a0005c0005t0005g0124 a0005c0005t0005g0284 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.997-597C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69595846 | |||||||
chr4:69596111 | A | C | 1 | a0001c0001t0001g0256 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.997-862T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596111 | |||||||
chr4:69596324 | C | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.997-1075G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596324 | |||||||
chr4:69596532 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.997-1283A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596532 | |||||||
chr4:69596579 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.997-1330C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596579 | |||||||
chr4:69596674 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0115 |
2 | NA18950.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.997-1425T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596674 | |||||||
chr4:69596804 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.997-1555C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596804 | |||||||
chr4:69596903 | A | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(271): Show |
289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.997-1654T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596903 | |||||||
chr4:69596950 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.997-1701G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596950 | |||||||
chr4:69596951 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.997-1702A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69596951 | |||||||
chr4:69597085 | T | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(237): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.997-1836A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597085 | |||||||
chr4:69597175 | C | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(237): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.997-1926G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597175 | |||||||
chr4:69597299 | C | T | 1 | a0004c0004t0001g0193 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.996+1947G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597299 | |||||||
chr4:69597422 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.996+1824G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597422 | |||||||
chr4:69597466 | T | C | 1 | a0004c0004t0001g0307 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.996+1780A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597466 | |||||||
chr4:69597500 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.996+1746G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597500 | |||||||
chr4:69597606 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.996+1640C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597606 | |||||||
chr4:69597715 | A | AAC | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(142): Show |
151 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.996+1529_996+1530d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597715 | |||||||
chr4:69597715 | A | AACACAC | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+1525_996+1530d others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597715 | |||||||
chr4:69597882 | T | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.996+1364A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597882 | |||||||
chr4:69597908 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.996+1338A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597908 | |||||||
chr4:69597944 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.996+1302A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597944 | |||||||
chr4:69597945 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.996+1301C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69597945 | |||||||
chr4:69598136 | T | A | 88 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(85): Show |
95 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.996+1110A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598136 | |||||||
chr4:69598149 | G | T | 1 | a0005c0005t0002g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.996+1097C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598149 | |||||||
chr4:69598154 | C | A | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.996+1092G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598154 | |||||||
chr4:69598406 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.996+840G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598406 | |||||||
chr4:69598438 | T | C | 1 | a0002c0002t0001g0346 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.996+808A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598438 | |||||||
chr4:69598631 | C | A | 4 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0008c0018t0001g0273 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.996+615G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598631 | |||||||
chr4:69598695 | T | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.996+551A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598695 | |||||||
chr4:69598793 | C | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.996+453G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598793 | |||||||
chr4:69598854 | C | A | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+392G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598854 | |||||||
chr4:69598983 | A | G | 88 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(85): Show |
95 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.996+263T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69598983 | |||||||
chr4:69599202 | T | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.996+44A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 4/6 | chr4 | 69599202 | |||||||
chr4:69599435 | A | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.848-41T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599435 | |||||||
chr4:69599523 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.848-129A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599523 | |||||||
chr4:69599689 | TAAAG | T | 19 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(16): Show |
20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.848-299_848-296del others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599689 | |||||||
chr4:69599695 | A | AAGAG | 74 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0030 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.848-305_848-302dup others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599695 | |||||||
chr4:69599695 | A | AAGAGAG | 7 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG01167.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.848-307_848-302dup others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599695 | |||||||
chr4:69599695 | A | G | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-301T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599695 | |||||||
chr4:69599723 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(233): Show |
249 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.848-329A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599723 | |||||||
chr4:69599775 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.848-381C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599775 | |||||||
chr4:69599866 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-472T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599866 | |||||||
chr4:69599896 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.848-502A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599896 | |||||||
chr4:69599908 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(237): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.848-514C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599908 | |||||||
chr4:69599974 | A | T | 1 | a0001c0001t0003g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.848-580T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69599974 | |||||||
chr4:69600019 | G | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(152): Show |
161 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.848-625C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600019 | |||||||
chr4:69600087 | G | A | 1 | a0005c0005t0002g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.848-693C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600087 | |||||||
chr4:69600132 | C | T | 1 | a0002c0002t0003g0312 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.848-738G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600132 | |||||||
chr4:69600261 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(173): Show |
183 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.848-867G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600261 | |||||||
chr4:69600303 | C | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-909G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600303 | |||||||
chr4:69600321 | C | A | 1 | a0001c0001t0002g0278 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.848-927G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600321 | |||||||
chr4:69600353 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0141 a0001c0001t0001g0155 others(2): Show |
5 | HG00639.hp2 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.848-959T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600353 | |||||||
chr4:69600502 | G | A | 6 | a0001c0001t0003g0014 a0001c0001t0003g0113 a0001c0001t0003g0114 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-1108C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600502 | |||||||
chr4:69600519 | C | G | 1 | a0004c0004t0002g0315 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.848-1125G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600519 | |||||||
chr4:69600527 | T | C | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-1133A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600527 | |||||||
chr4:69600539 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.848-1145C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600539 | |||||||
chr4:69600561 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.848-1167G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600561 | |||||||
chr4:69600562 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(173): Show |
183 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.848-1168A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600562 | |||||||
chr4:69600566 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0161 |
2 | NA18977.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.848-1172A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600566 | |||||||
chr4:69600568 | G | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-1174C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600568 | |||||||
chr4:69600620 | A | T | 3 | a0001c0001t0001g0319 a0008c0018t0001g0273 a0012c0016t0011g0225 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.848-1226T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600620 | |||||||
chr4:69600631 | T | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0112 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.848-1237A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600631 | |||||||
chr4:69600649 | G | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-1255C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600649 | |||||||
chr4:69600658 | C | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-1264G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600658 | |||||||
chr4:69600809 | T | TA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(115): Show |
124 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.848-1416dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600809 | |||||||
chr4:69600809 | T | TAA | 27 | a0001c0001t0001g0150 a0002c0002t0008g0289 a0002c0002t0008g0348 others(24): Show |
28 | HG01109.hp2 HG01346.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.848-1417_848-1416d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600809 | |||||||
chr4:69600875 | C | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-1481G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600875 | |||||||
chr4:69600916 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0075 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.848-1522G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600916 | |||||||
chr4:69600924 | T | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-1530A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69600924 | |||||||
chr4:69601066 | C | T | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.848-1672G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601066 | |||||||
chr4:69601072 | C | T | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.848-1678G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601072 | |||||||
chr4:69601081 | T | C | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-1687A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601081 | |||||||
chr4:69601092 | T | G | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-1698A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601092 | |||||||
chr4:69601187 | G | A | 113 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(110): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.848-1793C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601187 | |||||||
chr4:69601191 | G | A | 4 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-1797C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601191 | |||||||
chr4:69601218 | C | T | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-1824G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601218 | |||||||
chr4:69601308 | C | T | 1 | a0001c0001t0003g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.848-1914G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601308 | |||||||
chr4:69601313 | T | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-1919A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601313 | |||||||
chr4:69601364 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0349 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.848-1970C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601364 | |||||||
chr4:69601384 | C | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-1990G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601384 | |||||||
chr4:69601391 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-1997G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601391 | |||||||
chr4:69601392 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02280.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.848-1998C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601392 | |||||||
chr4:69601526 | C | G | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-2132G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601526 | |||||||
chr4:69601617 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0144 |
2 | NA19003.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.848-2223G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601617 | |||||||
chr4:69601741 | T | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2347A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601741 | |||||||
chr4:69601743 | T | A | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2349A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601743 | |||||||
chr4:69601746 | A | AG | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2353_848-2352i others(3): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601746 | |||||||
chr4:69601746 | A | G | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-2352T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601746 | |||||||
chr4:69601750 | A | G | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2356T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601750 | |||||||
chr4:69601753 | G | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2359C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601753 | |||||||
chr4:69601754 | G | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2360C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601754 | |||||||
chr4:69601755 | AG | A | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-2362delC | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601755 | |||||||
chr4:69601758 | CTAGAGGA others(5319): Show |
C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-7690_848-2365d others(2): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69601758 | |||||||
chr4:69602031 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.848-2637T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602031 | |||||||
chr4:69602112 | T | C | 4 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-2718A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602112 | |||||||
chr4:69602216 | A | AAACTC | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-2823_848-2822i others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602216 | |||||||
chr4:69602359 | C | T | 32 | a0001c0001t0001g0112 a0001c0007t0001g0106 a0001c0007t0001g0211 others(29): Show |
33 | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.848-2965G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602359 | |||||||
chr4:69602459 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.848-3065C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602459 | |||||||
chr4:69602462 | TTTA | T | 4 | a0003c0003t0004g0011 a0003c0010t0002g0145 a0005c0005t0002g0271 others(1): Show |
5 | HG02165.hp1 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.848-3071_848-3069d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602462 | |||||||
chr4:69602462 | TTTATCTA | T | 21 | a0003c0003t0002g0148 a0003c0003t0002g0149 a0003c0003t0002g0186 others(18): Show |
21 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-3075_848-3069d others(9): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602462 | |||||||
chr4:69602462 | TTTATCTA others(4): Show |
T | 3 | a0003c0003t0002g0132 a0009c0013t0007g0345 a0010c0012t0007g0202 |
3 | HG01884.hp1 HG02630.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.848-3079_848-3069d others(13): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602462 | |||||||
chr4:69602463 | T | TTATC | 11 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0001g0173 others(8): Show |
11 | HG00099.hp2 HG01167.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.848-3073_848-3070d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602463 | |||||||
chr4:69602463 | TTATC | T | 35 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0118 others(32): Show |
39 | HG01255.hp1 HG01255.hp2 HG01993.hp1 others(36): Show |
intron_variant | MODIFIER | c.848-3073_848-3070d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602463 | |||||||
chr4:69602463 | TTATCTAT others(1): Show |
T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0023 others(40): Show |
48 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.848-3077_848-3070d others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602463 | |||||||
chr4:69602463 | TTATCTAT others(5): Show |
T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0001g0228 |
3 | HG02970.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.848-3081_848-3070d others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602463 | |||||||
chr4:69602587 | G | A | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.848-3193C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602587 | |||||||
chr4:69602594 | A | G | 3 | a0001c0007t0001g0106 a0001c0007t0001g0211 a0006c0008t0001g0064 |
3 | HG00735.hp1 HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.848-3200T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602594 | |||||||
chr4:69602713 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0153 |
2 | NA18992.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.848-3319G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602713 | |||||||
chr4:69602955 | A | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-3561T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69602955 | |||||||
chr4:69603038 | C | G | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-3644G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603038 | |||||||
chr4:69603065 | T | G | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-3671A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603065 | |||||||
chr4:69603183 | G | A | 5 | a0001c0001t0001g0256 a0005c0005t0002g0206 a0005c0005t0002g0271 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.848-3789C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603183 | |||||||
chr4:69603196 | G | C | 1 | a0001c0001t0001g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.848-3802C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603196 | |||||||
chr4:69603288 | T | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0320 |
3 | NA18965.hp1 NA18967.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.848-3894A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603288 | |||||||
chr4:69603352 | C | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-3958G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603352 | |||||||
chr4:69603535 | T | G | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-4141A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603535 | |||||||
chr4:69603542 | A | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4148T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603542 | |||||||
chr4:69603558 | C | G | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4164G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603558 | |||||||
chr4:69603614 | G | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4220C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603614 | |||||||
chr4:69603618 | C | T | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-4224G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603618 | |||||||
chr4:69603630 | A | G | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4236T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603630 | |||||||
chr4:69603673 | A | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4279T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603673 | |||||||
chr4:69603699 | C | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4305G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603699 | |||||||
chr4:69603847 | C | T | 2 | a0005c0005t0005g0124 a0005c0005t0005g0284 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.848-4453G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603847 | |||||||
chr4:69603935 | G | A | 19 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(16): Show |
20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.848-4541C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603935 | |||||||
chr4:69603979 | T | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4585A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603979 | |||||||
chr4:69603983 | A | G | 1 | a0004c0004t0001g0308 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.848-4589T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69603983 | |||||||
chr4:69604131 | A | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4737T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604131 | |||||||
chr4:69604190 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-4796C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604190 | |||||||
chr4:69604320 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-4926G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604320 | |||||||
chr4:69604327 | AGAG | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-4936_848-4934d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604327 | |||||||
chr4:69604465 | C | T | 1 | a0004c0004t0001g0308 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.848-5071G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604465 | |||||||
chr4:69604479 | C | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-5085G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604479 | |||||||
chr4:69604507 | A | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-5113T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604507 | |||||||
chr4:69604556 | G | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-5162C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604556 | |||||||
chr4:69604719 | G | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-5325C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604719 | |||||||
chr4:69604890 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.848-5496T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604890 | |||||||
chr4:69604972 | A | G | 1 | a0004c0004t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5578T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604972 | |||||||
chr4:69604977 | C | A | 6 | a0004c0004t0001g0039 a0004c0004t0001g0181 a0004c0004t0001g0219 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.848-5583G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604977 | |||||||
chr4:69604981 | G | A | 29 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(26): Show |
30 | HG00741.hp2 HG01346.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.848-5587C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604981 | |||||||
chr4:69604998 | G | A | 29 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(26): Show |
30 | HG00741.hp2 HG01346.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.848-5604C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69604998 | |||||||
chr4:69605012 | T | C | 1 | a0004c0004t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5618A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605012 | |||||||
chr4:69605014 | A | G | 1 | a0004c0004t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5620T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605014 | |||||||
chr4:69605024 | A | T | 1 | a0004c0004t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5630T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605024 | |||||||
chr4:69605032 | T | G | 1 | a0004c0004t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5638A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605032 | |||||||
chr4:69605036 | T | C | 1 | a0004c0004t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848-5642A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605036 | |||||||
chr4:69605265 | A | T | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848-5871T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605265 | |||||||
chr4:69605266 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848-5872A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605266 | |||||||
chr4:69605276 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848-5882T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605276 | |||||||
chr4:69605279 | G | A | 2 | a0004c0004t0001g0074 a0004c0004t0001g0308 |
2 | HG00741.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.848-5885C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605279 | |||||||
chr4:69605334 | C | G | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-5940G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605334 | |||||||
chr4:69605497 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-6103A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605497 | |||||||
chr4:69605560 | A | G | 1 | a0001c0001t0002g0111 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.848-6166T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605560 | |||||||
chr4:69605802 | C | A | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-6408G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605802 | |||||||
chr4:69605848 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.848-6454C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605848 | |||||||
chr4:69605991 | A | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6597T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69605991 | |||||||
chr4:69606004 | G | C | 1 | a0005c0005t0005g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848-6610C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606004 | |||||||
chr4:69606035 | G | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6641C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606035 | |||||||
chr4:69606047 | G | C | 1 | a0006c0006t0002g0081 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.848-6653C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606047 | |||||||
chr4:69606117 | C | CA | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-6724dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606117 | |||||||
chr4:69606157 | C | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6763G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606157 | |||||||
chr4:69606160 | G | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6766C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606160 | |||||||
chr4:69606219 | C | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6825G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606219 | |||||||
chr4:69606224 | C | T | 2 | a0003c0003t0004g0011 a0003c0003t0004g0142 |
3 | NA18970.hp2 NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.848-6830G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606224 | |||||||
chr4:69606247 | T | G | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-6853A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606247 | |||||||
chr4:69606416 | T | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7022A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606416 | |||||||
chr4:69606421 | C | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7027G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606421 | |||||||
chr4:69606440 | T | C | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.848-7046A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606440 | |||||||
chr4:69606500 | T | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7106A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606500 | |||||||
chr4:69606573 | T | G | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7179A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606573 | |||||||
chr4:69606592 | G | A | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.848-7198C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606592 | |||||||
chr4:69606601 | G | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7207C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606601 | |||||||
chr4:69606678 | G | A | 1 | a0004c0004t0001g0307 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.848-7284C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606678 | |||||||
chr4:69606756 | C | G | 1 | a0001c0001t0001g0302 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.848-7362G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606756 | |||||||
chr4:69606761 | A | G | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-7367T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606761 | |||||||
chr4:69606869 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.848-7475G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606869 | |||||||
chr4:69606874 | G | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7480C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606874 | |||||||
chr4:69606932 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.848-7538A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606932 | |||||||
chr4:69606973 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.848-7579G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69606973 | |||||||
chr4:69607055 | T | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7661A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607055 | |||||||
chr4:69607101 | G | A | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-7707C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607101 | |||||||
chr4:69607122 | GC | G | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7729delG | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607122 | |||||||
chr4:69607132 | C | T | 1 | a0007c0014t0002g0086 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.848-7738G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607132 | |||||||
chr4:69607167 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.848-7773A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607167 | |||||||
chr4:69607184 | G | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7790C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607184 | |||||||
chr4:69607186 | A | AACCAAAA others(15): Show |
36 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0002c0002t0001g0324 others(33): Show |
37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.848-7814_848-7793d others(24): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607186 | |||||||
chr4:69607194 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0175 |
3 | HG00642.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.848-7800G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607194 | |||||||
chr4:69607223 | A | G | 4 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0008c0018t0001g0273 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-7829T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607223 | |||||||
chr4:69607224 | A | T | 2 | a0001c0001t0002g0102 a0001c0001t0002g0223 |
2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.848-7830T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607224 | |||||||
chr4:69607228 | C | T | 2 | a0001c0001t0002g0102 a0001c0001t0002g0223 |
2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.848-7834G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607228 | |||||||
chr4:69607248 | C | T | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-7854G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607248 | |||||||
chr4:69607265 | C | T | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-7871G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607265 | |||||||
chr4:69607266 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(271): Show |
289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.848-7872C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607266 | |||||||
chr4:69607286 | T | G | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-7892A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607286 | |||||||
chr4:69607309 | G | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.848-7915C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607309 | |||||||
chr4:69607367 | T | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-7973A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607367 | |||||||
chr4:69607368 | G | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-7974C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607368 | |||||||
chr4:69607381 | C | A | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-7987G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607381 | |||||||
chr4:69607386 | A | G | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-7992T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607386 | |||||||
chr4:69607403 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.848-8009A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607403 | |||||||
chr4:69607444 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.848-8050A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607444 | |||||||
chr4:69607488 | C | T | 1 | a0006c0006t0002g0080 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.848-8094G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607488 | |||||||
chr4:69607521 | T | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-8127A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607521 | |||||||
chr4:69607522 | G | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-8128C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607522 | |||||||
chr4:69607530 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.848-8136G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607530 | |||||||
chr4:69607598 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.848-8204T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607598 | |||||||
chr4:69607610 | A | C | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-8216T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607610 | |||||||
chr4:69607644 | G | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-8250C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607644 | |||||||
chr4:69607824 | C | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8430G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607824 | |||||||
chr4:69607835 | G | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8441C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607835 | |||||||
chr4:69607897 | G | A | 30 | a0001c0001t0001g0141 a0001c0001t0001g0241 a0003c0003t0002g0132 others(27): Show |
31 | HG01258.hp2 HG01346.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.848-8503C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607897 | |||||||
chr4:69607976 | T | G | 4 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0008c0018t0001g0273 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-8582A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69607976 | |||||||
chr4:69608070 | G | A | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8676C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608070 | |||||||
chr4:69608137 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.848-8743C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608137 | |||||||
chr4:69608141 | T | G | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8747A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608141 | |||||||
chr4:69608143 | C | A | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8749G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608143 | |||||||
chr4:69608145 | C | G | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.848-8751G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608145 | |||||||
chr4:69608168 | C | G | 1 | a0001c0001t0001g0277 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.848-8774G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608168 | |||||||
chr4:69608263 | C | G | 1 | a0005c0005t0005g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848-8869G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608263 | |||||||
chr4:69608321 | CA | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8928delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608321 | |||||||
chr4:69608362 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.848-8968A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608362 | |||||||
chr4:69608379 | A | G | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-8985T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608379 | |||||||
chr4:69608409 | G | A | 28 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(25): Show |
29 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.848-9015C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608409 | |||||||
chr4:69608431 | G | A | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-9037C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608431 | |||||||
chr4:69608434 | G | T | 4 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0008c0018t0001g0273 others(1): Show |
4 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-9040C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608434 | |||||||
chr4:69608451 | G | A | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-9057C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608451 | |||||||
chr4:69608529 | C | T | 3 | a0002c0002t0001g0214 a0002c0002t0001g0215 a0002c0002t0001g0323 |
3 | HG02895.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.848-9135G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608529 | |||||||
chr4:69608530 | G | A | 1 | a0005c0005t0002g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.848-9136C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608530 | |||||||
chr4:69608592 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(265): Show |
282 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.848-9198C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608592 | |||||||
chr4:69608756 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.848-9362G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608756 | |||||||
chr4:69608767 | C | T | 3 | a0001c0001t0002g0111 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | NA18980.hp2 NA19058.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.848-9373G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608767 | |||||||
chr4:69608989 | A | T | 1 | a0002c0002t0008g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.848-9595T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608989 | |||||||
chr4:69608992 | T | C | 3 | a0001c0001t0001g0319 a0008c0018t0001g0273 a0012c0016t0011g0225 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.848-9598A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69608992 | |||||||
chr4:69609051 | C | T | 1 | a0005c0005t0005g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848-9657G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609051 | |||||||
chr4:69609052 | G | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-9658C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609052 | |||||||
chr4:69609080 | G | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-9686C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609080 | |||||||
chr4:69609099 | G | T | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-9705C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609099 | |||||||
chr4:69609155 | A | AT | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(126): Show |
135 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.848-9762dupA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609155 | |||||||
chr4:69609155 | A | ATT | 10 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0105 others(7): Show |
10 | HG01261.hp1 HG01496.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.848-9763_848-9762d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609155 | |||||||
chr4:69609155 | A | ATTT | 100 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(97): Show |
107 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.848-9764_848-9762d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609155 | |||||||
chr4:69609155 | AT | A | 27 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(24): Show |
28 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.848-9762delA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609155 | |||||||
chr4:69609232 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-9838T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609232 | |||||||
chr4:69609290 | C | G | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-9896G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609290 | |||||||
chr4:69609338 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(271): Show |
289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.848-9944G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609338 | |||||||
chr4:69609378 | G | T | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-9984C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609378 | |||||||
chr4:69609382 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.848-9988A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609382 | |||||||
chr4:69609412 | C | G | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-10018G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609412 | |||||||
chr4:69609555 | G | A | 1 | a0004c0004t0001g0193 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.848-10161C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609555 | |||||||
chr4:69609610 | G | A | 116 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(113): Show |
124 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.848-10216C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609610 | |||||||
chr4:69609657 | C | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-10263G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609657 | |||||||
chr4:69609658 | C | G | 1 | a0008c0018t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.848-10264G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609658 | |||||||
chr4:69609685 | CACCTAT | C | 121 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(118): Show |
129 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.848-10297_848-1029 others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609685 | |||||||
chr4:69609750 | C | A | 30 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0003c0003t0002g0132 others(27): Show |
31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.848-10356G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609750 | |||||||
chr4:69609800 | A | C | 4 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-10406T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609800 | |||||||
chr4:69609929 | A | G | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-10535T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69609929 | |||||||
chr4:69610015 | C | A | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-10621G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610015 | |||||||
chr4:69610070 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.848-10676C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610070 | |||||||
chr4:69610148 | A | C | 114 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(111): Show |
122 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.848-10754T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610148 | |||||||
chr4:69610170 | G | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-10776C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610170 | |||||||
chr4:69610246 | C | CA | 115 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(112): Show |
123 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.848-10853dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610246 | |||||||
chr4:69610246 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.848-10852G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610246 | |||||||
chr4:69610328 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.848-10934G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610328 | |||||||
chr4:69610481 | C | A | 6 | a0001c0001t0003g0014 a0001c0001t0003g0113 a0001c0001t0003g0114 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-11087G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610481 | |||||||
chr4:69610590 | C | G | 1 | a0001c0001t0001g0330 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848-11196G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610590 | |||||||
chr4:69610591 | C | G | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.848-11197G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610591 | |||||||
chr4:69610591 | C | T | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-11197G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610591 | |||||||
chr4:69610651 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0139 |
3 | NA18985.hp1 NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.848-11257C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610651 | |||||||
chr4:69610675 | T | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0256 |
2 | NA18747.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.848-11281A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610675 | |||||||
chr4:69610762 | T | C | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-11368A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610762 | |||||||
chr4:69610817 | G | C | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-11423C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610817 | |||||||
chr4:69610847 | T | C | 5 | a0001c0001t0002g0018 a0001c0001t0002g0192 a0001c0001t0002g0204 others(2): Show |
6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-11453A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610847 | |||||||
chr4:69610870 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(116): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.848-11476C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610870 | |||||||
chr4:69610877 | C | T | 30 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0003c0003t0002g0132 others(27): Show |
31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.848-11483G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69610877 | |||||||
chr4:69611005 | C | G | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-11611G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611005 | |||||||
chr4:69611025 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.848-11631C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611025 | |||||||
chr4:69611113 | T | TA | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-11720dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611113 | |||||||
chr4:69611208 | C | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-11814G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611208 | |||||||
chr4:69611264 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.848-11870T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611264 | |||||||
chr4:69611265 | T | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-11871A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611265 | |||||||
chr4:69611287 | G | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-11893C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611287 | |||||||
chr4:69611288 | T | TCCAGCTA others(302): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0279 |
2 | HG03710.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.848-11895_848-1189 others(313): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | |||||||
chr4:69611288 | T | TCCAGCTA others(303): Show |
5 | a0001c0001t0001g0033 a0001c0001t0001g0141 a0001c0001t0001g0155 others(2): Show |
5 | HG00639.hp2 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.848-11895_848-1189 others(314): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | |||||||
chr4:69611288 | T | TCCAGCTA others(303): Show |
72 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(69): Show |
79 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.848-11895_848-1189 others(314): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | |||||||
chr4:69611288 | T | TCCAGCTA others(304): Show |
2 | a0001c0001t0001g0060 a0001c0001t0001g0139 |
2 | NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.848-11895_848-1189 others(315): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | |||||||
chr4:69611288 | T | TCCAGCTA others(323): Show |
1 | a0002c0002t0001g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.848-11895_848-1189 others(334): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | |||||||
chr4:69611288 | T | TCCAGCTA others(324): Show |
1 | a0002c0002t0001g0295 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.848-11895_848-1189 others(335): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | |||||||
chr4:69611288 | T | TCCAGCTA others(342): Show |
1 | a0002c0002t0001g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.848-11895_848-1189 others(353): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611288 | |||||||
chr4:69611290 | C | T | 1 | a0008c0018t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.848-11896G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611290 | |||||||
chr4:69611390 | C | A | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.848-11996G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611390 | |||||||
chr4:69611398 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.848-12004A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611398 | |||||||
chr4:69611610 | G | T | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-12216C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611610 | |||||||
chr4:69611854 | G | T | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-12460C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611854 | |||||||
chr4:69611860 | G | C | 1 | a0002c0002t0001g0324 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.848-12466C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611860 | |||||||
chr4:69611879 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848-12485G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611879 | |||||||
chr4:69611940 | A | G | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-12546T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611940 | |||||||
chr4:69611949 | T | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-12555A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611949 | |||||||
chr4:69611972 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.848-12578A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69611972 | |||||||
chr4:69612147 | G | A | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-12753C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612147 | |||||||
chr4:69612192 | C | G | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-12798G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612192 | |||||||
chr4:69612266 | C | T | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-12872G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612266 | |||||||
chr4:69612408 | T | G | 40 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(37): Show |
42 | HG00438.hp2 HG00609.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.848-13014A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612408 | |||||||
chr4:69612451 | C | T | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-13057G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612451 | |||||||
chr4:69612465 | C | T | 30 | a0001c0001t0001g0319 a0002c0002t0001g0122 a0003c0003t0002g0132 others(27): Show |
31 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.848-13071G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612465 | |||||||
chr4:69612486 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.848-13092A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612486 | |||||||
chr4:69612498 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.848-13104C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612498 | |||||||
chr4:69612534 | CAGAT | C | 84 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
91 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-13144_848-1314 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612534 | |||||||
chr4:69612592 | G | C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-13198C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612592 | |||||||
chr4:69612673 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-13279G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612673 | |||||||
chr4:69612677 | T | C | 2 | a0004c0004t0001g0309 a0004c0004t0001g0316 |
2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.848-13283A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612677 | |||||||
chr4:69612715 | T | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-13321A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612715 | |||||||
chr4:69612857 | C | T | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-13463G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612857 | |||||||
chr4:69612869 | T | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-13475A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612869 | |||||||
chr4:69612874 | A | G | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-13480T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612874 | |||||||
chr4:69612907 | G | GA | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(230): Show |
249 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.848-13514dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612907 | |||||||
chr4:69612907 | G | GAA | 17 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0127 others(14): Show |
18 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.848-13515_848-1351 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612907 | |||||||
chr4:69612907 | G | GAAA | 25 | a0002c0002t0001g0122 a0003c0003t0002g0148 a0003c0003t0002g0149 others(22): Show |
26 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.848-13516_848-1351 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612907 | |||||||
chr4:69612950 | T | G | 122 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(119): Show |
130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-13556A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612950 | |||||||
chr4:69612961 | A | T | 122 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(119): Show |
130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-13567T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69612961 | |||||||
chr4:69613054 | TA | T | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-13661delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613054 | |||||||
chr4:69613066 | G | A | 83 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(80): Show |
90 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.848-13672C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613066 | |||||||
chr4:69613090 | A | G | 3 | a0001c0001t0001g0319 a0008c0018t0001g0273 a0012c0016t0011g0225 |
3 | HG01192.hp2 HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.848-13696T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613090 | |||||||
chr4:69613095 | A | G | 120 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
128 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.848-13701T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613095 | |||||||
chr4:69613194 | T | C | 19 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(16): Show |
20 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.848-13800A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613194 | |||||||
chr4:69613253 | T | C | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-13859A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613253 | |||||||
chr4:69613304 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.848-13910G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613304 | |||||||
chr4:69613355 | A | C | 1 | a0001c0001t0001g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.848-13961T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613355 | |||||||
chr4:69613507 | CACA | C | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-14116_848-1411 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613507 | |||||||
chr4:69613693 | T | C | 29 | a0001c0001t0001g0319 a0003c0003t0002g0132 a0003c0003t0002g0148 others(26): Show |
30 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.848-14299A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613693 | |||||||
chr4:69613829 | A | G | 6 | a0001c0001t0003g0014 a0001c0001t0003g0113 a0001c0001t0003g0114 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-14435T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613829 | |||||||
chr4:69613900 | C | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-14506G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613900 | |||||||
chr4:69613948 | C | T | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-14554G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613948 | |||||||
chr4:69613967 | T | C | 1 | a0005c0005t0002g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.848-14573A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69613967 | |||||||
chr4:69614065 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(273): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.848-14671C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614065 | |||||||
chr4:69614112 | T | A | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14718A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614112 | |||||||
chr4:69614113 | A | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14719T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614113 | |||||||
chr4:69614114 | A | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14720T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614114 | |||||||
chr4:69614116 | C | CTGAATGG others(2): Show |
92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14723_848-1472 others(13): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614116 | |||||||
chr4:69614117 | C | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14723G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614117 | |||||||
chr4:69614118 | C | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-14724G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614118 | |||||||
chr4:69614149 | T | C | 1 | a0001c0007t0001g0211 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.848-14755A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614149 | |||||||
chr4:69614410 | A | G | 21 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.848-15016T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614410 | |||||||
chr4:69614415 | T | A | 122 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(119): Show |
130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-15021A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614415 | |||||||
chr4:69614418 | C | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.848-15024G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614418 | |||||||
chr4:69614436 | C | T | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-15042G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614436 | |||||||
chr4:69614461 | A | AT | 122 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(119): Show |
130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-15068_848-1506 others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614461 | |||||||
chr4:69614501 | C | G | 1 | a0001c0001t0006g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.848-15107G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614501 | |||||||
chr4:69614609 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(267): Show |
284 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.848-15215A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614609 | |||||||
chr4:69614617 | A | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(267): Show |
284 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.848-15223T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614617 | |||||||
chr4:69614630 | C | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-15236G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614630 | |||||||
chr4:69614760 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.848-15366A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614760 | |||||||
chr4:69614836 | T | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-15442A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69614836 | |||||||
chr4:69615039 | C | A | 27 | a0003c0003t0002g0132 a0003c0003t0002g0148 a0003c0003t0002g0149 others(24): Show |
28 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.848-15645G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615039 | |||||||
chr4:69615107 | T | G | 1 | a0001c0001t0002g0208 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.848-15713A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615107 | |||||||
chr4:69615157 | C | T | 8 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-15763G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615157 | |||||||
chr4:69615174 | C | A | 1 | a0001c0001t0002g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.848-15780G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615174 | |||||||
chr4:69615199 | C | A | 3 | a0009c0013t0007g0345 a0010c0012t0007g0202 a0012c0016t0011g0225 |
3 | HG01884.hp1 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.848-15805G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615199 | |||||||
chr4:69615208 | A | G | 122 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(119): Show |
130 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.848-15814T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615208 | |||||||
chr4:69615275 | G | A | 3 | a0009c0013t0007g0345 a0010c0012t0007g0202 a0012c0016t0011g0225 |
3 | HG01884.hp1 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.848-15881C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615275 | |||||||
chr4:69615484 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.848-16090C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615484 | |||||||
chr4:69615564 | T | C | 2 | a0001c0001t0001g0319 a0008c0018t0001g0273 |
2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.848-16170A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615564 | |||||||
chr4:69615702 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.848-16308T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615702 | |||||||
chr4:69615724 | G | A | 123 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(120): Show |
131 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.848-16330C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615724 | |||||||
chr4:69615731 | A | G | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-16337T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615731 | |||||||
chr4:69615786 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0342 a0011c0015t0001g0166 |
3 | NA18939.hp1 NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.848-16392C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615786 | |||||||
chr4:69615858 | C | CA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(64): Show |
73 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.848-16465dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615858 | |||||||
chr4:69615890 | C | T | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.848-16496G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615890 | |||||||
chr4:69615935 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.848-16541A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615935 | |||||||
chr4:69615969 | C | T | 1 | a0002c0002t0003g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.848-16575G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615969 | |||||||
chr4:69615987 | C | T | 101 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(98): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.848-16593G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69615987 | |||||||
chr4:69616115 | C | T | 26 | a0002c0002t0001g0122 a0003c0003t0002g0132 a0003c0003t0002g0148 others(23): Show |
27 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.848-16721G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616115 | |||||||
chr4:69616118 | G | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.848-16724C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616118 | |||||||
chr4:69616119 | G | A | 1 | a0003c0003t0002g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.848-16725C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616119 | |||||||
chr4:69616162 | A | G | 136 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(133): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.848-16768T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616162 | |||||||
chr4:69616292 | A | G | 4 | a0001c0001t0001g0141 a0001c0001t0001g0155 a0001c0001t0001g0241 others(1): Show |
4 | HG00639.hp2 HG00741.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-16898T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616292 | |||||||
chr4:69616379 | T | C | 115 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(112): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.848-16985A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616379 | |||||||
chr4:69616382 | G | C | 1 | a0001c0001t0001g0333 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.848-16988C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616382 | |||||||
chr4:69616604 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.848-17210T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616604 | |||||||
chr4:69616667 | T | C | 5 | a0001c0001t0002g0018 a0001c0001t0002g0192 a0001c0001t0002g0204 others(2): Show |
6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-17273A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616667 | |||||||
chr4:69616751 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.848-17357T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616751 | |||||||
chr4:69616833 | C | CT | 17 | a0001c0001t0001g0153 a0001c0001t0002g0013 a0001c0001t0002g0018 others(14): Show |
19 | HG01243.hp1 HG01934.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.848-17440dupA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | |||||||
chr4:69616833 | C | CTT | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0023 others(31): Show |
39 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.848-17441_848-1744 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | |||||||
chr4:69616833 | C | CTTT | 108 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(105): Show |
109 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.848-17442_848-1744 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | |||||||
chr4:69616833 | CT | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(20): Show |
25 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.848-17440delA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | |||||||
chr4:69616833 | CTT | C | 77 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(74): Show |
82 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.848-17441_848-1744 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616833 | |||||||
chr4:69616850 | T | G | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.848-17456A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69616850 | |||||||
chr4:69617324 | G | A | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.848-17930C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617324 | |||||||
chr4:69617448 | T | C | 6 | a0001c0001t0003g0014 a0001c0001t0003g0113 a0001c0001t0003g0114 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-18054A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617448 | |||||||
chr4:69617469 | G | A | 1 | a0002c0002t0001g0346 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.848-18075C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617469 | |||||||
chr4:69617482 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.848-18088G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617482 | |||||||
chr4:69617511 | A | C | 1 | a0002c0002t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.848-18117T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617511 | |||||||
chr4:69617532 | A | G | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.848-18138T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617532 | |||||||
chr4:69617605 | A | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+18086T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617605 | |||||||
chr4:69617630 | C | T | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+18061G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617630 | |||||||
chr4:69617733 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+17958G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617733 | |||||||
chr4:69617771 | C | G | 5 | a0001c0001t0002g0018 a0001c0001t0002g0192 a0001c0001t0002g0204 others(2): Show |
6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.847+17920G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617771 | |||||||
chr4:69617969 | T | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+17722A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69617969 | |||||||
chr4:69618187 | A | ATG | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(191): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.847+17502_847+1750 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618187 | |||||||
chr4:69618187 | A | ATGTG | 17 | a0001c0001t0001g0115 a0001c0001t0001g0129 a0001c0001t0001g0130 others(14): Show |
17 | HG00423.hp2 HG01192.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.847+17500_847+1750 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618187 | |||||||
chr4:69618187 | ATGTGTG | A | 3 | a0002c0002t0008g0289 a0002c0002t0008g0348 a0003c0009t0002g0212 |
3 | HG01109.hp2 HG02602.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.847+17498_847+1750 others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618187 | |||||||
chr4:69618201 | G | GTGTGTGT others(5): Show |
8 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0165 others(5): Show |
9 | HG00423.hp1 HG02615.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+17489_847+1749 others(16): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618201 | |||||||
chr4:69618203 | G | GTGTGTAT others(3): Show |
4 | a0001c0001t0001g0033 a0001c0001t0001g0275 a0001c0001t0006g0172 others(1): Show |
4 | HG01106.hp1 HG01891.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.847+17487_847+1748 others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618203 | |||||||
chr4:69618205 | G | GTGTATGT others(1): Show |
8 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0035 others(5): Show |
9 | HG01099.hp1 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+17485_847+1748 others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618205 | |||||||
chr4:69618205 | G | GTGTGTGT others(5): Show |
1 | a0002c0002t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.847+17485_847+1748 others(16): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618205 | |||||||
chr4:69618207 | G | GTGTA | 24 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0058 others(21): Show |
24 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.847+17483_847+1748 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618207 | |||||||
chr4:69618207 | G | GTGTATGT others(1): Show |
12 | a0001c0001t0001g0010 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
13 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.847+17483_847+1748 others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618207 | |||||||
chr4:69618209 | G | GTA | 9 | a0001c0001t0001g0049 a0002c0002t0001g0177 a0004c0004t0001g0061 others(6): Show |
9 | HG01496.hp1 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+17481_847+1748 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618209 | |||||||
chr4:69618209 | G | GTATGTT | 39 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0052 others(36): Show |
43 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.847+17481_847+1748 others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618209 | |||||||
chr4:69618209 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.847+17482C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618209 | |||||||
chr4:69618211 | G | A | 7 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(4): Show |
7 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+17480C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618211 | |||||||
chr4:69618211 | G | T | 24 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0058 others(21): Show |
24 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.847+17480C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618211 | |||||||
chr4:69618213 | G | A | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847+17478C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618213 | |||||||
chr4:69618213 | G | T | 9 | a0001c0001t0001g0049 a0002c0002t0001g0177 a0004c0004t0001g0061 others(6): Show |
9 | HG01496.hp1 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+17478C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618213 | |||||||
chr4:69618213 | GTGTA | G | 7 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(4): Show |
7 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+17474_847+1747 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618213 | |||||||
chr4:69618217 | A | G | 107 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(104): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.847+17474T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618217 | |||||||
chr4:69618217 | A | T | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847+17474T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618217 | |||||||
chr4:69618219 | G | T | 7 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(4): Show |
7 | HG02922.hp1 HG02976.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+17472C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618219 | |||||||
chr4:69618221 | T | G | 116 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(113): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.847+17470A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618221 | |||||||
chr4:69618221 | T | TTG | 86 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(83): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.847+17468_847+1746 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618221 | |||||||
chr4:69618221 | T | TTGTG | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(142): Show |
152 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.847+17466_847+1746 others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618221 | |||||||
chr4:69618239 | A | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+17452T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618239 | |||||||
chr4:69618328 | C | A | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+17363G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618328 | |||||||
chr4:69618350 | CATA | C | 78 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(75): Show |
83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+17338_847+1734 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618350 | |||||||
chr4:69618471 | T | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+17220A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618471 | |||||||
chr4:69618512 | T | A | 2 | a0001c0001t0001g0243 a0001c0011t0001g0131 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.847+17179A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618512 | |||||||
chr4:69618512 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.847+17179A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618512 | |||||||
chr4:69618532 | G | A | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+17159C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618532 | |||||||
chr4:69618674 | G | T | 1 | a0008c0018t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+17017C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618674 | |||||||
chr4:69618777 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.847+16914T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618777 | |||||||
chr4:69618915 | T | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0059 others(6): Show |
10 | NA18950.hp2 NA18964.hp1 NA18982.hp1 others(7): Show |
intron_variant | MODIFIER | c.847+16776A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618915 | |||||||
chr4:69618960 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.847+16731A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618960 | |||||||
chr4:69618993 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.847+16698A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69618993 | |||||||
chr4:69619079 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.847+16612T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619079 | |||||||
chr4:69619122 | C | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+16569G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619122 | |||||||
chr4:69619395 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0165 others(2): Show |
6 | NA18968.hp2 NA18988.hp2 NA19067.hp1 others(3): Show |
intron_variant | MODIFIER | c.847+16296C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619395 | |||||||
chr4:69619420 | C | CATAAA | 98 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(95): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.847+16266_847+1627 others(9): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619420 | |||||||
chr4:69619420 | C | CATAAAAT others(3): Show |
5 | a0001c0001t0002g0050 a0002c0002t0008g0289 a0002c0002t0008g0348 others(2): Show |
5 | HG00597.hp2 HG01109.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.847+16261_847+1627 others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619420 | |||||||
chr4:69619420 | C | CATAAAAT others(8): Show |
5 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0005c0005t0002g0206 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+16256_847+1627 others(19): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619420 | |||||||
chr4:69619470 | T | C | 109 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(106): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.847+16221A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619470 | |||||||
chr4:69619517 | C | T | 5 | a0001c0001t0001g0319 a0001c0001t0002g0227 a0001c0001t0002g0331 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+16174G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619517 | |||||||
chr4:69619518 | G | T | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+16173C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619518 | |||||||
chr4:69619551 | A | T | 1 | a0005c0005t0002g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.847+16140T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619551 | |||||||
chr4:69619909 | C | T | 265 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(262): Show |
279 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.847+15782G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619909 | |||||||
chr4:69619945 | T | C | 78 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(75): Show |
83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+15746A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619945 | |||||||
chr4:69619990 | T | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+15701A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69619990 | |||||||
chr4:69620125 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+15566G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620125 | |||||||
chr4:69620189 | A | G | 1 | a0008c0018t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+15502T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620189 | |||||||
chr4:69620221 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.847+15470A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620221 | |||||||
chr4:69620288 | C | G | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+15403G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620288 | |||||||
chr4:69620291 | G | GA | 110 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(107): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.847+15399dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620291 | |||||||
chr4:69620341 | G | A | 1 | a0005c0005t0005g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.847+15350C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620341 | |||||||
chr4:69620379 | A | AAAATGCC others(37): Show |
8 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(5): Show |
8 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+15311_847+1531 others(48): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620379 | |||||||
chr4:69620381 | T | A | 8 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(5): Show |
8 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+15310A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620381 | |||||||
chr4:69620655 | CA | C | 80 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0041 others(77): Show |
85 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.847+15035delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620655 | |||||||
chr4:69620655 | CAA | C | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+15034_847+1503 others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620655 | |||||||
chr4:69620772 | T | C | 1 | a0002c0002t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.847+14919A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620772 | |||||||
chr4:69620794 | A | G | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+14897T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620794 | |||||||
chr4:69620932 | C | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+14759G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69620932 | |||||||
chr4:69621091 | G | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+14600C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621091 | |||||||
chr4:69621114 | C | T | 5 | a0001c0001t0002g0317 a0003c0003t0002g0296 a0003c0003t0002g0334 others(2): Show |
5 | HG01358.hp1 HG02451.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+14577G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621114 | |||||||
chr4:69621291 | C | G | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+14400G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621291 | |||||||
chr4:69621371 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.847+14320C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621371 | |||||||
chr4:69621384 | A | T | 1 | a0004c0004t0001g0061 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.847+14307T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621384 | |||||||
chr4:69621491 | A | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+14200T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621491 | |||||||
chr4:69621585 | C | T | 4 | a0001c0001t0001g0112 a0001c0007t0001g0106 a0001c0007t0001g0211 others(1): Show |
4 | HG02602.hp2 HG03834.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.847+14106G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621585 | |||||||
chr4:69621621 | T | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(143): Show |
153 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.847+14070A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621621 | |||||||
chr4:69621656 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+14035G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621656 | |||||||
chr4:69621679 | C | T | 20 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(17): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+14012G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621679 | |||||||
chr4:69621711 | T | C | 2 | a0002c0002t0001g0065 a0005c0005t0005g0284 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.847+13980A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621711 | |||||||
chr4:69621894 | A | G | 2 | a0004c0004t0001g0063 a0004c0004t0001g0307 |
2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.847+13797T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69621894 | |||||||
chr4:69622043 | T | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+13648A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622043 | |||||||
chr4:69622044 | A | C | 79 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(76): Show |
84 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.847+13647T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622044 | |||||||
chr4:69622244 | A | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+13447T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622244 | |||||||
chr4:69622271 | GTAA | G | 3 | a0001c0007t0001g0106 a0001c0007t0001g0211 a0003c0009t0002g0212 |
3 | HG02602.hp2 HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.847+13417_847+1341 others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622271 | |||||||
chr4:69622304 | G | C | 100 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(97): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.847+13387C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622304 | |||||||
chr4:69622389 | A | G | 11 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.847+13302T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622389 | |||||||
chr4:69622559 | A | G | 1 | a0012c0016t0011g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.847+13132T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622559 | |||||||
chr4:69622642 | C | A | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+13049G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622642 | |||||||
chr4:69622662 | G | C | 11 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.847+13029C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622662 | |||||||
chr4:69622689 | T | C | 1 | a0002c0002t0008g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.847+13002A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622689 | |||||||
chr4:69622735 | T | A | 7 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0302 others(4): Show |
7 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+12956A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622735 | |||||||
chr4:69622823 | C | G | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+12868G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622823 | |||||||
chr4:69622860 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.847+12831A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69622860 | |||||||
chr4:69623025 | T | G | 1 | a0003c0003t0002g0296 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.847+12666A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623025 | |||||||
chr4:69623068 | T | G | 78 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(75): Show |
83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+12623A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623068 | |||||||
chr4:69623086 | A | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(274): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.847+12605T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623086 | |||||||
chr4:69623131 | T | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12560A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623131 | |||||||
chr4:69623168 | C | T | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.847+12523G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623168 | |||||||
chr4:69623324 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.847+12367A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623324 | |||||||
chr4:69623421 | A | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12270T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623421 | |||||||
chr4:69623434 | A | G | 78 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(75): Show |
83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+12257T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623434 | |||||||
chr4:69623436 | A | C | 1 | a0002c0002t0001g0325 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.847+12255T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623436 | |||||||
chr4:69623534 | A | G | 16 | a0002c0002t0001g0066 a0002c0002t0001g0176 a0002c0002t0001g0177 others(13): Show |
18 | HG00642.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.847+12157T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623534 | |||||||
chr4:69623563 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12128G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623563 | |||||||
chr4:69623564 | A | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12127T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623564 | |||||||
chr4:69623667 | C | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+12024G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623667 | |||||||
chr4:69623701 | A | G | 79 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(76): Show |
84 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.847+11990T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623701 | |||||||
chr4:69623728 | G | A | 78 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(75): Show |
83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+11963C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69623728 | |||||||
chr4:69624013 | A | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+11678T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624013 | |||||||
chr4:69624075 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.847+11616C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624075 | |||||||
chr4:69624231 | C | T | 20 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(17): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+11460G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624231 | |||||||
chr4:69624399 | T | A | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+11292A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624399 | |||||||
chr4:69624488 | A | G | 1 | a0008c0018t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+11203T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624488 | |||||||
chr4:69624514 | G | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+11177C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624514 | |||||||
chr4:69624588 | T | C | 2 | a0002c0002t0001g0017 a0002c0002t0001g0073 |
3 | NA18967.hp2 NA18986.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.847+11103A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624588 | |||||||
chr4:69624620 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.847+11071A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624620 | |||||||
chr4:69624803 | G | T | 78 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(75): Show |
83 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+10888C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624803 | |||||||
chr4:69624867 | T | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+10824A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624867 | |||||||
chr4:69624908 | G | A | 2 | a0002c0002t0001g0292 a0002c0002t0001g0295 |
2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.847+10783C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624908 | |||||||
chr4:69624971 | T | C | 1 | a0001c0001t0002g0317 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.847+10720A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69624971 | |||||||
chr4:69625003 | C | CA | 110 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(107): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.847+10687dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625003 | |||||||
chr4:69625022 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.847+10669A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625022 | |||||||
chr4:69625074 | A | G | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.847+10617T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625074 | |||||||
chr4:69625165 | CT | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+10525delA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625165 | |||||||
chr4:69625185 | T | G | 5 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+10506A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625185 | |||||||
chr4:69625220 | T | A | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+10471A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625220 | |||||||
chr4:69625236 | C | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+10455G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625236 | |||||||
chr4:69625551 | A | G | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+10140T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625551 | |||||||
chr4:69625613 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.847+10078A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625613 | |||||||
chr4:69625661 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.847+10030G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625661 | |||||||
chr4:69625790 | C | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9901G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625790 | |||||||
chr4:69625896 | T | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9795A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69625896 | |||||||
chr4:69626039 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.847+9652A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626039 | |||||||
chr4:69626077 | C | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9614G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626077 | |||||||
chr4:69626090 | T | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9601A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626090 | |||||||
chr4:69626155 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.847+9536A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626155 | |||||||
chr4:69626173 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(143): Show |
153 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.847+9518T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626173 | |||||||
chr4:69626252 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9439G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626252 | |||||||
chr4:69626267 | T | G | 1 | a0001c0001t0006g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.847+9424A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626267 | |||||||
chr4:69626303 | C | T | 8 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0184 others(5): Show |
8 | HG02602.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+9388G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626303 | |||||||
chr4:69626313 | G | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+9378C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626313 | |||||||
chr4:69626323 | G | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9368C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626323 | |||||||
chr4:69626337 | G | A | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+9354C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626337 | |||||||
chr4:69626424 | A | G | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+9267T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626424 | |||||||
chr4:69626587 | G | A | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9104C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626587 | |||||||
chr4:69626669 | TA | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+9021delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626669 | |||||||
chr4:69626714 | A | C | 1 | a0002c0002t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.847+8977T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626714 | |||||||
chr4:69626760 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0116 a0001c0001t0001g0252 others(4): Show |
7 | HG00621.hp2 HG02165.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+8931A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626760 | |||||||
chr4:69626827 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.847+8864A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626827 | |||||||
chr4:69626861 | C | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(262): Show |
279 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.847+8830G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626861 | |||||||
chr4:69626988 | A | G | 3 | a0006c0006t0002g0080 a0006c0006t0002g0081 a0006c0008t0001g0064 |
3 | HG00735.hp1 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.847+8703T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69626988 | |||||||
chr4:69627004 | C | T | 112 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(109): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.847+8687G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627004 | |||||||
chr4:69627095 | T | C | 2 | a0001c0001t0002g0204 a0001c0001t0002g0213 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.847+8596A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627095 | |||||||
chr4:69627215 | A | C | 20 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(17): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+8476T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627215 | |||||||
chr4:69627254 | A | C | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+8437T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627254 | |||||||
chr4:69627361 | T | C | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+8330A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627361 | |||||||
chr4:69627456 | ACAGGCAA others(13): Show |
A | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+8215_847+8234d others(22): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627456 | |||||||
chr4:69627486 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0226 |
3 | NA18954.hp2 NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.847+8205T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627486 | |||||||
chr4:69627534 | A | AAG | 86 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(83): Show |
91 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.847+8155_847+8156d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627534 | |||||||
chr4:69627538 | GAGAGAGA others(3): Show |
G | 1 | a0001c0001t0002g0286 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847+8143_847+8152d others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627538 | |||||||
chr4:69627540 | GAGAGAGA others(1): Show |
G | 64 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(61): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.847+8143_847+8150d others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627540 | |||||||
chr4:69627542 | G | A | 19 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(16): Show |
21 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.847+8149C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627542 | |||||||
chr4:69627542 | GAGAGAA | G | 4 | a0001c0001t0002g0018 a0001c0001t0002g0192 a0001c0001t0002g0204 others(1): Show |
5 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.847+8143_847+8148d others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627542 | |||||||
chr4:69627544 | GAGAA | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0090 a0001c0001t0002g0096 others(1): Show |
4 | NA18963.hp1 NA18968.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.847+8143_847+8146d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627544 | |||||||
chr4:69627546 | GAA | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(15): Show |
20 | HG00140.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.847+8143_847+8144d others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627546 | |||||||
chr4:69627548 | A | G | 5 | a0001c0001t0001g0276 a0001c0001t0002g0032 a0001c0001t0002g0297 others(2): Show |
5 | HG00423.hp1 HG02004.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.847+8143T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627548 | |||||||
chr4:69627550 | G | A | 1 | a0002c0002t0001g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.847+8141C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627550 | |||||||
chr4:69627552 | G | A | 1 | a0005c0005t0002g0271 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.847+8139C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627552 | |||||||
chr4:69627566 | G | A | 6 | a0004c0004t0001g0039 a0004c0004t0001g0181 a0004c0004t0001g0219 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.847+8125C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627566 | |||||||
chr4:69627568 | A | G | 22 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(19): Show |
24 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.847+8123T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627568 | |||||||
chr4:69627572 | A | G | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+8119T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627572 | |||||||
chr4:69627581 | A | T | 1 | a0001c0001t0001g0339 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.847+8110T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627581 | |||||||
chr4:69627597 | G | GGAAA | 3 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0002c0002t0001g0347 |
3 | HG02615.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.847+8093_847+8094i others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627597 | |||||||
chr4:69627598 | A | AAAAG | 81 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(78): Show |
86 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.847+8089_847+8092d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627598 | |||||||
chr4:69627598 | A | AAAAGAAA others(5): Show |
2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+8081_847+8092d others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627598 | |||||||
chr4:69627598 | A | G | 3 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0002c0002t0001g0347 |
3 | HG02615.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.847+8093T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627598 | |||||||
chr4:69627868 | A | G | 90 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(87): Show |
95 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.847+7823T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627868 | |||||||
chr4:69627912 | T | C | 6 | a0002c0002t0003g0002 a0002c0002t0003g0067 a0002c0002t0003g0068 others(3): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.847+7779A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627912 | |||||||
chr4:69627949 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+7742G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627949 | |||||||
chr4:69627960 | C | A | 2 | a0002c0002t0001g0292 a0002c0002t0001g0295 |
2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.847+7731G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627960 | |||||||
chr4:69627997 | G | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+7694C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69627997 | |||||||
chr4:69628009 | C | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+7682G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628009 | |||||||
chr4:69628108 | C | A | 1 | a0001c0001t0002g0098 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.847+7583G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628108 | |||||||
chr4:69628108 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.847+7583G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628108 | |||||||
chr4:69628275 | T | G | 32 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(29): Show |
34 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.847+7416A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628275 | |||||||
chr4:69628283 | C | CA | 112 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(109): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.847+7407dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628283 | |||||||
chr4:69628369 | G | A | 1 | a0001c0001t0002g0008 | 2 | NA18941.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.847+7322C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628369 | |||||||
chr4:69628401 | G | A | 2 | a0002c0002t0001g0292 a0002c0002t0001g0295 |
2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.847+7290C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628401 | |||||||
chr4:69628521 | G | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+7170C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628521 | |||||||
chr4:69628617 | A | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+7074T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628617 | |||||||
chr4:69628653 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.847+7038C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628653 | |||||||
chr4:69628691 | T | C | 3 | a0001c0001t0002g0079 a0001c0001t0002g0084 a0001c0001t0002g0099 |
3 | NA18945.hp2 NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.847+7000A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628691 | |||||||
chr4:69628696 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.847+6995C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628696 | |||||||
chr4:69628745 | A | G | 1 | a0008c0018t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+6946T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628745 | |||||||
chr4:69628757 | A | C | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+6934T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628757 | |||||||
chr4:69628796 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+6895G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628796 | |||||||
chr4:69628913 | T | G | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+6778A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69628913 | |||||||
chr4:69629006 | G | T | 12 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.847+6685C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629006 | |||||||
chr4:69629015 | T | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+6676A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629015 | |||||||
chr4:69629123 | T | C | 112 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(109): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.847+6568A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629123 | |||||||
chr4:69629183 | G | A | 90 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(87): Show |
95 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.847+6508C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629183 | |||||||
chr4:69629215 | G | A | 72 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(69): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.847+6476C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629215 | |||||||
chr4:69629266 | C | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.847+6425G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629266 | |||||||
chr4:69629476 | T | C | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0272 |
3 | HG02886.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.847+6215A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629476 | |||||||
chr4:69629635 | T | C | 18 | a0004c0004t0001g0039 a0004c0004t0001g0061 a0004c0004t0001g0062 others(15): Show |
18 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.847+6056A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629635 | |||||||
chr4:69629656 | A | T | 43 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.847+6035T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629656 | |||||||
chr4:69629694 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.847+5997A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629694 | |||||||
chr4:69629704 | C | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+5987G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629704 | |||||||
chr4:69629776 | G | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(13): Show |
18 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.847+5915C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629776 | |||||||
chr4:69629801 | G | C | 75 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(72): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.847+5890C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629801 | |||||||
chr4:69629934 | C | A | 19 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(16): Show |
21 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.847+5757G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69629934 | |||||||
chr4:69630021 | A | G | 5 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+5670T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630021 | |||||||
chr4:69630022 | A | G | 1 | a0012c0016t0011g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.847+5669T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630022 | |||||||
chr4:69630243 | C | T | 55 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(52): Show |
58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.847+5448G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630243 | |||||||
chr4:69630254 | C | T | 6 | a0003c0003t0002g0148 a0003c0003t0002g0149 a0003c0003t0002g0186 others(3): Show |
6 | HG01346.hp2 HG01928.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.847+5437G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630254 | |||||||
chr4:69630269 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | NA18612.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.847+5422C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630269 | |||||||
chr4:69630339 | G | A | 73 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(70): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.847+5352C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630339 | |||||||
chr4:69630400 | T | C | 1 | a0008c0018t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+5291A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630400 | |||||||
chr4:69630464 | T | C | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.847+5227A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630464 | |||||||
chr4:69630525 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.847+5166T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630525 | |||||||
chr4:69630544 | C | T | 55 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(52): Show |
58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.847+5147G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630544 | |||||||
chr4:69630558 | A | G | 2 | a0001c0001t0001g0108 a0011c0015t0001g0166 |
2 | NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.847+5133T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630558 | |||||||
chr4:69630591 | G | C | 1 | a0004c0004t0001g0285 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.847+5100C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630591 | |||||||
chr4:69630922 | AAAG | A | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+4766_847+4768d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69630922 | |||||||
chr4:69631077 | T | G | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+4614A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631077 | |||||||
chr4:69631157 | T | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+4534A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631157 | |||||||
chr4:69631318 | A | ATC | 269 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(266): Show |
283 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.847+4372_847+4373i others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631318 | |||||||
chr4:69631435 | A | C | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+4256T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631435 | |||||||
chr4:69631468 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.847+4223C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631468 | |||||||
chr4:69631517 | T | A | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.847+4174A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631517 | |||||||
chr4:69631666 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0328 a0001c0001t0001g0329 |
3 | HG02145.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.847+4025C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631666 | |||||||
chr4:69631873 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.847+3818A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631873 | |||||||
chr4:69631883 | C | T | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.847+3808G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631883 | |||||||
chr4:69631895 | T | G | 1 | a0002c0002t0001g0288 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.847+3796A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69631895 | |||||||
chr4:69632188 | G | A | 37 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0051 others(34): Show |
39 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.847+3503C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632188 | |||||||
chr4:69632194 | T | C | 37 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0051 others(34): Show |
39 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.847+3497A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632194 | |||||||
chr4:69632196 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+3495C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632196 | |||||||
chr4:69632315 | C | G | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+3376G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632315 | |||||||
chr4:69632430 | T | C | 10 | a0002c0002t0001g0122 a0002c0002t0001g0324 a0002c0002t0001g0325 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.847+3261A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632430 | |||||||
chr4:69632447 | C | T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0051 others(34): Show |
39 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.847+3244G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632447 | |||||||
chr4:69632574 | T | C | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+3117A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632574 | |||||||
chr4:69632672 | A | G | 10 | a0002c0002t0001g0122 a0002c0002t0001g0324 a0002c0002t0001g0325 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.847+3019T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632672 | |||||||
chr4:69632705 | G | T | 1 | a0001c0001t0002g0267 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.847+2986C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632705 | |||||||
chr4:69632885 | C | CA | 47 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(44): Show |
47 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.847+2805dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632885 | |||||||
chr4:69632885 | CA | C | 7 | a0001c0001t0001g0335 a0001c0001t0002g0082 a0001c0001t0002g0196 others(4): Show |
7 | HG00642.hp1 HG02004.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+2805delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632885 | |||||||
chr4:69632888 | A | C | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+2803T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632888 | |||||||
chr4:69632889 | A | G | 1 | a0005c0005t0005g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.847+2802T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632889 | |||||||
chr4:69632921 | C | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0341 |
2 | NA18963.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.847+2770G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69632921 | |||||||
chr4:69633058 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.847+2633A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633058 | |||||||
chr4:69633221 | C | T | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+2470G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633221 | |||||||
chr4:69633260 | A | T | 20 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(17): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+2431T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633260 | |||||||
chr4:69633268 | T | C | 4 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.847+2423A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633268 | |||||||
chr4:69633307 | A | T | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+2384T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633307 | |||||||
chr4:69633485 | T | C | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+2206A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633485 | |||||||
chr4:69633516 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(55): Show |
64 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.847+2175A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633516 | |||||||
chr4:69633578 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.847+2113A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633578 | |||||||
chr4:69633630 | T | C | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.847+2061A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633630 | |||||||
chr4:69633723 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0120 |
2 | HG02056.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.847+1968A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633723 | |||||||
chr4:69633747 | T | G | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG00438.hp1 HG02015.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.847+1944A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69633747 | |||||||
chr4:69634031 | C | T | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+1660G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634031 | |||||||
chr4:69634032 | T | G | 16 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(13): Show |
18 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.847+1659A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634032 | |||||||
chr4:69634106 | T | G | 62 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(59): Show |
67 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.847+1585A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634106 | |||||||
chr4:69634145 | T | C | 2 | a0002c0002t0001g0292 a0002c0002t0001g0295 |
2 | HG02004.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.847+1546A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634145 | |||||||
chr4:69634153 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.847+1538C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634153 | |||||||
chr4:69634172 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.847+1519C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634172 | |||||||
chr4:69634251 | CAAACAAA others(3): Show |
C | 53 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(50): Show |
56 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.847+1430_847+1439d others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634251 | |||||||
chr4:69634335 | T | C | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847+1356A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634335 | |||||||
chr4:69634589 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.847+1102G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634589 | |||||||
chr4:69634662 | G | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0297 |
2 | HG00423.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.847+1029C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634662 | |||||||
chr4:69634802 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.847+889T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634802 | |||||||
chr4:69634809 | A | T | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.847+882T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634809 | |||||||
chr4:69634843 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.847+848C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69634843 | |||||||
chr4:69635112 | T | C | 59 | a0001c0001t0001g0290 a0001c0001t0002g0018 a0001c0001t0002g0192 others(56): Show |
63 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.847+579A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635112 | |||||||
chr4:69635130 | A | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0099 |
2 | NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.847+561T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635130 | |||||||
chr4:69635131 | A | C | 1 | a0004c0004t0001g0193 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.847+560T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635131 | |||||||
chr4:69635131 | A | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0099 |
2 | NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.847+560T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635131 | |||||||
chr4:69635268 | T | A | 59 | a0001c0001t0001g0290 a0001c0001t0002g0018 a0001c0001t0002g0192 others(56): Show |
63 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.847+423A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635268 | |||||||
chr4:69635443 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
7 | HG01993.hp1 HG02027.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+248G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635443 | |||||||
chr4:69635555 | T | C | 1 | a0001c0001t0002g0097 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.847+136A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635555 | |||||||
chr4:69635656 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0087 a0007c0014t0002g0086 |
5 | HG00099.hp2 HG00140.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.847+35G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 3/6 | chr4 | 69635656 | |||||||
chr4:69635825 | C | CA | 26 | a0001c0001t0001g0143 a0002c0002t0001g0017 a0002c0002t0001g0065 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.716-4dupT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635825 | |||||||
chr4:69635825 | C | CAA | 3 | a0002c0002t0001g0017 a0002c0002t0001g0214 a0002c0002t0001g0215 |
3 | HG02895.hp1 NA18906.hp1 NA19009.hp1 |
splice_region_variant&intron_variant | LOW | c.716-4_716-3insTT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635825 | |||||||
chr4:69635825 | CACCAAAA others(4): Show |
C | 11 | a0002c0002t0001g0066 a0002c0002t0001g0177 a0002c0002t0001g0287 others(8): Show |
13 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.716-14_716-4delTTT others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635825 | |||||||
chr4:69635826 | ACC | A | 6 | a0001c0001t0002g0069 a0001c0001t0002g0079 a0001c0001t0002g0082 others(3): Show |
6 | HG01516.hp1 HG03239.hp2 NA18968.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.716-6_716-5delGG | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635826 | |||||||
chr4:69635827 | C | A | 327 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
splice_region_variant&intron_variant | LOW | c.716-5G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635827 | |||||||
chr4:69635828 | C | A | 40 | a0001c0001t0001g0143 a0002c0002t0001g0017 a0002c0002t0001g0065 others(37): Show |
41 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(38): Show |
splice_region_variant&intron_variant | LOW | c.716-6G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA | 27 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(24): Show |
29 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.716-13_716-7dupTTT others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0049 a0001c0001t0001g0059 a0001c0001t0001g0105 others(4): Show |
7 | HG00597.hp2 HG01106.hp2 HG01361.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.716-14_716-7dupTTT others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(2): Show |
5 | a0001c0001t0001g0060 a0001c0001t0003g0014 a0001c0001t0003g0217 others(2): Show |
6 | HG01884.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.716-15_716-7dupTTT others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0003g0326 a0012c0016t0011g0225 |
2 | HG06807.hp1 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.716-16_716-7dupTTT others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0330 | 1 | HG01891.hp1 | splice_region_variant&intron_variant | LOW | c.716-19_716-7dupTTT others(10): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0129 a0001c0001t0001g0220 a0001c0001t0001g0327 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.716-20_716-7dupTTT others(11): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(8): Show |
17 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0123 others(14): Show |
17 | HG01167.hp1 HG01517.hp2 HG02258.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.716-21_716-7dupTTT others(12): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(9): Show |
59 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0024 others(56): Show |
63 | HG00438.hp2 HG01167.hp2 HG01258.hp1 others(60): Show |
splice_region_variant&intron_variant | LOW | c.716-22_716-7dupTTT others(13): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(10): Show |
44 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0026 others(41): Show |
46 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(43): Show |
splice_region_variant&intron_variant | LOW | c.716-23_716-7dupTTT others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(11): Show |
10 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0119 others(7): Show |
10 | HG01261.hp1 HG01358.hp1 HG02818.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.716-24_716-7dupTTT others(15): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0138 a0001c0001t0001g0229 a0001c0001t0001g0234 others(1): Show |
4 | HG02145.hp2 HG02818.hp1 HG03710.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.716-25_716-7dupTTT others(16): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0263 | 1 | HG00544.hp1 | splice_region_variant&intron_variant | LOW | c.716-26_716-7dupTTT others(17): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0319 | 1 | HG01192.hp2 | splice_region_variant&intron_variant | LOW | c.716-27_716-7dupTTT others(18): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635828 | CA | C | 66 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(63): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
splice_region_variant&intron_variant | LOW | c.716-7delT | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635828 | |||||||
chr4:69635830 | A | C | 5 | a0001c0001t0002g0069 a0001c0001t0002g0079 a0001c0001t0002g0082 others(2): Show |
5 | HG03239.hp2 NA18968.hp1 NA18982.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.716-8T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635830 | |||||||
chr4:69635831 | A | C | 1 | a0001c0001t0002g0301 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.716-9T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635831 | |||||||
chr4:69635835 | A | C | 1 | a0001c0001t0006g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.716-13T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635835 | |||||||
chr4:69635849 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0146 a0003c0010t0002g0145 |
2 | HG02165.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.716-28_716-27insCT others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | |||||||
chr4:69635849 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0165 |
2 | NA18968.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.716-28_716-27insCT others(9): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | |||||||
chr4:69635849 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.716-28_716-27insGT others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | |||||||
chr4:69635849 | A | AAAAAAAA others(3): Show |
13 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0035 others(10): Show |
14 | HG00423.hp1 HG01106.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.716-28_716-27insCT others(8): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | |||||||
chr4:69635849 | A | G | 1 | a0001c0001t0006g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.716-27T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | |||||||
chr4:69635849 | AAGAGAG | A | 8 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0348 others(5): Show |
8 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.716-33_716-28delCT others(4): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635849 | |||||||
chr4:69635851 | G | A | 83 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(80): Show |
88 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.716-29C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635851 | |||||||
chr4:69635853 | G | A | 2 | a0002c0002t0001g0195 a0002c0002t0001g0314 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.716-31C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635853 | |||||||
chr4:69635855 | G | A | 2 | a0002c0002t0001g0195 a0002c0002t0001g0314 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.716-33C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635855 | |||||||
chr4:69635960 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.716-138T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69635960 | |||||||
chr4:69636038 | T | C | 12 | a0002c0002t0001g0122 a0002c0002t0001g0324 a0002c0002t0001g0325 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.716-216A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636038 | |||||||
chr4:69636043 | A | G | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.716-221T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636043 | |||||||
chr4:69636069 | A | G | 9 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.716-247T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636069 | |||||||
chr4:69636262 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(268): Show |
286 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.716-440G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636262 | |||||||
chr4:69636278 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.716-456G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636278 | |||||||
chr4:69636375 | G | A | 1 | a0002c0002t0001g0325 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.716-553C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636375 | |||||||
chr4:69636396 | A | G | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.716-574T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636396 | |||||||
chr4:69636527 | GATT | G | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.716-708_716-706del others(3): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636527 | |||||||
chr4:69636564 | C | A | 39 | a0002c0002t0001g0017 a0002c0002t0001g0066 a0002c0002t0001g0073 others(36): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.716-742G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636564 | |||||||
chr4:69636577 | C | A | 5 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.716-755G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636577 | |||||||
chr4:69636668 | T | G | 50 | a0001c0001t0001g0290 a0001c0001t0002g0018 a0001c0001t0002g0192 others(47): Show |
54 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.716-846A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636668 | |||||||
chr4:69636755 | T | A | 43 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(40): Show |
45 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.716-933A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636755 | |||||||
chr4:69636949 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.716-1127G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69636949 | |||||||
chr4:69637061 | G | A | 87 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(84): Show |
92 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.716-1239C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637061 | |||||||
chr4:69637231 | A | G | 1 | a0003c0003t0004g0142 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.716-1409T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637231 | |||||||
chr4:69637537 | C | A | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.716-1715G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637537 | |||||||
chr4:69637657 | C | T | 5 | a0001c0001t0001g0078 a0001c0001t0001g0249 a0001c0001t0001g0250 others(2): Show |
5 | HG02071.hp2 NA18963.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.716-1835G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637657 | |||||||
chr4:69637671 | A | G | 1 | a0001c0001t0006g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.716-1849T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637671 | |||||||
chr4:69637678 | A | G | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.716-1856T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637678 | |||||||
chr4:69637710 | T | G | 1 | a0002c0002t0001g0325 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.716-1888A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637710 | |||||||
chr4:69637729 | C | T | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.716-1907G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637729 | |||||||
chr4:69637757 | G | C | 7 | a0001c0001t0001g0123 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.716-1935C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637757 | |||||||
chr4:69637891 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.716-2069C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637891 | |||||||
chr4:69637908 | AAGGC | A | 28 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0021 others(25): Show |
30 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.716-2090_716-2087d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637908 | |||||||
chr4:69637908 | AAGGCAGG others(5): Show |
A | 3 | a0001c0001t0001g0290 a0001c0001t0002g0204 a0001c0001t0002g0213 |
3 | HG02717.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.716-2098_716-2087d others(14): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637908 | |||||||
chr4:69637997 | C | CAGGA | 6 | a0001c0001t0003g0014 a0001c0001t0003g0113 a0001c0001t0003g0114 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.716-2179_716-2176d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637997 | |||||||
chr4:69637997 | CAGGA | C | 4 | a0002c0002t0001g0122 a0002c0002t0008g0289 a0002c0002t0008g0348 others(1): Show |
4 | HG01109.hp2 HG01175.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-2179_716-2176d others(6): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69637997 | |||||||
chr4:69638001 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.716-2179T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638001 | |||||||
chr4:69638076 | G | T | 81 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0051 others(78): Show |
86 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.716-2254C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638076 | |||||||
chr4:69638184 | G | A | 1 | a0002c0002t0001g0295 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.716-2362C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638184 | |||||||
chr4:69638260 | G | C | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.716-2438C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638260 | |||||||
chr4:69638305 | G | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0139 |
3 | NA18985.hp1 NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.716-2483C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638305 | |||||||
chr4:69638309 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.716-2487T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638309 | |||||||
chr4:69638402 | T | C | 6 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-2580A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638402 | |||||||
chr4:69638488 | T | C | 1 | a0001c0001t0002g0170 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.716-2666A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638488 | |||||||
chr4:69638571 | T | C | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.716-2749A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638571 | |||||||
chr4:69638595 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(149): Show |
159 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.716-2773A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638595 | |||||||
chr4:69638640 | G | T | 1 | a0001c0001t0001g0330 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.716-2818C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638640 | |||||||
chr4:69638910 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.716-3088G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69638910 | |||||||
chr4:69639033 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.716-3211C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639033 | |||||||
chr4:69639105 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.716-3283C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639105 | |||||||
chr4:69639168 | G | A | 1 | a0003c0003t0002g0340 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.716-3346C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639168 | |||||||
chr4:69639318 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0272 |
3 | HG02886.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.716-3496C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639318 | |||||||
chr4:69639444 | G | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0033 others(14): Show |
19 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.716-3622C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639444 | |||||||
chr4:69639637 | C | T | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.716-3815G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639637 | |||||||
chr4:69639722 | G | A | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.716-3900C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639722 | |||||||
chr4:69639747 | A | G | 2 | a0002c0002t0001g0065 a0005c0005t0005g0284 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.716-3925T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639747 | |||||||
chr4:69639829 | A | G | 2 | a0009c0013t0007g0345 a0010c0012t0007g0202 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.716-4007T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639829 | |||||||
chr4:69639861 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.716-4039C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69639861 | |||||||
chr4:69640139 | C | A | 47 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(44): Show |
49 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.716-4317G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640139 | |||||||
chr4:69640186 | T | C | 49 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(46): Show |
51 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.716-4364A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640186 | |||||||
chr4:69640303 | A | AT | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(271): Show |
288 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.716-4482_716-4481i others(3): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640303 | |||||||
chr4:69640308 | T | C | 3 | a0001c0001t0002g0079 a0001c0001t0002g0084 a0001c0001t0002g0099 |
3 | NA18945.hp2 NA18968.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.716-4486A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640308 | |||||||
chr4:69640340 | T | C | 50 | a0001c0001t0001g0290 a0001c0001t0002g0018 a0001c0001t0002g0192 others(47): Show |
54 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.716-4518A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640340 | |||||||
chr4:69640348 | G | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.716-4526C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640348 | |||||||
chr4:69640388 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.716-4566C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640388 | |||||||
chr4:69640402 | G | A | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.716-4580C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640402 | |||||||
chr4:69640454 | G | A | 1 | a0002c0002t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.716-4632C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640454 | |||||||
chr4:69640665 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(271): Show |
288 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.716-4843C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640665 | |||||||
chr4:69640722 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.716-4900G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640722 | |||||||
chr4:69640761 | G | C | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.716-4939C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640761 | |||||||
chr4:69640800 | T | C | 98 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(95): Show |
104 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.716-4978A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640800 | |||||||
chr4:69640804 | C | A | 1 | a0001c0001t0002g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.716-4982G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640804 | |||||||
chr4:69640825 | A | T | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.716-5003T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69640825 | |||||||
chr4:69641110 | A | G | 49 | a0001c0001t0001g0290 a0001c0001t0002g0018 a0001c0001t0002g0192 others(46): Show |
53 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.716-5288T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641110 | |||||||
chr4:69641160 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0230 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.716-5338G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641160 | |||||||
chr4:69641169 | C | A | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.716-5347G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641169 | |||||||
chr4:69641197 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.716-5375T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641197 | |||||||
chr4:69641215 | C | T | 14 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(11): Show |
14 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.716-5393G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641215 | |||||||
chr4:69641238 | A | T | 1 | a0001c0001t0001g0281 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.716-5416T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641238 | |||||||
chr4:69641301 | T | C | 40 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0077 others(37): Show |
40 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.716-5479A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641301 | |||||||
chr4:69641340 | C | G | 96 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(93): Show |
102 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.716-5518G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641340 | |||||||
chr4:69641438 | G | T | 95 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(92): Show |
101 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.715+5492C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641438 | |||||||
chr4:69641461 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(148): Show |
158 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.715+5469G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641461 | |||||||
chr4:69641702 | C | T | 3 | a0001c0007t0001g0106 a0001c0007t0001g0211 a0003c0009t0002g0212 |
3 | HG02602.hp2 HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.715+5228G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641702 | |||||||
chr4:69641824 | A | C | 1 | a0001c0001t0002g0084 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.715+5106T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641824 | |||||||
chr4:69641827 | C | G | 5 | a0002c0002t0001g0017 a0002c0002t0001g0073 a0002c0002t0001g0195 others(2): Show |
6 | HG00733.hp1 HG01516.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.715+5103G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69641827 | |||||||
chr4:69642076 | C | T | 90 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0051 others(87): Show |
95 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.715+4854G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642076 | |||||||
chr4:69642143 | C | T | 1 | a0001c0001t0003g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.715+4787G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642143 | |||||||
chr4:69642346 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.715+4584A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642346 | |||||||
chr4:69642434 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | NA18612.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.715+4496T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642434 | |||||||
chr4:69642610 | T | C | 1 | a0001c0001t0002g0101 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715+4320A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642610 | |||||||
chr4:69642752 | A | G | 1 | a0006c0008t0001g0064 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.715+4178T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642752 | |||||||
chr4:69642953 | T | A | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715+3977A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69642953 | |||||||
chr4:69643151 | T | C | 62 | a0001c0001t0001g0290 a0001c0001t0001g0306 a0001c0001t0002g0018 others(59): Show |
66 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.715+3779A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643151 | |||||||
chr4:69643160 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(248): Show |
264 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(261): Show |
intron_variant | MODIFIER | c.715+3770C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643160 | |||||||
chr4:69643171 | A | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+3759T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643171 | |||||||
chr4:69643189 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0205 |
2 | NA19003.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.715+3741G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643189 | |||||||
chr4:69643414 | A | G | 5 | a0004c0004t0001g0039 a0004c0004t0001g0181 a0004c0004t0001g0219 others(2): Show |
5 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+3516T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643414 | |||||||
chr4:69643468 | T | C | 11 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.715+3462A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643468 | |||||||
chr4:69643519 | T | G | 61 | a0001c0001t0001g0290 a0001c0001t0001g0306 a0001c0001t0002g0018 others(58): Show |
65 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.715+3411A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643519 | |||||||
chr4:69643739 | T | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(32): Show |
37 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.715+3191A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643739 | |||||||
chr4:69643812 | A | C | 21 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
23 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.715+3118T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643812 | |||||||
chr4:69643996 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0223 |
2 | HG00738.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.715+2934A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69643996 | |||||||
chr4:69644284 | T | G | 1 | a0001c0001t0001g0342 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.715+2646A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644284 | |||||||
chr4:69644360 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.715+2570A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644360 | |||||||
chr4:69644440 | T | C | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+2490A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644440 | |||||||
chr4:69644446 | C | T | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.715+2484G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644446 | |||||||
chr4:69644457 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.715+2473G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644457 | |||||||
chr4:69644570 | T | G | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+2360A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644570 | |||||||
chr4:69644607 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.715+2323G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644607 | |||||||
chr4:69644691 | CTCT | C | 7 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0005c0005t0002g0206 others(4): Show |
7 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.715+2236_715+2238d others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644691 | |||||||
chr4:69644799 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.715+2131C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644799 | |||||||
chr4:69644847 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0327 others(1): Show |
4 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+2083G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644847 | |||||||
chr4:69644911 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+2019C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644911 | |||||||
chr4:69644930 | T | C | 20 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(17): Show |
22 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.715+2000A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69644930 | |||||||
chr4:69645000 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+1930G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645000 | |||||||
chr4:69645034 | T | C | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715+1896A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645034 | |||||||
chr4:69645072 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.715+1858G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645072 | |||||||
chr4:69645166 | G | A | 1 | a0002c0002t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.715+1764C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645166 | |||||||
chr4:69645482 | G | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0033 others(14): Show |
19 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.715+1448C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645482 | |||||||
chr4:69645628 | TCTCAA | T | 7 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0005c0005t0002g0206 others(4): Show |
7 | HG02717.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.715+1297_715+1301d others(7): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645628 | |||||||
chr4:69645709 | G | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(271): Show |
289 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.715+1221C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645709 | |||||||
chr4:69645842 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.715+1088C>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645842 | |||||||
chr4:69645907 | T | C | 18 | a0004c0004t0001g0039 a0004c0004t0001g0061 a0004c0004t0001g0062 others(15): Show |
18 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.715+1023A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645907 | |||||||
chr4:69645928 | A | C | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715+1002T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69645928 | |||||||
chr4:69646075 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.715+855A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646075 | |||||||
chr4:69646078 | A | T | 1 | a0001c0001t0002g0082 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.715+852T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646078 | |||||||
chr4:69646288 | T | G | 48 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0047 others(45): Show |
50 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.715+642A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646288 | |||||||
chr4:69646347 | C | T | 1 | a0005c0005t0005g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715+583G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646347 | |||||||
chr4:69646354 | A | G | 1 | a0006c0006t0002g0080 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.715+576T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646354 | |||||||
chr4:69646382 | T | C | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.715+548A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646382 | |||||||
chr4:69646395 | G | A | 51 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0030 others(48): Show |
51 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.715+535C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646395 | |||||||
chr4:69646430 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0235 a0001c0001t0001g0335 |
3 | HG02258.hp2 HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.715+500G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646430 | |||||||
chr4:69646590 | C | T | 1 | a0005c0005t0005g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.715+340G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646590 | |||||||
chr4:69646816 | A | G | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.715+114T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646816 | |||||||
chr4:69646892 | T | G | 2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.715+38A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 2/6 | chr4 | 69646892 | |||||||
chr4:69647833 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(146): Show |
156 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.-54-135C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69647833 | |||||||
chr4:69647875 | G | A | 8 | a0001c0001t0001g0112 a0001c0001t0003g0014 a0001c0001t0003g0113 others(5): Show |
9 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-54-177C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69647875 | |||||||
chr4:69647979 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02280.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-54-281A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69647979 | |||||||
chr4:69647992 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(239): Show |
254 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.-54-294G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69647992 | |||||||
chr4:69648129 | A | C | 2 | a0004c0004t0001g0061 a0004c0004t0001g0062 |
2 | HG01496.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-54-431T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648129 | |||||||
chr4:69648170 | T | G | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-472A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648170 | |||||||
chr4:69648174 | T | C | 44 | a0001c0001t0001g0306 a0002c0002t0001g0017 a0002c0002t0001g0065 others(41): Show |
47 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-54-476A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648174 | |||||||
chr4:69648251 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-54-553G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648251 | |||||||
chr4:69648268 | C | T | 1 | a0001c0017t0001g0274 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-54-570G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648268 | |||||||
chr4:69648307 | C | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(268): Show |
286 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.-54-609G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648307 | |||||||
chr4:69648505 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-54-807C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648505 | |||||||
chr4:69648524 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-54-826A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648524 | |||||||
chr4:69648553 | G | A | 4 | a0001c0001t0001g0164 a0001c0001t0001g0265 a0001c0001t0001g0343 others(1): Show |
4 | HG01952.hp1 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54-855C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648553 | |||||||
chr4:69648640 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(149): Show |
160 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.-54-942G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648640 | |||||||
chr4:69648650 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-54-952A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648650 | |||||||
chr4:69648770 | A | G | 6 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54-1072T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648770 | |||||||
chr4:69648995 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-54-1297T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69648995 | |||||||
chr4:69649047 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-54-1349C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649047 | |||||||
chr4:69649047 | G | T | 1 | a0001c0001t0002g0079 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-54-1349C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649047 | |||||||
chr4:69649093 | G | A | 63 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(60): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-54-1395C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649093 | |||||||
chr4:69649094 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
7 | HG01993.hp1 HG02027.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-54-1396G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649094 | |||||||
chr4:69649111 | T | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(150): Show |
161 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.-54-1413A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649111 | |||||||
chr4:69649185 | C | G | 44 | a0001c0001t0001g0306 a0002c0002t0001g0017 a0002c0002t0001g0065 others(41): Show |
47 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-54-1487G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649185 | |||||||
chr4:69649243 | A | G | 4 | a0002c0002t0001g0324 a0002c0002t0001g0325 a0002c0002t0008g0289 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54-1545T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649243 | |||||||
chr4:69649290 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-1592C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649290 | |||||||
chr4:69649307 | T | G | 78 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(75): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-54-1609A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649307 | |||||||
chr4:69649423 | A | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG00609.hp1 HG02155.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-1725T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649423 | |||||||
chr4:69649448 | T | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-1750A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649448 | |||||||
chr4:69649449 | A | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-1751T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649449 | |||||||
chr4:69649589 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-54-1891T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649589 | |||||||
chr4:69649620 | T | G | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-54-1922A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649620 | |||||||
chr4:69649646 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-54-1948C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649646 | |||||||
chr4:69649685 | C | T | 7 | a0005c0005t0002g0206 a0005c0005t0002g0271 a0005c0005t0002g0291 others(4): Show |
7 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54-1987G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649685 | |||||||
chr4:69649793 | C | A | 1 | a0004c0004t0001g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-54-2095G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649793 | |||||||
chr4:69649871 | G | A | 10 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54-2173C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69649871 | |||||||
chr4:69650070 | T | C | 63 | a0001c0001t0001g0290 a0001c0001t0001g0306 a0001c0001t0002g0018 others(60): Show |
67 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.-54-2372A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650070 | |||||||
chr4:69650242 | G | A | 1 | a0011c0015t0001g0166 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-54-2544C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650242 | |||||||
chr4:69650390 | T | A | 1 | a0002c0002t0003g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-54-2692A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650390 | |||||||
chr4:69650395 | T | A | 1 | a0001c0007t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-54-2697A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650395 | |||||||
chr4:69650507 | A | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0120 others(6): Show |
9 | HG01261.hp1 HG02056.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-55+2681T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650507 | |||||||
chr4:69650609 | A | T | 63 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(60): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-55+2579T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650609 | |||||||
chr4:69650683 | C | T | 1 | a0004c0004t0001g0193 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-55+2505G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650683 | |||||||
chr4:69650713 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(205): Show |
219 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.-55+2475G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650713 | |||||||
chr4:69650790 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(172): Show |
185 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.-55+2398A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650790 | |||||||
chr4:69650791 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | NA18960.hp1 NA18970.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-55+2397C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650791 | |||||||
chr4:69650802 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(151): Show |
162 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.-55+2386C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650802 | |||||||
chr4:69650805 | A | G | 1 | a0003c0003t0002g0296 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-55+2383T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650805 | |||||||
chr4:69650953 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(149): Show |
160 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.-55+2235G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69650953 | |||||||
chr4:69651018 | A | G | 1 | a0003c0003t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-55+2170T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651018 | |||||||
chr4:69651042 | G | A | 44 | a0001c0001t0001g0306 a0002c0002t0001g0017 a0002c0002t0001g0065 others(41): Show |
47 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-55+2146C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651042 | |||||||
chr4:69651088 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-55+2100G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651088 | |||||||
chr4:69651160 | C | T | 1 | a0001c0001t0001g0016 | 2 | NA18988.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-55+2028G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651160 | |||||||
chr4:69651390 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(151): Show |
163 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.-55+1798G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651390 | |||||||
chr4:69651425 | G | A | 43 | a0002c0002t0001g0017 a0002c0002t0001g0065 a0002c0002t0001g0066 others(40): Show |
46 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-55+1763C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651425 | |||||||
chr4:69651430 | A | T | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-55+1758T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651430 | |||||||
chr4:69651480 | C | T | 2 | a0001c0001t0001g0333 a0003c0003t0002g0334 |
2 | HG02451.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-55+1708G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651480 | |||||||
chr4:69651744 | C | G | 2 | a0002c0002t0001g0195 a0002c0002t0001g0314 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-55+1444G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651744 | |||||||
chr4:69651794 | T | C | 2 | a0002c0002t0008g0289 a0002c0002t0008g0348 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-55+1394A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651794 | |||||||
chr4:69651823 | A | C | 9 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-55+1365T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651823 | |||||||
chr4:69651932 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0226 |
2 | NA18954.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-55+1256G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69651932 | |||||||
chr4:69652074 | C | G | 4 | a0004c0004t0001g0039 a0004c0004t0001g0181 a0004c0004t0001g0285 others(1): Show |
4 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-55+1114G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652074 | |||||||
chr4:69652184 | G | GT | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(237): Show |
255 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.-55+1003dupA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652184 | |||||||
chr4:69652234 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(165): Show |
180 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-55+954A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652234 | |||||||
chr4:69652282 | C | CT | 18 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(15): Show |
18 | HG01109.hp2 HG01243.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.-55+905dupA | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652282 | |||||||
chr4:69652282 | C | CTT | 77 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0078 others(74): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-55+904_-55+905dup others(2): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652282 | |||||||
chr4:69652282 | C | CTTT | 86 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0041 others(83): Show |
90 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-55+903_-55+905dup others(3): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652282 | |||||||
chr4:69652282 | C | CTTTTT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(16): Show |
21 | HG00140.hp1 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-55+901_-55+905dup others(5): Show |
UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652282 | |||||||
chr4:69652368 | C | G | 1 | a0003c0003t0002g0296 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-55+820G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652368 | |||||||
chr4:69652388 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-55+800T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652388 | |||||||
chr4:69652441 | A | T | 1 | a0001c0001t0002g0297 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-55+747T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652441 | |||||||
chr4:69652452 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-55+736A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652452 | |||||||
chr4:69652466 | T | C | 1 | a0001c0001t0001g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-55+722A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652466 | |||||||
chr4:69652542 | A | G | 3 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 |
3 | NA18951.hp2 NA18984.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-55+646T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652542 | |||||||
chr4:69652562 | C | T | 2 | a0003c0003t0002g0296 a0004c0004t0001g0181 |
2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-55+626G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652562 | |||||||
chr4:69652626 | A | G | 3 | a0001c0001t0001g0026 a0002c0002t0001g0295 a0005c0005t0005g0284 |
3 | HG02004.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-55+562T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652626 | |||||||
chr4:69652667 | T | G | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0272 others(3): Show |
6 | HG01243.hp1 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-55+521A>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652667 | |||||||
chr4:69652741 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-55+447G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652741 | |||||||
chr4:69652767 | A | G | 1 | a0005c0005t0002g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-55+421T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652767 | |||||||
chr4:69652881 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | HG02155.hp2 NA18948.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-55+307T>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652881 | |||||||
chr4:69652976 | G | A | 4 | a0001c0001t0001g0349 a0001c0001t0001g0350 a0002c0002t0001g0347 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-55+212C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652976 | |||||||
chr4:69652994 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0180 a0001c0001t0001g0275 others(10): Show |
15 | HG01123.hp2 HG01361.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.-55+194A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69652994 | |||||||
chr4:69653025 | C | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(181): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-55+163G>C | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653025 | |||||||
chr4:69653036 | G | A | 69 | a0001c0001t0001g0019 a0001c0001t0001g0290 a0001c0001t0001g0298 others(66): Show |
71 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-55+152C>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653036 | |||||||
chr4:69653130 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-55+58T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653130 | |||||||
chr4:69653133 | A | T | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+55T>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653133 | |||||||
chr4:69653138 | T | A | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+50A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653138 | |||||||
chr4:69653155 | T | A | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+33A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653155 | |||||||
chr4:69653159 | G | T | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+29C>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653159 | |||||||
chr4:69653161 | T | A | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+27A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653161 | |||||||
chr4:69653162 | T | A | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+26A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653162 | |||||||
chr4:69653175 | T | C | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+13A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653175 | |||||||
chr4:69653176 | C | T | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-55+12G>A | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653176 | |||||||
chr4:69653180 | T | C | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.-55+8A>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653180 | |||||||
chr4:69653181 | T | A | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.-55+7A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653181 | |||||||
chr4:69653185 | T | A | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.-55+3A>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653185 | |||||||
chr4:69653186 | A | C | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | splice_donor_variant&intron_variant | HIGH | c.-55+2T>G | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653186 | |||||||
chr4:69653187 | C | A | 1 | a0001c0001t0009g0020 | 1 | HG01192.hp1 | splice_donor_variant&intron_variant | HIGH | c.-55+1G>T | UGT2A1 | ENSG00000173610.13 | transcript | ENST00000286604.9 | protein_coding | 1/6 | chr4 | 69653187 |