Item | Value |
---|---|
geneid | 11227 |
ensemblid | ENSG00000136542.9 |
hgncid | 4127 |
symbol | GALNT5 |
name | polypeptide N-acetylgalactosaminyltransferase 5 |
refseq_nuc | NM_014568.3 |
refseq_prot | NP_055383.1 |
ensembl_nuc | ENST00000259056.5 |
ensembl_prot | ENSP00000259056.4 |
mane_status | MANE Select |
chr | chr2 |
start | 157257705 |
end | 157318491 |
strand | + |
ver | v1.2 |
region | chr2:157257705-157318491 |
region5000 | chr2:157252705-157323491 |
regionname0 | GALNT5_chr2_157257705_157318491 |
regionname5000 | GALNT5_chr2_157252705_157323491 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 940 | 205 | 40 | 47 | 89 | 5 | 22 | 65 | GALNT5_chr2_157252705_157323491 | GALNT5 | MNRIR others(935): Show |
chr2 | 157252705 | 157323491 |
a0002 | 0/0 | 940 | 33 | 28 | 3 | 0 | 0 | 2 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | MNRIR others(935): Show |
chr2 | 157252705 | 157323491 |
a0003 | 0/0 | 940 | 25 | 0 | 0 | 25 | 0 | 0 | 21 | GALNT5_chr2_157252705_157323491 | GALNT5 | MNRIR others(935): Show |
chr2 | 157252705 | 157323491 |
a0004 | 0/0 | 940 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | MNRIR others(935): Show |
chr2 | 157252705 | 157323491 |
a0005 | 0/0 | 940 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | MNRIR others(935): Show |
chr2 | 157252705 | 157323491 |
a0006 | 0/0 | 940 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | MNRIR others(935): Show |
chr2 | 157252705 | 157323491 |
a0007 | 0/0 | 940 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | MNRIR others(935): Show |
chr2 | 157252705 | 157323491 |
a0008 | 0/0 | 940 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | MNRIR others(935): Show |
chr2 | 157252705 | 157323491 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2820 | 164 | 21 | 39 | 79 | 5 | 19 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0001c0002 | 1/0 | 2820 | 38 | 16 | 8 | 10 | 0 | 3 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0001c0009 | 0/0 | 2820 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0002c0003 | 0/0 | 2820 | 20 | 15 | 3 | 0 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0002c0005 | 0/0 | 2820 | 13 | 13 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0003c0004 | 0/0 | 2820 | 17 | 0 | 0 | 17 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0003c0007 | 0/0 | 2820 | 8 | 0 | 0 | 8 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0004c0006 | 0/0 | 2820 | 8 | 8 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0004c0011 | 0/0 | 2820 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0005c0008 | 0/0 | 2820 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0006c0010 | 0/0 | 2820 | 3 | 1 | 1 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0007c0012 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 | ||
a0008c0013 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | ATGAA others(2815): Show |
chr2 | 157252705 | 157323491 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 10344 | 89 | 4 | 19 | 51 | 4 | 10 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0002 | 0/0 | 10343 | 12 | 0 | 10 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0003 | 0/0 | 10344 | 6 | 1 | 0 | 1 | 0 | 4 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0004 | 0/0 | 10346 | 5 | 1 | 0 | 2 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10341): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0005 | 0/0 | 10353 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0006 | 0/0 | 10346 | 3 | 0 | 1 | 1 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10341): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0007 | 0/0 | 10344 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0010 | 0/0 | 10345 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10340): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0015 | 0/0 | 10329 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10324): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0016 | 0/0 | 10344 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0017 | 0/0 | 10344 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0019 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0020 | 0/0 | 10370 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10365): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0021 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0023 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0027 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0028 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0029 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0032 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10337): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0034 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0035 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0036 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0037 | 0/0 | 10343 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0041 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0043 | 0/0 | 10343 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0044 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0045 | 0/0 | 10345 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10340): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0046 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0047 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0048 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0049 | 0/0 | 10340 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10335): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0050 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0051 | 0/0 | 10346 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10341): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0052 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0057 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0058 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0061 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10335): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0063 | 0/0 | 10343 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0068 | 0/0 | 10353 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0069 | 0/0 | 10357 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10352): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0074 | 0/0 | 10348 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10343): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0078 | 0/0 | 10359 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10354): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0079 | 0/0 | 10356 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10351): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0080 | 0/0 | 10363 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10358): Show |
chr2 | 157252705 | 157323491 |
a0001c0001t0082 | 0/0 | 10354 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10349): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0001 | 1/0 | 10344 | 16 | 0 | 7 | 6 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0002 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0005 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0010 | 0/0 | 10345 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10340): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0014 | 0/0 | 10351 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10346): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0019 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0028 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0029 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0030 | 0/0 | 10353 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0033 | 0/0 | 10344 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0042 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0054 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10336): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0064 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0065 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0066 | 0/0 | 10349 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10344): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0071 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0072 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0076 | 0/0 | 10354 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10349): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0077 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0081 | 0/0 | 10359 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10354): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0083 | 0/0 | 10357 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10352): Show |
chr2 | 157252705 | 157323491 |
a0001c0002t0084 | 0/0 | 10362 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10357): Show |
chr2 | 157252705 | 157323491 |
a0001c0009t0024 | 0/0 | 10343 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0001c0009t0059 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10336): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0001 | 0/0 | 10344 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0003 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0006 | 0/0 | 10346 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10341): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0008 | 0/0 | 10342 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10337): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0011 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0022 | 0/0 | 10346 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10341): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0023 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0025 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10335): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0027 | 0/0 | 10343 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0038 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10336): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0053 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0055 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10337): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0060 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10337): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0085 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10337): Show |
chr2 | 157252705 | 157323491 |
a0002c0003t0086 | 0/0 | 10345 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10340): Show |
chr2 | 157252705 | 157323491 |
a0002c0005t0001 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0002c0005t0002 | 0/0 | 10343 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0002c0005t0008 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10337): Show |
chr2 | 157252705 | 157323491 |
a0002c0005t0012 | 0/0 | 10347 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10342): Show |
chr2 | 157252705 | 157323491 |
a0002c0005t0018 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0002c0005t0025 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10335): Show |
chr2 | 157252705 | 157323491 |
a0002c0005t0026 | 0/0 | 10339 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10334): Show |
chr2 | 157252705 | 157323491 |
a0002c0005t0039 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0003c0004t0001 | 0/0 | 10344 | 11 | 0 | 0 | 11 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0003c0004t0004 | 0/0 | 10346 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10341): Show |
chr2 | 157252705 | 157323491 |
a0003c0004t0009 | 0/0 | 10344 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0003c0004t0056 | 0/0 | 10345 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10340): Show |
chr2 | 157252705 | 157323491 |
a0003c0004t0062 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0003c0007t0001 | 0/0 | 10344 | 6 | 0 | 0 | 6 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0003c0007t0002 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0003c0007t0040 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10338): Show |
chr2 | 157252705 | 157323491 |
a0004c0006t0005 | 0/0 | 10353 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0004c0006t0013 | 0/0 | 10353 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0004c0006t0014 | 0/0 | 10351 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10346): Show |
chr2 | 157252705 | 157323491 |
a0004c0006t0075 | 0/0 | 10352 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10347): Show |
chr2 | 157252705 | 157323491 |
a0004c0011t0067 | 0/0 | 10352 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10347): Show |
chr2 | 157252705 | 157323491 |
a0004c0011t0073 | 0/0 | 10350 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10345): Show |
chr2 | 157252705 | 157323491 |
a0005c0008t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0005c0008t0009 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0005c0008t0011 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0006c0010t0005 | 0/0 | 10353 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10348): Show |
chr2 | 157252705 | 157323491 |
a0006c0010t0070 | 0/0 | 10352 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10347): Show |
chr2 | 157252705 | 157323491 |
a0007c0012t0021 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
a0008c0013t0031 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | AATCT others(10339): Show |
chr2 | 157252705 | 157323491 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0006g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0007g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0015g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0015g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0016g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0016g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0017g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0019g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0020g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0021g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0023g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0027g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0028g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0029g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0032g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0034g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0035g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0036g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0037g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0041g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0043g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0044g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0045g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0046g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0047g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0048g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0049g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0050g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0051g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0052g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0057g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0058g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0061g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0063g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0068g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0069g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0074g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0078g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0079g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0080g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0082g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0009 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0010g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0014g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0019g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0028g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0029g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0030g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0033g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0042g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0054g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0064g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0065g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0066g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0071g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0072g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0076g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0077g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0081g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0083g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0084g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0009t0024g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0009t0024g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0009t0059g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0022g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0022g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0023g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0025g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0027g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0038g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0053g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0055g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0060g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0085g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0086g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0012g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0018g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0025g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0026g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0026g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0039g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0009g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0056g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0062g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0040g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0014g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0075g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0011t0067g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0011t0073g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0005c0008t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0005c0008t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0005c0008t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0005c0008t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0006c0010t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0006c0010t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0006c0010t0070g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0007c0012t0021g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0008c0013t0031g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0049 | EUR | GBR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00438 | hp1 | a0001 | c0001 | t0019 | g0037 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00438 | hp2 | a0001 | c0001 | t0045 | g0147 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00544 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00597 | hp2 | a0003 | c0004 | t0001 | g0229 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00609 | hp2 | a0001 | c0001 | t0029 | g0036 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00639 | hp1 | a0002 | c0003 | t0022 | g0189 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00673 | hp1 | a0003 | c0004 | t0004 | g0221 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00673 | hp2 | a0001 | c0001 | t0020 | g0013 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00735 | hp2 | a0002 | c0003 | t0001 | g0191 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00741 | hp2 | a0001 | c0002 | t0010 | g0003 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01071 | hp2 | a0001 | c0001 | t0021 | g0117 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01074 | hp2 | a0001 | c0001 | t0068 | g0235 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0056 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01109 | hp2 | a0001 | c0001 | t0047 | g0011 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01168 | hp1 | a0001 | c0001 | t0063 | g0076 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01243 | hp1 | a0006 | c0010 | t0005 | g0208 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01243 | hp2 | a0001 | c0001 | t0044 | g0157 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01256 | hp1 | a0001 | c0001 | t0017 | g0005 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01258 | hp1 | a0001 | c0001 | t0017 | g0005 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01261 | hp1 | a0001 | c0001 | t0049 | g0006 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01261 | hp2 | a0002 | c0003 | t0023 | g0206 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01433 | hp1 | a0001 | c0001 | t0052 | g0078 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01884 | hp1 | a0004 | c0006 | t0075 | g0186 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01891 | hp1 | a0002 | c0005 | t0001 | g0203 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01891 | hp2 | a0004 | c0011 | t0067 | g0177 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02040 | hp2 | a0001 | c0001 | t0028 | g0061 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02055 | hp1 | a0002 | c0003 | t0055 | g0163 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02055 | hp2 | a0002 | c0003 | t0011 | g0164 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02071 | hp1 | a0003 | c0004 | t0004 | g0226 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02083 | hp1 | a0003 | c0007 | t0001 | g0230 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | CDX | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02257 | hp1 | a0002 | c0005 | t0026 | g0205 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02258 | hp1 | a0001 | c0002 | t0005 | g0250 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02258 | hp2 | a0002 | c0005 | t0012 | g0014 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02572 | hp1 | a0001 | c0002 | t0076 | g0240 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02572 | hp2 | a0001 | c0002 | t0014 | g0257 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02602 | hp1 | a0001 | c0002 | t0033 | g0093 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02615 | hp1 | a0001 | c0001 | t0061 | g0089 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02615 | hp2 | a0002 | c0005 | t0008 | g0204 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02622 | hp1 | a0001 | c0001 | t0015 | g0247 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02622 | hp2 | a0002 | c0005 | t0026 | g0202 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02630 | hp1 | a0005 | c0008 | t0011 | g0173 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02630 | hp2 | a0002 | c0005 | t0012 | g0188 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02647 | hp1 | a0004 | c0006 | t0013 | g0183 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02647 | hp2 | a0005 | c0008 | t0011 | g0172 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02683 | hp2 | a0001 | c0001 | t0016 | g0152 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02698 | hp2 | a0002 | c0003 | t0006 | g0175 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02717 | hp1 | a0005 | c0008 | t0003 | g0170 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02717 | hp2 | a0002 | c0003 | t0085 | g0198 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02723 | hp1 | a0004 | c0006 | t0014 | g0184 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02723 | hp2 | a0001 | c0002 | t0064 | g0249 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02809 | hp1 | a0005 | c0008 | t0009 | g0171 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0253 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02886 | hp1 | a0002 | c0005 | t0039 | g0168 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0256 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02895 | hp1 | a0001 | c0002 | t0077 | g0238 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02895 | hp2 | a0001 | c0002 | t0030 | g0016 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02896 | hp1 | a0001 | c0009 | t0024 | g0138 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02896 | hp2 | a0002 | c0003 | t0027 | g0161 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02897 | hp1 | a0001 | c0002 | t0030 | g0016 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02897 | hp2 | a0002 | c0003 | t0003 | g0162 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02965 | hp1 | a0001 | c0001 | t0043 | g0072 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02965 | hp2 | a0001 | c0002 | t0084 | g0255 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02970 | hp1 | a0001 | c0002 | t0083 | g0243 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02976 | hp1 | a0002 | c0005 | t0025 | g0200 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02976 | hp2 | a0001 | c0009 | t0059 | g0010 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03017 | hp2 | a0001 | c0001 | t0016 | g0115 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03130 | hp1 | a0001 | c0002 | t0065 | g0248 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03130 | hp2 | a0001 | c0002 | t0066 | g0245 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03139 | hp1 | a0004 | c0011 | t0073 | g0178 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03139 | hp2 | a0002 | c0005 | t0012 | g0014 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03195 | hp2 | a0002 | c0003 | t0038 | g0196 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03209 | hp1 | a0001 | c0002 | t0054 | g0097 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03209 | hp2 | a0004 | c0006 | t0013 | g0180 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03225 | hp1 | a0002 | c0003 | t0022 | g0192 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03225 | hp2 | a0001 | c0001 | t0082 | g0241 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03239 | hp1 | a0001 | c0001 | t0037 | g0083 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03453 | hp1 | a0002 | c0005 | t0002 | g0201 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03453 | hp2 | a0006 | c0010 | t0070 | g0185 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03486 | hp1 | a0002 | c0003 | t0053 | g0195 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03490 | hp1 | a0002 | c0003 | t0006 | g0174 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03516 | hp1 | a0002 | c0005 | t0001 | g0199 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03516 | hp2 | a0002 | c0003 | t0003 | g0193 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03540 | hp1 | a0001 | c0001 | t0078 | g0242 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03579 | hp2 | a0004 | c0006 | t0005 | g0179 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | BEB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | BEB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0128 | SAS | BEB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | STU | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18522 | hp1 | a0001 | c0002 | t0072 | g0246 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18522 | hp2 | a0002 | c0005 | t0018 | g0167 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18747 | hp2 | a0001 | c0002 | t0019 | g0051 | EAS | CHB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18906 | hp1 | a0001 | c0002 | t0042 | g0092 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18906 | hp2 | a0001 | c0001 | t0074 | g0244 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18946 | hp1 | a0003 | c0004 | t0001 | g0219 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18959 | hp1 | a0001 | c0001 | t0058 | g0119 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18960 | hp2 | a0001 | c0002 | t0028 | g0154 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18961 | hp1 | a0003 | c0007 | t0040 | g0209 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18961 | hp2 | a0003 | c0007 | t0001 | g0231 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18963 | hp2 | a0003 | c0004 | t0001 | g0210 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18964 | hp1 | a0003 | c0004 | t0001 | g0212 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18964 | hp2 | a0001 | c0001 | t0027 | g0148 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18965 | hp1 | a0003 | c0007 | t0001 | g0232 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18965 | hp2 | a0001 | c0001 | t0046 | g0023 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18970 | hp1 | a0001 | c0002 | t0029 | g0032 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18971 | hp2 | a0001 | c0001 | t0036 | g0124 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18973 | hp1 | a0003 | c0004 | t0001 | g0222 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18977 | hp1 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18979 | hp2 | a0003 | c0007 | t0001 | g0215 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18981 | hp2 | a0003 | c0004 | t0001 | g0015 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18982 | hp1 | a0003 | c0004 | t0056 | g0216 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18985 | hp2 | a0001 | c0001 | t0035 | g0081 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18990 | hp2 | a0001 | c0001 | t0034 | g0135 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18991 | hp1 | a0001 | c0001 | t0048 | g0022 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18991 | hp2 | a0003 | c0004 | t0001 | g0214 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18992 | hp2 | a0003 | c0007 | t0002 | g0223 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18999 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18999 | hp2 | a0001 | c0001 | t0020 | g0126 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19002 | hp1 | a0001 | c0001 | t0050 | g0024 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19002 | hp2 | a0003 | c0004 | t0001 | g0228 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19003 | hp1 | a0003 | c0004 | t0001 | g0227 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19011 | hp2 | a0003 | c0004 | t0009 | g0224 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19030 | hp1 | a0001 | c0002 | t0081 | g0237 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19030 | hp2 | a0002 | c0003 | t0060 | g0165 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19043 | hp1 | a0004 | c0006 | t0014 | g0166 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19043 | hp2 | a0002 | c0003 | t0008 | g0190 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19058 | hp1 | a0003 | c0004 | t0001 | g0015 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19062 | hp1 | a0001 | c0001 | t0057 | g0094 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19064 | hp2 | a0001 | c0001 | t0051 | g0111 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19065 | hp2 | a0003 | c0004 | t0009 | g0217 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19068 | hp2 | a0003 | c0007 | t0001 | g0220 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19074 | hp1 | a0003 | c0007 | t0001 | g0211 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19076 | hp2 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19084 | hp1 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19088 | hp1 | a0003 | c0004 | t0062 | g0218 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19088 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19091 | hp2 | a0003 | c0004 | t0001 | g0225 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19240 | hp1 | a0004 | c0006 | t0005 | g0182 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19240 | hp2 | a0001 | c0009 | t0024 | g0010 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20129 | hp1 | a0002 | c0003 | t0086 | g0197 | AFR | ASW | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20129 | hp2 | a0004 | c0006 | t0013 | g0181 | AFR | ASW | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20752 | hp2 | a0006 | c0010 | t0005 | g0176 | EUR | TSI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01123 | hp2 | a0007 | c0012 | t0021 | g0141 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02109 | hp1 | a0008 | c0013 | t0031 | g0259 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02109 | hp2 | a0002 | c0003 | t0008 | g0194 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02486 | hp1 | a0001 | c0001 | t0023 | g0060 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02486 | hp2 | a0002 | c0005 | t0018 | g0169 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0207 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02559 | hp2 | a0002 | c0003 | t0025 | g0187 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03471 | hp1 | a0001 | c0002 | t0071 | g0258 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03471 | hp2 | a0001 | c0001 | t0080 | g0236 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20300 | hp1 | a0001 | c0001 | t0032 | g0254 | AFR | USA | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20300 | hp2 | a0001 | c0001 | t0041 | g0107 | AFR | USA | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA21309 | hp1 | a0001 | c0001 | t0069 | g0239 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA21309 | hp2 | a0001 | c0001 | t0079 | g0251 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0145 | REF | REF | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0009 | REF | REF | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:157258312 | C | T | 1 | a0003 | 25 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(22): Show |
missense_variant | MODERATE | c.230C>T | p.Pro77Leu | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 608/10344 | 230/2823 | 77/940 | chr2 | 157258312 | |||
chr2:157258518 | G | A | 1 | a0005 | 4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
missense_variant | MODERATE | c.436G>A | p.Gly146Arg | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 814/10344 | 436/2823 | 146/940 | chr2 | 157258518 | |||
chr2:157258540 | C | T | 1 | a0008 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.458C>T | p.Ala153Val | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 836/10344 | 458/2823 | 153/940 | chr2 | 157258540 | |||
chr2:157258617 | A | T | 2 | a0004 a0006 |
13 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
missense_variant | MODERATE | c.535A>T | p.Thr179Ser | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 913/10344 | 535/2823 | 179/940 | chr2 | 157258617 | |||
chr2:157284294 | G | C | 3 | a0002 a0004 a0005 |
47 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(44): Show |
missense_variant | MODERATE | c.1467G>C | p.Gln489His | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/10 | 1845/10344 | 1467/2823 | 489/940 | chr2 | 157284294 | |||
chr2:157296405 | T | C | 1 | a0007 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.1889T>C | p.Val630Ala | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/10 | 2267/10344 | 1889/2823 | 630/940 | chr2 | 157296405 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:157258247 | A | C | 1 | a0008c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.165A>C | p.Ile55Ile | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 543/10344 | 165/2823 | 55/940 | chr2 | 157258247 | |||
chr2:157258517 | C | T | 1 | a0008c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.435C>T | p.Asp145Asp | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 813/10344 | 435/2823 | 145/940 | chr2 | 157258517 | |||
chr2:157258535 | T | C | 1 | a0008c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.453T>C | p.Pro151Pro | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 831/10344 | 453/2823 | 151/940 | chr2 | 157258535 | |||
chr2:157300849 | C | T | 9 | a0001c0001 a0001c0009 a0002c0003 others(6): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
synonymous_variant | LOW | c.2289C>T | p.His763His | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/10 | 2667/10344 | 2289/2823 | 763/940 | chr2 | 157300849 | |||
chr2:157300948 | G | A | 1 | a0001c0009 | 3 | HG02896.hp1 HG02976.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2388G>A | p.Leu796Leu | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/10 | 2766/10344 | 2388/2823 | 796/940 | chr2 | 157300948 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:157257756 | C | T | 2 | a0002c0003t0085 a0002c0003t0086 |
2 | HG02717.hp2 NA20129.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-327C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | chr2 | 157257756 | |||||||
chr2:157257836 | T | C | 1 | a0008c0013t0031 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-247T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 247 | chr2 | 157257836 | ||||||
chr2:157257986 | T | TCTG | 1 | a0002c0005t0012 | 3 | HG02258.hp2 HG02630.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73_-71dupGCT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | |||||
chr2:157257986 | T | TCTGCTGC others(2): Show |
20 | a0001c0001t0005 a0001c0001t0068 a0001c0001t0069 others(17): Show |
27 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-79_-71dupGCTGCTGC others(1): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | |||||
chr2:157257986 | T | TCTGCTGC others(5): Show |
2 | a0001c0002t0076 a0001c0002t0077 |
2 | HG02572.hp1 HG02895.hp1 |
5_prime_UTR_variant | MODIFIER | c.-82_-71dupGCTGCTGC others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | |||||
chr2:157257986 | T | TCTGCTGC others(8): Show |
6 | a0001c0001t0078 a0001c0001t0079 a0001c0001t0080 others(3): Show |
6 | HG02970.hp1 HG03225.hp2 HG03471.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-85_-71dupGCTGCTGC others(7): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | |||||
chr2:157257986 | T | TCTGCTGC others(11): Show |
1 | a0001c0002t0084 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88_-71dupGCTGCTGC others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | |||||
chr2:157257986 | TCTGCTG | T | 2 | a0001c0001t0015 a0001c0001t0032 |
3 | HG02622.hp1 HG02809.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-76_-71delGCTGCT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 71 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | |||||
chr2:157311472 | T | A | 2 | a0001c0001t0015 a0001c0002t0064 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*124T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 124 | chr2 | 157311472 | ||||||
chr2:157311530 | T | C | 2 | a0001c0001t0016 a0001c0002t0033 |
3 | HG02602.hp1 HG02683.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*182T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 182 | chr2 | 157311530 | ||||||
chr2:157311588 | A | G | 4 | a0001c0001t0028 a0001c0001t0029 a0001c0002t0028 others(1): Show |
4 | HG00609.hp2 HG02040.hp2 NA18960.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*240A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 240 | chr2 | 157311588 | ||||||
chr2:157311834 | C | T | 1 | a0001c0001t0063 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*486C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 486 | chr2 | 157311834 | ||||||
chr2:157311837 | T | C | 1 | a0001c0001t0017 | 2 | HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*489T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 489 | chr2 | 157311837 | ||||||
chr2:157311908 | C | T | 1 | a0003c0004t0062 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*560C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 560 | chr2 | 157311908 | ||||||
chr2:157311986 | G | A | 1 | a0001c0001t0034 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*638G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 638 | chr2 | 157311986 | ||||||
chr2:157312033 | C | T | 1 | a0001c0001t0061 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 685 | chr2 | 157312033 | ||||||
chr2:157312169 | G | A | 1 | a0001c0001t0035 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 821 | chr2 | 157312169 | ||||||
chr2:157312228 | A | G | 1 | a0008c0013t0031 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 880 | chr2 | 157312228 | ||||||
chr2:157312328 | G | A | 1 | a0001c0001t0078 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 980 | chr2 | 157312328 | ||||||
chr2:157312682 | C | T | 1 | a0002c0003t0060 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1334C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1334 | chr2 | 157312682 | ||||||
chr2:157312716 | A | G | 2 | a0001c0001t0015 a0001c0002t0064 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1368A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1368 | chr2 | 157312716 | ||||||
chr2:157312753 | A | T | 2 | a0001c0001t0015 a0001c0002t0064 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1405A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1405 | chr2 | 157312753 | ||||||
chr2:157312815 | A | G | 1 | a0001c0002t0033 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1467A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1467 | chr2 | 157312815 | ||||||
chr2:157312875 | T | C | 1 | a0001c0001t0036 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1527T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1527 | chr2 | 157312875 | ||||||
chr2:157312987 | A | G | 2 | a0001c0001t0015 a0001c0002t0064 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1639A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1639 | chr2 | 157312987 | ||||||
chr2:157313100 | G | A | 20 | a0001c0001t0015 a0001c0001t0028 a0001c0001t0037 others(17): Show |
27 | HG02040.hp2 HG02109.hp2 HG02258.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1752G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1752 | chr2 | 157313100 | ||||||
chr2:157313154 | C | T | 1 | a0001c0002t0084 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1806C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1806 | chr2 | 157313154 | ||||||
chr2:157313275 | T | G | 3 | a0001c0001t0028 a0001c0001t0037 a0001c0002t0028 |
3 | HG02040.hp2 HG03239.hp1 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1927T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1927 | chr2 | 157313275 | ||||||
chr2:157313321 | G | A | 3 | a0001c0001t0041 a0001c0001t0043 a0001c0002t0042 |
3 | HG02965.hp1 NA18906.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1973G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1973 | chr2 | 157313321 | ||||||
chr2:157313505 | T | C | 2 | a0001c0001t0015 a0001c0002t0064 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2157T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 2157 | chr2 | 157313505 | ||||||
chr2:157313566 | T | C | 1 | a0001c0001t0044 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2218T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 2218 | chr2 | 157313566 | ||||||
chr2:157314211 | T | TA | 11 | a0001c0001t0010 a0001c0001t0045 a0001c0001t0061 others(8): Show |
13 | HG00438.hp2 HG00741.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2880dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 2881 | INFO_REALIGN_3_PRIME | chr2 | 157314211 | |||||
chr2:157314211 | TA | T | 13 | a0001c0001t0027 a0001c0001t0028 a0001c0001t0037 others(10): Show |
13 | HG01168.hp1 HG01884.hp1 HG02040.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2880delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 2880 | INFO_REALIGN_3_PRIME | chr2 | 157314211 | |||||
chr2:157314348 | C | T | 5 | a0001c0002t0014 a0001c0002t0083 a0002c0003t0055 others(2): Show |
6 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3000C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3000 | chr2 | 157314348 | ||||||
chr2:157314404 | G | A | 1 | a0001c0001t0068 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3056G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3056 | chr2 | 157314404 | ||||||
chr2:157314586 | T | C | 2 | a0001c0001t0019 a0001c0002t0019 |
2 | HG00438.hp1 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3238T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3238 | chr2 | 157314586 | ||||||
chr2:157314983 | CAGG | C | 2 | a0001c0001t0015 a0001c0002t0064 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3638_*3640delGAG | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3638 | INFO_REALIGN_3_PRIME | chr2 | 157314983 | |||||
chr2:157315002 | C | T | 1 | a0001c0001t0068 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3654C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3654 | chr2 | 157315002 | ||||||
chr2:157315029 | A | G | 40 | a0001c0001t0015 a0001c0001t0023 a0001c0001t0028 others(37): Show |
47 | HG00639.hp1 HG01261.hp2 HG01891.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3681A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3681 | chr2 | 157315029 | ||||||
chr2:157315081 | AAAT | A | 8 | a0001c0001t0015 a0001c0001t0061 a0001c0002t0064 others(5): Show |
10 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3746_*3748delAAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3746 | INFO_REALIGN_3_PRIME | chr2 | 157315081 | |||||
chr2:157315083 | A | T | 1 | a0001c0001t0001 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3735A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3735 | chr2 | 157315083 | ||||||
chr2:157315440 | A | T | 2 | a0001c0001t0015 a0001c0002t0064 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4092A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 4092 | chr2 | 157315440 | ||||||
chr2:157315456 | A | C | 1 | a0002c0003t0053 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4108A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 4108 | chr2 | 157315456 | ||||||
chr2:157316235 | A | G | 3 | a0001c0001t0021 a0001c0001t0052 a0007c0012t0021 |
3 | HG01071.hp2 HG01123.hp2 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4887A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 4887 | chr2 | 157316235 | ||||||
chr2:157316619 | A | G | 1 | a0001c0002t0030 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5271A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5271 | chr2 | 157316619 | ||||||
chr2:157316638 | T | C | 2 | a0001c0001t0061 a0001c0002t0066 |
2 | HG02615.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5290T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5290 | chr2 | 157316638 | ||||||
chr2:157316697 | T | C | 1 | a0001c0001t0046 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5349T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5349 | chr2 | 157316697 | ||||||
chr2:157316735 | G | A | 1 | a0001c0001t0047 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5387G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5387 | chr2 | 157316735 | ||||||
chr2:157316946 | A | G | 2 | a0001c0001t0007 a0001c0001t0051 |
5 | HG00544.hp2 NA18999.hp1 NA19064.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5598A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5598 | chr2 | 157316946 | ||||||
chr2:157317109 | A | C | 3 | a0002c0005t0012 a0002c0005t0018 a0002c0005t0039 |
6 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5761A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5761 | chr2 | 157317109 | ||||||
chr2:157317174 | G | GTA | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0051 others(4): Show |
16 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5850_*5851dupAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5852 | INFO_REALIGN_3_PRIME | chr2 | 157317174 | |||||
chr2:157317174 | G | GTATA | 3 | a0001c0001t0032 a0001c0001t0069 a0001c0001t0080 |
3 | HG03471.hp2 NA20300.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5848_*5851dupATAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5852 | INFO_REALIGN_3_PRIME | chr2 | 157317174 | |||||
chr2:157317174 | GTA | G | 10 | a0001c0001t0061 a0001c0002t0014 a0001c0002t0066 others(7): Show |
11 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5850_*5851delAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5850 | INFO_REALIGN_3_PRIME | chr2 | 157317174 | |||||
chr2:157317174 | GTATA | G | 3 | a0001c0001t0049 a0002c0003t0025 a0002c0005t0025 |
3 | HG01261.hp1 HG02559.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5848_*5851delATAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5848 | INFO_REALIGN_3_PRIME | chr2 | 157317174 | |||||
chr2:157317176 | A | G | 1 | a0001c0001t0050 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5828A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5828 | chr2 | 157317176 | ||||||
chr2:157317191 | TATA | T | 6 | a0001c0001t0015 a0001c0001t0079 a0001c0002t0054 others(3): Show |
7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5844_*5846delATA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5844 | chr2 | 157317191 | ||||||
chr2:157317191 | TATATA | T | 3 | a0001c0001t0074 a0001c0001t0082 a0002c0005t0026 |
4 | HG02257.hp1 HG02622.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5844_*5848delATAT others(1): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5844 | chr2 | 157317191 | ||||||
chr2:157317194 | A | T | 2 | a0001c0002t0076 a0004c0006t0005 |
2 | HG02572.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5846A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5846 | chr2 | 157317194 | ||||||
chr2:157317196 | A | T | 21 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0046 others(18): Show |
24 | HG00735.hp2 HG01891.hp2 HG01952.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5848A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5848 | chr2 | 157317196 | ||||||
chr2:157317197 | TA | T | 7 | a0001c0001t0002 a0001c0002t0002 a0001c0009t0024 others(4): Show |
19 | HG01106.hp1 HG01361.hp1 HG01361.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5850delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5850 | chr2 | 157317197 | ||||||
chr2:157317198 | A | AT | 5 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0020 others(2): Show |
7 | HG00280.hp2 HG00673.hp2 HG01258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5861dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5862 | INFO_REALIGN_3_PRIME | chr2 | 157317198 | |||||
chr2:157317198 | A | ATT | 8 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0017 others(5): Show |
9 | HG01256.hp1 HG02040.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5860_*5861dupTT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5862 | INFO_REALIGN_3_PRIME | chr2 | 157317198 | |||||
chr2:157317198 | A | T | 41 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0020 others(38): Show |
82 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*5850A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5850 | chr2 | 157317198 | ||||||
chr2:157317198 | ATT | A | 5 | a0002c0005t0012 a0002c0005t0018 a0002c0005t0039 others(2): Show |
8 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5860_*5861delTT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5860 | INFO_REALIGN_3_PRIME | chr2 | 157317198 | |||||
chr2:157317200 | T | A | 13 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0027 others(10): Show |
25 | HG00099.hp2 HG00438.hp2 HG01106.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5852T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5852 | chr2 | 157317200 | ||||||
chr2:157317247 | C | T | 1 | a0001c0001t0052 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5899C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5899 | chr2 | 157317247 | ||||||
chr2:157317286 | T | C | 4 | a0002c0003t0008 a0002c0003t0038 a0002c0003t0085 others(1): Show |
5 | HG02109.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5938T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5938 | chr2 | 157317286 | ||||||
chr2:157317362 | T | C | 1 | a0001c0001t0050 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6014T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6014 | chr2 | 157317362 | ||||||
chr2:157317382 | T | G | 1 | a0001c0002t0071 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6034T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6034 | chr2 | 157317382 | ||||||
chr2:157317414 | T | G | 1 | a0001c0001t0048 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6066T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6066 | chr2 | 157317414 | ||||||
chr2:157317960 | C | G | 1 | a0001c0002t0030 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6612C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6612 | chr2 | 157317960 | ||||||
chr2:157318122 | A | T | 3 | a0001c0001t0023 a0002c0003t0022 a0002c0003t0023 |
4 | HG00639.hp1 HG01261.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6774A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6774 | chr2 | 157318122 | ||||||
chr2:157318149 | A | T | 1 | a0001c0001t0020 | 2 | HG00673.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6801A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6801 | chr2 | 157318149 | ||||||
chr2:157318154 | T | TTATTTTT others(19): Show |
1 | a0001c0001t0020 | 2 | HG00673.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6806_*6807insTATT others(22): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6807 | chr2 | 157318154 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:157259616 | C | T | 26 | a0001c0001t0005g0252 a0001c0001t0005g0256 a0001c0001t0015g0247 others(23): Show |
27 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1454+80C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157259616 | |||||||
chr2:157259729 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1454+193T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157259729 | |||||||
chr2:157260183 | A | G | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1454+647A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260183 | |||||||
chr2:157260260 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | NA18959.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1454+724A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260260 | |||||||
chr2:157260788 | C | T | 74 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(71): Show |
76 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1454+1252C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260788 | |||||||
chr2:157260893 | T | C | 74 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(71): Show |
76 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1454+1357T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260893 | |||||||
chr2:157260977 | T | C | 1 | a0001c0001t0068g0235 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1454+1441T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260977 | |||||||
chr2:157261171 | C | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0002g0020 others(1): Show |
4 | HG00741.hp1 HG01106.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+1635C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261171 | |||||||
chr2:157261242 | G | T | 26 | a0001c0001t0001g0213 a0001c0002t0002g0160 a0003c0004t0001g0015 others(23): Show |
27 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1454+1706G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261242 | |||||||
chr2:157261317 | G | A | 8 | a0001c0001t0069g0239 a0001c0001t0078g0242 a0001c0001t0080g0236 others(5): Show |
8 | HG02572.hp1 HG02895.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1454+1781G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261317 | |||||||
chr2:157261357 | C | T | 3 | a0003c0007t0001g0230 a0003c0007t0001g0231 a0003c0007t0001g0232 |
3 | HG02083.hp1 NA18961.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1454+1821C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261357 | |||||||
chr2:157261479 | G | A | 1 | a0001c0001t0048g0022 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1454+1943G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261479 | |||||||
chr2:157261538 | C | T | 13 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(10): Show |
13 | HG00438.hp2 HG01243.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1454+2002C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261538 | |||||||
chr2:157262112 | G | A | 74 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(71): Show |
76 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1454+2576G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262112 | |||||||
chr2:157262155 | ACATAACT others(2): Show |
A | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+2624_1454+263 others(13): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262155 | ||||||
chr2:157262207 | T | TA | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(56): Show |
65 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1454+2689dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262207 | ||||||
chr2:157262207 | T | TAA | 6 | a0001c0001t0046g0023 a0001c0001t0050g0024 a0001c0002t0001g0025 others(3): Show |
6 | NA18961.hp1 NA18963.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454+2688_1454+268 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262207 | ||||||
chr2:157262207 | TA | T | 9 | a0001c0001t0001g0146 a0001c0001t0001g0159 a0001c0002t0030g0016 others(6): Show |
10 | HG01358.hp1 HG01891.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454+2689delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262207 | ||||||
chr2:157262225 | A | T | 2 | a0002c0003t0001g0207 a0002c0003t0023g0206 |
2 | HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1454+2689A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262225 | |||||||
chr2:157262287 | G | A | 1 | a0001c0001t0006g0049 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1454+2751G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262287 | |||||||
chr2:157262362 | C | CA | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1454+2827dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262362 | ||||||
chr2:157262454 | T | C | 2 | a0001c0001t0005g0252 a0001c0001t0079g0251 |
2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1454+2918T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262454 | |||||||
chr2:157262484 | AAAAATTA others(784): Show |
A | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+2953_1454+374 others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262484 | ||||||
chr2:157262658 | CAACAAT | C | 71 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(68): Show |
73 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1454+3125_1454+313 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262658 | ||||||
chr2:157262661 | CAAT | C | 4 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0032g0254 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3128_1454+313 others(7): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262661 | ||||||
chr2:157262819 | C | CT | 17 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0066 others(14): Show |
18 | HG00544.hp1 HG00544.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1454+3310dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262819 | ||||||
chr2:157262819 | CTTTTT | C | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0212 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1454+3306_1454+331 others(9): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262819 | ||||||
chr2:157262819 | CTTTTTT | C | 47 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(44): Show |
48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1454+3305_1454+331 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262819 | ||||||
chr2:157262897 | G | A | 1 | a0001c0001t0051g0111 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1454+3361G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262897 | |||||||
chr2:157262921 | G | C | 4 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0032g0254 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3385G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262921 | |||||||
chr2:157262972 | C | A | 1 | a0002c0005t0026g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1454+3436C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262972 | |||||||
chr2:157262990 | G | A | 4 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0032g0254 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3454G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262990 | |||||||
chr2:157263027 | C | A | 2 | a0001c0002t0014g0257 a0001c0002t0071g0258 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1454+3491C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263027 | |||||||
chr2:157263046 | C | T | 2 | a0001c0001t0005g0252 a0001c0001t0079g0251 |
2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1454+3510C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263046 | |||||||
chr2:157263107 | G | A | 2 | a0002c0003t0003g0162 a0002c0003t0027g0161 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1454+3571G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263107 | |||||||
chr2:157263123 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1454+3587G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263123 | |||||||
chr2:157263222 | T | C | 4 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0032g0254 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3686T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263222 | |||||||
chr2:157263268 | A | G | 2 | a0002c0005t0018g0167 a0002c0005t0018g0169 |
2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1454+3732A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263268 | |||||||
chr2:157263273 | A | G | 4 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0032g0254 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3737A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263273 | |||||||
chr2:157263422 | G | A | 24 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(21): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+3886G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263422 | |||||||
chr2:157263480 | T | C | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1454+3944T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263480 | |||||||
chr2:157263670 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1454+4134C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263670 | |||||||
chr2:157263891 | T | G | 2 | a0001c0001t0007g0149 a0001c0001t0045g0147 |
2 | HG00438.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1454+4355T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263891 | |||||||
chr2:157263913 | G | C | 3 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0032g0254 |
3 | HG02622.hp1 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1454+4377G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263913 | |||||||
chr2:157263962 | A | G | 1 | a0001c0002t0072g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1454+4426A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263962 | |||||||
chr2:157264122 | T | C | 24 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(21): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+4586T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264122 | |||||||
chr2:157264148 | T | C | 1 | a0004c0006t0014g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1454+4612T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264148 | |||||||
chr2:157264174 | T | TAC | 9 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
10 | HG01106.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1454+4667_1454+466 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264174 | ||||||
chr2:157264174 | TAC | T | 15 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0032g0254 others(12): Show |
15 | HG01123.hp2 HG02083.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1454+4667_1454+466 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264174 | ||||||
chr2:157264174 | TACAC | T | 80 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0142 others(77): Show |
83 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1454+4665_1454+466 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264174 | ||||||
chr2:157264174 | TACACAC | T | 4 | a0001c0001t0001g0048 a0001c0002t0005g0250 a0001c0002t0064g0249 others(1): Show |
4 | HG02258.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454+4663_1454+466 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264174 | ||||||
chr2:157264333 | T | C | 1 | a0001c0001t0074g0244 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1454+4797T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264333 | |||||||
chr2:157264414 | C | A | 6 | a0002c0005t0001g0203 a0002c0005t0002g0201 a0002c0005t0008g0204 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454+4878C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264414 | |||||||
chr2:157264456 | C | T | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+4920C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264456 | |||||||
chr2:157264568 | T | G | 2 | a0002c0003t0006g0174 a0002c0003t0006g0175 |
2 | HG02698.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1454+5032T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264568 | |||||||
chr2:157264597 | GT | G | 17 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(14): Show |
18 | HG01074.hp2 HG02572.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1454+5070delT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264597 | ||||||
chr2:157264692 | C | T | 24 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(21): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+5156C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264692 | |||||||
chr2:157264953 | C | T | 97 | a0001c0001t0001g0026 a0001c0001t0001g0213 a0001c0001t0005g0252 others(94): Show |
100 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1454+5417C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264953 | |||||||
chr2:157265175 | T | C | 70 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(67): Show |
72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1454+5639T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157265175 | |||||||
chr2:157265332 | T | C | 1 | a0001c0001t0004g0028 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1454+5796T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157265332 | |||||||
chr2:157265806 | C | T | 24 | a0001c0001t0001g0213 a0001c0002t0001g0140 a0003c0004t0001g0015 others(21): Show |
25 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+6270C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157265806 | |||||||
chr2:157266192 | T | C | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1454+6656T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266192 | |||||||
chr2:157266234 | A | G | 1 | a0002c0005t0026g0205 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1454+6698A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266234 | |||||||
chr2:157266241 | T | G | 1 | a0001c0001t0045g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1454+6705T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266241 | |||||||
chr2:157266312 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1454+6776G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266312 | |||||||
chr2:157266417 | C | T | 2 | a0001c0002t0081g0237 a0001c0002t0083g0243 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1454+6881C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266417 | |||||||
chr2:157266509 | A | G | 2 | a0001c0001t0005g0252 a0001c0001t0079g0251 |
2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1454+6973A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266509 | |||||||
chr2:157266792 | C | T | 1 | a0002c0005t0001g0199 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1454+7256C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266792 | |||||||
chr2:157266835 | C | T | 2 | a0001c0002t0014g0257 a0001c0002t0071g0258 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1454+7299C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266835 | |||||||
chr2:157267019 | C | G | 8 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(5): Show |
9 | HG01074.hp2 HG02572.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1454+7483C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267019 | |||||||
chr2:157267020 | A | G | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+7484A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267020 | |||||||
chr2:157267058 | G | A | 71 | a0001c0001t0001g0057 a0001c0001t0001g0213 a0002c0003t0001g0191 others(68): Show |
73 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1454+7522G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267058 | |||||||
chr2:157267180 | G | C | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+7644G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267180 | |||||||
chr2:157267315 | G | A | 1 | a0002c0003t0055g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1454+7779G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267315 | |||||||
chr2:157267482 | A | G | 4 | a0005c0008t0003g0170 a0005c0008t0009g0171 a0005c0008t0011g0172 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454+7946A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267482 | |||||||
chr2:157267765 | C | T | 47 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(44): Show |
48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1454+8229C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267765 | |||||||
chr2:157267783 | T | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0007c0012t0021g0141 |
3 | HG01123.hp2 HG01192.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1454+8247T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267783 | |||||||
chr2:157268045 | G | T | 10 | a0001c0001t0032g0254 a0001c0001t0069g0239 a0001c0001t0078g0242 others(7): Show |
10 | HG02572.hp1 HG02895.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454+8509G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268045 | |||||||
chr2:157268176 | C | T | 1 | a0001c0001t0074g0244 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1454+8640C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268176 | |||||||
chr2:157268375 | T | A | 1 | a0001c0001t0027g0148 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1454+8839T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268375 | |||||||
chr2:157268401 | G | A | 9 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(6): Show |
10 | HG01074.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454+8865G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268401 | |||||||
chr2:157268792 | CCAAGA | C | 70 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(67): Show |
72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1454+9260_1454+926 others(9): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157268792 | ||||||
chr2:157268793 | CA | C | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+9259delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157268793 | ||||||
chr2:157268826 | T | C | 1 | a0001c0001t0028g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1454+9290T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268826 | |||||||
chr2:157268827 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1454+9291A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268827 | |||||||
chr2:157268932 | C | T | 1 | a0003c0004t0001g0229 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1454+9396C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268932 | |||||||
chr2:157268999 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1454+9463C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268999 | |||||||
chr2:157269077 | T | C | 2 | a0001c0001t0015g0247 a0001c0001t0015g0253 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1454+9541T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269077 | |||||||
chr2:157269199 | C | T | 2 | a0001c0001t0001g0139 a0001c0002t0002g0160 |
2 | HG02074.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1454+9663C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269199 | |||||||
chr2:157269263 | A | G | 1 | a0001c0009t0024g0138 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1454+9727A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269263 | |||||||
chr2:157269393 | T | G | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+9857T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269393 | |||||||
chr2:157269918 | C | T | 4 | a0001c0001t0007g0136 a0001c0001t0028g0061 a0001c0002t0001g0025 others(1): Show |
4 | HG00544.hp2 HG02040.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+10382C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269918 | |||||||
chr2:157269946 | C | T | 97 | a0001c0001t0001g0026 a0001c0001t0001g0213 a0001c0001t0005g0252 others(94): Show |
100 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1454+10410C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269946 | |||||||
chr2:157269950 | A | G | 19 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0193 others(16): Show |
20 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454+10414A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269950 | |||||||
chr2:157270006 | A | T | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1454+10470A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270006 | |||||||
chr2:157270083 | C | T | 3 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0008c0013t0031g0259 |
3 | HG02109.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1454+10547C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270083 | |||||||
chr2:157270153 | G | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0050 a0001c0001t0001g0052 others(8): Show |
11 | HG00544.hp1 HG02071.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1454+10617G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270153 | |||||||
chr2:157270177 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1454+10641G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270177 | |||||||
chr2:157270389 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1454+10853C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270389 | |||||||
chr2:157270414 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1454+10878T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270414 | |||||||
chr2:157270606 | G | A | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1454+11070G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270606 | |||||||
chr2:157271032 | C | T | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1454+11496C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271032 | |||||||
chr2:157271041 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0003g0143 |
2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1454+11505G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271041 | |||||||
chr2:157271048 | G | A | 4 | a0005c0008t0003g0170 a0005c0008t0009g0171 a0005c0008t0011g0172 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454+11512G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271048 | |||||||
chr2:157271102 | CA | C | 53 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0002t0005g0250 others(50): Show |
54 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(51): Show |
intron_variant | MODIFIER | c.1454+11580delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157271102 | ||||||
chr2:157271214 | T | C | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1454+11678T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271214 | |||||||
chr2:157271216 | G | T | 1 | a0001c0001t0001g0047 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1454+11680G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271216 | |||||||
chr2:157271322 | T | A | 3 | a0001c0001t0001g0053 a0001c0001t0004g0054 a0001c0002t0001g0070 |
3 | HG02738.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1454+11786T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271322 | |||||||
chr2:157271719 | G | A | 24 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(21): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+12183G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271719 | |||||||
chr2:157271808 | A | G | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+12272A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271808 | |||||||
chr2:157272109 | G | A | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-12173G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157272109 | |||||||
chr2:157272121 | T | C | 4 | a0005c0008t0003g0170 a0005c0008t0009g0171 a0005c0008t0011g0172 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-12161T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157272121 | |||||||
chr2:157272247 | G | A | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-12035G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157272247 | |||||||
chr2:157272622 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-11660C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157272622 | |||||||
chr2:157273477 | A | G | 2 | a0001c0002t0014g0257 a0001c0002t0071g0258 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1455-10805A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273477 | |||||||
chr2:157273520 | A | G | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1455-10762A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273520 | |||||||
chr2:157273630 | C | CT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
85 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1455-10623dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTT | 15 | a0001c0001t0001g0013 a0001c0001t0001g0131 a0001c0001t0001g0132 others(12): Show |
15 | HG00621.hp1 HG00673.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1455-10624_1455-10 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTT | 12 | a0001c0001t0001g0213 a0001c0001t0005g0252 a0001c0001t0023g0060 others(9): Show |
12 | HG00099.hp1 HG02083.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1455-10626_1455-10 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTTT | 13 | a0001c0002t0030g0016 a0002c0003t0006g0175 a0003c0004t0001g0015 others(10): Show |
15 | HG00597.hp2 HG00673.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1455-10627_1455-10 others(11): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTTTT | 8 | a0001c0001t0001g0026 a0001c0002t0066g0245 a0002c0003t0022g0189 others(5): Show |
9 | HG00639.hp1 HG02071.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-10628_1455-10 others(12): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTTTTT | 12 | a0001c0001t0068g0235 a0001c0002t0072g0246 a0002c0003t0001g0191 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1455-10629_1455-10 others(13): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0074g0244 a0002c0003t0003g0162 a0002c0003t0003g0193 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1455-10630_1455-10 others(14): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTTTTT others(2): Show |
11 | a0002c0003t0011g0164 a0002c0003t0038g0196 a0002c0003t0055g0163 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1455-10631_1455-10 others(15): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTTTTT others(3): Show |
12 | a0002c0003t0086g0197 a0002c0005t0001g0203 a0002c0005t0002g0201 others(9): Show |
12 | HG01891.hp1 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1455-10632_1455-10 others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTTTTT others(4): Show |
2 | a0002c0005t0026g0205 a0004c0006t0075g0186 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1455-10633_1455-10 others(17): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | C | CTTTTTTT others(5): Show |
1 | a0002c0003t0085g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1455-10634_1455-10 others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273630 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0071 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1455-10632_1455-10 others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | ||||||
chr2:157273688 | G | A | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-10594G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273688 | |||||||
chr2:157273750 | C | T | 1 | a0004c0006t0014g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1455-10532C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273750 | |||||||
chr2:157273791 | C | T | 1 | a0001c0001t0017g0005 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1455-10491C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273791 | |||||||
chr2:157273873 | G | A | 2 | a0004c0011t0067g0177 a0004c0011t0073g0178 |
2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1455-10409G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273873 | |||||||
chr2:157273926 | C | G | 47 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(44): Show |
48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-10356C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273926 | |||||||
chr2:157273967 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-10315C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273967 | |||||||
chr2:157273983 | C | T | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-10299C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273983 | |||||||
chr2:157273986 | C | A | 47 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(44): Show |
48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-10296C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273986 | |||||||
chr2:157274124 | T | C | 2 | a0001c0002t0076g0240 a0001c0002t0077g0238 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1455-10158T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274124 | |||||||
chr2:157274225 | T | C | 2 | a0002c0005t0025g0200 a0002c0005t0039g0168 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1455-10057T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274225 | |||||||
chr2:157274229 | C | T | 2 | a0002c0003t0001g0207 a0002c0003t0023g0206 |
2 | HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1455-10053C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274229 | |||||||
chr2:157274638 | C | CGT | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-9643_1455-964 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157274638 | ||||||
chr2:157274955 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
73 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1455-9327C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274955 | |||||||
chr2:157274971 | G | A | 1 | a0001c0001t0023g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1455-9311G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274971 | |||||||
chr2:157275021 | A | T | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-9261A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275021 | |||||||
chr2:157275068 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1455-9214C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275068 | |||||||
chr2:157275216 | G | C | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-9066G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275216 | |||||||
chr2:157275287 | G | A | 1 | a0004c0011t0067g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1455-8995G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275287 | |||||||
chr2:157275597 | G | A | 3 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0008c0013t0031g0259 |
3 | HG02109.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1455-8685G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275597 | |||||||
chr2:157275638 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0051g0111 |
2 | NA19064.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1455-8644G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275638 | |||||||
chr2:157275722 | T | G | 1 | a0001c0001t0005g0256 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1455-8560T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275722 | |||||||
chr2:157275769 | A | C | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-8513A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275769 | |||||||
chr2:157275788 | T | A | 2 | a0002c0003t0003g0162 a0002c0003t0027g0161 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1455-8494T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275788 | |||||||
chr2:157275810 | C | G | 1 | a0003c0004t0001g0225 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1455-8472C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275810 | |||||||
chr2:157276064 | A | T | 1 | a0002c0005t0008g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1455-8218A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276064 | |||||||
chr2:157276114 | G | A | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-8168G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276114 | |||||||
chr2:157276321 | G | A | 1 | a0003c0007t0001g0211 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1455-7961G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276321 | |||||||
chr2:157276361 | T | C | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-7921T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276361 | |||||||
chr2:157276362 | G | T | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-7920G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276362 | |||||||
chr2:157276369 | G | C | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-7913G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276369 | |||||||
chr2:157276460 | T | C | 47 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(44): Show |
48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-7822T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276460 | |||||||
chr2:157276578 | T | C | 47 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(44): Show |
48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-7704T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276578 | |||||||
chr2:157276580 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1455-7702C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276580 | |||||||
chr2:157276637 | G | A | 2 | a0002c0003t0003g0162 a0002c0003t0027g0161 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1455-7645G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276637 | |||||||
chr2:157276671 | T | C | 2 | a0001c0001t0015g0247 a0001c0001t0015g0253 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1455-7611T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276671 | |||||||
chr2:157276780 | T | TTCATTGA others(277): Show |
3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-7499_1455-749 others(288): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157276780 | ||||||
chr2:157276784 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-7498C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276784 | |||||||
chr2:157276888 | G | C | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-7394G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276888 | |||||||
chr2:157277033 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0133 a0001c0001t0001g0139 |
3 | NA18941.hp1 NA18963.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1455-7249G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277033 | |||||||
chr2:157277091 | T | C | 1 | a0003c0004t0001g0229 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1455-7191T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277091 | |||||||
chr2:157277107 | T | A | 1 | a0001c0002t0030g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1455-7175T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277107 | |||||||
chr2:157277253 | A | T | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-7029A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277253 | |||||||
chr2:157277271 | T | C | 41 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0193 others(38): Show |
42 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.1455-7011T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277271 | |||||||
chr2:157277278 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0130 |
2 | HG01496.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1455-7004C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277278 | |||||||
chr2:157277288 | T | A | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-6994T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277288 | |||||||
chr2:157277343 | G | C | 1 | a0001c0001t0043g0072 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1455-6939G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277343 | |||||||
chr2:157277392 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1455-6890A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277392 | |||||||
chr2:157277546 | G | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0074 others(4): Show |
9 | HG00280.hp2 HG00639.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-6736G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277546 | |||||||
chr2:157277605 | G | C | 3 | a0001c0001t0005g0252 a0001c0001t0079g0251 a0001c0002t0030g0016 |
4 | HG02895.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455-6677G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277605 | |||||||
chr2:157277691 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0068g0235 |
2 | HG01074.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1455-6591C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277691 | |||||||
chr2:157277802 | G | A | 10 | a0001c0001t0032g0254 a0001c0001t0069g0239 a0001c0001t0078g0242 others(7): Show |
10 | HG02572.hp1 HG02895.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1455-6480G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277802 | |||||||
chr2:157277837 | G | T | 20 | a0002c0005t0001g0203 a0002c0005t0002g0201 a0002c0005t0008g0204 others(17): Show |
20 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1455-6445G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277837 | |||||||
chr2:157277917 | C | T | 1 | a0002c0003t0022g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1455-6365C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277917 | |||||||
chr2:157278317 | A | C | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-5965A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278317 | |||||||
chr2:157278328 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
94 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1455-5954T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278328 | |||||||
chr2:157278417 | T | C | 1 | a0001c0001t0044g0157 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1455-5865T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278417 | |||||||
chr2:157278419 | G | A | 1 | a0002c0005t0039g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1455-5863G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278419 | |||||||
chr2:157278668 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-5614C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278668 | |||||||
chr2:157278691 | G | A | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-5591G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278691 | |||||||
chr2:157278718 | T | C | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-5564T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278718 | |||||||
chr2:157278947 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1455-5335G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278947 | |||||||
chr2:157279286 | C | T | 1 | a0001c0001t0078g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1455-4996C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279286 | |||||||
chr2:157279298 | G | A | 70 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(67): Show |
72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1455-4984G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279298 | |||||||
chr2:157279318 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1455-4964G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279318 | |||||||
chr2:157279326 | G | A | 70 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(67): Show |
72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1455-4956G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279326 | |||||||
chr2:157279468 | C | T | 43 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(40): Show |
44 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.1455-4814C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279468 | |||||||
chr2:157279481 | C | A | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-4801C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279481 | |||||||
chr2:157279530 | G | A | 1 | a0001c0001t0028g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1455-4752G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279530 | |||||||
chr2:157279718 | T | A | 1 | a0001c0001t0029g0036 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1455-4564T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279718 | |||||||
chr2:157279767 | C | T | 1 | a0001c0002t0005g0250 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1455-4515C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279767 | |||||||
chr2:157279768 | G | A | 70 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(67): Show |
72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1455-4514G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279768 | |||||||
chr2:157279831 | T | C | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-4451T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279831 | |||||||
chr2:157279889 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1455-4393G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279889 | |||||||
chr2:157279943 | C | T | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-4339C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279943 | |||||||
chr2:157279992 | T | C | 1 | a0001c0001t0063g0076 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1455-4290T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279992 | |||||||
chr2:157280003 | C | G | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-4279C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280003 | |||||||
chr2:157280053 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-4229C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280053 | |||||||
chr2:157280421 | C | T | 47 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(44): Show |
48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-3861C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280421 | |||||||
chr2:157280437 | A | G | 1 | a0001c0001t0004g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1455-3845A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280437 | |||||||
chr2:157280491 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-3791C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280491 | |||||||
chr2:157280531 | A | G | 3 | a0001c0001t0032g0254 a0001c0001t0080g0236 a0001c0001t0082g0241 |
3 | HG03225.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1455-3751A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280531 | |||||||
chr2:157280755 | G | C | 4 | a0005c0008t0003g0170 a0005c0008t0009g0171 a0005c0008t0011g0172 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-3527G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280755 | |||||||
chr2:157280915 | C | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-3367C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280915 | |||||||
chr2:157280973 | G | C | 2 | a0001c0002t0081g0237 a0001c0002t0083g0243 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1455-3309G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280973 | |||||||
chr2:157280990 | C | T | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-3292C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280990 | |||||||
chr2:157281004 | G | A | 2 | a0001c0002t0014g0257 a0001c0002t0071g0258 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1455-3278G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281004 | |||||||
chr2:157281114 | C | T | 97 | a0001c0001t0001g0026 a0001c0001t0001g0213 a0001c0001t0005g0252 others(94): Show |
100 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1455-3168C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281114 | |||||||
chr2:157281115 | A | G | 97 | a0001c0001t0001g0026 a0001c0001t0001g0213 a0001c0001t0005g0252 others(94): Show |
100 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1455-3167A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281115 | |||||||
chr2:157281218 | C | T | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-3064C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281218 | |||||||
chr2:157281219 | G | A | 1 | a0002c0005t0012g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1455-3063G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281219 | |||||||
chr2:157281272 | C | T | 70 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(67): Show |
72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1455-3010C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281272 | |||||||
chr2:157281421 | C | T | 24 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(21): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1455-2861C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281421 | |||||||
chr2:157281532 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0068g0235 |
2 | HG01074.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1455-2750C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281532 | |||||||
chr2:157281563 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1455-2719C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281563 | |||||||
chr2:157281612 | A | G | 1 | a0001c0001t0034g0135 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1455-2670A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281612 | |||||||
chr2:157281612 | AAAAG | A | 24 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(21): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1455-2653_1455-265 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157281612 | ||||||
chr2:157281919 | C | T | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-2363C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281919 | |||||||
chr2:157282079 | A | G | 3 | a0001c0002t0005g0250 a0001c0002t0064g0249 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-2203A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282079 | |||||||
chr2:157282079 | A | T | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-2203A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282079 | |||||||
chr2:157282133 | C | T | 48 | a0001c0001t0001g0044 a0002c0003t0001g0191 a0002c0003t0001g0207 others(45): Show |
49 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(46): Show |
intron_variant | MODIFIER | c.1455-2149C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282133 | |||||||
chr2:157282162 | A | T | 2 | a0002c0003t0001g0207 a0002c0003t0023g0206 |
2 | HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1455-2120A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282162 | |||||||
chr2:157282226 | TA | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0139 a0001c0002t0005g0250 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1455-2055delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282226 | |||||||
chr2:157282227 | A | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(84): Show |
95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1455-2055A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282227 | |||||||
chr2:157282253 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(5): Show |
9 | HG01074.hp2 HG02572.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-2029A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282253 | |||||||
chr2:157282298 | CCAAT | C | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-1979_1455-197 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157282298 | ||||||
chr2:157282337 | G | T | 27 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(24): Show |
28 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.1455-1945G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282337 | |||||||
chr2:157282654 | A | T | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-1628A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282654 | |||||||
chr2:157282719 | C | A | 24 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(21): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1455-1563C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282719 | |||||||
chr2:157282733 | C | CA | 67 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(64): Show |
69 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1455-1541dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157282733 | ||||||
chr2:157282991 | G | A | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-1291G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282991 | |||||||
chr2:157283000 | A | T | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-1282A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283000 | |||||||
chr2:157283142 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1455-1140T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283142 | |||||||
chr2:157283329 | G | A | 8 | a0001c0001t0001g0026 a0001c0001t0005g0252 a0001c0001t0005g0256 others(5): Show |
9 | HG01074.hp2 HG02572.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-953G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283329 | |||||||
chr2:157283331 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1455-951G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283331 | |||||||
chr2:157283354 | T | C | 73 | a0001c0001t0001g0213 a0001c0001t0074g0244 a0001c0002t0066g0245 others(70): Show |
75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-928T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283354 | |||||||
chr2:157283598 | T | C | 3 | a0001c0001t0032g0254 a0001c0001t0080g0236 a0001c0001t0082g0241 |
3 | HG03225.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1455-684T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283598 | |||||||
chr2:157283652 | T | C | 1 | a0005c0008t0003g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1455-630T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283652 | |||||||
chr2:157283696 | AC | A | 69 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(66): Show |
71 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1455-585delC | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283696 | |||||||
chr2:157283852 | C | T | 1 | a0002c0003t0053g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1455-430C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283852 | |||||||
chr2:157284112 | A | G | 2 | a0001c0001t0015g0247 a0001c0001t0015g0253 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1455-170A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157284112 | |||||||
chr2:157284205 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
101 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1455-77C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157284205 | |||||||
chr2:157284459 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1621+11C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284459 | |||||||
chr2:157284559 | C | T | 69 | a0001c0001t0001g0213 a0002c0003t0001g0191 a0002c0003t0001g0207 others(66): Show |
71 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1621+111C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284559 | |||||||
chr2:157284567 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
84 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1621+119T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284567 | |||||||
chr2:157284580 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1621+132G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284580 | |||||||
chr2:157284580 | G | T | 46 | a0002c0003t0001g0191 a0002c0003t0001g0207 a0002c0003t0003g0162 others(43): Show |
47 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(44): Show |
intron_variant | MODIFIER | c.1621+132G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284580 | |||||||
chr2:157284612 | A | G | 1 | a0001c0001t0004g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1621+164A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284612 | |||||||
chr2:157284618 | G | A | 1 | a0001c0002t0084g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1621+170G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284618 | |||||||
chr2:157284650 | T | C | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1621+202T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284650 | |||||||
chr2:157284674 | C | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(89): Show |
98 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1621+226C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284674 | |||||||
chr2:157284769 | G | T | 23 | a0001c0001t0001g0213 a0003c0004t0001g0015 a0003c0004t0001g0210 others(20): Show |
24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1621+321G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284769 | |||||||
chr2:157284790 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1621+342C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284790 | |||||||
chr2:157285175 | T | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
97 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1621+727T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285175 | |||||||
chr2:157285241 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1622-774T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285241 | |||||||
chr2:157285437 | G | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
99 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1622-578G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285437 | |||||||
chr2:157285509 | G | A | 1 | a0002c0005t0026g0205 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-506G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285509 | |||||||
chr2:157285577 | G | A | 1 | a0001c0002t0030g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1622-438G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285577 | |||||||
chr2:157285619 | T | C | 2 | a0002c0003t0003g0162 a0002c0003t0027g0161 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1622-396T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285619 | |||||||
chr2:157285663 | G | A | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-352G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285663 | |||||||
chr2:157285974 | T | C | 3 | a0001c0001t0074g0244 a0001c0002t0066g0245 a0001c0002t0072g0246 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1622-41T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285974 | |||||||
chr2:157286004 | C | T | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-11C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157286004 | |||||||
chr2:157286241 | C | T | 2 | a0002c0005t0012g0014 a0002c0005t0012g0188 |
3 | HG02258.hp2 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1741+107C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157286241 | |||||||
chr2:157286301 | CAT | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0044 others(4): Show |
10 | HG01361.hp1 HG01433.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1741+169_1741+170d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286301 | ||||||
chr2:157286634 | G | A | 1 | a0001c0001t0016g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1741+500G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157286634 | |||||||
chr2:157286737 | C | T | 2 | a0001c0002t0076g0240 a0001c0002t0077g0238 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1741+603C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157286737 | |||||||
chr2:157286872 | C | A | 2 | a0001c0002t0076g0240 a0001c0002t0077g0238 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1741+738C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157286872 | |||||||
chr2:157286893 | A | AGT | 40 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0052 others(37): Show |
42 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1741+802_1741+803d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | A | AGTGT | 31 | a0001c0001t0001g0055 a0001c0001t0001g0109 a0001c0001t0002g0033 others(28): Show |
32 | HG00639.hp1 HG00735.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.1741+800_1741+803d others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | A | AGTGTGT | 4 | a0001c0001t0001g0074 a0001c0001t0003g0073 a0002c0005t0001g0203 others(1): Show |
4 | HG01891.hp1 HG02074.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+798_1741+803d others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | A | AGTGTGTG others(5): Show |
1 | a0001c0002t0014g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1741+792_1741+803d others(14): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | A | AGTGTGTG others(9): Show |
1 | a0001c0002t0071g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1741+788_1741+803d others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | AGT | A | 28 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0062 others(25): Show |
29 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1741+802_1741+803d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | AGTGT | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(46): Show |
51 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1741+800_1741+803d others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | AGTGTGT | A | 5 | a0001c0001t0001g0116 a0001c0001t0015g0247 a0001c0001t0015g0253 others(2): Show |
5 | HG00280.hp1 HG00438.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1741+798_1741+803d others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | AGTGTGTG others(7): Show |
A | 1 | a0001c0002t0064g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+790_1741+803d others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157286893 | AGTGTGTG others(9): Show |
A | 3 | a0001c0001t0005g0256 a0001c0002t0005g0250 a0001c0002t0065g0248 |
3 | HG02258.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1741+788_1741+803d others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | ||||||
chr2:157287097 | T | A | 2 | a0002c0003t0003g0162 a0002c0003t0027g0161 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1741+963T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287097 | |||||||
chr2:157287129 | A | G | 1 | a0001c0001t0004g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1741+995A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287129 | |||||||
chr2:157287237 | T | C | 1 | a0002c0003t0008g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1741+1103T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287237 | |||||||
chr2:157287246 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1741+1112C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287246 | |||||||
chr2:157287251 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1741+1117G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287251 | |||||||
chr2:157287272 | T | C | 1 | a0003c0007t0001g0211 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1741+1138T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287272 | |||||||
chr2:157287295 | A | C | 2 | a0002c0003t0038g0196 a0002c0003t0055g0163 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1741+1161A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287295 | |||||||
chr2:157287339 | T | C | 3 | a0001c0001t0005g0256 a0001c0001t0015g0247 a0001c0001t0015g0253 |
3 | HG02622.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1741+1205T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287339 | |||||||
chr2:157287422 | T | A | 2 | a0004c0011t0067g0177 a0004c0011t0073g0178 |
2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1741+1288T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287422 | |||||||
chr2:157287423 | C | T | 3 | a0001c0001t0005g0256 a0001c0001t0015g0247 a0001c0001t0015g0253 |
3 | HG02622.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1741+1289C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287423 | |||||||
chr2:157287682 | C | T | 11 | a0001c0002t0005g0250 a0001c0002t0065g0248 a0002c0003t0003g0162 others(8): Show |
11 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1741+1548C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287682 | |||||||
chr2:157287683 | G | A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
88 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1741+1549G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287683 | |||||||
chr2:157287746 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1741+1612T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287746 | |||||||
chr2:157287757 | A | T | 32 | a0001c0001t0001g0057 a0001c0001t0057g0094 a0001c0002t0001g0069 others(29): Show |
33 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1741+1623A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287757 | |||||||
chr2:157287797 | A | G | 2 | a0001c0002t0071g0258 a0001c0002t0084g0255 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1741+1663A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287797 | |||||||
chr2:157287845 | A | G | 31 | a0001c0001t0001g0057 a0001c0001t0057g0094 a0001c0002t0001g0069 others(28): Show |
32 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1741+1711A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287845 | |||||||
chr2:157287878 | A | C | 1 | a0003c0007t0001g0232 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1741+1744A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287878 | |||||||
chr2:157287884 | T | C | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1741+1750T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287884 | |||||||
chr2:157288192 | T | C | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1741+2058T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288192 | |||||||
chr2:157288253 | T | C | 1 | a0001c0002t0001g0140 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1741+2119T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288253 | |||||||
chr2:157288270 | A | G | 57 | a0001c0001t0005g0252 a0001c0002t0001g0069 a0001c0002t0001g0075 others(54): Show |
59 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(56): Show |
intron_variant | MODIFIER | c.1741+2136A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288270 | |||||||
chr2:157288401 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1741+2267C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288401 | |||||||
chr2:157288480 | A | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0137 |
2 | NA18977.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1741+2346A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288480 | |||||||
chr2:157288579 | G | T | 1 | a0001c0002t0064g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+2445G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288579 | |||||||
chr2:157288592 | GATTC | G | 7 | a0004c0006t0005g0179 a0004c0006t0013g0180 a0004c0006t0013g0181 others(4): Show |
7 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1741+2462_1741+246 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157288592 | ||||||
chr2:157288697 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0151 |
2 | HG02074.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1741+2563T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288697 | |||||||
chr2:157288731 | G | A | 1 | a0001c0002t0064g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+2597G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288731 | |||||||
chr2:157288731 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1741+2597G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288731 | |||||||
chr2:157288747 | C | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0063 |
2 | NA19064.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1741+2613C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288747 | |||||||
chr2:157288865 | C | T | 1 | a0001c0002t0014g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1741+2731C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288865 | |||||||
chr2:157288877 | T | C | 33 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(30): Show |
34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1741+2743T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288877 | |||||||
chr2:157288906 | G | A | 1 | a0001c0002t0066g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1741+2772G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288906 | |||||||
chr2:157288913 | A | C | 2 | a0001c0002t0071g0258 a0001c0002t0084g0255 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1741+2779A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288913 | |||||||
chr2:157288927 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1741+2793A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288927 | |||||||
chr2:157288931 | G | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1741+2797G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288931 | |||||||
chr2:157288935 | G | A | 1 | a0005c0008t0009g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1741+2801G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288935 | |||||||
chr2:157289136 | C | A | 1 | a0002c0003t0001g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1741+3002C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289136 | |||||||
chr2:157289146 | GCA | G | 59 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(56): Show |
61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.1741+3015_1741+301 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157289146 | ||||||
chr2:157289318 | T | A | 1 | a0001c0001t0037g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1741+3184T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289318 | |||||||
chr2:157289422 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1741+3288A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289422 | |||||||
chr2:157289462 | A | T | 3 | a0001c0009t0024g0010 a0001c0009t0024g0138 a0001c0009t0059g0010 |
3 | HG02896.hp1 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1741+3328A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289462 | |||||||
chr2:157289571 | C | T | 59 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(56): Show |
61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.1741+3437C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289571 | |||||||
chr2:157289674 | T | C | 4 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0003c0004t0009g0217 others(1): Show |
4 | NA18982.hp2 NA18985.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1741+3540T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289674 | |||||||
chr2:157289710 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0050 others(16): Show |
19 | HG00597.hp1 HG00609.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1741+3576A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289710 | |||||||
chr2:157289751 | A | G | 33 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(30): Show |
34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1741+3617A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289751 | |||||||
chr2:157289787 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1741+3653T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289787 | |||||||
chr2:157290062 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1741+3928A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290062 | |||||||
chr2:157290073 | C | CA | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741+3951dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290073 | ||||||
chr2:157290080 | A | T | 2 | a0001c0001t0001g0012 a0001c0001t0007g0012 |
2 | NA19003.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1741+3946A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290080 | |||||||
chr2:157290083 | AAATGTAT | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0105 others(5): Show |
8 | HG00621.hp2 HG02027.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1741+3951_1741+395 others(11): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290083 | ||||||
chr2:157290084 | A | AAAATATA others(3): Show |
1 | a0001c0002t0064g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+3951_1741+395 others(14): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290084 | ||||||
chr2:157290087 | G | A | 1 | a0001c0002t0064g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+3953G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290087 | |||||||
chr2:157290087 | G | GTA | 3 | a0001c0002t0001g0140 a0001c0002t0030g0016 a0004c0006t0005g0182 |
4 | HG01256.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+3978_1741+397 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290087 | ||||||
chr2:157290087 | GTA | G | 5 | a0002c0005t0012g0014 a0002c0005t0012g0188 a0002c0005t0018g0167 others(2): Show |
6 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+3978_1741+397 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290087 | ||||||
chr2:157290087 | GTATA | G | 18 | a0001c0001t0001g0213 a0001c0001t0005g0252 a0001c0001t0016g0115 others(15): Show |
18 | HG00099.hp1 HG00639.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1741+3976_1741+397 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290087 | ||||||
chr2:157290087 | GTATATA | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(168): Show |
179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1741+3974_1741+397 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290087 | ||||||
chr2:157290093 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0105 others(5): Show |
8 | HG00621.hp2 HG02027.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1741+3959A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290093 | |||||||
chr2:157290095 | A | T | 14 | a0001c0001t0005g0252 a0001c0001t0068g0235 a0001c0001t0079g0251 others(11): Show |
14 | HG00639.hp1 HG01074.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1741+3961A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290095 | |||||||
chr2:157290099 | A | G | 9 | a0001c0002t0033g0093 a0002c0005t0001g0199 a0004c0006t0005g0179 others(6): Show |
9 | HG01884.hp1 HG02602.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1741+3965A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290099 | |||||||
chr2:157290108 | T | C | 5 | a0002c0005t0012g0014 a0002c0005t0012g0188 a0002c0005t0018g0167 others(2): Show |
6 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+3974T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290108 | |||||||
chr2:157290110 | T | C | 5 | a0002c0005t0012g0014 a0002c0005t0012g0188 a0002c0005t0018g0167 others(2): Show |
6 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+3976T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290110 | |||||||
chr2:157290112 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1741+3978T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290112 | |||||||
chr2:157290112 | T | TATATATA others(5): Show |
1 | a0001c0002t0001g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(7): Show |
6 | a0003c0004t0001g0212 a0003c0004t0001g0222 a0003c0004t0001g0227 others(3): Show |
6 | HG00673.hp1 HG02071.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(7): Show |
8 | a0001c0002t0002g0160 a0001c0002t0019g0051 a0003c0004t0001g0015 others(5): Show |
9 | HG00597.hp2 HG02074.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(9): Show |
6 | a0001c0002t0001g0025 a0001c0002t0001g0075 a0001c0002t0001g0125 others(3): Show |
6 | NA18960.hp2 NA18977.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(20): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(11): Show |
2 | a0002c0005t0001g0203 a0002c0005t0002g0201 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(22): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(11): Show |
5 | a0001c0002t0001g0156 a0001c0002t0029g0032 a0002c0005t0026g0205 others(2): Show |
5 | HG02165.hp2 HG02257.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(22): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(13): Show |
2 | a0001c0002t0083g0243 a0003c0004t0001g0225 |
2 | HG02970.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(24): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(15): Show |
3 | a0001c0002t0076g0240 a0001c0002t0077g0238 a0001c0002t0081g0237 |
3 | HG02572.hp1 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(26): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(19): Show |
3 | a0001c0002t0005g0250 a0001c0002t0065g0248 a0004c0006t0075g0186 |
3 | HG01884.hp1 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(30): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(21): Show |
2 | a0001c0002t0042g0092 a0004c0006t0013g0181 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(32): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(23): Show |
1 | a0001c0002t0072g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(34): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(19): Show |
1 | a0001c0002t0084g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(30): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(21): Show |
1 | a0002c0005t0026g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(32): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(23): Show |
3 | a0001c0002t0054g0097 a0002c0005t0001g0199 a0004c0006t0014g0166 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(34): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(23): Show |
1 | a0002c0005t0025g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(34): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(25): Show |
1 | a0004c0006t0013g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(36): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(23): Show |
1 | a0001c0002t0071g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(34): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(25): Show |
1 | a0002c0005t0008g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(36): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(27): Show |
3 | a0004c0006t0005g0179 a0004c0006t0013g0180 a0004c0006t0014g0184 |
3 | HG02723.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(38): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(29): Show |
1 | a0001c0002t0066g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(40): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290112 | T | TATATATA others(29): Show |
1 | a0001c0002t0033g0093 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(40): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | ||||||
chr2:157290116 | T | C | 1 | a0004c0006t0013g0181 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1741+3982T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290116 | |||||||
chr2:157290134 | C | CAT | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741+4007_1741+400 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290134 | ||||||
chr2:157290164 | T | C | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741+4030T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290164 | |||||||
chr2:157290175 | A | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1741+4041A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290175 | |||||||
chr2:157290347 | G | A | 1 | a0002c0005t0025g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1741+4213G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290347 | |||||||
chr2:157290450 | G | T | 2 | a0001c0001t0003g0104 a0001c0001t0006g0049 |
2 | HG00099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1741+4316G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290450 | |||||||
chr2:157290668 | C | G | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741+4534C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290668 | |||||||
chr2:157290804 | G | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1741+4670G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290804 | |||||||
chr2:157291070 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1742-4593C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291070 | |||||||
chr2:157291252 | T | C | 1 | a0001c0002t0014g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1742-4411T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291252 | |||||||
chr2:157291269 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0153 |
2 | HG03239.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1742-4394C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291269 | |||||||
chr2:157291432 | C | T | 3 | a0001c0002t0064g0249 a0001c0002t0071g0258 a0001c0002t0084g0255 |
3 | HG02723.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-4231C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291432 | |||||||
chr2:157291474 | C | T | 1 | a0003c0007t0002g0223 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1742-4189C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291474 | |||||||
chr2:157291633 | A | AC | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(177): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1742-4021dupC | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157291633 | ||||||
chr2:157291633 | A | ACC | 17 | a0001c0001t0001g0074 a0001c0001t0002g0020 a0001c0001t0002g0040 others(14): Show |
18 | HG01433.hp2 HG01884.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1742-4022_1742-402 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157291633 | ||||||
chr2:157291637 | C | A | 2 | a0002c0003t0011g0164 a0002c0003t0060g0165 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1742-4026C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291637 | |||||||
chr2:157291640 | C | CT | 4 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0003c0004t0009g0217 others(1): Show |
4 | NA18982.hp2 NA18985.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1742-4023_1742-402 others(5): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291640 | |||||||
chr2:157291655 | T | C | 30 | a0001c0001t0001g0103 a0001c0002t0001g0025 a0001c0002t0001g0069 others(27): Show |
31 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1742-4008T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291655 | |||||||
chr2:157291843 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1742-3820T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291843 | |||||||
chr2:157291947 | C | A | 3 | a0001c0002t0064g0249 a0001c0002t0071g0258 a0001c0002t0084g0255 |
3 | HG02723.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-3716C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291947 | |||||||
chr2:157292125 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
2 | HG00621.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1742-3538T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292125 | |||||||
chr2:157292200 | G | C | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1742-3463G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292200 | |||||||
chr2:157292321 | A | G | 3 | a0001c0002t0064g0249 a0001c0002t0071g0258 a0001c0002t0084g0255 |
3 | HG02723.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-3342A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292321 | |||||||
chr2:157292365 | C | T | 2 | a0001c0002t0030g0016 a0004c0006t0005g0182 |
3 | HG02895.hp2 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1742-3298C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292365 | |||||||
chr2:157292712 | A | AT | 27 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(24): Show |
28 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1742-2939dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157292712 | ||||||
chr2:157292715 | T | A | 3 | a0001c0001t0001g0146 a0001c0002t0076g0240 a0001c0002t0077g0238 |
3 | HG01358.hp1 HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1742-2948T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292715 | |||||||
chr2:157292861 | G | A | 2 | a0002c0003t0003g0162 a0002c0003t0027g0161 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1742-2802G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292861 | |||||||
chr2:157292866 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1742-2797A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292866 | |||||||
chr2:157292871 | T | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1742-2792T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292871 | |||||||
chr2:157292998 | G | C | 1 | a0001c0001t0063g0076 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1742-2665G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292998 | |||||||
chr2:157293246 | A | G | 2 | a0001c0002t0071g0258 a0001c0002t0084g0255 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-2417A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293246 | |||||||
chr2:157293275 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0017g0005 |
3 | HG00099.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1742-2388G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293275 | |||||||
chr2:157293279 | C | T | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1742-2384C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293279 | |||||||
chr2:157293464 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1742-2199G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293464 | |||||||
chr2:157293503 | A | G | 59 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(56): Show |
61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.1742-2160A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293503 | |||||||
chr2:157293534 | A | G | 32 | a0001c0001t0005g0252 a0001c0001t0005g0256 a0001c0001t0015g0247 others(29): Show |
32 | HG00639.hp1 HG01074.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1742-2129A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293534 | |||||||
chr2:157293605 | C | A | 1 | a0001c0001t0006g0056 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1742-2058C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293605 | |||||||
chr2:157293606 | C | G | 1 | a0001c0001t0006g0056 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1742-2057C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293606 | |||||||
chr2:157293764 | AG | A | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1742-1898delG | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293764 | |||||||
chr2:157293797 | C | G | 1 | a0001c0001t0005g0256 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1742-1866C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293797 | |||||||
chr2:157293839 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1742-1824C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293839 | |||||||
chr2:157293884 | T | G | 1 | a0002c0003t0053g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1742-1779T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293884 | |||||||
chr2:157293932 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1742-1731T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293932 | |||||||
chr2:157293988 | G | A | 2 | a0001c0002t0071g0258 a0001c0002t0084g0255 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-1675G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293988 | |||||||
chr2:157294248 | C | T | 1 | a0002c0005t0008g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1742-1415C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294248 | |||||||
chr2:157294500 | G | A | 1 | a0002c0003t0003g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1742-1163G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294500 | |||||||
chr2:157294504 | T | G | 1 | a0002c0003t0003g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1742-1159T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294504 | |||||||
chr2:157294553 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1742-1110A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294553 | |||||||
chr2:157294608 | C | T | 2 | a0001c0002t0071g0258 a0001c0002t0084g0255 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-1055C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294608 | |||||||
chr2:157294674 | G | A | 2 | a0002c0003t0085g0198 a0002c0003t0086g0197 |
2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1742-989G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294674 | |||||||
chr2:157294694 | G | A | 2 | a0001c0002t0005g0250 a0001c0002t0065g0248 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1742-969G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294694 | |||||||
chr2:157294784 | C | CCA | 3 | a0001c0002t0001g0070 a0001c0002t0001g0080 a0001c0002t0064g0249 |
3 | HG01943.hp2 HG02723.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1742-841_1742-840d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294784 | CCA | C | 11 | a0001c0002t0001g0075 a0001c0002t0019g0051 a0001c0002t0077g0238 others(8): Show |
11 | HG00673.hp1 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1742-841_1742-840d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294784 | CCACA | C | 23 | a0001c0002t0001g0025 a0001c0002t0001g0125 a0001c0002t0001g0137 others(20): Show |
25 | HG01891.hp1 HG02257.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1742-843_1742-840d others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294784 | CCACACA | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(44): Show |
54 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.1742-845_1742-840d others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294784 | CCACACAC others(1): Show |
C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(125): Show |
129 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1742-847_1742-840d others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294784 | CCACACAC others(3): Show |
C | 8 | a0001c0001t0005g0256 a0001c0001t0015g0247 a0001c0001t0015g0253 others(5): Show |
8 | HG02109.hp2 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1742-849_1742-840d others(12): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294784 | CCACACAC others(5): Show |
C | 18 | a0001c0001t0001g0011 a0001c0001t0005g0252 a0001c0001t0043g0072 others(15): Show |
18 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1742-851_1742-840d others(14): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294784 | CCACACAC others(7): Show |
C | 4 | a0001c0001t0061g0089 a0004c0011t0067g0177 a0004c0011t0073g0178 others(1): Show |
4 | HG01891.hp2 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1742-853_1742-840d others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294784 | CCACACAC others(11): Show |
C | 2 | a0002c0003t0085g0198 a0002c0003t0086g0197 |
2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1742-857_1742-840d others(20): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | ||||||
chr2:157294827 | A | G | 1 | a0001c0001t0004g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1742-836A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294827 | |||||||
chr2:157294941 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1742-722C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294941 | |||||||
chr2:157294965 | C | CT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1742-688dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294965 | ||||||
chr2:157295092 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1742-571G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295092 | |||||||
chr2:157295100 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1742-563G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295100 | |||||||
chr2:157295157 | T | TC | 30 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(27): Show |
31 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1742-502dupC | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157295157 | ||||||
chr2:157295202 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1742-461T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295202 | |||||||
chr2:157295435 | A | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0131 a0001c0001t0001g0233 |
3 | NA18947.hp1 NA18959.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1742-228A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295435 | |||||||
chr2:157295517 | T | C | 2 | a0001c0002t0071g0258 a0001c0002t0084g0255 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-146T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295517 | |||||||
chr2:157295534 | GA | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1742-116delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157295534 | ||||||
chr2:157295608 | C | T | 4 | a0001c0001t0023g0060 a0001c0001t0082g0241 a0002c0003t0003g0162 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1742-55C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295608 | |||||||
chr2:157296145 | A | AT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1878-241dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 157296145 | ||||||
chr2:157296962 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1997+449G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157296962 | |||||||
chr2:157297163 | T | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0063 others(4): Show |
7 | HG00544.hp1 NA18968.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1997+650T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297163 | |||||||
chr2:157297173 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0137 |
2 | NA18977.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1997+660T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297173 | |||||||
chr2:157297233 | C | A | 1 | a0001c0002t0014g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1997+720C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297233 | |||||||
chr2:157297337 | A | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0137 |
2 | NA18977.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1997+824A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297337 | |||||||
chr2:157297464 | G | A | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1997+951G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297464 | |||||||
chr2:157297498 | C | G | 59 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(56): Show |
61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.1997+985C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297498 | |||||||
chr2:157297534 | T | C | 3 | a0002c0005t0018g0167 a0002c0005t0018g0169 a0002c0005t0039g0168 |
3 | HG02486.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1997+1021T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297534 | |||||||
chr2:157297694 | G | A | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1997+1181G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297694 | |||||||
chr2:157297718 | G | T | 2 | a0001c0002t0066g0245 a0001c0002t0072g0246 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1997+1205G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297718 | |||||||
chr2:157297831 | C | T | 28 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(25): Show |
29 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1997+1318C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297831 | |||||||
chr2:157298106 | G | A | 2 | a0001c0001t0001g0105 a0003c0007t0002g0223 |
2 | NA18948.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1998-1442G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298106 | |||||||
chr2:157298280 | A | C | 2 | a0001c0001t0003g0104 a0001c0001t0006g0049 |
2 | HG00099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1998-1268A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298280 | |||||||
chr2:157298294 | A | G | 2 | a0001c0002t0066g0245 a0001c0002t0072g0246 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1998-1254A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298294 | |||||||
chr2:157298414 | G | A | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1998-1134G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298414 | |||||||
chr2:157298514 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1998-1034C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298514 | |||||||
chr2:157298544 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1998-1004A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298544 | |||||||
chr2:157298739 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1998-809T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298739 | |||||||
chr2:157298782 | G | A | 1 | a0001c0001t0005g0256 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1998-766G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298782 | |||||||
chr2:157298912 | C | T | 2 | a0001c0001t0041g0107 a0001c0001t0043g0072 |
2 | HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1998-636C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298912 | |||||||
chr2:157298926 | T | C | 6 | a0002c0003t0038g0196 a0002c0003t0055g0163 a0005c0008t0003g0170 others(3): Show |
6 | HG02055.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1998-622T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298926 | |||||||
chr2:157298934 | ACGGAAGA others(1): Show |
A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1998-588_1998-581d others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 157298934 | ||||||
chr2:157298983 | C | T | 1 | a0001c0001t0058g0119 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1998-565C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298983 | |||||||
chr2:157299036 | G | T | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1998-512G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299036 | |||||||
chr2:157299064 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1998-484G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299064 | |||||||
chr2:157299074 | C | G | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1998-474C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299074 | |||||||
chr2:157299182 | G | A | 2 | a0002c0003t0085g0198 a0002c0003t0086g0197 |
2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1998-366G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299182 | |||||||
chr2:157299219 | A | G | 1 | a0008c0013t0031g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1998-329A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299219 | |||||||
chr2:157299285 | T | A | 32 | a0001c0001t0005g0252 a0001c0001t0005g0256 a0001c0001t0015g0247 others(29): Show |
32 | HG00639.hp1 HG01074.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1998-263T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299285 | |||||||
chr2:157299337 | T | G | 33 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(30): Show |
34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1998-211T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299337 | |||||||
chr2:157299356 | A | G | 1 | a0004c0011t0073g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1998-192A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299356 | |||||||
chr2:157300155 | T | A | 33 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(30): Show |
34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.2115+490T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300155 | |||||||
chr2:157300205 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2116-471T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300205 | |||||||
chr2:157300223 | G | T | 32 | a0001c0001t0005g0252 a0001c0001t0005g0256 a0001c0001t0015g0247 others(29): Show |
32 | HG00639.hp1 HG01074.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.2116-453G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300223 | |||||||
chr2:157300231 | G | A | 1 | a0001c0002t0064g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2116-445G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300231 | |||||||
chr2:157300338 | G | A | 25 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(22): Show |
26 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2116-338G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300338 | |||||||
chr2:157300379 | A | T | 2 | a0001c0002t0071g0258 a0001c0002t0084g0255 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2116-297A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300379 | |||||||
chr2:157300404 | A | G | 24 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(21): Show |
25 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2116-272A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300404 | |||||||
chr2:157300405 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2116-271T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300405 | |||||||
chr2:157301233 | G | C | 33 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(30): Show |
34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.2439+234G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301233 | |||||||
chr2:157301282 | T | C | 28 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(25): Show |
29 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.2439+283T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301282 | |||||||
chr2:157301333 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0068 |
2 | NA18968.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.2439+334C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301333 | |||||||
chr2:157301387 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(227): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2439+388G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301387 | |||||||
chr2:157301651 | C | T | 10 | a0001c0001t0061g0089 a0001c0001t0074g0244 a0002c0003t0001g0207 others(7): Show |
10 | HG01261.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2439+652C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301651 | |||||||
chr2:157301753 | A | C | 1 | a0001c0001t0003g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2439+754A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301753 | |||||||
chr2:157301957 | A | G | 14 | a0001c0001t0005g0252 a0001c0001t0068g0235 a0001c0001t0079g0251 others(11): Show |
14 | HG00639.hp1 HG01074.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2439+958A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301957 | |||||||
chr2:157302002 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2439+1003C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302002 | |||||||
chr2:157302128 | C | T | 3 | a0001c0001t0061g0089 a0004c0011t0067g0177 a0004c0011t0073g0178 |
3 | HG01891.hp2 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2439+1129C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302128 | |||||||
chr2:157302350 | T | C | 1 | a0002c0003t0003g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2439+1351T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302350 | |||||||
chr2:157302384 | T | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2439+1385T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302384 | |||||||
chr2:157302460 | C | A | 1 | a0001c0001t0005g0256 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2439+1461C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302460 | |||||||
chr2:157302582 | G | GA | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2439+1595dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 157302582 | ||||||
chr2:157302925 | G | C | 59 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(56): Show |
61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.2439+1926G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302925 | |||||||
chr2:157303009 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2439+2010G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303009 | |||||||
chr2:157303323 | C | T | 2 | a0001c0001t0032g0254 a0001c0001t0080g0236 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2439+2324C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303323 | |||||||
chr2:157303324 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.2439+2325A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303324 | |||||||
chr2:157303340 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2439+2341G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303340 | |||||||
chr2:157303496 | CTAT | C | 30 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(27): Show |
31 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.2440-2251_2440-224 others(7): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 157303496 | ||||||
chr2:157303619 | GAGATGAT others(4): Show |
G | 2 | a0001c0002t0071g0258 a0001c0002t0084g0255 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2440-2128_2440-211 others(15): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 157303619 | ||||||
chr2:157303633 | A | G | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2440-2116A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303633 | |||||||
chr2:157303730 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2440-2019A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303730 | |||||||
chr2:157303758 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2440-1991G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303758 | |||||||
chr2:157303794 | C | A | 2 | a0002c0003t0006g0174 a0002c0003t0006g0175 |
2 | HG02698.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2440-1955C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303794 | |||||||
chr2:157303800 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2440-1949G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303800 | |||||||
chr2:157304072 | G | A | 6 | a0002c0005t0001g0203 a0002c0005t0002g0201 a0002c0005t0008g0204 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-1677G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304072 | |||||||
chr2:157304390 | C | A | 1 | a0001c0001t0004g0065 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2440-1359C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304390 | |||||||
chr2:157304511 | C | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.2440-1238C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304511 | |||||||
chr2:157304519 | C | G | 90 | a0001c0001t0005g0252 a0001c0001t0015g0247 a0001c0001t0015g0253 others(87): Show |
92 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.2440-1230C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304519 | |||||||
chr2:157304519 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.2440-1230C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304519 | |||||||
chr2:157304774 | A | G | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2440-975A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304774 | |||||||
chr2:157304795 | T | C | 5 | a0003c0004t0001g0222 a0003c0004t0001g0227 a0003c0004t0004g0221 others(2): Show |
5 | HG00673.hp1 HG02071.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440-954T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304795 | |||||||
chr2:157304804 | A | C | 4 | a0005c0008t0003g0170 a0005c0008t0009g0171 a0005c0008t0011g0172 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-945A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304804 | |||||||
chr2:157304978 | A | G | 14 | a0001c0001t0005g0252 a0001c0001t0068g0235 a0001c0001t0079g0251 others(11): Show |
14 | HG00639.hp1 HG01074.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2440-771A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304978 | |||||||
chr2:157304992 | C | T | 33 | a0001c0002t0005g0250 a0001c0002t0033g0093 a0001c0002t0042g0092 others(30): Show |
34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.2440-757C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304992 | |||||||
chr2:157305011 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2440-738G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305011 | |||||||
chr2:157305023 | A | G | 1 | a0003c0004t0004g0221 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2440-726A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305023 | |||||||
chr2:157305098 | T | C | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2440-651T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305098 | |||||||
chr2:157305115 | G | C | 59 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(56): Show |
61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.2440-634G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305115 | |||||||
chr2:157305187 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2440-562G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305187 | |||||||
chr2:157305225 | C | A | 2 | a0001c0001t0001g0134 a0003c0007t0001g0230 |
2 | HG00621.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.2440-524C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305225 | |||||||
chr2:157305250 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2440-499G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305250 | |||||||
chr2:157305345 | G | T | 1 | a0002c0003t0003g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2440-404G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305345 | |||||||
chr2:157305521 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2440-228A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305521 | |||||||
chr2:157305619 | G | A | 10 | a0001c0001t0061g0089 a0001c0001t0074g0244 a0002c0003t0001g0207 others(7): Show |
10 | HG01261.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2440-130G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305619 | |||||||
chr2:157305650 | C | A | 2 | a0001c0001t0015g0247 a0001c0001t0015g0253 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2440-99C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305650 | |||||||
chr2:157305963 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2520+134C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157305963 | |||||||
chr2:157306009 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2520+180T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306009 | |||||||
chr2:157306106 | G | T | 2 | a0001c0001t0041g0107 a0001c0001t0043g0072 |
2 | HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2520+277G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306106 | |||||||
chr2:157306126 | C | T | 1 | a0001c0001t0006g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2520+297C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306126 | |||||||
chr2:157306140 | G | A | 4 | a0001c0002t0042g0092 a0001c0002t0054g0097 a0001c0002t0081g0237 others(1): Show |
4 | HG02970.hp1 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2520+311G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306140 | |||||||
chr2:157306498 | G | A | 6 | a0001c0002t0001g0003 a0001c0002t0001g0030 a0001c0002t0001g0080 others(3): Show |
7 | HG00741.hp2 HG01192.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2520+669G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306498 | |||||||
chr2:157306525 | C | T | 2 | a0001c0001t0003g0104 a0001c0001t0006g0049 |
2 | HG00099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2520+696C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306525 | |||||||
chr2:157306914 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2520+1085A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306914 | |||||||
chr2:157307010 | AT | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(226): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2520+1194delT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 157307010 | ||||||
chr2:157307106 | T | C | 1 | a0003c0004t0004g0221 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2520+1277T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307106 | |||||||
chr2:157307155 | G | A | 26 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(23): Show |
27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2520+1326G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307155 | |||||||
chr2:157307155 | G | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2520+1326G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307155 | |||||||
chr2:157307292 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0142 a0001c0001t0003g0143 |
3 | HG03195.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2521-1275G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307292 | |||||||
chr2:157307351 | C | G | 1 | a0004c0006t0014g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2521-1216C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307351 | |||||||
chr2:157307424 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.2521-1143A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307424 | |||||||
chr2:157307597 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2521-970G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307597 | |||||||
chr2:157307624 | C | T | 1 | a0003c0004t0009g0224 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2521-943C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307624 | |||||||
chr2:157307730 | T | A | 58 | a0001c0002t0001g0025 a0001c0002t0001g0069 a0001c0002t0001g0075 others(55): Show |
60 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(57): Show |
intron_variant | MODIFIER | c.2521-837T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307730 | |||||||
chr2:157307733 | G | A | 1 | a0001c0001t0005g0256 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2521-834G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307733 | |||||||
chr2:157307766 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2521-801C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307766 | |||||||
chr2:157307802 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2521-765G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307802 | |||||||
chr2:157307843 | C | A | 1 | a0001c0002t0064g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2521-724C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307843 | |||||||
chr2:157307924 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2521-643C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307924 | |||||||
chr2:157307939 | G | A | 7 | a0001c0001t0005g0252 a0001c0001t0068g0235 a0002c0003t0006g0174 others(4): Show |
7 | HG00639.hp1 HG01074.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.2521-628G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307939 | |||||||
chr2:157307964 | A | G | 1 | a0001c0001t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2521-603A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307964 | |||||||
chr2:157308012 | T | C | 2 | a0002c0003t0085g0198 a0002c0003t0086g0197 |
2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2521-555T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308012 | |||||||
chr2:157308228 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0049g0006 |
2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2521-339A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308228 | |||||||
chr2:157308347 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2521-220T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308347 | |||||||
chr2:157308373 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2521-194A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308373 | |||||||
chr2:157308492 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.2521-75C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308492 | |||||||
chr2:157308889 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2682+161A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157308889 | |||||||
chr2:157308903 | C | CT | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(221): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2682+185dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 157308903 | ||||||
chr2:157309011 | C | T | 1 | a0004c0006t0013g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2682+283C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309011 | |||||||
chr2:157309028 | G | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0050 others(15): Show |
18 | HG00597.hp1 HG00609.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.2682+300G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309028 | |||||||
chr2:157309082 | G | A | 1 | a0004c0006t0013g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2682+354G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309082 | |||||||
chr2:157309306 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(179): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2682+578T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309306 | |||||||
chr2:157309441 | T | A | 76 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0050 others(73): Show |
78 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2682+713T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309441 | |||||||
chr2:157309443 | G | T | 76 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0050 others(73): Show |
78 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2682+715G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309443 | |||||||
chr2:157309720 | G | A | 2 | a0001c0002t0076g0240 a0001c0002t0077g0238 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2682+992G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309720 | |||||||
chr2:157309745 | G | C | 69 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0041 others(66): Show |
71 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2682+1017G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309745 | |||||||
chr2:157309877 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0017 others(126): Show |
135 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.2682+1149A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309877 | |||||||
chr2:157309953 | C | T | 1 | a0001c0001t0051g0111 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2682+1225C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309953 | |||||||
chr2:157310097 | A | T | 4 | a0001c0002t0065g0248 a0001c0002t0066g0245 a0001c0002t0072g0246 others(1): Show |
4 | HG03130.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-1111A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310097 | |||||||
chr2:157310109 | T | C | 2 | a0001c0002t0081g0237 a0001c0002t0083g0243 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2683-1099T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310109 | |||||||
chr2:157310424 | T | C | 7 | a0001c0001t0003g0143 a0002c0003t0003g0162 a0002c0003t0003g0193 others(4): Show |
7 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2683-784T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310424 | |||||||
chr2:157310426 | G | A | 3 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0002t0064g0249 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2683-782G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310426 | |||||||
chr2:157310466 | C | G | 3 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0002t0064g0249 |
3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2683-742C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310466 | |||||||
chr2:157310682 | C | T | 4 | a0001c0002t0066g0245 a0001c0002t0072g0246 a0002c0003t0011g0164 others(1): Show |
4 | HG02055.hp2 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-526C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310682 | |||||||
chr2:157310775 | C | T | 5 | a0002c0003t0008g0190 a0002c0003t0008g0194 a0002c0003t0038g0196 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2683-433C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310775 | |||||||
chr2:157310792 | T | G | 20 | a0001c0001t0001g0039 a0001c0001t0001g0110 a0001c0001t0001g0121 others(17): Show |
21 | HG00609.hp2 HG00673.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.2683-416T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310792 | |||||||
chr2:157310846 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2683-362C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310846 | |||||||
chr2:157310875 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2683-333A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310875 | |||||||
chr2:157311026 | T | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0091 a0001c0001t0001g0106 others(5): Show |
8 | HG00621.hp1 HG02165.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2683-182T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311026 | |||||||
chr2:157311082 | T | C | 4 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0079g0251 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-126T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311082 | |||||||
chr2:157311107 | A | G | 3 | a0001c0001t0016g0115 a0001c0001t0016g0152 a0001c0002t0033g0093 |
3 | HG02602.hp1 HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2683-101A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311107 | |||||||
chr2:157311124 | A | AT | 4 | a0001c0001t0015g0247 a0001c0001t0015g0253 a0001c0001t0079g0251 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-77dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 157311124 | ||||||
chr2:157311131 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2683-77T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311131 | |||||||
chr2:157311136 | G | A | 1 | a0003c0004t0062g0218 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2683-72G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311136 |