Item | Value |
---|---|
geneid | 57147 |
ensemblid | ENSG00000000457.14 |
hgncid | 19285 |
symbol | SCYL3 |
name | SCY1 like pseudokinase 3 |
refseq_nuc | NM_020423.7 |
refseq_prot | NP_065156.5 |
ensembl_nuc | ENST00000367771.11 |
ensembl_prot | ENSP00000356745.5 |
mane_status | MANE Select |
chr | chr1 |
start | 169849631 |
end | 169893896 |
strand | - |
ver | v1.2 |
region | chr1:169849631-169893896 |
region5000 | chr1:169844631-169898896 |
regionname0 | SCYL3_chr1_169849631_169893896 |
regionname5000 | SCYL3_chr1_169844631_169898896 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 688 | 293 | 73 | 42 | 132 | 11 | 34 | 104 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
a0002 | 1/0 | 688 | 92 | 7 | 15 | 61 | 3 | 5 | 43 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
a0003 | 0/0 | 688 | 16 | 0 | 6 | 5 | 2 | 3 | 3 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
a0004 | 0/0 | 688 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
a0005 | 0/0 | 688 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
a0006 | 0/0 | 688 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
a0007 | 0/0 | 688 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
a0008 | 0/0 | 688 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
a0009 | 0/0 | 688 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | MGSEN others(683): Show |
chr1 | 169844631 | 169898896 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2064 | 254 | 53 | 32 | 132 | 7 | 29 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0001c0003 | 0/0 | 2064 | 32 | 14 | 10 | 0 | 4 | 4 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0001c0006 | 0/0 | 2064 | 3 | 3 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0001c0007 | 0/0 | 2064 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0001c0010 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0001c0016 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0002c0002 | 1/0 | 2064 | 91 | 6 | 15 | 61 | 3 | 5 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0002c0015 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0003c0004 | 0/0 | 2064 | 15 | 0 | 5 | 5 | 2 | 3 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0003c0011 | 0/0 | 2064 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0004c0005 | 0/0 | 2064 | 12 | 12 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0005c0012 | 0/0 | 2064 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0006c0008 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0007c0009 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0008c0014 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 | ||
a0009c0013 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | ATGGG others(2059): Show |
chr1 | 169844631 | 169898896 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6311 | 67 | 13 | 4 | 33 | 5 | 12 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0003 | 0/0 | 6320 | 58 | 3 | 2 | 48 | 1 | 4 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6315): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0005 | 0/0 | 6316 | 17 | 0 | 5 | 11 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6311): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0007 | 0/0 | 6315 | 12 | 1 | 3 | 7 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6310): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0008 | 0/0 | 6317 | 10 | 0 | 4 | 3 | 0 | 3 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6312): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0009 | 0/0 | 6304 | 10 | 0 | 8 | 0 | 1 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6299): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0011 | 0/0 | 6311 | 9 | 4 | 0 | 3 | 0 | 2 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0012 | 0/0 | 6311 | 6 | 0 | 3 | 0 | 0 | 3 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0013 | 0/0 | 6311 | 7 | 6 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0014 | 0/0 | 6318 | 6 | 0 | 2 | 3 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6313): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0015 | 0/0 | 6311 | 5 | 5 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0016 | 0/0 | 6322 | 5 | 0 | 0 | 5 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6317): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0017 | 0/0 | 6320 | 4 | 4 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6315): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0019 | 0/0 | 6311 | 3 | 0 | 0 | 3 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0021 | 0/0 | 6312 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6307): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0022 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0023 | 0/0 | 6320 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6315): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0028 | 0/0 | 6323 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6318): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0029 | 0/0 | 6315 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6310): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0030 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6309): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0031 | 0/0 | 6312 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6307): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0034 | 0/0 | 6316 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6311): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0035 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6309): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0036 | 0/0 | 6320 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6315): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0037 | 0/0 | 6320 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6315): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0038 | 0/0 | 6320 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6315): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0039 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6319): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0040 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6318): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0047 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6310): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0048 | 0/0 | 6316 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6311): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0049 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0050 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0052 | 0/0 | 6341 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6336): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0053 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6329): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0054 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6329): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0055 | 0/0 | 6332 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6327): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0056 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6325): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0057 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6322): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0058 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6319): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0059 | 0/0 | 6321 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6316): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0060 | 0/0 | 6317 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6312): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0061 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0001t0064 | 0/1 | 6287 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6282): Show |
chr1 | 169844631 | 169898896 |
a0001c0003t0004 | 0/0 | 6311 | 30 | 13 | 10 | 0 | 3 | 4 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0003t0015 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0003t0051 | 0/0 | 6248 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6243): Show |
chr1 | 169844631 | 169898896 |
a0001c0006t0002 | 0/0 | 6311 | 3 | 3 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0007t0012 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0007t0062 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0010t0004 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0001c0016t0063 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6307): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0001 | 1/0 | 6308 | 74 | 2 | 9 | 56 | 3 | 3 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0010 | 0/0 | 6308 | 7 | 1 | 2 | 2 | 0 | 2 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0026 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0027 | 0/0 | 6308 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0032 | 0/0 | 6308 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0041 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6308): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0042 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6307): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0066 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0067 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0002c0002t0068 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0002c0015t0046 | 0/0 | 6308 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0003c0004t0006 | 0/0 | 6244 | 12 | 0 | 4 | 5 | 0 | 3 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6239): Show |
chr1 | 169844631 | 169898896 |
a0003c0004t0020 | 0/0 | 6244 | 2 | 0 | 0 | 0 | 2 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6239): Show |
chr1 | 169844631 | 169898896 |
a0003c0004t0033 | 0/0 | 6245 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6240): Show |
chr1 | 169844631 | 169898896 |
a0003c0011t0001 | 0/0 | 6308 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0004c0005t0010 | 0/0 | 6308 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0004c0005t0018 | 0/0 | 6315 | 4 | 4 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6310): Show |
chr1 | 169844631 | 169898896 |
a0004c0005t0024 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6309): Show |
chr1 | 169844631 | 169898896 |
a0004c0005t0025 | 0/0 | 6313 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6308): Show |
chr1 | 169844631 | 169898896 |
a0004c0005t0043 | 0/0 | 6319 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6314): Show |
chr1 | 169844631 | 169898896 |
a0004c0005t0044 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6307): Show |
chr1 | 169844631 | 169898896 |
a0004c0005t0065 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6308): Show |
chr1 | 169844631 | 169898896 |
a0005c0012t0045 | 0/0 | 6309 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6304): Show |
chr1 | 169844631 | 169898896 |
a0006c0008t0004 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0007c0009t0010 | 0/0 | 6308 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6303): Show |
chr1 | 169844631 | 169898896 |
a0008c0014t0002 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6306): Show |
chr1 | 169844631 | 169898896 |
a0009c0013t0030 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | GTAGT others(6309): Show |
chr1 | 169844631 | 169898896 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0002 | 0/0 | 20 | 0 | 1 | 12 | 3 | 4 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0003 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0004 | 0/0 | 8 | 2 | 0 | 3 | 0 | 3 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0007g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0007g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0007g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0007g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0008g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0009g0006 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0009g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0009g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0011g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0011g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0011g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0011g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0011g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0012g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0012g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0012g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0012g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0012g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0013g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0013g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0013g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0013g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0013g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0014g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0014g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0014g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0014g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0014g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0015g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0015g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0015g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0016g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0016g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0016g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0016g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0017g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0019g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0021g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0021g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0022g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0022g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0023g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0023g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0028g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0028g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0029g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0029g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0030g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0031g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0031g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0034g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0035g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0036g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0037g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0038g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0039g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0040g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0047g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0048g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0049g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0050g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0052g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0053g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0054g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0055g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0056g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0057g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0058g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0059g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0060g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0061g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0001t0064g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0015g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0003t0051g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0006t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0006t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0006t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0007t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0007t0062g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0010t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0001c0016t0063g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0001 | 0/0 | 22 | 0 | 0 | 22 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0008 | 1/0 | 5 | 0 | 1 | 0 | 2 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0010 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0010g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0010g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0010g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0010g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0026g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0026g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0027g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0032g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0041g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0042g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0066g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0067g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0002t0068g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0002c0015t0046g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0020g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0004t0033g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0003c0011t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0010g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0018g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0018g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0018g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0018g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0024g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0024g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0025g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0025g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0043g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0044g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0004c0005t0065g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0005c0012t0045g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0006c0008t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0007c0009t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0008c0014t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
a0009c0013t0030g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0003 | t0004 | g0200 | EUR | GBR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00140 | hp2 | a0001 | c0003 | t0004 | g0044 | EUR | GBR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0165 | EUR | FIN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0008 | EUR | FIN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00323 | hp1 | a0001 | c0001 | t0009 | g0006 | EUR | FIN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0145 | EUR | FIN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00408 | hp2 | a0001 | c0001 | t0007 | g0249 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00438 | hp1 | a0001 | c0001 | t0036 | g0058 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00544 | hp1 | a0002 | c0002 | t0010 | g0027 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00544 | hp2 | a0001 | c0001 | t0029 | g0086 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00597 | hp2 | a0001 | c0001 | t0011 | g0047 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0261 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00642 | hp1 | a0001 | c0003 | t0004 | g0207 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0235 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | CHS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0252 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0197 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00735 | hp1 | a0002 | c0002 | t0010 | g0110 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00735 | hp2 | a0001 | c0003 | t0004 | g0194 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG00741 | hp2 | a0003 | c0004 | t0033 | g0210 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01069 | hp1 | a0001 | c0003 | t0004 | g0040 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01069 | hp2 | a0002 | c0002 | t0027 | g0028 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01071 | hp1 | a0002 | c0002 | t0027 | g0028 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01071 | hp2 | a0001 | c0003 | t0004 | g0040 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01074 | hp1 | a0001 | c0001 | t0012 | g0209 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01081 | hp1 | a0001 | c0003 | t0004 | g0039 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01099 | hp1 | a0003 | c0011 | t0001 | g0220 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01099 | hp2 | a0001 | c0003 | t0004 | g0039 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01109 | hp1 | a0002 | c0002 | t0010 | g0103 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01109 | hp2 | a0005 | c0012 | t0045 | g0123 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01167 | hp2 | a0001 | c0001 | t0012 | g0208 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01168 | hp1 | a0003 | c0004 | t0006 | g0045 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01169 | hp1 | a0003 | c0004 | t0006 | g0045 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0258 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01192 | hp2 | a0001 | c0001 | t0013 | g0075 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01243 | hp2 | a0002 | c0002 | t0042 | g0227 | AMR | PUR | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01255 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01256 | hp1 | a0001 | c0003 | t0004 | g0198 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0274 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01257 | hp1 | a0001 | c0001 | t0009 | g0006 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01258 | hp1 | a0001 | c0001 | t0014 | g0273 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01261 | hp1 | a0001 | c0001 | t0014 | g0049 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01358 | hp2 | a0001 | c0001 | t0009 | g0037 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01361 | hp2 | a0003 | c0004 | t0006 | g0211 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01433 | hp1 | a0001 | c0003 | t0004 | g0196 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | IBS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01516 | hp1 | a0003 | c0004 | t0020 | g0046 | EUR | IBS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | IBS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01517 | hp1 | a0003 | c0004 | t0020 | g0046 | EUR | IBS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01884 | hp1 | a0001 | c0001 | t0015 | g0026 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01891 | hp1 | a0001 | c0003 | t0004 | g0043 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01978 | hp1 | a0001 | c0003 | t0004 | g0195 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0276 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0011 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01981 | hp2 | a0003 | c0004 | t0006 | g0214 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02004 | hp2 | a0001 | c0001 | t0009 | g0166 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02027 | hp1 | a0001 | c0001 | t0011 | g0047 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02040 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02055 | hp1 | a0001 | c0003 | t0004 | g0193 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02055 | hp2 | a0001 | c0001 | t0013 | g0076 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02074 | hp2 | a0003 | c0004 | t0006 | g0017 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0262 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02132 | hp1 | a0001 | c0001 | t0014 | g0263 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02145 | hp1 | a0001 | c0007 | t0012 | g0098 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02145 | hp2 | a0004 | c0005 | t0018 | g0233 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | CDX | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CDX | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02257 | hp1 | a0001 | c0016 | t0063 | g0082 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02258 | hp1 | a0004 | c0005 | t0018 | g0231 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02258 | hp2 | a0001 | c0003 | t0004 | g0206 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02273 | hp1 | a0001 | c0001 | t0009 | g0006 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02273 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02280 | hp1 | a0001 | c0001 | t0021 | g0187 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02280 | hp2 | a0001 | c0001 | t0031 | g0179 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02293 | hp1 | a0002 | c0002 | t0032 | g0131 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02293 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | PEL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02451 | hp1 | a0001 | c0001 | t0017 | g0013 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02451 | hp2 | a0001 | c0001 | t0049 | g0248 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02523 | hp2 | a0003 | c0004 | t0006 | g0017 | EAS | KHV | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02572 | hp1 | a0004 | c0005 | t0025 | g0234 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02622 | hp2 | a0004 | c0005 | t0010 | g0230 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02630 | hp1 | a0006 | c0008 | t0004 | g0186 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02630 | hp2 | a0001 | c0001 | t0021 | g0151 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02647 | hp1 | a0002 | c0002 | t0041 | g0226 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02647 | hp2 | a0001 | c0003 | t0004 | g0185 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02683 | hp2 | a0001 | c0003 | t0004 | g0038 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02717 | hp1 | a0001 | c0001 | t0047 | g0246 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02717 | hp2 | a0001 | c0001 | t0013 | g0073 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02723 | hp1 | a0001 | c0003 | t0004 | g0043 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02723 | hp2 | a0001 | c0006 | t0002 | g0159 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02735 | hp1 | a0001 | c0001 | t0008 | g0255 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02738 | hp2 | a0001 | c0003 | t0004 | g0190 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02809 | hp1 | a0001 | c0001 | t0013 | g0079 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02818 | hp2 | a0001 | c0003 | t0004 | g0042 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02886 | hp1 | a0001 | c0003 | t0004 | g0204 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02886 | hp2 | a0001 | c0006 | t0002 | g0174 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02895 | hp1 | a0007 | c0009 | t0010 | g0104 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02895 | hp2 | a0001 | c0003 | t0004 | g0042 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02896 | hp1 | a0004 | c0005 | t0024 | g0229 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02896 | hp2 | a0002 | c0002 | t0026 | g0106 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02897 | hp1 | a0002 | c0002 | t0026 | g0105 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02897 | hp2 | a0001 | c0003 | t0004 | g0205 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02922 | hp1 | a0004 | c0005 | t0018 | g0232 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0074 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02965 | hp1 | a0001 | c0001 | t0017 | g0064 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02970 | hp1 | a0004 | c0005 | t0043 | g0080 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02970 | hp2 | a0001 | c0001 | t0023 | g0065 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02976 | hp1 | a0002 | c0015 | t0046 | g0222 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02976 | hp2 | a0001 | c0001 | t0015 | g0162 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03017 | hp1 | a0001 | c0001 | t0012 | g0095 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03041 | hp1 | a0004 | c0005 | t0024 | g0228 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03041 | hp2 | a0001 | c0001 | t0015 | g0026 | AFR | GWD | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03098 | hp1 | a0002 | c0002 | t0010 | g0102 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03098 | hp2 | a0001 | c0001 | t0039 | g0067 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0203 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0013 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03195 | hp1 | a0004 | c0005 | t0018 | g0223 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03209 | hp2 | a0004 | c0005 | t0025 | g0224 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03239 | hp1 | a0003 | c0004 | t0006 | g0213 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03239 | hp2 | a0001 | c0001 | t0011 | g0257 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03453 | hp1 | a0001 | c0001 | t0022 | g0152 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03453 | hp2 | a0001 | c0001 | t0023 | g0068 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03486 | hp1 | a0004 | c0005 | t0065 | g0217 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03486 | hp2 | a0001 | c0003 | t0004 | g0201 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03491 | hp2 | a0003 | c0004 | t0006 | g0212 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0154 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03516 | hp2 | a0001 | c0001 | t0040 | g0066 | AFR | ESN | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03579 | hp1 | a0001 | c0001 | t0055 | g0182 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03579 | hp2 | a0001 | c0007 | t0062 | g0097 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03654 | hp2 | a0001 | c0001 | t0052 | g0089 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03688 | hp1 | a0008 | c0014 | t0002 | g0168 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03688 | hp2 | a0001 | c0001 | t0012 | g0093 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03704 | hp2 | a0009 | c0013 | t0030 | g0087 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03710 | hp1 | a0002 | c0002 | t0010 | g0129 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03710 | hp2 | a0001 | c0003 | t0004 | g0038 | SAS | PJL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03831 | hp1 | a0001 | c0003 | t0004 | g0041 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0247 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03834 | hp2 | a0001 | c0001 | t0007 | g0251 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03927 | hp2 | a0001 | c0001 | t0014 | g0049 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0265 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04115 | hp1 | a0001 | c0001 | t0012 | g0100 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04115 | hp2 | a0001 | c0001 | t0009 | g0037 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04184 | hp2 | a0001 | c0001 | t0008 | g0138 | SAS | BEB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04199 | hp1 | a0001 | c0001 | t0011 | g0256 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04199 | hp2 | a0003 | c0004 | t0006 | g0215 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04204 | hp1 | a0001 | c0010 | t0004 | g0191 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | STU | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18522 | hp1 | a0001 | c0001 | t0015 | g0101 | AFR | YRI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18522 | hp2 | a0001 | c0006 | t0002 | g0158 | AFR | YRI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | CHB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18747 | hp2 | a0002 | c0002 | t0066 | g0121 | EAS | CHB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18906 | hp2 | a0001 | c0003 | t0004 | g0189 | AFR | YRI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18940 | hp2 | a0001 | c0001 | t0008 | g0277 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18943 | hp1 | a0003 | c0004 | t0006 | g0216 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18943 | hp2 | a0002 | c0002 | t0068 | g0281 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18953 | hp1 | a0001 | c0001 | t0034 | g0253 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18953 | hp2 | a0003 | c0004 | t0006 | g0130 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18959 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18961 | hp1 | a0002 | c0002 | t0010 | g0027 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18962 | hp2 | a0001 | c0001 | t0059 | g0267 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18963 | hp2 | a0001 | c0001 | t0014 | g0269 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18964 | hp1 | a0001 | c0001 | t0029 | g0237 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18965 | hp1 | a0001 | c0001 | t0019 | g0015 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18973 | hp1 | a0001 | c0001 | t0016 | g0096 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18974 | hp1 | a0001 | c0001 | t0019 | g0015 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18974 | hp2 | a0001 | c0001 | t0030 | g0238 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18975 | hp2 | a0001 | c0001 | t0019 | g0015 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18977 | hp2 | a0001 | c0001 | t0056 | g0091 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18978 | hp2 | a0001 | c0001 | t0058 | g0092 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18982 | hp2 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18985 | hp1 | a0001 | c0001 | t0016 | g0083 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18986 | hp2 | a0001 | c0001 | t0060 | g0239 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18988 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18994 | hp1 | a0001 | c0001 | t0016 | g0099 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18995 | hp2 | a0001 | c0001 | t0008 | g0279 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18997 | hp1 | a0001 | c0001 | t0007 | g0271 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18997 | hp2 | a0002 | c0002 | t0067 | g0135 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18999 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19002 | hp2 | a0001 | c0001 | t0054 | g0090 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19009 | hp1 | a0001 | c0001 | t0028 | g0085 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19010 | hp2 | a0001 | c0001 | t0016 | g0025 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19030 | hp2 | a0001 | c0001 | t0050 | g0156 | AFR | LWK | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19043 | hp1 | a0001 | c0001 | t0038 | g0169 | AFR | LWK | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0240 | AFR | LWK | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19054 | hp2 | a0001 | c0001 | t0008 | g0242 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19055 | hp2 | a0001 | c0001 | t0035 | g0266 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19062 | hp1 | a0001 | c0001 | t0014 | g0275 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19063 | hp2 | a0001 | c0001 | t0011 | g0245 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19065 | hp1 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19068 | hp2 | a0001 | c0001 | t0016 | g0025 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19072 | hp2 | a0001 | c0001 | t0028 | g0084 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19083 | hp2 | a0001 | c0001 | t0037 | g0144 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19085 | hp1 | a0001 | c0001 | t0061 | g0088 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19087 | hp1 | a0001 | c0001 | t0057 | g0094 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19240 | hp1 | a0001 | c0003 | t0051 | g0202 | AFR | YRI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | YRI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA20752 | hp1 | a0001 | c0003 | t0004 | g0044 | EUR | TSI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA20752 | hp2 | a0001 | c0003 | t0015 | g0199 | EUR | TSI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0124 | EUR | TSI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA20905 | hp1 | a0002 | c0002 | t0010 | g0147 | SAS | GIH | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | GIH | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01123 | hp1 | a0001 | c0003 | t0004 | g0192 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG01123 | hp2 | a0001 | c0001 | t0008 | g0268 | AMR | CLM | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02109 | hp2 | a0001 | c0001 | t0022 | g0188 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02486 | hp1 | a0001 | c0001 | t0017 | g0013 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02486 | hp2 | a0001 | c0001 | t0053 | g0181 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0019 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG02559 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | ACB | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03471 | hp1 | a0001 | c0001 | t0031 | g0180 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG03471 | hp2 | a0001 | c0001 | t0048 | g0254 | AFR | MSL | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
HG06807 | hp2 | a0001 | c0003 | t0004 | g0041 | AFR | USA | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA18955 | hp2 | a0003 | c0004 | t0006 | g0017 | EAS | JPT | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA20300 | hp1 | a0004 | c0005 | t0044 | g0225 | AFR | USA | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | USA | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
homoSapiens | chm13v2 | a0001 | c0001 | t0064 | g0163 | REF | REF | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0008 | REF | REF | SCYL3_chr1_169844631_169898896 | SCYL3 | chr1 | 169844631 | 169898896 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:169853751 | C | G | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2029G>C | p.Glu677Gln | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2188/6308 | 2029/2067 | 677/688 | chr1 | 169853751 | |||
chr1:169854380 | C | T | 1 | a0004 | 12 | HG02145.hp2 HG02258.hp1 HG02572.hp1 others(9): Show |
missense_variant | MODERATE | c.1897G>A | p.Ala633Thr | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 2056/6308 | 1897/2067 | 633/688 | chr1 | 169854380 | |||
chr1:169854545 | C | T | 1 | a0008 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1732G>A | p.Ala578Thr | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1891/6308 | 1732/2067 | 578/688 | chr1 | 169854545 | |||
chr1:169854556 | C | T | 1 | a0009 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1721G>A | p.Arg574Lys | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1880/6308 | 1721/2067 | 574/688 | chr1 | 169854556 | |||
chr1:169854577 | T | C | 4 | a0001 a0006 a0008 others(1): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
missense_variant | MODERATE | c.1700A>G | p.Gln567Arg | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1859/6308 | 1700/2067 | 567/688 | chr1 | 169854577 | |||
chr1:169854649 | C | G | 1 | a0003 | 15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
missense_variant | MODERATE | c.1628G>C | p.Gly543Ala | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1787/6308 | 1628/2067 | 543/688 | chr1 | 169854649 | |||
chr1:169854650 | C | T | 1 | a0003 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1627G>A | p.Gly543Arg | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1786/6308 | 1627/2067 | 543/688 | chr1 | 169854650 | |||
chr1:169870330 | A | G | 1 | a0007 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.550T>C | p.Cys184Arg | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 6/13 | 709/6308 | 550/2067 | 184/688 | chr1 | 169870330 | |||
chr1:169888756 | C | T | 1 | a0006 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.85G>A | p.Ala29Thr | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/13 | 244/6308 | 85/2067 | 29/688 | chr1 | 169888756 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:169854519 | C | T | 3 | a0001c0003 a0001c0010 a0006c0008 |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
synonymous_variant | LOW | c.1758G>A | p.Val586Val | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1917/6308 | 1758/2067 | 586/688 | chr1 | 169854519 | |||
chr1:169854900 | C | T | 1 | a0001c0010 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.1377G>A | p.Ser459Ser | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1536/6308 | 1377/2067 | 459/688 | chr1 | 169854900 | |||
chr1:169854927 | A | G | 1 | a0003c0004 | 15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
synonymous_variant | LOW | c.1350T>C | p.Asn450Asn | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1509/6308 | 1350/2067 | 450/688 | chr1 | 169854927 | |||
chr1:169854963 | G | A | 1 | a0003c0004 | 15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
splice_region_variant&synonymous_variant | LOW | c.1314C>T | p.Gly438Gly | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/13 | 1473/6308 | 1314/2067 | 438/688 | chr1 | 169854963 | |||
chr1:169859186 | G | A | 1 | a0003c0004 | 15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
synonymous_variant | LOW | c.1167C>T | p.Ser389Ser | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/13 | 1326/6308 | 1167/2067 | 389/688 | chr1 | 169859186 | |||
chr1:169862625 | G | C | 1 | a0002c0015 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1128C>G | p.Val376Val | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/13 | 1287/6308 | 1128/2067 | 376/688 | chr1 | 169862625 | |||
chr1:169878679 | A | T | 2 | a0001c0006 a0006c0008 |
4 | HG02630.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.306T>A | p.Ala102Ala | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/13 | 465/6308 | 306/2067 | 102/688 | chr1 | 169878679 | |||
chr1:169878703 | T | C | 1 | a0001c0007 | 2 | HG02145.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.282A>G | p.Thr94Thr | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/13 | 441/6308 | 282/2067 | 94/688 | chr1 | 169878703 | |||
chr1:169878754 | G | A | 1 | a0001c0016 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.231C>T | p.Gly77Gly | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/13 | 390/6308 | 231/2067 | 77/688 | chr1 | 169878754 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:169849717 | T | C | 1 | a0001c0016t0063 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3996A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3996 | chr1 | 169849717 | ||||||
chr1:169849739 | G | A | 19 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0028 others(16): Show |
59 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3974C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3974 | chr1 | 169849739 | ||||||
chr1:169849785 | T | C | 15 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0028 others(12): Show |
26 | HG00544.hp2 HG00733.hp2 HG01074.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3928A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3928 | chr1 | 169849785 | ||||||
chr1:169849924 | A | G | 17 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(14): Show |
68 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3789T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3789 | chr1 | 169849924 | ||||||
chr1:169849976 | C | G | 2 | a0001c0001t0021 a0001c0001t0022 |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3737G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3737 | chr1 | 169849976 | ||||||
chr1:169850035 | C | T | 7 | a0001c0001t0016 a0001c0001t0028 a0001c0001t0054 others(4): Show |
12 | NA18973.hp1 NA18977.hp2 NA18978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3678G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3678 | chr1 | 169850035 | ||||||
chr1:169850143 | G | A | 6 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0013 others(3): Show |
89 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*3570C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3570 | chr1 | 169850143 | ||||||
chr1:169850417 | C | T | 1 | a0002c0015t0046 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3296G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3296 | chr1 | 169850417 | ||||||
chr1:169850464 | A | G | 53 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(50): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*3249T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3249 | chr1 | 169850464 | ||||||
chr1:169850525 | C | T | 1 | a0001c0001t0019 | 3 | NA18965.hp1 NA18974.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3188G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3188 | chr1 | 169850525 | ||||||
chr1:169850529 | G | A | 3 | a0003c0004t0006 a0003c0004t0020 a0003c0004t0033 |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3184C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3184 | chr1 | 169850529 | ||||||
chr1:169850641 | C | G | 1 | a0001c0001t0038 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3072G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3072 | chr1 | 169850641 | ||||||
chr1:169850689 | G | A | 53 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(50): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*3024C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 3024 | chr1 | 169850689 | ||||||
chr1:169850751 | A | G | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(67): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*2962T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2962 | chr1 | 169850751 | ||||||
chr1:169850870 | A | G | 1 | a0001c0001t0037 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2843T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2843 | chr1 | 169850870 | ||||||
chr1:169850912 | T | C | 1 | a0002c0015t0046 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2801A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2801 | chr1 | 169850912 | ||||||
chr1:169850936 | G | GAGA | 53 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(50): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*2774_*2776dupTCT | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2776 | chr1 | 169850936 | ||||||
chr1:169850974 | G | A | 14 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0028 others(11): Show |
25 | HG00544.hp2 HG00733.hp2 HG01074.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2739C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2739 | chr1 | 169850974 | ||||||
chr1:169850980 | C | CT | 4 | a0001c0001t0021 a0001c0001t0031 a0001c0016t0063 others(1): Show |
6 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2732dupA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTT | 5 | a0001c0001t0030 a0001c0001t0035 a0001c0001t0040 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG03516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2730_*2732dupAAA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTT | 6 | a0001c0001t0007 a0001c0001t0029 a0001c0001t0039 others(3): Show |
18 | HG00408.hp2 HG00544.hp2 HG01192.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2729_*2732dupAAAA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTT | 6 | a0001c0001t0005 a0001c0001t0034 a0001c0001t0048 others(3): Show |
23 | HG00621.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2728_*2732dupAAAA others(1): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTT | 3 | a0001c0001t0008 a0001c0001t0060 a0004c0005t0024 |
13 | HG00642.hp2 HG00733.hp1 HG01123.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2727_*2732dupAAAA others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT | 2 | a0001c0001t0014 a0004c0005t0018 |
10 | HG01258.hp1 HG01261.hp1 HG02132.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2726_*2732dupAAAA others(3): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0059 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2723_*2732dupAAAA others(6): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0016 a0004c0005t0043 |
6 | HG02970.hp1 NA18973.hp1 NA18985.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2722_*2732dupAAAA others(7): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0028 | 2 | NA19009.hp1 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2721_*2732dupAAAA others(8): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0058 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2720_*2732dupAAAA others(9): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0057 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2717_*2732dupAAAA others(12): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0056 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2714_*2732dupAAAA others(15): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0055 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2712_*2732dupAAAA others(17): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0053 a0001c0001t0054 |
2 | HG02486.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2710_*2732dupAAAA others(19): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0052 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2732_*2733insAAAA others(26): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2732 | chr1 | 169850980 | ||||||
chr1:169850980 | CTTTTTTT others(61): Show |
C | 1 | a0003c0004t0033 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2665_*2732delAAAG others(64): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2665 | chr1 | 169850980 | ||||||
chr1:169850980 | CTTTTTTT others(62): Show |
C | 2 | a0003c0004t0006 a0003c0004t0020 |
14 | HG01168.hp1 HG01169.hp1 HG01361.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2664_*2732delAAAA others(65): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2664 | chr1 | 169850980 | ||||||
chr1:169850982 | TTTTTTTT others(56): Show |
T | 1 | a0001c0003t0051 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2668_*2730delGGGC others(59): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2668 | chr1 | 169850982 | ||||||
chr1:169850985 | TTTTTTTT others(53): Show |
T | 2 | a0001c0003t0004 a0001c0003t0015 |
12 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2668_*2727delGGGC others(56): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2668 | chr1 | 169850985 | ||||||
chr1:169850986 | TTTTTTTT others(52): Show |
T | 1 | a0001c0003t0004 | 10 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2668_*2726delGGGC others(55): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2668 | chr1 | 169850986 | ||||||
chr1:169850987 | TTTTTTTT others(51): Show |
T | 2 | a0001c0003t0004 a0006c0008t0004 |
7 | HG02055.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2668_*2725delGGGC others(54): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2668 | chr1 | 169850987 | ||||||
chr1:169850988 | TTTTTTTT others(50): Show |
T | 1 | a0001c0003t0004 | 2 | HG03130.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2668_*2724delGGGC others(53): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2668 | chr1 | 169850988 | ||||||
chr1:169850989 | TTTTTTTT others(49): Show |
T | 1 | a0001c0010t0004 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2668_*2723delGGGC others(52): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2668 | chr1 | 169850989 | ||||||
chr1:169850990 | TTTTTTTT others(48): Show |
T | 1 | a0001c0003t0004 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2668_*2722delGGGC others(51): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2668 | chr1 | 169850990 | ||||||
chr1:169850996 | TTTTTTTT others(8): Show |
T | 1 | a0001c0001t0015 | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2702_*2716delCAAA others(11): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2702 | chr1 | 169850996 | ||||||
chr1:169850997 | TTTTTTTT others(7): Show |
T | 2 | a0001c0001t0011 a0001c0001t0061 |
2 | NA19063.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2702_*2715delCAAA others(10): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2702 | chr1 | 169850997 | ||||||
chr1:169850998 | TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0049 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2702_*2714delCAAA others(9): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2702 | chr1 | 169850998 | ||||||
chr1:169851001 | TTTTTTAT others(3): Show |
T | 1 | a0001c0001t0012 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2702_*2711delCAAA others(6): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2702 | chr1 | 169851001 | ||||||
chr1:169851003 | TTTTA | T | 5 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(2): Show |
45 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2706_*2709delTAAA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2706 | chr1 | 169851003 | ||||||
chr1:169851004 | TTTA | T | 10 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0017 others(7): Show |
72 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2706_*2708delTAA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2706 | chr1 | 169851004 | ||||||
chr1:169851004 | TTTATTTG | T | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0013 others(2): Show |
72 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2702_*2708delCAAA others(3): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2702 | chr1 | 169851004 | ||||||
chr1:169851005 | TTA | T | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0007t0062 others(4): Show |
28 | HG01109.hp1 HG02071.hp1 HG02129.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2706_*2707delTA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2706 | chr1 | 169851005 | ||||||
chr1:169851005 | TTATTTG | T | 4 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0013 others(1): Show |
15 | HG01361.hp1 HG02004.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2702_*2707delCAAA others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2702 | chr1 | 169851005 | ||||||
chr1:169851006 | TA | T | 3 | a0001c0007t0012 a0002c0002t0010 a0002c0002t0032 |
4 | HG00544.hp1 HG00735.hp1 HG02145.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2706delT | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2706 | chr1 | 169851006 | ||||||
chr1:169851007 | A | T | 40 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(37): Show |
104 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2706T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2706 | chr1 | 169851007 | ||||||
chr1:169851011 | G | T | 40 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(37): Show |
161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*2702C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2702 | chr1 | 169851011 | ||||||
chr1:169851045 | C | CT | 15 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(12): Show |
48 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2667dupA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTT | 4 | a0001c0001t0005 a0001c0001t0008 a0002c0002t0001 others(1): Show |
7 | HG02040.hp2 HG02293.hp1 NA18983.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2666_*2667dupAA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0014 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2658_*2667dupAAAA others(6): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0011 a0001c0001t0059 |
2 | HG00597.hp2 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2657_*2667dupAAAA others(7): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0014 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2656_*2667dupAAAA others(8): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0011 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2654_*2667dupAAAA others(10): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0014 |
3 | HG03239.hp2 HG03834.hp2 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2651_*2667dupAAAA others(13): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0008 a0001c0001t0014 |
3 | HG00733.hp1 HG01261.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2650_*2667dupAAAA others(14): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0007 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2649_*2667dupAAAA others(15): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0008 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2647_*2667dupAAAA others(17): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0047 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2643_*2667dupAAAA others(21): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0005 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2642_*2667dupAAAA others(22): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0005 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2667_*2668insAAAA others(27): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0008 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2667_*2668insAAAA others(28): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0014 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667_*2668insAAAA others(29): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0014 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667_*2668insAAAA others(32): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | CT | C | 14 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0022 others(11): Show |
24 | HG00544.hp2 HG00733.hp2 HG01069.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2667delA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2667 | chr1 | 169851045 | ||||||
chr1:169851045 | CTTTTT | C | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(4): Show |
15 | HG00408.hp2 HG01123.hp2 HG01192.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2663_*2667delAAAA others(1): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2663 | chr1 | 169851045 | ||||||
chr1:169851045 | CTTTTTT | C | 6 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(3): Show |
65 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2662_*2667delAAAA others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2662 | chr1 | 169851045 | ||||||
chr1:169851045 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0050 others(1): Show |
63 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2658_*2667delAAAA others(6): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2658 | chr1 | 169851045 | ||||||
chr1:169851045 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002 a0001c0001t0013 |
24 | HG01192.hp2 HG01891.hp2 HG02015.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2657_*2667delAAAA others(7): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2657 | chr1 | 169851045 | ||||||
chr1:169851077 | A | G | 1 | a0001c0001t0050 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2636T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2636 | chr1 | 169851077 | ||||||
chr1:169851173 | C | A | 1 | a0001c0007t0062 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2540G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2540 | chr1 | 169851173 | ||||||
chr1:169851270 | A | C | 1 | a0001c0001t0036 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2443T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2443 | chr1 | 169851270 | ||||||
chr1:169851293 | TTTACATA others(2): Show |
T | 1 | a0001c0001t0019 | 3 | NA18965.hp1 NA18974.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2411_*2419delTATA others(5): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2411 | chr1 | 169851293 | ||||||
chr1:169851374 | G | C | 1 | a0001c0016t0063 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2339C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2339 | chr1 | 169851374 | ||||||
chr1:169851416 | C | T | 1 | a0003c0004t0020 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2297G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2297 | chr1 | 169851416 | ||||||
chr1:169851499 | A | G | 2 | a0001c0001t0048 a0001c0001t0049 |
2 | HG02451.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2214T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2214 | chr1 | 169851499 | ||||||
chr1:169851541 | C | T | 1 | a0001c0001t0017 | 4 | HG02451.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2172G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2172 | chr1 | 169851541 | ||||||
chr1:169851569 | A | T | 2 | a0002c0002t0041 a0002c0002t0042 |
2 | HG01243.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2144T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 2144 | chr1 | 169851569 | ||||||
chr1:169851858 | T | A | 1 | a0002c0002t0027 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1855A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 1855 | chr1 | 169851858 | ||||||
chr1:169851914 | A | C | 1 | a0001c0001t0047 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1799T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 1799 | chr1 | 169851914 | ||||||
chr1:169851994 | C | T | 6 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(3): Show |
68 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1719G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 1719 | chr1 | 169851994 | ||||||
chr1:169852261 | T | C | 1 | a0001c0001t0013 | 7 | HG01192.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1452A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 1452 | chr1 | 169852261 | ||||||
chr1:169852347 | T | C | 53 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(50): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*1366A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 1366 | chr1 | 169852347 | ||||||
chr1:169852395 | ATAGTAAT | A | 1 | a0001c0001t0009 | 10 | HG00323.hp1 HG00741.hp1 HG01243.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1311_*1317delATTA others(3): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 1311 | chr1 | 169852395 | ||||||
chr1:169852527 | T | C | 1 | a0004c0005t0065 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1186A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 1186 | chr1 | 169852527 | ||||||
chr1:169852709 | T | C | 1 | a0002c0002t0066 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 1004 | chr1 | 169852709 | ||||||
chr1:169852999 | A | AGGCAGAA others(2): Show |
9 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(6): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*705_*713dupAGTTCT others(3): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 713 | chr1 | 169852999 | ||||||
chr1:169853231 | A | G | 2 | a0001c0001t0021 a0001c0001t0022 |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*482T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 482 | chr1 | 169853231 | ||||||
chr1:169853312 | A | G | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | NA18953.hp1 NA19055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*401T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 401 | chr1 | 169853312 | ||||||
chr1:169853344 | T | G | 1 | a0002c0002t0067 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*369A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 369 | chr1 | 169853344 | ||||||
chr1:169853347 | T | TAAAGA | 3 | a0003c0004t0006 a0003c0004t0020 a0003c0004t0033 |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*361_*365dupTCTTT | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 365 | chr1 | 169853347 | ||||||
chr1:169853402 | A | G | 3 | a0003c0004t0006 a0003c0004t0020 a0003c0004t0033 |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*311T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 311 | chr1 | 169853402 | ||||||
chr1:169853415 | A | T | 1 | a0002c0002t0032 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 298 | chr1 | 169853415 | ||||||
chr1:169853709 | A | G | 1 | a0001c0001t0017 | 4 | HG02451.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 13/13 | 4 | chr1 | 169853709 | ||||||
chr1:169893844 | C | A | 1 | a0002c0002t0068 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-107G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/13 | 5004 | chr1 | 169893844 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:169853819 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2008-47A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169853819 | |||||||
chr1:169853842 | A | T | 5 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2008-70T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169853842 | |||||||
chr1:169853890 | C | T | 1 | a0002c0002t0001g0218 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2008-118G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169853890 | |||||||
chr1:169853905 | AACTTAGA others(8): Show |
A | 4 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2008-148_2008-134d others(17): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169853905 | |||||||
chr1:169854036 | T | TTTTTC | 7 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0011g0183 others(4): Show |
9 | HG01891.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2007+229_2007+233d others(7): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169854036 | |||||||
chr1:169854094 | CATTTTTC others(37): Show |
C | 4 | a0001c0001t0015g0026 a0001c0001t0015g0101 a0001c0001t0015g0154 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2007+132_2007+175d others(46): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169854094 | |||||||
chr1:169854126 | A | ATGAT | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.2007+140_2007+143d others(6): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169854126 | |||||||
chr1:169854155 | G | GCTTGA | 169 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(166): Show |
254 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.2007+110_2007+114d others(7): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169854155 | |||||||
chr1:169854155 | G | GCTTGACT others(3): Show |
6 | a0001c0001t0011g0019 a0001c0001t0011g0257 a0001c0001t0023g0065 others(3): Show |
8 | HG02559.hp1 HG02809.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2007+105_2007+114d others(12): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169854155 | |||||||
chr1:169854237 | T | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
4 | HG01891.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2007+33A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169854237 | |||||||
chr1:169854254 | C | T | 1 | a0001c0001t0008g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2007+16G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 12/12 | chr1 | 169854254 | |||||||
chr1:169855062 | A | G | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1313-98T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855062 | |||||||
chr1:169855064 | T | C | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(33): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1313-100A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855064 | |||||||
chr1:169855127 | A | T | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(33): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1313-163T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855127 | |||||||
chr1:169855204 | T | C | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1313-240A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855204 | |||||||
chr1:169855238 | G | A | 27 | a0001c0003t0004g0038 a0001c0003t0004g0039 a0001c0003t0004g0040 others(24): Show |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1313-274C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855238 | |||||||
chr1:169855254 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1313-290T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855254 | |||||||
chr1:169855265 | C | T | 1 | a0001c0001t0011g0019 | 3 | HG02559.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1313-301G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855265 | |||||||
chr1:169855374 | A | G | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(33): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1313-410T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855374 | |||||||
chr1:169855685 | A | C | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1313-721T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855685 | |||||||
chr1:169855768 | A | G | 1 | a0003c0004t0006g0213 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1313-804T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169855768 | |||||||
chr1:169856159 | A | G | 3 | a0003c0004t0006g0045 a0003c0004t0006g0211 a0003c0004t0006g0215 |
4 | HG01168.hp1 HG01169.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-1195T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856159 | |||||||
chr1:169856199 | T | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
4 | HG01891.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-1235A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856199 | |||||||
chr1:169856200 | A | T | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | HG01081.hp2 HG01884.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1313-1236T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856200 | |||||||
chr1:169856239 | T | C | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1313-1275A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856239 | |||||||
chr1:169856278 | T | G | 202 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(199): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1313-1314A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856278 | |||||||
chr1:169856388 | A | G | 50 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(47): Show |
88 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1313-1424T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856388 | |||||||
chr1:169856586 | C | T | 3 | a0001c0001t0015g0026 a0001c0001t0015g0101 a0001c0001t0015g0154 |
4 | HG01884.hp1 HG03041.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-1622G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856586 | |||||||
chr1:169856590 | C | G | 1 | a0001c0001t0002g0077 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1313-1626G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856590 | |||||||
chr1:169856939 | A | G | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1313-1975T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169856939 | |||||||
chr1:169857132 | A | G | 1 | a0001c0001t0011g0019 | 3 | HG02559.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1312+1909T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857132 | |||||||
chr1:169857180 | C | CAAGAAA | 4 | a0004c0005t0018g0223 a0004c0005t0025g0224 a0004c0005t0044g0225 others(1): Show |
4 | HG03195.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312+1855_1312+186 others(10): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857180 | |||||||
chr1:169857259 | A | G | 1 | a0001c0001t0007g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1312+1782T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857259 | |||||||
chr1:169857415 | G | A | 1 | a0001c0001t0003g0059 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1312+1626C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857415 | |||||||
chr1:169857503 | C | T | 18 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(15): Show |
25 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1312+1538G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857503 | |||||||
chr1:169857504 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1312+1537C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857504 | |||||||
chr1:169857645 | T | G | 1 | a0001c0001t0003g0062 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1312+1396A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857645 | |||||||
chr1:169857726 | G | A | 61 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(58): Show |
75 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1312+1315C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857726 | |||||||
chr1:169857755 | TAAC | T | 151 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(148): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1312+1283_1312+128 others(7): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857755 | |||||||
chr1:169857830 | T | C | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1312+1211A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857830 | |||||||
chr1:169857882 | G | C | 1 | a0001c0001t0007g0258 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1312+1159C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857882 | |||||||
chr1:169857889 | A | G | 1 | a0002c0002t0010g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1312+1152T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169857889 | |||||||
chr1:169858032 | G | A | 12 | a0004c0005t0010g0230 a0004c0005t0018g0223 a0004c0005t0018g0231 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1312+1009C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858032 | |||||||
chr1:169858241 | C | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0101 a0001c0001t0015g0154 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312+800G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858241 | |||||||
chr1:169858252 | T | C | 1 | a0001c0001t0029g0237 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1312+789A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858252 | |||||||
chr1:169858310 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0050g0156 |
3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1312+731A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858310 | |||||||
chr1:169858496 | A | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0161 |
3 | HG03130.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1312+545T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858496 | |||||||
chr1:169858521 | T | C | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1312+520A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858521 | |||||||
chr1:169858572 | GTAT | G | 5 | a0001c0003t0004g0039 a0001c0003t0004g0041 a0001c0003t0004g0195 others(2): Show |
7 | HG01081.hp1 HG01099.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312+466_1312+468d others(5): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858572 | |||||||
chr1:169858615 | A | G | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1312+426T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858615 | |||||||
chr1:169858717 | G | A | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1312+324C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858717 | |||||||
chr1:169858753 | ACAGT | A | 24 | a0001c0001t0012g0093 a0001c0001t0012g0095 a0001c0001t0012g0100 others(21): Show |
25 | HG00544.hp2 HG00733.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1312+284_1312+287d others(6): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858753 | |||||||
chr1:169858897 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1312+144G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858897 | |||||||
chr1:169858957 | A | G | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1312+84T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 11/12 | chr1 | 169858957 | |||||||
chr1:169859427 | A | T | 11 | a0001c0003t0004g0042 a0001c0003t0004g0043 a0001c0003t0004g0185 others(8): Show |
13 | HG01891.hp1 HG02258.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1141-215T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859427 | |||||||
chr1:169859460 | T | A | 275 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(272): Show |
408 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(405): Show |
intron_variant | MODIFIER | c.1141-248A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859460 | |||||||
chr1:169859485 | C | T | 1 | a0002c0002t0010g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1141-273G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859485 | |||||||
chr1:169859486 | G | A | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1141-274C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859486 | |||||||
chr1:169859518 | C | T | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1141-306G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859518 | |||||||
chr1:169859641 | T | G | 1 | a0001c0010t0004g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1141-429A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859641 | |||||||
chr1:169859702 | T | C | 1 | a0002c0002t0001g0126 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1141-490A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859702 | |||||||
chr1:169859768 | C | T | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | HG01081.hp2 HG01884.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1141-556G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859768 | |||||||
chr1:169859782 | C | T | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1141-570G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859782 | |||||||
chr1:169859930 | G | A | 51 | a0001c0001t0012g0093 a0001c0001t0012g0095 a0001c0001t0012g0100 others(48): Show |
59 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1141-718C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169859930 | |||||||
chr1:169860059 | A | AT | 55 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(52): Show |
65 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1141-848dupA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860059 | |||||||
chr1:169860156 | A | C | 1 | a0001c0001t0002g0069 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1141-944T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860156 | |||||||
chr1:169860331 | A | G | 1 | a0001c0001t0002g0164 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1141-1119T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860331 | |||||||
chr1:169860442 | G | A | 1 | a0001c0001t0002g0050 | 2 | NA18955.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1141-1230C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860442 | |||||||
chr1:169860674 | C | T | 58 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(55): Show |
96 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1141-1462G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860674 | |||||||
chr1:169860679 | T | C | 1 | a0001c0001t0003g0020 | 2 | NA19062.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1141-1467A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860679 | |||||||
chr1:169860681 | T | G | 1 | a0002c0002t0010g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1141-1469A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860681 | |||||||
chr1:169860689 | A | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0101 a0001c0001t0015g0154 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1141-1477T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860689 | |||||||
chr1:169860963 | G | C | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1140+1650C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860963 | |||||||
chr1:169860974 | T | C | 50 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(47): Show |
60 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1140+1639A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169860974 | |||||||
chr1:169861030 | A | T | 1 | a0001c0016t0063g0082 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1140+1583T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861030 | |||||||
chr1:169861045 | A | T | 1 | a0002c0002t0001g0137 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1140+1568T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861045 | |||||||
chr1:169861137 | T | C | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(33): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+1476A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861137 | |||||||
chr1:169861180 | G | A | 1 | a0001c0003t0004g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1140+1433C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861180 | |||||||
chr1:169861205 | C | T | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1140+1408G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861205 | |||||||
chr1:169861233 | T | C | 1 | a0001c0001t0013g0075 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1140+1380A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861233 | |||||||
chr1:169861255 | G | A | 5 | a0001c0001t0011g0019 a0001c0001t0023g0065 a0001c0001t0023g0068 others(2): Show |
7 | HG02559.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1140+1358C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861255 | |||||||
chr1:169861541 | T | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0053 a0001c0001t0003g0055 others(2): Show |
11 | NA18947.hp2 NA18948.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1140+1072A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861541 | |||||||
chr1:169861609 | A | G | 232 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(229): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1140+1004T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861609 | |||||||
chr1:169861706 | A | G | 1 | a0001c0003t0004g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1140+907T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861706 | |||||||
chr1:169861849 | G | C | 4 | a0002c0002t0001g0029 a0002c0002t0001g0127 a0002c0002t0001g0133 others(1): Show |
5 | HG01975.hp1 NA18612.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+764C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861849 | |||||||
chr1:169861952 | A | C | 2 | a0002c0002t0041g0226 a0002c0002t0042g0227 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1140+661T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169861952 | |||||||
chr1:169862045 | G | T | 4 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+568C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169862045 | |||||||
chr1:169862062 | T | C | 52 | a0001c0001t0012g0093 a0001c0001t0012g0095 a0001c0001t0012g0100 others(49): Show |
60 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1140+551A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169862062 | |||||||
chr1:169862069 | C | G | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1140+544G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169862069 | |||||||
chr1:169862303 | T | C | 1 | a0001c0001t0003g0062 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1140+310A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169862303 | |||||||
chr1:169862381 | C | T | 5 | a0002c0002t0010g0102 a0002c0002t0010g0103 a0002c0002t0026g0105 others(2): Show |
5 | HG01109.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+232G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169862381 | |||||||
chr1:169862390 | A | G | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1140+223T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169862390 | |||||||
chr1:169862468 | T | G | 19 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(16): Show |
26 | HG01081.hp2 HG01192.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1140+145A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169862468 | |||||||
chr1:169862549 | CTCTT | C | 27 | a0001c0003t0004g0038 a0001c0003t0004g0039 a0001c0003t0004g0040 others(24): Show |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1140+60_1140+63del others(4): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 10/12 | chr1 | 169862549 | |||||||
chr1:169862852 | A | G | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.956-55T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169862852 | |||||||
chr1:169862922 | T | C | 3 | a0001c0001t0007g0240 a0001c0001t0008g0235 a0001c0001t0047g0246 |
3 | HG00642.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.956-125A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169862922 | |||||||
chr1:169863006 | A | G | 4 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-209T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863006 | |||||||
chr1:169863043 | G | C | 2 | a0001c0003t0004g0203 a0001c0003t0004g0206 |
2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.956-246C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863043 | |||||||
chr1:169863044 | C | A | 3 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0188 |
3 | HG02109.hp2 HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.956-247G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863044 | |||||||
chr1:169863073 | C | T | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.956-276G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863073 | |||||||
chr1:169863199 | C | T | 13 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0031 others(10): Show |
31 | HG00323.hp2 HG00673.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.956-402G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863199 | |||||||
chr1:169863203 | G | A | 201 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(198): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.956-406C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863203 | |||||||
chr1:169863279 | G | T | 201 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(198): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.956-482C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863279 | |||||||
chr1:169863303 | C | T | 2 | a0001c0003t0004g0038 a0001c0003t0004g0192 |
3 | HG01123.hp1 HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.956-506G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863303 | |||||||
chr1:169863476 | G | A | 1 | a0003c0004t0006g0130 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.956-679C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863476 | |||||||
chr1:169863777 | C | T | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.955+592G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863777 | |||||||
chr1:169863907 | C | CTA | 4 | a0001c0001t0031g0179 a0001c0001t0031g0180 a0001c0001t0053g0181 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+460_955+461dup others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169863907 | |||||||
chr1:169864012 | AAAAT | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(36): Show |
70 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.955+353_955+356del others(4): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169864012 | |||||||
chr1:169864154 | A | G | 1 | a0001c0001t0008g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.955+215T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169864154 | |||||||
chr1:169864171 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.955+198G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169864171 | |||||||
chr1:169864200 | C | T | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.955+169G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169864200 | |||||||
chr1:169864256 | C | T | 13 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0072 others(10): Show |
18 | HG01192.hp2 HG02015.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.955+113G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169864256 | |||||||
chr1:169864257 | G | A | 1 | a0003c0004t0033g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.955+112C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169864257 | |||||||
chr1:169864283 | C | T | 1 | a0001c0001t0011g0019 | 3 | HG02559.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.955+86G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 9/12 | chr1 | 169864283 | |||||||
chr1:169864681 | T | C | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.816-173A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169864681 | |||||||
chr1:169864714 | C | T | 1 | a0001c0001t0005g0048 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.816-206G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169864714 | |||||||
chr1:169864804 | A | T | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.816-296T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169864804 | |||||||
chr1:169864805 | C | A | 1 | a0001c0003t0015g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.816-297G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169864805 | |||||||
chr1:169864955 | G | A | 4 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-447C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169864955 | |||||||
chr1:169864969 | C | CAA | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.816-463_816-462dup others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169864969 | |||||||
chr1:169864969 | CA | C | 61 | a0001c0001t0002g0050 a0001c0001t0002g0072 a0001c0001t0002g0219 others(58): Show |
73 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.816-462delT | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169864969 | |||||||
chr1:169864969 | CAA | C | 137 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(134): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.816-463_816-462del others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169864969 | |||||||
chr1:169865075 | T | C | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.816-567A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169865075 | |||||||
chr1:169865164 | A | G | 1 | a0001c0001t0017g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816-656T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169865164 | |||||||
chr1:169865210 | A | G | 19 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(16): Show |
26 | HG01081.hp2 HG01192.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.816-702T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169865210 | |||||||
chr1:169865225 | G | A | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.816-717C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169865225 | |||||||
chr1:169865363 | G | A | 1 | a0004c0005t0025g0234 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.816-855C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169865363 | |||||||
chr1:169865410 | T | C | 5 | a0004c0005t0010g0230 a0004c0005t0018g0223 a0004c0005t0025g0224 others(2): Show |
5 | HG02622.hp2 HG03195.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.816-902A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169865410 | |||||||
chr1:169865907 | A | G | 5 | a0001c0003t0004g0042 a0001c0003t0004g0185 a0001c0003t0004g0204 others(2): Show |
6 | HG02630.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.815+989T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169865907 | |||||||
chr1:169866063 | T | G | 212 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(209): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.815+833A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866063 | |||||||
chr1:169866069 | G | T | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.815+827C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866069 | |||||||
chr1:169866205 | T | C | 1 | a0002c0002t0010g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.815+691A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866205 | |||||||
chr1:169866214 | T | G | 1 | a0002c0002t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.815+682A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866214 | |||||||
chr1:169866260 | T | G | 201 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(198): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.815+636A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866260 | |||||||
chr1:169866540 | T | C | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.815+356A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866540 | |||||||
chr1:169866736 | T | A | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.815+160A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866736 | |||||||
chr1:169866772 | T | C | 1 | a0002c0002t0001g0030 | 2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.815+124A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866772 | |||||||
chr1:169866809 | A | C | 214 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(211): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.815+87T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866809 | |||||||
chr1:169866813 | C | A | 1 | a0003c0004t0006g0045 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.815+83G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866813 | |||||||
chr1:169866871 | T | G | 1 | a0001c0001t0002g0260 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.815+25A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 8/12 | chr1 | 169866871 | |||||||
chr1:169867034 | T | C | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.738-61A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867034 | |||||||
chr1:169867123 | G | T | 1 | a0001c0010t0004g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.738-150C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867123 | |||||||
chr1:169867286 | C | T | 4 | a0003c0004t0006g0213 a0003c0004t0006g0214 a0003c0004t0020g0046 others(1): Show |
5 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-313G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867286 | |||||||
chr1:169867289 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
4 | HG01891.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-316C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867289 | |||||||
chr1:169867314 | A | G | 1 | a0001c0001t0003g0052 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.738-341T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867314 | |||||||
chr1:169867344 | A | G | 1 | a0002c0002t0001g0148 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.738-371T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867344 | |||||||
chr1:169867506 | T | C | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.738-533A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867506 | |||||||
chr1:169867519 | T | C | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.738-546A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867519 | |||||||
chr1:169867624 | A | G | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.738-651T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867624 | |||||||
chr1:169867626 | C | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0101 a0001c0001t0015g0154 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.738-653G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867626 | |||||||
chr1:169867727 | T | C | 2 | a0001c0001t0005g0261 a0001c0001t0007g0262 |
2 | HG00621.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.738-754A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867727 | |||||||
chr1:169867731 | G | A | 3 | a0004c0005t0018g0232 a0004c0005t0024g0228 a0004c0005t0024g0229 |
3 | HG02896.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.738-758C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867731 | |||||||
chr1:169867759 | C | T | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.738-786G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867759 | |||||||
chr1:169867805 | T | C | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.738-832A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867805 | |||||||
chr1:169867911 | G | C | 1 | a0001c0001t0002g0165 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.738-938C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867911 | |||||||
chr1:169867914 | C | T | 2 | a0002c0002t0010g0110 a0002c0002t0032g0131 |
2 | HG00735.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.738-941G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169867914 | |||||||
chr1:169868284 | A | G | 1 | a0001c0016t0063g0082 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.737+644T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169868284 | |||||||
chr1:169868650 | A | G | 34 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(31): Show |
65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.737+278T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169868650 | |||||||
chr1:169868694 | C | T | 1 | a0001c0001t0005g0048 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.737+234G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169868694 | |||||||
chr1:169868727 | A | G | 4 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+201T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169868727 | |||||||
chr1:169868875 | G | A | 32 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(29): Show |
68 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.737+53C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169868875 | |||||||
chr1:169868905 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.737+23C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 7/12 | chr1 | 169868905 | |||||||
chr1:169869137 | G | A | 27 | a0001c0003t0004g0038 a0001c0003t0004g0039 a0001c0003t0004g0040 others(24): Show |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.626-98C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 6/12 | chr1 | 169869137 | |||||||
chr1:169869382 | T | C | 1 | a0001c0003t0004g0040 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.626-343A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 6/12 | chr1 | 169869382 | |||||||
chr1:169869574 | C | T | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.626-535G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 6/12 | chr1 | 169869574 | |||||||
chr1:169869742 | G | A | 4 | a0001c0001t0015g0026 a0001c0001t0015g0101 a0001c0001t0015g0154 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.625+513C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 6/12 | chr1 | 169869742 | |||||||
chr1:169870069 | T | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(31): Show |
70 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.625+186A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 6/12 | chr1 | 169870069 | |||||||
chr1:169870454 | A | G | 39 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(36): Show |
70 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.523-97T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169870454 | |||||||
chr1:169870618 | C | T | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.523-261G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169870618 | |||||||
chr1:169870654 | A | G | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(33): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.523-297T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169870654 | |||||||
chr1:169870684 | T | C | 34 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(31): Show |
65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.523-327A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169870684 | |||||||
chr1:169870711 | C | G | 1 | a0009c0013t0030g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.523-354G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169870711 | |||||||
chr1:169870732 | G | A | 2 | a0001c0001t0015g0154 a0001c0001t0015g0162 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.523-375C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169870732 | |||||||
chr1:169870755 | CT | C | 26 | a0001c0001t0005g0264 a0001c0001t0012g0093 a0001c0001t0012g0095 others(23): Show |
27 | HG00544.hp2 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.523-399delA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169870755 | |||||||
chr1:169870817 | C | T | 2 | a0002c0002t0001g0107 a0002c0002t0001g0108 |
2 | HG02056.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.523-460G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169870817 | |||||||
chr1:169871044 | A | G | 30 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(27): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.523-687T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871044 | |||||||
chr1:169871072 | C | T | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-715G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871072 | |||||||
chr1:169871079 | A | AAT | 55 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(52): Show |
65 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.523-724_523-723dup others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871079 | |||||||
chr1:169871298 | C | T | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-941G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871298 | |||||||
chr1:169871304 | C | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0101 a0001c0001t0015g0154 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-947G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871304 | |||||||
chr1:169871352 | A | G | 1 | a0001c0001t0022g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.523-995T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871352 | |||||||
chr1:169871366 | C | T | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(33): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.523-1009G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871366 | |||||||
chr1:169871405 | C | T | 40 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(37): Show |
71 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.523-1048G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871405 | |||||||
chr1:169871562 | T | C | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.523-1205A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871562 | |||||||
chr1:169871563 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.523-1206C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871563 | |||||||
chr1:169871986 | G | C | 1 | a0001c0001t0015g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.523-1629C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169871986 | |||||||
chr1:169872177 | G | A | 1 | a0001c0001t0009g0166 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.522+1519C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169872177 | |||||||
chr1:169872248 | G | A | 1 | a0004c0005t0024g0229 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.522+1448C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169872248 | |||||||
chr1:169872372 | T | C | 13 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0004c0005t0010g0230 others(10): Show |
13 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.522+1324A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169872372 | |||||||
chr1:169872744 | C | T | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.522+952G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169872744 | |||||||
chr1:169872848 | G | A | 1 | a0001c0001t0028g0085 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.522+848C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169872848 | |||||||
chr1:169872944 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.522+752T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169872944 | |||||||
chr1:169872996 | G | T | 2 | a0001c0001t0005g0272 a0001c0001t0014g0275 |
2 | NA18988.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.522+700C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169872996 | |||||||
chr1:169873003 | T | G | 1 | a0002c0002t0010g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.522+693A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873003 | |||||||
chr1:169873151 | A | G | 202 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(199): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.522+545T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873151 | |||||||
chr1:169873224 | A | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0101 a0001c0001t0015g0154 others(1): Show |
5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+472T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873224 | |||||||
chr1:169873292 | A | T | 3 | a0001c0003t0004g0042 a0001c0003t0004g0185 a0001c0003t0004g0205 |
4 | HG02647.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+404T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873292 | |||||||
chr1:169873386 | G | T | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.522+310C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873386 | |||||||
chr1:169873437 | C | T | 1 | a0001c0001t0003g0057 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.522+259G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873437 | |||||||
chr1:169873438 | G | A | 4 | a0001c0001t0023g0065 a0001c0001t0023g0068 a0001c0001t0039g0067 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+258C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873438 | |||||||
chr1:169873453 | T | C | 1 | a0002c0002t0001g0150 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.522+243A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873453 | |||||||
chr1:169873528 | G | A | 50 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(47): Show |
60 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.522+168C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873528 | |||||||
chr1:169873529 | C | T | 1 | a0001c0001t0011g0019 | 3 | HG02559.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.522+167G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873529 | |||||||
chr1:169873680 | A | C | 20 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(17): Show |
27 | HG01081.hp2 HG01192.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.522+16T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 5/12 | chr1 | 169873680 | |||||||
chr1:169873876 | C | T | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-124G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169873876 | |||||||
chr1:169873938 | C | T | 1 | a0001c0001t0011g0019 | 3 | HG02559.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.466-186G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169873938 | |||||||
chr1:169873962 | T | C | 1 | a0001c0001t0029g0237 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.466-210A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169873962 | |||||||
chr1:169873984 | C | G | 25 | a0001c0001t0012g0093 a0001c0001t0012g0095 a0001c0001t0012g0100 others(22): Show |
26 | HG00544.hp2 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.466-232G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169873984 | |||||||
chr1:169874046 | T | C | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(33): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.466-294A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874046 | |||||||
chr1:169874057 | G | C | 2 | a0001c0001t0005g0261 a0001c0001t0007g0262 |
2 | HG00621.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.466-305C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874057 | |||||||
chr1:169874199 | A | C | 1 | a0001c0001t0007g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.466-447T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874199 | |||||||
chr1:169874249 | C | T | 5 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-497G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874249 | |||||||
chr1:169874253 | G | A | 49 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(46): Show |
59 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.466-501C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874253 | |||||||
chr1:169874295 | A | G | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-543T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874295 | |||||||
chr1:169874307 | C | T | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.466-555G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874307 | |||||||
chr1:169874435 | A | G | 1 | a0001c0003t0004g0194 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.466-683T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874435 | |||||||
chr1:169874468 | A | G | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-716T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874468 | |||||||
chr1:169874482 | G | A | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-730C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874482 | |||||||
chr1:169874545 | AAAG | A | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-796_466-794del others(3): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874545 | |||||||
chr1:169874598 | A | G | 5 | a0001c0001t0011g0019 a0001c0001t0023g0065 a0001c0001t0023g0068 others(2): Show |
7 | HG02559.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-846T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874598 | |||||||
chr1:169874653 | C | T | 4 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-901G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874653 | |||||||
chr1:169874664 | A | G | 1 | a0001c0001t0008g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.466-912T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874664 | |||||||
chr1:169874695 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.466-943C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874695 | |||||||
chr1:169874732 | C | T | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-980G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874732 | |||||||
chr1:169874743 | C | T | 273 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(270): Show |
405 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.466-991G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874743 | |||||||
chr1:169874952 | T | C | 11 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0130 others(8): Show |
15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.465+1026A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169874952 | |||||||
chr1:169875017 | A | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0161 |
5 | HG02965.hp2 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+961T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875017 | |||||||
chr1:169875046 | C | T | 4 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+932G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875046 | |||||||
chr1:169875265 | G | A | 15 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(12): Show |
22 | HG01192.hp2 HG01891.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.465+713C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875265 | |||||||
chr1:169875374 | T | G | 115 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(112): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.465+604A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875374 | |||||||
chr1:169875381 | C | T | 32 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(29): Show |
68 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.465+597G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875381 | |||||||
chr1:169875667 | G | A | 2 | a0001c0001t0015g0026 a0001c0001t0015g0101 |
3 | HG01884.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.465+311C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875667 | |||||||
chr1:169875696 | T | C | 1 | a0001c0001t0005g0244 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.465+282A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875696 | |||||||
chr1:169875736 | G | A | 212 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(209): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.465+242C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875736 | |||||||
chr1:169875755 | C | T | 1 | a0001c0001t0008g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.465+223G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875755 | |||||||
chr1:169875874 | A | G | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.465+104T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 4/12 | chr1 | 169875874 | |||||||
chr1:169876302 | A | G | 1 | a0002c0002t0001g0118 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.352-211T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876302 | |||||||
chr1:169876502 | T | C | 34 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(31): Show |
65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.352-411A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876502 | |||||||
chr1:169876565 | C | T | 1 | a0001c0001t0013g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.352-474G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876565 | |||||||
chr1:169876615 | T | A | 27 | a0001c0003t0004g0038 a0001c0003t0004g0039 a0001c0003t0004g0040 others(24): Show |
34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.352-524A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876615 | |||||||
chr1:169876651 | C | T | 1 | a0001c0001t0007g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-560G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876651 | |||||||
chr1:169876879 | C | T | 1 | a0001c0001t0007g0249 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.352-788G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876879 | |||||||
chr1:169876934 | G | A | 5 | a0003c0004t0006g0213 a0003c0004t0006g0214 a0003c0004t0020g0046 others(2): Show |
6 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-843C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876934 | |||||||
chr1:169876958 | T | TA | 43 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(40): Show |
51 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.352-868dupT | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876958 | |||||||
chr1:169876958 | TA | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0036 others(37): Show |
49 | HG00544.hp2 HG00733.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.352-868delT | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876958 | |||||||
chr1:169876958 | TAA | T | 37 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(34): Show |
70 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.352-869_352-868del others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876958 | |||||||
chr1:169876958 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0003g0143 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.352-879_352-868del others(12): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876958 | |||||||
chr1:169876958 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0003g0056 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.352-880_352-868del others(13): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876958 | |||||||
chr1:169876976 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.352-885T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169876976 | |||||||
chr1:169877128 | A | AT | 3 | a0001c0001t0007g0240 a0001c0001t0008g0235 a0001c0001t0047g0246 |
3 | HG00642.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.352-1038dupA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877128 | |||||||
chr1:169877142 | T | C | 1 | a0001c0016t0063g0082 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.352-1051A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877142 | |||||||
chr1:169877215 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.352-1124C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877215 | |||||||
chr1:169877285 | AG | A | 13 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0004c0005t0010g0230 others(10): Show |
13 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.352-1195delC | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877285 | |||||||
chr1:169877395 | C | T | 1 | a0001c0001t0003g0141 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.351+1239G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877395 | |||||||
chr1:169877396 | G | A | 1 | a0006c0008t0004g0186 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.351+1238C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877396 | |||||||
chr1:169877432 | A | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(31): Show |
70 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.351+1202T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877432 | |||||||
chr1:169877742 | T | C | 56 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0069 others(53): Show |
68 | HG00140.hp1 HG00733.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.351+892A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877742 | |||||||
chr1:169877862 | A | C | 1 | a0001c0001t0061g0088 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.351+772T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877862 | |||||||
chr1:169877913 | T | A | 1 | a0001c0001t0007g0271 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.351+721A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169877913 | |||||||
chr1:169878005 | C | T | 196 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(193): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.351+629G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878005 | |||||||
chr1:169878010 | A | C | 1 | a0001c0006t0002g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.351+624T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878010 | |||||||
chr1:169878020 | C | A | 2 | a0002c0002t0010g0110 a0002c0002t0032g0131 |
2 | HG00735.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.351+614G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878020 | |||||||
chr1:169878087 | A | G | 25 | a0001c0001t0002g0170 a0001c0001t0008g0247 a0001c0001t0012g0093 others(22): Show |
26 | HG00544.hp2 HG01074.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.351+547T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878087 | |||||||
chr1:169878218 | A | G | 1 | a0002c0002t0001g0116 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.351+416T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878218 | |||||||
chr1:169878345 | T | C | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.351+289A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878345 | |||||||
chr1:169878346 | G | T | 213 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(210): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.351+288C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878346 | |||||||
chr1:169878447 | A | G | 2 | a0003c0004t0006g0017 a0003c0004t0006g0216 |
4 | HG02074.hp2 HG02523.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+187T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878447 | |||||||
chr1:169878542 | G | A | 214 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(211): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.351+92C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 3/12 | chr1 | 169878542 | |||||||
chr1:169878824 | A | G | 1 | a0001c0003t0004g0204 | 1 | HG02886.hp1 | splice_region_variant&intron_variant | LOW | c.166-5T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169878824 | |||||||
chr1:169878872 | A | T | 1 | a0001c0003t0004g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.166-53T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169878872 | |||||||
chr1:169879189 | C | T | 52 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(49): Show |
64 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.166-370G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169879189 | |||||||
chr1:169879226 | T | G | 204 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(201): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.166-407A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169879226 | |||||||
chr1:169879336 | T | C | 1 | a0002c0002t0042g0227 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.166-517A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169879336 | |||||||
chr1:169879365 | G | A | 32 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(29): Show |
68 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.166-546C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169879365 | |||||||
chr1:169879496 | C | T | 5 | a0002c0002t0010g0102 a0002c0002t0010g0103 a0002c0002t0026g0105 others(2): Show |
5 | HG01109.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-677G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169879496 | |||||||
chr1:169879634 | T | G | 1 | a0001c0001t0005g0265 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.166-815A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169879634 | |||||||
chr1:169879650 | T | C | 204 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(201): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.166-831A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169879650 | |||||||
chr1:169880000 | A | G | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-1181T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880000 | |||||||
chr1:169880086 | A | G | 204 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(201): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.166-1267T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880086 | |||||||
chr1:169880095 | T | C | 215 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(212): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.166-1276A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880095 | |||||||
chr1:169880123 | A | C | 2 | a0001c0001t0023g0065 a0001c0001t0040g0066 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.166-1304T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880123 | |||||||
chr1:169880221 | A | T | 1 | a0003c0004t0033g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-1402T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880221 | |||||||
chr1:169880330 | A | T | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-1511T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880330 | |||||||
chr1:169880374 | TAAATATC others(231): Show |
T | 28 | a0001c0001t0012g0197 a0001c0003t0004g0038 a0001c0003t0004g0039 others(25): Show |
35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.166-1793_166-1556d others(2): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880374 | |||||||
chr1:169880404 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.166-1585G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880404 | |||||||
chr1:169880561 | T | A | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.166-1742A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880561 | |||||||
chr1:169880598 | CA | C | 53 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(50): Show |
65 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.166-1780delT | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880598 | |||||||
chr1:169880616 | A | C | 28 | a0001c0001t0012g0197 a0001c0003t0004g0038 a0001c0003t0004g0039 others(25): Show |
35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.166-1797T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880616 | |||||||
chr1:169880624 | C | A | 1 | a0002c0002t0001g0137 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.166-1805G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880624 | |||||||
chr1:169880759 | C | T | 1 | a0001c0001t0047g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.166-1940G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880759 | |||||||
chr1:169880762 | C | CT | 100 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0003g0055 others(97): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.166-1944dupA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880762 | |||||||
chr1:169880762 | CT | C | 15 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0002c0002t0001g0132 others(12): Show |
19 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.166-1944delA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880762 | |||||||
chr1:169880784 | C | T | 2 | a0002c0002t0001g0107 a0002c0002t0001g0108 |
2 | HG02056.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.166-1965G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880784 | |||||||
chr1:169880823 | G | A | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-2004C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880823 | |||||||
chr1:169880870 | C | T | 214 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(211): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.166-2051G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880870 | |||||||
chr1:169880877 | T | C | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-2058A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880877 | |||||||
chr1:169880952 | G | A | 10 | a0004c0005t0010g0230 a0004c0005t0018g0223 a0004c0005t0018g0231 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-2133C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169880952 | |||||||
chr1:169881005 | G | A | 35 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(32): Show |
66 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.166-2186C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881005 | |||||||
chr1:169881030 | G | T | 1 | a0001c0006t0002g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166-2211C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881030 | |||||||
chr1:169881035 | T | C | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.166-2216A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881035 | |||||||
chr1:169881096 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.166-2277G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881096 | |||||||
chr1:169881162 | A | G | 1 | a0001c0001t0031g0180 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.166-2343T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881162 | |||||||
chr1:169881203 | A | G | 1 | a0004c0005t0010g0230 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.166-2384T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881203 | |||||||
chr1:169881210 | C | A | 1 | a0001c0001t0002g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.166-2391G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881210 | |||||||
chr1:169881219 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.166-2400C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881219 | |||||||
chr1:169881233 | T | C | 28 | a0001c0001t0012g0197 a0001c0003t0004g0038 a0001c0003t0004g0039 others(25): Show |
35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.166-2414A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881233 | |||||||
chr1:169881269 | T | C | 35 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(32): Show |
71 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.166-2450A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881269 | |||||||
chr1:169881293 | T | C | 1 | a0001c0001t0002g0172 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.166-2474A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881293 | |||||||
chr1:169881307 | A | C | 5 | a0001c0001t0011g0183 a0001c0001t0031g0179 a0001c0001t0031g0180 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-2488T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881307 | |||||||
chr1:169881357 | G | A | 3 | a0001c0001t0016g0083 a0001c0001t0028g0084 a0001c0001t0028g0085 |
3 | NA18985.hp1 NA19009.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.166-2538C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881357 | |||||||
chr1:169881472 | C | T | 1 | a0001c0001t0011g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.166-2653G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881472 | |||||||
chr1:169881525 | A | T | 183 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(180): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.166-2706T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881525 | |||||||
chr1:169881666 | T | A | 1 | a0003c0004t0006g0216 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.166-2847A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881666 | |||||||
chr1:169881701 | T | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
4 | HG01891.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-2882A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881701 | |||||||
chr1:169881701 | T | G | 1 | a0001c0001t0016g0099 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.166-2882A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881701 | |||||||
chr1:169881809 | G | T | 1 | a0001c0001t0002g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.166-2990C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169881809 | |||||||
chr1:169882008 | C | T | 1 | a0002c0002t0010g0110 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.166-3189G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882008 | |||||||
chr1:169882018 | G | A | 95 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(92): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.166-3199C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882018 | |||||||
chr1:169882029 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.166-3210C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882029 | |||||||
chr1:169882092 | C | G | 1 | a0001c0001t0011g0245 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.166-3273G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882092 | |||||||
chr1:169882196 | C | T | 19 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(16): Show |
26 | HG01081.hp2 HG01192.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.166-3377G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882196 | |||||||
chr1:169882224 | A | G | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-3405T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882224 | |||||||
chr1:169882228 | G | A | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-3409C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882228 | |||||||
chr1:169882282 | C | T | 1 | a0002c0002t0001g0114 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.166-3463G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882282 | |||||||
chr1:169882347 | C | T | 32 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(29): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-3528G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882347 | |||||||
chr1:169882383 | G | A | 1 | a0001c0001t0012g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.166-3564C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882383 | |||||||
chr1:169882432 | C | A | 1 | a0001c0001t0014g0269 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.166-3613G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882432 | |||||||
chr1:169882438 | C | T | 15 | a0001c0001t0012g0197 a0001c0003t0004g0038 a0001c0003t0004g0039 others(12): Show |
19 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.166-3619G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882438 | |||||||
chr1:169882493 | C | T | 1 | a0009c0013t0030g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.166-3674G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882493 | |||||||
chr1:169882494 | G | A | 6 | a0001c0001t0005g0270 a0001c0001t0005g0278 a0001c0001t0005g0280 others(3): Show |
6 | NA18940.hp2 NA18979.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-3675C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882494 | |||||||
chr1:169882581 | G | T | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-3762C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882581 | |||||||
chr1:169882590 | G | A | 53 | a0001c0001t0002g0050 a0001c0001t0002g0184 a0001c0001t0002g0260 others(50): Show |
65 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.166-3771C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882590 | |||||||
chr1:169882625 | A | T | 1 | a0002c0002t0001g0114 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.166-3806T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882625 | |||||||
chr1:169882631 | C | A | 1 | a0001c0016t0063g0082 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.166-3812G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882631 | |||||||
chr1:169882715 | A | G | 5 | a0001c0001t0002g0184 a0001c0001t0023g0065 a0001c0001t0023g0068 others(2): Show |
5 | HG02615.hp2 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-3896T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882715 | |||||||
chr1:169882718 | C | G | 1 | a0001c0001t0003g0142 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.166-3899G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882718 | |||||||
chr1:169882794 | G | C | 1 | a0001c0001t0003g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.166-3975C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882794 | |||||||
chr1:169882829 | T | C | 2 | a0002c0002t0010g0102 a0007c0009t0010g0104 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.166-4010A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882829 | |||||||
chr1:169882849 | G | A | 53 | a0001c0001t0002g0050 a0001c0001t0002g0184 a0001c0001t0002g0260 others(50): Show |
65 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.166-4030C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882849 | |||||||
chr1:169882898 | C | T | 1 | a0002c0002t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.166-4079G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882898 | |||||||
chr1:169882907 | T | G | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.166-4088A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882907 | |||||||
chr1:169882953 | A | G | 214 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(211): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.166-4134T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882953 | |||||||
chr1:169882968 | T | C | 64 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(61): Show |
102 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.166-4149A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169882968 | |||||||
chr1:169883100 | C | T | 2 | a0004c0005t0024g0228 a0004c0005t0024g0229 |
2 | HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.166-4281G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883100 | |||||||
chr1:169883131 | A | G | 4 | a0001c0001t0005g0243 a0001c0001t0005g0244 a0001c0001t0008g0242 others(1): Show |
4 | HG00673.hp1 HG02040.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-4312T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883131 | |||||||
chr1:169883158 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.166-4339G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883158 | |||||||
chr1:169883159 | A | G | 214 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(211): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.166-4340T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883159 | |||||||
chr1:169883194 | G | A | 30 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0035 others(27): Show |
59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.166-4375C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883194 | |||||||
chr1:169883209 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.166-4390T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883209 | |||||||
chr1:169883220 | A | G | 4 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-4401T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883220 | |||||||
chr1:169883225 | G | A | 51 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(48): Show |
63 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.166-4406C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883225 | |||||||
chr1:169883372 | G | A | 52 | a0001c0001t0012g0093 a0001c0001t0012g0095 a0001c0001t0012g0100 others(49): Show |
60 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.166-4553C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883372 | |||||||
chr1:169883375 | T | C | 2 | a0001c0001t0003g0031 a0001c0001t0003g0141 |
3 | NA18965.hp2 NA18985.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.166-4556A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883375 | |||||||
chr1:169883472 | A | G | 56 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(53): Show |
68 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.166-4653T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883472 | |||||||
chr1:169883525 | A | G | 1 | a0001c0001t0013g0073 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166-4706T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883525 | |||||||
chr1:169883679 | G | A | 4 | a0001c0001t0021g0151 a0001c0001t0021g0187 a0001c0001t0022g0152 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-4860C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883679 | |||||||
chr1:169883710 | T | C | 28 | a0001c0001t0012g0197 a0001c0003t0004g0038 a0001c0003t0004g0039 others(25): Show |
35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.166-4891A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883710 | |||||||
chr1:169883714 | AT | A | 169 | a0001c0001t0002g0002 a0001c0001t0002g0034 a0001c0001t0002g0035 others(166): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.166-4896delA | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883714 | |||||||
chr1:169883714 | ATT | A | 9 | a0001c0001t0002g0175 a0001c0001t0002g0184 a0001c0001t0003g0145 others(6): Show |
9 | HG00323.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-4897_166-4896d others(4): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883714 | |||||||
chr1:169883714 | ATTT | A | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-4898_166-4896d others(5): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883714 | |||||||
chr1:169883789 | G | A | 4 | a0001c0001t0023g0065 a0001c0001t0023g0068 a0001c0001t0039g0067 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+4887C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883789 | |||||||
chr1:169883863 | C | T | 1 | a0002c0002t0001g0112 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.165+4813G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169883863 | |||||||
chr1:169884024 | A | G | 2 | a0001c0001t0021g0187 a0001c0001t0022g0188 |
2 | HG02109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.165+4652T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884024 | |||||||
chr1:169884049 | C | T | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+4627G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884049 | |||||||
chr1:169884179 | C | A | 1 | a0001c0003t0004g0044 | 2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.165+4497G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884179 | |||||||
chr1:169884298 | C | T | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | HG01081.hp2 HG01884.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.165+4378G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884298 | |||||||
chr1:169884318 | A | T | 2 | a0001c0001t0015g0026 a0001c0001t0015g0101 |
3 | HG01884.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.165+4358T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884318 | |||||||
chr1:169884332 | T | C | 1 | a0001c0001t0003g0053 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.165+4344A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884332 | |||||||
chr1:169884517 | C | CTT | 16 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(13): Show |
23 | HG01192.hp2 HG01891.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.165+4158_165+4159i others(4): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884517 | |||||||
chr1:169884573 | T | C | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+4103A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884573 | |||||||
chr1:169884590 | G | C | 12 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0004c0005t0010g0230 others(9): Show |
12 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+4086C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884590 | |||||||
chr1:169884616 | T | C | 5 | a0001c0001t0011g0183 a0001c0001t0031g0179 a0001c0001t0031g0180 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+4060A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884616 | |||||||
chr1:169884618 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.165+4058G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884618 | |||||||
chr1:169884972 | T | C | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+3704A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169884972 | |||||||
chr1:169885016 | A | G | 1 | a0002c0002t0001g0111 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.165+3660T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169885016 | |||||||
chr1:169885179 | C | A | 1 | a0001c0001t0002g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.165+3497G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169885179 | |||||||
chr1:169885448 | G | C | 1 | a0001c0001t0002g0177 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.165+3228C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169885448 | |||||||
chr1:169885526 | G | A | 2 | a0001c0001t0023g0068 a0001c0001t0039g0067 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+3150C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169885526 | |||||||
chr1:169885570 | A | C | 1 | a0001c0001t0002g0072 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.165+3106T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169885570 | |||||||
chr1:169885878 | G | C | 1 | a0001c0003t0004g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.165+2798C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169885878 | |||||||
chr1:169885924 | G | C | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+2752C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169885924 | |||||||
chr1:169885966 | C | T | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+2710G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169885966 | |||||||
chr1:169886034 | C | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(28): Show |
67 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.165+2642G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886034 | |||||||
chr1:169886050 | T | C | 5 | a0001c0001t0005g0272 a0001c0001t0005g0276 a0001c0001t0008g0274 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+2626A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886050 | |||||||
chr1:169886095 | G | A | 4 | a0001c0001t0023g0065 a0001c0001t0023g0068 a0001c0001t0039g0067 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2581C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886095 | |||||||
chr1:169886292 | CAG | C | 203 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(200): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.165+2382_165+2383d others(4): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886292 | |||||||
chr1:169886383 | A | G | 1 | a0007c0009t0010g0104 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.165+2293T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886383 | |||||||
chr1:169886384 | T | C | 1 | a0007c0009t0010g0104 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.165+2292A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886384 | |||||||
chr1:169886435 | A | G | 227 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(224): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.165+2241T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886435 | |||||||
chr1:169886484 | A | C | 1 | a0002c0002t0010g0110 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.165+2192T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886484 | |||||||
chr1:169886505 | T | C | 1 | a0002c0002t0001g0137 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.165+2171A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886505 | |||||||
chr1:169886612 | G | C | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.165+2064C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886612 | |||||||
chr1:169886659 | G | A | 2 | a0002c0002t0026g0105 a0002c0002t0026g0106 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.165+2017C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886659 | |||||||
chr1:169886887 | T | C | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+1789A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169886887 | |||||||
chr1:169887181 | G | T | 1 | a0001c0001t0031g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.165+1495C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887181 | |||||||
chr1:169887287 | C | T | 1 | a0001c0001t0007g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165+1389G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887287 | |||||||
chr1:169887323 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0146 |
4 | HG00673.hp2 HG02129.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+1353C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887323 | |||||||
chr1:169887327 | G | GGTCT | 35 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(32): Show |
66 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.165+1345_165+1348d others(6): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887327 | |||||||
chr1:169887397 | T | C | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+1279A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887397 | |||||||
chr1:169887423 | T | C | 3 | a0001c0001t0005g0278 a0001c0001t0008g0277 a0001c0001t0060g0239 |
3 | NA18940.hp2 NA18986.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.165+1253A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887423 | |||||||
chr1:169887464 | G | A | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.165+1212C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887464 | |||||||
chr1:169887481 | A | T | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+1195T>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887481 | |||||||
chr1:169887503 | A | C | 1 | a0001c0001t0003g0054 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.165+1173T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887503 | |||||||
chr1:169887520 | G | A | 1 | a0002c0002t0001g0030 | 2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.165+1156C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887520 | |||||||
chr1:169887602 | A | G | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+1074T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887602 | |||||||
chr1:169887727 | A | G | 5 | a0001c0001t0011g0183 a0001c0001t0031g0179 a0001c0001t0031g0180 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+949T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887727 | |||||||
chr1:169887876 | T | C | 35 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(32): Show |
71 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.165+800A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887876 | |||||||
chr1:169887954 | A | C | 5 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0004c0005t0018g0223 others(2): Show |
5 | HG01243.hp2 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+722T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887954 | |||||||
chr1:169887971 | T | C | 215 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(212): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.165+705A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169887971 | |||||||
chr1:169888094 | A | C | 1 | a0002c0002t0001g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.165+582T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169888094 | |||||||
chr1:169888237 | G | A | 2 | a0001c0001t0005g0280 a0001c0001t0008g0279 |
2 | NA18995.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.165+439C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169888237 | |||||||
chr1:169888262 | A | G | 1 | a0001c0001t0003g0053 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.165+414T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169888262 | |||||||
chr1:169888349 | C | T | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+327G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169888349 | |||||||
chr1:169888377 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.165+299A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169888377 | |||||||
chr1:169888503 | T | C | 1 | a0002c0002t0010g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.165+173A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169888503 | |||||||
chr1:169888611 | A | G | 2 | a0002c0002t0001g0107 a0002c0002t0001g0108 |
2 | HG02056.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.165+65T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 2/12 | chr1 | 169888611 | |||||||
chr1:169889051 | G | A | 51 | a0001c0001t0002g0050 a0001c0001t0002g0260 a0001c0001t0005g0018 others(48): Show |
63 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-50-161C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169889051 | |||||||
chr1:169889262 | A | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
4 | HG01891.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-372T>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169889262 | |||||||
chr1:169889559 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-50-669G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169889559 | |||||||
chr1:169889587 | T | A | 200 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(197): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-50-697A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169889587 | |||||||
chr1:169889591 | TA | T | 21 | a0001c0001t0012g0093 a0001c0001t0012g0095 a0001c0001t0012g0100 others(18): Show |
22 | HG00544.hp2 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-50-702delT | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169889591 | |||||||
chr1:169889833 | G | T | 20 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(17): Show |
27 | HG01081.hp2 HG01192.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-50-943C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169889833 | |||||||
chr1:169890070 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-50-1180A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169890070 | |||||||
chr1:169890136 | C | G | 5 | a0002c0002t0010g0102 a0002c0002t0010g0103 a0002c0002t0026g0105 others(2): Show |
5 | HG01109.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50-1246G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169890136 | |||||||
chr1:169890235 | A | G | 2 | a0001c0001t0003g0012 a0001c0001t0003g0052 |
4 | HG02015.hp2 HG02080.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-1345T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169890235 | |||||||
chr1:169890576 | C | G | 190 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(187): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-50-1686G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169890576 | |||||||
chr1:169890695 | G | C | 3 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0150 |
3 | NA18950.hp1 NA19009.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-50-1805C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169890695 | |||||||
chr1:169890819 | C | G | 3 | a0002c0002t0010g0102 a0002c0002t0010g0103 a0007c0009t0010g0104 |
3 | HG01109.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-50-1929G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169890819 | |||||||
chr1:169890871 | G | A | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50-1981C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169890871 | |||||||
chr1:169891012 | G | T | 200 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(197): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-50-2122C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891012 | |||||||
chr1:169891058 | C | T | 32 | a0001c0001t0012g0197 a0001c0001t0021g0151 a0001c0001t0021g0187 others(29): Show |
39 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-50-2168G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891058 | |||||||
chr1:169891195 | C | T | 3 | a0001c0001t0016g0083 a0001c0001t0028g0084 a0001c0001t0028g0085 |
3 | NA18985.hp1 NA19009.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-50-2305G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891195 | |||||||
chr1:169891214 | G | C | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50-2324C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891214 | |||||||
chr1:169891259 | A | G | 1 | a0001c0003t0051g0202 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-50-2369T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891259 | |||||||
chr1:169891313 | T | C | 12 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0004c0005t0010g0230 others(9): Show |
12 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-2423A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891313 | |||||||
chr1:169891332 | G | A | 95 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0021 others(92): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-50-2442C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891332 | |||||||
chr1:169891387 | C | A | 60 | a0001c0001t0002g0050 a0001c0001t0002g0184 a0001c0001t0002g0236 others(57): Show |
72 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.-51+2401G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891387 | |||||||
chr1:169891647 | T | G | 15 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0072 others(12): Show |
20 | HG01192.hp2 HG02015.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-51+2141A>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891647 | |||||||
chr1:169891843 | T | A | 4 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1945A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891843 | |||||||
chr1:169891992 | A | G | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-51+1796T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169891992 | |||||||
chr1:169892025 | G | C | 2 | a0004c0005t0018g0233 a0004c0005t0025g0234 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-51+1763C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892025 | |||||||
chr1:169892060 | C | G | 1 | a0001c0003t0004g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-51+1728G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892060 | |||||||
chr1:169892071 | T | C | 47 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(44): Show |
61 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-51+1717A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892071 | |||||||
chr1:169892133 | T | A | 1 | a0003c0004t0020g0046 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-51+1655A>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892133 | |||||||
chr1:169892250 | TTTTG | T | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-51+1534_-51+1537d others(6): Show |
SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892250 | |||||||
chr1:169892297 | C | T | 22 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0003c0004t0006g0017 others(19): Show |
26 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51+1491G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892297 | |||||||
chr1:169892497 | C | T | 21 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0022 others(18): Show |
28 | HG01081.hp2 HG01192.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-51+1291G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892497 | |||||||
chr1:169892758 | G | A | 2 | a0001c0001t0012g0208 a0001c0001t0012g0209 |
2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-51+1030C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892758 | |||||||
chr1:169892887 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG02602.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-51+901G>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892887 | |||||||
chr1:169892923 | C | G | 22 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0003c0004t0006g0017 others(19): Show |
26 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51+865G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892923 | |||||||
chr1:169892930 | T | C | 10 | a0003c0004t0006g0017 a0003c0004t0006g0045 a0003c0004t0006g0211 others(7): Show |
14 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-51+858A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892930 | |||||||
chr1:169892983 | C | G | 1 | a0001c0001t0008g0235 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51+805G>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169892983 | |||||||
chr1:169893021 | G | T | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-51+767C>A | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893021 | |||||||
chr1:169893191 | T | C | 13 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0004c0005t0010g0230 others(10): Show |
13 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+597A>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893191 | |||||||
chr1:169893262 | G | A | 1 | a0002c0002t0001g0218 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-51+526C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893262 | |||||||
chr1:169893328 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-51+460C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893328 | |||||||
chr1:169893347 | C | A | 7 | a0004c0005t0010g0230 a0004c0005t0018g0231 a0004c0005t0018g0232 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51+441G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893347 | |||||||
chr1:169893444 | G | C | 3 | a0002c0002t0001g0010 a0002c0002t0001g0221 a0003c0011t0001g0220 |
6 | HG01099.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+344C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893444 | |||||||
chr1:169893514 | C | A | 1 | a0002c0015t0046g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-51+274G>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893514 | |||||||
chr1:169893598 | G | A | 12 | a0002c0002t0041g0226 a0002c0002t0042g0227 a0004c0005t0010g0230 others(9): Show |
12 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+190C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893598 | |||||||
chr1:169893600 | G | C | 7 | a0004c0005t0010g0230 a0004c0005t0018g0231 a0004c0005t0018g0232 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51+188C>G | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893600 | |||||||
chr1:169893652 | G | A | 54 | a0001c0001t0002g0050 a0001c0001t0002g0236 a0001c0001t0002g0260 others(51): Show |
66 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-51+136C>T | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893652 | |||||||
chr1:169893773 | A | G | 22 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0012 others(19): Show |
40 | HG00423.hp2 HG00438.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.-51+15T>C | SCYL3 | ENSG00000000457.14 | transcript | ENST00000367771.11 | protein_coding | 1/12 | chr1 | 169893773 |