Item | Value |
---|---|
geneid | 57185 |
ensemblid | ENSG00000001461.17 |
hgncid | 25233 |
symbol | NIPAL3 |
name | NIPA like domain containing 3 |
refseq_nuc | NM_020448.5 |
refseq_prot | NP_065181.1 |
ensembl_nuc | ENST00000374399.9 |
ensembl_prot | ENSP00000363520.4 |
mane_status | MANE Select |
chr | chr1 |
start | 24415802 |
end | 24472976 |
strand | + |
ver | v1.2 |
region | chr1:24415802-24472976 |
region5000 | chr1:24410802-24477976 |
regionname0 | NIPAL3_chr1_24415802_24472976 |
regionname5000 | NIPAL3_chr1_24410802_24477976 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 406 | 377 | 87 | 68 | 162 | 16 | 42 | 122 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | MDGSH others(401): Show |
chr1 | 24410802 | 24477976 |
a0002 | 0/0 | 196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | MDGSH others(191): Show |
chr1 | 24410802 | 24477976 |
a0003 | 0/0 | 406 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | MDGSH others(401): Show |
chr1 | 24410802 | 24477976 |
a0004 | 0/0 | 406 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | MDGSH others(401): Show |
chr1 | 24410802 | 24477976 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1218 | 241 | 70 | 46 | 89 | 10 | 25 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0001c0002 | 0/1 | 1218 | 121 | 14 | 22 | 61 | 6 | 17 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0001c0003 | 0/0 | 1218 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0001c0004 | 0/0 | 1218 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0001c0005 | 0/0 | 1218 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0001c0008 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0001c0010 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0002c0009 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0003c0006 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 | ||
a0004c0007 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | ATGGA others(1213): Show |
chr1 | 24410802 | 24477976 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5372 | 50 | 2 | 5 | 34 | 2 | 7 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0002 | 1/0 | 5372 | 45 | 6 | 6 | 17 | 5 | 10 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0003 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0004 | 0/0 | 5371 | 21 | 18 | 2 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0005 | 0/0 | 5372 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0006 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0007 | 0/0 | 5371 | 8 | 7 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0008 | 0/0 | 5372 | 8 | 0 | 5 | 0 | 2 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0009 | 0/0 | 5372 | 6 | 0 | 6 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0010 | 0/0 | 5372 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0011 | 0/0 | 5371 | 5 | 2 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0012 | 0/0 | 5372 | 3 | 0 | 1 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0013 | 0/0 | 5371 | 4 | 2 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0014 | 0/0 | 5372 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0015 | 0/0 | 5373 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0016 | 0/0 | 5370 | 4 | 1 | 1 | 0 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0017 | 0/0 | 5374 | 4 | 1 | 3 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5369): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0018 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0020 | 0/0 | 5371 | 4 | 3 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0021 | 0/0 | 5374 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5369): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0022 | 0/0 | 5373 | 3 | 0 | 0 | 1 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0023 | 0/0 | 5371 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0024 | 0/0 | 5372 | 2 | 0 | 0 | 1 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0025 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0026 | 0/0 | 5372 | 2 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0028 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0029 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0030 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0031 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0032 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0034 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0035 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0037 | 0/0 | 5371 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0038 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0039 | 0/0 | 5383 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5378): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0040 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0041 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0042 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0043 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0046 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0047 | 0/0 | 5374 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5369): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0049 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0050 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0051 | 0/0 | 5370 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0052 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0053 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0054 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0055 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0056 | 0/0 | 5370 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0057 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0059 | 0/0 | 5371 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0060 | 0/0 | 5374 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5369): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0064 | 0/0 | 5370 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0065 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0066 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0068 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0069 | 0/0 | 5372 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0071 | 0/0 | 5372 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0072 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0073 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0074 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0075 | 0/0 | 5371 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0001t0076 | 0/0 | 5371 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0001 | 0/1 | 5372 | 38 | 1 | 8 | 18 | 2 | 8 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0002 | 0/0 | 5372 | 8 | 0 | 0 | 6 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0003 | 0/0 | 5372 | 41 | 6 | 12 | 17 | 2 | 4 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0005 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0006 | 0/0 | 5371 | 8 | 3 | 0 | 1 | 2 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0012 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0015 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0018 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0019 | 0/0 | 5373 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0024 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0027 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0028 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0029 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0033 | 0/0 | 5373 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0036 | 0/0 | 5372 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0044 | 0/0 | 5374 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5369): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0045 | 0/0 | 5372 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0048 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0058 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0061 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0062 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0063 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0001c0002t0067 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0003t0001 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0003t0003 | 0/0 | 5372 | 5 | 0 | 0 | 5 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0004t0005 | 0/0 | 5372 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0005t0004 | 0/0 | 5371 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5366): Show |
chr1 | 24410802 | 24477976 |
a0001c0008t0003 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0001c0010t0003 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0002c0009t0012 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5367): Show |
chr1 | 24410802 | 24477976 |
a0003c0006t0070 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5368): Show |
chr1 | 24410802 | 24477976 |
a0004c0007t0030 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | GAATT others(5365): Show |
chr1 | 24410802 | 24477976 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 0 | 8 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0010g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0012g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0012g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0012g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0013g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0013g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0014g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0014g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0014g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0014g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0015g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0015g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0015g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0016g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0016g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0016g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0017g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0017g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0017g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0018g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0020g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0020g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0020g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0021g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0021g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0021g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0022g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0022g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0022g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0023g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0023g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0023g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0024g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0024g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0025g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0025g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0026g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0029g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0030g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0031g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0031g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0032g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0032g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0034g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0035g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0037g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0038g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0039g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0040g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0041g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0042g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0043g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0046g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0047g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0049g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0050g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0051g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0052g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0053g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0054g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0055g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0056g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0057g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0059g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0060g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0064g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0065g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0066g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0068g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0069g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0071g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0072g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0073g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0074g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0075g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0076g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0012g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0015g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0018g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0018g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0019g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0019g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0019g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0019g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0024g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0027g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0027g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0028g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0029g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0033g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0033g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0036g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0044g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0045g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0048g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0058g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0061g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0062g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0063g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0067g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0004t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0004t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0004t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0004t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0005t0004g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0008t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0010t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0002c0009t0012g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0003c0006t0070g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0004c0007t0030g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0232 | EUR | GBR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0068 | EUR | GBR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0064 | EUR | GBR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | GBR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0223 | EUR | FIN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00323 | hp1 | a0001 | c0002 | t0003 | g0069 | EUR | FIN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00438 | hp2 | a0001 | c0003 | t0003 | g0075 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00544 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00544 | hp2 | a0001 | c0001 | t0018 | g0008 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00597 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0291 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0224 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00609 | hp2 | a0001 | c0008 | t0003 | g0307 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00621 | hp2 | a0001 | c0002 | t0003 | g0066 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00639 | hp1 | a0001 | c0001 | t0013 | g0322 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00639 | hp2 | a0001 | c0001 | t0064 | g0138 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00673 | hp1 | a0001 | c0001 | t0012 | g0318 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00673 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0183 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0305 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00741 | hp1 | a0001 | c0001 | t0047 | g0163 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01069 | hp1 | a0001 | c0001 | t0013 | g0191 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01069 | hp2 | a0001 | c0001 | t0017 | g0029 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01070 | hp1 | a0001 | c0001 | t0008 | g0026 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0256 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01071 | hp2 | a0001 | c0001 | t0017 | g0029 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0013 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01081 | hp2 | a0001 | c0001 | t0026 | g0017 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01099 | hp1 | a0001 | c0001 | t0020 | g0156 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0084 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01106 | hp1 | a0001 | c0001 | t0035 | g0143 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01106 | hp2 | a0001 | c0002 | t0012 | g0260 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01109 | hp1 | a0001 | c0001 | t0016 | g0166 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01109 | hp2 | a0001 | c0001 | t0037 | g0189 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0230 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01168 | hp2 | a0001 | c0001 | t0075 | g0288 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01175 | hp2 | a0001 | c0001 | t0076 | g0176 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01192 | hp1 | a0001 | c0001 | t0043 | g0242 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01192 | hp2 | a0001 | c0001 | t0053 | g0167 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01243 | hp1 | a0001 | c0001 | t0059 | g0020 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01243 | hp2 | a0001 | c0001 | t0017 | g0261 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01255 | hp1 | a0001 | c0001 | t0008 | g0297 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01255 | hp2 | a0001 | c0001 | t0051 | g0164 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01257 | hp1 | a0001 | c0001 | t0008 | g0264 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01257 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0016 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01346 | hp1 | a0001 | c0001 | t0056 | g0243 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0290 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0093 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0198 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01496 | hp2 | a0001 | c0001 | t0074 | g0286 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0169 | EUR | IBS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01515 | hp2 | a0001 | c0001 | t0008 | g0289 | EUR | IBS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01517 | hp1 | a0001 | c0001 | t0008 | g0287 | EUR | IBS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0058 | EUR | IBS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01884 | hp1 | a0001 | c0002 | t0033 | g0177 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01891 | hp1 | a0001 | c0005 | t0004 | g0003 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01952 | hp1 | a0001 | c0002 | t0044 | g0024 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01952 | hp2 | a0001 | c0001 | t0009 | g0219 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01975 | hp2 | a0001 | c0001 | t0009 | g0220 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0053 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01993 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0091 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02004 | hp2 | a0001 | c0001 | t0008 | g0026 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0122 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02027 | hp1 | a0001 | c0003 | t0003 | g0088 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02056 | hp1 | a0001 | c0001 | t0060 | g0212 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02056 | hp2 | a0001 | c0001 | t0046 | g0316 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02074 | hp1 | a0001 | c0010 | t0003 | g0225 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02080 | hp1 | a0001 | c0001 | t0011 | g0181 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02083 | hp1 | a0001 | c0001 | t0018 | g0008 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02129 | hp2 | a0001 | c0002 | t0018 | g0218 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02145 | hp1 | a0001 | c0001 | t0073 | g0036 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02145 | hp2 | a0001 | c0002 | t0006 | g0100 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0013 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02257 | hp1 | a0001 | c0001 | t0023 | g0262 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02258 | hp1 | a0001 | c0001 | t0025 | g0193 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02258 | hp2 | a0001 | c0001 | t0032 | g0157 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02273 | hp2 | a0001 | c0001 | t0009 | g0231 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02280 | hp1 | a0001 | c0002 | t0036 | g0050 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02280 | hp2 | a0001 | c0001 | t0025 | g0192 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02300 | hp1 | a0001 | c0001 | t0009 | g0234 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0098 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02451 | hp1 | a0001 | c0001 | t0050 | g0160 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02523 | hp2 | a0001 | c0002 | t0018 | g0114 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0145 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02615 | hp2 | a0001 | c0001 | t0020 | g0155 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02647 | hp1 | a0001 | c0005 | t0004 | g0003 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02717 | hp2 | a0001 | c0001 | t0017 | g0153 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02723 | hp1 | a0001 | c0001 | t0021 | g0325 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02723 | hp2 | a0001 | c0001 | t0068 | g0182 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02735 | hp1 | a0001 | c0002 | t0006 | g0102 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0078 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02809 | hp1 | a0001 | c0001 | t0052 | g0173 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02818 | hp2 | a0001 | c0002 | t0045 | g0147 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02886 | hp1 | a0001 | c0001 | t0055 | g0033 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02886 | hp2 | a0001 | c0002 | t0006 | g0089 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0180 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02896 | hp2 | a0001 | c0002 | t0006 | g0253 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0188 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02965 | hp1 | a0001 | c0001 | t0013 | g0194 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02965 | hp2 | a0001 | c0001 | t0023 | g0034 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02970 | hp2 | a0001 | c0001 | t0032 | g0161 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0179 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02976 | hp2 | a0001 | c0001 | t0038 | g0199 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0129 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03041 | hp2 | a0001 | c0001 | t0030 | g0159 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03098 | hp2 | a0001 | c0001 | t0021 | g0324 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03139 | hp2 | a0001 | c0005 | t0004 | g0003 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03195 | hp2 | a0001 | c0001 | t0065 | g0139 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0107 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03209 | hp2 | a0001 | c0001 | t0031 | g0137 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03225 | hp1 | a0001 | c0001 | t0049 | g0257 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03239 | hp1 | a0001 | c0001 | t0069 | g0245 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03453 | hp2 | a0001 | c0002 | t0033 | g0178 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03486 | hp1 | a0001 | c0001 | t0020 | g0037 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03490 | hp1 | a0001 | c0001 | t0016 | g0018 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03492 | hp1 | a0001 | c0001 | t0016 | g0018 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03516 | hp1 | a0001 | c0001 | t0016 | g0165 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03516 | hp2 | a0001 | c0001 | t0021 | g0327 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03540 | hp2 | a0001 | c0001 | t0071 | g0170 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03579 | hp1 | a0001 | c0001 | t0039 | g0187 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03688 | hp2 | a0001 | c0002 | t0063 | g0083 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03710 | hp2 | a0001 | c0001 | t0008 | g0239 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | BEB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | BEB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03942 | hp1 | a0001 | c0001 | t0026 | g0017 | SAS | BEB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04115 | hp1 | a0001 | c0001 | t0040 | g0267 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04199 | hp1 | a0001 | c0001 | t0022 | g0202 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04199 | hp2 | a0001 | c0001 | t0022 | g0023 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0277 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04228 | hp1 | a0001 | c0002 | t0006 | g0077 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0115 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18522 | hp1 | a0001 | c0001 | t0072 | g0039 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18522 | hp2 | a0001 | c0001 | t0057 | g0007 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18612 | hp1 | a0001 | c0003 | t0003 | g0041 | EAS | CHB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0126 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18940 | hp1 | a0001 | c0002 | t0019 | g0011 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18942 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18942 | hp2 | a0001 | c0002 | t0029 | g0061 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18943 | hp1 | a0001 | c0001 | t0014 | g0266 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18946 | hp1 | a0001 | c0004 | t0005 | g0238 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18950 | hp2 | a0001 | c0002 | t0003 | g0313 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18952 | hp1 | a0001 | c0002 | t0058 | g0042 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18952 | hp2 | a0001 | c0001 | t0028 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18953 | hp1 | a0001 | c0001 | t0015 | g0281 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18953 | hp2 | a0001 | c0001 | t0024 | g0207 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18956 | hp1 | a0001 | c0002 | t0019 | g0296 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18956 | hp2 | a0002 | c0009 | t0012 | g0092 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18960 | hp1 | a0001 | c0002 | t0027 | g0085 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18962 | hp1 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18963 | hp2 | a0001 | c0002 | t0024 | g0067 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18964 | hp1 | a0001 | c0001 | t0014 | g0025 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18964 | hp2 | a0001 | c0001 | t0011 | g0184 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18967 | hp2 | a0001 | c0002 | t0019 | g0094 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18968 | hp1 | a0001 | c0001 | t0029 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18970 | hp1 | a0001 | c0001 | t0014 | g0320 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18970 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18972 | hp2 | a0001 | c0004 | t0005 | g0252 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18973 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18975 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18975 | hp2 | a0001 | c0002 | t0067 | g0222 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18979 | hp1 | a0001 | c0002 | t0006 | g0227 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18979 | hp2 | a0001 | c0001 | t0041 | g0278 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18986 | hp1 | a0001 | c0002 | t0061 | g0106 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18986 | hp2 | a0001 | c0004 | t0005 | g0215 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18987 | hp2 | a0001 | c0002 | t0003 | g0134 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18990 | hp1 | a0001 | c0001 | t0015 | g0293 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18990 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18994 | hp1 | a0001 | c0002 | t0048 | g0118 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18998 | hp2 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19000 | hp1 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19000 | hp2 | a0003 | c0006 | t0070 | g0010 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19004 | hp1 | a0001 | c0002 | t0005 | g0051 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19004 | hp2 | a0001 | c0001 | t0042 | g0314 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19010 | hp1 | a0001 | c0002 | t0027 | g0014 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19010 | hp2 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19011 | hp2 | a0001 | c0001 | t0011 | g0185 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19012 | hp2 | a0001 | c0001 | t0066 | g0133 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19043 | hp1 | a0001 | c0001 | t0031 | g0140 | AFR | LWK | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19043 | hp2 | a0004 | c0007 | t0030 | g0172 | AFR | LWK | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19058 | hp1 | a0001 | c0001 | t0012 | g0044 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19058 | hp2 | a0001 | c0002 | t0005 | g0097 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19062 | hp2 | a0001 | c0001 | t0014 | g0315 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19063 | hp1 | a0001 | c0002 | t0028 | g0065 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19063 | hp2 | a0001 | c0004 | t0005 | g0221 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19067 | hp2 | a0001 | c0002 | t0015 | g0049 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19068 | hp2 | a0001 | c0001 | t0010 | g0206 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19074 | hp2 | a0001 | c0002 | t0062 | g0062 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19078 | hp1 | a0001 | c0002 | t0019 | g0040 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19078 | hp2 | a0001 | c0001 | t0010 | g0208 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19084 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19086 | hp1 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19090 | hp2 | a0001 | c0001 | t0022 | g0004 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0130 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0174 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20129 | hp1 | a0001 | c0001 | t0054 | g0326 | AFR | ASW | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ASW | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20752 | hp1 | a0001 | c0001 | t0024 | g0236 | EUR | TSI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20752 | hp2 | a0001 | c0002 | t0006 | g0104 | EUR | TSI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0210 | EUR | TSI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20805 | hp2 | a0001 | c0002 | t0006 | g0101 | EUR | TSI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0072 | SAS | GIH | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0081 | SAS | GIH | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0079 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0190 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02109 | hp2 | a0001 | c0001 | t0034 | g0323 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02486 | hp2 | a0001 | c0001 | t0020 | g0158 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0186 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | USA | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | USA | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0128 | AFR | USA | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | USA | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA21309 | hp1 | a0001 | c0001 | t0023 | g0035 | AFR | LWK | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | LWK | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0059 | REF | REF | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0209 | REF | REF | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:24419566 | G | A | 1 | a0003 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.19G>A | p.Ala7Thr | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/12 | 379/5372 | 19/1221 | 7/406 | chr1 | 24419566 | |||
chr1:24442071 | G | A | 1 | a0004 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.179G>A | p.Arg60His | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/12 | 539/5372 | 179/1221 | 60/406 | chr1 | 24442071 | |||
chr1:24453456 | A | T | 1 | a0002 | 1 | NA18956.hp2 | stop_gained | HIGH | c.589A>T | p.Lys197* | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/12 | 949/5372 | 589/1221 | 197/406 | chr1 | 24453456 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:24419637 | C | T | 2 | a0001c0004 a0001c0010 |
5 | HG02074.hp1 NA18946.hp1 NA18972.hp2 others(2): Show |
synonymous_variant | LOW | c.90C>T | p.Tyr30Tyr | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/12 | 450/5372 | 90/1221 | 30/406 | chr1 | 24419637 | |||
chr1:24456220 | C | T | 1 | a0001c0003 | 6 | HG00423.hp1 HG00438.hp2 HG02027.hp1 others(3): Show |
synonymous_variant | LOW | c.720C>T | p.Pro240Pro | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/12 | 1080/5372 | 720/1221 | 240/406 | chr1 | 24456220 | |||
chr1:24456256 | C | T | 1 | a0001c0008 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.756C>T | p.Thr252Thr | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/12 | 1116/5372 | 756/1221 | 252/406 | chr1 | 24456256 | |||
chr1:24458903 | C | T | 5 | a0001c0002 a0001c0003 a0001c0008 others(2): Show |
129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
synonymous_variant | LOW | c.789C>T | p.Ala263Ala | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/12 | 1149/5372 | 789/1221 | 263/406 | chr1 | 24458903 | |||
chr1:24469140 | C | T | 1 | a0001c0005 | 3 | HG01891.hp1 HG02647.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.1176C>T | p.Ala392Ala | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1536/5372 | 1176/1221 | 392/406 | chr1 | 24469140 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:24415834 | C | T | 2 | a0001c0001t0076 a0001c0002t0033 |
3 | HG01175.hp2 HG01884.hp1 HG03453.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-328C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/12 | chr1 | 24415834 | |||||||
chr1:24469374 | T | G | 4 | a0001c0001t0013 a0001c0001t0025 a0001c0001t0034 others(1): Show |
8 | HG00639.hp1 HG01069.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*189T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 189 | chr1 | 24469374 | ||||||
chr1:24469527 | T | G | 1 | a0001c0002t0036 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 342 | chr1 | 24469527 | ||||||
chr1:24469577 | G | A | 5 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0037 others(2): Show |
16 | HG00733.hp1 HG01109.hp2 HG02080.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*392G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 392 | chr1 | 24469577 | ||||||
chr1:24469579 | A | C | 3 | a0001c0001t0008 a0001c0001t0074 a0001c0001t0075 |
10 | HG01070.hp1 HG01168.hp2 HG01255.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 394 | chr1 | 24469579 | ||||||
chr1:24469639 | C | G | 7 | a0001c0001t0020 a0001c0001t0025 a0001c0001t0032 others(4): Show |
12 | HG01099.hp1 HG01106.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*454C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 454 | chr1 | 24469639 | ||||||
chr1:24469653 | G | A | 1 | a0001c0001t0040 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 468 | chr1 | 24469653 | ||||||
chr1:24469837 | G | A | 1 | a0001c0001t0074 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*652G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 652 | chr1 | 24469837 | ||||||
chr1:24469876 | GAAGTTAA others(94): Show |
G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*693_*793del | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 693 | INFO_REALIGN_3_PRIME | chr1 | 24469876 | |||||
chr1:24469946 | A | G | 1 | a0001c0001t0022 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*761A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 761 | chr1 | 24469946 | ||||||
chr1:24469997 | G | C | 3 | a0001c0001t0014 a0001c0001t0041 a0001c0001t0042 |
6 | NA18943.hp1 NA18964.hp1 NA18970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*812G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 812 | chr1 | 24469997 | ||||||
chr1:24470041 | C | T | 1 | a0003c0006t0070 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*856C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 856 | chr1 | 24470041 | ||||||
chr1:24470108 | C | T | 1 | a0001c0001t0069 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 923 | chr1 | 24470108 | ||||||
chr1:24470196 | A | G | 1 | a0001c0001t0034 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1011A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1011 | chr1 | 24470196 | ||||||
chr1:24470348 | A | G | 23 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(20): Show |
82 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1163A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1163 | chr1 | 24470348 | ||||||
chr1:24470382 | A | G | 1 | a0001c0001t0059 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1197 | chr1 | 24470382 | ||||||
chr1:24470893 | A | G | 2 | a0001c0001t0034 a0001c0001t0068 |
2 | HG02109.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1708A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1708 | chr1 | 24470893 | ||||||
chr1:24470904 | G | A | 1 | a0001c0001t0043 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1719G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1719 | chr1 | 24470904 | ||||||
chr1:24470968 | C | G | 1 | a0001c0001t0010 | 6 | NA18942.hp1 NA18970.hp2 NA18973.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1783C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1783 | chr1 | 24470968 | ||||||
chr1:24471070 | T | TCGGTATG others(106): Show |
1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888_*1889insTATG others(109): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1889 | INFO_REALIGN_3_PRIME | chr1 | 24471070 | |||||
chr1:24471074 | A | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1889A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1889 | chr1 | 24471074 | ||||||
chr1:24471076 | C | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1891 | chr1 | 24471076 | ||||||
chr1:24471077 | C | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1892 | chr1 | 24471077 | ||||||
chr1:24471080 | A | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1895A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1895 | chr1 | 24471080 | ||||||
chr1:24471081 | G | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1896G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1896 | chr1 | 24471081 | ||||||
chr1:24471082 | C | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1897C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1897 | chr1 | 24471082 | ||||||
chr1:24471084 | C | T | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1899 | chr1 | 24471084 | ||||||
chr1:24471085 | A | G | 5 | a0001c0001t0005 a0001c0001t0042 a0001c0002t0005 others(2): Show |
14 | HG00408.hp1 HG00609.hp1 NA18946.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1900A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1900 | chr1 | 24471085 | ||||||
chr1:24471112 | T | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1927 | chr1 | 24471112 | ||||||
chr1:24471116 | G | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1931G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1931 | chr1 | 24471116 | ||||||
chr1:24471120 | C | T | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1935C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1935 | chr1 | 24471120 | ||||||
chr1:24471122 | C | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1937C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1937 | chr1 | 24471122 | ||||||
chr1:24471145 | A | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1960A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1960 | chr1 | 24471145 | ||||||
chr1:24471148 | T | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1963T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1963 | chr1 | 24471148 | ||||||
chr1:24471161 | T | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1976T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1976 | chr1 | 24471161 | ||||||
chr1:24471163 | T | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1978T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1978 | chr1 | 24471163 | ||||||
chr1:24471164 | A | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1979A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1979 | chr1 | 24471164 | ||||||
chr1:24471165 | A | T | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1980 | chr1 | 24471165 | ||||||
chr1:24471166 | A | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1981A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1981 | chr1 | 24471166 | ||||||
chr1:24471168 | T | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1983 | chr1 | 24471168 | ||||||
chr1:24471170 | G | A | 1 | a0001c0001t0037 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1985G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1985 | chr1 | 24471170 | ||||||
chr1:24471173 | T | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1988T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1988 | chr1 | 24471173 | ||||||
chr1:24471174 | G | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1989G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1989 | chr1 | 24471174 | ||||||
chr1:24471175 | A | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1990A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1990 | chr1 | 24471175 | ||||||
chr1:24471177 | C | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1992C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1992 | chr1 | 24471177 | ||||||
chr1:24471186 | G | T | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2001G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2001 | chr1 | 24471186 | ||||||
chr1:24471247 | G | C | 5 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0037 others(2): Show |
16 | HG00733.hp1 HG01109.hp2 HG02080.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2062G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2062 | chr1 | 24471247 | ||||||
chr1:24471421 | A | C | 2 | a0001c0001t0018 a0001c0002t0018 |
4 | HG00544.hp2 HG02083.hp1 HG02129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2236A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2236 | chr1 | 24471421 | ||||||
chr1:24471511 | G | A | 55 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(52): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*2326G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2326 | chr1 | 24471511 | ||||||
chr1:24471530 | A | G | 1 | a0001c0001t0053 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2345A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2345 | chr1 | 24471530 | ||||||
chr1:24471578 | C | CA | 11 | a0001c0001t0022 a0001c0001t0029 a0001c0001t0034 others(8): Show |
13 | HG01106.hp1 HG01168.hp2 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2413dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2414 | INFO_REALIGN_3_PRIME | chr1 | 24471578 | |||||
chr1:24471578 | C | CAA | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(26): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2412_*2413dupAA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2414 | INFO_REALIGN_3_PRIME | chr1 | 24471578 | |||||
chr1:24471578 | C | CAAA | 10 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0021 others(7): Show |
20 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2411_*2413dupAAA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2414 | INFO_REALIGN_3_PRIME | chr1 | 24471578 | |||||
chr1:24471694 | T | C | 2 | a0001c0001t0023 a0001c0001t0055 |
4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2509T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2509 | chr1 | 24471694 | ||||||
chr1:24471720 | C | A | 1 | a0001c0002t0045 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2535C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2535 | chr1 | 24471720 | ||||||
chr1:24471746 | T | C | 2 | a0001c0001t0064 a0001c0001t0065 |
2 | HG00639.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2561T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2561 | chr1 | 24471746 | ||||||
chr1:24471893 | C | T | 39 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(36): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*2708C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2708 | chr1 | 24471893 | ||||||
chr1:24471906 | C | T | 1 | a0001c0002t0048 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2721C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2721 | chr1 | 24471906 | ||||||
chr1:24471946 | G | A | 4 | a0001c0001t0030 a0001c0001t0050 a0001c0001t0064 others(1): Show |
4 | HG00639.hp2 HG02451.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2761G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2761 | chr1 | 24471946 | ||||||
chr1:24472008 | CT | C | 33 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(30): Show |
90 | HG00558.hp1 HG00639.hp1 HG00733.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2841delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2841 | INFO_REALIGN_3_PRIME | chr1 | 24472008 | |||||
chr1:24472008 | CTT | C | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(41): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2840_*2841delTT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2840 | INFO_REALIGN_3_PRIME | chr1 | 24472008 | |||||
chr1:24472025 | T | C | 1 | a0001c0001t0051 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2840T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2840 | chr1 | 24472025 | ||||||
chr1:24472169 | C | T | 1 | a0001c0001t0056 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2984C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2984 | chr1 | 24472169 | ||||||
chr1:24472206 | C | T | 5 | a0001c0001t0007 a0001c0001t0031 a0001c0001t0037 others(2): Show |
13 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3021C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3021 | chr1 | 24472206 | ||||||
chr1:24472236 | G | A | 2 | a0001c0001t0009 a0001c0001t0043 |
7 | HG01168.hp1 HG01192.hp1 HG01496.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3051G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3051 | chr1 | 24472236 | ||||||
chr1:24472290 | G | A | 1 | a0001c0002t0027 | 2 | NA18960.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3105G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3105 | chr1 | 24472290 | ||||||
chr1:24472332 | A | G | 1 | a0001c0002t0067 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3147A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3147 | chr1 | 24472332 | ||||||
chr1:24472379 | A | C | 2 | a0001c0001t0021 a0001c0001t0054 |
4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3194A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3194 | chr1 | 24472379 | ||||||
chr1:24472555 | A | T | 15 | a0001c0001t0016 a0001c0001t0018 a0001c0001t0023 others(12): Show |
24 | HG00544.hp2 HG01081.hp2 HG01109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3370A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3370 | chr1 | 24472555 | ||||||
chr1:24472741 | G | A | 1 | a0001c0001t0046 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3556G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3556 | chr1 | 24472741 | ||||||
chr1:24472887 | C | G | 1 | a0001c0001t0057 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3702C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3702 | chr1 | 24472887 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:24415925 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0004g0030 a0001c0001t0004g0031 |
3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-258+21G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24415925 | |||||||
chr1:24416308 | C | G | 5 | a0001c0001t0017g0029 a0001c0001t0021g0324 a0001c0001t0021g0325 others(2): Show |
6 | HG01069.hp2 HG01071.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-258+404C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416308 | |||||||
chr1:24416496 | T | C | 122 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(119): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-258+592T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416496 | |||||||
chr1:24416532 | C | G | 2 | a0001c0002t0002g0141 a0001c0002t0003g0142 |
2 | NA19086.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-258+628C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416532 | |||||||
chr1:24416609 | A | G | 1 | a0001c0001t0034g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-258+705A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416609 | |||||||
chr1:24416616 | C | T | 3 | a0001c0001t0001g0321 a0001c0001t0013g0322 a0001c0001t0034g0323 |
3 | HG00639.hp1 HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-258+712C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416616 | |||||||
chr1:24416724 | G | A | 5 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0035g0143 others(2): Show |
5 | HG01106.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-258+820G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416724 | |||||||
chr1:24416733 | T | G | 10 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0148 others(7): Show |
15 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-258+829T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416733 | |||||||
chr1:24416824 | A | G | 4 | a0001c0001t0031g0137 a0001c0001t0031g0140 a0001c0001t0064g0138 others(1): Show |
4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-258+920A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416824 | |||||||
chr1:24417003 | G | A | 21 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0002g0169 others(18): Show |
24 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.-258+1099G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417003 | |||||||
chr1:24417090 | C | T | 1 | a0001c0001t0014g0320 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-258+1186C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417090 | |||||||
chr1:24417113 | C | A | 26 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(23): Show |
29 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-258+1209C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417113 | |||||||
chr1:24417142 | A | G | 1 | a0004c0007t0030g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-258+1238A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417142 | |||||||
chr1:24417272 | G | C | 7 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0023g0034 others(4): Show |
7 | HG02145.hp1 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-258+1368G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417272 | |||||||
chr1:24417293 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(67): Show |
83 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-258+1389C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417293 | |||||||
chr1:24417389 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(70): Show |
86 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-258+1485C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417389 | |||||||
chr1:24417941 | A | G | 2 | a0001c0001t0002g0258 a0001c0001t0002g0259 |
2 | NA18967.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-257-1350A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417941 | |||||||
chr1:24417959 | AAAAT | A | 4 | a0001c0001t0031g0137 a0001c0001t0031g0140 a0001c0001t0064g0138 others(1): Show |
4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-257-1325_-257-132 others(8): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 24417959 | ||||||
chr1:24417968 | A | G | 7 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-257-1323A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417968 | |||||||
chr1:24418111 | G | A | 2 | a0001c0001t0011g0174 a0001c0001t0052g0173 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-257-1180G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418111 | |||||||
chr1:24418502 | G | A | 2 | a0001c0001t0011g0174 a0001c0001t0052g0173 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-257-789G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418502 | |||||||
chr1:24418580 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(271): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-257-711T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418580 | |||||||
chr1:24418622 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(253): Show |
285 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.-257-669T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418622 | |||||||
chr1:24418672 | T | A | 1 | a0001c0001t0001g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-257-619T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418672 | |||||||
chr1:24418709 | C | A | 1 | a0001c0001t0008g0264 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-257-582C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418709 | |||||||
chr1:24418920 | G | GT | 10 | a0001c0001t0001g0317 a0001c0001t0001g0319 a0001c0001t0002g0250 others(7): Show |
10 | HG00673.hp1 HG02056.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.-257-355dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 24418920 | ||||||
chr1:24418920 | GT | G | 106 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(103): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-257-355delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 24418920 | ||||||
chr1:24418941 | C | T | 1 | a0001c0001t0031g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-257-350C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418941 | |||||||
chr1:24418948 | A | G | 1 | a0001c0002t0001g0125 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-257-343A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418948 | |||||||
chr1:24419006 | G | C | 1 | a0001c0002t0003g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-257-285G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24419006 | |||||||
chr1:24419096 | G | A | 2 | a0001c0001t0020g0155 a0001c0001t0020g0156 |
2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-257-195G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24419096 | |||||||
chr1:24419125 | G | A | 149 | a0001c0001t0001g0032 a0001c0001t0001g0070 a0001c0001t0001g0109 others(146): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-257-166G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24419125 | |||||||
chr1:24419214 | T | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(70): Show |
86 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-257-77T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24419214 | |||||||
chr1:24419715 | C | T | 124 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(121): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.93+75C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24419715 | |||||||
chr1:24419943 | G | A | 21 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0002g0169 others(18): Show |
24 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.93+303G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24419943 | |||||||
chr1:24420086 | G | GA | 26 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0001g0265 others(23): Show |
29 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.93+462dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24420086 | ||||||
chr1:24420086 | G | GAA | 6 | a0001c0001t0001g0032 a0001c0001t0004g0030 a0001c0001t0004g0031 others(3): Show |
6 | HG01099.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+461_93+462dupAA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24420086 | ||||||
chr1:24420087 | A | G | 1 | a0001c0001t0049g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.93+447A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420087 | |||||||
chr1:24420384 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.93+744C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420384 | |||||||
chr1:24420520 | T | C | 1 | a0001c0001t0014g0266 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.93+880T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420520 | |||||||
chr1:24420594 | T | G | 2 | a0001c0001t0007g0020 a0001c0001t0059g0020 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.93+954T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420594 | |||||||
chr1:24420672 | T | G | 3 | a0001c0001t0001g0032 a0001c0001t0004g0030 a0001c0001t0004g0031 |
3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.93+1032T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420672 | |||||||
chr1:24420695 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(69): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+1055G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420695 | |||||||
chr1:24420738 | C | G | 24 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(21): Show |
27 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.93+1098C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420738 | |||||||
chr1:24420778 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.93+1138G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420778 | |||||||
chr1:24420977 | A | G | 24 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(21): Show |
27 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.93+1337A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420977 | |||||||
chr1:24421067 | C | G | 14 | a0001c0001t0002g0038 a0001c0001t0002g0254 a0001c0001t0004g0007 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.93+1427C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421067 | |||||||
chr1:24421102 | G | C | 4 | a0001c0001t0031g0137 a0001c0001t0031g0140 a0001c0001t0064g0138 others(1): Show |
4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1462G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421102 | |||||||
chr1:24421134 | C | T | 117 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(114): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.93+1494C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421134 | |||||||
chr1:24421163 | A | G | 13 | a0001c0001t0001g0321 a0001c0001t0004g0003 a0001c0001t0004g0006 others(10): Show |
18 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+1523A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421163 | |||||||
chr1:24421192 | C | T | 131 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(128): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.93+1552C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421192 | |||||||
chr1:24421281 | G | A | 1 | a0001c0001t0040g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.93+1641G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421281 | |||||||
chr1:24421351 | C | CA | 7 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0023g0034 others(4): Show |
7 | HG02145.hp1 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+1720dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24421351 | ||||||
chr1:24421353 | A | C | 1 | a0001c0001t0001g0312 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.93+1713A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421353 | |||||||
chr1:24421393 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.93+1753G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421393 | |||||||
chr1:24421820 | G | A | 24 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(21): Show |
27 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.93+2180G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421820 | |||||||
chr1:24421847 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0002g0196 a0001c0001t0004g0197 |
3 | HG00558.hp1 HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.93+2207T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421847 | |||||||
chr1:24421979 | G | A | 2 | a0001c0001t0020g0158 a0001c0001t0032g0157 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.93+2339G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421979 | |||||||
chr1:24422090 | T | C | 1 | a0001c0001t0055g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.93+2450T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422090 | |||||||
chr1:24422094 | A | C | 1 | a0001c0001t0002g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93+2454A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422094 | |||||||
chr1:24422149 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93+2509C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422149 | |||||||
chr1:24422210 | C | T | 2 | a0001c0002t0003g0122 a0001c0002t0003g0123 |
2 | HG02015.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.93+2570C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422210 | |||||||
chr1:24422284 | G | A | 24 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(21): Show |
27 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.93+2644G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422284 | |||||||
chr1:24422339 | A | G | 113 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(110): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.93+2699A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422339 | |||||||
chr1:24422520 | C | T | 1 | a0001c0001t0049g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.93+2880C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422520 | |||||||
chr1:24422589 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(69): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+2949C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422589 | |||||||
chr1:24422590 | G | A | 1 | a0001c0002t0006g0253 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93+2950G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422590 | |||||||
chr1:24422837 | A | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(271): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.93+3197A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422837 | |||||||
chr1:24422887 | A | G | 131 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(128): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.93+3247A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422887 | |||||||
chr1:24423216 | G | A | 117 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(114): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.93+3576G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423216 | |||||||
chr1:24423406 | C | T | 1 | a0001c0001t0001g0319 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.93+3766C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423406 | |||||||
chr1:24423445 | G | A | 18 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(15): Show |
19 | HG00733.hp1 HG01069.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.93+3805G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423445 | |||||||
chr1:24423456 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(239): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.93+3816A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423456 | |||||||
chr1:24423463 | C | G | 2 | a0001c0002t0001g0146 a0001c0002t0045g0147 |
2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.93+3823C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423463 | |||||||
chr1:24423552 | C | T | 1 | a0001c0002t0001g0028 | 2 | NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.93+3912C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423552 | |||||||
chr1:24423572 | G | A | 3 | a0001c0001t0012g0044 a0001c0002t0001g0043 a0001c0002t0058g0042 |
3 | HG01358.hp1 NA18952.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.93+3932G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423572 | |||||||
chr1:24423579 | G | A | 1 | a0001c0001t0049g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.93+3939G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423579 | |||||||
chr1:24423585 | G | A | 1 | a0001c0001t0009g0198 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.93+3945G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423585 | |||||||
chr1:24423641 | C | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(269): Show |
302 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.93+4001C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423641 | |||||||
chr1:24423864 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.93+4224C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423864 | |||||||
chr1:24423986 | A | G | 10 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0148 others(7): Show |
15 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.93+4346A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423986 | |||||||
chr1:24424103 | T | C | 1 | a0001c0001t0068g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.93+4463T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424103 | |||||||
chr1:24424356 | T | C | 2 | a0001c0001t0001g0321 a0001c0001t0034g0323 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.93+4716T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424356 | |||||||
chr1:24424388 | T | C | 12 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(9): Show |
13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.93+4748T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424388 | |||||||
chr1:24424484 | C | T | 2 | a0001c0001t0011g0174 a0001c0001t0052g0173 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.93+4844C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424484 | |||||||
chr1:24424502 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0002g0269 |
2 | HG00735.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.93+4862G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424502 | |||||||
chr1:24424512 | G | A | 1 | a0001c0001t0042g0314 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.93+4872G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424512 | |||||||
chr1:24424707 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(271): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.93+5067T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424707 | |||||||
chr1:24425005 | A | G | 3 | a0001c0002t0002g0121 a0001c0002t0002g0141 a0001c0002t0003g0142 |
3 | NA19062.hp1 NA19086.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.93+5365A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425005 | |||||||
chr1:24425164 | A | G | 1 | a0001c0001t0004g0197 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.93+5524A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425164 | |||||||
chr1:24425202 | G | C | 1 | a0001c0001t0003g0200 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.93+5562G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425202 | |||||||
chr1:24425283 | T | C | 113 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(110): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.93+5643T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425283 | |||||||
chr1:24425319 | AT | A | 131 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(128): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.93+5687delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24425319 | ||||||
chr1:24425387 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | NA18980.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.93+5747T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425387 | |||||||
chr1:24425430 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(253): Show |
285 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.93+5790A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425430 | |||||||
chr1:24425497 | C | T | 2 | a0001c0001t0011g0174 a0001c0001t0052g0173 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.93+5857C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425497 | |||||||
chr1:24425527 | G | A | 5 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0035g0143 others(2): Show |
5 | HG01106.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+5887G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425527 | |||||||
chr1:24425544 | A | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0002t0001g0116 others(2): Show |
5 | HG02027.hp2 NA18943.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+5904A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425544 | |||||||
chr1:24425829 | C | G | 9 | a0001c0001t0001g0321 a0001c0001t0002g0254 a0001c0001t0004g0007 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.93+6189C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425829 | |||||||
chr1:24426083 | C | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(277): Show |
310 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.93+6443C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426083 | |||||||
chr1:24426092 | C | T | 2 | a0001c0001t0017g0261 a0001c0001t0023g0262 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.93+6452C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426092 | |||||||
chr1:24426227 | G | A | 4 | a0001c0001t0007g0183 a0001c0001t0011g0181 a0001c0001t0011g0184 others(1): Show |
4 | HG00733.hp1 HG02080.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+6587G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426227 | |||||||
chr1:24426240 | G | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(69): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+6600G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426240 | |||||||
chr1:24426270 | C | A | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.93+6630C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426270 | |||||||
chr1:24426294 | CT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(70): Show |
86 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.93+6667delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24426294 | ||||||
chr1:24426376 | C | A | 113 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(110): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.93+6736C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426376 | |||||||
chr1:24426453 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(277): Show |
310 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.93+6813T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426453 | |||||||
chr1:24426674 | G | A | 113 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(110): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.93+7034G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426674 | |||||||
chr1:24426808 | G | A | 1 | a0001c0001t0007g0021 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.93+7168G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426808 | |||||||
chr1:24426820 | G | A | 131 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(128): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.93+7180G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426820 | |||||||
chr1:24426839 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.93+7199C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426839 | |||||||
chr1:24426860 | T | C | 1 | a0001c0001t0050g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.93+7220T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426860 | |||||||
chr1:24426999 | G | A | 1 | a0001c0002t0001g0270 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.93+7359G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426999 | |||||||
chr1:24427271 | G | T | 1 | a0001c0001t0013g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93+7631G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427271 | |||||||
chr1:24427708 | A | G | 1 | a0001c0002t0001g0046 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.93+8068A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427708 | |||||||
chr1:24427764 | G | T | 2 | a0001c0001t0005g0246 a0001c0001t0005g0247 |
2 | HG00408.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.93+8124G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427764 | |||||||
chr1:24427778 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(69): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+8138A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427778 | |||||||
chr1:24427916 | T | A | 117 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(114): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.93+8276T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427916 | |||||||
chr1:24427936 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(239): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.93+8296G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427936 | |||||||
chr1:24427979 | C | G | 2 | a0001c0001t0001g0321 a0001c0001t0034g0323 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.93+8339C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427979 | |||||||
chr1:24427993 | C | T | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8353C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427993 | |||||||
chr1:24428030 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(154): Show |
181 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.93+8390A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428030 | |||||||
chr1:24428104 | A | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0310 a0001c0001t0002g0269 |
3 | HG00735.hp1 HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.93+8464A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428104 | |||||||
chr1:24428197 | G | A | 1 | a0001c0001t0038g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93+8557G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428197 | |||||||
chr1:24428216 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0308 |
3 | HG02129.hp1 NA18612.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.93+8576A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428216 | |||||||
chr1:24428237 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.93+8597C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428237 | |||||||
chr1:24428254 | A | AAAAAGAG others(10): Show |
1 | a0001c0002t0015g0049 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.93+8615_93+8616ins others(17): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428254 | ||||||
chr1:24428254 | A | AGAGAGAG others(4): Show |
1 | a0001c0001t0002g0259 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.93+8614_93+8615ins others(11): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428254 | |||||||
chr1:24428258 | A | AAG | 16 | a0001c0001t0002g0057 a0001c0001t0002g0213 a0001c0001t0002g0214 others(13): Show |
18 | HG00597.hp1 HG01070.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.93+8662_93+8663dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAG | 14 | a0001c0001t0001g0217 a0001c0001t0002g0216 a0001c0001t0002g0248 others(11): Show |
14 | HG01952.hp2 HG02109.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+8660_93+8663dup others(4): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAG | 15 | a0001c0001t0002g0249 a0001c0001t0009g0220 a0001c0001t0038g0199 others(12): Show |
15 | HG00099.hp2 HG00140.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.93+8658_93+8663dup others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(1): Show |
21 | a0001c0001t0001g0070 a0001c0001t0002g0196 a0001c0001t0002g0223 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.93+8656_93+8663dup others(8): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(3): Show |
23 | a0001c0001t0001g0195 a0001c0001t0002g0022 a0001c0001t0002g0226 others(20): Show |
26 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.93+8654_93+8663dup others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(5): Show |
18 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0007g0183 others(15): Show |
18 | HG00733.hp1 HG01069.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.93+8652_93+8663dup others(12): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(7): Show |
13 | a0001c0001t0002g0124 a0001c0001t0002g0240 a0001c0001t0008g0239 others(10): Show |
13 | HG01099.hp2 HG01496.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+8650_93+8663dup others(14): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(9): Show |
14 | a0001c0001t0001g0119 a0001c0001t0002g0241 a0001c0001t0005g0247 others(11): Show |
14 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+8648_93+8663dup others(16): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(11): Show |
9 | a0001c0001t0002g0023 a0001c0001t0002g0203 a0001c0001t0022g0023 others(6): Show |
9 | HG02300.hp2 HG03579.hp2 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.93+8646_93+8663dup others(18): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(13): Show |
6 | a0001c0002t0001g0099 a0001c0002t0001g0103 a0001c0002t0003g0016 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+8644_93+8663dup others(20): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(15): Show |
1 | a0001c0001t0011g0184 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.93+8642_93+8663dup others(22): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(19): Show |
2 | a0001c0002t0003g0105 a0001c0002t0006g0104 |
2 | NA19066.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.93+8638_93+8663dup others(26): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AAGAGAGA others(27): Show |
1 | a0001c0002t0061g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.93+8630_93+8663dup others(34): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | A | AGAG | 3 | a0001c0001t0004g0256 a0001c0002t0003g0107 a0001c0002t0003g0108 |
3 | HG00438.hp1 HG01071.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.93+8618_93+8619ins others(3): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | A | AGAGAGAG others(2): Show |
5 | a0001c0001t0001g0109 a0001c0001t0002g0175 a0001c0001t0003g0200 others(2): Show |
5 | HG01346.hp1 HG02132.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+8618_93+8619ins others(9): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | A | AGAGAGAG others(4): Show |
1 | a0001c0001t0069g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(11): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | A | AGAGAGAG others(6): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0001c0002t0001g0110 others(1): Show |
4 | HG00280.hp2 HG03491.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+8618_93+8619ins others(13): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | A | AGAGAGAG others(8): Show |
1 | a0001c0002t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(15): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | A | AGAGAGAG others(10): Show |
1 | a0001c0008t0003g0307 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(17): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | A | AGAGAGAG others(12): Show |
1 | a0001c0002t0018g0114 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(19): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | A | AGAGAGAG others(22): Show |
1 | a0001c0001t0011g0185 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(29): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | A | G | 3 | a0001c0001t0002g0259 a0001c0002t0003g0115 a0001c0002t0015g0049 |
3 | HG04228.hp2 NA18968.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.93+8618A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | |||||||
chr1:24428258 | AAG | A | 16 | a0001c0001t0002g0002 a0001c0001t0002g0205 a0001c0001t0002g0250 others(13): Show |
22 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+8662_93+8663del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | AAGAG | A | 4 | a0001c0001t0004g0154 a0001c0001t0007g0186 a0001c0002t0001g0146 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+8660_93+8663del others(4): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | AAGAGAG | A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0038 a0001c0001t0004g0003 others(6): Show |
14 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.93+8658_93+8663del others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | AAGAGAGA others(1): Show |
A | 24 | a0001c0001t0001g0301 a0001c0001t0001g0304 a0001c0001t0001g0306 others(21): Show |
26 | HG00639.hp1 HG00673.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.93+8656_93+8663del others(8): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | AAGAGAGA others(3): Show |
A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(79): Show |
98 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.93+8654_93+8663del others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | AAGAGAGA others(5): Show |
A | 1 | a0001c0001t0005g0272 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.93+8652_93+8663del others(12): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | AAGAGAGA others(7): Show |
A | 4 | a0001c0001t0001g0309 a0001c0001t0002g0204 a0001c0001t0014g0320 others(1): Show |
4 | HG01981.hp2 NA18970.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+8650_93+8663del others(14): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | AAGAGAGA others(9): Show |
A | 1 | a0001c0001t0021g0324 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.93+8648_93+8663del others(16): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428258 | AAGAGAGA others(13): Show |
A | 1 | a0001c0001t0001g0271 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.93+8644_93+8663del others(20): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | ||||||
chr1:24428294 | GAGAGAGA others(3): Show |
G | 2 | a0001c0001t0049g0257 a0001c0002t0036g0050 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.93+8656_93+8665del others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428294 | ||||||
chr1:24428299 | A | C | 26 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(23): Show |
29 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.93+8659A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428299 | |||||||
chr1:24428300 | G | GAGAGAGA others(3): Show |
1 | a0001c0002t0003g0005 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.93+8663_93+8664ins others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428300 | ||||||
chr1:24428302 | GAC | G | 3 | a0001c0002t0001g0054 a0001c0002t0003g0005 a0001c0002t0003g0122 |
3 | HG01975.hp1 HG02015.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.93+8665_93+8666del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428302 | ||||||
chr1:24428304 | C | G | 110 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(107): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.93+8664C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428304 | |||||||
chr1:24428307 | C | G | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8667C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428307 | |||||||
chr1:24428312 | C | A | 3 | a0001c0002t0001g0028 a0001c0002t0001g0270 a0001c0002t0001g0273 |
4 | NA18944.hp2 NA18999.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+8672C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428312 | |||||||
chr1:24428312 | C | G | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8672C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428312 | |||||||
chr1:24428313 | C | A | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8673C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428313 | |||||||
chr1:24428314 | T | G | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8674T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428314 | |||||||
chr1:24428315 | T | A | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8675T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428315 | |||||||
chr1:24428316 | T | G | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8676T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428316 | |||||||
chr1:24428317 | C | A | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8677C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428317 | |||||||
chr1:24428318 | C | G | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8678C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428318 | |||||||
chr1:24428319 | C | A | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8679C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428319 | |||||||
chr1:24428320 | C | G | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8680C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428320 | |||||||
chr1:24428322 | A | G | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8682A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428322 | |||||||
chr1:24428325 | C | A | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8685C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428325 | |||||||
chr1:24428326 | C | G | 1 | a0001c0001t0011g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8686C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428326 | |||||||
chr1:24428429 | A | C | 39 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(36): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.93+8789A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428429 | |||||||
chr1:24428502 | C | T | 1 | a0001c0002t0002g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.93+8862C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428502 | |||||||
chr1:24428513 | G | A | 32 | a0001c0001t0006g0144 a0001c0001t0007g0020 a0001c0001t0007g0021 others(29): Show |
34 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.93+8873G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428513 | |||||||
chr1:24428518 | G | A | 115 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(112): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.93+8878G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428518 | |||||||
chr1:24428575 | A | G | 1 | a0001c0002t0003g0313 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.93+8935A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428575 | |||||||
chr1:24428714 | G | A | 115 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(112): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.93+9074G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428714 | |||||||
chr1:24428791 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(139): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.93+9151G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428791 | |||||||
chr1:24428796 | C | A | 3 | a0001c0001t0017g0261 a0001c0001t0023g0262 a0001c0002t0012g0260 |
3 | HG01106.hp2 HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.93+9156C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428796 | |||||||
chr1:24428948 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(140): Show |
166 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.93+9308G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428948 | |||||||
chr1:24428994 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.93+9354C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428994 | |||||||
chr1:24429043 | G | A | 1 | a0001c0001t0038g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93+9403G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429043 | |||||||
chr1:24429044 | C | T | 15 | a0001c0001t0001g0321 a0001c0001t0004g0003 a0001c0001t0004g0006 others(12): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.93+9404C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429044 | |||||||
chr1:24429214 | A | G | 1 | a0001c0001t0038g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93+9574A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429214 | |||||||
chr1:24429354 | C | CA | 339 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(336): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.93+9714_93+9715ins others(1): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429354 | |||||||
chr1:24429503 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(153): Show |
180 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.93+9863C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429503 | |||||||
chr1:24429724 | T | C | 2 | a0001c0002t0003g0069 a0001c0002t0003g0081 |
2 | HG00323.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.93+10084T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429724 | |||||||
chr1:24429840 | C | G | 1 | a0001c0001t0002g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.93+10200C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429840 | |||||||
chr1:24429942 | G | C | 1 | a0001c0001t0007g0183 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.94-10230G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429942 | |||||||
chr1:24429952 | T | C | 7 | a0001c0001t0005g0211 a0001c0001t0005g0224 a0001c0004t0005g0215 others(4): Show |
7 | HG00609.hp1 HG02074.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-10220T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429952 | |||||||
chr1:24429984 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(139): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-10188G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429984 | |||||||
chr1:24430214 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0004g0030 a0001c0001t0004g0031 |
3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.94-9958G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430214 | |||||||
chr1:24430235 | CT | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(146): Show |
173 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.94-9923delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24430235 | ||||||
chr1:24430235 | CTT | C | 8 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0023g0034 others(5): Show |
8 | HG02145.hp1 HG02886.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-9924_94-9923del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24430235 | ||||||
chr1:24430290 | T | TGGAGTGC others(1): Show |
118 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(115): Show |
139 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.94-9873_94-9866dup others(8): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24430290 | ||||||
chr1:24430313 | C | T | 45 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(42): Show |
53 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.94-9859C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430313 | |||||||
chr1:24430314 | G | A | 1 | a0001c0001t0034g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.94-9858G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430314 | |||||||
chr1:24430377 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(139): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-9795A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430377 | |||||||
chr1:24430450 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(139): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-9722G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430450 | |||||||
chr1:24430534 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(272): Show |
305 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.94-9638A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430534 | |||||||
chr1:24430540 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.94-9632G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430540 | |||||||
chr1:24430639 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(139): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-9533C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430639 | |||||||
chr1:24430701 | T | C | 1 | a0001c0001t0050g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-9471T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430701 | |||||||
chr1:24430718 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(67): Show |
83 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.94-9454A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430718 | |||||||
chr1:24430729 | G | A | 12 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(9): Show |
18 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.94-9443G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430729 | |||||||
chr1:24430851 | C | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(139): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-9321C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430851 | |||||||
chr1:24430859 | G | A | 7 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-9313G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430859 | |||||||
chr1:24431277 | A | G | 4 | a0001c0001t0031g0137 a0001c0001t0031g0140 a0001c0001t0064g0138 others(1): Show |
4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-8895A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431277 | |||||||
chr1:24431316 | C | T | 19 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0002g0169 others(16): Show |
21 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.94-8856C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431316 | |||||||
chr1:24431504 | A | G | 3 | a0001c0001t0001g0300 a0001c0001t0001g0309 a0001c0001t0012g0305 |
3 | HG00733.hp2 HG01981.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.94-8668A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431504 | |||||||
chr1:24431803 | AC | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0255 a0001c0001t0004g0256 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-8364delC | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24431803 | ||||||
chr1:24431813 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.94-8359C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431813 | |||||||
chr1:24431844 | C | T | 1 | a0001c0003t0003g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.94-8328C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431844 | |||||||
chr1:24432001 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0020g0037 |
2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.94-8171C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432001 | |||||||
chr1:24432002 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94-8170G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432002 | |||||||
chr1:24432038 | C | T | 14 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0017g0029 others(11): Show |
15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-8134C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432038 | |||||||
chr1:24432114 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(139): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-8058C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432114 | |||||||
chr1:24432117 | A | G | 30 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(27): Show |
37 | HG00733.hp1 HG01069.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.94-8055A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432117 | |||||||
chr1:24432158 | T | C | 4 | a0001c0002t0001g0082 a0001c0002t0001g0087 a0001c0002t0001g0099 others(1): Show |
4 | HG03490.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-8014T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432158 | |||||||
chr1:24432193 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(139): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-7979A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432193 | |||||||
chr1:24432244 | C | T | 2 | a0001c0001t0011g0174 a0001c0001t0052g0173 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94-7928C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432244 | |||||||
chr1:24432449 | T | C | 1 | a0001c0001t0011g0145 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94-7723T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432449 | |||||||
chr1:24432535 | C | T | 1 | a0001c0001t0049g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94-7637C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432535 | |||||||
chr1:24432569 | T | C | 114 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(111): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.94-7603T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432569 | |||||||
chr1:24432723 | G | T | 2 | a0001c0001t0001g0265 a0001c0001t0002g0299 |
2 | HG01123.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.94-7449G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432723 | |||||||
chr1:24432849 | G | C | 3 | a0001c0002t0002g0121 a0001c0002t0002g0141 a0001c0002t0003g0142 |
3 | NA19062.hp1 NA19086.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.94-7323G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432849 | |||||||
chr1:24432913 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(138): Show |
164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-7259G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432913 | |||||||
chr1:24432919 | A | G | 2 | a0001c0001t0011g0174 a0001c0001t0052g0173 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94-7253A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432919 | |||||||
chr1:24432939 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(138): Show |
164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-7233G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432939 | |||||||
chr1:24432985 | A | G | 14 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0017g0029 others(11): Show |
15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-7187A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432985 | |||||||
chr1:24433124 | C | T | 1 | a0001c0001t0024g0207 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.94-7048C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433124 | |||||||
chr1:24433125 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.94-7047G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433125 | |||||||
chr1:24433195 | G | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(114): Show |
138 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.94-6977G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433195 | |||||||
chr1:24433440 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(66): Show |
82 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.94-6732C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433440 | |||||||
chr1:24433629 | G | A | 7 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0023g0034 others(4): Show |
7 | HG02145.hp1 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-6543G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433629 | |||||||
chr1:24433633 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(138): Show |
164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-6539C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433633 | |||||||
chr1:24433708 | T | C | 1 | a0001c0001t0060g0212 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.94-6464T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433708 | |||||||
chr1:24433759 | A | G | 12 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(9): Show |
18 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.94-6413A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433759 | |||||||
chr1:24433809 | G | T | 12 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(9): Show |
13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.94-6363G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433809 | |||||||
chr1:24433823 | TG | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(138): Show |
164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-6346delG | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24433823 | ||||||
chr1:24433826 | G | A | 5 | a0001c0003t0001g0131 a0001c0003t0003g0012 a0001c0003t0003g0041 others(2): Show |
6 | HG00423.hp1 HG00438.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-6346G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433826 | |||||||
chr1:24433927 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(138): Show |
164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-6245C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433927 | |||||||
chr1:24433940 | A | C | 1 | a0001c0002t0003g0093 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-6232A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433940 | |||||||
chr1:24434001 | T | C | 1 | a0001c0001t0007g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94-6171T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434001 | |||||||
chr1:24434164 | T | C | 45 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(42): Show |
53 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.94-6008T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434164 | |||||||
chr1:24434309 | A | G | 14 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0017g0029 others(11): Show |
15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-5863A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434309 | |||||||
chr1:24434489 | G | A | 2 | a0001c0002t0006g0089 a0001c0002t0006g0100 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.94-5683G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434489 | |||||||
chr1:24434553 | T | C | 1 | a0001c0001t0030g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94-5619T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434553 | |||||||
chr1:24434812 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(271): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.94-5360C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434812 | |||||||
chr1:24434853 | T | G | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.94-5319T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434853 | |||||||
chr1:24434901 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(138): Show |
164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-5271A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434901 | |||||||
chr1:24435345 | A | G | 1 | a0001c0010t0003g0225 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.94-4827A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435345 | |||||||
chr1:24435500 | C | A | 3 | a0001c0001t0001g0195 a0001c0001t0002g0196 a0001c0001t0004g0197 |
3 | HG00558.hp1 HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.94-4672C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435500 | |||||||
chr1:24435572 | C | T | 1 | a0001c0002t0003g0098 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.94-4600C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435572 | |||||||
chr1:24435573 | G | A | 1 | a0001c0002t0003g0098 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.94-4599G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435573 | |||||||
chr1:24435574 | C | T | 1 | a0001c0002t0003g0098 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.94-4598C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435574 | |||||||
chr1:24435579 | A | G | 24 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(21): Show |
26 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.94-4593A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435579 | |||||||
chr1:24435605 | C | T | 1 | a0001c0002t0002g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.94-4567C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435605 | |||||||
chr1:24435660 | A | G | 1 | a0001c0001t0049g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94-4512A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435660 | |||||||
chr1:24435769 | G | A | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.94-4403G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435769 | |||||||
chr1:24435896 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.94-4276G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435896 | |||||||
chr1:24435970 | G | A | 8 | a0001c0001t0017g0029 a0001c0001t0021g0324 a0001c0001t0021g0325 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-4202G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435970 | |||||||
chr1:24436041 | A | G | 1 | a0001c0002t0001g0028 | 2 | NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.94-4131A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436041 | |||||||
chr1:24436068 | G | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(270): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.94-4104G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436068 | |||||||
chr1:24436086 | C | T | 14 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0017g0029 others(11): Show |
15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-4086C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436086 | |||||||
chr1:24436149 | G | A | 23 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(20): Show |
25 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.94-4023G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436149 | |||||||
chr1:24436221 | G | A | 1 | a0001c0001t0032g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.94-3951G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436221 | |||||||
chr1:24436251 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(137): Show |
163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3921C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436251 | |||||||
chr1:24436252 | A | T | 2 | a0001c0001t0025g0192 a0001c0001t0025g0193 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.94-3920A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436252 | |||||||
chr1:24436309 | T | A | 1 | a0001c0001t0014g0266 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.94-3863T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436309 | |||||||
chr1:24436359 | A | G | 1 | a0001c0001t0068g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.94-3813A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436359 | |||||||
chr1:24436444 | A | G | 13 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(10): Show |
14 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.94-3728A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436444 | |||||||
chr1:24436497 | T | C | 1 | a0001c0002t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.94-3675T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436497 | |||||||
chr1:24436510 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(136): Show |
162 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.94-3662C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436510 | |||||||
chr1:24436522 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.94-3650C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436522 | |||||||
chr1:24436572 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(137): Show |
163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3600T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436572 | |||||||
chr1:24436640 | C | G | 4 | a0001c0001t0031g0137 a0001c0001t0031g0140 a0001c0001t0064g0138 others(1): Show |
4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3532C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436640 | |||||||
chr1:24436645 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(66): Show |
82 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.94-3527C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436645 | |||||||
chr1:24436653 | T | TAA | 45 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(42): Show |
53 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.94-3518_94-3517dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24436653 | ||||||
chr1:24436679 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(270): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.94-3493G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436679 | |||||||
chr1:24436765 | C | T | 4 | a0001c0001t0031g0137 a0001c0001t0031g0140 a0001c0001t0064g0138 others(1): Show |
4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3407C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436765 | |||||||
chr1:24436791 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(137): Show |
163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3381G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436791 | |||||||
chr1:24436795 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(137): Show |
163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3377A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436795 | |||||||
chr1:24436841 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(137): Show |
163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3331A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436841 | |||||||
chr1:24436857 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.94-3315G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436857 | |||||||
chr1:24437023 | G | T | 1 | a0004c0007t0030g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94-3149G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437023 | |||||||
chr1:24437061 | A | C | 1 | a0001c0001t0049g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94-3111A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437061 | |||||||
chr1:24437120 | C | T | 103 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0112 others(100): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.94-3052C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437120 | |||||||
chr1:24437125 | G | A | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.94-3047G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437125 | |||||||
chr1:24437176 | C | T | 9 | a0001c0001t0001g0032 a0001c0001t0004g0030 a0001c0001t0004g0031 others(6): Show |
9 | HG01099.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-2996C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437176 | |||||||
chr1:24437201 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.94-2971G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437201 | |||||||
chr1:24437304 | T | G | 2 | a0001c0001t0001g0301 a0001c0001t0005g0272 |
2 | NA18994.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.94-2868T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437304 | |||||||
chr1:24437361 | A | G | 1 | a0001c0001t0008g0297 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.94-2811A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437361 | |||||||
chr1:24437447 | G | C | 1 | a0001c0001t0002g0250 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.94-2725G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437447 | |||||||
chr1:24437580 | A | AAGGTCTG others(8): Show |
3 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0055g0033 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.94-2575_94-2561dup others(15): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24437580 | ||||||
chr1:24437802 | T | G | 2 | a0001c0001t0006g0144 a0001c0001t0035g0143 |
2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.94-2370T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437802 | |||||||
chr1:24437807 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94-2365G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437807 | |||||||
chr1:24437841 | G | A | 1 | a0001c0002t0006g0253 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.94-2331G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437841 | |||||||
chr1:24438199 | C | T | 131 | a0001c0001t0001g0112 a0001c0001t0002g0057 a0001c0001t0002g0124 others(128): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.94-1973C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438199 | |||||||
chr1:24438211 | G | A | 1 | a0001c0001t0022g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94-1961G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438211 | |||||||
chr1:24438229 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0016g0165 a0001c0001t0047g0163 others(1): Show |
4 | HG00735.hp2 HG00741.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-1943G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438229 | |||||||
chr1:24438252 | T | C | 1 | a0001c0001t0068g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.94-1920T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438252 | |||||||
chr1:24438254 | G | A | 2 | a0001c0001t0002g0235 a0001c0001t0056g0243 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.94-1918G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438254 | |||||||
chr1:24438255 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0004g0030 a0001c0001t0004g0031 |
3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.94-1917G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438255 | |||||||
chr1:24438264 | G | A | 130 | a0001c0001t0001g0112 a0001c0001t0002g0057 a0001c0001t0002g0124 others(127): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.94-1908G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438264 | |||||||
chr1:24438350 | G | GT | 5 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(2): Show |
5 | HG01069.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-1821dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24438350 | ||||||
chr1:24438367 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.94-1805C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438367 | |||||||
chr1:24438425 | A | G | 119 | a0001c0001t0001g0112 a0001c0001t0002g0057 a0001c0001t0002g0124 others(116): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.94-1747A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438425 | |||||||
chr1:24438436 | A | T | 1 | a0001c0001t0037g0189 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.94-1736A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438436 | |||||||
chr1:24438473 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0004g0030 others(3): Show |
6 | HG00639.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-1699C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438473 | |||||||
chr1:24438475 | G | A | 3 | a0001c0001t0001g0321 a0001c0001t0013g0322 a0001c0001t0034g0323 |
3 | HG00639.hp1 HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.94-1697G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438475 | |||||||
chr1:24438533 | G | A | 1 | a0001c0001t0032g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.94-1639G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438533 | |||||||
chr1:24438623 | G | A | 23 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0002g0038 others(20): Show |
25 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.94-1549G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438623 | |||||||
chr1:24438813 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94-1359A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438813 | |||||||
chr1:24438888 | TA | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(198): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.94-1281delA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24438888 | ||||||
chr1:24438923 | T | C | 1 | a0001c0001t0004g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.94-1249T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438923 | |||||||
chr1:24439032 | G | A | 117 | a0001c0001t0001g0112 a0001c0001t0002g0057 a0001c0001t0002g0124 others(114): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.94-1140G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439032 | |||||||
chr1:24439047 | G | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(198): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.94-1125G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439047 | |||||||
chr1:24439217 | G | A | 7 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-955G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439217 | |||||||
chr1:24439249 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.94-923C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439249 | |||||||
chr1:24439390 | A | G | 1 | a0001c0001t0020g0156 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.94-782A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439390 | |||||||
chr1:24439624 | AAT | A | 8 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0021g0324 others(5): Show |
8 | HG01106.hp1 HG01175.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.94-543_94-542delAT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24439624 | ||||||
chr1:24439693 | G | A | 1 | a0001c0001t0007g0183 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.94-479G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439693 | |||||||
chr1:24439741 | G | T | 1 | a0001c0001t0020g0158 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.94-431G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439741 | |||||||
chr1:24439863 | T | G | 3 | a0001c0001t0001g0032 a0001c0001t0004g0030 a0001c0001t0004g0031 |
3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.94-309T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439863 | |||||||
chr1:24440009 | C | CT | 3 | a0001c0001t0001g0032 a0001c0001t0004g0030 a0001c0001t0004g0031 |
3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.94-161dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24440009 | ||||||
chr1:24440296 | G | A | 5 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(2): Show |
5 | HG01069.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+56G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440296 | |||||||
chr1:24440347 | A | C | 1 | a0001c0001t0008g0264 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.162+107A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440347 | |||||||
chr1:24440431 | G | A | 1 | a0001c0001t0011g0145 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+191G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440431 | |||||||
chr1:24440500 | C | G | 3 | a0001c0001t0001g0321 a0001c0001t0013g0322 a0001c0001t0034g0323 |
3 | HG00639.hp1 HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.162+260C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440500 | |||||||
chr1:24440715 | C | G | 37 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(34): Show |
45 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.162+475C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440715 | |||||||
chr1:24440758 | G | C | 3 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0055g0033 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.162+518G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440758 | |||||||
chr1:24440828 | G | A | 1 | a0001c0001t0068g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.162+588G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440828 | |||||||
chr1:24440884 | A | G | 1 | a0001c0001t0060g0212 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.162+644A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440884 | |||||||
chr1:24440936 | C | T | 119 | a0001c0001t0001g0112 a0001c0001t0002g0057 a0001c0001t0002g0124 others(116): Show |
126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.162+696C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440936 | |||||||
chr1:24440947 | C | T | 1 | a0001c0001t0003g0200 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.162+707C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440947 | |||||||
chr1:24441005 | G | A | 4 | a0001c0001t0007g0180 a0001c0001t0007g0186 a0001c0001t0007g0188 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+765G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441005 | |||||||
chr1:24441128 | C | T | 23 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0002g0038 others(20): Show |
25 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+888C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441128 | |||||||
chr1:24441255 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(79): Show |
95 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.163-800C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441255 | |||||||
chr1:24441284 | T | A | 2 | a0001c0002t0006g0089 a0001c0002t0006g0100 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.163-771T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441284 | |||||||
chr1:24441298 | C | A | 1 | a0001c0001t0002g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.163-757C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441298 | |||||||
chr1:24441472 | C | T | 1 | a0001c0001t0038g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163-583C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441472 | |||||||
chr1:24441473 | C | T | 11 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(8): Show |
12 | HG00733.hp1 HG01243.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-582C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441473 | |||||||
chr1:24441610 | C | T | 5 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(2): Show |
5 | HG01069.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-445C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441610 | |||||||
chr1:24441612 | AAC | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0195 others(6): Show |
11 | HG00544.hp2 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-437_163-436del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 24441612 | ||||||
chr1:24441670 | G | A | 11 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0017g0029 others(8): Show |
12 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-385G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441670 | |||||||
chr1:24441979 | G | A | 34 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0168 others(31): Show |
36 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.163-76G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441979 | |||||||
chr1:24442288 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(268): Show |
301 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.334+62G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442288 | |||||||
chr1:24442367 | C | T | 1 | a0001c0002t0001g0043 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.334+141C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442367 | |||||||
chr1:24442477 | G | C | 12 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(9): Show |
13 | HG00733.hp1 HG01243.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.334+251G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442477 | |||||||
chr1:24442578 | G | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02027.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.334+352G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442578 | |||||||
chr1:24442694 | T | C | 7 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+468T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442694 | |||||||
chr1:24442743 | G | C | 3 | a0001c0002t0006g0089 a0001c0002t0006g0100 a0001c0002t0006g0253 |
3 | HG02145.hp2 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.334+517G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442743 | |||||||
chr1:24442815 | A | G | 2 | a0001c0001t0001g0319 a0001c0001t0015g0293 |
2 | NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.334+589A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442815 | |||||||
chr1:24442844 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(269): Show |
302 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.334+618T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442844 | |||||||
chr1:24442926 | C | T | 23 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0002g0038 others(20): Show |
25 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.334+700C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442926 | |||||||
chr1:24443269 | T | C | 36 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(33): Show |
43 | HG00733.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.334+1043T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443269 | |||||||
chr1:24443439 | T | C | 7 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+1213T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443439 | |||||||
chr1:24443531 | C | T | 7 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+1305C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443531 | |||||||
chr1:24443545 | A | T | 1 | a0001c0001t0013g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.334+1319A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443545 | |||||||
chr1:24443649 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(60): Show |
75 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.334+1423C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443649 | |||||||
chr1:24443663 | C | T | 1 | a0001c0001t0004g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.334+1437C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443663 | |||||||
chr1:24443967 | G | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(218): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.335-1218G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443967 | |||||||
chr1:24444018 | C | CT | 248 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(245): Show |
276 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.335-1155dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 24444018 | ||||||
chr1:24444018 | C | CTT | 14 | a0001c0001t0001g0112 a0001c0001t0001g0162 a0001c0001t0001g0168 others(11): Show |
16 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.335-1156_335-1155d others(4): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 24444018 | ||||||
chr1:24444063 | A | G | 2 | a0001c0001t0031g0137 a0001c0001t0031g0140 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.335-1122A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444063 | |||||||
chr1:24444104 | G | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(218): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.335-1081G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444104 | |||||||
chr1:24444252 | A | G | 2 | a0001c0001t0064g0138 a0001c0001t0065g0139 |
2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.335-933A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444252 | |||||||
chr1:24444341 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.335-844A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444341 | |||||||
chr1:24444370 | GA | G | 3 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0055g0033 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.335-811delA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 24444370 | ||||||
chr1:24444406 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.335-779A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444406 | |||||||
chr1:24444409 | G | T | 3 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0055g0033 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.335-776G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444409 | |||||||
chr1:24444703 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.335-482T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444703 | |||||||
chr1:24444944 | T | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.335-241T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444944 | |||||||
chr1:24444951 | C | T | 6 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.335-234C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444951 | |||||||
chr1:24445116 | C | T | 1 | a0001c0001t0005g0074 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.335-69C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24445116 | |||||||
chr1:24445302 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0034g0323 |
3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.394+58G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445302 | |||||||
chr1:24445440 | C | T | 3 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0055g0033 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.394+196C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445440 | |||||||
chr1:24445493 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0034g0323 |
3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.394+249C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445493 | |||||||
chr1:24445719 | C | G | 1 | a0001c0001t0022g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.394+475C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445719 | |||||||
chr1:24445776 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.394+532G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445776 | |||||||
chr1:24445975 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(267): Show |
300 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.394+731T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445975 | |||||||
chr1:24446069 | C | CGT | 9 | a0001c0001t0001g0321 a0001c0001t0002g0299 a0001c0001t0013g0190 others(6): Show |
9 | HG00639.hp2 HG01069.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+862_394+863dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | ||||||
chr1:24446069 | C | CT | 3 | a0001c0001t0020g0158 a0001c0001t0023g0035 a0001c0001t0032g0161 |
3 | HG02486.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.394+825_394+826ins others(1): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | |||||||
chr1:24446069 | C | CTGT | 7 | a0001c0001t0001g0274 a0001c0001t0002g0038 a0001c0001t0020g0037 others(4): Show |
7 | HG02145.hp1 HG02965.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+825_394+826ins others(3): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | |||||||
chr1:24446069 | C | CTGTGT | 6 | a0001c0001t0015g0291 a0001c0001t0020g0155 a0001c0001t0020g0156 others(3): Show |
6 | HG00597.hp2 HG00741.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.394+825_394+826ins others(5): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | |||||||
chr1:24446069 | C | CTGTGTGT | 57 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0027 others(54): Show |
70 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.394+825_394+826ins others(7): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | |||||||
chr1:24446069 | C | CTGTGTGT others(2): Show |
16 | a0001c0001t0001g0025 a0001c0001t0001g0070 a0001c0001t0001g0271 others(13): Show |
18 | HG00673.hp1 HG00733.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.394+825_394+826ins others(9): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | |||||||
chr1:24446069 | C | CTGTGTGT others(4): Show |
2 | a0001c0001t0050g0160 a0004c0007t0030g0172 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.394+825_394+826ins others(11): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | |||||||
chr1:24446069 | C | CTGTGTGT others(6): Show |
2 | a0001c0001t0001g0280 a0001c0001t0002g0254 |
2 | HG00423.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.394+825_394+826ins others(13): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | |||||||
chr1:24446069 | C | CTGTGTGT others(10): Show |
1 | a0001c0001t0049g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.394+825_394+826ins others(17): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | |||||||
chr1:24446069 | CGT | C | 65 | a0001c0001t0001g0032 a0001c0001t0001g0217 a0001c0001t0002g0002 others(62): Show |
73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.394+862_394+863del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | ||||||
chr1:24446069 | CGTGT | C | 8 | a0001c0001t0002g0203 a0001c0001t0009g0234 a0001c0002t0001g0063 others(5): Show |
8 | HG02300.hp1 HG03579.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.394+860_394+863del others(4): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | ||||||
chr1:24446069 | CGTGTGT | C | 114 | a0001c0001t0012g0044 a0001c0001t0017g0029 a0001c0002t0001g0010 others(111): Show |
122 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.394+858_394+863del others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | ||||||
chr1:24446069 | CGTGTGTG others(13): Show |
C | 2 | a0001c0001t0031g0137 a0001c0001t0031g0140 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.394+844_394+863del others(20): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | ||||||
chr1:24446069 | CGTGTGTG others(15): Show |
C | 36 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(33): Show |
43 | HG01106.hp1 HG01109.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.394+842_394+863del others(22): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | ||||||
chr1:24446069 | CGTGTGTG others(17): Show |
C | 1 | a0001c0001t0007g0183 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.394+840_394+863del others(24): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | ||||||
chr1:24446196 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.394+952G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446196 | |||||||
chr1:24446204 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.394+960G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446204 | |||||||
chr1:24446210 | T | C | 1 | a0001c0001t0004g0149 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.394+966T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446210 | |||||||
chr1:24446233 | C | T | 1 | a0001c0002t0001g0028 | 2 | NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.394+989C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446233 | |||||||
chr1:24446373 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.394+1129A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446373 | |||||||
chr1:24446519 | A | G | 21 | a0001c0001t0001g0112 a0001c0001t0001g0162 a0001c0001t0001g0168 others(18): Show |
23 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.394+1275A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446519 | |||||||
chr1:24446543 | T | C | 39 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(36): Show |
46 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.394+1299T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446543 | |||||||
chr1:24446546 | A | G | 22 | a0001c0001t0001g0112 a0001c0001t0001g0162 a0001c0001t0001g0168 others(19): Show |
24 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.394+1302A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446546 | |||||||
chr1:24446572 | T | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(335): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.394+1328T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446572 | |||||||
chr1:24446601 | T | C | 124 | a0001c0001t0012g0044 a0001c0001t0017g0029 a0001c0002t0001g0010 others(121): Show |
132 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.394+1357T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446601 | |||||||
chr1:24446613 | T | A | 2 | a0001c0001t0031g0137 a0001c0001t0031g0140 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.394+1369T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446613 | |||||||
chr1:24446638 | G | A | 39 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(36): Show |
46 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.394+1394G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446638 | |||||||
chr1:24446880 | C | G | 1 | a0001c0001t0068g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.394+1636C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446880 | |||||||
chr1:24447115 | A | G | 2 | a0001c0001t0017g0261 a0001c0001t0023g0262 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.394+1871A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447115 | |||||||
chr1:24447144 | G | A | 27 | a0001c0001t0006g0144 a0001c0001t0007g0020 a0001c0001t0007g0021 others(24): Show |
28 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.394+1900G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447144 | |||||||
chr1:24447222 | C | T | 4 | a0001c0001t0002g0022 a0001c0001t0002g0233 a0001c0001t0002g0240 others(1): Show |
5 | HG00140.hp2 HG00741.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+1978C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447222 | |||||||
chr1:24447286 | A | G | 39 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(36): Show |
46 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.394+2042A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447286 | |||||||
chr1:24447313 | T | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(267): Show |
300 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.394+2069T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447313 | |||||||
chr1:24447486 | C | G | 1 | a0001c0001t0004g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395-1995C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447486 | |||||||
chr1:24447782 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.395-1699G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447782 | |||||||
chr1:24447783 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.395-1698A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447783 | |||||||
chr1:24447798 | A | C | 2 | a0001c0001t0023g0034 a0001c0001t0023g0035 |
2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.395-1683A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447798 | |||||||
chr1:24447986 | G | T | 2 | a0001c0001t0006g0144 a0001c0001t0035g0143 |
2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.395-1495G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447986 | |||||||
chr1:24448009 | C | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.395-1472C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448009 | |||||||
chr1:24448284 | G | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(217): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.395-1197G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448284 | |||||||
chr1:24448370 | C | A | 1 | a0001c0001t0013g0322 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.395-1111C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448370 | |||||||
chr1:24448424 | ATAGTAAT | A | 2 | a0001c0003t0001g0131 a0001c0003t0003g0012 |
3 | HG00423.hp1 NA19000.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.395-1054_395-1048d others(9): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24448424 | ||||||
chr1:24448510 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(92): Show |
110 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.395-971C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448510 | |||||||
chr1:24448590 | A | G | 1 | a0001c0002t0062g0062 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.395-891A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448590 | |||||||
chr1:24448604 | A | G | 8 | a0001c0001t0002g0232 a0001c0001t0009g0198 a0001c0001t0009g0219 others(5): Show |
8 | HG00099.hp1 HG01168.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-877A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448604 | |||||||
chr1:24448673 | C | CAAGAATG others(2903): Show |
3 | a0001c0001t0008g0264 a0001c0001t0008g0289 a0001c0001t0075g0288 |
3 | HG01168.hp2 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.395-793_395-792ins others(2910): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24448673 | ||||||
chr1:24448673 | C | CAAGAATG others(2904): Show |
3 | a0001c0001t0008g0287 a0001c0001t0008g0297 a0001c0001t0074g0286 |
3 | HG01255.hp1 HG01496.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.395-793_395-792ins others(2911): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24448673 | ||||||
chr1:24448673 | C | CAAGAATG others(2904): Show |
2 | a0001c0001t0008g0026 a0001c0001t0008g0290 |
3 | HG01070.hp1 HG01361.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.395-793_395-792ins others(2911): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24448673 | ||||||
chr1:24449002 | C | T | 1 | a0001c0001t0049g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395-479C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449002 | |||||||
chr1:24449081 | A | G | 2 | a0001c0001t0008g0287 a0001c0001t0008g0289 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.395-400A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449081 | |||||||
chr1:24449232 | A | G | 2 | a0001c0001t0001g0304 a0001c0001t0012g0318 |
2 | HG00673.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.395-249A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449232 | |||||||
chr1:24449392 | G | A | 5 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-89G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449392 | |||||||
chr1:24449457 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0034g0323 |
3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.395-24C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449457 | |||||||
chr1:24449477 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(60): Show |
75 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(72): Show |
splice_region_variant&intron_variant | LOW | c.395-4G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449477 | |||||||
chr1:24449695 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.540+69G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24449695 | |||||||
chr1:24449755 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.540+129C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24449755 | |||||||
chr1:24450087 | A | G | 2 | a0001c0001t0008g0026 a0001c0001t0008g0290 |
3 | HG01070.hp1 HG01361.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.540+461A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450087 | |||||||
chr1:24450095 | G | A | 12 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0016g0165 others(9): Show |
12 | HG01106.hp1 HG01175.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.540+469G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450095 | |||||||
chr1:24450108 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.540+482C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450108 | |||||||
chr1:24450114 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0034g0323 |
3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.540+488C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450114 | |||||||
chr1:24450237 | G | A | 10 | a0001c0001t0006g0144 a0001c0001t0011g0145 a0001c0001t0016g0165 others(7): Show |
10 | HG01106.hp1 HG01175.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+611G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450237 | |||||||
chr1:24450307 | C | T | 27 | a0001c0001t0006g0144 a0001c0001t0007g0020 a0001c0001t0007g0021 others(24): Show |
28 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.540+681C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450307 | |||||||
chr1:24450452 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.540+826C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450452 | |||||||
chr1:24450481 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(60): Show |
75 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.540+855T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450481 | |||||||
chr1:24450609 | C | T | 12 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(9): Show |
13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+983C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450609 | |||||||
chr1:24450677 | G | C | 1 | a0001c0001t0004g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.540+1051G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450677 | |||||||
chr1:24450723 | G | A | 1 | a0001c0001t0032g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.540+1097G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450723 | |||||||
chr1:24451026 | A | T | 1 | a0001c0002t0001g0058 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.540+1400A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451026 | |||||||
chr1:24451083 | G | A | 15 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0004g0003 others(12): Show |
21 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.540+1457G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451083 | |||||||
chr1:24451155 | T | C | 39 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(36): Show |
46 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.540+1529T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451155 | |||||||
chr1:24451351 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.540+1725C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451351 | |||||||
chr1:24451356 | A | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.540+1730A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451356 | |||||||
chr1:24451525 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.541-1883G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451525 | |||||||
chr1:24451799 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(336): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.541-1609A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451799 | |||||||
chr1:24451917 | A | G | 1 | a0001c0002t0003g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.541-1491A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451917 | |||||||
chr1:24451970 | C | T | 1 | a0001c0002t0001g0125 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.541-1438C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451970 | |||||||
chr1:24452145 | T | C | 1 | a0001c0001t0017g0029 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.541-1263T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452145 | |||||||
chr1:24452321 | A | G | 124 | a0001c0001t0012g0044 a0001c0001t0017g0029 a0001c0002t0001g0010 others(121): Show |
132 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.541-1087A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452321 | |||||||
chr1:24452335 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(62): Show |
77 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.541-1073G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452335 | |||||||
chr1:24452369 | C | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.541-1039C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452369 | |||||||
chr1:24452372 | C | T | 1 | a0001c0002t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.541-1036C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452372 | |||||||
chr1:24452458 | C | T | 23 | a0001c0001t0001g0112 a0001c0001t0001g0162 a0001c0001t0001g0168 others(20): Show |
25 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.541-950C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452458 | |||||||
chr1:24452675 | T | A | 3 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0055g0033 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.541-733T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452675 | |||||||
chr1:24452748 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.541-660C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452748 | |||||||
chr1:24452778 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.541-630C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452778 | |||||||
chr1:24452843 | C | T | 8 | a0001c0002t0001g0015 a0001c0002t0001g0076 a0001c0002t0002g0015 others(5): Show |
8 | NA18942.hp2 NA18963.hp2 NA19005.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-565C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452843 | |||||||
chr1:24452853 | A | AT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(192): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.541-535dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 24452853 | ||||||
chr1:24452853 | A | ATT | 32 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0294 others(29): Show |
33 | HG00621.hp2 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.541-536_541-535dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 24452853 | ||||||
chr1:24452853 | A | ATTT | 28 | a0001c0001t0001g0112 a0001c0001t0001g0162 a0001c0001t0001g0168 others(25): Show |
30 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.541-537_541-535dup others(3): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 24452853 | ||||||
chr1:24452892 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(94): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.541-516G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452892 | |||||||
chr1:24452894 | G | A | 156 | a0001c0001t0006g0144 a0001c0001t0007g0020 a0001c0001t0007g0021 others(153): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.541-514G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452894 | |||||||
chr1:24452969 | T | G | 8 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0158 others(5): Show |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-439T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452969 | |||||||
chr1:24452992 | G | A | 1 | a0001c0001t0024g0207 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.541-416G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452992 | |||||||
chr1:24453189 | C | G | 124 | a0001c0001t0012g0044 a0001c0001t0066g0133 a0001c0002t0001g0010 others(121): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.541-219C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453189 | |||||||
chr1:24453359 | G | A | 1 | a0001c0001t0038g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.541-49G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453359 | |||||||
chr1:24453365 | T | C | 125 | a0001c0001t0001g0162 a0001c0001t0012g0044 a0001c0001t0017g0029 others(122): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.541-43T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453365 | |||||||
chr1:24453383 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(96): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.541-25C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453383 | |||||||
chr1:24453397 | G | T | 1 | a0002c0009t0012g0092 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.541-11G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453397 | |||||||
chr1:24453404 | A | C | 1 | a0002c0009t0012g0092 | 1 | NA18956.hp2 | splice_region_variant&intron_variant | LOW | c.541-4A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453404 | |||||||
chr1:24453508 | A | C | 1 | a0002c0009t0012g0092 | 1 | NA18956.hp2 | splice_region_variant&intron_variant | LOW | c.637+4A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453508 | |||||||
chr1:24453586 | A | G | 1 | a0001c0001t0008g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637+82A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453586 | |||||||
chr1:24453710 | A | C | 1 | a0002c0009t0012g0092 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.637+206A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453710 | |||||||
chr1:24453746 | T | C | 2 | a0001c0002t0003g0126 a0001c0002t0003g0127 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+242T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453746 | |||||||
chr1:24453856 | C | T | 1 | a0001c0002t0028g0065 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.637+352C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453856 | |||||||
chr1:24453866 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(58): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.637+362C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453866 | |||||||
chr1:24454031 | C | CT | 125 | a0001c0001t0002g0203 a0001c0001t0012g0044 a0001c0001t0017g0029 others(122): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.637+542dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 24454031 | ||||||
chr1:24454031 | C | CTT | 7 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(4): Show |
7 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.637+541_637+542dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 24454031 | ||||||
chr1:24454031 | CT | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(132): Show |
157 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.637+542delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 24454031 | ||||||
chr1:24454253 | A | G | 6 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(3): Show |
6 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+749A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454253 | |||||||
chr1:24454260 | A | C | 1 | a0002c0009t0012g0092 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.637+756A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454260 | |||||||
chr1:24454380 | G | C | 12 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(9): Show |
13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.637+876G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454380 | |||||||
chr1:24454437 | G | A | 13 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(10): Show |
14 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+933G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454437 | |||||||
chr1:24454674 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(87): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.637+1170T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454674 | |||||||
chr1:24454757 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(220): Show |
244 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.637+1253T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454757 | |||||||
chr1:24454903 | G | A | 1 | a0001c0001t0051g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.638-1235G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454903 | |||||||
chr1:24454933 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0034g0323 |
3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-1205G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454933 | |||||||
chr1:24454992 | A | G | 1 | a0001c0001t0016g0018 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.638-1146A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454992 | |||||||
chr1:24455163 | G | A | 1 | a0001c0001t0068g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.638-975G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455163 | |||||||
chr1:24455319 | G | A | 3 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0055g0033 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.638-819G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455319 | |||||||
chr1:24455364 | T | C | 37 | a0001c0001t0001g0112 a0001c0001t0001g0162 a0001c0001t0001g0168 others(34): Show |
40 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.638-774T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455364 | |||||||
chr1:24455607 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0006g0144 others(2): Show |
5 | HG01106.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-531C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455607 | |||||||
chr1:24455668 | A | G | 4 | a0001c0002t0001g0082 a0001c0002t0001g0087 a0001c0002t0001g0099 others(1): Show |
4 | HG03490.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-470A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455668 | |||||||
chr1:24455722 | C | A | 2 | a0001c0001t0006g0144 a0001c0001t0035g0143 |
2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.638-416C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455722 | |||||||
chr1:24455796 | C | T | 4 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(1): Show |
4 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-342C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455796 | |||||||
chr1:24455800 | T | C | 1 | a0001c0001t0038g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.638-338T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455800 | |||||||
chr1:24455850 | C | A | 2 | a0001c0002t0001g0055 a0001c0002t0001g0125 |
2 | HG01993.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.638-288C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455850 | |||||||
chr1:24455998 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.638-140G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455998 | |||||||
chr1:24456036 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.638-102C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24456036 | |||||||
chr1:24456078 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.638-60C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24456078 | |||||||
chr1:24456079 | G | A | 1 | a0001c0002t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.638-59G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24456079 | |||||||
chr1:24456133 | T | C | 2 | a0001c0001t0064g0138 a0001c0001t0065g0139 |
2 | HG00639.hp2 HG03195.hp2 |
splice_region_variant&intron_variant | LOW | c.638-5T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24456133 | |||||||
chr1:24456278 | G | A | 1 | a0001c0001t0008g0290 | 1 | HG01361.hp2 | splice_region_variant&intron_variant | LOW | c.773+5G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456278 | |||||||
chr1:24456440 | G | A | 10 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+167G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456440 | |||||||
chr1:24456493 | G | C | 2 | a0001c0001t0031g0137 a0001c0001t0031g0140 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.773+220G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456493 | |||||||
chr1:24456532 | C | T | 1 | a0001c0001t0005g0272 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.773+259C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456532 | |||||||
chr1:24456656 | A | G | 1 | a0001c0001t0002g0298 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.773+383A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456656 | |||||||
chr1:24456701 | G | A | 10 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+428G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456701 | |||||||
chr1:24456821 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(255): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.773+548A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456821 | |||||||
chr1:24456902 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(67): Show |
82 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.773+629A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456902 | |||||||
chr1:24456910 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(218): Show |
242 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.773+637A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456910 | |||||||
chr1:24457195 | T | A | 1 | a0001c0001t0002g0205 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.773+922T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457195 | |||||||
chr1:24457379 | T | G | 1 | a0001c0001t0001g0295 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.773+1106T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457379 | |||||||
chr1:24457428 | G | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02027.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.773+1155G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457428 | |||||||
chr1:24457501 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.773+1228C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457501 | |||||||
chr1:24457545 | T | C | 12 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(9): Show |
18 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.773+1272T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457545 | |||||||
chr1:24457616 | C | T | 1 | a0001c0002t0061g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.774-1272C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457616 | |||||||
chr1:24457649 | A | G | 145 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0002g0038 others(142): Show |
153 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.774-1239A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457649 | |||||||
chr1:24457707 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(218): Show |
242 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.774-1181T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457707 | |||||||
chr1:24457724 | G | A | 15 | a0001c0001t0001g0112 a0001c0001t0001g0162 a0001c0001t0001g0168 others(12): Show |
17 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.774-1164G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457724 | |||||||
chr1:24457785 | A | C | 1 | a0001c0001t0010g0206 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.774-1103A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457785 | |||||||
chr1:24457796 | A | G | 10 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-1092A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457796 | |||||||
chr1:24457831 | C | T | 1 | a0001c0002t0067g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.774-1057C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457831 | |||||||
chr1:24458276 | G | A | 2 | a0001c0001t0064g0138 a0001c0001t0065g0139 |
2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.774-612G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458276 | |||||||
chr1:24458368 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.774-520G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458368 | |||||||
chr1:24458447 | C | T | 122 | a0001c0002t0001g0010 a0001c0002t0001g0014 a0001c0002t0001g0015 others(119): Show |
129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.774-441C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458447 | |||||||
chr1:24458572 | G | A | 10 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-316G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458572 | |||||||
chr1:24458577 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(73): Show |
89 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.774-311C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458577 | |||||||
chr1:24458579 | G | A | 68 | a0001c0002t0001g0015 a0001c0002t0001g0043 a0001c0002t0001g0056 others(65): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.774-309G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458579 | |||||||
chr1:24458616 | G | A | 1 | a0001c0001t0008g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.774-272G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458616 | |||||||
chr1:24458690 | G | T | 10 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-198G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458690 | |||||||
chr1:24459130 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.862+154G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459130 | |||||||
chr1:24459336 | G | A | 10 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.862+360G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459336 | |||||||
chr1:24459414 | A | T | 1 | a0001c0001t0020g0158 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.862+438A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459414 | |||||||
chr1:24459456 | A | AT | 7 | a0001c0002t0003g0107 a0001c0002t0003g0126 a0001c0002t0003g0127 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.862+489dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 24459456 | ||||||
chr1:24459868 | G | T | 13 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0204 others(10): Show |
20 | HG02056.hp1 NA18942.hp1 NA18947.hp1 others(17): Show |
intron_variant | MODIFIER | c.863-613G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459868 | |||||||
chr1:24459944 | C | G | 37 | a0001c0001t0001g0112 a0001c0001t0001g0162 a0001c0001t0001g0168 others(34): Show |
41 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.863-537C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459944 | |||||||
chr1:24459973 | C | T | 13 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0180 others(10): Show |
14 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.863-508C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459973 | |||||||
chr1:24460108 | G | C | 1 | a0001c0003t0003g0088 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.863-373G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24460108 | |||||||
chr1:24460273 | A | G | 10 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.863-208A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24460273 | |||||||
chr1:24460879 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.926+335C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24460879 | |||||||
chr1:24461088 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.926+544A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461088 | |||||||
chr1:24461283 | T | C | 4 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0021g0327 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.926+739T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461283 | |||||||
chr1:24461307 | CGAGGCAG others(318): Show |
C | 5 | a0001c0001t0004g0006 a0001c0001t0004g0148 a0001c0001t0004g0149 others(2): Show |
7 | HG01884.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+777_926+1101de others(1): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24461307 | ||||||
chr1:24461389 | A | G | 5 | a0001c0001t0007g0021 a0001c0001t0007g0180 a0001c0001t0007g0186 others(2): Show |
6 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.926+845A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461389 | |||||||
chr1:24461457 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(239): Show |
266 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.926+913A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461457 | |||||||
chr1:24461489 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(101): Show |
120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.926+945C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461489 | |||||||
chr1:24461542 | C | CA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0008g0297 others(6): Show |
9 | HG00639.hp1 HG01069.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.926+1014dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24461542 | ||||||
chr1:24461542 | CA | C | 11 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0008g0287 others(8): Show |
11 | HG00639.hp2 HG01517.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.926+1014delA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24461542 | ||||||
chr1:24461638 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(189): Show |
211 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.926+1094A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461638 | |||||||
chr1:24461701 | T | A | 1 | a0001c0001t0023g0262 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.926+1157T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461701 | |||||||
chr1:24461865 | C | CA | 6 | a0001c0001t0004g0030 a0001c0001t0064g0138 a0001c0001t0065g0139 others(3): Show |
6 | HG00639.hp2 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.926+1335dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24461865 | ||||||
chr1:24462065 | G | A | 7 | a0001c0002t0003g0107 a0001c0002t0003g0126 a0001c0002t0003g0127 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+1521G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462065 | |||||||
chr1:24462344 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0321 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.927-1682G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462344 | |||||||
chr1:24462374 | C | T | 1 | a0001c0002t0001g0273 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.927-1652C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462374 | |||||||
chr1:24462460 | G | A | 22 | a0001c0001t0006g0144 a0001c0002t0003g0016 a0001c0002t0003g0053 others(19): Show |
23 | HG00099.hp2 HG01123.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.927-1566G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462460 | |||||||
chr1:24462558 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.927-1468G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462558 | |||||||
chr1:24462565 | G | A | 4 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0072g0039 others(1): Show |
4 | HG02145.hp1 HG03486.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-1461G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462565 | |||||||
chr1:24462692 | G | T | 5 | a0001c0001t0002g0254 a0001c0001t0004g0007 a0001c0001t0004g0255 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.927-1334G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462692 | |||||||
chr1:24462700 | G | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.927-1326G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462700 | |||||||
chr1:24462869 | G | A | 7 | a0001c0001t0017g0153 a0001c0001t0023g0034 a0001c0001t0023g0035 others(4): Show |
7 | HG00639.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.927-1157G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462869 | |||||||
chr1:24462895 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(96): Show |
114 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.927-1131C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462895 | |||||||
chr1:24462983 | TAAAATAC others(9): Show |
T | 4 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0021g0327 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.927-1028_927-1013d others(18): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24462983 | ||||||
chr1:24463124 | G | C | 8 | a0001c0001t0016g0018 a0001c0001t0016g0165 a0001c0001t0016g0166 others(5): Show |
10 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.927-902G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463124 | |||||||
chr1:24463154 | C | A | 1 | a0001c0001t0050g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927-872C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463154 | |||||||
chr1:24463264 | G | C | 1 | a0001c0001t0005g0272 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.927-762G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463264 | |||||||
chr1:24463299 | G | T | 1 | a0001c0001t0002g0299 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.927-727G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463299 | |||||||
chr1:24463363 | G | A | 2 | a0001c0001t0016g0165 a0001c0001t0051g0164 |
2 | HG01255.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.927-663G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463363 | |||||||
chr1:24463472 | G | A | 14 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(11): Show |
14 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.927-554G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463472 | |||||||
chr1:24463519 | A | G | 14 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(11): Show |
14 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.927-507A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463519 | |||||||
chr1:24463576 | C | G | 1 | a0001c0001t0004g0006 | 3 | HG01884.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.927-450C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463576 | |||||||
chr1:24463583 | G | C | 1 | a0001c0002t0002g0060 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.927-443G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463583 | |||||||
chr1:24463651 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.927-375A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463651 | |||||||
chr1:24463681 | G | A | 4 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(1): Show |
4 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-345G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463681 | |||||||
chr1:24463854 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0321 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.927-172C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463854 | |||||||
chr1:24463946 | C | T | 4 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0021g0327 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.927-80C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463946 | |||||||
chr1:24463974 | C | T | 4 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0023g0262 others(1): Show |
4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.927-52C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463974 | |||||||
chr1:24464021 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG01515.hp1 | splice_region_variant&intron_variant | LOW | c.927-5C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24464021 | |||||||
chr1:24464167 | A | C | 1 | a0001c0002t0006g0077 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1021+47A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464167 | |||||||
chr1:24464208 | C | T | 1 | a0001c0001t0054g0326 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1021+88C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464208 | |||||||
chr1:24464221 | G | T | 1 | a0001c0001t0075g0288 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1021+101G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464221 | |||||||
chr1:24464299 | G | A | 1 | a0001c0001t0021g0325 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1021+179G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464299 | |||||||
chr1:24464460 | G | T | 4 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0023g0262 others(1): Show |
4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+340G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464460 | |||||||
chr1:24464550 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1021+430C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464550 | |||||||
chr1:24464934 | T | A | 1 | a0001c0001t0025g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1021+814T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464934 | |||||||
chr1:24464976 | C | T | 1 | a0001c0002t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1021+856C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464976 | |||||||
chr1:24465196 | A | AGTGCATG others(7): Show |
105 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(102): Show |
121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1021+1085_1021+109 others(18): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465196 | ||||||
chr1:24465342 | C | G | 2 | a0001c0001t0011g0145 a0001c0001t0011g0174 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1021+1222C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465342 | |||||||
chr1:24465417 | T | TTG | 4 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0004g0030 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1305_1021+130 others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465417 | ||||||
chr1:24465425 | G | GTA | 24 | a0001c0001t0002g0038 a0001c0001t0002g0057 a0001c0001t0004g0003 others(21): Show |
30 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1021+1322_1021+132 others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465425 | ||||||
chr1:24465425 | G | GTATATA | 4 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0021g0327 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1318_1021+132 others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465425 | ||||||
chr1:24465425 | GTA | G | 8 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(5): Show |
8 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021+1322_1021+132 others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465425 | ||||||
chr1:24465427 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(112): Show |
131 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1021+1307A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465427 | |||||||
chr1:24465441 | A | G | 2 | a0001c0001t0017g0153 a0001c0001t0017g0261 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1021+1321A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465441 | |||||||
chr1:24465617 | C | T | 3 | a0001c0001t0001g0265 a0001c0001t0017g0153 a0001c0001t0017g0261 |
3 | HG01123.hp1 HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1021+1497C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465617 | |||||||
chr1:24465775 | T | A | 4 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0023g0262 others(1): Show |
4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1655T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465775 | |||||||
chr1:24465834 | A | T | 11 | a0001c0001t0004g0003 a0001c0001t0004g0006 a0001c0001t0004g0019 others(8): Show |
17 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1021+1714A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465834 | |||||||
chr1:24465927 | T | C | 2 | a0001c0001t0017g0153 a0001c0001t0017g0261 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1021+1807T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465927 | |||||||
chr1:24466127 | T | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(233): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1021+2007T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466127 | |||||||
chr1:24466164 | C | A | 1 | a0001c0001t0002g0233 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1021+2044C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466164 | |||||||
chr1:24466241 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1021+2121C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466241 | |||||||
chr1:24466285 | A | G | 1 | a0001c0001t0002g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1021+2165A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466285 | |||||||
chr1:24466438 | G | T | 10 | a0001c0001t0016g0018 a0001c0001t0016g0165 a0001c0001t0016g0166 others(7): Show |
12 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021+2318G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466438 | |||||||
chr1:24466473 | C | T | 1 | a0001c0002t0001g0276 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1021+2353C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466473 | |||||||
chr1:24466629 | C | A | 4 | a0001c0001t0013g0190 a0001c0001t0013g0191 a0001c0001t0013g0194 others(1): Show |
4 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-2357C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466629 | |||||||
chr1:24466666 | C | T | 1 | a0001c0001t0068g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1022-2320C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466666 | |||||||
chr1:24466764 | A | G | 1 | a0001c0001t0002g0254 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1022-2222A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466764 | |||||||
chr1:24466795 | T | A | 1 | a0001c0001t0009g0230 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1022-2191T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466795 | |||||||
chr1:24466803 | G | A | 1 | a0001c0002t0003g0123 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1022-2183G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466803 | |||||||
chr1:24466807 | C | A | 2 | a0001c0001t0017g0153 a0001c0001t0017g0261 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1022-2179C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466807 | |||||||
chr1:24466838 | C | T | 14 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(11): Show |
14 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1022-2148C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466838 | |||||||
chr1:24466841 | C | G | 1 | a0001c0001t0002g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1022-2145C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466841 | |||||||
chr1:24466856 | G | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(243): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1022-2130G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466856 | |||||||
chr1:24466933 | A | G | 15 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(12): Show |
15 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1022-2053A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466933 | |||||||
chr1:24466949 | G | A | 1 | a0001c0001t0009g0230 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1022-2037G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466949 | |||||||
chr1:24466978 | C | T | 15 | a0001c0001t0002g0038 a0001c0001t0020g0037 a0001c0001t0020g0155 others(12): Show |
15 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1022-2008C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466978 | |||||||
chr1:24466990 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(238): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1022-1996T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466990 | |||||||
chr1:24467202 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1022-1784G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467202 | |||||||
chr1:24467234 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1022-1752C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467234 | |||||||
chr1:24467307 | CA | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(216): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1022-1666delA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24467307 | ||||||
chr1:24467347 | G | A | 10 | a0001c0002t0001g0015 a0001c0002t0001g0076 a0001c0002t0002g0015 others(7): Show |
10 | HG02132.hp1 HG02135.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1022-1639G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467347 | |||||||
chr1:24467441 | G | T | 2 | a0001c0001t0031g0137 a0001c0001t0031g0140 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1022-1545G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467441 | |||||||
chr1:24467481 | A | T | 70 | a0001c0001t0001g0032 a0001c0001t0001g0321 a0001c0001t0002g0213 others(67): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1022-1505A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467481 | |||||||
chr1:24467520 | C | G | 4 | a0001c0001t0025g0192 a0001c0001t0025g0193 a0001c0001t0034g0323 others(1): Show |
4 | HG01106.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-1466C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467520 | |||||||
chr1:24467529 | T | C | 1 | a0001c0001t0002g0299 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1022-1457T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467529 | |||||||
chr1:24467638 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1022-1348G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467638 | |||||||
chr1:24467912 | T | C | 1 | a0001c0001t0001g0283 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1022-1074T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467912 | |||||||
chr1:24467943 | A | T | 1 | a0001c0002t0001g0277 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1022-1043A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467943 | |||||||
chr1:24468009 | G | A | 1 | a0001c0001t0034g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1022-977G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468009 | |||||||
chr1:24468064 | T | G | 1 | a0001c0002t0001g0136 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1022-922T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468064 | |||||||
chr1:24468071 | T | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0031 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1022-915T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468071 | |||||||
chr1:24468314 | C | CAATA | 11 | a0001c0001t0002g0204 a0001c0001t0004g0031 a0001c0001t0016g0165 others(8): Show |
11 | HG02257.hp2 HG02723.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1022-649_1022-646d others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24468314 | ||||||
chr1:24468352 | C | T | 9 | a0001c0001t0001g0311 a0001c0001t0002g0038 a0001c0001t0020g0037 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-634C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468352 | |||||||
chr1:24468353 | G | A | 4 | a0001c0001t0023g0034 a0001c0001t0023g0035 a0001c0001t0023g0262 others(1): Show |
4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-633G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468353 | |||||||
chr1:24468489 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1022-497T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468489 | |||||||
chr1:24468591 | T | C | 1 | a0001c0001t0052g0173 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1022-395T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468591 | |||||||
chr1:24468604 | G | T | 13 | a0001c0001t0020g0037 a0001c0001t0020g0155 a0001c0001t0020g0156 others(10): Show |
13 | HG01099.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1022-382G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468604 | |||||||
chr1:24468700 | C | T | 1 | a0001c0001t0073g0036 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1022-286C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468700 | |||||||
chr1:24468702 | C | T | 1 | a0001c0002t0003g0073 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1022-284C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468702 | |||||||
chr1:24468855 | A | T | 1 | a0001c0002t0003g0096 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1022-131A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468855 | |||||||
chr1:24468873 | G | T | 1 | a0001c0001t0002g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1022-113G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468873 | |||||||
chr1:24468878 | T | G | 1 | a0001c0001t0002g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1022-108T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468878 | |||||||
chr1:24468882 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1022-104T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468882 | |||||||
chr1:24468906 | C | T | 1 | a0001c0001t0030g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1022-80C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468906 | |||||||
chr1:24468982 | T | A | 1 | a0001c0001t0052g0173 | 1 | HG02809.hp1 | splice_region_variant&intron_variant | LOW | c.1022-4T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468982 |