Item | Value |
---|---|
geneid | 283464 |
ensemblid | ENSG00000151233.11 |
hgncid | 27482 |
symbol | GXYLT1 |
name | glucoside xylosyltransferase 1 |
refseq_nuc | NM_173601.2 |
refseq_prot | NP_775872.1 |
ensembl_nuc | ENST00000398675.8 |
ensembl_prot | ENSP00000381666.3 |
mane_status | MANE Select |
chr | chr12 |
start | 42081845 |
end | 42144874 |
strand | - |
ver | v1.2 |
region | chr12:42081845-42144874 |
region5000 | chr12:42076845-42149874 |
regionname0 | GXYLT1_chr12_42081845_42144874 |
regionname5000 | GXYLT1_chr12_42076845_42149874 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 440 | 395 | 91 | 72 | 184 | 14 | 32 | 145 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | MRRYL others(435): Show |
chr12 | 42076845 | 42149874 |
a0002 | 0/0 | 427 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | MRRYL others(422): Show |
chr12 | 42076845 | 42149874 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1320 | 180 | 58 | 32 | 70 | 6 | 12 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | ATGCG others(1315): Show |
chr12 | 42076845 | 42149874 | ||
a0001c0002 | 0/0 | 1320 | 127 | 16 | 22 | 71 | 4 | 14 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | ATGCG others(1315): Show |
chr12 | 42076845 | 42149874 | ||
a0001c0003 | 0/0 | 1320 | 85 | 16 | 16 | 43 | 4 | 6 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | ATGCG others(1315): Show |
chr12 | 42076845 | 42149874 | ||
a0001c0005 | 0/0 | 1320 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | ATGCG others(1315): Show |
chr12 | 42076845 | 42149874 | ||
a0001c0006 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | ATGCG others(1315): Show |
chr12 | 42076845 | 42149874 | ||
a0002c0004 | 0/0 | 1281 | 3 | 1 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | ATGCG others(1276): Show |
chr12 | 42076845 | 42149874 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/1 | 7492 | 63 | 5 | 15 | 33 | 4 | 4 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0005 | 0/0 | 7493 | 20 | 1 | 3 | 15 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0006 | 0/0 | 7490 | 14 | 0 | 3 | 11 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7485): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0007 | 0/0 | 7504 | 12 | 9 | 2 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7499): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0008 | 0/0 | 7507 | 10 | 0 | 6 | 1 | 2 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7502): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0009 | 0/0 | 7493 | 8 | 8 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0010 | 0/0 | 7490 | 6 | 0 | 0 | 2 | 0 | 4 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7485): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0011 | 0/0 | 7493 | 6 | 6 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0012 | 0/0 | 7504 | 6 | 0 | 0 | 6 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7499): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0014 | 0/0 | 7494 | 4 | 4 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7489): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0016 | 0/0 | 7494 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7489): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0017 | 0/0 | 7492 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0018 | 0/0 | 7493 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0021 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0022 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0024 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0026 | 0/0 | 7492 | 2 | 1 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0027 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0028 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0037 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0038 | 0/0 | 7493 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0041 | 0/0 | 7492 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0043 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0044 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0045 | 0/0 | 7492 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0052 | 0/0 | 7504 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7499): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0053 | 0/0 | 7504 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7499): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0054 | 0/0 | 7504 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7499): Show |
chr12 | 42076845 | 42149874 |
a0001c0001t0055 | 0/0 | 7504 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7499): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0003 | 0/0 | 7493 | 55 | 5 | 9 | 35 | 1 | 5 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0004 | 0/0 | 7493 | 52 | 7 | 11 | 29 | 2 | 3 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0015 | 0/0 | 7493 | 4 | 0 | 1 | 0 | 1 | 2 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0019 | 0/0 | 7493 | 2 | 0 | 0 | 0 | 0 | 2 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0020 | 0/0 | 7493 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0025 | 0/0 | 7493 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0030 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0031 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0032 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0033 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0034 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0046 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0047 | 0/0 | 7493 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0048 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0049 | 0/0 | 7493 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0002t0050 | 0/0 | 7493 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0001 | 0/0 | 7493 | 71 | 14 | 14 | 39 | 3 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0013 | 0/0 | 7492 | 5 | 0 | 0 | 0 | 0 | 5 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7487): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0023 | 0/0 | 7493 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0029 | 0/0 | 7493 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0035 | 0/0 | 7493 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0036 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0039 | 0/0 | 7493 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0040 | 0/0 | 7493 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0003t0042 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0005t0004 | 0/0 | 7493 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0001c0006t0056 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7488): Show |
chr12 | 42076845 | 42149874 |
a0002c0004t0002 | 0/0 | 7453 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7448): Show |
chr12 | 42076845 | 42149874 |
a0002c0004t0051 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | AGAGG others(7460): Show |
chr12 | 42076845 | 42149874 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0280 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0321 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0008g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0009g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0009g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0009g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0010g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0011g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0012g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0012g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0012g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0012g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0012g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0012g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0014g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0014g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0014g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0016g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0016g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0016g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0017g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0017g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0017g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0018g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0018g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0018g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0021g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0022g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0022g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0024g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0024g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0026g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0026g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0027g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0027g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0028g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0028g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0037g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0038g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0041g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0043g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0044g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0045g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0052g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0053g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0054g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0001t0055g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0015g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0015g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0015g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0015g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0019g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0019g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0020g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0020g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0025g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0025g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0030g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0031g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0032g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0033g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0034g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0046g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0047g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0048g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0049g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0002t0050g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0013g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0013g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0013g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0013g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0013g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0023g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0023g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0029g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0029g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0035g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0036g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0039g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0040g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0003t0042g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0005t0004g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0001c0006t0056g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0002c0004t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
a0002c0004t0051g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0327 | EUR | GBR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0124 | EUR | GBR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00140 | hp1 | a0001 | c0002 | t0015 | g0236 | EUR | GBR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0323 | EUR | GBR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00323 | hp1 | a0001 | c0002 | t0004 | g0080 | EUR | FIN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00323 | hp2 | a0001 | c0003 | t0039 | g0249 | EUR | FIN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00408 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00423 | hp1 | a0001 | c0001 | t0006 | g0244 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0132 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00438 | hp2 | a0001 | c0002 | t0030 | g0024 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0271 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0199 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00621 | hp2 | a0001 | c0002 | t0004 | g0050 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0332 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00639 | hp2 | a0001 | c0002 | t0003 | g0196 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00642 | hp1 | a0001 | c0001 | t0008 | g0356 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0142 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00733 | hp1 | a0001 | c0002 | t0004 | g0042 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0210 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00738 | hp1 | a0001 | c0001 | t0007 | g0343 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0197 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0352 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0043 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01071 | hp1 | a0001 | c0002 | t0004 | g0044 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0123 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01081 | hp1 | a0001 | c0002 | t0004 | g0045 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0243 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0214 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01099 | hp2 | a0001 | c0002 | t0004 | g0079 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01106 | hp1 | a0001 | c0005 | t0004 | g0008 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0250 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01168 | hp2 | a0001 | c0003 | t0001 | g0131 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01169 | hp1 | a0001 | c0001 | t0026 | g0310 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01175 | hp1 | a0001 | c0001 | t0008 | g0353 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01175 | hp2 | a0001 | c0002 | t0003 | g0098 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0160 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0112 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01243 | hp2 | a0001 | c0002 | t0004 | g0047 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01255 | hp2 | a0001 | c0003 | t0035 | g0113 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01256 | hp1 | a0001 | c0001 | t0008 | g0358 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01257 | hp1 | a0001 | c0002 | t0004 | g0062 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01258 | hp2 | a0001 | c0001 | t0008 | g0357 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01346 | hp1 | a0001 | c0002 | t0015 | g0179 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01346 | hp2 | a0001 | c0001 | t0008 | g0355 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01433 | hp2 | a0001 | c0002 | t0047 | g0181 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01496 | hp1 | a0001 | c0005 | t0004 | g0008 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0351 | EUR | IBS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0215 | EUR | IBS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01517 | hp1 | a0001 | c0001 | t0008 | g0350 | EUR | IBS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0306 | EUR | IBS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01884 | hp1 | a0001 | c0001 | t0014 | g0231 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0094 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01891 | hp1 | a0001 | c0001 | t0011 | g0257 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0346 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01928 | hp1 | a0001 | c0001 | t0045 | g0287 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01928 | hp2 | a0001 | c0003 | t0040 | g0122 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0144 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0164 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0117 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01975 | hp1 | a0001 | c0002 | t0004 | g0082 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0266 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0262 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01981 | hp1 | a0001 | c0002 | t0004 | g0046 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG01981 | hp2 | a0001 | c0002 | t0003 | g0169 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0193 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0118 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02015 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02015 | hp2 | a0002 | c0004 | t0002 | g0009 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02040 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0251 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02055 | hp2 | a0001 | c0002 | t0034 | g0032 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0247 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02071 | hp2 | a0001 | c0002 | t0025 | g0105 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02080 | hp1 | a0001 | c0002 | t0048 | g0237 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02080 | hp2 | a0001 | c0002 | t0004 | g0067 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02083 | hp1 | a0001 | c0002 | t0004 | g0061 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02135 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02135 | hp2 | a0001 | c0001 | t0008 | g0359 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0170 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02155 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | CDX | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02165 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | CDX | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | CDX | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02258 | hp1 | a0001 | c0001 | t0022 | g0238 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02258 | hp2 | a0001 | c0002 | t0004 | g0054 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0264 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02280 | hp1 | a0001 | c0001 | t0014 | g0227 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02280 | hp2 | a0001 | c0001 | t0055 | g0349 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02293 | hp2 | a0001 | c0002 | t0004 | g0083 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02300 | hp1 | a0001 | c0001 | t0038 | g0275 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02300 | hp2 | a0001 | c0002 | t0004 | g0089 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02451 | hp1 | a0001 | c0001 | t0017 | g0240 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0269 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02523 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02572 | hp1 | a0001 | c0002 | t0003 | g0095 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02572 | hp2 | a0001 | c0003 | t0023 | g0208 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0253 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02615 | hp2 | a0001 | c0002 | t0004 | g0052 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0221 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0222 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0216 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02630 | hp2 | a0001 | c0001 | t0016 | g0091 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02647 | hp1 | a0001 | c0001 | t0017 | g0233 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0344 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02717 | hp1 | a0001 | c0001 | t0037 | g0103 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02717 | hp2 | a0001 | c0002 | t0020 | g0034 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0258 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02723 | hp2 | a0001 | c0002 | t0004 | g0066 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0162 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02738 | hp1 | a0001 | c0002 | t0049 | g0183 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02738 | hp2 | a0001 | c0001 | t0041 | g0320 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0226 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02809 | hp2 | a0002 | c0004 | t0051 | g0329 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0217 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02818 | hp2 | a0001 | c0001 | t0011 | g0102 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02886 | hp1 | a0001 | c0001 | t0028 | g0309 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0056 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0314 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0037 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02897 | hp2 | a0001 | c0001 | t0011 | g0101 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0331 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02922 | hp2 | a0001 | c0001 | t0018 | g0260 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02965 | hp1 | a0001 | c0002 | t0031 | g0025 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0254 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02970 | hp1 | a0001 | c0001 | t0053 | g0337 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0334 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02976 | hp2 | a0001 | c0003 | t0023 | g0207 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0206 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03041 | hp2 | a0001 | c0002 | t0020 | g0033 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0092 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0252 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0055 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0097 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0219 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03209 | hp1 | a0001 | c0001 | t0043 | g0100 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03225 | hp1 | a0001 | c0001 | t0024 | g0224 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03225 | hp2 | a0001 | c0001 | t0022 | g0239 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03239 | hp1 | a0001 | c0003 | t0013 | g0139 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03239 | hp2 | a0001 | c0002 | t0004 | g0069 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03453 | hp1 | a0001 | c0001 | t0016 | g0093 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03453 | hp2 | a0001 | c0001 | t0027 | g0230 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03486 | hp1 | a0001 | c0001 | t0021 | g0229 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0096 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0223 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03579 | hp1 | a0001 | c0001 | t0017 | g0232 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0209 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03654 | hp1 | a0001 | c0003 | t0013 | g0143 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0182 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03704 | hp1 | a0001 | c0001 | t0010 | g0031 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0277 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03831 | hp2 | a0001 | c0001 | t0010 | g0027 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0014 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03927 | hp1 | a0001 | c0002 | t0004 | g0068 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03927 | hp2 | a0001 | c0002 | t0015 | g0198 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03942 | hp1 | a0001 | c0002 | t0003 | g0109 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03942 | hp2 | a0001 | c0001 | t0010 | g0030 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04115 | hp1 | a0001 | c0002 | t0050 | g0158 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0029 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04184 | hp1 | a0001 | c0002 | t0004 | g0041 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04184 | hp2 | a0001 | c0003 | t0013 | g0256 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04199 | hp1 | a0001 | c0002 | t0019 | g0075 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04199 | hp2 | a0001 | c0003 | t0013 | g0138 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0211 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0340 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04228 | hp1 | a0001 | c0002 | t0019 | g0053 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG04228 | hp2 | a0001 | c0003 | t0013 | g0140 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0348 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18612 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | CHB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | CHB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18747 | hp2 | a0001 | c0003 | t0029 | g0360 | EAS | CHB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0255 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0261 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18940 | hp1 | a0001 | c0001 | t0006 | g0248 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18940 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18941 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0245 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18943 | hp2 | a0001 | c0002 | t0004 | g0035 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18944 | hp2 | a0001 | c0002 | t0004 | g0087 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18946 | hp1 | a0001 | c0001 | t0012 | g0335 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18947 | hp1 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18948 | hp1 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18949 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18950 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18950 | hp2 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18952 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18957 | hp1 | a0001 | c0001 | t0012 | g0333 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18957 | hp2 | a0001 | c0002 | t0004 | g0072 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18959 | hp1 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18960 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18961 | hp2 | a0001 | c0001 | t0012 | g0339 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0246 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18966 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18972 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18973 | hp2 | a0001 | c0002 | t0004 | g0073 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18975 | hp2 | a0001 | c0003 | t0029 | g0361 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18978 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18980 | hp2 | a0001 | c0002 | t0046 | g0178 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18982 | hp2 | a0001 | c0002 | t0004 | g0057 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18983 | hp2 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18984 | hp1 | a0001 | c0001 | t0012 | g0338 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18984 | hp2 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18987 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18989 | hp1 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18989 | hp2 | a0001 | c0001 | t0010 | g0026 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18990 | hp1 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18991 | hp1 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18991 | hp2 | a0001 | c0001 | t0012 | g0342 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18992 | hp2 | a0001 | c0002 | t0025 | g0104 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18993 | hp2 | a0001 | c0002 | t0004 | g0076 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18994 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0273 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18995 | hp1 | a0001 | c0002 | t0033 | g0064 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18998 | hp1 | a0001 | c0002 | t0004 | g0065 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19003 | hp1 | a0001 | c0001 | t0054 | g0341 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19003 | hp2 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19006 | hp1 | a0001 | c0002 | t0003 | g0235 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19011 | hp1 | a0001 | c0001 | t0044 | g0268 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19011 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19012 | hp2 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0099 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19030 | hp2 | a0001 | c0001 | t0027 | g0157 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19043 | hp1 | a0001 | c0001 | t0014 | g0234 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0107 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19055 | hp2 | a0001 | c0001 | t0006 | g0241 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19057 | hp1 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19057 | hp2 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19058 | hp1 | a0001 | c0002 | t0004 | g0084 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19060 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19060 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19062 | hp1 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19062 | hp2 | a0002 | c0004 | t0002 | g0009 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19066 | hp2 | a0001 | c0002 | t0004 | g0051 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19067 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19068 | hp1 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19068 | hp2 | a0001 | c0003 | t0042 | g0127 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19070 | hp1 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19070 | hp2 | a0001 | c0002 | t0004 | g0086 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19074 | hp1 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19076 | hp1 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19076 | hp2 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19077 | hp2 | a0001 | c0002 | t0004 | g0071 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0267 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19082 | hp1 | a0001 | c0002 | t0004 | g0088 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19084 | hp1 | a0001 | c0002 | t0032 | g0048 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19084 | hp2 | a0001 | c0003 | t0036 | g0145 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19086 | hp1 | a0001 | c0001 | t0012 | g0345 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19086 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19088 | hp1 | a0001 | c0002 | t0004 | g0074 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19091 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA19240 | hp2 | a0001 | c0001 | t0026 | g0313 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20129 | hp1 | a0001 | c0001 | t0021 | g0228 | AFR | ASW | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0202 | AFR | ASW | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0325 | EUR | TSI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0185 | EUR | TSI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0213 | EUR | TSI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20805 | hp2 | a0001 | c0002 | t0004 | g0090 | EUR | TSI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20905 | hp1 | a0001 | c0001 | t0008 | g0354 | SAS | GIH | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20905 | hp2 | a0001 | c0002 | t0015 | g0180 | SAS | GIH | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0205 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02109 | hp2 | a0001 | c0001 | t0028 | g0311 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02486 | hp1 | a0001 | c0001 | t0024 | g0225 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02486 | hp2 | a0001 | c0002 | t0004 | g0059 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0347 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03471 | hp1 | a0001 | c0001 | t0018 | g0259 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG03471 | hp2 | a0001 | c0001 | t0052 | g0330 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0336 | AFR | USA | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | USA | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18955 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0019 | AFR | USA | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0328 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
NA21309 | hp2 | a0001 | c0006 | t0056 | g0362 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0321 | REF | REF | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0280 | REF | REF | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42144454 | GGCCCGCG others(32): Show |
G | 1 | a0002 | 3 | HG02015.hp2 HG02809.hp2 NA19062.hp2 |
conservative_inframe_deletion | MODERATE | c.154_192delGGCGGACG others(31): Show |
p.Gly52_Gly64del | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 420/7492 | 154/1323 | 52/440 | chr12 | 42144454 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42087930 | G | A | 1 | a0001c0003 | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
synonymous_variant | LOW | c.1179C>T | p.Asp393Asp | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1407/7492 | 1179/1323 | 393/440 | chr12 | 42087930 | |||
chr12:42097577 | T | A | 1 | a0001c0005 | 2 | HG01106.hp1 HG01496.hp1 |
synonymous_variant | LOW | c.1026A>T | p.Arg342Arg | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/8 | 1254/7492 | 1026/1323 | 342/440 | chr12 | 42097577 | |||
chr12:42109665 | T | C | 2 | a0001c0002 a0001c0005 |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
synonymous_variant | LOW | c.513A>G | p.Thr171Thr | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/8 | 741/7492 | 513/1323 | 171/440 | chr12 | 42109665 | |||
chr12:42119162 | C | T | 1 | a0001c0006 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.324G>A | p.Leu108Leu | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/8 | 552/7492 | 324/1323 | 108/440 | chr12 | 42119162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42081850 | G | A | 2 | a0001c0001t0014 a0001c0001t0021 |
6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5936C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5936 | chr12 | 42081850 | ||||||
chr12:42081899 | T | C | 1 | a0001c0006t0056 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5887A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5887 | chr12 | 42081899 | ||||||
chr12:42081946 | G | A | 1 | a0001c0001t0009 | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5840C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5840 | chr12 | 42081946 | ||||||
chr12:42082086 | G | A | 16 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0015 others(13): Show |
128 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*5700C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5700 | chr12 | 42082086 | ||||||
chr12:42082139 | G | A | 1 | a0001c0001t0038 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5647C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5647 | chr12 | 42082139 | ||||||
chr12:42082182 | T | A | 2 | a0001c0001t0006 a0001c0001t0010 |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5604A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5604 | chr12 | 42082182 | ||||||
chr12:42082222 | T | A | 2 | a0001c0001t0026 a0001c0001t0028 |
4 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5564A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5564 | chr12 | 42082222 | ||||||
chr12:42082233 | G | A | 1 | a0001c0002t0050 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5553C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5553 | chr12 | 42082233 | ||||||
chr12:42082411 | A | G | 3 | a0001c0001t0005 a0001c0001t0038 a0001c0001t0044 |
22 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5375T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5375 | chr12 | 42082411 | ||||||
chr12:42082684 | C | A | 1 | a0001c0001t0054 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5102G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5102 | chr12 | 42082684 | ||||||
chr12:42082811 | A | C | 30 | a0001c0001t0016 a0001c0001t0026 a0001c0001t0027 others(27): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*4975T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4975 | chr12 | 42082811 | ||||||
chr12:42082877 | C | A | 1 | a0001c0001t0009 | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4909G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4909 | chr12 | 42082877 | ||||||
chr12:42082996 | T | C | 2 | a0001c0001t0006 a0001c0001t0010 |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4790A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4790 | chr12 | 42082996 | ||||||
chr12:42083043 | T | C | 1 | a0001c0001t0017 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4743A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4743 | chr12 | 42083043 | ||||||
chr12:42083174 | C | T | 1 | a0001c0001t0043 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4612G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4612 | chr12 | 42083174 | ||||||
chr12:42083185 | T | A | 11 | a0001c0001t0024 a0001c0001t0053 a0001c0002t0003 others(8): Show |
70 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*4601A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4601 | chr12 | 42083185 | ||||||
chr12:42083186 | A | T | 4 | a0001c0001t0018 a0001c0001t0026 a0001c0001t0052 others(1): Show |
7 | HG00323.hp2 HG01169.hp1 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4600T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4600 | chr12 | 42083186 | ||||||
chr12:42083554 | T | A | 2 | a0001c0001t0012 a0001c0001t0054 |
7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4232A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4232 | chr12 | 42083554 | ||||||
chr12:42083602 | T | C | 2 | a0001c0001t0006 a0001c0001t0010 |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4184A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4184 | chr12 | 42083602 | ||||||
chr12:42083625 | A | G | 1 | a0001c0001t0009 | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4161T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4161 | chr12 | 42083625 | ||||||
chr12:42083725 | T | C | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4061A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4061 | chr12 | 42083725 | ||||||
chr12:42083768 | T | C | 4 | a0001c0002t0015 a0001c0002t0047 a0001c0002t0049 others(1): Show |
7 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4018A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4018 | chr12 | 42083768 | ||||||
chr12:42083873 | A | T | 1 | a0001c0002t0047 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3913T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3913 | chr12 | 42083873 | ||||||
chr12:42083978 | T | TA | 12 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0011 others(9): Show |
51 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3807dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3807 | chr12 | 42083978 | ||||||
chr12:42083978 | TA | T | 1 | a0001c0003t0013 | 5 | HG03239.hp1 HG03654.hp1 HG04184.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3807delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3807 | chr12 | 42083978 | ||||||
chr12:42084013 | A | G | 1 | a0001c0001t0037 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3773T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3773 | chr12 | 42084013 | ||||||
chr12:42084261 | C | T | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3525G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3525 | chr12 | 42084261 | ||||||
chr12:42084416 | G | A | 1 | a0001c0006t0056 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3370C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3370 | chr12 | 42084416 | ||||||
chr12:42084462 | C | CA | 27 | a0001c0001t0016 a0001c0002t0003 a0001c0002t0004 others(24): Show |
217 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*3323_*3324insT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3323 | chr12 | 42084462 | ||||||
chr12:42084513 | C | T | 1 | a0001c0001t0041 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3273G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3273 | chr12 | 42084513 | ||||||
chr12:42084611 | G | T | 53 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(50): Show |
330 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*3175C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3175 | chr12 | 42084611 | ||||||
chr12:42084737 | T | C | 3 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0028 |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3049A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3049 | chr12 | 42084737 | ||||||
chr12:42084754 | A | C | 7 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0012 others(4): Show |
32 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3032T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3032 | chr12 | 42084754 | ||||||
chr12:42084855 | T | C | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2931A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2931 | chr12 | 42084855 | ||||||
chr12:42084881 | C | A | 1 | a0001c0002t0019 | 2 | HG04199.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2905G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2905 | chr12 | 42084881 | ||||||
chr12:42084937 | A | C | 1 | a0001c0002t0047 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2849T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2849 | chr12 | 42084937 | ||||||
chr12:42084993 | CTA | C | 3 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0021 |
22 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2791_*2792delTA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2791 | chr12 | 42084993 | ||||||
chr12:42085032 | C | T | 1 | a0001c0003t0023 | 2 | HG02572.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2754G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2754 | chr12 | 42085032 | ||||||
chr12:42085377 | G | A | 1 | a0001c0003t0042 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2409C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2409 | chr12 | 42085377 | ||||||
chr12:42085385 | C | T | 1 | a0001c0002t0046 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2401G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2401 | chr12 | 42085385 | ||||||
chr12:42085538 | G | A | 1 | a0001c0001t0043 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2248C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2248 | chr12 | 42085538 | ||||||
chr12:42085570 | T | G | 1 | a0001c0001t0044 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2216A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2216 | chr12 | 42085570 | ||||||
chr12:42085648 | A | G | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(8): Show |
55 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2138T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2138 | chr12 | 42085648 | ||||||
chr12:42085791 | G | C | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1995C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1995 | chr12 | 42085791 | ||||||
chr12:42086067 | C | T | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1719G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1719 | chr12 | 42086067 | ||||||
chr12:42086175 | A | G | 1 | a0001c0003t0036 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1611T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1611 | chr12 | 42086175 | ||||||
chr12:42086434 | G | A | 1 | a0001c0001t0045 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1352C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1352 | chr12 | 42086434 | ||||||
chr12:42086570 | G | C | 1 | a0001c0002t0034 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1216C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1216 | chr12 | 42086570 | ||||||
chr12:42087088 | A | G | 1 | a0001c0001t0009 | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*698T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 698 | chr12 | 42087088 | ||||||
chr12:42087299 | A | G | 1 | a0001c0003t0035 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 487 | chr12 | 42087299 | ||||||
chr12:42087335 | A | G | 1 | a0001c0002t0032 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*451T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 451 | chr12 | 42087335 | ||||||
chr12:42087562 | G | GT | 2 | a0001c0001t0014 a0001c0001t0021 |
6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*223dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 223 | chr12 | 42087562 | ||||||
chr12:42087641 | A | G | 8 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0012 others(5): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*145T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 145 | chr12 | 42087641 | ||||||
chr12:42087722 | G | A | 1 | a0001c0002t0020 | 2 | HG02717.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*64C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 64 | chr12 | 42087722 | ||||||
chr12:42087743 | T | C | 8 | a0001c0002t0003 a0001c0002t0015 a0001c0002t0030 others(5): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*43A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 43 | chr12 | 42087743 | ||||||
chr12:42144661 | T | TCCTCCTT others(5): Show |
1 | a0002c0004t0051 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-27_-16dupCGGCGAAG others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 16 | chr12 | 42144661 | ||||||
chr12:42144668 | T | TCGCCGCC others(5): Show |
6 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0052 others(3): Show |
22 | HG00639.hp1 HG00738.hp1 HG01891.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-34_-23dupGCGGCGGC others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 23 | chr12 | 42144668 | ||||||
chr12:42144668 | T | TCGCCGCC others(8): Show |
1 | a0001c0001t0008 | 10 | HG00642.hp1 HG01069.hp1 HG01175.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-23dupGCGGCGGC others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 23 | chr12 | 42144668 | ||||||
chr12:42144700 | T | C | 1 | a0001c0003t0029 | 2 | NA18747.hp2 NA18975.hp2 |
5_prime_UTR_variant | MODIFIER | c.-54A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 54 | chr12 | 42144700 | ||||||
chr12:42144728 | C | G | 8 | a0001c0002t0004 a0001c0002t0019 a0001c0002t0020 others(5): Show |
62 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-82G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 82 | chr12 | 42144728 | ||||||
chr12:42144766 | C | A | 1 | a0001c0006t0056 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-120G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 120 | chr12 | 42144766 | ||||||
chr12:42144767 | C | T | 1 | a0001c0001t0010 | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-121G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 121 | chr12 | 42144767 | ||||||
chr12:42144788 | C | T | 1 | a0001c0002t0031 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-142G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 142 | chr12 | 42144788 | ||||||
chr12:42144833 | G | T | 1 | a0001c0002t0030 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 187 | chr12 | 42144833 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42088001 | G | A | 303 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(300): Show |
325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.1162-54C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088001 | |||||||
chr12:42088099 | T | G | 1 | a0001c0001t0028g0311 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1162-152A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088099 | |||||||
chr12:42088199 | T | C | 24 | a0001c0002t0004g0035 a0001c0002t0004g0036 a0001c0002t0004g0038 others(21): Show |
24 | HG00621.hp2 HG01975.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1162-252A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088199 | |||||||
chr12:42088222 | A | C | 1 | a0001c0001t0002g0291 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1162-275T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088222 | |||||||
chr12:42088292 | C | T | 1 | a0001c0003t0036g0145 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1162-345G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088292 | |||||||
chr12:42088510 | G | A | 1 | a0001c0002t0004g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1162-563C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088510 | |||||||
chr12:42088625 | C | T | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-678G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088625 | |||||||
chr12:42088883 | G | GAAAGAAC others(70): Show |
1 | a0001c0003t0001g0150 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1162-937_1162-936i others(79): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | |||||||
chr12:42088883 | G | GAAAGAAC others(80): Show |
2 | a0001c0002t0004g0036 a0001c0002t0020g0033 |
2 | HG03041.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1162-937_1162-936i others(89): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | |||||||
chr12:42088883 | G | GAAAGAAC others(81): Show |
49 | a0001c0002t0004g0035 a0001c0002t0004g0037 a0001c0002t0004g0038 others(46): Show |
49 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1162-937_1162-936i others(90): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | |||||||
chr12:42088883 | G | GAAAGAAC others(82): Show |
120 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(117): Show |
130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1162-937_1162-936i others(91): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | |||||||
chr12:42088883 | G | GAAAGAAC others(83): Show |
22 | a0001c0002t0003g0170 a0001c0002t0003g0182 a0001c0002t0003g0193 others(19): Show |
22 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1162-937_1162-936i others(92): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | |||||||
chr12:42088883 | G | GAAAGAAC others(84): Show |
5 | a0001c0002t0003g0195 a0001c0002t0004g0045 a0001c0002t0004g0047 others(2): Show |
5 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162-937_1162-936i others(93): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | |||||||
chr12:42088883 | G | GAAAGAAC others(85): Show |
2 | a0001c0003t0001g0116 a0001c0005t0004g0008 |
3 | HG01106.hp1 HG01496.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1162-937_1162-936i others(94): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | |||||||
chr12:42088883 | G | GAAAGAAC others(86): Show |
2 | a0001c0003t0001g0128 a0001c0003t0001g0160 |
2 | HG01192.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1162-937_1162-936i others(95): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | |||||||
chr12:42089000 | A | G | 1 | a0001c0001t0007g0334 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1162-1053T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089000 | |||||||
chr12:42089176 | A | G | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1162-1229T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089176 | |||||||
chr12:42089306 | G | A | 1 | a0001c0001t0005g0328 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1162-1359C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089306 | |||||||
chr12:42089312 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1162-1365C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089312 | |||||||
chr12:42089342 | T | A | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162-1395A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089342 | |||||||
chr12:42089466 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-1519G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089466 | |||||||
chr12:42089477 | A | G | 1 | a0001c0001t0006g0243 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1162-1530T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089477 | |||||||
chr12:42089516 | T | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0285 a0001c0001t0002g0292 others(1): Show |
6 | HG01496.hp2 HG01928.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1569A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089516 | |||||||
chr12:42089573 | C | T | 1 | a0002c0004t0051g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1162-1626G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089573 | |||||||
chr12:42089633 | C | T | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162-1686G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089633 | |||||||
chr12:42089669 | T | C | 1 | a0001c0002t0004g0041 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1162-1722A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089669 | |||||||
chr12:42089786 | G | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0285 a0001c0001t0002g0292 others(1): Show |
6 | HG01496.hp2 HG01928.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1839C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089786 | |||||||
chr12:42089888 | A | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-1941T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089888 | |||||||
chr12:42090032 | T | C | 1 | a0001c0001t0017g0240 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1162-2085A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090032 | |||||||
chr12:42090114 | G | GA | 347 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(344): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.1162-2168dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090114 | |||||||
chr12:42090114 | G | GAA | 11 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(8): Show |
11 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162-2169_1162-216 others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090114 | |||||||
chr12:42090129 | T | C | 59 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(56): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1162-2182A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090129 | |||||||
chr12:42090205 | T | A | 1 | a0001c0001t0008g0353 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1162-2258A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090205 | |||||||
chr12:42090388 | T | A | 1 | a0001c0001t0027g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1162-2441A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090388 | |||||||
chr12:42090568 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-2621A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090568 | |||||||
chr12:42090771 | T | A | 2 | a0001c0002t0020g0033 a0001c0002t0020g0034 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1162-2824A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090771 | |||||||
chr12:42090865 | A | C | 1 | a0001c0003t0001g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1162-2918T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090865 | |||||||
chr12:42090886 | T | C | 8 | a0001c0002t0004g0035 a0001c0002t0004g0040 a0001c0002t0004g0049 others(5): Show |
8 | HG00621.hp2 HG02129.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162-2939A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090886 | |||||||
chr12:42090954 | T | C | 1 | a0001c0002t0020g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1162-3007A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090954 | |||||||
chr12:42090956 | A | AATTT | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162-3010_1162-300 others(8): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090956 | |||||||
chr12:42090978 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-3031A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090978 | |||||||
chr12:42091052 | G | A | 59 | a0001c0002t0004g0035 a0001c0002t0004g0036 a0001c0002t0004g0037 others(56): Show |
60 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.1162-3105C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091052 | |||||||
chr12:42091287 | AT | A | 8 | a0001c0002t0003g0191 a0001c0002t0015g0179 a0001c0002t0015g0180 others(5): Show |
8 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162-3341delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091287 | |||||||
chr12:42091292 | T | A | 1 | a0001c0002t0004g0049 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1162-3345A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091292 | |||||||
chr12:42091293 | T | A | 15 | a0001c0001t0016g0092 a0001c0001t0016g0093 a0001c0002t0003g0165 others(12): Show |
15 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1162-3346A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091293 | |||||||
chr12:42091294 | T | A | 199 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0016g0091 others(196): Show |
210 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1162-3347A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091294 | |||||||
chr12:42091295 | A | T | 6 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 others(3): Show |
6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-3348T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091295 | |||||||
chr12:42091361 | T | C | 1 | a0001c0001t0002g0300 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1162-3414A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091361 | |||||||
chr12:42091414 | GAT | G | 4 | a0001c0002t0015g0179 a0001c0002t0015g0180 a0001c0002t0015g0198 others(1): Show |
4 | HG00140.hp1 HG01346.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-3469_1162-346 others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091414 | |||||||
chr12:42091415 | A | AT | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-3469dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091415 | |||||||
chr12:42091434 | G | A | 1 | a0001c0002t0031g0025 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1162-3487C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091434 | |||||||
chr12:42091486 | A | G | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-3539T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091486 | |||||||
chr12:42091503 | C | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-3556G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091503 | |||||||
chr12:42091633 | TC | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-3687delG | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091633 | |||||||
chr12:42091649 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-3702A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091649 | |||||||
chr12:42091665 | T | C | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1162-3718A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091665 | |||||||
chr12:42091717 | C | A | 303 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(300): Show |
325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.1162-3770G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091717 | |||||||
chr12:42091856 | C | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1162-3909G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091856 | |||||||
chr12:42091885 | T | C | 6 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 others(3): Show |
6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-3938A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091885 | |||||||
chr12:42092670 | A | G | 42 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(39): Show |
48 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.1162-4723T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092670 | |||||||
chr12:42092686 | T | C | 1 | a0001c0003t0001g0219 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1162-4739A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092686 | |||||||
chr12:42092693 | G | A | 3 | a0001c0001t0021g0228 a0001c0001t0021g0229 a0002c0004t0051g0329 |
3 | HG02809.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1162-4746C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092693 | |||||||
chr12:42092774 | C | T | 1 | a0001c0001t0022g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1161+4668G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092774 | |||||||
chr12:42092800 | C | T | 303 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(300): Show |
325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.1161+4642G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092800 | |||||||
chr12:42092840 | G | A | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+4602C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092840 | |||||||
chr12:42092905 | T | C | 1 | a0001c0001t0008g0354 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1161+4537A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092905 | |||||||
chr12:42092920 | G | T | 1 | a0001c0002t0003g0163 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1161+4522C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092920 | |||||||
chr12:42092960 | G | A | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161+4482C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092960 | |||||||
chr12:42092986 | A | G | 1 | a0001c0001t0037g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1161+4456T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092986 | |||||||
chr12:42093037 | T | C | 1 | a0001c0002t0004g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1161+4405A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093037 | |||||||
chr12:42093200 | C | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161+4242G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093200 | |||||||
chr12:42093344 | G | A | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+4098C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093344 | |||||||
chr12:42093346 | C | A | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1161+4096G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093346 | |||||||
chr12:42093348 | G | A | 1 | a0001c0003t0001g0123 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1161+4094C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093348 | |||||||
chr12:42093415 | A | C | 5 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+4027T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093415 | |||||||
chr12:42093466 | T | C | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+3976A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093466 | |||||||
chr12:42093495 | T | C | 1 | a0001c0002t0003g0174 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1161+3947A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093495 | |||||||
chr12:42093517 | C | A | 81 | a0001c0003t0001g0010 a0001c0003t0001g0011 a0001c0003t0001g0012 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1161+3925G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093517 | |||||||
chr12:42093853 | A | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1161+3589T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093853 | |||||||
chr12:42094055 | T | TAAA | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+3384_1161+338 others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094055 | |||||||
chr12:42094067 | A | G | 6 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+3375T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094067 | |||||||
chr12:42094275 | C | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1161+3167G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094275 | |||||||
chr12:42094351 | C | CA | 46 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0028g0309 others(43): Show |
50 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1161+3090dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094351 | |||||||
chr12:42094351 | C | CAA | 15 | a0001c0002t0003g0015 a0001c0002t0003g0016 a0001c0002t0003g0108 others(12): Show |
17 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1161+3089_1161+309 others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094351 | |||||||
chr12:42094351 | CA | C | 35 | a0001c0001t0002g0290 a0001c0001t0002g0293 a0001c0001t0002g0315 others(32): Show |
38 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1161+3090delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094351 | |||||||
chr12:42094461 | C | G | 2 | a0001c0001t0011g0257 a0001c0001t0011g0258 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1161+2981G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094461 | |||||||
chr12:42094505 | A | G | 2 | a0001c0001t0007g0331 a0001c0001t0052g0330 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1161+2937T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094505 | |||||||
chr12:42094734 | A | T | 1 | a0001c0001t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1161+2708T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094734 | |||||||
chr12:42094832 | G | T | 2 | a0001c0001t0011g0257 a0001c0001t0011g0258 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1161+2610C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094832 | |||||||
chr12:42094847 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1161+2595G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094847 | |||||||
chr12:42094867 | T | C | 2 | a0001c0002t0004g0089 a0001c0002t0004g0090 |
2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1161+2575A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094867 | |||||||
chr12:42094914 | T | C | 2 | a0001c0002t0020g0033 a0001c0002t0020g0034 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1161+2528A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094914 | |||||||
chr12:42094940 | T | C | 2 | a0001c0001t0002g0279 a0001c0001t0002g0302 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1161+2502A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094940 | |||||||
chr12:42095009 | A | AC | 209 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(206): Show |
220 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1161+2432dupG | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095009 | |||||||
chr12:42095155 | T | C | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1161+2287A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095155 | |||||||
chr12:42095354 | C | T | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+2088G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095354 | |||||||
chr12:42095357 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1161+2085A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095357 | |||||||
chr12:42095393 | C | T | 9 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(6): Show |
9 | HG01169.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1161+2049G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095393 | |||||||
chr12:42095680 | T | C | 1 | a0001c0003t0001g0212 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1161+1762A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095680 | |||||||
chr12:42095718 | CT | C | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161+1723delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095718 | |||||||
chr12:42095720 | AT | A | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+1721delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095720 | |||||||
chr12:42095798 | T | C | 1 | a0001c0001t0014g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1161+1644A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095798 | |||||||
chr12:42095811 | A | G | 211 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(208): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1161+1631T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095811 | |||||||
chr12:42095875 | T | G | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1567A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095875 | |||||||
chr12:42095876 | A | T | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1566T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095876 | |||||||
chr12:42095877 | T | A | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1565A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095877 | |||||||
chr12:42095886 | C | T | 1 | a0001c0001t0021g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1161+1556G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095886 | |||||||
chr12:42095902 | C | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161+1540G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095902 | |||||||
chr12:42095991 | C | T | 2 | a0001c0001t0002g0282 a0001c0001t0002g0289 |
2 | NA18969.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1161+1451G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095991 | |||||||
chr12:42096017 | G | A | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1425C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096017 | |||||||
chr12:42096110 | A | C | 1 | a0001c0001t0014g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1161+1332T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096110 | |||||||
chr12:42096125 | T | C | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1161+1317A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096125 | |||||||
chr12:42096199 | C | T | 201 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(198): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1161+1243G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096199 | |||||||
chr12:42096283 | T | A | 1 | a0001c0002t0004g0054 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1161+1159A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096283 | |||||||
chr12:42096336 | G | T | 6 | a0001c0001t0008g0350 a0001c0001t0008g0351 a0001c0001t0008g0352 others(3): Show |
6 | HG00642.hp1 HG01069.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+1106C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096336 | |||||||
chr12:42096410 | A | C | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1161+1032T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096410 | |||||||
chr12:42096420 | G | T | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1022C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096420 | |||||||
chr12:42096464 | A | G | 6 | a0001c0001t0007g0023 a0001c0001t0007g0334 a0001c0001t0007g0336 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161+978T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096464 | |||||||
chr12:42096478 | A | C | 1 | a0001c0003t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1161+964T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096478 | |||||||
chr12:42096502 | C | A | 81 | a0001c0003t0001g0010 a0001c0003t0001g0011 a0001c0003t0001g0012 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1161+940G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096502 | |||||||
chr12:42096504 | T | G | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+938A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096504 | |||||||
chr12:42096578 | G | A | 1 | a0001c0002t0003g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1161+864C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096578 | |||||||
chr12:42096610 | G | A | 202 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(199): Show |
213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1161+832C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096610 | |||||||
chr12:42096618 | T | C | 1 | a0001c0003t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1161+824A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096618 | |||||||
chr12:42096673 | A | G | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+769T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096673 | |||||||
chr12:42096746 | C | T | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+696G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096746 | |||||||
chr12:42096747 | T | C | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+695A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096747 | |||||||
chr12:42096749 | C | T | 1 | a0001c0002t0003g0191 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+693G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096749 | |||||||
chr12:42096914 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1161+528C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096914 | |||||||
chr12:42097004 | T | C | 4 | a0001c0002t0004g0035 a0001c0002t0004g0058 a0001c0002t0004g0063 others(1): Show |
4 | NA18943.hp2 NA18998.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161+438A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097004 | |||||||
chr12:42097030 | A | C | 2 | a0001c0001t0011g0257 a0001c0001t0011g0258 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1161+412T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097030 | |||||||
chr12:42097073 | C | T | 2 | a0001c0001t0026g0310 a0001c0001t0026g0313 |
2 | HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1161+369G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097073 | |||||||
chr12:42097149 | G | A | 204 | a0001c0001t0024g0224 a0001c0001t0024g0225 a0001c0002t0003g0004 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1161+293C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097149 | |||||||
chr12:42097153 | G | A | 1 | a0001c0002t0003g0173 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1161+289C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097153 | |||||||
chr12:42097214 | T | C | 32 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(29): Show |
36 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.1161+228A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097214 | |||||||
chr12:42097234 | A | G | 1 | a0001c0001t0053g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1161+208T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097234 | |||||||
chr12:42097283 | T | C | 5 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+159A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097283 | |||||||
chr12:42097301 | G | A | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1161+141C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097301 | |||||||
chr12:42097388 | A | G | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+54T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097388 | |||||||
chr12:42097390 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1161+52G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097390 | |||||||
chr12:42098383 | T | G | 3 | a0001c0002t0020g0033 a0001c0002t0020g0034 a0001c0002t0034g0032 |
3 | HG02055.hp2 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.865-350A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098383 | |||||||
chr12:42098456 | T | TCA | 304 | a0001c0001t0002g0299 a0001c0001t0005g0003 a0001c0001t0005g0262 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.865-424_865-423ins others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098456 | |||||||
chr12:42098760 | C | CAT | 21 | a0001c0001t0005g0269 a0001c0001t0005g0328 a0001c0001t0007g0023 others(18): Show |
22 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.865-729_865-728dup others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATAT | 22 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(19): Show |
25 | HG00544.hp1 HG00597.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.865-731_865-728dup others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATAT | 9 | a0001c0001t0005g0265 a0001c0001t0007g0340 a0001c0001t0010g0031 others(6): Show |
10 | HG01106.hp1 HG01496.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.865-733_865-728dup others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(1): Show |
11 | a0001c0001t0006g0243 a0001c0001t0007g0332 a0001c0001t0009g0253 others(8): Show |
11 | HG00639.hp1 HG01081.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.865-735_865-728dup others(8): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(3): Show |
11 | a0001c0001t0006g0242 a0001c0001t0014g0231 a0001c0002t0004g0037 others(8): Show |
11 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.865-737_865-728dup others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(5): Show |
27 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(24): Show |
31 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.865-739_865-728dup others(12): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(7): Show |
20 | a0001c0002t0003g0175 a0001c0002t0004g0042 a0001c0002t0004g0049 others(17): Show |
20 | HG00733.hp1 HG01074.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.865-741_865-728dup others(14): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(9): Show |
36 | a0001c0001t0006g0245 a0001c0001t0006g0247 a0001c0001t0006g0248 others(33): Show |
40 | HG00438.hp1 HG00438.hp2 HG01975.hp1 others(37): Show |
intron_variant | MODIFIER | c.865-743_865-728dup others(16): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(11): Show |
12 | a0001c0002t0003g0096 a0001c0002t0003g0173 a0001c0002t0003g0182 others(9): Show |
12 | HG00323.hp2 HG00621.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.865-745_865-728dup others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(13): Show |
20 | a0001c0001t0010g0029 a0001c0002t0003g0004 a0001c0002t0003g0014 others(17): Show |
24 | HG00408.hp2 HG00609.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.865-747_865-728dup others(20): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(15): Show |
22 | a0001c0001t0010g0026 a0001c0001t0014g0226 a0001c0002t0003g0016 others(19): Show |
23 | HG00544.hp2 HG00597.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.865-749_865-728dup others(22): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(17): Show |
17 | a0001c0001t0009g0254 a0001c0002t0003g0015 a0001c0002t0003g0097 others(14): Show |
18 | HG01099.hp1 HG01981.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.865-751_865-728dup others(24): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(19): Show |
20 | a0001c0001t0009g0252 a0001c0001t0014g0227 a0001c0001t0014g0234 others(17): Show |
22 | HG00099.hp2 HG01074.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(26): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(21): Show |
12 | a0001c0001t0010g0028 a0001c0002t0003g0170 a0001c0002t0003g0187 others(9): Show |
12 | HG00140.hp1 HG01346.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(28): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(23): Show |
6 | a0001c0001t0009g0251 a0001c0002t0003g0108 a0001c0002t0003g0159 others(3): Show |
6 | HG00609.hp1 HG00733.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(30): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(25): Show |
4 | a0001c0002t0003g0197 a0001c0003t0001g0128 a0001c0003t0001g0130 others(1): Show |
4 | HG00738.hp2 HG02083.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(32): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(27): Show |
6 | a0001c0002t0003g0196 a0001c0002t0004g0043 a0001c0002t0004g0044 others(3): Show |
6 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(34): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | C | CATATATA others(29): Show |
1 | a0001c0002t0003g0185 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.865-728_865-727ins others(36): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | CAT | C | 55 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(52): Show |
69 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.865-729_865-728del others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | CATAT | C | 3 | a0001c0001t0002g0307 a0001c0001t0027g0157 a0001c0001t0027g0230 |
3 | HG00423.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.865-731_865-728del others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | CATATAT | C | 4 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-733_865-728del others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | CATATATA others(3): Show |
C | 1 | a0001c0002t0003g0161 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.865-737_865-728del others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098760 | CATATATA others(11): Show |
C | 1 | a0001c0003t0001g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.865-745_865-728del others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | |||||||
chr12:42098762 | T | TATATATA others(45): Show |
1 | a0001c0003t0001g0220 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.865-730_865-729ins others(52): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098762 | |||||||
chr12:42098782 | T | TAA | 3 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 |
3 | HG02717.hp1 HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.865-750_865-749ins others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098782 | |||||||
chr12:42098782 | T | TATATATA others(13): Show |
1 | a0001c0003t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.865-750_865-749ins others(20): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098782 | |||||||
chr12:42098784 | T | A | 10 | a0001c0001t0002g0281 a0001c0001t0002g0295 a0001c0001t0011g0101 others(7): Show |
10 | HG01169.hp1 HG01256.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.865-751A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098784 | |||||||
chr12:42098784 | T | TATATATA others(3): Show |
1 | a0001c0001t0043g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.865-752_865-751ins others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098784 | |||||||
chr12:42098784 | T | TATATATA others(3): Show |
1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.865-752_865-751ins others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098784 | |||||||
chr12:42098784 | T | TATATATA others(8): Show |
1 | a0001c0002t0003g0186 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.865-752_865-751ins others(15): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098784 | |||||||
chr12:42099009 | G | T | 1 | a0001c0001t0002g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.865-976C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099009 | |||||||
chr12:42099102 | C | G | 1 | a0001c0003t0001g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.865-1069G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099102 | |||||||
chr12:42099159 | T | C | 1 | a0001c0001t0002g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.865-1126A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099159 | |||||||
chr12:42099619 | G | A | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.865-1586C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099619 | |||||||
chr12:42099651 | G | A | 2 | a0001c0003t0001g0160 a0001c0006t0056g0362 |
2 | HG01192.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.865-1618C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099651 | |||||||
chr12:42099710 | C | A | 1 | a0001c0005t0004g0008 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.865-1677G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099710 | |||||||
chr12:42099875 | T | C | 3 | a0001c0003t0001g0213 a0001c0003t0001g0214 a0001c0003t0001g0215 |
3 | HG01099.hp1 HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.865-1842A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099875 | |||||||
chr12:42100151 | A | G | 26 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(23): Show |
30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.865-2118T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100151 | |||||||
chr12:42100264 | T | G | 7 | a0001c0001t0012g0333 a0001c0001t0012g0335 a0001c0001t0012g0338 others(4): Show |
7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.865-2231A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100264 | |||||||
chr12:42100314 | A | T | 1 | a0001c0003t0001g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.865-2281T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100314 | |||||||
chr12:42100429 | T | C | 50 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(47): Show |
55 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.865-2396A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100429 | |||||||
chr12:42100440 | T | C | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.865-2407A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100440 | |||||||
chr12:42100554 | GA | G | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-2522delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100554 | |||||||
chr12:42100655 | A | T | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-2622T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100655 | |||||||
chr12:42100704 | A | C | 1 | a0001c0005t0004g0008 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.865-2671T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100704 | |||||||
chr12:42100886 | TATACACA others(3): Show |
T | 19 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(16): Show |
22 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.865-2863_865-2854d others(12): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100886 | |||||||
chr12:42101098 | C | T | 1 | a0001c0001t0002g0288 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.865-3065G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101098 | |||||||
chr12:42101125 | A | G | 1 | a0001c0003t0001g0144 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.865-3092T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101125 | |||||||
chr12:42101303 | G | C | 1 | a0001c0003t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.865-3270C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101303 | |||||||
chr12:42101324 | G | A | 2 | a0001c0001t0011g0257 a0001c0001t0011g0258 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.865-3291C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101324 | |||||||
chr12:42101459 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.865-3426T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101459 | |||||||
chr12:42101562 | T | C | 1 | a0001c0003t0001g0148 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.865-3529A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101562 | |||||||
chr12:42101575 | C | CT | 6 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(3): Show |
6 | HG02630.hp2 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.865-3543dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101575 | |||||||
chr12:42101575 | CT | C | 34 | a0001c0001t0005g0266 a0001c0001t0007g0023 a0001c0001t0007g0331 others(31): Show |
35 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.865-3543delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101575 | |||||||
chr12:42101582 | T | A | 1 | a0001c0002t0003g0192 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.865-3549A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101582 | |||||||
chr12:42101585 | T | A | 1 | a0001c0001t0014g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.865-3552A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101585 | |||||||
chr12:42101657 | C | T | 1 | a0001c0001t0014g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.865-3624G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101657 | |||||||
chr12:42101696 | C | T | 2 | a0001c0001t0018g0259 a0001c0001t0018g0261 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.865-3663G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101696 | |||||||
chr12:42101728 | T | C | 1 | a0001c0002t0025g0104 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.865-3695A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101728 | |||||||
chr12:42101873 | CAAAATGC others(7): Show |
C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.865-3854_865-3841d others(16): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101873 | |||||||
chr12:42102022 | C | T | 3 | a0001c0001t0008g0352 a0001c0001t0008g0354 a0001c0001t0008g0356 |
3 | HG00642.hp1 HG01069.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.864+3796G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102022 | |||||||
chr12:42102114 | A | C | 5 | a0001c0003t0013g0138 a0001c0003t0013g0139 a0001c0003t0013g0140 others(2): Show |
5 | HG03239.hp1 HG03654.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.864+3704T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102114 | |||||||
chr12:42102175 | T | C | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.864+3643A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102175 | |||||||
chr12:42102238 | T | C | 2 | a0001c0002t0025g0104 a0001c0002t0025g0105 |
2 | HG02071.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.864+3580A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102238 | |||||||
chr12:42102256 | C | G | 5 | a0001c0002t0004g0036 a0001c0002t0004g0070 a0001c0002t0004g0071 others(2): Show |
5 | NA18957.hp2 NA18959.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.864+3562G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102256 | |||||||
chr12:42102270 | T | C | 1 | a0001c0001t0012g0345 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.864+3548A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102270 | |||||||
chr12:42102389 | C | T | 11 | a0001c0003t0001g0106 a0001c0003t0001g0116 a0001c0003t0001g0120 others(8): Show |
11 | NA18948.hp2 NA18952.hp1 NA18983.hp1 others(8): Show |
intron_variant | MODIFIER | c.864+3429G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102389 | |||||||
chr12:42102401 | T | G | 10 | a0001c0003t0001g0211 a0001c0003t0001g0212 a0001c0003t0001g0213 others(7): Show |
10 | HG01099.hp1 HG01515.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.864+3417A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102401 | |||||||
chr12:42102436 | A | G | 26 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(23): Show |
30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.864+3382T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102436 | |||||||
chr12:42102486 | G | C | 3 | a0001c0002t0020g0033 a0001c0002t0020g0034 a0001c0002t0034g0032 |
3 | HG02055.hp2 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.864+3332C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102486 | |||||||
chr12:42102500 | A | G | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.864+3318T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102500 | |||||||
chr12:42102840 | A | G | 1 | a0001c0003t0001g0126 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.864+2978T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102840 | |||||||
chr12:42102891 | TATTTA | T | 5 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+2922_864+2926d others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102891 | |||||||
chr12:42102949 | T | A | 3 | a0001c0002t0003g0189 a0001c0002t0003g0194 a0001c0002t0003g0199 |
3 | HG00621.hp1 NA19067.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.864+2869A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102949 | |||||||
chr12:42103061 | A | G | 1 | a0001c0003t0001g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.864+2757T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103061 | |||||||
chr12:42103062 | G | C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.864+2756C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103062 | |||||||
chr12:42103111 | C | G | 1 | a0001c0001t0002g0283 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.864+2707G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103111 | |||||||
chr12:42103211 | G | A | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.864+2607C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103211 | |||||||
chr12:42103239 | G | A | 1 | a0001c0001t0012g0339 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.864+2579C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103239 | |||||||
chr12:42103266 | A | T | 1 | a0001c0002t0004g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.864+2552T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103266 | |||||||
chr12:42103303 | G | A | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+2515C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103303 | |||||||
chr12:42103318 | A | G | 304 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.864+2500T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103318 | |||||||
chr12:42103322 | A | G | 309 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(306): Show |
331 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.864+2496T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103322 | |||||||
chr12:42103350 | T | C | 10 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(7): Show |
14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.864+2468A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103350 | |||||||
chr12:42103581 | T | C | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.864+2237A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103581 | |||||||
chr12:42104025 | G | A | 7 | a0001c0002t0015g0179 a0001c0002t0015g0180 a0001c0002t0015g0198 others(4): Show |
7 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1793C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104025 | |||||||
chr12:42104081 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.864+1737G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104081 | |||||||
chr12:42104254 | C | CT | 25 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(22): Show |
26 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.864+1563_864+1564i others(3): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104254 | |||||||
chr12:42104254 | C | CTT | 7 | a0001c0001t0012g0333 a0001c0001t0012g0335 a0001c0001t0012g0338 others(4): Show |
7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1563_864+1564i others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104254 | |||||||
chr12:42104255 | A | AT | 247 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(244): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.864+1562dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104255 | |||||||
chr12:42104255 | A | ATT | 19 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(16): Show |
23 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.864+1561_864+1562d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104255 | |||||||
chr12:42104255 | A | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.864+1563T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104255 | |||||||
chr12:42104298 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0020 a0001c0001t0002g0022 others(4): Show |
11 | HG01496.hp2 HG01928.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.864+1520T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104298 | |||||||
chr12:42104435 | G | C | 1 | a0001c0001t0002g0325 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.864+1383C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104435 | |||||||
chr12:42104557 | TA | T | 289 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(286): Show |
311 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.864+1260delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104557 | |||||||
chr12:42104598 | A | G | 304 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.864+1220T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104598 | |||||||
chr12:42104672 | GC | G | 3 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0156 |
3 | NA18953.hp1 NA18972.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.864+1145delG | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104672 | |||||||
chr12:42104779 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.864+1039C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104779 | |||||||
chr12:42105146 | C | T | 1 | a0001c0003t0001g0130 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.864+672G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105146 | |||||||
chr12:42105156 | A | G | 2 | a0001c0001t0021g0228 a0001c0001t0021g0229 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.864+662T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105156 | |||||||
chr12:42105274 | A | C | 1 | a0001c0002t0031g0025 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864+544T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105274 | |||||||
chr12:42105280 | G | C | 1 | a0001c0003t0001g0133 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.864+538C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105280 | |||||||
chr12:42105405 | AT | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.864+412delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105405 | |||||||
chr12:42105412 | G | A | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.864+406C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105412 | |||||||
chr12:42105553 | G | C | 1 | a0001c0001t0043g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.864+265C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105553 | |||||||
chr12:42105593 | C | T | 304 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.864+225G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105593 | |||||||
chr12:42105599 | T | C | 1 | a0001c0002t0003g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.864+219A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105599 | |||||||
chr12:42105670 | C | G | 2 | a0001c0001t0009g0005 a0001c0001t0009g0255 |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+148G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105670 | |||||||
chr12:42105736 | T | A | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.864+82A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105736 | |||||||
chr12:42105737 | T | C | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.864+81A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105737 | |||||||
chr12:42106207 | C | T | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-138G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106207 | |||||||
chr12:42106212 | A | G | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.613-143T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106212 | |||||||
chr12:42106255 | C | T | 2 | a0001c0001t0053g0337 a0002c0004t0051g0329 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.613-186G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106255 | |||||||
chr12:42106388 | G | C | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.613-319C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106388 | |||||||
chr12:42106408 | C | G | 1 | a0001c0002t0004g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.613-339G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106408 | |||||||
chr12:42106520 | T | C | 20 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(17): Show |
24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.613-451A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106520 | |||||||
chr12:42106692 | T | C | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-623A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106692 | |||||||
chr12:42106742 | T | C | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-673A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106742 | |||||||
chr12:42106743 | C | CT | 19 | a0001c0001t0002g0278 a0001c0001t0002g0283 a0001c0001t0002g0286 others(16): Show |
19 | HG01192.hp1 HG02055.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.613-675dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106743 | |||||||
chr12:42106743 | C | T | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-674G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106743 | |||||||
chr12:42106743 | CT | C | 10 | a0001c0001t0002g0294 a0001c0001t0006g0241 a0001c0001t0014g0226 others(7): Show |
10 | HG01515.hp2 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-675delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106743 | |||||||
chr12:42106748 | T | C | 31 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(28): Show |
35 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.613-679A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106748 | |||||||
chr12:42106808 | T | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.613-739A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106808 | |||||||
chr12:42106855 | C | T | 2 | a0001c0002t0004g0043 a0001c0002t0004g0044 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.613-786G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106855 | |||||||
chr12:42106907 | G | A | 1 | a0001c0001t0014g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.613-838C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106907 | |||||||
chr12:42106985 | G | A | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-916C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106985 | |||||||
chr12:42107028 | C | T | 1 | a0001c0002t0004g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.613-959G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107028 | |||||||
chr12:42107029 | G | A | 1 | a0001c0002t0034g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.613-960C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107029 | |||||||
chr12:42107115 | C | T | 1 | a0001c0003t0042g0127 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.613-1046G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107115 | |||||||
chr12:42107344 | C | T | 304 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.613-1275G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107344 | |||||||
chr12:42107438 | C | T | 26 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(23): Show |
30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.613-1369G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107438 | |||||||
chr12:42107461 | C | T | 1 | a0001c0003t0001g0116 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.613-1392G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107461 | |||||||
chr12:42107471 | A | G | 240 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(237): Show |
258 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.613-1402T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107471 | |||||||
chr12:42107808 | C | G | 1 | a0001c0002t0004g0081 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.613-1739G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107808 | |||||||
chr12:42107838 | G | C | 1 | a0001c0002t0050g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.612+1728C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107838 | |||||||
chr12:42107881 | C | A | 1 | a0001c0002t0004g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.612+1685G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107881 | |||||||
chr12:42108043 | AT | A | 3 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 |
3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.612+1522delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108043 | |||||||
chr12:42108200 | C | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.612+1366G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108200 | |||||||
chr12:42108255 | G | C | 1 | a0001c0003t0001g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.612+1311C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108255 | |||||||
chr12:42108320 | T | C | 24 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(21): Show |
28 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.612+1246A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108320 | |||||||
chr12:42108489 | A | ACC | 4 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0028g0309 others(1): Show |
4 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+1076_612+1077i others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108489 | |||||||
chr12:42108757 | T | A | 81 | a0001c0003t0001g0010 a0001c0003t0001g0011 a0001c0003t0001g0012 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.612+809A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108757 | |||||||
chr12:42108817 | G | A | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.612+749C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108817 | |||||||
chr12:42108980 | C | T | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+586G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108980 | |||||||
chr12:42108993 | T | C | 1 | a0001c0001t0010g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.612+573A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108993 | |||||||
chr12:42109232 | G | A | 7 | a0001c0001t0005g0270 a0001c0001t0026g0310 a0001c0001t0026g0313 others(4): Show |
7 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+334C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109232 | |||||||
chr12:42109309 | C | T | 1 | a0001c0002t0004g0070 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.612+257G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109309 | |||||||
chr12:42109452 | C | T | 313 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(310): Show |
335 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.612+114G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109452 | |||||||
chr12:42109523 | T | A | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.612+43A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109523 | |||||||
chr12:42109523 | T | TA | 7 | a0001c0001t0011g0102 a0001c0001t0014g0231 a0001c0001t0037g0103 others(4): Show |
7 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+42dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109523 | |||||||
chr12:42109523 | TA | T | 35 | a0001c0001t0002g0282 a0001c0001t0002g0314 a0001c0001t0002g0322 others(32): Show |
35 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.612+42delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109523 | |||||||
chr12:42109702 | T | TA | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.487-12_487-11insT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109702 | |||||||
chr12:42109703 | T | A | 359 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(356): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.487-12A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109703 | |||||||
chr12:42109798 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-107G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109798 | |||||||
chr12:42109838 | C | T | 1 | a0001c0002t0004g0089 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.487-147G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109838 | |||||||
chr12:42109927 | C | A | 6 | a0001c0001t0007g0023 a0001c0001t0007g0334 a0001c0001t0007g0336 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-236G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109927 | |||||||
chr12:42109933 | C | A | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.487-242G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109933 | |||||||
chr12:42109992 | C | A | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-301G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109992 | |||||||
chr12:42110142 | G | C | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-451C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110142 | |||||||
chr12:42110145 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-454A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110145 | |||||||
chr12:42110195 | T | C | 5 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-504A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110195 | |||||||
chr12:42110198 | C | T | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-507G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110198 | |||||||
chr12:42110270 | C | A | 1 | a0001c0002t0003g0177 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.487-579G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110270 | |||||||
chr12:42110395 | G | A | 2 | a0001c0001t0024g0224 a0001c0001t0024g0225 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.487-704C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110395 | |||||||
chr12:42110396 | A | G | 1 | a0001c0002t0003g0187 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.487-705T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110396 | |||||||
chr12:42110523 | T | C | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-832A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110523 | |||||||
chr12:42110553 | T | G | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-862A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110553 | |||||||
chr12:42110633 | T | C | 81 | a0001c0003t0001g0010 a0001c0003t0001g0011 a0001c0003t0001g0012 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.487-942A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110633 | |||||||
chr12:42110681 | G | A | 1 | a0001c0001t0014g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.487-990C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110681 | |||||||
chr12:42110765 | T | G | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-1074A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110765 | |||||||
chr12:42110877 | T | G | 122 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(119): Show |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.487-1186A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110877 | |||||||
chr12:42111051 | T | C | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-1360A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111051 | |||||||
chr12:42111181 | G | A | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-1490C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111181 | |||||||
chr12:42111185 | G | A | 24 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(21): Show |
28 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.487-1494C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111185 | |||||||
chr12:42111185 | G | T | 1 | a0001c0002t0003g0192 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.487-1494C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111185 | |||||||
chr12:42111198 | G | A | 3 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 |
3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.487-1507C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111198 | |||||||
chr12:42111215 | C | G | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-1524G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111215 | |||||||
chr12:42111247 | G | A | 2 | a0001c0001t0009g0254 a0001c0001t0016g0092 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.487-1556C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111247 | |||||||
chr12:42111259 | C | A | 1 | a0001c0001t0002g0326 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.487-1568G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111259 | |||||||
chr12:42111289 | A | T | 1 | a0002c0004t0051g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.487-1598T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111289 | |||||||
chr12:42111291 | T | A | 3 | a0001c0001t0007g0334 a0001c0001t0007g0336 a0001c0001t0007g0343 |
3 | HG00738.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.487-1600A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111291 | |||||||
chr12:42111305 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.487-1614G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111305 | |||||||
chr12:42111309 | C | T | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-1618G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111309 | |||||||
chr12:42111321 | C | T | 1 | a0001c0001t0002g0301 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.487-1630G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111321 | |||||||
chr12:42111434 | T | A | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-1743A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111434 | |||||||
chr12:42111440 | G | A | 3 | a0001c0001t0005g0263 a0001c0001t0005g0273 a0001c0001t0005g0318 |
3 | NA18994.hp2 NA19058.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.487-1749C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111440 | |||||||
chr12:42111546 | C | T | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-1855G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111546 | |||||||
chr12:42111559 | C | T | 1 | a0001c0002t0004g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.487-1868G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111559 | |||||||
chr12:42111582 | C | A | 304 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.487-1891G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111582 | |||||||
chr12:42111603 | G | A | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.487-1912C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111603 | |||||||
chr12:42111644 | G | A | 7 | a0001c0001t0002g0306 a0001c0001t0024g0224 a0001c0001t0024g0225 others(4): Show |
7 | HG01169.hp1 HG01517.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-1953C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111644 | |||||||
chr12:42111659 | C | A | 1 | a0001c0002t0003g0166 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.487-1968G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111659 | |||||||
chr12:42111702 | T | G | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.487-2011A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111702 | |||||||
chr12:42111717 | C | T | 2 | a0001c0001t0027g0157 a0001c0001t0027g0230 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.487-2026G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111717 | |||||||
chr12:42111718 | G | A | 3 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.487-2027C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111718 | |||||||
chr12:42111725 | CAA | C | 8 | a0001c0002t0004g0061 a0001c0002t0004g0076 a0001c0002t0004g0077 others(5): Show |
8 | HG02083.hp1 NA18944.hp2 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-2036_487-2035d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111725 | |||||||
chr12:42111748 | C | T | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.487-2057G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111748 | |||||||
chr12:42111773 | G | A | 6 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-2082C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111773 | |||||||
chr12:42111794 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.487-2103G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111794 | |||||||
chr12:42111803 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-2112G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111803 | |||||||
chr12:42111804 | G | A | 1 | a0001c0001t0002g0326 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.487-2113C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111804 | |||||||
chr12:42111813 | G | C | 80 | a0001c0003t0001g0010 a0001c0003t0001g0011 a0001c0003t0001g0012 others(77): Show |
84 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.487-2122C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111813 | |||||||
chr12:42111823 | C | T | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.487-2132G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111823 | |||||||
chr12:42111824 | G | A | 1 | a0001c0002t0046g0178 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.487-2133C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111824 | |||||||
chr12:42111860 | T | C | 212 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(209): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.487-2169A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111860 | |||||||
chr12:42111884 | C | G | 1 | a0001c0002t0034g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.487-2193G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111884 | |||||||
chr12:42111913 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-2222G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111913 | |||||||
chr12:42111914 | A | G | 218 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(215): Show |
229 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.487-2223T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111914 | |||||||
chr12:42111935 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-2244T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111935 | |||||||
chr12:42111972 | G | T | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-2281C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111972 | |||||||
chr12:42112019 | G | A | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-2328C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112019 | |||||||
chr12:42112044 | TAGCAAAC others(21): Show |
T | 1 | a0001c0005t0004g0008 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.487-2381_487-2354d others(30): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112044 | |||||||
chr12:42112157 | C | A | 1 | a0001c0001t0002g0295 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.487-2466G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112157 | |||||||
chr12:42112277 | G | C | 6 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 others(3): Show |
6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-2586C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112277 | |||||||
chr12:42112346 | G | C | 1 | a0001c0002t0047g0181 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.487-2655C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112346 | |||||||
chr12:42112363 | G | A | 21 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(18): Show |
25 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.487-2672C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112363 | |||||||
chr12:42112380 | A | G | 9 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(6): Show |
9 | HG01169.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-2689T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112380 | |||||||
chr12:42112468 | C | T | 6 | a0001c0001t0007g0023 a0001c0001t0007g0334 a0001c0001t0007g0336 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-2777G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112468 | |||||||
chr12:42112513 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-2822T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112513 | |||||||
chr12:42112517 | C | T | 6 | a0001c0002t0003g0094 a0001c0002t0003g0095 a0001c0002t0003g0096 others(3): Show |
6 | HG01175.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-2826G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112517 | |||||||
chr12:42112609 | C | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.487-2918G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112609 | |||||||
chr12:42112610 | G | A | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-2919C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112610 | |||||||
chr12:42112647 | G | C | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-2956C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112647 | |||||||
chr12:42112684 | C | T | 1 | a0001c0003t0001g0211 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.487-2993G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112684 | |||||||
chr12:42112686 | G | C | 1 | a0001c0003t0001g0211 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.487-2995C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112686 | |||||||
chr12:42112687 | A | G | 1 | a0001c0003t0001g0211 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.487-2996T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112687 | |||||||
chr12:42112735 | GAACTTCC others(1139): Show |
G | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-4190_487-3045d others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112735 | |||||||
chr12:42112898 | T | A | 9 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(6): Show |
9 | HG01169.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-3207A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112898 | |||||||
chr12:42112949 | A | C | 2 | a0001c0001t0010g0030 a0001c0001t0010g0031 |
2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.487-3258T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112949 | |||||||
chr12:42112996 | T | A | 212 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(209): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.487-3305A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112996 | |||||||
chr12:42113016 | A | T | 18 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(15): Show |
21 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.487-3325T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113016 | |||||||
chr12:42113090 | T | G | 1 | a0001c0002t0004g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.487-3399A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113090 | |||||||
chr12:42113113 | A | T | 1 | a0001c0003t0001g0211 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.487-3422T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113113 | |||||||
chr12:42113151 | C | T | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-3460G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113151 | |||||||
chr12:42113168 | A | C | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-3477T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113168 | |||||||
chr12:42113201 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-3510T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113201 | |||||||
chr12:42113220 | G | C | 212 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(209): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.487-3529C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113220 | |||||||
chr12:42113251 | G | A | 1 | a0001c0002t0003g0169 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.487-3560C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113251 | |||||||
chr12:42113315 | C | A | 2 | a0001c0001t0007g0334 a0001c0001t0007g0336 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.487-3624G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113315 | |||||||
chr12:42113326 | C | A | 5 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-3635G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113326 | |||||||
chr12:42113390 | T | C | 1 | a0001c0001t0007g0332 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.487-3699A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113390 | |||||||
chr12:42113393 | C | T | 1 | a0001c0001t0002g0307 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.487-3702G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113393 | |||||||
chr12:42113400 | A | G | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.487-3709T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113400 | |||||||
chr12:42113499 | A | G | 20 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(17): Show |
24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.487-3808T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113499 | |||||||
chr12:42113522 | G | A | 1 | a0001c0001t0006g0248 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.487-3831C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113522 | |||||||
chr12:42113556 | C | G | 4 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(1): Show |
4 | HG02040.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-3865G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113556 | |||||||
chr12:42113556 | C | T | 1 | a0001c0002t0003g0196 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.487-3865G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113556 | |||||||
chr12:42113624 | T | G | 2 | a0001c0001t0007g0331 a0001c0001t0052g0330 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.487-3933A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113624 | |||||||
chr12:42113637 | C | T | 11 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(8): Show |
15 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.487-3946G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113637 | |||||||
chr12:42113672 | C | CAAT | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-3984_487-3982d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113672 | |||||||
chr12:42113678 | T | A | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.487-3987A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113678 | |||||||
chr12:42113699 | T | C | 1 | a0001c0002t0004g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.487-4008A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113699 | |||||||
chr12:42113707 | T | C | 43 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(40): Show |
47 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.487-4016A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113707 | |||||||
chr12:42113712 | C | A | 14 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(11): Show |
14 | HG02630.hp2 HG03098.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-4021G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113712 | |||||||
chr12:42113740 | G | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-4049C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113740 | |||||||
chr12:42113775 | G | A | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.487-4084C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113775 | |||||||
chr12:42113887 | T | C | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-4196A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113887 | |||||||
chr12:42113899 | T | C | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-4208A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113899 | |||||||
chr12:42113917 | A | G | 5 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-4226T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113917 | |||||||
chr12:42113959 | C | T | 1 | a0001c0001t0005g0267 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.487-4268G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113959 | |||||||
chr12:42113987 | A | G | 15 | a0001c0001t0007g0332 a0001c0001t0007g0340 a0001c0001t0007g0346 others(12): Show |
17 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.487-4296T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113987 | |||||||
chr12:42113996 | C | T | 1 | a0001c0002t0004g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.487-4305G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113996 | |||||||
chr12:42114061 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-4370T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114061 | |||||||
chr12:42114084 | G | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.487-4393C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114084 | |||||||
chr12:42114118 | A | G | 2 | a0001c0003t0001g0154 a0001c0003t0001g0155 |
2 | HG00544.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.487-4427T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114118 | |||||||
chr12:42114149 | C | T | 304 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.487-4458G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114149 | |||||||
chr12:42114183 | G | A | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-4492C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114183 | |||||||
chr12:42114252 | T | G | 1 | a0001c0002t0003g0017 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.487-4561A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114252 | |||||||
chr12:42114278 | T | A | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.487-4587A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114278 | |||||||
chr12:42114377 | C | T | 1 | a0001c0002t0003g0169 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.486+4623G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114377 | |||||||
chr12:42114381 | A | G | 1 | a0001c0003t0001g0152 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.486+4619T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114381 | |||||||
chr12:42114410 | A | C | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.486+4590T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114410 | |||||||
chr12:42114433 | C | A | 1 | a0001c0001t0002g0281 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.486+4567G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114433 | |||||||
chr12:42114568 | A | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.486+4432T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114568 | |||||||
chr12:42114576 | C | G | 1 | a0001c0003t0013g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.486+4424G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114576 | |||||||
chr12:42114600 | T | A | 4 | a0001c0003t0001g0216 a0001c0003t0001g0217 a0001c0003t0001g0222 others(1): Show |
4 | HG02622.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+4400A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114600 | |||||||
chr12:42114600 | T | C | 7 | a0001c0001t0012g0333 a0001c0001t0012g0335 a0001c0001t0012g0338 others(4): Show |
7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+4400A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114600 | |||||||
chr12:42114654 | A | G | 2 | a0001c0001t0026g0310 a0001c0001t0026g0313 |
2 | HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.486+4346T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114654 | |||||||
chr12:42114696 | G | A | 2 | a0001c0001t0027g0157 a0001c0001t0027g0230 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.486+4304C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114696 | |||||||
chr12:42114756 | A | G | 1 | a0001c0001t0053g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.486+4244T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114756 | |||||||
chr12:42114796 | A | G | 1 | a0001c0001t0014g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.486+4204T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114796 | |||||||
chr12:42114855 | G | C | 1 | a0001c0001t0002g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.486+4145C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114855 | |||||||
chr12:42114864 | C | T | 205 | a0001c0001t0021g0228 a0001c0001t0021g0229 a0001c0002t0003g0004 others(202): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.486+4136G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114864 | |||||||
chr12:42114997 | A | G | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+4003T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114997 | |||||||
chr12:42115060 | G | T | 1 | a0001c0001t0041g0320 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486+3940C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115060 | |||||||
chr12:42115062 | T | C | 1 | a0001c0001t0041g0320 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486+3938A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115062 | |||||||
chr12:42115084 | T | C | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+3916A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115084 | |||||||
chr12:42115125 | G | A | 33 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(30): Show |
34 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.486+3875C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115125 | |||||||
chr12:42115213 | C | A | 7 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(4): Show |
7 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+3787G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115213 | |||||||
chr12:42115254 | C | G | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.486+3746G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115254 | |||||||
chr12:42115259 | T | C | 2 | a0001c0001t0027g0157 a0001c0001t0027g0230 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.486+3741A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115259 | |||||||
chr12:42115311 | C | T | 1 | a0001c0001t0012g0345 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.486+3689G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115311 | |||||||
chr12:42115339 | T | C | 5 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+3661A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115339 | |||||||
chr12:42115343 | T | C | 18 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(15): Show |
22 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.486+3657A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115343 | |||||||
chr12:42115364 | T | C | 1 | a0001c0001t0012g0333 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.486+3636A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115364 | |||||||
chr12:42115416 | A | C | 1 | a0001c0001t0002g0323 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.486+3584T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115416 | |||||||
chr12:42115419 | A | C | 1 | a0001c0001t0002g0153 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.486+3581T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115419 | |||||||
chr12:42115431 | T | G | 2 | a0001c0001t0011g0257 a0001c0001t0011g0258 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.486+3569A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115431 | |||||||
chr12:42115480 | G | C | 212 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(209): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.486+3520C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115480 | |||||||
chr12:42115494 | C | A | 312 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(309): Show |
334 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.486+3506G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115494 | |||||||
chr12:42115521 | T | C | 1 | a0001c0002t0003g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.486+3479A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115521 | |||||||
chr12:42115577 | T | C | 32 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(29): Show |
36 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.486+3423A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115577 | |||||||
chr12:42115578 | G | A | 32 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(29): Show |
36 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.486+3422C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115578 | |||||||
chr12:42115598 | C | G | 2 | a0001c0002t0004g0037 a0001c0003t0042g0127 |
2 | HG02896.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.486+3402G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115598 | |||||||
chr12:42115767 | T | C | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+3233A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115767 | |||||||
chr12:42115814 | G | A | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+3186C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115814 | |||||||
chr12:42115828 | G | C | 309 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(306): Show |
331 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.486+3172C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115828 | |||||||
chr12:42115839 | A | G | 1 | a0001c0001t0002g0300 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.486+3161T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115839 | |||||||
chr12:42115845 | A | C | 1 | a0001c0003t0001g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.486+3155T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115845 | |||||||
chr12:42115860 | T | C | 122 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(119): Show |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.486+3140A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115860 | |||||||
chr12:42115895 | A | G | 205 | a0001c0001t0007g0331 a0001c0001t0052g0330 a0001c0002t0003g0004 others(202): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.486+3105T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115895 | |||||||
chr12:42115901 | A | G | 205 | a0001c0001t0007g0331 a0001c0001t0052g0330 a0001c0002t0003g0004 others(202): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.486+3099T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115901 | |||||||
chr12:42115919 | T | C | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+3081A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115919 | |||||||
chr12:42115936 | A | C | 2 | a0001c0001t0007g0331 a0001c0001t0052g0330 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486+3064T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115936 | |||||||
chr12:42115939 | C | T | 208 | a0001c0001t0007g0331 a0001c0001t0016g0091 a0001c0001t0016g0092 others(205): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.486+3061G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115939 | |||||||
chr12:42115949 | T | A | 309 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(306): Show |
331 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.486+3051A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115949 | |||||||
chr12:42115960 | C | T | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+3040G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115960 | |||||||
chr12:42115962 | C | G | 48 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(45): Show |
53 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.486+3038G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115962 | |||||||
chr12:42115962 | C | T | 1 | a0001c0003t0001g0219 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.486+3038G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115962 | |||||||
chr12:42115977 | A | G | 2 | a0001c0001t0007g0331 a0001c0001t0052g0330 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486+3023T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115977 | |||||||
chr12:42115984 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0052g0330 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486+3016A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115984 | |||||||
chr12:42115985 | A | C | 2 | a0001c0001t0007g0331 a0001c0001t0052g0330 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486+3015T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115985 | |||||||
chr12:42116011 | C | G | 2 | a0001c0001t0027g0157 a0001c0001t0027g0230 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.486+2989G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116011 | |||||||
chr12:42116071 | A | T | 1 | a0001c0003t0001g0219 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.486+2929T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116071 | |||||||
chr12:42116078 | C | T | 23 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(20): Show |
29 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.486+2922G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116078 | |||||||
chr12:42116150 | C | A | 3 | a0001c0001t0002g0294 a0001c0003t0001g0204 a0001c0003t0001g0205 |
3 | HG02109.hp1 HG03130.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.486+2850G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116150 | |||||||
chr12:42116192 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.486+2808C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116192 | |||||||
chr12:42116211 | T | G | 2 | a0001c0002t0004g0056 a0001c0002t0031g0025 |
2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.486+2789A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116211 | |||||||
chr12:42116237 | A | G | 1 | a0001c0002t0004g0062 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.486+2763T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116237 | |||||||
chr12:42116251 | A | T | 42 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(39): Show |
48 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.486+2749T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116251 | |||||||
chr12:42116327 | A | G | 1 | a0001c0001t0014g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486+2673T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116327 | |||||||
chr12:42116339 | C | A | 2 | a0001c0001t0012g0339 a0001c0003t0036g0145 |
2 | NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.486+2661G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116339 | |||||||
chr12:42116340 | G | A | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+2660C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116340 | |||||||
chr12:42116345 | C | T | 3 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 |
3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.486+2655G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116345 | |||||||
chr12:42116360 | A | T | 1 | a0001c0002t0004g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.486+2640T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116360 | |||||||
chr12:42116363 | A | G | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+2637T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116363 | |||||||
chr12:42116392 | G | A | 26 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(23): Show |
30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.486+2608C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116392 | |||||||
chr12:42116400 | C | G | 6 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+2600G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116400 | |||||||
chr12:42116414 | T | G | 350 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(347): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.486+2586A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116414 | |||||||
chr12:42116419 | CA | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.486+2580delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116419 | |||||||
chr12:42116432 | C | A | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+2568G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116432 | |||||||
chr12:42116463 | C | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(53): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.486+2537G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116463 | |||||||
chr12:42116463 | C | T | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.486+2537G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116463 | |||||||
chr12:42116498 | A | G | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.486+2502T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116498 | |||||||
chr12:42116522 | A | G | 1 | a0001c0001t0006g0244 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.486+2478T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116522 | |||||||
chr12:42116534 | C | T | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.486+2466G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116534 | |||||||
chr12:42116543 | G | A | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.486+2457C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116543 | |||||||
chr12:42116574 | C | A | 10 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(7): Show |
14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.486+2426G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116574 | |||||||
chr12:42116574 | C | T | 12 | a0001c0002t0004g0057 a0001c0002t0004g0060 a0001c0002t0004g0061 others(9): Show |
12 | HG00323.hp1 HG01099.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.486+2426G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116574 | |||||||
chr12:42116591 | C | G | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.486+2409G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116591 | |||||||
chr12:42116604 | C | A | 1 | a0002c0004t0002g0009 | 2 | HG02015.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.486+2396G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116604 | |||||||
chr12:42116605 | A | G | 1 | a0002c0004t0002g0009 | 2 | HG02015.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.486+2395T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116605 | |||||||
chr12:42116608 | C | T | 2 | a0001c0002t0020g0033 a0001c0002t0020g0034 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.486+2392G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116608 | |||||||
chr12:42116641 | A | C | 1 | a0001c0001t0018g0259 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486+2359T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116641 | |||||||
chr12:42116685 | G | C | 10 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(7): Show |
14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.486+2315C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116685 | |||||||
chr12:42116687 | A | G | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.486+2313T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116687 | |||||||
chr12:42116806 | C | A | 1 | a0001c0001t0002g0317 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.486+2194G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116806 | |||||||
chr12:42116849 | T | C | 1 | a0001c0001t0027g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.486+2151A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116849 | |||||||
chr12:42116851 | C | T | 3 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.486+2149G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116851 | |||||||
chr12:42116872 | C | A | 1 | a0001c0001t0005g0273 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.486+2128G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116872 | |||||||
chr12:42116872 | C | G | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.486+2128G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116872 | |||||||
chr12:42116891 | A | G | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.486+2109T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116891 | |||||||
chr12:42116944 | A | G | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+2056T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116944 | |||||||
chr12:42116969 | T | C | 1 | a0001c0001t0005g0271 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.486+2031A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116969 | |||||||
chr12:42117022 | A | G | 304 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.486+1978T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117022 | |||||||
chr12:42117045 | A | G | 304 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(301): Show |
326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.486+1955T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117045 | |||||||
chr12:42117226 | T | C | 1 | a0001c0001t0007g0340 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486+1774A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117226 | |||||||
chr12:42117291 | T | A | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.486+1709A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117291 | |||||||
chr12:42117292 | A | T | 1 | a0001c0001t0002g0282 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.486+1708T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117292 | |||||||
chr12:42117323 | A | T | 20 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(17): Show |
24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.486+1677T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117323 | |||||||
chr12:42117446 | A | G | 3 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02896.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.486+1554T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117446 | |||||||
chr12:42117469 | G | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.486+1531C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117469 | |||||||
chr12:42117491 | G | GT | 63 | a0001c0002t0003g0168 a0001c0002t0003g0186 a0001c0002t0003g0189 others(60): Show |
64 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.486+1508dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117491 | |||||||
chr12:42117502 | C | T | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.486+1498G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117502 | |||||||
chr12:42117522 | G | T | 1 | a0001c0001t0007g0332 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486+1478C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117522 | |||||||
chr12:42117785 | G | C | 1 | a0001c0003t0001g0123 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.486+1215C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117785 | |||||||
chr12:42117925 | G | T | 1 | a0001c0003t0001g0126 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.486+1075C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117925 | |||||||
chr12:42118046 | C | T | 1 | a0001c0001t0018g0259 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486+954G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118046 | |||||||
chr12:42118238 | C | T | 5 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+762G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118238 | |||||||
chr12:42118282 | A | G | 1 | a0001c0003t0001g0147 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.486+718T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118282 | |||||||
chr12:42118322 | A | T | 6 | a0001c0001t0007g0023 a0001c0001t0007g0334 a0001c0001t0007g0336 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+678T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118322 | |||||||
chr12:42118476 | G | A | 1 | a0001c0001t0041g0320 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486+524C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118476 | |||||||
chr12:42118502 | A | G | 49 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(46): Show |
54 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.486+498T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118502 | |||||||
chr12:42118506 | A | T | 2 | a0001c0003t0001g0115 a0001c0003t0001g0141 |
2 | HG02040.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.486+494T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118506 | |||||||
chr12:42118590 | T | C | 31 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0334 others(28): Show |
32 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.486+410A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118590 | |||||||
chr12:42119189 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.315-18G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119189 | |||||||
chr12:42119298 | C | T | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-127G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119298 | |||||||
chr12:42119325 | G | A | 122 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(119): Show |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.315-154C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119325 | |||||||
chr12:42119371 | A | G | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-200T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119371 | |||||||
chr12:42119444 | GAAAGGGA others(5): Show |
G | 2 | a0001c0001t0009g0005 a0001c0001t0009g0255 |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-285_315-274del others(12): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119444 | |||||||
chr12:42119476 | G | A | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-305C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119476 | |||||||
chr12:42119615 | C | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.315-444G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119615 | |||||||
chr12:42119791 | T | G | 2 | a0001c0001t0026g0310 a0001c0001t0026g0313 |
2 | HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.315-620A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119791 | |||||||
chr12:42119812 | G | A | 6 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-641C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119812 | |||||||
chr12:42120007 | C | T | 31 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0334 others(28): Show |
32 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.315-836G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120007 | |||||||
chr12:42120080 | T | C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.315-909A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120080 | |||||||
chr12:42120091 | A | G | 261 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(258): Show |
277 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.315-920T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120091 | |||||||
chr12:42120336 | A | G | 1 | a0001c0001t0007g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.315-1165T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120336 | |||||||
chr12:42120392 | A | G | 2 | a0001c0001t0027g0157 a0001c0001t0027g0230 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.315-1221T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120392 | |||||||
chr12:42120458 | T | C | 302 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(299): Show |
324 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.315-1287A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120458 | |||||||
chr12:42120571 | C | G | 1 | a0001c0001t0002g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.315-1400G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120571 | |||||||
chr12:42120747 | G | C | 3 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 |
3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.315-1576C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120747 | |||||||
chr12:42120748 | C | T | 3 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 |
3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.315-1577G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120748 | |||||||
chr12:42120793 | C | T | 1 | a0001c0001t0006g0243 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.315-1622G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120793 | |||||||
chr12:42120945 | A | C | 1 | a0001c0001t0006g0246 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.315-1774T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120945 | |||||||
chr12:42121082 | T | C | 2 | a0001c0001t0011g0101 a0001c0001t0011g0102 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.315-1911A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121082 | |||||||
chr12:42121121 | A | C | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.315-1950T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121121 | |||||||
chr12:42121310 | G | A | 1 | a0001c0002t0046g0178 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.315-2139C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121310 | |||||||
chr12:42121361 | G | A | 2 | a0001c0001t0053g0337 a0002c0004t0051g0329 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.315-2190C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121361 | |||||||
chr12:42121453 | G | A | 7 | a0001c0001t0011g0257 a0001c0001t0011g0258 a0001c0001t0014g0226 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-2282C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121453 | |||||||
chr12:42121504 | G | A | 81 | a0001c0003t0001g0010 a0001c0003t0001g0011 a0001c0003t0001g0012 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.315-2333C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121504 | |||||||
chr12:42121600 | C | G | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-2429G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121600 | |||||||
chr12:42121656 | G | GA | 25 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(22): Show |
29 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.315-2486dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121656 | |||||||
chr12:42121656 | GA | G | 59 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(56): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.315-2486delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121656 | |||||||
chr12:42122046 | G | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.315-2875C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122046 | |||||||
chr12:42122236 | G | A | 1 | a0001c0001t0002g0294 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.315-3065C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122236 | |||||||
chr12:42122304 | C | T | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.315-3133G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122304 | |||||||
chr12:42122341 | G | A | 1 | a0001c0003t0001g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.315-3170C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122341 | |||||||
chr12:42122397 | C | T | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-3226G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122397 | |||||||
chr12:42122406 | A | C | 1 | a0001c0002t0003g0108 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.315-3235T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122406 | |||||||
chr12:42122418 | C | T | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-3247G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122418 | |||||||
chr12:42122450 | C | T | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-3279G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122450 | |||||||
chr12:42122574 | A | G | 60 | a0001c0002t0004g0035 a0001c0002t0004g0036 a0001c0002t0004g0037 others(57): Show |
61 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.315-3403T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122574 | |||||||
chr12:42122826 | A | G | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.315-3655T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122826 | |||||||
chr12:42122889 | T | C | 20 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(17): Show |
24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.315-3718A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122889 | |||||||
chr12:42122931 | C | G | 1 | a0001c0001t0014g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.315-3760G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122931 | |||||||
chr12:42122967 | G | C | 31 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0334 others(28): Show |
32 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.315-3796C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122967 | |||||||
chr12:42122983 | CTAATAA | C | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-3818_315-3813d others(8): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122983 | |||||||
chr12:42123128 | T | C | 1 | a0001c0001t0005g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.315-3957A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123128 | |||||||
chr12:42123153 | G | A | 1 | a0001c0002t0004g0060 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.315-3982C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123153 | |||||||
chr12:42123273 | T | C | 1 | a0001c0002t0003g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.315-4102A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123273 | |||||||
chr12:42123347 | C | T | 31 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0334 others(28): Show |
32 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.315-4176G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123347 | |||||||
chr12:42123580 | ACTT | A | 6 | a0001c0002t0015g0179 a0001c0002t0015g0180 a0001c0002t0015g0198 others(3): Show |
6 | HG01346.hp1 HG01433.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-4412_315-4410d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123580 | |||||||
chr12:42123617 | CATA | C | 5 | a0001c0002t0004g0061 a0001c0002t0004g0084 a0001c0002t0004g0085 others(2): Show |
5 | HG02083.hp1 NA18944.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-4449_315-4447d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123617 | |||||||
chr12:42123621 | A | G | 1 | a0001c0002t0003g0195 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.315-4450T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123621 | |||||||
chr12:42123715 | ATAAT | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.315-4548_315-4545d others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123715 | |||||||
chr12:42123952 | GA | G | 20 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(17): Show |
23 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.315-4782delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123952 | |||||||
chr12:42124014 | T | C | 2 | a0001c0001t0028g0309 a0001c0001t0028g0311 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.315-4843A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124014 | |||||||
chr12:42124041 | T | TA | 10 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(7): Show |
14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.315-4871dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124041 | |||||||
chr12:42124165 | G | A | 59 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(56): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.315-4994C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124165 | |||||||
chr12:42124300 | T | C | 60 | a0001c0002t0004g0035 a0001c0002t0004g0036 a0001c0002t0004g0037 others(57): Show |
61 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.315-5129A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124300 | |||||||
chr12:42124397 | G | T | 3 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02896.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.315-5226C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124397 | |||||||
chr12:42124461 | T | C | 5 | a0001c0003t0013g0138 a0001c0003t0013g0139 a0001c0003t0013g0140 others(2): Show |
5 | HG03239.hp1 HG03654.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-5290A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124461 | |||||||
chr12:42124462 | A | G | 1 | a0001c0002t0003g0188 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.315-5291T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124462 | |||||||
chr12:42124485 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+5274T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124485 | |||||||
chr12:42124502 | T | C | 1 | a0001c0001t0009g0253 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.314+5257A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124502 | |||||||
chr12:42124514 | G | A | 2 | a0001c0003t0001g0201 a0001c0003t0001g0209 |
2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.314+5245C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124514 | |||||||
chr12:42124526 | C | A | 303 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(300): Show |
325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.314+5233G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124526 | |||||||
chr12:42124667 | T | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+5092A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124667 | |||||||
chr12:42124732 | T | C | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+5027A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124732 | |||||||
chr12:42124784 | TA | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0299 |
3 | HG00408.hp1 NA18961.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.314+4974delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124784 | |||||||
chr12:42124997 | T | C | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.314+4762A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124997 | |||||||
chr12:42125083 | G | A | 1 | a0001c0003t0023g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.314+4676C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125083 | |||||||
chr12:42125098 | T | C | 2 | a0001c0001t0021g0228 a0001c0001t0021g0229 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.314+4661A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125098 | |||||||
chr12:42125138 | T | C | 4 | a0001c0002t0004g0037 a0001c0002t0004g0054 a0001c0002t0004g0055 others(1): Show |
4 | HG02258.hp2 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+4621A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125138 | |||||||
chr12:42125220 | T | C | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.314+4539A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125220 | |||||||
chr12:42125245 | T | C | 3 | a0001c0003t0001g0123 a0001c0003t0001g0210 a0001c0003t0040g0122 |
3 | HG00733.hp2 HG01074.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.314+4514A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125245 | |||||||
chr12:42125379 | C | G | 1 | a0001c0002t0003g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.314+4380G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125379 | |||||||
chr12:42125394 | G | C | 1 | a0001c0003t0001g0137 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.314+4365C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125394 | |||||||
chr12:42125843 | C | T | 5 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+3916G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125843 | |||||||
chr12:42125852 | G | A | 1 | a0001c0003t0001g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.314+3907C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125852 | |||||||
chr12:42125886 | C | G | 309 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(306): Show |
331 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.314+3873G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125886 | |||||||
chr12:42126032 | C | A | 59 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(56): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.314+3727G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126032 | |||||||
chr12:42126037 | A | C | 24 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(21): Show |
28 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.314+3722T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126037 | |||||||
chr12:42126073 | C | CT | 38 | a0001c0001t0002g0283 a0001c0001t0002g0284 a0001c0001t0006g0002 others(35): Show |
44 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.314+3685dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126073 | |||||||
chr12:42126073 | C | CTT | 39 | a0001c0001t0006g0242 a0001c0001t0007g0023 a0001c0001t0007g0331 others(36): Show |
40 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.314+3684_314+3685d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126073 | |||||||
chr12:42126096 | C | T | 203 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(200): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.314+3663G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126096 | |||||||
chr12:42126123 | G | A | 5 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+3636C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126123 | |||||||
chr12:42126186 | G | A | 1 | a0001c0001t0053g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.314+3573C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126186 | |||||||
chr12:42126221 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.314+3538C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126221 | |||||||
chr12:42126255 | G | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.314+3504C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126255 | |||||||
chr12:42126320 | A | G | 1 | a0001c0003t0001g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.314+3439T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126320 | |||||||
chr12:42126450 | T | C | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+3309A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126450 | |||||||
chr12:42126721 | C | A | 1 | a0001c0003t0001g0114 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.314+3038G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126721 | |||||||
chr12:42126765 | C | T | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+2994G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126765 | |||||||
chr12:42126880 | G | GA | 8 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0002t0003g0235 others(5): Show |
9 | HG00621.hp2 HG02572.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+2878dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126880 | |||||||
chr12:42126880 | GA | G | 20 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(17): Show |
24 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.314+2878delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126880 | |||||||
chr12:42126948 | G | GT | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+2810_314+2811i others(3): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126948 | |||||||
chr12:42126959 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+2800A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126959 | |||||||
chr12:42126998 | T | G | 2 | a0001c0002t0020g0034 a0001c0002t0034g0032 |
2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.314+2761A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126998 | |||||||
chr12:42127287 | G | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+2472C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127287 | |||||||
chr12:42127352 | C | CT | 26 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(23): Show |
30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.314+2406dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127352 | |||||||
chr12:42127359 | T | TA | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+2399dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127359 | |||||||
chr12:42127600 | C | T | 1 | a0001c0001t0027g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.314+2159G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127600 | |||||||
chr12:42127756 | T | C | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+2003A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127756 | |||||||
chr12:42127764 | C | A | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+1995G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127764 | |||||||
chr12:42127786 | G | A | 6 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+1973C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127786 | |||||||
chr12:42127991 | A | C | 1 | a0001c0002t0004g0084 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.314+1768T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127991 | |||||||
chr12:42128071 | T | C | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.314+1688A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128071 | |||||||
chr12:42128135 | A | G | 1 | a0001c0002t0003g0187 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.314+1624T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128135 | |||||||
chr12:42128156 | C | A | 1 | a0001c0002t0020g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.314+1603G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128156 | |||||||
chr12:42128244 | G | T | 1 | a0001c0001t0002g0307 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314+1515C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128244 | |||||||
chr12:42128329 | T | A | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.314+1430A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128329 | |||||||
chr12:42128397 | T | G | 1 | a0001c0001t0053g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.314+1362A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128397 | |||||||
chr12:42128429 | T | C | 3 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.314+1330A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128429 | |||||||
chr12:42128599 | C | T | 2 | a0001c0001t0011g0101 a0001c0001t0011g0102 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.314+1160G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128599 | |||||||
chr12:42128803 | C | A | 1 | a0001c0001t0002g0300 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.314+956G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128803 | |||||||
chr12:42128809 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+950G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128809 | |||||||
chr12:42128810 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+949T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128810 | |||||||
chr12:42128853 | T | A | 1 | a0001c0003t0001g0221 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.314+906A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128853 | |||||||
chr12:42128955 | C | T | 2 | a0001c0003t0001g0012 a0001c0003t0001g0146 |
3 | NA19007.hp2 NA19079.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.314+804G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128955 | |||||||
chr12:42129083 | G | A | 303 | a0001c0001t0002g0153 a0001c0001t0005g0003 a0001c0001t0005g0262 others(300): Show |
325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.314+676C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129083 | |||||||
chr12:42129131 | A | G | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+628T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129131 | |||||||
chr12:42129147 | T | C | 1 | a0001c0003t0001g0219 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.314+612A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129147 | |||||||
chr12:42129213 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+546A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129213 | |||||||
chr12:42129358 | G | T | 207 | a0001c0001t0002g0153 a0001c0001t0016g0091 a0001c0001t0016g0092 others(204): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.314+401C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129358 | |||||||
chr12:42129443 | C | A | 1 | a0001c0001t0005g0266 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.314+316G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129443 | |||||||
chr12:42129525 | T | C | 1 | a0001c0001t0011g0019 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.314+234A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129525 | |||||||
chr12:42129533 | G | C | 6 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 others(3): Show |
6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+226C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129533 | |||||||
chr12:42129564 | T | C | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+195A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129564 | |||||||
chr12:42129640 | G | A | 1 | a0001c0002t0003g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.314+119C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129640 | |||||||
chr12:42130073 | T | G | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.222-222A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130073 | |||||||
chr12:42130090 | T | C | 1 | a0001c0001t0002g0303 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.222-239A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130090 | |||||||
chr12:42130095 | G | A | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-244C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130095 | |||||||
chr12:42130133 | C | T | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.222-282G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130133 | |||||||
chr12:42130204 | G | A | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222-353C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130204 | |||||||
chr12:42130249 | C | T | 2 | a0001c0001t0016g0092 a0001c0001t0016g0093 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-398G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130249 | |||||||
chr12:42130277 | T | C | 1 | a0001c0001t0002g0297 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.222-426A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130277 | |||||||
chr12:42130359 | A | C | 1 | a0001c0001t0002g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.222-508T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130359 | |||||||
chr12:42130360 | T | C | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-509A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130360 | |||||||
chr12:42130444 | T | C | 1 | a0001c0001t0002g0298 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.222-593A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130444 | |||||||
chr12:42130529 | A | C | 10 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(7): Show |
14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.222-678T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130529 | |||||||
chr12:42130564 | T | C | 1 | a0001c0002t0049g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.222-713A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130564 | |||||||
chr12:42130570 | T | G | 81 | a0001c0001t0002g0153 a0001c0003t0001g0010 a0001c0003t0001g0011 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.222-719A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130570 | |||||||
chr12:42130713 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0299 |
3 | HG00408.hp1 NA18961.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.222-862C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130713 | |||||||
chr12:42130779 | C | T | 2 | a0001c0001t0011g0101 a0001c0001t0011g0102 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.222-928G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130779 | |||||||
chr12:42130898 | G | C | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.222-1047C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130898 | |||||||
chr12:42131037 | T | C | 1 | a0001c0001t0002g0304 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.222-1186A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131037 | |||||||
chr12:42131173 | T | C | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-1322A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131173 | |||||||
chr12:42131406 | T | C | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.222-1555A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131406 | |||||||
chr12:42131606 | T | C | 2 | a0001c0002t0004g0045 a0001c0002t0004g0047 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.222-1755A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131606 | |||||||
chr12:42131657 | G | T | 2 | a0001c0002t0003g0014 a0001c0002t0003g0164 |
3 | HG01943.hp2 HG02132.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.222-1806C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131657 | |||||||
chr12:42131899 | G | A | 1 | a0001c0002t0003g0184 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.222-2048C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131899 | |||||||
chr12:42132046 | A | T | 7 | a0001c0001t0012g0333 a0001c0001t0012g0335 a0001c0001t0012g0338 others(4): Show |
7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-2195T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132046 | |||||||
chr12:42132071 | A | C | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-2220T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132071 | |||||||
chr12:42132182 | T | A | 2 | a0001c0001t0016g0092 a0001c0001t0016g0093 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-2331A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132182 | |||||||
chr12:42132197 | T | C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-2346A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132197 | |||||||
chr12:42132275 | G | C | 305 | a0001c0001t0002g0153 a0001c0001t0005g0003 a0001c0001t0005g0262 others(302): Show |
327 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.222-2424C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132275 | |||||||
chr12:42132343 | G | T | 2 | a0001c0001t0024g0224 a0001c0001t0024g0225 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.222-2492C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132343 | |||||||
chr12:42132386 | C | T | 1 | a0001c0003t0001g0151 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.222-2535G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132386 | |||||||
chr12:42132447 | A | G | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.222-2596T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132447 | |||||||
chr12:42132591 | G | A | 1 | a0001c0002t0034g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.222-2740C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132591 | |||||||
chr12:42132593 | G | A | 1 | a0001c0002t0004g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.222-2742C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132593 | |||||||
chr12:42132635 | T | C | 1 | a0001c0003t0001g0011 | 2 | NA19012.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.222-2784A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132635 | |||||||
chr12:42132688 | C | G | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.222-2837G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132688 | |||||||
chr12:42132784 | G | GT | 6 | a0001c0001t0021g0228 a0001c0001t0021g0229 a0001c0002t0004g0050 others(3): Show |
6 | HG00621.hp2 HG01192.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-2934dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132784 | |||||||
chr12:42132784 | G | T | 1 | a0001c0003t0001g0211 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.222-2933C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132784 | |||||||
chr12:42132826 | A | G | 1 | a0001c0001t0037g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.222-2975T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132826 | |||||||
chr12:42132856 | T | C | 1 | a0001c0002t0020g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.222-3005A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132856 | |||||||
chr12:42132873 | G | A | 4 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 others(1): Show |
4 | HG00099.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-3022C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132873 | |||||||
chr12:42132875 | G | C | 1 | a0001c0001t0027g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.222-3024C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132875 | |||||||
chr12:42132938 | G | C | 1 | a0001c0005t0004g0008 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.222-3087C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132938 | |||||||
chr12:42132971 | C | T | 1 | a0001c0002t0003g0163 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.222-3120G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132971 | |||||||
chr12:42133035 | C | T | 1 | a0001c0001t0009g0254 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.222-3184G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133035 | |||||||
chr12:42133041 | G | C | 1 | a0001c0002t0004g0068 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.222-3190C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133041 | |||||||
chr12:42133135 | A | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-3284T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133135 | |||||||
chr12:42133147 | G | A | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-3296C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133147 | |||||||
chr12:42133192 | C | T | 2 | a0001c0001t0011g0257 a0001c0001t0011g0258 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.222-3341G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133192 | |||||||
chr12:42133193 | G | A | 1 | a0001c0003t0001g0220 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.222-3342C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133193 | |||||||
chr12:42133300 | C | A | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-3449G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133300 | |||||||
chr12:42133459 | T | G | 1 | a0001c0001t0002g0327 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.222-3608A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133459 | |||||||
chr12:42133608 | T | C | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-3757A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133608 | |||||||
chr12:42133609 | C | G | 2 | a0001c0001t0053g0337 a0002c0004t0051g0329 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.222-3758G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133609 | |||||||
chr12:42133690 | T | C | 1 | a0001c0001t0007g0344 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.222-3839A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133690 | |||||||
chr12:42133751 | T | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-3900A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133751 | |||||||
chr12:42133837 | C | A | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-3986G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133837 | |||||||
chr12:42133900 | A | C | 6 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0027g0157 others(3): Show |
6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-4049T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133900 | |||||||
chr12:42133919 | G | A | 1 | a0001c0002t0003g0185 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.222-4068C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133919 | |||||||
chr12:42133963 | G | A | 1 | a0001c0001t0005g0272 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.222-4112C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133963 | |||||||
chr12:42134028 | C | T | 1 | a0001c0002t0003g0193 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.222-4177G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134028 | |||||||
chr12:42134062 | T | C | 3 | a0001c0002t0003g0109 a0001c0002t0003g0196 a0001c0002t0003g0197 |
3 | HG00639.hp2 HG00738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.222-4211A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134062 | |||||||
chr12:42134066 | GGT | G | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-4217_222-4216d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134066 | |||||||
chr12:42134105 | TAGG | T | 58 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(55): Show |
64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.222-4257_222-4255d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134105 | |||||||
chr12:42134143 | T | A | 7 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(4): Show |
9 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-4292A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134143 | |||||||
chr12:42134215 | AAG | A | 5 | a0001c0003t0013g0138 a0001c0003t0013g0139 a0001c0003t0013g0140 others(2): Show |
5 | HG03239.hp1 HG03654.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-4366_222-4365d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134215 | |||||||
chr12:42134329 | T | C | 1 | a0001c0002t0003g0186 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.222-4478A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134329 | |||||||
chr12:42134472 | A | C | 3 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.222-4621T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134472 | |||||||
chr12:42134485 | T | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-4634A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134485 | |||||||
chr12:42134546 | G | A | 3 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 |
3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.222-4695C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134546 | |||||||
chr12:42134599 | G | T | 3 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.222-4748C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134599 | |||||||
chr12:42134600 | C | T | 3 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.222-4749G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134600 | |||||||
chr12:42134604 | A | G | 1 | a0001c0001t0017g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.222-4753T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134604 | |||||||
chr12:42134728 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.222-4877C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134728 | |||||||
chr12:42134811 | T | A | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222-4960A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134811 | |||||||
chr12:42134896 | T | G | 114 | a0001c0001t0002g0153 a0001c0001t0007g0023 a0001c0001t0007g0331 others(111): Show |
119 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.222-5045A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134896 | |||||||
chr12:42134982 | C | G | 81 | a0001c0001t0002g0153 a0001c0003t0001g0010 a0001c0003t0001g0011 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.222-5131G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134982 | |||||||
chr12:42135081 | G | C | 1 | a0001c0001t0054g0341 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.222-5230C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135081 | |||||||
chr12:42135088 | T | C | 1 | a0001c0002t0004g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.222-5237A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135088 | |||||||
chr12:42135349 | G | A | 1 | a0001c0001t0041g0320 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.222-5498C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135349 | |||||||
chr12:42135350 | T | C | 1 | a0001c0001t0007g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.222-5499A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135350 | |||||||
chr12:42135400 | T | G | 1 | a0001c0001t0002g0300 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.222-5549A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135400 | |||||||
chr12:42135434 | T | A | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-5583A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135434 | |||||||
chr12:42135568 | G | A | 3 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0043g0100 |
3 | HG02818.hp2 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.222-5717C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135568 | |||||||
chr12:42135575 | AAAT | A | 58 | a0001c0002t0003g0200 a0001c0002t0004g0035 a0001c0002t0004g0036 others(55): Show |
59 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.222-5727_222-5725d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135575 | |||||||
chr12:42135642 | A | G | 4 | a0001c0001t0026g0310 a0001c0001t0026g0313 a0001c0001t0028g0309 others(1): Show |
4 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-5791T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135642 | |||||||
chr12:42135670 | C | T | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.222-5819G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135670 | |||||||
chr12:42135692 | A | C | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.222-5841T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135692 | |||||||
chr12:42135727 | C | G | 1 | a0001c0001t0041g0320 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.222-5876G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135727 | |||||||
chr12:42135775 | T | C | 11 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(8): Show |
13 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.222-5924A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135775 | |||||||
chr12:42135919 | T | C | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.222-6068A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135919 | |||||||
chr12:42135966 | T | C | 3 | a0001c0001t0014g0226 a0001c0001t0014g0227 a0001c0001t0014g0231 |
3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.222-6115A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135966 | |||||||
chr12:42135986 | A | G | 1 | a0001c0002t0003g0166 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.222-6135T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135986 | |||||||
chr12:42136003 | C | T | 1 | a0001c0002t0004g0079 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.222-6152G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136003 | |||||||
chr12:42136017 | T | C | 1 | a0001c0001t0028g0309 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.222-6166A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136017 | |||||||
chr12:42136126 | A | C | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222-6275T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136126 | |||||||
chr12:42136134 | G | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-6283C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136134 | |||||||
chr12:42136299 | G | A | 2 | a0001c0001t0027g0157 a0001c0001t0027g0230 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.222-6448C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136299 | |||||||
chr12:42136380 | C | T | 2 | a0001c0003t0001g0201 a0001c0003t0001g0209 |
2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.222-6529G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136380 | |||||||
chr12:42136604 | A | G | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.222-6753T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136604 | |||||||
chr12:42136683 | A | C | 6 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 others(3): Show |
6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-6832T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136683 | |||||||
chr12:42136751 | T | TATAC | 9 | a0001c0001t0002g0322 a0001c0001t0005g0328 a0001c0001t0007g0348 others(6): Show |
9 | HG01255.hp1 HG02886.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-6904_222-6901d others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | |||||||
chr12:42136751 | T | TATACATA others(1): Show |
43 | a0001c0001t0002g0282 a0001c0001t0005g0262 a0001c0001t0005g0264 others(40): Show |
45 | HG00733.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.222-6908_222-6901d others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | |||||||
chr12:42136751 | T | TATACATA others(5): Show |
196 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0020 others(193): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.222-6912_222-6901d others(14): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | |||||||
chr12:42136751 | T | TATACATA others(9): Show |
87 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0301 others(84): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.222-6916_222-6901d others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | |||||||
chr12:42136751 | T | TATACATA others(13): Show |
10 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0001t0016g0091 others(7): Show |
10 | HG00642.hp2 HG01517.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.222-6920_222-6901d others(22): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | |||||||
chr12:42136751 | T | TTATACAT others(6): Show |
1 | a0001c0003t0001g0220 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.222-6901_222-6900i others(15): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | |||||||
chr12:42136751 | TATACATA others(9): Show |
T | 3 | a0001c0001t0009g0251 a0001c0001t0009g0252 a0001c0001t0009g0253 |
3 | HG02055.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.222-6916_222-6901d others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | |||||||
chr12:42136785 | T | TACATACA others(9): Show |
2 | a0001c0001t0002g0307 a0002c0004t0002g0009 |
3 | HG00423.hp2 HG02015.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.222-6935_222-6934i others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136785 | |||||||
chr12:42136789 | A | T | 6 | a0001c0001t0002g0279 a0001c0001t0011g0257 a0001c0001t0011g0258 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-6938T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136789 | |||||||
chr12:42136793 | A | C | 3 | a0001c0001t0022g0238 a0001c0001t0022g0239 a0001c0002t0019g0053 |
3 | HG02258.hp1 HG03225.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.222-6942T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136793 | |||||||
chr12:42136797 | C | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-6946G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136797 | |||||||
chr12:42136837 | G | A | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-6986C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136837 | |||||||
chr12:42137028 | T | C | 1 | a0001c0001t0016g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.222-7177A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137028 | |||||||
chr12:42137132 | G | C | 5 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-7281C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137132 | |||||||
chr12:42137209 | C | T | 1 | a0001c0002t0004g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221+7217G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137209 | |||||||
chr12:42137235 | G | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+7191C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137235 | |||||||
chr12:42137236 | C | T | 1 | a0001c0002t0004g0051 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.221+7190G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137236 | |||||||
chr12:42137335 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+7091A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137335 | |||||||
chr12:42137344 | T | C | 2 | a0001c0002t0020g0033 a0001c0002t0020g0034 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.221+7082A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137344 | |||||||
chr12:42137503 | C | CA | 126 | a0001c0001t0002g0308 a0001c0001t0005g0273 a0001c0001t0005g0276 others(123): Show |
133 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.221+6922dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | |||||||
chr12:42137503 | C | CAA | 21 | a0001c0001t0024g0224 a0001c0001t0024g0225 a0001c0002t0003g0098 others(18): Show |
21 | HG00140.hp1 HG00609.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.221+6921_221+6922d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | |||||||
chr12:42137503 | C | CAAA | 63 | a0001c0001t0002g0153 a0001c0002t0003g0195 a0001c0002t0025g0105 others(60): Show |
66 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.221+6920_221+6922d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | |||||||
chr12:42137503 | C | CAAAA | 8 | a0001c0003t0001g0012 a0001c0003t0001g0144 a0001c0003t0001g0146 others(5): Show |
9 | HG01255.hp2 HG01934.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.221+6919_221+6922d others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | |||||||
chr12:42137503 | CA | C | 7 | a0001c0001t0002g0278 a0001c0001t0005g0263 a0001c0001t0007g0331 others(4): Show |
7 | HG02922.hp1 HG02922.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+6922delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | |||||||
chr12:42137529 | G | A | 1 | a0001c0001t0024g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.221+6897C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137529 | |||||||
chr12:42137549 | G | A | 1 | a0001c0006t0056g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.221+6877C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137549 | |||||||
chr12:42137574 | G | A | 2 | a0001c0003t0001g0154 a0001c0003t0001g0155 |
2 | HG00544.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.221+6852C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137574 | |||||||
chr12:42137617 | C | G | 1 | a0001c0001t0027g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+6809G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137617 | |||||||
chr12:42137705 | C | A | 1 | a0001c0001t0043g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.221+6721G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137705 | |||||||
chr12:42137749 | T | C | 3 | a0001c0002t0003g0109 a0001c0002t0003g0196 a0001c0002t0003g0197 |
3 | HG00639.hp2 HG00738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.221+6677A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137749 | |||||||
chr12:42137750 | C | T | 4 | a0001c0003t0001g0202 a0001c0003t0001g0203 a0001c0003t0001g0204 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+6676G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137750 | |||||||
chr12:42137751 | C | A | 3 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02896.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.221+6675G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137751 | |||||||
chr12:42137762 | G | GAAAAA | 19 | a0001c0001t0005g0318 a0001c0001t0007g0334 a0001c0001t0009g0251 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.221+6659_221+6663d others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137762 | |||||||
chr12:42137762 | G | GAAAAAA | 272 | a0001c0001t0002g0153 a0001c0001t0002g0312 a0001c0001t0005g0003 others(269): Show |
293 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.221+6658_221+6663d others(8): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137762 | |||||||
chr12:42137762 | G | GAAAAAAA | 7 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0002g0316 others(4): Show |
8 | HG02896.hp1 HG02897.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+6657_221+6663d others(9): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137762 | |||||||
chr12:42137762 | G | GGAAAAAA | 10 | a0001c0001t0007g0347 a0001c0001t0008g0350 a0001c0001t0008g0351 others(7): Show |
10 | HG00642.hp1 HG01069.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+6663_221+6664i others(9): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137762 | |||||||
chr12:42137821 | G | A | 2 | a0001c0002t0004g0079 a0001c0002t0004g0080 |
2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.221+6605C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137821 | |||||||
chr12:42137852 | T | C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.221+6574A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137852 | |||||||
chr12:42137864 | G | A | 122 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(119): Show |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.221+6562C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137864 | |||||||
chr12:42137872 | A | T | 1 | a0001c0002t0004g0081 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.221+6554T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137872 | |||||||
chr12:42137976 | A | G | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221+6450T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137976 | |||||||
chr12:42137990 | G | A | 1 | a0001c0002t0004g0081 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.221+6436C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137990 | |||||||
chr12:42138136 | A | G | 1 | a0001c0002t0020g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.221+6290T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138136 | |||||||
chr12:42138218 | G | A | 2 | a0001c0003t0001g0106 a0001c0003t0001g0147 |
2 | NA18990.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.221+6208C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138218 | |||||||
chr12:42138306 | C | T | 1 | a0001c0002t0003g0161 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.221+6120G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138306 | |||||||
chr12:42138337 | C | T | 301 | a0001c0001t0002g0153 a0001c0001t0005g0003 a0001c0001t0005g0262 others(298): Show |
323 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.221+6089G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138337 | |||||||
chr12:42138399 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+6027A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138399 | |||||||
chr12:42138442 | T | G | 26 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(23): Show |
30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.221+5984A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138442 | |||||||
chr12:42138482 | C | G | 2 | a0001c0001t0011g0101 a0001c0001t0011g0102 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.221+5944G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138482 | |||||||
chr12:42138546 | G | GA | 297 | a0001c0001t0002g0153 a0001c0001t0005g0003 a0001c0001t0005g0262 others(294): Show |
319 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.221+5879dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138546 | |||||||
chr12:42138557 | G | A | 2 | a0001c0001t0021g0228 a0001c0001t0021g0229 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.221+5869C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138557 | |||||||
chr12:42138584 | G | A | 2 | a0001c0001t0027g0157 a0001c0001t0027g0230 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.221+5842C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138584 | |||||||
chr12:42138660 | C | A | 1 | a0001c0003t0001g0148 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.221+5766G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138660 | |||||||
chr12:42138673 | T | A | 6 | a0001c0002t0003g0094 a0001c0002t0003g0095 a0001c0002t0003g0096 others(3): Show |
6 | HG01175.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+5753A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138673 | |||||||
chr12:42138819 | A | C | 82 | a0001c0001t0002g0153 a0001c0003t0001g0010 a0001c0003t0001g0011 others(79): Show |
86 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.221+5607T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138819 | |||||||
chr12:42138913 | C | G | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.221+5513G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138913 | |||||||
chr12:42138986 | C | T | 3 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 |
3 | HG01081.hp1 HG01243.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.221+5440G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138986 | |||||||
chr12:42139037 | C | CA | 76 | a0001c0001t0011g0257 a0001c0001t0011g0258 a0001c0003t0001g0010 others(73): Show |
79 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.221+5388dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139037 | |||||||
chr12:42139037 | C | CAA | 7 | a0001c0001t0002g0153 a0001c0003t0001g0013 a0001c0003t0001g0149 others(4): Show |
8 | NA18962.hp1 NA18969.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+5387_221+5388d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139037 | |||||||
chr12:42139121 | A | G | 3 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0156 |
3 | NA18953.hp1 NA18972.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.221+5305T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139121 | |||||||
chr12:42139203 | T | TA | 7 | a0001c0001t0011g0257 a0001c0001t0011g0258 a0001c0001t0016g0091 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+5222dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139203 | |||||||
chr12:42139262 | T | TTTCTCCT others(11): Show |
3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+5146_221+5163d others(20): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139262 | |||||||
chr12:42139348 | T | A | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221+5078A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139348 | |||||||
chr12:42139442 | G | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+4984C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139442 | |||||||
chr12:42139552 | A | T | 1 | a0001c0001t0043g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.221+4874T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139552 | |||||||
chr12:42139594 | T | C | 6 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 others(3): Show |
6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+4832A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139594 | |||||||
chr12:42139617 | G | C | 1 | a0001c0001t0038g0275 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.221+4809C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139617 | |||||||
chr12:42139696 | C | A | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221+4730G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139696 | |||||||
chr12:42139789 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+4637G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139789 | |||||||
chr12:42139877 | C | A | 1 | a0001c0002t0015g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.221+4549G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139877 | |||||||
chr12:42139892 | G | A | 1 | a0001c0002t0004g0041 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.221+4534C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139892 | |||||||
chr12:42139895 | A | G | 2 | a0001c0002t0004g0043 a0001c0002t0004g0044 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.221+4531T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139895 | |||||||
chr12:42140063 | C | A | 2 | a0001c0002t0004g0082 a0001c0002t0004g0083 |
2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.221+4363G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140063 | |||||||
chr12:42140163 | A | C | 1 | a0001c0002t0004g0042 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.221+4263T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140163 | |||||||
chr12:42140180 | C | CA | 81 | a0001c0001t0002g0316 a0001c0001t0005g0003 a0001c0001t0005g0263 others(78): Show |
92 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.221+4245dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140180 | |||||||
chr12:42140197 | A | C | 1 | a0001c0001t0016g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.221+4229T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140197 | |||||||
chr12:42140197 | A | G | 2 | a0001c0001t0016g0091 a0001c0001t0016g0092 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.221+4229T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140197 | |||||||
chr12:42140198 | G | A | 60 | a0001c0001t0005g0276 a0001c0001t0007g0348 a0001c0001t0027g0230 others(57): Show |
61 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.221+4228C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140198 | |||||||
chr12:42140199 | GC | G | 5 | a0001c0002t0003g0200 a0001c0002t0004g0084 a0001c0002t0004g0085 others(2): Show |
5 | NA18944.hp2 NA18991.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+4226delG | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140199 | |||||||
chr12:42140200 | C | CG | 95 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0020 others(92): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.221+4225dupC | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140200 | |||||||
chr12:42140200 | C | CGG | 72 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(69): Show |
76 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.221+4224_221+4225d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140200 | |||||||
chr12:42140200 | C | G | 62 | a0001c0001t0005g0276 a0001c0001t0007g0348 a0001c0001t0010g0026 others(59): Show |
63 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.221+4226G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140200 | |||||||
chr12:42140200 | CG | C | 62 | a0001c0001t0008g0352 a0001c0001t0011g0257 a0001c0001t0011g0258 others(59): Show |
67 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.221+4225delC | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140200 | |||||||
chr12:42140201 | G | C | 55 | a0001c0001t0005g0276 a0001c0001t0007g0348 a0001c0001t0027g0230 others(52): Show |
56 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.221+4225C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140201 | |||||||
chr12:42140202 | G | C | 5 | a0001c0002t0003g0200 a0001c0002t0004g0084 a0001c0002t0004g0085 others(2): Show |
5 | NA18944.hp2 NA18991.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+4224C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140202 | |||||||
chr12:42140261 | T | C | 1 | a0001c0001t0014g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.221+4165A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140261 | |||||||
chr12:42140272 | A | G | 1 | a0001c0002t0003g0159 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.221+4154T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140272 | |||||||
chr12:42140283 | G | C | 81 | a0001c0001t0002g0153 a0001c0003t0001g0010 a0001c0003t0001g0011 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.221+4143C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140283 | |||||||
chr12:42140296 | A | C | 1 | a0001c0002t0050g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.221+4130T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140296 | |||||||
chr12:42140437 | A | G | 1 | a0001c0001t0043g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.221+3989T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140437 | |||||||
chr12:42140569 | A | ACAGT | 207 | a0001c0001t0002g0153 a0001c0001t0016g0091 a0001c0001t0016g0092 others(204): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.221+3853_221+3856d others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140569 | |||||||
chr12:42140580 | C | T | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.221+3846G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140580 | |||||||
chr12:42140640 | A | C | 1 | a0001c0001t0007g0331 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.221+3786T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140640 | |||||||
chr12:42140689 | C | T | 204 | a0001c0001t0002g0153 a0001c0002t0003g0004 a0001c0002t0003g0014 others(201): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.221+3737G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140689 | |||||||
chr12:42140704 | A | G | 1 | a0001c0001t0027g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+3722T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140704 | |||||||
chr12:42140827 | T | A | 3 | a0001c0001t0017g0232 a0001c0001t0017g0233 a0001c0001t0017g0240 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.221+3599A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140827 | |||||||
chr12:42140941 | T | C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(13): Show |
20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.221+3485A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140941 | |||||||
chr12:42141017 | T | C | 1 | a0001c0001t0014g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221+3409A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141017 | |||||||
chr12:42141047 | C | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+3379G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141047 | |||||||
chr12:42141403 | T | C | 1 | a0001c0001t0005g0277 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.221+3023A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141403 | |||||||
chr12:42141498 | C | T | 1 | a0001c0003t0001g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221+2928G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141498 | |||||||
chr12:42141547 | C | CA | 11 | a0001c0001t0002g0317 a0001c0001t0002g0319 a0001c0001t0009g0005 others(8): Show |
13 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.221+2878dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141547 | |||||||
chr12:42141578 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+2848T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141578 | |||||||
chr12:42141601 | T | C | 1 | a0001c0002t0015g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.221+2825A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141601 | |||||||
chr12:42141672 | T | C | 1 | a0001c0002t0048g0237 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.221+2754A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141672 | |||||||
chr12:42141798 | G | A | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+2628C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141798 | |||||||
chr12:42141870 | G | A | 19 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(16): Show |
22 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.221+2556C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141870 | |||||||
chr12:42141895 | GTTCCT | G | 6 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 others(3): Show |
6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+2526_221+2530d others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141895 | |||||||
chr12:42141975 | A | G | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.221+2451T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141975 | |||||||
chr12:42142019 | C | T | 20 | a0001c0001t0005g0003 a0001c0001t0005g0262 a0001c0001t0005g0263 others(17): Show |
24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.221+2407G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142019 | |||||||
chr12:42142254 | T | C | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.221+2172A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142254 | |||||||
chr12:42142262 | G | A | 50 | a0001c0001t0006g0002 a0001c0001t0006g0018 a0001c0001t0006g0241 others(47): Show |
55 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.221+2164C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142262 | |||||||
chr12:42142320 | G | A | 2 | a0001c0001t0022g0238 a0001c0001t0022g0239 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.221+2106C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142320 | |||||||
chr12:42142337 | A | AT | 71 | a0001c0001t0002g0153 a0001c0001t0008g0350 a0001c0001t0008g0351 others(68): Show |
75 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.221+2088dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142337 | |||||||
chr12:42142337 | A | ATT | 8 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0011g0257 others(5): Show |
8 | HG01891.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+2087_221+2088d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142337 | |||||||
chr12:42142337 | AT | A | 20 | a0001c0001t0005g0318 a0001c0001t0006g0002 a0001c0001t0006g0018 others(17): Show |
24 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.221+2088delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142337 | |||||||
chr12:42142381 | G | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+2045C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142381 | |||||||
chr12:42142395 | G | A | 10 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(7): Show |
12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+2031C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142395 | |||||||
chr12:42142462 | A | C | 1 | a0001c0002t0034g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.221+1964T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142462 | |||||||
chr12:42142504 | T | A | 1 | a0001c0002t0003g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221+1922A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142504 | |||||||
chr12:42142507 | T | C | 1 | a0001c0001t0002g0319 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.221+1919A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142507 | |||||||
chr12:42142522 | A | AT | 62 | a0001c0002t0004g0035 a0001c0002t0004g0036 a0001c0002t0004g0037 others(59): Show |
63 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.221+1903dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142522 | |||||||
chr12:42142695 | T | C | 1 | a0001c0001t0016g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.221+1731A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142695 | |||||||
chr12:42142711 | C | T | 3 | a0001c0001t0018g0259 a0001c0001t0018g0260 a0001c0001t0018g0261 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.221+1715G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142711 | |||||||
chr12:42142805 | C | T | 4 | a0001c0001t0011g0101 a0001c0001t0011g0102 a0001c0001t0037g0103 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+1621G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142805 | |||||||
chr12:42142825 | G | A | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+1601C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142825 | |||||||
chr12:42142882 | A | T | 32 | a0001c0001t0007g0023 a0001c0001t0007g0331 a0001c0001t0007g0332 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.221+1544T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142882 | |||||||
chr12:42143217 | C | A | 2 | a0001c0003t0001g0250 a0001c0003t0039g0249 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.221+1209G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143217 | |||||||
chr12:42143254 | A | G | 6 | a0001c0002t0003g0094 a0001c0002t0003g0095 a0001c0002t0003g0096 others(3): Show |
6 | HG01175.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+1172T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143254 | |||||||
chr12:42143335 | A | C | 3 | a0001c0001t0016g0091 a0001c0001t0016g0092 a0001c0001t0016g0093 |
3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+1091T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143335 | |||||||
chr12:42143582 | G | C | 6 | a0001c0001t0009g0005 a0001c0001t0009g0251 a0001c0001t0009g0252 others(3): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+844C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143582 | |||||||
chr12:42143748 | C | G | 2 | a0001c0001t0008g0350 a0001c0001t0008g0351 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.221+678G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143748 | |||||||
chr12:42143816 | G | A | 1 | a0001c0003t0013g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.221+610C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143816 | |||||||
chr12:42143869 | T | A | 1 | a0001c0001t0041g0320 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.221+557A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143869 | |||||||
chr12:42143870 | G | A | 2 | a0001c0002t0004g0089 a0001c0002t0004g0090 |
2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.221+556C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143870 | |||||||
chr12:42143952 | G | A | 1 | a0001c0001t0008g0359 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.221+474C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143952 | |||||||
chr12:42144004 | A | T | 2 | a0001c0001t0011g0257 a0001c0001t0011g0258 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.221+422T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42144004 | |||||||
chr12:42144260 | A | G | 280 | a0001c0001t0002g0153 a0001c0001t0006g0002 a0001c0001t0006g0018 others(277): Show |
298 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.221+166T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42144260 | |||||||
chr12:42144317 | G | A | 6 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 others(3): Show |
6 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+109C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42144317 | |||||||
chr12:42144351 | G | GCAGCCCG others(9): Show |
1 | a0001c0001t0005g0328 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.221+59_221+74dupGG others(14): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42144351 |