Item | Value |
---|---|
geneid | 9688 |
ensemblid | ENSG00000102900.13 |
hgncid | 28958 |
symbol | NUP93 |
name | nucleoporin 93 |
refseq_nuc | NM_014669.5 |
refseq_prot | NP_055484.3 |
ensembl_nuc | ENST00000308159.10 |
ensembl_prot | ENSP00000310668.5 |
mane_status | MANE Select |
chr | chr16 |
start | 56730129 |
end | 56850286 |
strand | + |
ver | v1.2 |
region | chr16:56730129-56850286 |
region5000 | chr16:56725129-56855286 |
regionname0 | NUP93_chr16_56730129_56850286 |
regionname5000 | NUP93_chr16_56725129_56855286 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 819 | 366 | 87 | 65 | 161 | 14 | 37 | 118 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0002 | 0/0 | 819 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0003 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0004 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0005 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0006 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0007 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0008 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0009 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
a0010 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | MDTEG others(814): Show |
chr16 | 56725129 | 56855286 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2457 | 189 | 42 | 29 | 88 | 9 | 21 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0002 | 0/0 | 2457 | 68 | 12 | 14 | 32 | 3 | 7 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0003 | 0/1 | 2457 | 42 | 4 | 11 | 24 | 1 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0004 | 1/0 | 2457 | 39 | 4 | 11 | 15 | 1 | 7 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0005 | 0/0 | 2457 | 8 | 8 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0006 | 0/0 | 2457 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0007 | 0/0 | 2457 | 4 | 4 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0009 | 0/0 | 2457 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0010 | 0/0 | 2457 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0011 | 0/0 | 2457 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0012 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0014 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0016 | 0/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0017 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0001c0019 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0002c0008 | 0/0 | 2457 | 4 | 0 | 0 | 4 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0003c0015 | 0/0 | 2457 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0004c0022 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0005c0024 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0006c0020 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0007c0013 | 0/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0008c0023 | 0/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0009c0021 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 | ||
a0010c0018 | 0/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | ATGGA others(2452): Show |
chr16 | 56725129 | 56855286 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8235 | 86 | 15 | 8 | 45 | 7 | 11 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0002 | 0/0 | 8235 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0003 | 0/0 | 8207 | 26 | 2 | 10 | 11 | 1 | 2 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8202): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0004 | 0/0 | 8235 | 21 | 1 | 4 | 16 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0006 | 0/0 | 8235 | 19 | 4 | 5 | 6 | 1 | 3 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0007 | 0/0 | 8209 | 3 | 0 | 2 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8204): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0011 | 0/0 | 8235 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0013 | 0/0 | 8235 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0014 | 0/0 | 8235 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0016 | 0/0 | 8209 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8204): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0017 | 0/0 | 8235 | 3 | 0 | 0 | 3 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0023 | 0/0 | 8235 | 2 | 0 | 0 | 2 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0025 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0027 | 0/0 | 8207 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8202): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0028 | 0/0 | 8207 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8202): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0029 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0031 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0034 | 0/0 | 8209 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8204): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0035 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0036 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0038 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0039 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0043 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0001t0046 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0002t0001 | 0/0 | 8235 | 60 | 11 | 8 | 32 | 3 | 6 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0002t0010 | 0/0 | 8235 | 5 | 0 | 5 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0002t0037 | 0/0 | 8235 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0002t0040 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0002t0041 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0003t0002 | 0/1 | 8235 | 35 | 4 | 9 | 20 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0003t0020 | 0/0 | 8235 | 2 | 0 | 2 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0003t0021 | 0/0 | 8235 | 2 | 0 | 0 | 2 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0003t0030 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0003t0032 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0003t0042 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0004t0005 | 0/0 | 8230 | 22 | 0 | 6 | 15 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8225): Show |
chr16 | 56725129 | 56855286 |
a0001c0004t0008 | 0/0 | 8234 | 7 | 1 | 3 | 0 | 0 | 3 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8229): Show |
chr16 | 56725129 | 56855286 |
a0001c0004t0015 | 0/0 | 8235 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0004t0019 | 1/0 | 8234 | 3 | 0 | 0 | 0 | 0 | 2 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8229): Show |
chr16 | 56725129 | 56855286 |
a0001c0004t0024 | 0/0 | 8234 | 2 | 0 | 2 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8229): Show |
chr16 | 56725129 | 56855286 |
a0001c0004t0044 | 0/0 | 8234 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8229): Show |
chr16 | 56725129 | 56855286 |
a0001c0004t0045 | 0/0 | 8234 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8229): Show |
chr16 | 56725129 | 56855286 |
a0001c0005t0007 | 0/0 | 8209 | 8 | 8 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8204): Show |
chr16 | 56725129 | 56855286 |
a0001c0006t0009 | 0/0 | 8236 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8231): Show |
chr16 | 56725129 | 56855286 |
a0001c0007t0012 | 0/0 | 8235 | 4 | 4 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0009t0018 | 0/0 | 8235 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0010t0022 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0010t0033 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0011t0001 | 0/0 | 8235 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0012t0001 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0014t0001 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0016t0001 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0017t0001 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0001c0019t0001 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0002c0008t0002 | 0/0 | 8235 | 4 | 0 | 0 | 4 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0003c0015t0004 | 0/0 | 8235 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0004c0022t0022 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0005c0024t0018 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0006c0020t0001 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0007c0013t0007 | 0/0 | 8209 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8204): Show |
chr16 | 56725129 | 56855286 |
a0008c0023t0026 | 0/0 | 8207 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8202): Show |
chr16 | 56725129 | 56855286 |
a0009c0021t0001 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
a0010c0018t0004 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | AGGAA others(8230): Show |
chr16 | 56725129 | 56855286 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0003g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0007g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0014g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0014g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0016g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0016g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0017g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0017g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0017g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0023g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0023g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0025g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0027g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0028g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0029g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0031g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0034g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0035g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0036g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0038g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0039g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0043g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0001t0046g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0010g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0010g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0010g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0037g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0040g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0002t0041g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0020g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0020g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0021g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0021g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0030g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0032g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0003t0042g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0008g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0008g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0008g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0015g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0019g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0019g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0019g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0024g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0024g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0044g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0004t0045g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0005t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0005t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0005t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0005t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0005t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0005t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0005t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0005t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0006t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0006t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0006t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0006t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0006t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0007t0012g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0007t0012g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0007t0012g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0007t0012g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0009t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0009t0018g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0010t0022g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0010t0033g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0011t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0011t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0012t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0014t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0016t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0017t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0001c0019t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0002c0008t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0002c0008t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0002c0008t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0002c0008t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0003c0015t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0004c0022t0022g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0005c0024t0018g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0006c0020t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0007c0013t0007g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0008c0023t0026g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0009c0021t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
a0010c0018t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00099 | hp2 | a0001 | c0004 | t0044 | g0179 | EUR | GBR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0110 | EUR | GBR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0303 | EUR | GBR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0365 | EUR | FIN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0072 | EUR | FIN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00423 | hp1 | a0001 | c0003 | t0021 | g0260 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00423 | hp2 | a0001 | c0004 | t0005 | g0045 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00438 | hp2 | a0001 | c0004 | t0005 | g0042 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00544 | hp2 | a0001 | c0003 | t0002 | g0286 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00558 | hp2 | a0001 | c0004 | t0005 | g0039 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00597 | hp1 | a0001 | c0003 | t0002 | g0291 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00621 | hp2 | a0001 | c0001 | t0017 | g0305 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0363 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00639 | hp2 | a0001 | c0004 | t0024 | g0041 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00673 | hp1 | a0001 | c0003 | t0002 | g0288 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00733 | hp2 | a0001 | c0002 | t0010 | g0113 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00741 | hp1 | a0001 | c0004 | t0008 | g0002 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG00741 | hp2 | a0001 | c0004 | t0005 | g0036 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01069 | hp1 | a0001 | c0003 | t0002 | g0256 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01069 | hp2 | a0001 | c0002 | t0010 | g0051 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0350 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0212 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0349 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01071 | hp2 | a0001 | c0003 | t0002 | g0255 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0364 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01099 | hp1 | a0001 | c0003 | t0002 | g0278 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01099 | hp2 | a0001 | c0004 | t0005 | g0032 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01106 | hp1 | a0001 | c0004 | t0008 | g0175 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0340 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0253 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01167 | hp1 | a0001 | c0002 | t0010 | g0050 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0374 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01168 | hp1 | a0001 | c0003 | t0020 | g0295 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0216 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01169 | hp1 | a0001 | c0003 | t0020 | g0281 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0373 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0279 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0210 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01243 | hp2 | a0001 | c0003 | t0002 | g0262 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01255 | hp1 | a0001 | c0002 | t0010 | g0052 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0211 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01258 | hp2 | a0001 | c0004 | t0008 | g0177 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01261 | hp1 | a0001 | c0004 | t0005 | g0037 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01261 | hp2 | a0001 | c0003 | t0002 | g0246 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01346 | hp1 | a0001 | c0004 | t0005 | g0035 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01346 | hp2 | a0001 | c0002 | t0010 | g0114 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01358 | hp1 | a0001 | c0004 | t0024 | g0044 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0348 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0220 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0234 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0213 | EUR | IBS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01884 | hp1 | a0001 | c0001 | t0011 | g0007 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01884 | hp2 | a0001 | c0001 | t0014 | g0217 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01891 | hp1 | a0001 | c0007 | t0012 | g0067 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0264 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0215 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0361 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01978 | hp2 | a0003 | c0015 | t0004 | g0233 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01981 | hp1 | a0001 | c0002 | t0037 | g0086 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0360 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01993 | hp1 | a0001 | c0004 | t0005 | g0033 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02015 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0344 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02027 | hp1 | a0001 | c0001 | t0028 | g0358 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02056 | hp1 | a0001 | c0003 | t0002 | g0289 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02074 | hp2 | a0001 | c0003 | t0021 | g0292 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02080 | hp2 | a0001 | c0003 | t0032 | g0269 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0204 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02132 | hp2 | a0004 | c0022 | t0022 | g0252 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02145 | hp1 | a0001 | c0001 | t0029 | g0243 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02145 | hp2 | a0001 | c0007 | t0012 | g0345 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0362 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02155 | hp1 | a0001 | c0003 | t0002 | g0276 | EAS | CDX | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CDX | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | CDX | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02257 | hp2 | a0001 | c0005 | t0007 | g0183 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02258 | hp2 | a0001 | c0001 | t0016 | g0193 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02293 | hp2 | a0001 | c0004 | t0005 | g0034 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0287 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02451 | hp2 | a0005 | c0024 | t0018 | g0012 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02572 | hp2 | a0001 | c0001 | t0034 | g0196 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02602 | hp1 | a0001 | c0004 | t0045 | g0182 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0271 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02615 | hp2 | a0001 | c0006 | t0009 | g0248 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0283 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02630 | hp1 | a0001 | c0001 | t0011 | g0011 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02630 | hp2 | a0001 | c0003 | t0002 | g0275 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02698 | hp1 | a0001 | c0004 | t0008 | g0174 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02717 | hp2 | a0001 | c0005 | t0007 | g0188 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0194 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0353 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02809 | hp2 | a0001 | c0005 | t0007 | g0185 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02818 | hp1 | a0001 | c0004 | t0015 | g0019 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02818 | hp2 | a0001 | c0006 | t0009 | g0250 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02886 | hp2 | a0001 | c0007 | t0012 | g0347 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02895 | hp1 | a0001 | c0011 | t0001 | g0091 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02895 | hp2 | a0001 | c0014 | t0001 | g0139 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02896 | hp1 | a0001 | c0005 | t0007 | g0197 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02896 | hp2 | a0001 | c0006 | t0009 | g0251 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02897 | hp1 | a0001 | c0006 | t0009 | g0249 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02897 | hp2 | a0001 | c0011 | t0001 | g0092 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02922 | hp1 | a0001 | c0005 | t0007 | g0187 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02965 | hp1 | a0006 | c0020 | t0001 | g0065 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02965 | hp2 | a0001 | c0004 | t0015 | g0018 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02970 | hp1 | a0001 | c0002 | t0040 | g0099 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03017 | hp2 | a0001 | c0004 | t0005 | g0023 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0015 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03041 | hp2 | a0001 | c0005 | t0007 | g0189 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03130 | hp2 | a0001 | c0001 | t0016 | g0191 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03139 | hp1 | a0001 | c0003 | t0002 | g0280 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03139 | hp2 | a0001 | c0010 | t0022 | g0258 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0241 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03209 | hp1 | a0001 | c0009 | t0018 | g0020 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0016 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0214 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03239 | hp2 | a0001 | c0001 | t0036 | g0150 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03453 | hp1 | a0001 | c0001 | t0014 | g0219 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03453 | hp2 | a0001 | c0005 | t0007 | g0184 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03486 | hp1 | a0001 | c0007 | t0012 | g0346 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03491 | hp1 | a0001 | c0004 | t0019 | g0180 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0203 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0208 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03516 | hp2 | a0001 | c0009 | t0018 | g0021 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03540 | hp2 | a0001 | c0017 | t0001 | g0160 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03579 | hp1 | a0001 | c0010 | t0033 | g0259 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03654 | hp2 | a0001 | c0002 | t0041 | g0115 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03669 | hp2 | a0001 | c0004 | t0008 | g0176 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03688 | hp1 | a0007 | c0013 | t0007 | g0190 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03704 | hp1 | a0001 | c0016 | t0001 | g0119 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03704 | hp2 | a0001 | c0004 | t0008 | g0178 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03834 | hp2 | a0001 | c0003 | t0002 | g0049 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03927 | hp1 | a0001 | c0004 | t0019 | g0181 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03942 | hp2 | a0001 | c0001 | t0027 | g0369 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG04184 | hp2 | a0001 | c0001 | t0043 | g0156 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG04199 | hp2 | a0001 | c0001 | t0031 | g0209 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG04204 | hp2 | a0008 | c0023 | t0026 | g0370 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18522 | hp2 | a0009 | c0021 | t0001 | g0013 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18612 | hp1 | a0001 | c0003 | t0002 | g0261 | EAS | CHB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18612 | hp2 | a0001 | c0004 | t0005 | g0027 | EAS | CHB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | CHB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0206 | EAS | CHB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18906 | hp1 | a0001 | c0004 | t0015 | g0017 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18906 | hp2 | a0001 | c0001 | t0013 | g0014 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18939 | hp1 | a0001 | c0003 | t0002 | g0244 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18940 | hp1 | a0001 | c0003 | t0002 | g0245 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18941 | hp1 | a0001 | c0001 | t0035 | g0003 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18941 | hp2 | a0001 | c0003 | t0002 | g0274 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0366 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18942 | hp2 | a0001 | c0003 | t0002 | g0273 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18943 | hp1 | a0001 | c0004 | t0005 | g0038 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18945 | hp1 | a0001 | c0003 | t0002 | g0266 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18946 | hp1 | a0001 | c0001 | t0039 | g0317 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18948 | hp2 | a0001 | c0004 | t0005 | g0028 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18949 | hp2 | a0001 | c0003 | t0002 | g0254 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18951 | hp1 | a0001 | c0004 | t0005 | g0026 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0368 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18954 | hp1 | a0002 | c0008 | t0002 | g0296 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0371 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18966 | hp1 | a0002 | c0008 | t0002 | g0297 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18967 | hp1 | a0001 | c0004 | t0005 | g0040 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18969 | hp1 | a0001 | c0001 | t0017 | g0342 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18971 | hp2 | a0001 | c0004 | t0005 | g0029 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18972 | hp1 | a0001 | c0004 | t0005 | g0030 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18977 | hp2 | a0001 | c0004 | t0005 | g0022 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18981 | hp2 | a0001 | c0003 | t0002 | g0294 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18983 | hp1 | a0001 | c0003 | t0002 | g0263 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18988 | hp1 | a0001 | c0001 | t0038 | g0152 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18988 | hp2 | a0001 | c0004 | t0005 | g0024 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18989 | hp1 | a0001 | c0004 | t0005 | g0043 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18991 | hp1 | a0001 | c0001 | t0023 | g0329 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19000 | hp2 | a0001 | c0003 | t0002 | g0285 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19001 | hp1 | a0001 | c0003 | t0002 | g0267 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19011 | hp2 | a0001 | c0001 | t0017 | g0341 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19012 | hp1 | a0001 | c0003 | t0002 | g0270 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19057 | hp2 | a0001 | c0001 | t0025 | g0310 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19066 | hp1 | a0001 | c0012 | t0001 | g0081 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19066 | hp2 | a0001 | c0003 | t0002 | g0265 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19068 | hp2 | a0001 | c0001 | t0023 | g0330 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19070 | hp2 | a0001 | c0003 | t0030 | g0272 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19074 | hp1 | a0001 | c0003 | t0002 | g0277 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0355 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19079 | hp1 | a0001 | c0004 | t0005 | g0031 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19079 | hp2 | a0002 | c0008 | t0002 | g0298 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19081 | hp1 | a0001 | c0004 | t0005 | g0025 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19081 | hp2 | a0001 | c0003 | t0002 | g0268 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19087 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19087 | hp2 | a0001 | c0019 | t0001 | g0080 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19090 | hp1 | a0002 | c0008 | t0002 | g0299 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0199 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | ASW | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | ASW | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20752 | hp1 | a0001 | c0003 | t0042 | g0284 | EUR | TSI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | TSI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | TSI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20905 | hp2 | a0010 | c0018 | t0004 | g0226 | SAS | GIH | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02109 | hp2 | a0001 | c0006 | t0009 | g0247 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG02559 | hp2 | a0001 | c0005 | t0007 | g0186 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03471 | hp1 | a0001 | c0001 | t0046 | g0010 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0359 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG06807 | hp1 | a0001 | c0004 | t0008 | g0002 | AFR | USA | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | USA | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | USA | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA20300 | hp2 | a0001 | c0001 | t0016 | g0192 | AFR | USA | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA21309 | hp1 | a0001 | c0001 | t0014 | g0218 | AFR | LWK | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0257 | REF | REF | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
homoSapiens | grch38p0 | a0001 | c0004 | t0019 | g0173 | REF | REF | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:56748383 | C | T | 1 | a0005 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.136C>T | p.Arg46Cys | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/22 | 233/8234 | 136/2460 | 46/819 | chr16 | 56748383 | |||
chr16:56758644 | A | G | 1 | a0008 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.286A>G | p.Thr96Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/22 | 383/8234 | 286/2460 | 96/819 | chr16 | 56758644 | |||
chr16:56821545 | G | C | 1 | a0004 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.606G>C | p.Gln202His | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/22 | 703/8234 | 606/2460 | 202/819 | chr16 | 56821545 | |||
chr16:56823768 | C | T | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.716C>T | p.Thr239Met | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/22 | 813/8234 | 716/2460 | 239/819 | chr16 | 56823768 | |||
chr16:56823842 | C | G | 1 | a0006 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.790C>G | p.Gln264Glu | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/22 | 887/8234 | 790/2460 | 264/819 | chr16 | 56823842 | |||
chr16:56830600 | G | A | 1 | a0007 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1000G>A | p.Ala334Thr | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/22 | 1097/8234 | 1000/2460 | 334/819 | chr16 | 56830600 | |||
chr16:56831966 | A | G | 1 | a0010 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1210A>G | p.Ser404Gly | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 11/22 | 1307/8234 | 1210/2460 | 404/819 | chr16 | 56831966 | |||
chr16:56836715 | A | C | 1 | a0002 | 4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1897A>C | p.Lys633Gln | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/22 | 1994/8234 | 1897/2460 | 633/819 | chr16 | 56836715 | |||
chr16:56837649 | C | A | 1 | a0003 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1941C>A | p.Ser647Arg | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/22 | 2038/8234 | 1941/2460 | 647/819 | chr16 | 56837649 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:56748364 | G | A | 1 | a0001c0006 | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.117G>A | p.Ala39Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/22 | 214/8234 | 117/2460 | 39/819 | chr16 | 56748364 | |||
chr16:56805527 | C | T | 3 | a0001c0003 a0002c0008 a0004c0022 |
46 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(43): Show |
synonymous_variant | LOW | c.384C>T | p.Tyr128Tyr | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/22 | 481/8234 | 384/2460 | 128/819 | chr16 | 56805527 | |||
chr16:56818732 | G | A | 1 | a0001c0005 | 8 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.558G>A | p.Ala186Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/22 | 655/8234 | 558/2460 | 186/819 | chr16 | 56818732 | |||
chr16:56821584 | C | G | 21 | a0001c0001 a0001c0002 a0001c0003 others(18): Show |
335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
synonymous_variant | LOW | c.645C>G | p.Leu215Leu | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/22 | 742/8234 | 645/2460 | 215/819 | chr16 | 56821584 | |||
chr16:56823748 | C | T | 1 | a0001c0011 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.696C>T | p.Asp232Asp | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/22 | 793/8234 | 696/2460 | 232/819 | chr16 | 56823748 | |||
chr16:56823841 | G | A | 1 | a0001c0007 | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.789G>A | p.Glu263Glu | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/22 | 886/8234 | 789/2460 | 263/819 | chr16 | 56823841 | |||
chr16:56830560 | G | A | 1 | a0001c0012 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.960G>A | p.Ala320Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/22 | 1057/8234 | 960/2460 | 320/819 | chr16 | 56830560 | |||
chr16:56831956 | C | T | 1 | a0001c0019 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.1200C>T | p.Thr400Thr | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 11/22 | 1297/8234 | 1200/2460 | 400/819 | chr16 | 56831956 | |||
chr16:56832315 | C | T | 1 | a0001c0017 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1272C>T | p.Asp424Asp | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/22 | 1369/8234 | 1272/2460 | 424/819 | chr16 | 56832315 | |||
chr16:56833279 | G | A | 1 | a0001c0014 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1410G>A | p.Ala470Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/22 | 1507/8234 | 1410/2460 | 470/819 | chr16 | 56833279 | |||
chr16:56833348 | A | G | 1 | a0001c0010 | 2 | HG03139.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.1479A>G | p.Ala493Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/22 | 1576/8234 | 1479/2460 | 493/819 | chr16 | 56833348 | |||
chr16:56834397 | C | T | 2 | a0001c0009 a0005c0024 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1692C>T | p.Asn564Asn | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 15/22 | 1789/8234 | 1692/2460 | 564/819 | chr16 | 56834397 | |||
chr16:56839583 | C | T | 5 | a0001c0002 a0001c0011 a0001c0012 others(2): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
synonymous_variant | LOW | c.2199C>T | p.Ala733Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/22 | 2296/8234 | 2199/2460 | 733/819 | chr16 | 56839583 | |||
chr16:56844549 | A | G | 1 | a0001c0016 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2400A>G | p.Pro800Pro | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2497/8234 | 2400/2460 | 800/819 | chr16 | 56844549 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:56730172 | C | G | 2 | a0001c0001t0011 a0001c0001t0046 |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/22 | chr16 | 56730172 | |||||||
chr16:56844630 | C | G | 1 | a0001c0004t0045 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 21 | chr16 | 56844630 | ||||||
chr16:56844637 | G | A | 2 | a0001c0001t0011 a0001c0001t0046 |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 28 | chr16 | 56844637 | ||||||
chr16:56844729 | T | C | 1 | a0001c0001t0025 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 120 | chr16 | 56844729 | ||||||
chr16:56844802 | T | TC | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(55): Show |
363 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*194dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 195 | INFO_REALIGN_3_PRIME | chr16 | 56844802 | |||||
chr16:56844823 | T | C | 1 | a0001c0001t0013 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*214T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 214 | chr16 | 56844823 | ||||||
chr16:56845150 | A | G | 2 | a0001c0001t0011 a0001c0001t0046 |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*541A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 541 | chr16 | 56845150 | ||||||
chr16:56845284 | A | G | 1 | a0001c0001t0043 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 675 | chr16 | 56845284 | ||||||
chr16:56845290 | T | C | 4 | a0001c0001t0003 a0001c0001t0027 a0001c0001t0028 others(1): Show |
29 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*681T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 681 | chr16 | 56845290 | ||||||
chr16:56845302 | C | T | 2 | a0001c0009t0018 a0005c0024t0018 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 693 | chr16 | 56845302 | ||||||
chr16:56845350 | C | A | 1 | a0001c0003t0020 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*741C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 741 | chr16 | 56845350 | ||||||
chr16:56845364 | C | T | 1 | a0001c0003t0042 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 755 | chr16 | 56845364 | ||||||
chr16:56845409 | C | T | 1 | a0001c0002t0041 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*800C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 800 | chr16 | 56845409 | ||||||
chr16:56845413 | C | T | 1 | a0001c0001t0023 | 2 | NA18991.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*804C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 804 | chr16 | 56845413 | ||||||
chr16:56845516 | C | A | 1 | a0001c0001t0014 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*907C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 907 | chr16 | 56845516 | ||||||
chr16:56845559 | G | T | 2 | a0001c0009t0018 a0005c0024t0018 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 950 | chr16 | 56845559 | ||||||
chr16:56845620 | G | A | 1 | a0001c0001t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1011G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1011 | chr16 | 56845620 | ||||||
chr16:56845659 | G | C | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(38): Show |
201 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1050G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1050 | chr16 | 56845659 | ||||||
chr16:56845726 | G | C | 7 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0027 others(4): Show |
41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1117G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1117 | chr16 | 56845726 | ||||||
chr16:56845948 | C | G | 4 | a0001c0001t0004 a0001c0001t0035 a0003c0015t0004 others(1): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1339C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1339 | chr16 | 56845948 | ||||||
chr16:56846187 | GATCACC | G | 9 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0016 others(6): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1579_*1584delATCA others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1579 | chr16 | 56846187 | ||||||
chr16:56846236 | C | T | 1 | a0001c0001t0034 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1627C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1627 | chr16 | 56846236 | ||||||
chr16:56846239 | C | T | 1 | a0001c0007t0012 | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1630C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1630 | chr16 | 56846239 | ||||||
chr16:56846246 | A | G | 22 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0023 others(19): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1637A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1637 | chr16 | 56846246 | ||||||
chr16:56846493 | T | C | 9 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0016 others(6): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1884T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1884 | chr16 | 56846493 | ||||||
chr16:56846497 | G | T | 1 | a0001c0001t0035 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1888 | chr16 | 56846497 | ||||||
chr16:56846536 | C | T | 2 | a0001c0001t0011 a0001c0001t0046 |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1927C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1927 | chr16 | 56846536 | ||||||
chr16:56846659 | G | A | 1 | a0001c0001t0029 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2050 | chr16 | 56846659 | ||||||
chr16:56846700 | G | T | 2 | a0001c0009t0018 a0005c0024t0018 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2091G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2091 | chr16 | 56846700 | ||||||
chr16:56846924 | C | G | 1 | a0001c0001t0028 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2315C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2315 | chr16 | 56846924 | ||||||
chr16:56846925 | T | G | 1 | a0001c0001t0028 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2316T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2316 | chr16 | 56846925 | ||||||
chr16:56846930 | T | C | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*2321T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2321 | chr16 | 56846930 | ||||||
chr16:56846969 | AGGTTCTT others(13): Show |
A | 9 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0016 others(6): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2364_*2383delTCTT others(16): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2364 | INFO_REALIGN_3_PRIME | chr16 | 56846969 | |||||
chr16:56847045 | G | A | 1 | a0001c0001t0016 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2436G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2436 | chr16 | 56847045 | ||||||
chr16:56847363 | A | G | 1 | a0001c0010t0033 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2754A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2754 | chr16 | 56847363 | ||||||
chr16:56847375 | C | T | 1 | a0001c0003t0032 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2766C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2766 | chr16 | 56847375 | ||||||
chr16:56847479 | A | G | 4 | a0001c0004t0005 a0001c0004t0015 a0001c0009t0018 others(1): Show |
28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2870A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2870 | chr16 | 56847479 | ||||||
chr16:56847518 | C | G | 1 | a0001c0002t0040 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2909C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2909 | chr16 | 56847518 | ||||||
chr16:56847732 | T | A | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*3123T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3123 | chr16 | 56847732 | ||||||
chr16:56847804 | C | T | 1 | a0001c0001t0031 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3195C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3195 | chr16 | 56847804 | ||||||
chr16:56847822 | G | A | 1 | a0001c0003t0021 | 2 | HG00423.hp1 HG02074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3213G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3213 | chr16 | 56847822 | ||||||
chr16:56847829 | C | G | 1 | a0001c0001t0027 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3220C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3220 | chr16 | 56847829 | ||||||
chr16:56847948 | A | G | 1 | a0001c0001t0013 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3339A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3339 | chr16 | 56847948 | ||||||
chr16:56848237 | G | C | 2 | a0001c0001t0011 a0001c0001t0046 |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3628G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3628 | chr16 | 56848237 | ||||||
chr16:56848277 | C | G | 1 | a0001c0006t0009 | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3668C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3668 | chr16 | 56848277 | ||||||
chr16:56848298 | G | A | 1 | a0001c0004t0044 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3689G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3689 | chr16 | 56848298 | ||||||
chr16:56848313 | G | T | 1 | a0008c0023t0026 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3704G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3704 | chr16 | 56848313 | ||||||
chr16:56848649 | A | G | 1 | a0001c0001t0029 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4040A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4040 | chr16 | 56848649 | ||||||
chr16:56848891 | G | GT | 1 | a0001c0006t0009 | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4289dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4290 | INFO_REALIGN_3_PRIME | chr16 | 56848891 | |||||
chr16:56848952 | AAG | A | 4 | a0001c0001t0003 a0001c0001t0027 a0001c0001t0028 others(1): Show |
29 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4346_*4347delAG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4346 | INFO_REALIGN_3_PRIME | chr16 | 56848952 | |||||
chr16:56848958 | A | G | 1 | a0001c0006t0009 | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4349A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4349 | chr16 | 56848958 | ||||||
chr16:56849027 | C | G | 1 | a0001c0001t0017 | 3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4418C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4418 | chr16 | 56849027 | ||||||
chr16:56849057 | T | C | 1 | a0001c0001t0014 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4448T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4448 | chr16 | 56849057 | ||||||
chr16:56849063 | G | A | 1 | a0001c0001t0029 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4454G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4454 | chr16 | 56849063 | ||||||
chr16:56849172 | T | C | 4 | a0001c0001t0004 a0001c0001t0035 a0003c0015t0004 others(1): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4563T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4563 | chr16 | 56849172 | ||||||
chr16:56849350 | C | T | 1 | a0001c0001t0039 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4741C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4741 | chr16 | 56849350 | ||||||
chr16:56849393 | A | G | 1 | a0001c0001t0038 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4784A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4784 | chr16 | 56849393 | ||||||
chr16:56849510 | G | A | 1 | a0001c0001t0036 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4901G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4901 | chr16 | 56849510 | ||||||
chr16:56849522 | T | A | 1 | a0001c0002t0037 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4913T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4913 | chr16 | 56849522 | ||||||
chr16:56849526 | G | A | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0013 others(37): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*4917G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4917 | chr16 | 56849526 | ||||||
chr16:56849574 | G | C | 1 | a0008c0023t0026 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4965G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4965 | chr16 | 56849574 | ||||||
chr16:56849623 | G | C | 4 | a0001c0001t0004 a0001c0001t0035 a0003c0015t0004 others(1): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5014G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5014 | chr16 | 56849623 | ||||||
chr16:56849649 | GACACT | G | 1 | a0001c0004t0005 | 22 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5041_*5045delACAC others(1): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5041 | chr16 | 56849649 | ||||||
chr16:56849748 | C | T | 2 | a0001c0002t0010 a0001c0002t0041 |
6 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5139C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5139 | chr16 | 56849748 | ||||||
chr16:56849792 | C | T | 3 | a0001c0002t0010 a0001c0002t0041 a0001c0003t0030 |
7 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5183C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5183 | chr16 | 56849792 | ||||||
chr16:56849797 | G | C | 21 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0023 others(18): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*5188G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5188 | chr16 | 56849797 | ||||||
chr16:56850012 | A | G | 21 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0023 others(18): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*5403A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5403 | chr16 | 56850012 | ||||||
chr16:56850169 | G | C | 9 | a0001c0001t0002 a0001c0003t0002 a0001c0003t0020 others(6): Show |
50 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5560G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5560 | chr16 | 56850169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:56730269 | C | A | 1 | a0001c0001t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-15+58C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730269 | |||||||
chr16:56730563 | A | G | 28 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(25): Show |
29 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15+352A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730563 | |||||||
chr16:56730566 | C | T | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+355C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730566 | |||||||
chr16:56730648 | C | T | 1 | a0001c0002t0001g0344 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+437C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730648 | |||||||
chr16:56730749 | A | T | 1 | a0001c0001t0001g0343 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-15+538A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730749 | |||||||
chr16:56730773 | C | T | 2 | a0001c0001t0017g0341 a0001c0001t0017g0342 |
2 | NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-15+562C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730773 | |||||||
chr16:56730971 | C | T | 1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-15+760C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730971 | |||||||
chr16:56731087 | A | G | 1 | a0001c0002t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-15+876A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731087 | |||||||
chr16:56731168 | C | T | 97 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(94): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-15+957C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731168 | |||||||
chr16:56731191 | T | C | 271 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(268): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.-15+980T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731191 | |||||||
chr16:56731202 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15+991C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731202 | |||||||
chr16:56731314 | C | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(165): Show |
169 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-15+1103C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731314 | |||||||
chr16:56731434 | C | T | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+1223C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731434 | |||||||
chr16:56731650 | C | T | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-15+1439C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731650 | |||||||
chr16:56731774 | A | T | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-15+1563A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731774 | |||||||
chr16:56731890 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-15+1679C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731890 | |||||||
chr16:56731915 | A | G | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02155.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-15+1704A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731915 | |||||||
chr16:56732036 | G | A | 1 | a0001c0002t0001g0046 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-15+1825G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732036 | |||||||
chr16:56732119 | T | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-15+1908T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732119 | |||||||
chr16:56732146 | C | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15+1935C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732146 | |||||||
chr16:56732522 | G | A | 1 | a0005c0024t0018g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15+2311G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732522 | |||||||
chr16:56732576 | C | T | 3 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0002t0001g0170 |
3 | HG00408.hp1 HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-15+2365C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732576 | |||||||
chr16:56732581 | A | G | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+2370A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732581 | |||||||
chr16:56732622 | C | T | 1 | a0001c0002t0001g0169 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-15+2411C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732622 | |||||||
chr16:56732692 | G | A | 1 | a0001c0001t0001g0337 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-15+2481G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732692 | |||||||
chr16:56732919 | C | T | 92 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(89): Show |
93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.-15+2708C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732919 | |||||||
chr16:56733179 | G | A | 44 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(41): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+2968G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733179 | |||||||
chr16:56733213 | T | A | 44 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(41): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+3002T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733213 | |||||||
chr16:56733369 | G | A | 2 | a0001c0003t0002g0244 a0001c0003t0002g0245 |
2 | NA18939.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.-15+3158G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733369 | |||||||
chr16:56733424 | AAGTAGAG others(1): Show |
A | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+3214_-15+3221d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733424 | |||||||
chr16:56733469 | G | A | 1 | a0001c0003t0002g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-15+3258G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733469 | |||||||
chr16:56733687 | G | T | 97 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(94): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-15+3476G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733687 | |||||||
chr16:56733873 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-15+3662G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733873 | |||||||
chr16:56733890 | C | T | 44 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(41): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+3679C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733890 | |||||||
chr16:56733900 | A | C | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-15+3689A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733900 | |||||||
chr16:56733916 | T | A | 1 | a0001c0006t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-15+3705T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733916 | |||||||
chr16:56734635 | CAT | C | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-15+4425_-15+4426d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56734635 | |||||||
chr16:56734967 | G | A | 1 | a0001c0001t0003g0348 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-15+4756G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56734967 | |||||||
chr16:56735103 | A | G | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-15+4892A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735103 | |||||||
chr16:56735193 | G | C | 2 | a0001c0001t0003g0349 a0001c0001t0003g0350 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-15+4982G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735193 | |||||||
chr16:56735543 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-15+5332C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735543 | |||||||
chr16:56735549 | A | C | 4 | a0002c0008t0002g0296 a0002c0008t0002g0297 a0002c0008t0002g0298 others(1): Show |
4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5338A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735549 | |||||||
chr16:56735582 | C | T | 1 | a0001c0001t0001g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-15+5371C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735582 | |||||||
chr16:56735721 | G | C | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-15+5510G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735721 | |||||||
chr16:56735828 | C | CA | 134 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(131): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-15+5632dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56735828 | ||||||
chr16:56735828 | C | CAA | 7 | a0001c0002t0001g0053 a0001c0002t0001g0169 a0001c0002t0010g0050 others(4): Show |
7 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+5631_-15+5632d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56735828 | ||||||
chr16:56735828 | CA | C | 6 | a0001c0001t0001g0333 a0001c0001t0003g0373 a0001c0001t0003g0374 others(3): Show |
6 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+5632delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56735828 | ||||||
chr16:56735990 | A | G | 52 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(49): Show |
52 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-15+5779A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735990 | |||||||
chr16:56736059 | G | T | 1 | a0001c0002t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-15+5848G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736059 | |||||||
chr16:56736081 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-15+5870G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736081 | |||||||
chr16:56736166 | C | T | 1 | a0001c0002t0001g0166 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-15+5955C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736166 | |||||||
chr16:56736186 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-15+5975C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736186 | |||||||
chr16:56736258 | G | A | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15+6047G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736258 | |||||||
chr16:56736328 | A | G | 1 | a0001c0004t0005g0045 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-15+6117A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736328 | |||||||
chr16:56736615 | G | T | 1 | a0001c0004t0005g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-15+6404G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736615 | |||||||
chr16:56736735 | G | A | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+6524G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736735 | |||||||
chr16:56736739 | A | C | 2 | a0001c0007t0012g0346 a0001c0007t0012g0347 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+6528A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736739 | |||||||
chr16:56737397 | T | C | 1 | a0001c0007t0012g0346 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+7186T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56737397 | |||||||
chr16:56737531 | A | G | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+7320A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56737531 | |||||||
chr16:56737613 | C | A | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-15+7402C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56737613 | |||||||
chr16:56737622 | CT | C | 215 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.-15+7423delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56737622 | ||||||
chr16:56737720 | CTG | C | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+7516_-15+7517d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56737720 | ||||||
chr16:56737879 | T | C | 68 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(65): Show |
69 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.-15+7668T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56737879 | |||||||
chr16:56738245 | T | C | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-15+8034T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738245 | |||||||
chr16:56738340 | T | C | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15+8129T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738340 | |||||||
chr16:56738428 | T | G | 14 | a0001c0004t0005g0024 a0001c0004t0005g0025 a0001c0004t0005g0026 others(11): Show |
14 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+8217T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738428 | |||||||
chr16:56738485 | T | C | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-15+8274T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738485 | |||||||
chr16:56738541 | T | C | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.-15+8330T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738541 | |||||||
chr16:56738600 | A | G | 1 | a0001c0009t0018g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+8389A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738600 | |||||||
chr16:56738643 | CAAT | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+8433_-15+8435d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738643 | |||||||
chr16:56738672 | T | G | 3 | a0001c0005t0007g0183 a0001c0005t0007g0184 a0001c0005t0007g0185 |
3 | HG02257.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+8461T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738672 | |||||||
chr16:56738742 | T | A | 1 | a0001c0001t0003g0004 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-15+8531T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738742 | |||||||
chr16:56738745 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-15+8534A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738745 | |||||||
chr16:56738764 | G | T | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-15+8553G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738764 | |||||||
chr16:56738835 | A | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-15+8624A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738835 | |||||||
chr16:56738893 | G | T | 132 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.-15+8682G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738893 | |||||||
chr16:56738945 | C | CT | 94 | a0001c0001t0001g0047 a0001c0001t0001g0300 a0001c0001t0001g0301 others(91): Show |
94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-15+8750dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | ||||||
chr16:56738945 | C | CTT | 92 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0116 others(89): Show |
93 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-15+8749_-15+8750d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | ||||||
chr16:56738945 | C | CTTT | 32 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(29): Show |
32 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-15+8748_-15+8750d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | ||||||
chr16:56738945 | C | CTTTT | 8 | a0001c0001t0001g0054 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+8747_-15+8750d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | ||||||
chr16:56738945 | CT | C | 54 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(51): Show |
54 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-15+8750delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | ||||||
chr16:56739130 | C | T | 4 | a0001c0001t0002g0293 a0001c0009t0018g0020 a0001c0009t0018g0021 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+8919C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739130 | |||||||
chr16:56739171 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-15+8960G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739171 | |||||||
chr16:56739257 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-14-8977G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739257 | |||||||
chr16:56739322 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | NA18939.hp2 NA18964.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-14-8912G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739322 | |||||||
chr16:56739326 | C | T | 1 | a0001c0004t0005g0037 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-14-8908C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739326 | |||||||
chr16:56739327 | G | A | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8907G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739327 | |||||||
chr16:56739339 | A | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8895A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739339 | |||||||
chr16:56739350 | C | CCCCCCAA others(802): Show |
1 | a0001c0001t0001g0303 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-14-8879_-14-8878i others(811): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(835): Show |
11 | a0001c0001t0004g0003 a0001c0001t0004g0220 a0001c0001t0004g0221 others(8): Show |
11 | HG00733.hp1 HG01175.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(844): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(786): Show |
2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | NA18952.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(795): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(836): Show |
1 | a0001c0001t0004g0231 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(845): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(836): Show |
3 | a0001c0001t0004g0232 a0001c0001t0004g0234 a0003c0015t0004g0233 |
3 | HG00408.hp2 HG01496.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(845): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(787): Show |
1 | a0001c0001t0004g0235 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(796): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(835): Show |
3 | a0001c0001t0004g0236 a0001c0001t0004g0237 a0001c0001t0004g0238 |
3 | NA18959.hp2 NA18972.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(844): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(837): Show |
1 | a0001c0001t0004g0239 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(846): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(657): Show |
1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(666): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(837): Show |
1 | a0001c0001t0004g0240 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(846): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739350 | C | CCCCCCCC others(835): Show |
1 | a0001c0001t0004g0198 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(844): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | ||||||
chr16:56739351 | C | CCCCCCCA others(332): Show |
1 | a0001c0001t0003g0351 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(341): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739351 | ||||||
chr16:56739351 | C | CCCCCCCA others(332): Show |
42 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(39): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(341): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739351 | ||||||
chr16:56739351 | C | CCCCCCCA others(332): Show |
3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(341): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739351 | ||||||
chr16:56739351 | C | CCCCCCCC others(333): Show |
20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-8877_-14-8876i others(342): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739351 | ||||||
chr16:56739351 | C | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8883C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739351 | |||||||
chr16:56739389 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14-8845C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739389 | |||||||
chr16:56739389 | C | T | 56 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(53): Show |
56 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.-14-8845C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739389 | |||||||
chr16:56739397 | T | C | 26 | a0001c0001t0001g0303 a0001c0001t0004g0003 a0001c0001t0004g0198 others(23): Show |
26 | HG00140.hp2 HG00408.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.-14-8837T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739397 | |||||||
chr16:56739401 | C | A | 67 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(64): Show |
68 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-14-8833C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739401 | |||||||
chr16:56739406 | A | AACCTCCC others(673): Show |
1 | a0001c0001t0013g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-14-8753_-14-8752i others(682): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | AACCTCCC others(673): Show |
2 | a0001c0001t0013g0015 a0001c0001t0013g0016 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-14-8753_-14-8752i others(682): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | AACCTCCC others(855): Show |
1 | a0001c0004t0045g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-14-8753_-14-8752i others(864): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | AACCTCCC others(676): Show |
3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-8753_-14-8752i others(685): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | AACCTCCC others(852): Show |
6 | a0001c0004t0008g0002 a0001c0004t0008g0174 a0001c0004t0008g0175 others(3): Show |
7 | HG00741.hp1 HG01106.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-8753_-14-8752i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | AACCTCCC others(852): Show |
1 | a0001c0004t0019g0180 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-14-8753_-14-8752i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | AACCTCCC others(836): Show |
6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8753_-14-8752i others(845): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | AACCTCCC others(349): Show |
3 | a0001c0002t0010g0113 a0001c0002t0010g0114 a0001c0002t0041g0115 |
3 | HG00733.hp2 HG01346.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-14-8768_-14-8767i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | AACCTCCC others(1901): Show |
1 | a0001c0001t0001g0328 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-14-8789_-14-8788i others(1910): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | ||||||
chr16:56739406 | A | C | 94 | a0001c0001t0001g0303 a0001c0001t0003g0004 a0001c0001t0003g0348 others(91): Show |
95 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.-14-8828A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739406 | |||||||
chr16:56739434 | C | T | 1 | a0001c0002t0001g0131 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-14-8800C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739434 | |||||||
chr16:56739471 | C | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8763C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739471 | |||||||
chr16:56739482 | A | G | 326 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(323): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-14-8752A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739482 | |||||||
chr16:56739504 | C | CGGCTGGC others(349): Show |
2 | a0001c0002t0001g0062 a0001c0002t0001g0063 |
2 | NA18983.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(349): Show |
100 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(97): Show |
101 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(350): Show |
1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(359): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(349): Show |
3 | a0001c0003t0002g0254 a0001c0003t0002g0255 a0001c0003t0002g0256 |
3 | HG01069.hp1 HG01071.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(171): Show |
1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(180): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(349): Show |
1 | a0001c0009t0018g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(349): Show |
21 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(18): Show |
21 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(348): Show |
6 | a0001c0004t0005g0032 a0001c0004t0005g0033 a0001c0004t0005g0034 others(3): Show |
6 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(357): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(171): Show |
3 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0130 |
3 | HG00140.hp1 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(180): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(349): Show |
2 | a0001c0009t0018g0020 a0005c0024t0018g0012 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGCTGGC others(350): Show |
1 | a0001c0002t0001g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14-8711_-14-8710i others(359): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | CGGGTGGC others(349): Show |
1 | a0001c0002t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-14-8728_-14-8727i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | ||||||
chr16:56739504 | C | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(66): Show |
70 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.-14-8730C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739504 | |||||||
chr16:56739516 | C | CGGGGGGG others(350): Show |
1 | a0001c0002t0001g0131 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(359): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739516 | ||||||
chr16:56739516 | C | CGGGGGGG others(853): Show |
1 | a0001c0004t0019g0181 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739516 | ||||||
chr16:56739516 | C | T | 3 | a0001c0001t0001g0303 a0001c0001t0001g0328 a0001c0001t0029g0243 |
3 | HG00140.hp2 HG02145.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-14-8718C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739516 | |||||||
chr16:56739517 | G | A | 3 | a0001c0001t0001g0303 a0001c0001t0001g0328 a0001c0002t0001g0060 |
3 | HG00140.hp2 HG02129.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.-14-8717G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739517 | |||||||
chr16:56739517 | G | GGGGGGGC others(801): Show |
1 | a0004c0022t0022g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(810): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(852): Show |
1 | a0001c0003t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(525): Show |
1 | a0001c0001t0001g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(534): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(852): Show |
34 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0304 others(31): Show |
34 | HG00609.hp1 HG00621.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(852): Show |
31 | a0001c0001t0002g0293 a0001c0003t0002g0244 a0001c0003t0002g0245 others(28): Show |
31 | HG00423.hp1 HG01099.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(1857): Show |
1 | a0002c0008t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(1866): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(853): Show |
1 | a0001c0001t0002g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(852): Show |
1 | a0001c0003t0002g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(853): Show |
1 | a0001c0003t0042g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(853): Show |
1 | a0001c0001t0001g0333 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(853): Show |
3 | a0001c0003t0002g0285 a0001c0003t0002g0294 a0002c0008t0002g0299 |
3 | NA18981.hp2 NA19000.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(853): Show |
4 | a0001c0003t0002g0286 a0001c0003t0002g0287 a0001c0003t0002g0288 others(1): Show |
4 | HG00544.hp2 HG00673.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(854): Show |
1 | a0001c0001t0001g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(863): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(856): Show |
1 | a0001c0001t0001g0301 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(865): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGC others(674): Show |
1 | a0001c0001t0002g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(683): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739517 | G | GGGGGGGG others(856): Show |
1 | a0001c0003t0021g0292 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-14-8711_-14-8710i others(865): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | ||||||
chr16:56739527 | A | ACTCCCCC others(350): Show |
10 | a0001c0001t0001g0054 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG00408.hp1 HG00544.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(359): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(351): Show |
1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(360): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(351): Show |
1 | a0001c0002t0001g0172 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(360): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(352): Show |
1 | a0001c0002t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(361): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(352): Show |
1 | a0001c0001t0001g0132 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(361): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(853): Show |
2 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
2 | HG00438.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(853): Show |
1 | a0001c0004t0044g0179 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(853): Show |
3 | a0001c0003t0002g0280 a0001c0003t0020g0281 a0001c0006t0009g0247 |
3 | HG01169.hp1 HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(856): Show |
1 | a0001c0003t0002g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(865): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(856): Show |
1 | a0001c0003t0002g0289 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(865): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739527 | A | ACTCCCCC others(857): Show |
1 | a0001c0003t0002g0291 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(866): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | ||||||
chr16:56739529 | C | T | 1 | a0001c0001t0043g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-14-8705C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739529 | |||||||
chr16:56739530 | C | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
5 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-8704C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739530 | |||||||
chr16:56739533 | C | A | 1 | a0001c0001t0004g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-14-8701C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739533 | |||||||
chr16:56739536 | C | A | 1 | a0001c0002t0001g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-14-8698C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739536 | |||||||
chr16:56739536 | C | T | 1 | a0001c0002t0001g0109 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-14-8698C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739536 | |||||||
chr16:56739547 | C | T | 25 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(22): Show |
25 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14-8687C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739547 | |||||||
chr16:56739552 | G | A | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-8682G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739552 | |||||||
chr16:56739556 | C | T | 226 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(223): Show |
228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-14-8678C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739556 | |||||||
chr16:56739569 | G | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
6 | HG04184.hp2 NA18939.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8665G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739569 | |||||||
chr16:56739578 | A | AC | 11 | a0001c0001t0001g0048 a0001c0001t0001g0125 a0001c0001t0001g0132 others(8): Show |
11 | HG00642.hp2 HG01261.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14-8649dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739578 | ||||||
chr16:56739578 | A | ACACCCCC others(301): Show |
4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8655_-14-8654i others(310): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739578 | ||||||
chr16:56739578 | A | ACACCCCC others(353): Show |
1 | a0001c0001t0043g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-14-8655_-14-8654i others(362): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739578 | ||||||
chr16:56739580 | C | A | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8654C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739580 | |||||||
chr16:56739600 | T | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
6 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-8634T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739600 | |||||||
chr16:56739605 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8629C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739605 | |||||||
chr16:56739614 | G | A | 7 | a0001c0002t0001g0066 a0001c0002t0001g0068 a0001c0002t0001g0069 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-8620G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739614 | |||||||
chr16:56739614 | G | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8620G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739614 | |||||||
chr16:56739617 | C | CAGAGGGG others(18): Show |
1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8617_-14-8616i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739617 | |||||||
chr16:56739617 | C | CG | 13 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0132 others(10): Show |
13 | HG00642.hp2 HG01261.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-8611dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739617 | ||||||
chr16:56739617 | C | T | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-14-8617C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739617 | |||||||
chr16:56739621 | G | C | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8613G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739621 | |||||||
chr16:56739625 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8609C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739625 | |||||||
chr16:56739628 | C | G | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8606C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739628 | |||||||
chr16:56739629 | A | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8605A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739629 | |||||||
chr16:56739630 | T | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8604T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739630 | |||||||
chr16:56739630 | T | G | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8604T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739630 | |||||||
chr16:56739630 | T | TCCCCACC others(447): Show |
2 | a0001c0003t0002g0255 a0001c0003t0002g0256 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-14-8568_-14-8567i others(456): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739630 | ||||||
chr16:56739631 | C | G | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8603C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739631 | |||||||
chr16:56739633 | C | G | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8601C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739633 | |||||||
chr16:56739635 | A | C | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8599A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739635 | |||||||
chr16:56739646 | G | A | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-14-8588G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739646 | |||||||
chr16:56739649 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8585C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739649 | |||||||
chr16:56739654 | C | CGGCTGGC others(170): Show |
1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8568_-14-8567i others(179): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739654 | ||||||
chr16:56739654 | C | CGGCTGGC others(170): Show |
1 | a0001c0003t0002g0254 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-14-8568_-14-8567i others(179): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739654 | ||||||
chr16:56739654 | C | CGGCTGGC others(172): Show |
1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-14-8568_-14-8567i others(181): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739654 | ||||||
chr16:56739662 | C | CGGGCAGG others(170): Show |
29 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(26): Show |
29 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-14-8568_-14-8567i others(179): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739662 | ||||||
chr16:56739662 | C | CGGGCAGG others(171): Show |
1 | a0001c0004t0005g0037 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-14-8568_-14-8567i others(180): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739662 | ||||||
chr16:56739662 | CGGGCGGA others(5): Show |
C | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-14-8570_-14-8559d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739662 | ||||||
chr16:56739666 | C | G | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8568C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739666 | |||||||
chr16:56739666 | C | T | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8568C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739666 | |||||||
chr16:56739667 | G | A | 195 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(192): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-14-8567G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739667 | |||||||
chr16:56739669 | A | G | 197 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-14-8565A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739669 | |||||||
chr16:56739674 | T | C | 196 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(193): Show |
198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-14-8560T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739674 | |||||||
chr16:56739692 | C | T | 3 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 |
3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-14-8542C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739692 | |||||||
chr16:56739695 | G | A | 6 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0072 others(3): Show |
7 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-8539G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739695 | |||||||
chr16:56739715 | C | CG | 12 | a0001c0001t0001g0127 a0001c0001t0001g0301 a0001c0001t0001g0327 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.-14-8513dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739715 | ||||||
chr16:56739723 | C | CGATCCCC others(397): Show |
2 | a0001c0001t0014g0217 a0001c0001t0014g0218 |
2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-8509_-14-8508i others(406): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | ||||||
chr16:56739723 | C | CGATCCCC others(397): Show |
1 | a0001c0001t0014g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-14-8509_-14-8508i others(406): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | ||||||
chr16:56739723 | C | CGATCCCC others(446): Show |
1 | a0001c0001t0006g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-14-8509_-14-8508i others(455): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | ||||||
chr16:56739723 | C | CGATCCCC others(447): Show |
14 | a0001c0001t0006g0203 a0001c0001t0006g0204 a0001c0001t0006g0205 others(11): Show |
14 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-8509_-14-8508i others(456): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | ||||||
chr16:56739723 | C | CGATCCCC others(448): Show |
1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-14-8509_-14-8508i others(457): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | ||||||
chr16:56739723 | C | T | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8511C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739723 | |||||||
chr16:56739725 | A | AT | 175 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(172): Show |
177 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-14-8509_-14-8508i others(3): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739725 | |||||||
chr16:56739727 | C | A | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8507C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739727 | |||||||
chr16:56739728 | C | T | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8506C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739728 | |||||||
chr16:56739748 | G | A | 46 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(43): Show |
47 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-8486G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739748 | |||||||
chr16:56739798 | G | A | 9 | a0001c0001t0004g0198 a0001c0001t0004g0229 a0001c0001t0004g0230 others(6): Show |
9 | HG00597.hp2 NA18952.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-8436G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739798 | |||||||
chr16:56739800 | G | A | 46 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(43): Show |
47 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-8434G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739800 | |||||||
chr16:56739807 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-14-8427C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739807 | |||||||
chr16:56739808 | G | A | 33 | a0001c0001t0007g0194 a0001c0001t0034g0196 a0001c0003t0002g0254 others(30): Show |
33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-8426G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739808 | |||||||
chr16:56739822 | A | G | 34 | a0001c0001t0007g0194 a0001c0001t0034g0196 a0001c0002t0001g0061 others(31): Show |
34 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-8412A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739822 | |||||||
chr16:56739825 | C | T | 1 | a0001c0004t0024g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-14-8409C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739825 | |||||||
chr16:56739830 | C | T | 43 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(40): Show |
44 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-14-8404C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739830 | |||||||
chr16:56739842 | C | A | 1 | a0001c0003t0002g0254 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-14-8392C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739842 | |||||||
chr16:56739842 | C | CG | 33 | a0001c0001t0007g0194 a0001c0001t0034g0196 a0001c0002t0001g0061 others(30): Show |
33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-8390dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739842 | ||||||
chr16:56739845 | A | G | 34 | a0001c0001t0007g0194 a0001c0001t0034g0196 a0001c0002t0001g0061 others(31): Show |
34 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-8389A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739845 | |||||||
chr16:56739850 | T | TGA | 29 | a0001c0001t0034g0196 a0001c0003t0002g0254 a0001c0004t0005g0023 others(26): Show |
29 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-14-8384_-14-8383i others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739850 | |||||||
chr16:56739850 | T | TGAC | 4 | a0001c0001t0007g0194 a0001c0004t0005g0022 a0001c0004t0005g0036 others(1): Show |
4 | HG00741.hp2 HG02738.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-8384_-14-8383i others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739850 | |||||||
chr16:56739851 | C | G | 43 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(40): Show |
44 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-14-8383C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739851 | |||||||
chr16:56739852 | A | AC | 8 | a0001c0001t0001g0132 a0001c0001t0001g0328 a0001c0001t0004g0234 others(5): Show |
8 | HG00597.hp1 HG00597.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-8376dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739852 | ||||||
chr16:56739852 | A | C | 33 | a0001c0001t0007g0194 a0001c0001t0034g0196 a0001c0003t0002g0254 others(30): Show |
33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-8382A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739852 | |||||||
chr16:56739855 | C | CCCCCCAC others(271): Show |
1 | a0007c0013t0007g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-14-8376_-14-8375i others(280): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739855 | ||||||
chr16:56739855 | C | CCCCCCAC others(272): Show |
1 | a0001c0001t0007g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-14-8376_-14-8375i others(281): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739855 | ||||||
chr16:56739855 | C | CCCCCCCA others(93): Show |
1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8376_-14-8375i others(102): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739855 | ||||||
chr16:56739859 | G | C | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.-14-8375G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739859 | |||||||
chr16:56739870 | C | T | 2 | a0001c0001t0007g0194 a0001c0001t0034g0196 |
2 | HG02572.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-14-8364C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739870 | |||||||
chr16:56739879 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-14-8355C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739879 | |||||||
chr16:56739888 | A | G | 210 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(207): Show |
212 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-14-8346A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739888 | |||||||
chr16:56739892 | G | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-14-8342G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739892 | |||||||
chr16:56739894 | G | A | 2 | a0001c0001t0007g0195 a0007c0013t0007g0190 |
2 | HG00642.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-14-8340G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739894 | |||||||
chr16:56739894 | G | GGGGCCGA others(270): Show |
38 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(35): Show |
39 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.-14-8336_-14-8335i others(279): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739894 | ||||||
chr16:56739894 | G | GGGGCCGA others(271): Show |
1 | a0008c0023t0026g0370 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-14-8336_-14-8335i others(280): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739894 | ||||||
chr16:56739894 | G | GGGGGCCG others(271): Show |
1 | a0001c0001t0003g0371 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-14-8337_-14-8336i others(280): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739894 | ||||||
chr16:56739899 | T | C | 1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8335T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739899 | |||||||
chr16:56739902 | C | G | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-8332C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739902 | |||||||
chr16:56739923 | C | T | 4 | a0001c0001t0007g0194 a0001c0001t0034g0196 a0001c0002t0001g0166 others(1): Show |
4 | HG02572.hp2 HG02738.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-8311C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739923 | |||||||
chr16:56739940 | C | CG | 8 | a0001c0001t0001g0127 a0001c0001t0001g0328 a0001c0002t0001g0071 others(5): Show |
8 | HG01175.hp2 HG01255.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-8288dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739940 | ||||||
chr16:56739940 | CG | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8288delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739940 | ||||||
chr16:56739946 | G | T | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8288G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739946 | |||||||
chr16:56739950 | A | AC | 27 | a0001c0001t0001g0047 a0001c0001t0001g0125 a0001c0001t0001g0127 others(24): Show |
27 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-8276dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739950 | ||||||
chr16:56739950 | AC | A | 42 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(39): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.-14-8276delC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739950 | ||||||
chr16:56739951 | C | CATCCCCA others(91): Show |
2 | a0001c0001t0034g0196 a0001c0003t0002g0254 |
2 | HG02572.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-14-8283_-14-8282i others(100): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739951 | |||||||
chr16:56739951 | C | CATCCCCA others(92): Show |
1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-14-8283_-14-8282i others(101): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739951 | |||||||
chr16:56739958 | C | T | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-14-8276C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739958 | |||||||
chr16:56739960 | C | A | 1 | a0001c0002t0010g0113 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-14-8274C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739960 | |||||||
chr16:56739986 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-14-8248C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739986 | |||||||
chr16:56740012 | G | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-14-8222G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740012 | |||||||
chr16:56740023 | G | C | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.-14-8211G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740023 | |||||||
chr16:56740067 | G | T | 1 | a0001c0002t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-14-8167G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740067 | |||||||
chr16:56740089 | T | C | 1 | a0001c0001t0004g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-14-8145T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740089 | |||||||
chr16:56740100 | C | T | 1 | a0001c0002t0001g0170 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-14-8134C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740100 | |||||||
chr16:56740111 | G | A | 2 | a0001c0001t0023g0329 a0001c0001t0023g0330 |
2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-14-8123G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740111 | |||||||
chr16:56740114 | A | G | 132 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.-14-8120A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740114 | |||||||
chr16:56740127 | A | ACCC | 100 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0055 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-14-8102_-14-8100d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | ||||||
chr16:56740127 | A | ACCCC | 28 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0122 others(25): Show |
28 | HG00609.hp2 HG01433.hp1 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-8103_-14-8100d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | ||||||
chr16:56740127 | A | ACCCCCCC others(44): Show |
28 | a0001c0004t0005g0023 a0001c0004t0005g0024 a0001c0004t0005g0025 others(25): Show |
28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-8081_-14-8080i others(53): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | ||||||
chr16:56740127 | A | ACCCCCCC others(45): Show |
4 | a0001c0004t0005g0022 a0001c0004t0005g0037 a0001c0007t0012g0346 others(1): Show |
4 | HG01261.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8081_-14-8080i others(54): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | ||||||
chr16:56740127 | A | ACCCCCCC others(46): Show |
1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-14-8081_-14-8080i others(55): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | ||||||
chr16:56740195 | GGCTGCCG others(33): Show |
G | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00621.hp1 HG02071.hp1 HG03239.hp2 others(16): Show |
intron_variant | MODIFIER | c.-14-8024_-14-7985d others(42): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740195 | ||||||
chr16:56740272 | G | C | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-14-7962G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740272 | |||||||
chr16:56740318 | C | T | 2 | a0001c0001t0016g0192 a0001c0001t0016g0193 |
2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-14-7916C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740318 | |||||||
chr16:56740346 | C | T | 48 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(45): Show |
48 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.-14-7888C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740346 | |||||||
chr16:56740386 | T | C | 1 | a0001c0003t0002g0286 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-14-7848T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740386 | |||||||
chr16:56740405 | C | T | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-14-7829C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740405 | |||||||
chr16:56740471 | G | A | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14-7763G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740471 | |||||||
chr16:56740524 | C | G | 1 | a0001c0001t0004g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-14-7710C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740524 | |||||||
chr16:56740587 | G | A | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-14-7647G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740587 | |||||||
chr16:56740827 | C | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-7407C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740827 | |||||||
chr16:56740875 | C | T | 97 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(94): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-14-7359C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740875 | |||||||
chr16:56740952 | C | G | 1 | a0001c0017t0001g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14-7282C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740952 | |||||||
chr16:56740985 | C | T | 2 | a0001c0007t0012g0346 a0001c0007t0012g0347 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-7249C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740985 | |||||||
chr16:56741004 | G | GGGGAGA | 161 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(158): Show |
162 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.-14-7204_-14-7199d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56741004 | ||||||
chr16:56741004 | G | GGGGAGAG others(5): Show |
5 | a0001c0001t0001g0128 a0001c0001t0013g0014 a0001c0001t0013g0015 others(2): Show |
5 | HG03041.hp1 HG03225.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-7210_-14-7199d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56741004 | ||||||
chr16:56741004 | G | GGGGAGAG others(11): Show |
3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-7216_-14-7199d others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56741004 | ||||||
chr16:56741004 | GGGGAGA | G | 5 | a0001c0001t0029g0243 a0001c0003t0002g0261 a0001c0003t0021g0260 others(2): Show |
5 | HG00423.hp1 HG02074.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-7204_-14-7199d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56741004 | ||||||
chr16:56741006 | G | A | 4 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-7228G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741006 | |||||||
chr16:56741144 | T | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-7090T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741144 | |||||||
chr16:56741155 | T | G | 1 | a0001c0003t0002g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-14-7079T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741155 | |||||||
chr16:56741205 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-14-7029A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741205 | |||||||
chr16:56741345 | A | G | 1 | a0001c0001t0027g0369 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-14-6889A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741345 | |||||||
chr16:56741605 | C | T | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.-14-6629C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741605 | |||||||
chr16:56742048 | A | G | 1 | a0001c0002t0001g0172 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-14-6186A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742048 | |||||||
chr16:56742096 | C | A | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-14-6138C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742096 | |||||||
chr16:56742118 | A | T | 2 | a0001c0010t0022g0258 a0001c0010t0033g0259 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-14-6116A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742118 | |||||||
chr16:56742275 | G | T | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.-14-5959G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742275 | |||||||
chr16:56742371 | A | G | 1 | a0001c0009t0018g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-5863A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742371 | |||||||
chr16:56742643 | A | G | 2 | a0001c0010t0022g0258 a0001c0010t0033g0259 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-14-5591A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742643 | |||||||
chr16:56742744 | C | T | 1 | a0001c0001t0014g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-5490C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742744 | |||||||
chr16:56742868 | C | T | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-5366C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742868 | |||||||
chr16:56742979 | A | G | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-5255A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742979 | |||||||
chr16:56743113 | G | A | 1 | a0001c0002t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-14-5121G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743113 | |||||||
chr16:56743125 | A | C | 2 | a0001c0002t0001g0001 a0001c0002t0001g0073 |
3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-14-5109A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743125 | |||||||
chr16:56743169 | A | G | 1 | a0001c0002t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-14-5065A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743169 | |||||||
chr16:56743345 | C | T | 1 | a0001c0001t0003g0368 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-14-4889C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743345 | |||||||
chr16:56743984 | C | T | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-14-4250C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743984 | |||||||
chr16:56744034 | G | C | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-4200G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744034 | |||||||
chr16:56744155 | G | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-14-4079G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744155 | |||||||
chr16:56744223 | C | T | 3 | a0001c0001t0004g0220 a0001c0001t0004g0227 a0001c0001t0004g0234 |
3 | HG01433.hp2 HG01496.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-14-4011C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744223 | |||||||
chr16:56744374 | G | T | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-14-3860G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744374 | |||||||
chr16:56744589 | C | T | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-14-3645C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744589 | |||||||
chr16:56744701 | G | A | 1 | a0001c0002t0001g0074 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-14-3533G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744701 | |||||||
chr16:56744706 | C | A | 1 | a0001c0002t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14-3528C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744706 | |||||||
chr16:56744734 | G | A | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14-3500G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744734 | |||||||
chr16:56744924 | G | A | 4 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-3310G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744924 | |||||||
chr16:56744994 | G | T | 2 | a0001c0001t0002g0290 a0001c0014t0001g0139 |
2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-14-3240G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744994 | |||||||
chr16:56745009 | A | G | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-3225A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745009 | |||||||
chr16:56745016 | TG | T | 3 | a0001c0002t0001g0095 a0001c0002t0001g0105 a0001c0002t0001g0106 |
3 | HG00673.hp2 HG02074.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-14-3215delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56745016 | ||||||
chr16:56745063 | C | T | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-3171C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745063 | |||||||
chr16:56745350 | GA | G | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-2883delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745350 | |||||||
chr16:56745356 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-14-2878G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745356 | |||||||
chr16:56745744 | T | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-14-2490T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745744 | |||||||
chr16:56745796 | T | C | 1 | a0001c0001t0003g0353 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-2438T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745796 | |||||||
chr16:56745888 | A | G | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-2346A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745888 | |||||||
chr16:56746214 | C | G | 2 | a0001c0002t0001g0103 a0001c0002t0001g0107 |
2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-14-2020C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56746214 | |||||||
chr16:56746347 | T | C | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-14-1887T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56746347 | |||||||
chr16:56746418 | G | A | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-14-1816G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56746418 | |||||||
chr16:56746479 | T | C | 92 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(89): Show |
93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.-14-1755T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56746479 | |||||||
chr16:56746997 | A | AT | 8 | a0001c0001t0001g0336 a0001c0001t0003g0368 a0001c0002t0001g0108 others(5): Show |
8 | HG01978.hp2 HG02145.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-1221dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56746997 | ||||||
chr16:56746997 | AT | A | 10 | a0001c0001t0001g0300 a0001c0001t0001g0304 a0001c0001t0004g0236 others(7): Show |
10 | HG00423.hp1 HG01993.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-1221delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56746997 | ||||||
chr16:56747019 | A | G | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(1): Show |
4 | HG00735.hp2 HG01081.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1215A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747019 | |||||||
chr16:56747065 | T | C | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-1169T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747065 | |||||||
chr16:56747123 | C | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-14-1111C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747123 | |||||||
chr16:56747350 | G | A | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-884G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747350 | |||||||
chr16:56747384 | A | G | 98 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-14-850A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747384 | |||||||
chr16:56747407 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-14-827C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747407 | |||||||
chr16:56747411 | A | G | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-14-823A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747411 | |||||||
chr16:56747608 | A | G | 1 | a0001c0001t0031g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-14-626A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747608 | |||||||
chr16:56747820 | A | G | 164 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(161): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-14-414A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747820 | |||||||
chr16:56747823 | G | A | 9 | a0001c0001t0003g0351 a0001c0001t0003g0352 a0001c0001t0003g0354 others(6): Show |
9 | HG02027.hp1 NA18961.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-411G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747823 | |||||||
chr16:56747918 | C | T | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.-14-316C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747918 | |||||||
chr16:56748053 | A | G | 23 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(20): Show |
23 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-181A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56748053 | |||||||
chr16:56748435 | T | G | 1 | a0001c0001t0003g0353 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.179+9T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748435 | |||||||
chr16:56748714 | A | T | 1 | a0001c0001t0004g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.179+288A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748714 | |||||||
chr16:56748732 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.179+306A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748732 | |||||||
chr16:56748924 | C | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.179+498C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748924 | |||||||
chr16:56748990 | G | A | 2 | a0001c0004t0005g0043 a0001c0004t0005g0045 |
2 | HG00423.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.179+564G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748990 | |||||||
chr16:56749091 | G | A | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.179+665G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749091 | |||||||
chr16:56749154 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.179+728A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749154 | |||||||
chr16:56749204 | A | T | 3 | a0001c0001t0003g0366 a0001c0001t0003g0367 a0001c0001t0003g0368 |
3 | NA18942.hp1 NA18952.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.179+778A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749204 | |||||||
chr16:56749318 | C | T | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179+892C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749318 | |||||||
chr16:56749465 | G | A | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.179+1039G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749465 | |||||||
chr16:56749476 | G | A | 3 | a0001c0001t0017g0305 a0001c0001t0017g0341 a0001c0001t0017g0342 |
3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.179+1050G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749476 | |||||||
chr16:56749569 | C | T | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.179+1143C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749569 | |||||||
chr16:56749605 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.179+1179A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749605 | |||||||
chr16:56749984 | C | T | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.179+1558C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749984 | |||||||
chr16:56749985 | C | T | 12 | a0001c0001t0003g0351 a0001c0001t0003g0352 a0001c0001t0003g0354 others(9): Show |
12 | HG02027.hp1 NA18942.hp1 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.179+1559C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749985 | |||||||
chr16:56750273 | A | G | 1 | a0001c0001t0004g0238 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.179+1847A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750273 | |||||||
chr16:56750489 | A | G | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.179+2063A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750489 | |||||||
chr16:56750598 | AT | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | NA18970.hp1 NA18988.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+2173delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750598 | |||||||
chr16:56750625 | C | T | 1 | a0010c0018t0004g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.179+2199C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750625 | |||||||
chr16:56750812 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.179+2386C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750812 | |||||||
chr16:56750888 | G | A | 11 | a0001c0002t0001g0061 a0001c0002t0001g0075 a0001c0002t0001g0077 others(8): Show |
11 | HG02071.hp2 HG02080.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.179+2462G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750888 | |||||||
chr16:56750899 | C | T | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+2473C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750899 | |||||||
chr16:56750939 | G | A | 1 | a0001c0002t0001g0172 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.179+2513G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750939 | |||||||
chr16:56751196 | A | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.179+2770A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751196 | |||||||
chr16:56751211 | C | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(52): Show |
55 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.179+2785C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751211 | |||||||
chr16:56751227 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.179+2801A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751227 | |||||||
chr16:56751311 | A | G | 1 | a0001c0001t0001g0321 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.179+2885A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751311 | |||||||
chr16:56751387 | G | A | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+2961G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751387 | |||||||
chr16:56751407 | C | T | 1 | a0001c0001t0003g0348 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.179+2981C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751407 | |||||||
chr16:56751408 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.179+2982G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751408 | |||||||
chr16:56751478 | A | G | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.179+3052A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751478 | |||||||
chr16:56752120 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179+3694T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56752120 | |||||||
chr16:56752668 | A | G | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.179+4242A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56752668 | |||||||
chr16:56752880 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.179+4454G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56752880 | |||||||
chr16:56752937 | G | A | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+4511G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56752937 | |||||||
chr16:56753041 | CAT | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+4618_179+4619d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56753041 | ||||||
chr16:56753103 | T | A | 3 | a0001c0001t0017g0305 a0001c0001t0017g0341 a0001c0001t0017g0342 |
3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.179+4677T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753103 | |||||||
chr16:56753195 | T | C | 271 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(268): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.179+4769T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753195 | |||||||
chr16:56753249 | A | G | 98 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.179+4823A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753249 | |||||||
chr16:56753420 | TATC | T | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.179+4997_179+4999d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56753420 | ||||||
chr16:56753434 | T | C | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.179+5008T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753434 | |||||||
chr16:56753460 | A | G | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+5034A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753460 | |||||||
chr16:56753514 | C | T | 1 | a0001c0002t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.180-5024C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753514 | |||||||
chr16:56753691 | C | T | 1 | a0001c0006t0009g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.180-4847C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753691 | |||||||
chr16:56753908 | A | T | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.180-4630A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753908 | |||||||
chr16:56753970 | T | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(20): Show |
23 | HG01433.hp1 HG01496.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.180-4568T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753970 | |||||||
chr16:56753973 | A | AT | 34 | a0001c0001t0001g0133 a0001c0001t0011g0006 a0001c0001t0011g0007 others(31): Show |
34 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.180-4552dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56753973 | ||||||
chr16:56753973 | AT | A | 8 | a0001c0001t0001g0117 a0001c0001t0004g0238 a0001c0001t0006g0203 others(5): Show |
8 | HG02451.hp2 HG03209.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.180-4552delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56753973 | ||||||
chr16:56753995 | A | T | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.180-4543A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753995 | |||||||
chr16:56754156 | A | G | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.180-4382A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754156 | |||||||
chr16:56754209 | CT | C | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.180-4327delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56754209 | ||||||
chr16:56754279 | G | T | 47 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(44): Show |
47 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.180-4259G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754279 | |||||||
chr16:56754442 | T | C | 1 | a0005c0024t0018g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.180-4096T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754442 | |||||||
chr16:56754675 | G | A | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.180-3863G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754675 | |||||||
chr16:56754842 | G | A | 44 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(41): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.180-3696G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754842 | |||||||
chr16:56754879 | T | C | 1 | a0001c0001t0002g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.180-3659T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754879 | |||||||
chr16:56754922 | C | T | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.180-3616C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754922 | |||||||
chr16:56754993 | G | A | 1 | a0007c0013t0007g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.180-3545G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754993 | |||||||
chr16:56754996 | G | A | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.180-3542G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754996 | |||||||
chr16:56755054 | A | G | 1 | a0001c0002t0001g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.180-3484A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755054 | |||||||
chr16:56755164 | C | G | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.180-3374C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755164 | |||||||
chr16:56755252 | G | A | 2 | a0001c0002t0010g0050 a0001c0002t0010g0052 |
2 | HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.180-3286G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755252 | |||||||
chr16:56755427 | A | G | 98 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.180-3111A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755427 | |||||||
chr16:56755595 | G | A | 2 | a0001c0007t0012g0346 a0001c0007t0012g0347 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.180-2943G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755595 | |||||||
chr16:56755677 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.180-2861C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755677 | |||||||
chr16:56756200 | A | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.180-2338A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756200 | |||||||
chr16:56756295 | G | GC | 71 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(68): Show |
71 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.180-2229dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | ||||||
chr16:56756295 | G | GCC | 64 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0054 others(61): Show |
65 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.180-2230_180-2229d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | ||||||
chr16:56756295 | G | GCCC | 24 | a0001c0001t0001g0128 a0001c0001t0006g0202 a0001c0001t0006g0204 others(21): Show |
24 | HG01070.hp2 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.180-2231_180-2229d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | ||||||
chr16:56756295 | GC | G | 26 | a0001c0001t0001g0123 a0001c0001t0001g0306 a0001c0001t0002g0290 others(23): Show |
27 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.180-2229delC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | ||||||
chr16:56756295 | GCC | G | 47 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(44): Show |
47 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.180-2230_180-2229d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | ||||||
chr16:56756299 | C | G | 9 | a0001c0001t0003g0351 a0001c0001t0003g0352 a0001c0001t0003g0354 others(6): Show |
9 | HG02027.hp1 NA18961.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.180-2239C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756299 | |||||||
chr16:56756300 | C | G | 1 | a0001c0003t0002g0278 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.180-2238C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756300 | |||||||
chr16:56756302 | C | G | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.180-2236C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756302 | |||||||
chr16:56756303 | C | A | 1 | a0001c0003t0002g0262 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.180-2235C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756303 | |||||||
chr16:56756303 | C | CG | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.180-2235_180-2234i others(3): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756303 | |||||||
chr16:56756304 | C | G | 4 | a0001c0001t0002g0290 a0001c0001t0013g0014 a0001c0001t0013g0015 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-2234C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756304 | |||||||
chr16:56756305 | C | G | 16 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(13): Show |
16 | HG00621.hp1 NA18943.hp2 NA18946.hp2 others(13): Show |
intron_variant | MODIFIER | c.180-2233C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756305 | |||||||
chr16:56756306 | C | T | 1 | a0001c0004t0005g0036 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.180-2232C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756306 | |||||||
chr16:56756310 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.180-2228G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756310 | |||||||
chr16:56756368 | G | A | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-2170G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756368 | |||||||
chr16:56756375 | T | C | 4 | a0002c0008t0002g0296 a0002c0008t0002g0297 a0002c0008t0002g0298 others(1): Show |
4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.180-2163T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756375 | |||||||
chr16:56756431 | A | G | 49 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(46): Show |
49 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.180-2107A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756431 | |||||||
chr16:56756440 | A | G | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.180-2098A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756440 | |||||||
chr16:56756545 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.180-1993G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756545 | |||||||
chr16:56756596 | G | A | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.180-1942G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756596 | |||||||
chr16:56756795 | C | T | 1 | a0001c0004t0008g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.180-1743C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756795 | |||||||
chr16:56756966 | T | C | 2 | a0001c0002t0001g0110 a0001c0002t0001g0111 |
2 | HG00140.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.180-1572T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756966 | |||||||
chr16:56757304 | A | G | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.180-1234A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757304 | |||||||
chr16:56757471 | C | G | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.180-1067C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757471 | |||||||
chr16:56757482 | C | T | 1 | a0001c0001t0003g0372 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.180-1056C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757482 | |||||||
chr16:56757540 | T | C | 2 | a0001c0003t0002g0255 a0001c0003t0002g0256 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.180-998T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757540 | |||||||
chr16:56757568 | T | C | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.180-970T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757568 | |||||||
chr16:56757572 | A | G | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.180-966A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757572 | |||||||
chr16:56757687 | C | T | 1 | a0001c0009t0018g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.180-851C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757687 | |||||||
chr16:56757767 | A | G | 17 | a0001c0001t0006g0202 a0001c0001t0006g0203 a0001c0001t0006g0204 others(14): Show |
17 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.180-771A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757767 | |||||||
chr16:56757829 | C | A | 2 | a0001c0010t0022g0258 a0001c0010t0033g0259 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.180-709C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757829 | |||||||
chr16:56757856 | C | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.180-682C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757856 | |||||||
chr16:56757951 | T | C | 7 | a0001c0002t0001g0066 a0001c0002t0001g0068 a0001c0002t0001g0069 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.180-587T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757951 | |||||||
chr16:56757963 | C | T | 20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.180-575C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757963 | |||||||
chr16:56757971 | T | C | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.180-567T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757971 | |||||||
chr16:56758020 | G | A | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.180-518G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758020 | |||||||
chr16:56758071 | AG | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.180-466delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758071 | |||||||
chr16:56758087 | T | C | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.180-451T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758087 | |||||||
chr16:56758087 | T | G | 129 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(126): Show |
131 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.180-451T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758087 | |||||||
chr16:56758104 | A | G | 164 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(161): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.180-434A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758104 | |||||||
chr16:56758527 | T | A | 6 | a0001c0001t0006g0202 a0001c0001t0006g0204 a0001c0001t0006g0205 others(3): Show |
6 | HG02015.hp1 HG02083.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-11T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758527 | |||||||
chr16:56758973 | C | T | 1 | a0001c0006t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.297+318C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56758973 | |||||||
chr16:56759015 | C | T | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+360C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759015 | |||||||
chr16:56759045 | T | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+390T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759045 | |||||||
chr16:56759155 | G | T | 1 | a0001c0014t0001g0139 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.297+500G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759155 | |||||||
chr16:56759192 | A | G | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+537A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759192 | |||||||
chr16:56759357 | G | T | 2 | a0001c0001t0006g0203 a0001c0001t0006g0208 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.297+702G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759357 | |||||||
chr16:56759434 | C | A | 103 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(100): Show |
103 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.297+779C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759434 | |||||||
chr16:56759713 | C | T | 2 | a0001c0003t0002g0244 a0001c0003t0002g0245 |
2 | NA18939.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.297+1058C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759713 | |||||||
chr16:56759720 | C | G | 1 | a0001c0003t0002g0270 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.297+1065C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759720 | |||||||
chr16:56759721 | G | A | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.297+1066G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759721 | |||||||
chr16:56759838 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.297+1183T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759838 | |||||||
chr16:56759903 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.297+1248A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759903 | |||||||
chr16:56760354 | C | A | 2 | a0001c0002t0001g0098 a0001c0002t0001g0112 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.297+1699C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760354 | |||||||
chr16:56760403 | G | C | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+1748G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760403 | |||||||
chr16:56760678 | C | G | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+2023C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760678 | |||||||
chr16:56760770 | C | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+2115C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760770 | |||||||
chr16:56760841 | G | A | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+2186G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760841 | |||||||
chr16:56760967 | C | A | 21 | a0001c0001t0001g0307 a0001c0001t0006g0199 a0001c0001t0006g0200 others(18): Show |
21 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.297+2312C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760967 | |||||||
chr16:56761025 | A | G | 104 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(101): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.297+2370A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761025 | |||||||
chr16:56761209 | T | C | 5 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(2): Show |
5 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+2554T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761209 | |||||||
chr16:56761380 | T | C | 25 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(22): Show |
25 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.297+2725T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761380 | |||||||
chr16:56761421 | T | C | 3 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 |
3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+2766T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761421 | |||||||
chr16:56761423 | A | C | 1 | a0001c0002t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.297+2768A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761423 | |||||||
chr16:56761561 | A | AT | 348 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(345): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.297+2916dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56761561 | ||||||
chr16:56761561 | A | ATT | 13 | a0001c0001t0001g0168 a0001c0001t0013g0014 a0001c0001t0013g0015 others(10): Show |
14 | HG00741.hp1 HG01106.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+2915_297+2916d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56761561 | ||||||
chr16:56761694 | G | A | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+3039G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761694 | |||||||
chr16:56761711 | A | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0161 |
2 | NA18961.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.297+3056A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761711 | |||||||
chr16:56762169 | T | C | 8 | a0001c0005t0007g0183 a0001c0005t0007g0184 a0001c0005t0007g0185 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+3514T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56762169 | |||||||
chr16:56762848 | G | T | 3 | a0001c0001t0003g0364 a0001c0001t0003g0373 a0001c0001t0003g0374 |
3 | HG01081.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.297+4193G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56762848 | |||||||
chr16:56762877 | G | A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.297+4222G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56762877 | |||||||
chr16:56762992 | A | G | 47 | a0001c0001t0001g0171 a0001c0001t0043g0156 a0001c0002t0001g0046 others(44): Show |
47 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.297+4337A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56762992 | |||||||
chr16:56763059 | T | C | 8 | a0001c0005t0007g0183 a0001c0005t0007g0184 a0001c0005t0007g0185 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+4404T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763059 | |||||||
chr16:56763289 | A | G | 1 | a0001c0002t0001g0076 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.297+4634A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763289 | |||||||
chr16:56763455 | G | A | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.297+4800G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763455 | |||||||
chr16:56763495 | T | G | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+4840T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763495 | |||||||
chr16:56763503 | G | GGT | 3 | a0001c0001t0003g0364 a0001c0001t0003g0373 a0001c0001t0003g0374 |
3 | HG01081.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.297+4859_297+4860d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56763503 | ||||||
chr16:56763503 | G | T | 1 | a0001c0003t0002g0266 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.297+4848G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763503 | |||||||
chr16:56763503 | GGTGTGTG others(17): Show |
G | 14 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0072 others(11): Show |
15 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.297+4865_297+4888d others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56763503 | ||||||
chr16:56763892 | A | G | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+5237A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763892 | |||||||
chr16:56764004 | A | G | 1 | a0005c0024t0018g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.297+5349A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764004 | |||||||
chr16:56764268 | A | C | 2 | a0001c0001t0003g0352 a0001c0001t0003g0372 |
2 | NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.297+5613A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764268 | |||||||
chr16:56764276 | A | T | 1 | a0001c0001t0001g0320 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.297+5621A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764276 | |||||||
chr16:56764319 | G | T | 1 | a0001c0001t0001g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.297+5664G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764319 | |||||||
chr16:56764377 | C | G | 2 | a0001c0001t0016g0192 a0001c0001t0016g0193 |
2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+5722C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764377 | |||||||
chr16:56764707 | T | TG | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.297+6054dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56764707 | ||||||
chr16:56765163 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.297+6508G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765163 | |||||||
chr16:56765315 | C | T | 2 | a0001c0002t0001g0098 a0001c0002t0001g0112 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.297+6660C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765315 | |||||||
chr16:56765379 | A | T | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.297+6724A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765379 | |||||||
chr16:56765441 | A | G | 1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.297+6786A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765441 | |||||||
chr16:56765838 | G | A | 1 | a0001c0001t0003g0359 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.297+7183G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765838 | |||||||
chr16:56765893 | T | G | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+7238T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765893 | |||||||
chr16:56765973 | T | TTAAAAAT others(13): Show |
10 | a0001c0004t0008g0002 a0001c0004t0008g0174 a0001c0004t0008g0175 others(7): Show |
11 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+7328_297+7347d others(22): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56765973 | ||||||
chr16:56766006 | G | A | 2 | a0001c0001t0001g0308 a0001c0003t0002g0286 |
2 | HG00544.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.297+7351G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766006 | |||||||
chr16:56766130 | A | G | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+7475A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766130 | |||||||
chr16:56766139 | G | T | 1 | a0001c0003t0002g0291 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.297+7484G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766139 | |||||||
chr16:56766193 | G | A | 4 | a0001c0001t0006g0204 a0001c0001t0006g0205 a0001c0001t0006g0206 others(1): Show |
4 | HG02083.hp1 NA18747.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+7538G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766193 | |||||||
chr16:56766271 | A | T | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+7616A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766271 | |||||||
chr16:56766415 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.297+7760C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766415 | |||||||
chr16:56766421 | T | A | 329 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(326): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.297+7766T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766421 | |||||||
chr16:56766599 | G | T | 1 | a0001c0001t0003g0367 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.297+7944G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766599 | |||||||
chr16:56766715 | C | T | 2 | a0001c0002t0001g0110 a0001c0002t0001g0111 |
2 | HG00140.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.297+8060C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766715 | |||||||
chr16:56766731 | C | A | 1 | a0001c0002t0001g0084 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.297+8076C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766731 | |||||||
chr16:56766831 | GA | G | 3 | a0001c0002t0010g0050 a0001c0002t0010g0051 a0001c0002t0010g0052 |
3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.297+8177delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766831 | |||||||
chr16:56767135 | C | T | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+8480C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767135 | |||||||
chr16:56767370 | A | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+8715A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767370 | |||||||
chr16:56767467 | T | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.297+8812T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767467 | |||||||
chr16:56767514 | T | A | 1 | a0001c0009t0018g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.297+8859T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767514 | |||||||
chr16:56767695 | G | A | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.297+9040G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767695 | |||||||
chr16:56767783 | C | T | 1 | a0001c0001t0006g0212 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.297+9128C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767783 | |||||||
chr16:56767784 | G | A | 98 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.297+9129G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767784 | |||||||
chr16:56767848 | C | T | 2 | a0001c0001t0016g0192 a0001c0001t0016g0193 |
2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+9193C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767848 | |||||||
chr16:56767946 | A | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+9291A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767946 | |||||||
chr16:56768013 | A | G | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+9358A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768013 | |||||||
chr16:56768080 | A | T | 1 | a0001c0001t0001g0327 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.297+9425A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768080 | |||||||
chr16:56768180 | A | G | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+9525A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768180 | |||||||
chr16:56768259 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0118 |
2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.297+9604G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768259 | |||||||
chr16:56768301 | C | T | 126 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(123): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.297+9646C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768301 | |||||||
chr16:56768302 | G | T | 1 | a0001c0001t0011g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.297+9647G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768302 | |||||||
chr16:56768334 | T | G | 48 | a0001c0001t0002g0282 a0001c0001t0002g0293 a0001c0003t0002g0049 others(45): Show |
48 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.297+9679T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768334 | |||||||
chr16:56768432 | G | A | 4 | a0001c0003t0002g0255 a0001c0003t0002g0256 a0001c0003t0002g0263 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+9777G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768432 | |||||||
chr16:56768450 | C | T | 28 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(25): Show |
28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+9795C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768450 | |||||||
chr16:56768455 | C | T | 2 | a0001c0004t0019g0180 a0001c0004t0019g0181 |
2 | HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.297+9800C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768455 | |||||||
chr16:56768519 | C | T | 1 | a0001c0001t0014g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.297+9864C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768519 | |||||||
chr16:56768574 | A | T | 2 | a0001c0001t0006g0211 a0001c0001t0006g0215 |
2 | HG01255.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.297+9919A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768574 | |||||||
chr16:56768575 | T | A | 6 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+9920T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768575 | |||||||
chr16:56768602 | T | C | 43 | a0001c0001t0001g0140 a0001c0001t0001g0300 a0001c0001t0001g0301 others(40): Show |
43 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.297+9947T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768602 | |||||||
chr16:56768638 | G | A | 1 | a0001c0007t0012g0346 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+9983G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768638 | |||||||
chr16:56768683 | G | A | 24 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0007g0194 others(21): Show |
24 | HG00642.hp2 HG01109.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+10028G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768683 | |||||||
chr16:56768693 | T | C | 14 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
14 | HG00621.hp1 NA18943.hp2 NA18961.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+10038T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768693 | |||||||
chr16:56768702 | TA | T | 15 | a0001c0001t0001g0054 a0001c0001t0001g0132 a0001c0001t0001g0134 others(12): Show |
15 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+10053delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768702 | ||||||
chr16:56768724 | T | A | 2 | a0001c0011t0001g0091 a0001c0011t0001g0092 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.297+10069T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768724 | |||||||
chr16:56768724 | T | G | 14 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
14 | HG00621.hp1 NA18943.hp2 NA18961.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+10069T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768724 | |||||||
chr16:56768727 | T | C | 14 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
14 | HG00621.hp1 NA18943.hp2 NA18961.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+10072T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768727 | |||||||
chr16:56768728 | G | A | 13 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(10): Show |
13 | HG00621.hp1 NA18943.hp2 NA18961.hp2 others(10): Show |
intron_variant | MODIFIER | c.297+10073G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768728 | |||||||
chr16:56768736 | G | A | 28 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0004g0003 others(25): Show |
28 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+10081G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768736 | |||||||
chr16:56768759 | C | T | 4 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+10104C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768759 | |||||||
chr16:56768866 | C | CAA | 8 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0322 others(5): Show |
8 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+10225_297+1022 others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768866 | ||||||
chr16:56768866 | C | CAAA | 243 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(240): Show |
244 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.297+10224_297+1022 others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768866 | ||||||
chr16:56768866 | C | CAAAA | 42 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0301 others(39): Show |
42 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.297+10223_297+1022 others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768866 | ||||||
chr16:56768866 | CA | C | 25 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(22): Show |
25 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.297+10226delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768866 | ||||||
chr16:56769113 | A | G | 3 | a0001c0004t0008g0002 a0001c0004t0008g0176 a0001c0004t0044g0179 |
4 | HG00099.hp2 HG00741.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+10458A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769113 | |||||||
chr16:56769209 | A | G | 2 | a0001c0002t0001g0169 a0001c0012t0001g0081 |
2 | NA19066.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.297+10554A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769209 | |||||||
chr16:56769226 | A | G | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+10571A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769226 | |||||||
chr16:56769287 | C | T | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+10632C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769287 | |||||||
chr16:56769288 | G | A | 7 | a0001c0002t0001g0066 a0001c0002t0001g0068 a0001c0002t0001g0069 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+10633G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769288 | |||||||
chr16:56769379 | G | A | 1 | a0001c0001t0036g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.297+10724G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769379 | |||||||
chr16:56769590 | A | AG | 24 | a0001c0001t0003g0360 a0001c0001t0006g0199 a0001c0001t0006g0200 others(21): Show |
24 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+10937dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56769590 | ||||||
chr16:56769717 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0128 |
2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.297+11062C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769717 | |||||||
chr16:56769746 | T | C | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.297+11091T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769746 | |||||||
chr16:56769794 | A | C | 98 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.297+11139A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769794 | |||||||
chr16:56770128 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.297+11473G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770128 | |||||||
chr16:56770282 | G | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+11627G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770282 | |||||||
chr16:56770492 | G | A | 2 | a0001c0002t0001g0100 a0001c0002t0040g0099 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.297+11837G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770492 | |||||||
chr16:56770526 | C | T | 1 | a0001c0001t0006g0213 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.297+11871C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770526 | |||||||
chr16:56770565 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.297+11910T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770565 | |||||||
chr16:56770780 | T | A | 2 | a0001c0001t0023g0329 a0001c0001t0023g0330 |
2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.297+12125T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770780 | |||||||
chr16:56770907 | T | TA | 97 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(94): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.297+12263dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56770907 | ||||||
chr16:56770982 | G | C | 4 | a0001c0002t0001g0078 a0001c0002t0001g0083 a0001c0002t0001g0169 others(1): Show |
4 | HG02071.hp2 HG02080.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+12327G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770982 | |||||||
chr16:56770999 | C | T | 1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.297+12344C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770999 | |||||||
chr16:56771162 | G | A | 1 | a0001c0009t0018g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.297+12507G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771162 | |||||||
chr16:56771453 | G | A | 12 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0072 others(9): Show |
13 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.297+12798G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771453 | |||||||
chr16:56771563 | G | A | 2 | a0001c0010t0022g0258 a0001c0010t0033g0259 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.297+12908G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771563 | |||||||
chr16:56771566 | G | A | 2 | a0001c0001t0011g0011 a0001c0001t0046g0010 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.297+12911G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771566 | |||||||
chr16:56771598 | A | T | 98 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.297+12943A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771598 | |||||||
chr16:56771642 | A | G | 3 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 |
3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+12987A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771642 | |||||||
chr16:56771670 | A | G | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.297+13015A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771670 | |||||||
chr16:56772167 | G | A | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+13512G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772167 | |||||||
chr16:56772358 | C | T | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+13703C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772358 | |||||||
chr16:56772549 | T | C | 3 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 |
3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+13894T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772549 | |||||||
chr16:56772627 | T | C | 1 | a0001c0002t0001g0129 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.297+13972T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772627 | |||||||
chr16:56772788 | G | T | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.297+14133G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772788 | |||||||
chr16:56772879 | T | C | 1 | a0001c0002t0001g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.297+14224T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772879 | |||||||
chr16:56772890 | G | A | 1 | a0001c0003t0002g0266 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.297+14235G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772890 | |||||||
chr16:56773016 | A | C | 2 | a0001c0011t0001g0091 a0001c0011t0001g0092 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.297+14361A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773016 | |||||||
chr16:56773051 | A | G | 1 | a0001c0001t0036g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.297+14396A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773051 | |||||||
chr16:56773461 | T | C | 1 | a0001c0009t0018g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.297+14806T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773461 | |||||||
chr16:56773478 | T | G | 1 | a0006c0020t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.297+14823T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773478 | |||||||
chr16:56773667 | G | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(161): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.297+15012G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773667 | |||||||
chr16:56773718 | G | A | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+15063G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773718 | |||||||
chr16:56773984 | C | A | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+15329C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773984 | |||||||
chr16:56774445 | T | C | 1 | a0001c0003t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.297+15790T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774445 | |||||||
chr16:56774624 | A | G | 4 | a0001c0002t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+15969A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774624 | |||||||
chr16:56774700 | T | C | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.297+16045T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774700 | |||||||
chr16:56774731 | G | A | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00621.hp1 HG02071.hp1 HG03239.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+16076G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774731 | |||||||
chr16:56774891 | G | T | 4 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+16236G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774891 | |||||||
chr16:56774903 | G | GT | 31 | a0001c0001t0001g0054 a0001c0001t0001g0149 a0001c0001t0001g0333 others(28): Show |
32 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.297+16262dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56774903 | ||||||
chr16:56774903 | GT | G | 7 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(4): Show |
7 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+16262delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56774903 | ||||||
chr16:56774909 | T | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.297+16254T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774909 | |||||||
chr16:56774931 | G | A | 98 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.297+16276G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774931 | |||||||
chr16:56775422 | T | C | 2 | a0001c0001t0001g0301 a0001c0001t0001g0309 |
2 | NA18971.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.297+16767T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775422 | |||||||
chr16:56775521 | G | A | 3 | a0001c0005t0007g0183 a0001c0005t0007g0184 a0001c0005t0007g0185 |
3 | HG02257.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.297+16866G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775521 | |||||||
chr16:56775541 | AG | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.297+16887delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775541 | |||||||
chr16:56775718 | A | G | 1 | a0001c0010t0033g0259 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.297+17063A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775718 | |||||||
chr16:56775834 | G | T | 23 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(20): Show |
23 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.297+17179G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775834 | |||||||
chr16:56775945 | T | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+17290T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775945 | |||||||
chr16:56776058 | AT | A | 160 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(157): Show |
161 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.297+17414delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56776058 | ||||||
chr16:56776219 | T | C | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+17564T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56776219 | |||||||
chr16:56776223 | GT | G | 98 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.297+17574delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56776223 | ||||||
chr16:56776360 | T | C | 1 | a0001c0002t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.297+17705T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56776360 | |||||||
chr16:56776633 | G | A | 1 | a0001c0003t0002g0049 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.297+17978G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56776633 | |||||||
chr16:56776810 | C | G | 1 | a0001c0001t0003g0372 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.297+18155C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56776810 | |||||||
chr16:56777022 | G | C | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.297+18367G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777022 | |||||||
chr16:56777038 | G | A | 3 | a0001c0001t0003g0349 a0001c0001t0003g0350 a0001c0001t0003g0353 |
3 | HG01070.hp1 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.297+18383G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777038 | |||||||
chr16:56777149 | G | A | 1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+18494G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777149 | |||||||
chr16:56777275 | A | G | 11 | a0001c0001t0007g0194 a0001c0001t0007g0195 a0001c0005t0007g0183 others(8): Show |
11 | HG00642.hp2 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.297+18620A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777275 | |||||||
chr16:56777362 | C | CT | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.297+18708dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56777362 | ||||||
chr16:56777501 | C | A | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.297+18846C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777501 | |||||||
chr16:56777506 | C | CT | 6 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(3): Show |
6 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+18859dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56777506 | ||||||
chr16:56777549 | A | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(54): Show |
57 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.297+18894A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777549 | |||||||
chr16:56777603 | T | G | 2 | a0001c0002t0001g0085 a0001c0002t0001g0344 |
2 | HG02015.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.297+18948T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777603 | |||||||
chr16:56777677 | C | T | 1 | a0001c0004t0005g0030 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.297+19022C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777677 | |||||||
chr16:56777692 | G | A | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.297+19037G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777692 | |||||||
chr16:56777717 | A | G | 1 | a0001c0001t0017g0305 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.297+19062A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777717 | |||||||
chr16:56777780 | T | C | 167 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(164): Show |
168 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.297+19125T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777780 | |||||||
chr16:56777913 | G | A | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.297+19258G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777913 | |||||||
chr16:56777955 | T | C | 1 | a0001c0003t0002g0254 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.297+19300T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777955 | |||||||
chr16:56778076 | A | G | 6 | a0001c0001t0004g0198 a0001c0001t0004g0236 a0001c0001t0004g0237 others(3): Show |
6 | HG00597.hp2 NA18959.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+19421A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778076 | |||||||
chr16:56778101 | C | T | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.297+19446C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778101 | |||||||
chr16:56778102 | G | A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.297+19447G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778102 | |||||||
chr16:56778199 | A | G | 3 | a0001c0003t0002g0265 a0001c0003t0002g0273 a0001c0003t0002g0294 |
3 | NA18942.hp2 NA18981.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.297+19544A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778199 | |||||||
chr16:56778388 | C | T | 167 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(164): Show |
168 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.297+19733C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778388 | |||||||
chr16:56778441 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.297+19786A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778441 | |||||||
chr16:56778559 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.297+19904G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778559 | |||||||
chr16:56778765 | A | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-19711A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778765 | |||||||
chr16:56778862 | C | T | 1 | a0001c0003t0002g0254 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.298-19614C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778862 | |||||||
chr16:56779653 | A | G | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-18823A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56779653 | |||||||
chr16:56779752 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.298-18724C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56779752 | |||||||
chr16:56780413 | A | T | 56 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(53): Show |
56 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.298-18063A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780413 | |||||||
chr16:56780583 | A | C | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-17893A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780583 | |||||||
chr16:56780927 | G | A | 1 | a0001c0001t0003g0353 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298-17549G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780927 | |||||||
chr16:56780935 | G | A | 182 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(179): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.298-17541G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780935 | |||||||
chr16:56780994 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18946.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.298-17482C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780994 | |||||||
chr16:56781052 | T | C | 1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.298-17424T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781052 | |||||||
chr16:56781288 | A | G | 10 | a0001c0004t0008g0002 a0001c0004t0008g0174 a0001c0004t0008g0175 others(7): Show |
11 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-17188A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781288 | |||||||
chr16:56781646 | C | T | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.298-16830C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781646 | |||||||
chr16:56781708 | G | A | 2 | a0001c0004t0019g0180 a0001c0004t0019g0181 |
2 | HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.298-16768G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781708 | |||||||
chr16:56781809 | C | A | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.298-16667C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781809 | |||||||
chr16:56782170 | G | A | 2 | a0001c0001t0003g0366 a0001c0001t0003g0367 |
2 | NA18942.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.298-16306G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56782170 | |||||||
chr16:56782183 | G | A | 1 | a0001c0002t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.298-16293G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56782183 | |||||||
chr16:56782540 | T | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.298-15936T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56782540 | |||||||
chr16:56783154 | G | T | 1 | a0001c0003t0002g0264 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.298-15322G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783154 | |||||||
chr16:56783250 | C | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.298-15226C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783250 | |||||||
chr16:56783383 | C | T | 2 | a0001c0002t0001g0085 a0001c0002t0001g0344 |
2 | HG02015.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.298-15093C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783383 | |||||||
chr16:56783465 | A | T | 2 | a0001c0001t0006g0203 a0001c0001t0006g0208 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.298-15011A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783465 | |||||||
chr16:56783585 | A | G | 1 | a0001c0001t0003g0352 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.298-14891A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783585 | |||||||
chr16:56783727 | C | G | 1 | a0001c0001t0036g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.298-14749C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783727 | |||||||
chr16:56783757 | G | C | 1 | a0001c0004t0005g0032 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.298-14719G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783757 | |||||||
chr16:56783992 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.298-14484C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783992 | |||||||
chr16:56784003 | AT | A | 10 | a0001c0004t0008g0002 a0001c0004t0008g0174 a0001c0004t0008g0175 others(7): Show |
11 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-14464delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56784003 | ||||||
chr16:56784329 | A | G | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.298-14147A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784329 | |||||||
chr16:56784347 | A | C | 48 | a0001c0001t0002g0282 a0001c0001t0002g0293 a0001c0003t0002g0049 others(45): Show |
48 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.298-14129A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784347 | |||||||
chr16:56784438 | T | C | 1 | a0001c0010t0033g0259 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.298-14038T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784438 | |||||||
chr16:56784635 | T | G | 329 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(326): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.298-13841T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784635 | |||||||
chr16:56784671 | G | T | 1 | a0001c0001t0006g0213 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.298-13805G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784671 | |||||||
chr16:56784879 | G | A | 1 | a0001c0001t0003g0353 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298-13597G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784879 | |||||||
chr16:56784942 | G | A | 3 | a0001c0001t0017g0305 a0001c0001t0017g0341 a0001c0001t0017g0342 |
3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.298-13534G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784942 | |||||||
chr16:56785075 | A | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.298-13401A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785075 | |||||||
chr16:56785107 | G | A | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298-13369G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785107 | |||||||
chr16:56785259 | T | G | 329 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(326): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.298-13217T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785259 | |||||||
chr16:56785328 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.298-13148G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785328 | |||||||
chr16:56785359 | T | G | 2 | a0001c0004t0005g0032 a0001c0004t0005g0034 |
2 | HG01099.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.298-13117T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785359 | |||||||
chr16:56785565 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.298-12911A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785565 | |||||||
chr16:56785671 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.298-12805T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785671 | |||||||
chr16:56786007 | C | T | 56 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(53): Show |
56 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.298-12469C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786007 | |||||||
chr16:56786024 | G | A | 1 | a0001c0001t0023g0329 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.298-12452G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786024 | |||||||
chr16:56786505 | G | A | 1 | a0001c0006t0009g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.298-11971G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786505 | |||||||
chr16:56786625 | C | G | 3 | a0001c0001t0004g0229 a0001c0001t0004g0230 a0001c0001t0004g0235 |
3 | NA18952.hp1 NA18967.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.298-11851C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786625 | |||||||
chr16:56786647 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0118 |
2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-11829A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786647 | |||||||
chr16:56786690 | T | C | 1 | a0001c0002t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.298-11786T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786690 | |||||||
chr16:56786728 | G | A | 281 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.298-11748G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786728 | |||||||
chr16:56786967 | T | C | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.298-11509T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786967 | |||||||
chr16:56787084 | G | A | 2 | a0001c0001t0003g0354 a0001c0001t0003g0371 |
2 | NA18961.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.298-11392G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787084 | |||||||
chr16:56787204 | GAAAGAAT others(8): Show |
G | 23 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(20): Show |
23 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.298-11269_298-1125 others(19): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56787204 | ||||||
chr16:56787360 | G | C | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298-11116G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787360 | |||||||
chr16:56787508 | T | G | 1 | a0001c0004t0005g0032 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.298-10968T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787508 | |||||||
chr16:56787557 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.298-10919T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787557 | |||||||
chr16:56787607 | C | G | 8 | a0001c0005t0007g0183 a0001c0005t0007g0184 a0001c0005t0007g0185 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-10869C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787607 | |||||||
chr16:56787747 | G | A | 6 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG00099.hp1 HG00735.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-10729G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787747 | |||||||
chr16:56788081 | C | T | 2 | a0001c0003t0002g0255 a0001c0003t0002g0256 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.298-10395C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788081 | |||||||
chr16:56788082 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.298-10394G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788082 | |||||||
chr16:56788127 | G | C | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.298-10349G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788127 | |||||||
chr16:56788156 | C | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298-10320C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788156 | |||||||
chr16:56788233 | G | T | 1 | a0001c0003t0002g0270 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.298-10243G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788233 | |||||||
chr16:56788497 | C | A | 1 | a0001c0003t0042g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.298-9979C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788497 | |||||||
chr16:56788581 | G | A | 2 | a0001c0002t0001g0066 a0001c0007t0012g0067 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.298-9895G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788581 | |||||||
chr16:56788699 | C | G | 1 | a0001c0001t0001g0318 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.298-9777C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788699 | |||||||
chr16:56788730 | C | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.298-9746C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788730 | |||||||
chr16:56788737 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298-9739G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788737 | |||||||
chr16:56788761 | C | G | 3 | a0001c0002t0010g0113 a0001c0002t0010g0114 a0001c0002t0041g0115 |
3 | HG00733.hp2 HG01346.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.298-9715C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788761 | |||||||
chr16:56789000 | G | A | 4 | a0001c0002t0001g0046 a0001c0002t0010g0050 a0001c0002t0010g0051 others(1): Show |
4 | HG00544.hp1 HG01069.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-9476G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789000 | |||||||
chr16:56789089 | T | G | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-9387T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789089 | |||||||
chr16:56789324 | T | A | 1 | a0004c0022t0022g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.298-9152T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789324 | |||||||
chr16:56789325 | A | G | 2 | a0001c0003t0002g0255 a0001c0003t0002g0256 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.298-9151A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789325 | |||||||
chr16:56789419 | T | G | 2 | a0001c0001t0004g0237 a0001c0001t0004g0239 |
2 | NA19083.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.298-9057T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789419 | |||||||
chr16:56789444 | C | T | 1 | a0001c0014t0001g0139 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.298-9032C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789444 | |||||||
chr16:56789614 | C | T | 16 | a0001c0001t0006g0202 a0001c0001t0006g0203 a0001c0001t0006g0204 others(13): Show |
16 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.298-8862C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789614 | |||||||
chr16:56789765 | C | A | 2 | a0001c0004t0024g0041 a0001c0004t0024g0044 |
2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.298-8711C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789765 | |||||||
chr16:56789785 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.298-8691G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789785 | |||||||
chr16:56789799 | G | T | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.298-8677G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789799 | |||||||
chr16:56789815 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.298-8661A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789815 | |||||||
chr16:56789836 | C | T | 2 | a0001c0009t0018g0020 a0005c0024t0018g0012 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298-8640C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789836 | |||||||
chr16:56789946 | A | G | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-8530A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789946 | |||||||
chr16:56789970 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.298-8506G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789970 | |||||||
chr16:56790096 | T | TCAAAA | 90 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(87): Show |
91 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.298-8349_298-8345d others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790096 | ||||||
chr16:56790096 | T | TCAAAACA others(3): Show |
63 | a0001c0001t0001g0309 a0001c0001t0002g0282 a0001c0001t0003g0352 others(60): Show |
63 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.298-8354_298-8345d others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790096 | ||||||
chr16:56790096 | T | TCAAAACA others(8): Show |
11 | a0001c0001t0002g0293 a0001c0003t0002g0254 a0001c0003t0002g0273 others(8): Show |
11 | HG01175.hp2 HG02109.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.298-8359_298-8345d others(17): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790096 | ||||||
chr16:56790096 | TCAAAA | T | 137 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(134): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.298-8349_298-8345d others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790096 | ||||||
chr16:56790115 | A | AACAAAAC others(3): Show |
1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298-8352_298-8351i others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790115 | ||||||
chr16:56790271 | T | G | 371 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(368): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.298-8205T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56790271 | |||||||
chr16:56790407 | A | T | 3 | a0001c0007t0012g0345 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.298-8069A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56790407 | |||||||
chr16:56790633 | T | A | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-7843T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56790633 | |||||||
chr16:56790794 | T | G | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.298-7682T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56790794 | |||||||
chr16:56791012 | C | T | 2 | a0001c0001t0017g0341 a0001c0001t0017g0342 |
2 | NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.298-7464C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791012 | |||||||
chr16:56791046 | A | G | 1 | a0001c0002t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.298-7430A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791046 | |||||||
chr16:56791149 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.298-7327C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791149 | |||||||
chr16:56791523 | C | T | 6 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(3): Show |
6 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-6953C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791523 | |||||||
chr16:56791668 | G | A | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298-6808G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791668 | |||||||
chr16:56791754 | G | A | 64 | a0001c0002t0001g0001 a0001c0002t0001g0046 a0001c0002t0001g0053 others(61): Show |
65 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.298-6722G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791754 | |||||||
chr16:56791818 | G | C | 1 | a0001c0003t0030g0272 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.298-6658G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791818 | |||||||
chr16:56791983 | A | G | 1 | a0001c0001t0003g0366 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.298-6493A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791983 | |||||||
chr16:56791989 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.298-6487A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791989 | |||||||
chr16:56792129 | G | A | 1 | a0001c0001t0043g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.298-6347G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792129 | |||||||
chr16:56792335 | G | GA | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-6140dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56792335 | ||||||
chr16:56792450 | A | C | 56 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(53): Show |
56 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.298-6026A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792450 | |||||||
chr16:56792521 | G | A | 20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-5955G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792521 | |||||||
chr16:56792531 | A | G | 1 | a0001c0003t0002g0278 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.298-5945A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792531 | |||||||
chr16:56792544 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.298-5932G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792544 | |||||||
chr16:56792665 | C | T | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-5811C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792665 | |||||||
chr16:56792706 | A | C | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-5770A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792706 | |||||||
chr16:56792854 | T | C | 173 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(170): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.298-5622T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792854 | |||||||
chr16:56793011 | A | G | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-5465A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793011 | |||||||
chr16:56793133 | A | C | 1 | a0001c0003t0002g0049 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.298-5343A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793133 | |||||||
chr16:56793350 | C | CTT | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-5125_298-5124d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56793350 | ||||||
chr16:56793455 | C | G | 1 | a0001c0001t0003g0359 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298-5021C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793455 | |||||||
chr16:56793458 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0118 |
2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-5018C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793458 | |||||||
chr16:56793542 | T | C | 271 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(268): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.298-4934T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793542 | |||||||
chr16:56793786 | G | C | 1 | a0001c0001t0006g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298-4690G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793786 | |||||||
chr16:56793839 | T | C | 4 | a0001c0004t0005g0033 a0001c0004t0005g0035 a0001c0004t0005g0036 others(1): Show |
4 | HG00741.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-4637T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793839 | |||||||
chr16:56793858 | G | A | 2 | a0001c0001t0006g0199 a0001c0001t0006g0200 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.298-4618G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793858 | |||||||
chr16:56794034 | G | A | 1 | a0001c0001t0003g0360 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.298-4442G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794034 | |||||||
chr16:56794070 | A | G | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.298-4406A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794070 | |||||||
chr16:56794070 | ATAGG | A | 127 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0123 others(124): Show |
128 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.298-4386_298-4383d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794070 | ||||||
chr16:56794074 | G | A | 1 | a0001c0001t0004g0003 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.298-4402G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794074 | |||||||
chr16:56794082 | GTAGGTAG others(5): Show |
G | 22 | a0001c0004t0005g0023 a0001c0004t0005g0024 a0001c0004t0005g0025 others(19): Show |
22 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.298-4390_298-4379d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794082 | ||||||
chr16:56794082 | GTAGGTAG others(9): Show |
G | 4 | a0001c0004t0005g0035 a0001c0009t0018g0020 a0001c0009t0018g0021 others(1): Show |
4 | HG01346.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-4390_298-4375d others(18): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794082 | ||||||
chr16:56794082 | GTAGGTAG others(13): Show |
G | 2 | a0001c0004t0015g0017 a0001c0004t0015g0019 |
2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.298-4390_298-4371d others(22): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794082 | ||||||
chr16:56794086 | G | GTAGA | 19 | a0001c0001t0001g0118 a0001c0001t0001g0143 a0001c0001t0011g0009 others(16): Show |
19 | HG01123.hp1 HG01175.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.298-4387_298-4386i others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794086 | ||||||
chr16:56794086 | GTAGGTAG others(1): Show |
G | 75 | a0001c0001t0001g0054 a0001c0001t0001g0116 a0001c0001t0001g0132 others(72): Show |
75 | HG00099.hp1 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.298-4386_298-4379d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794086 | ||||||
chr16:56794086 | GTAGGTAG others(5): Show |
G | 23 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(20): Show |
23 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.298-4386_298-4375d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794086 | ||||||
chr16:56794090 | G | A | 84 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0143 others(81): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.298-4386G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794090 | |||||||
chr16:56794090 | G | GTAGA | 9 | a0001c0002t0001g0066 a0001c0004t0008g0002 a0001c0006t0009g0247 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.298-4348_298-4345d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794090 | ||||||
chr16:56794090 | G | GTAGATAG others(5): Show |
2 | a0001c0004t0008g0002 a0001c0004t0008g0177 |
2 | HG00741.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.298-4356_298-4345d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794090 | ||||||
chr16:56794090 | GTAGA | G | 13 | a0001c0001t0001g0047 a0001c0001t0001g0055 a0001c0001t0001g0056 others(10): Show |
13 | HG00099.hp2 HG01106.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.298-4348_298-4345d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794090 | ||||||
chr16:56794136 | T | A | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298-4340T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794136 | |||||||
chr16:56794148 | A | C | 1 | a0001c0004t0005g0022 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.298-4328A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794148 | |||||||
chr16:56794409 | A | ATATTT | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.298-4065_298-4064i others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794409 | ||||||
chr16:56794421 | G | T | 2 | a0001c0001t0003g0362 a0001c0001t0003g0363 |
2 | HG00639.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.298-4055G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794421 | |||||||
chr16:56794563 | G | A | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-3913G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794563 | |||||||
chr16:56794584 | T | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.298-3892T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794584 | |||||||
chr16:56794584 | T | TAG | 8 | a0001c0001t0001g0303 a0001c0001t0011g0006 a0001c0001t0011g0007 others(5): Show |
8 | HG00140.hp2 HG01884.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-3864_298-3863d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | ||||||
chr16:56794584 | TAG | T | 71 | a0001c0001t0001g0047 a0001c0001t0003g0004 a0001c0001t0003g0348 others(68): Show |
72 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.298-3864_298-3863d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | ||||||
chr16:56794584 | TAGAG | T | 106 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(103): Show |
106 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.298-3866_298-3863d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | ||||||
chr16:56794584 | TAGAGAG | T | 7 | a0001c0001t0001g0334 a0001c0001t0003g0367 a0001c0007t0012g0346 others(4): Show |
7 | HG02451.hp2 HG02886.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-3868_298-3863d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | ||||||
chr16:56794584 | TAGAGAGA others(1): Show |
T | 45 | a0001c0001t0001g0171 a0001c0002t0001g0046 a0001c0002t0001g0059 others(42): Show |
45 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.298-3870_298-3863d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | ||||||
chr16:56794584 | TAGAGAGA others(3): Show |
T | 20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-3872_298-3863d others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | ||||||
chr16:56794592 | G | C | 1 | a0001c0002t0001g0131 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.298-3884G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794592 | |||||||
chr16:56794604 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298-3872G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794604 | |||||||
chr16:56794710 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.298-3766C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794710 | |||||||
chr16:56794785 | G | A | 1 | a0001c0001t0006g0242 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.298-3691G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794785 | |||||||
chr16:56794811 | C | T | 131 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.298-3665C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794811 | |||||||
chr16:56794826 | G | A | 6 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0212 others(3): Show |
6 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-3650G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794826 | |||||||
chr16:56794853 | G | A | 1 | a0001c0001t0006g0212 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.298-3623G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794853 | |||||||
chr16:56794858 | G | A | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-3618G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794858 | |||||||
chr16:56794927 | CAAAA | C | 20 | a0001c0001t0004g0003 a0001c0001t0004g0220 a0001c0001t0004g0221 others(17): Show |
20 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-3520_298-3517d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | ||||||
chr16:56794927 | CAAAAAAA | C | 41 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(38): Show |
41 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.298-3523_298-3517d others(9): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | ||||||
chr16:56794927 | CAAAAAAA others(1): Show |
C | 22 | a0001c0001t0001g0171 a0001c0001t0043g0156 a0001c0002t0001g0066 others(19): Show |
22 | HG01099.hp1 HG02080.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.298-3524_298-3517d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | ||||||
chr16:56794927 | CAAAAAAA others(2): Show |
C | 160 | a0001c0001t0001g0047 a0001c0001t0001g0141 a0001c0001t0001g0142 others(157): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.298-3525_298-3517d others(11): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | ||||||
chr16:56794927 | CAAAAAAA others(3): Show |
C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0054 others(54): Show |
57 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.298-3526_298-3517d others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | ||||||
chr16:56794927 | CAAAAAAA others(4): Show |
C | 13 | a0001c0001t0007g0194 a0001c0001t0011g0006 a0001c0001t0011g0007 others(10): Show |
13 | HG01884.hp1 HG02258.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.298-3527_298-3517d others(13): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | ||||||
chr16:56794927 | CAAAAAAA others(5): Show |
C | 39 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(36): Show |
40 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.298-3528_298-3517d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | ||||||
chr16:56794927 | CAAAAAAA others(6): Show |
C | 1 | a0001c0005t0007g0189 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.298-3529_298-3517d others(15): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | ||||||
chr16:56795116 | C | CA | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-3360_298-3359i others(3): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795116 | |||||||
chr16:56795212 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.298-3264A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795212 | |||||||
chr16:56795246 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.298-3230C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795246 | |||||||
chr16:56795266 | G | A | 20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-3210G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795266 | |||||||
chr16:56795380 | C | G | 1 | a0001c0001t0001g0307 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.298-3096C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795380 | |||||||
chr16:56795417 | T | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0154 |
3 | NA18992.hp1 NA19005.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.298-3059T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795417 | |||||||
chr16:56795510 | T | C | 6 | a0001c0001t0004g0198 a0001c0001t0004g0236 a0001c0001t0004g0237 others(3): Show |
6 | HG00597.hp2 NA18959.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-2966T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795510 | |||||||
chr16:56795628 | G | A | 67 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(64): Show |
68 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.298-2848G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795628 | |||||||
chr16:56795630 | A | ATATTTT | 156 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0054 others(153): Show |
157 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.298-2814_298-2809d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56795630 | ||||||
chr16:56795630 | A | ATATTTTT others(5): Show |
2 | a0001c0001t0001g0005 a0001c0002t0001g0077 |
2 | HG03098.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.298-2820_298-2809d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56795630 | ||||||
chr16:56795630 | ATATTTTT others(5): Show |
A | 1 | a0001c0002t0001g0169 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.298-2820_298-2809d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56795630 | ||||||
chr16:56795698 | G | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.298-2778G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795698 | |||||||
chr16:56795771 | C | T | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-2705C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795771 | |||||||
chr16:56795791 | C | T | 2 | a0001c0007t0012g0346 a0001c0007t0012g0347 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.298-2685C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795791 | |||||||
chr16:56795838 | G | T | 1 | a0001c0003t0002g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.298-2638G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795838 | |||||||
chr16:56795893 | C | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-2583C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795893 | |||||||
chr16:56796067 | T | C | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-2409T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796067 | |||||||
chr16:56796437 | C | A | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-2039C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796437 | |||||||
chr16:56796481 | C | G | 2 | a0001c0002t0001g0098 a0001c0002t0001g0112 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.298-1995C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796481 | |||||||
chr16:56796867 | G | C | 69 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(66): Show |
70 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.298-1609G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796867 | |||||||
chr16:56796987 | A | G | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-1489A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796987 | |||||||
chr16:56797234 | C | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.298-1242C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797234 | |||||||
chr16:56797254 | A | G | 2 | a0001c0002t0001g0001 a0001c0002t0001g0073 |
3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.298-1222A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797254 | |||||||
chr16:56797386 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.298-1090A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797386 | |||||||
chr16:56797415 | C | A | 2 | a0001c0001t0016g0192 a0001c0001t0016g0193 |
2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.298-1061C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797415 | |||||||
chr16:56797480 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.298-996C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797480 | |||||||
chr16:56797650 | A | G | 14 | a0001c0004t0005g0024 a0001c0004t0005g0025 a0001c0004t0005g0026 others(11): Show |
14 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.298-826A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797650 | |||||||
chr16:56797659 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298-817C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797659 | |||||||
chr16:56797757 | G | A | 2 | a0001c0003t0002g0263 a0001c0003t0002g0285 |
2 | NA18983.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.298-719G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797757 | |||||||
chr16:56797830 | A | G | 1 | a0001c0002t0041g0115 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.298-646A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797830 | |||||||
chr16:56797924 | C | T | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0025 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-552C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797924 | |||||||
chr16:56798299 | T | G | 1 | a0001c0001t0014g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.298-177T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56798299 | |||||||
chr16:56798381 | T | C | 4 | a0001c0007t0012g0067 a0001c0007t0012g0345 a0001c0007t0012g0346 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-95T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56798381 | |||||||
chr16:56798390 | C | T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(52): Show |
55 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.298-86C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56798390 | |||||||
chr16:56798594 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.360+56G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56798594 | |||||||
chr16:56798679 | G | A | 4 | a0001c0007t0012g0067 a0001c0007t0012g0345 a0001c0007t0012g0346 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+141G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56798679 | |||||||
chr16:56798741 | C | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.360+203C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56798741 | |||||||
chr16:56798844 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.360+306G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56798844 | |||||||
chr16:56798871 | C | CA | 7 | a0001c0001t0006g0204 a0001c0001t0013g0014 a0001c0003t0002g0253 others(4): Show |
7 | HG01109.hp2 HG02083.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+349dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56798871 | ||||||
chr16:56798871 | CA | C | 30 | a0001c0001t0001g0135 a0001c0001t0004g0003 a0001c0001t0004g0198 others(27): Show |
30 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.360+349delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56798871 | ||||||
chr16:56799583 | G | A | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.360+1045G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56799583 | |||||||
chr16:56799904 | C | G | 1 | a0001c0001t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.360+1366C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56799904 | |||||||
chr16:56800041 | G | A | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+1503G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800041 | |||||||
chr16:56800051 | C | T | 1 | a0001c0003t0002g0278 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.360+1513C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800051 | |||||||
chr16:56800124 | A | G | 1 | a0001c0003t0002g0278 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.360+1586A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800124 | |||||||
chr16:56800184 | A | G | 171 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(168): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.360+1646A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800184 | |||||||
chr16:56800295 | G | GT | 9 | a0001c0001t0003g0364 a0001c0001t0003g0371 a0001c0001t0028g0358 others(6): Show |
9 | HG01081.hp2 HG01106.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.360+1765dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56800295 | ||||||
chr16:56800322 | G | A | 56 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(53): Show |
56 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.360+1784G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800322 | |||||||
chr16:56800342 | C | G | 56 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(53): Show |
56 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.360+1804C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800342 | |||||||
chr16:56800416 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.360+1878C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800416 | |||||||
chr16:56800570 | A | G | 1 | a0001c0009t0018g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.360+2032A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800570 | |||||||
chr16:56801028 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0154 |
3 | NA18992.hp1 NA19005.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.360+2490C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801028 | |||||||
chr16:56801081 | C | T | 2 | a0001c0007t0012g0346 a0001c0007t0012g0347 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+2543C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801081 | |||||||
chr16:56801213 | CATT | C | 3 | a0001c0003t0002g0265 a0001c0003t0002g0273 a0001c0003t0002g0294 |
3 | NA18942.hp2 NA18981.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.360+2677_360+2679d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56801213 | ||||||
chr16:56801298 | C | G | 1 | a0001c0003t0002g0273 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.360+2760C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801298 | |||||||
chr16:56801570 | G | A | 1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.360+3032G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801570 | |||||||
chr16:56801635 | A | G | 2 | a0001c0005t0007g0186 a0001c0005t0007g0187 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.360+3097A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801635 | |||||||
chr16:56801799 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.360+3261C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801799 | |||||||
chr16:56801800 | G | T | 134 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(131): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.360+3262G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801800 | |||||||
chr16:56801983 | T | G | 2 | a0001c0009t0018g0020 a0005c0024t0018g0012 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.360+3445T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801983 | |||||||
chr16:56802077 | G | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.361-3427G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802077 | |||||||
chr16:56802140 | C | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361-3364C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802140 | |||||||
chr16:56802196 | T | C | 173 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(170): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.361-3308T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802196 | |||||||
chr16:56802305 | C | A | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.361-3199C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802305 | |||||||
chr16:56802410 | G | A | 1 | a0001c0004t0005g0024 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.361-3094G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802410 | |||||||
chr16:56802588 | CA | C | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.361-2915delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802588 | |||||||
chr16:56802647 | A | G | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.361-2857A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802647 | |||||||
chr16:56802826 | G | A | 2 | a0001c0002t0001g0001 a0001c0002t0001g0073 |
3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.361-2678G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802826 | |||||||
chr16:56802849 | G | C | 1 | a0001c0002t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.361-2655G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802849 | |||||||
chr16:56802910 | A | G | 1 | a0001c0001t0001g0304 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.361-2594A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802910 | |||||||
chr16:56803238 | C | T | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.361-2266C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803238 | |||||||
chr16:56803326 | G | A | 1 | a0001c0002t0001g0172 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.361-2178G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803326 | |||||||
chr16:56803382 | A | G | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.361-2122A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803382 | |||||||
chr16:56803456 | T | A | 4 | a0001c0003t0002g0274 a0001c0004t0005g0022 a0001c0004t0005g0042 others(1): Show |
4 | HG00438.hp2 NA18522.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-2048T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803456 | |||||||
chr16:56803676 | A | C | 1 | a0001c0010t0033g0259 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.361-1828A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803676 | |||||||
chr16:56803745 | AAAAT | A | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.361-1757_361-1754d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56803745 | ||||||
chr16:56803747 | AAT | A | 7 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 others(4): Show |
7 | HG00423.hp1 HG01884.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-1738_361-1737d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56803747 | ||||||
chr16:56803747 | AATAT | A | 353 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(350): Show |
355 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.361-1740_361-1737d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56803747 | ||||||
chr16:56803749 | T | A | 1 | a0001c0004t0008g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.361-1755T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803749 | |||||||
chr16:56803810 | C | T | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-1694C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803810 | |||||||
chr16:56803831 | A | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-1673A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803831 | |||||||
chr16:56803867 | G | T | 2 | a0001c0001t0023g0329 a0001c0001t0023g0330 |
2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.361-1637G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803867 | |||||||
chr16:56803963 | G | A | 1 | a0001c0002t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.361-1541G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803963 | |||||||
chr16:56804157 | C | T | 1 | a0001c0002t0010g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.361-1347C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804157 | |||||||
chr16:56804187 | CCTTGCAG others(5): Show |
C | 4 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-1301_361-1290d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56804187 | ||||||
chr16:56804189 | T | A | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.361-1315T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804189 | |||||||
chr16:56804595 | A | G | 4 | a0001c0002t0001g0046 a0001c0002t0001g0087 a0001c0002t0001g0089 others(1): Show |
4 | HG00544.hp1 HG00609.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-909A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804595 | |||||||
chr16:56804675 | G | A | 92 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(89): Show |
93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.361-829G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804675 | |||||||
chr16:56804691 | C | T | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.361-813C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804691 | |||||||
chr16:56804767 | G | A | 4 | a0002c0008t0002g0296 a0002c0008t0002g0297 a0002c0008t0002g0298 others(1): Show |
4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-737G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804767 | |||||||
chr16:56804861 | G | A | 1 | a0001c0001t0006g0211 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.361-643G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804861 | |||||||
chr16:56804905 | C | CA | 7 | a0001c0001t0001g0307 a0001c0001t0003g0353 a0001c0001t0023g0329 others(4): Show |
7 | HG00140.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-583dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56804905 | ||||||
chr16:56804905 | CA | C | 7 | a0001c0001t0001g0163 a0001c0002t0001g0131 a0001c0003t0002g0270 others(4): Show |
7 | HG02895.hp2 NA18940.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-583delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56804905 | ||||||
chr16:56804957 | A | G | 1 | a0001c0001t0043g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.361-547A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804957 | |||||||
chr16:56805015 | A | T | 3 | a0001c0002t0001g0087 a0001c0002t0001g0089 a0001c0002t0001g0097 |
3 | HG00609.hp2 HG02083.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.361-489A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805015 | |||||||
chr16:56805040 | C | G | 3 | a0001c0004t0008g0174 a0001c0004t0008g0175 a0001c0004t0008g0178 |
3 | HG01106.hp1 HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.361-464C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805040 | |||||||
chr16:56805066 | T | G | 206 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(203): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.361-438T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805066 | |||||||
chr16:56805107 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.361-397G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805107 | |||||||
chr16:56805114 | A | G | 2 | a0001c0001t0043g0156 a0001c0002t0001g0101 |
2 | HG03579.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.361-390A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805114 | |||||||
chr16:56805124 | C | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.361-380C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805124 | |||||||
chr16:56805284 | G | A | 1 | a0004c0022t0022g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.361-220G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805284 | |||||||
chr16:56805434 | T | A | 3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.361-70T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805434 | |||||||
chr16:56805725 | C | A | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+93C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56805725 | |||||||
chr16:56805908 | C | T | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.489+276C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56805908 | |||||||
chr16:56806115 | T | C | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.489+483T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806115 | |||||||
chr16:56806259 | A | G | 172 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(169): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.489+627A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806259 | |||||||
chr16:56806309 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.489+677A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806309 | |||||||
chr16:56806416 | G | A | 67 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(64): Show |
68 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.489+784G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806416 | |||||||
chr16:56806527 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.489+895G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806527 | |||||||
chr16:56806963 | C | T | 7 | a0001c0001t0039g0317 a0001c0002t0001g0066 a0001c0002t0001g0068 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+1331C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806963 | |||||||
chr16:56807042 | A | C | 1 | a0001c0001t0001g0308 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.489+1410A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807042 | |||||||
chr16:56807056 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.489+1424C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807056 | |||||||
chr16:56807067 | G | C | 1 | a0001c0010t0033g0259 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.489+1435G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807067 | |||||||
chr16:56807293 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.489+1661C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807293 | |||||||
chr16:56807356 | T | G | 6 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0322 others(3): Show |
6 | HG00140.hp2 HG00735.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+1724T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807356 | |||||||
chr16:56807748 | C | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.489+2116C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807748 | |||||||
chr16:56807802 | C | T | 170 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(167): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.489+2170C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807802 | |||||||
chr16:56807881 | G | A | 1 | a0001c0001t0014g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.489+2249G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807881 | |||||||
chr16:56807966 | T | G | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+2334T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807966 | |||||||
chr16:56808016 | C | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.489+2384C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808016 | |||||||
chr16:56808100 | C | A | 4 | a0002c0008t0002g0296 a0002c0008t0002g0297 a0002c0008t0002g0298 others(1): Show |
4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2468C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808100 | |||||||
chr16:56808115 | A | ATTATATA others(15): Show |
4 | a0001c0001t0011g0006 a0001c0001t0011g0008 a0001c0001t0011g0011 others(1): Show |
4 | HG02630.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2499_489+2520d others(24): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808115 | ||||||
chr16:56808124 | C | A | 160 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(157): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.489+2492C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808124 | |||||||
chr16:56808131 | A | AAAT | 53 | a0001c0001t0002g0282 a0001c0001t0002g0293 a0001c0002t0001g0089 others(50): Show |
53 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.489+2500_489+2501i others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | ||||||
chr16:56808131 | A | AAATATAT others(394): Show |
1 | a0001c0003t0002g0262 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489+2500_489+2501i others(403): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | ||||||
chr16:56808131 | A | AAATATAT others(286): Show |
1 | a0001c0001t0002g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.489+2500_489+2501i others(295): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | ||||||
chr16:56808131 | A | AAATATAT others(21): Show |
2 | a0001c0003t0002g0283 a0001c0003t0042g0284 |
2 | HG02622.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.489+2500_489+2501i others(30): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | ||||||
chr16:56808131 | A | AAATATAT others(344): Show |
1 | a0001c0003t0002g0245 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.489+2500_489+2501i others(353): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | ||||||
chr16:56808131 | A | AAATATAT others(369): Show |
1 | a0001c0003t0002g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.489+2500_489+2501i others(378): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | ||||||
chr16:56808137 | T | G | 59 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(56): Show |
59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.489+2505T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808137 | |||||||
chr16:56808137 | T | TTTATATA others(43): Show |
3 | a0001c0004t0015g0017 a0001c0004t0015g0018 a0001c0004t0015g0019 |
3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.489+2520_489+2521i others(52): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808137 | ||||||
chr16:56808137 | T | TTTATATA others(143): Show |
1 | a0001c0009t0018g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+2520_489+2521i others(152): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808137 | ||||||
chr16:56808137 | T | TTTATATA others(168): Show |
1 | a0001c0009t0018g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2520_489+2521i others(177): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808137 | ||||||
chr16:56808141 | T | C | 2 | a0001c0001t0002g0290 a0001c0003t0002g0262 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.489+2509T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808141 | |||||||
chr16:56808142 | A | G | 4 | a0001c0001t0002g0290 a0001c0003t0002g0245 a0001c0003t0002g0246 others(1): Show |
4 | HG01243.hp2 HG01261.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2510A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808142 | |||||||
chr16:56808146 | CT | C | 2 | a0001c0004t0008g0002 a0001c0004t0008g0176 |
3 | HG00741.hp1 HG03669.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.489+2515delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808146 | |||||||
chr16:56808153 | T | A | 269 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(266): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.489+2521T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | |||||||
chr16:56808153 | T | TAATATAT others(143): Show |
1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(152): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808153 | ||||||
chr16:56808153 | T | TAATATAT others(68): Show |
3 | a0001c0001t0003g0359 a0001c0001t0003g0372 a0008c0023t0026g0370 |
3 | HG03471.hp2 HG04204.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.489+2570_489+2571i others(77): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808153 | ||||||
chr16:56808153 | T | TAATATAT others(93): Show |
1 | a0001c0001t0003g0371 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.489+2570_489+2571i others(102): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808153 | ||||||
chr16:56808153 | T | TAATATAT others(93): Show |
1 | a0001c0001t0003g0004 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.489+2545_489+2546i others(102): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808153 | ||||||
chr16:56808153 | T | TTTTATAT others(18): Show |
1 | a0001c0001t0004g0228 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.489+2521_489+2522i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | |||||||
chr16:56808153 | T | TTTTATAT others(18): Show |
19 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0221 others(16): Show |
19 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.489+2521_489+2522i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | |||||||
chr16:56808153 | T | TTTTATAT others(68): Show |
1 | a0001c0001t0004g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.489+2521_489+2522i others(77): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | |||||||
chr16:56808153 | T | TTTTATAT others(93): Show |
3 | a0001c0001t0004g0220 a0001c0001t0004g0230 a0001c0001t0004g0234 |
3 | HG01433.hp2 HG01496.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.489+2521_489+2522i others(102): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | |||||||
chr16:56808155 | A | ATATATAG others(43): Show |
17 | a0001c0001t0003g0348 a0001c0001t0003g0349 a0001c0001t0003g0350 others(14): Show |
17 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+2570_489+2571i others(52): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808155 | ||||||
chr16:56808166 | T | C | 5 | a0001c0001t0002g0290 a0001c0003t0002g0262 a0001c0007t0012g0345 others(2): Show |
5 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2534T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808166 | |||||||
chr16:56808167 | A | ATAACTAT others(18): Show |
1 | a0001c0004t0008g0176 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.489+2559_489+2560i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808167 | ||||||
chr16:56808167 | A | G | 15 | a0001c0001t0002g0290 a0001c0001t0004g0220 a0001c0001t0004g0227 others(12): Show |
15 | HG01243.hp2 HG01261.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2535A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808167 | |||||||
chr16:56808180 | A | ATATATAG others(18): Show |
4 | a0001c0001t0003g0360 a0001c0001t0003g0364 a0001c0001t0003g0373 others(1): Show |
4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2570_489+2571i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808180 | ||||||
chr16:56808181 | TATATAGT others(116): Show |
T | 1 | a0001c0001t0006g0205 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.489+2555_489+2677d others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808181 | ||||||
chr16:56808182 | A | ATATAGTT others(16): Show |
1 | a0007c0013t0007g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.489+2570_489+2571i others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808182 | ||||||
chr16:56808191 | T | C | 5 | a0001c0001t0002g0290 a0001c0003t0002g0262 a0001c0007t0012g0345 others(2): Show |
5 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2559T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808191 | |||||||
chr16:56808192 | A | ATAACTAT others(218): Show |
1 | a0001c0001t0011g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+2583_489+2584i others(227): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(68): Show |
1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.489+2583_489+2584i others(77): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(168): Show |
1 | a0005c0024t0018g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(177): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(391): Show |
2 | a0001c0003t0002g0275 a0001c0003t0002g0280 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.489+2584_489+2585i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(466): Show |
2 | a0001c0003t0002g0255 a0001c0003t0002g0256 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.489+2584_489+2585i others(475): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(341): Show |
1 | a0001c0003t0002g0286 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(350): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(316): Show |
1 | a0001c0003t0002g0285 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(325): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(291): Show |
1 | a0001c0003t0002g0277 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(300): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(291): Show |
1 | a0001c0003t0002g0270 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(300): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(316): Show |
1 | a0001c0003t0002g0288 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(325): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(341): Show |
2 | a0001c0003t0002g0261 a0001c0003t0002g0276 |
2 | HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.489+2584_489+2585i others(350): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(391): Show |
1 | a0001c0003t0002g0265 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(416): Show |
2 | a0001c0003t0002g0254 a0001c0003t0002g0273 |
2 | NA18942.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.489+2584_489+2585i others(425): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(341): Show |
1 | a0001c0003t0002g0291 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(350): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(343): Show |
1 | a0001c0003t0021g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(352): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(368): Show |
1 | a0001c0003t0021g0292 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(377): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(18): Show |
5 | a0001c0004t0008g0002 a0001c0004t0008g0174 a0001c0004t0008g0175 others(2): Show |
6 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+2819_489+2843d others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(43): Show |
1 | a0001c0004t0019g0181 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.489+2794_489+2843d others(52): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(366): Show |
1 | a0001c0003t0002g0263 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.489+2793_489+2794i others(375): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(341): Show |
2 | a0001c0003t0002g0283 a0001c0003t0030g0272 |
2 | HG02622.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.489+2818_489+2819i others(350): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(366): Show |
2 | a0001c0003t0002g0244 a0001c0003t0002g0278 |
2 | HG01099.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.489+2818_489+2819i others(375): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(391): Show |
2 | a0001c0003t0002g0279 a0002c0008t0002g0296 |
2 | HG01175.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.489+2870_489+2871i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(416): Show |
1 | a0002c0008t0002g0297 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.489+2870_489+2871i others(425): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(566): Show |
1 | a0001c0003t0002g0294 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.489+2870_489+2871i others(575): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(468): Show |
1 | a0001c0003t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(477): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | ATAACTAT others(43): Show |
1 | a0001c0001t0003g0365 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.489+2570_489+2571i others(52): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808192 | A | G | 24 | a0001c0001t0002g0290 a0001c0001t0004g0220 a0001c0001t0004g0227 others(21): Show |
24 | HG01109.hp2 HG01243.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.489+2560A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808192 | |||||||
chr16:56808192 | ATAACTAT others(18): Show |
A | 1 | a0001c0004t0045g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.489+2819_489+2843d others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | ||||||
chr16:56808198 | A | ATATAAAA others(391): Show |
1 | a0001c0001t0002g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808198 | ||||||
chr16:56808203 | A | T | 12 | a0001c0001t0007g0194 a0001c0001t0007g0195 a0001c0001t0007g0340 others(9): Show |
12 | HG00642.hp2 HG01109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+2571A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808203 | |||||||
chr16:56808204 | A | T | 12 | a0001c0001t0007g0194 a0001c0001t0007g0195 a0001c0001t0007g0340 others(9): Show |
12 | HG00642.hp2 HG01109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+2572A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808204 | |||||||
chr16:56808205 | A | ATATATAG others(18): Show |
1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808205 | ||||||
chr16:56808205 | A | T | 10 | a0001c0001t0007g0194 a0001c0001t0007g0195 a0001c0001t0007g0340 others(7): Show |
10 | HG00642.hp2 HG01109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+2573A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808205 | |||||||
chr16:56808216 | T | C | 7 | a0001c0001t0002g0290 a0001c0001t0011g0007 a0001c0003t0002g0262 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+2584T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808216 | |||||||
chr16:56808217 | G | A | 263 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(260): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.489+2585G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808217 | |||||||
chr16:56808217 | G | GTAACTAT others(18): Show |
1 | a0001c0001t0002g0293 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.489+2609_489+2610i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808217 | ||||||
chr16:56808221 | CTA | C | 19 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(16): Show |
19 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.489+2594_489+2595d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808221 | ||||||
chr16:56808223 | A | ATATAAAA others(266): Show |
1 | a0004c0022t0022g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.489+2608_489+2609i others(275): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808223 | ||||||
chr16:56808223 | A | ATATAAAA others(16): Show |
1 | a0001c0002t0001g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.489+2609_489+2610i others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808223 | ||||||
chr16:56808228 | A | T | 3 | a0001c0001t0016g0192 a0001c0001t0016g0193 a0001c0001t0034g0196 |
3 | HG02258.hp2 HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.489+2596A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808228 | |||||||
chr16:56808229 | A | T | 3 | a0001c0001t0016g0192 a0001c0001t0016g0193 a0001c0001t0034g0196 |
3 | HG02258.hp2 HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.489+2597A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808229 | |||||||
chr16:56808230 | A | T | 3 | a0001c0001t0016g0192 a0001c0001t0016g0193 a0001c0001t0034g0196 |
3 | HG02258.hp2 HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.489+2598A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808230 | |||||||
chr16:56808231 | T | TATATAGT others(41): Show |
1 | a0001c0004t0005g0040 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.489+2609_489+2610i others(50): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808231 | ||||||
chr16:56808231 | T | TATATAGT others(285): Show |
1 | a0001c0002t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.489+2609_489+2610i others(294): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808231 | ||||||
chr16:56808233 | T | A | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.489+2601T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808233 | |||||||
chr16:56808241 | T | C | 15 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0003t0002g0262 others(12): Show |
15 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2609T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808241 | |||||||
chr16:56808242 | G | A | 252 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(249): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.489+2610G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808242 | |||||||
chr16:56808256 | T | TATATAGT others(164): Show |
1 | a0001c0001t0001g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.489+2634_489+2635i others(173): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808256 | ||||||
chr16:56808256 | T | TATATAGT others(212): Show |
1 | a0001c0002t0001g0110 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.489+2634_489+2635i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808256 | ||||||
chr16:56808256 | T | TATATAGT others(237): Show |
1 | a0001c0002t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.489+2634_489+2635i others(246): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808256 | ||||||
chr16:56808256 | T | TATATAGT others(212): Show |
1 | a0001c0002t0001g0088 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.489+2634_489+2635i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808256 | ||||||
chr16:56808266 | T | C | 15 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0003t0002g0262 others(12): Show |
15 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2634T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808266 | |||||||
chr16:56808267 | G | A | 233 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(230): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.489+2635G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808267 | |||||||
chr16:56808281 | T | TATAGTTA others(185): Show |
1 | a0001c0002t0001g0085 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.489+2652_489+2653i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | ||||||
chr16:56808281 | T | TATATAGT others(235): Show |
1 | a0001c0002t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.489+2659_489+2660i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | ||||||
chr16:56808281 | T | TATATAGT others(187): Show |
5 | a0001c0002t0001g0074 a0001c0002t0001g0107 a0001c0002t0001g0166 others(2): Show |
5 | HG00408.hp1 HG02027.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2659_489+2660i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | ||||||
chr16:56808281 | T | TATATAGT others(212): Show |
3 | a0001c0002t0001g0078 a0001c0002t0001g0082 a0001c0002t0001g0339 |
3 | HG02056.hp2 HG02071.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.489+2659_489+2660i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | ||||||
chr16:56808281 | T | TATATAGT others(235): Show |
2 | a0001c0002t0001g0077 a0001c0012t0001g0081 |
2 | NA19002.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.489+2659_489+2660i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | ||||||
chr16:56808288 | T | TTATATAA others(37): Show |
3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+2659_489+2660i others(46): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808288 | ||||||
chr16:56808291 | T | C | 15 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0003t0002g0262 others(12): Show |
15 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2659T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808291 | |||||||
chr16:56808292 | G | A | 216 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(213): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.489+2660G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808292 | |||||||
chr16:56808304 | AATATATA others(45): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.489+2678_489+2729d others(54): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808304 | ||||||
chr16:56808306 | T | TATATAGT others(114): Show |
1 | a0001c0001t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+2684_489+2685i others(123): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808306 | ||||||
chr16:56808306 | T | TATATAGT others(39): Show |
1 | a0001c0002t0001g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.489+2684_489+2685i others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808306 | ||||||
chr16:56808306 | T | TATATAGT others(210): Show |
5 | a0001c0002t0001g0096 a0001c0002t0001g0100 a0001c0002t0001g0101 others(2): Show |
5 | HG02886.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2684_489+2685i others(219): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808306 | ||||||
chr16:56808316 | T | C | 15 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0003t0002g0262 others(12): Show |
15 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2684T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808316 | |||||||
chr16:56808317 | G | A | 200 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(197): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.489+2685G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808317 | |||||||
chr16:56808321 | CTA | C | 17 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0303 others(14): Show |
17 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+2694_489+2695d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808321 | ||||||
chr16:56808331 | T | TATATAGT others(162): Show |
2 | a0001c0001t0001g0322 a0001c0001t0023g0330 |
2 | HG01123.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.489+2709_489+2710i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | ||||||
chr16:56808331 | T | TATATAGT others(162): Show |
3 | a0001c0001t0017g0305 a0001c0001t0017g0341 a0001c0001t0017g0342 |
3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.489+2709_489+2710i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | ||||||
chr16:56808331 | T | TATATAGT others(187): Show |
1 | a0001c0001t0001g0321 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.489+2709_489+2710i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | ||||||
chr16:56808331 | T | TATATAGT others(212): Show |
1 | a0001c0001t0001g0343 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.489+2709_489+2710i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | ||||||
chr16:56808331 | T | TATATAGT others(235): Show |
1 | a0001c0002t0001g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.489+2709_489+2710i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | ||||||
chr16:56808341 | T | C | 14 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0003t0002g0262 others(11): Show |
14 | HG01243.hp2 HG02132.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+2709T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808341 | |||||||
chr16:56808342 | G | A | 200 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(197): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.489+2710G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808342 | |||||||
chr16:56808346 | CTA | C | 29 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0146 others(26): Show |
29 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.489+2719_489+2720d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808346 | ||||||
chr16:56808348 | A | ATAAAATA others(185): Show |
1 | a0001c0002t0037g0086 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.489+2718_489+2719i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808348 | ||||||
chr16:56808348 | A | ATAAAATA others(185): Show |
2 | a0001c0001t0001g0316 a0001c0001t0001g0318 |
2 | HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.489+2718_489+2719i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808348 | ||||||
chr16:56808353 | A | T | 3 | a0001c0001t0001g0316 a0001c0001t0001g0318 a0001c0002t0037g0086 |
3 | HG01358.hp2 HG01981.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.489+2721A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808353 | |||||||
chr16:56808354 | AAT | A | 7 | a0001c0001t0001g0165 a0001c0001t0001g0336 a0001c0002t0001g0110 others(4): Show |
7 | HG00140.hp1 HG01891.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2728_489+2729d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808354 | ||||||
chr16:56808356 | T | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0318 a0001c0002t0037g0086 |
3 | HG01358.hp2 HG01981.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.489+2724T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808356 | |||||||
chr16:56808356 | T | TATATAGT others(114): Show |
1 | a0001c0001t0001g0149 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.489+2734_489+2735i others(123): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | ||||||
chr16:56808356 | T | TATATAGT others(162): Show |
7 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
7 | HG01496.hp1 HG02451.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2734_489+2735i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | ||||||
chr16:56808356 | T | TATATAGT others(187): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0118 a0001c0001t0001g0126 |
3 | HG01433.hp1 HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.489+2734_489+2735i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | ||||||
chr16:56808356 | T | TATATAGT others(187): Show |
1 | a0001c0001t0001g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489+2734_489+2735i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | ||||||
chr16:56808356 | T | TATATAGT others(212): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+2734_489+2735i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | ||||||
chr16:56808366 | T | C | 14 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0003t0002g0262 others(11): Show |
14 | HG01243.hp2 HG02132.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+2734T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808366 | |||||||
chr16:56808366 | T | TATAACTA others(235): Show |
1 | a0001c0002t0001g0062 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.489+2734_489+2735i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808366 | |||||||
chr16:56808366 | T | TATAACTA others(308): Show |
1 | a0001c0002t0001g0063 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.489+2734_489+2735i others(317): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808366 | |||||||
chr16:56808367 | G | A | 195 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(192): Show |
196 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.489+2735G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808367 | |||||||
chr16:56808371 | CTA | C | 21 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0141 others(18): Show |
21 | HG00621.hp1 HG01069.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.489+2744_489+2745d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808371 | ||||||
chr16:56808371 | CTATATAA others(70): Show |
C | 2 | a0001c0001t0006g0203 a0001c0001t0006g0208 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.489+2744_489+2820d others(79): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808371 | ||||||
chr16:56808373 | A | ATAAAATA others(83): Show |
1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.489+2743_489+2744i others(92): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | ||||||
chr16:56808373 | A | ATAAAATA others(185): Show |
2 | a0001c0002t0001g0068 a0006c0020t0001g0065 |
2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.489+2743_489+2744i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | ||||||
chr16:56808373 | A | ATAAAATA others(210): Show |
1 | a0001c0002t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.489+2743_489+2744i others(219): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | ||||||
chr16:56808373 | A | ATAAAATA others(306): Show |
2 | a0001c0002t0001g0075 a0001c0019t0001g0080 |
2 | NA18954.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.489+2743_489+2744i others(315): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | ||||||
chr16:56808373 | A | ATAAAATA others(235): Show |
2 | a0001c0002t0001g0103 a0001c0002t0001g0131 |
2 | HG02602.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.489+2743_489+2744i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | ||||||
chr16:56808373 | A | ATAAATAT others(135): Show |
1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+2743_489+2744i others(144): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | ||||||
chr16:56808378 | A | T | 8 | a0001c0001t0001g0163 a0001c0002t0001g0068 a0001c0002t0001g0075 others(5): Show |
8 | HG02074.hp1 HG02602.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+2746A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808378 | |||||||
chr16:56808379 | AAT | A | 25 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0343 others(22): Show |
25 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.489+2753_489+2754d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808379 | ||||||
chr16:56808381 | T | A | 8 | a0001c0001t0001g0163 a0001c0002t0001g0068 a0001c0002t0001g0075 others(5): Show |
8 | HG02074.hp1 HG02602.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+2749T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808381 | |||||||
chr16:56808381 | T | TATATAGT others(283): Show |
1 | a0001c0002t0001g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(292): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(185): Show |
1 | a0001c0002t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(137): Show |
1 | a0001c0001t0043g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(210): Show |
1 | a0001c0002t0001g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(219): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(285): Show |
1 | a0001c0002t0001g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(294): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(162): Show |
1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(281): Show |
1 | a0001c0002t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(290): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(187): Show |
1 | a0001c0001t0001g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(187): Show |
1 | a0001c0001t0001g0171 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(237): Show |
1 | a0001c0002t0001g0109 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(246): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(41): Show |
1 | a0001c0004t0005g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(50): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(231): Show |
1 | a0001c0002t0001g0169 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(240): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(185): Show |
2 | a0001c0002t0001g0076 a0001c0002t0001g0093 |
2 | HG01123.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.489+2759_489+2760i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(212): Show |
1 | a0001c0017t0001g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(210): Show |
4 | a0001c0002t0001g0084 a0001c0002t0001g0090 a0001c0002t0001g0094 others(1): Show |
4 | HG01258.hp1 HG02148.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2759_489+2760i others(219): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(162): Show |
6 | a0001c0001t0001g0301 a0001c0001t0001g0309 a0001c0001t0001g0312 others(3): Show |
6 | NA18944.hp2 NA18971.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2759_489+2760i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(262): Show |
1 | a0001c0001t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(271): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808381 | T | TATATAGT others(116): Show |
1 | a0001c0004t0005g0031 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(125): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | ||||||
chr16:56808391 | T | C | 16 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0002t0001g0062 others(13): Show |
16 | HG01243.hp2 HG02132.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+2759T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808391 | |||||||
chr16:56808392 | G | A | 178 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(175): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.489+2760G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808392 | |||||||
chr16:56808396 | CTA | C | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0318 others(3): Show |
6 | HG00609.hp1 HG01358.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2769_489+2770d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808396 | ||||||
chr16:56808398 | A | ATAAAATA others(137): Show |
1 | a0001c0001t0001g0161 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.489+2768_489+2769i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808398 | ||||||
chr16:56808398 | A | ATAAAATA others(233): Show |
1 | a0001c0002t0001g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.489+2768_489+2769i others(242): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808398 | ||||||
chr16:56808403 | A | T | 2 | a0001c0001t0001g0161 a0001c0002t0001g0098 |
2 | HG02280.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.489+2771A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808403 | |||||||
chr16:56808404 | AAT | A | 5 | a0001c0001t0001g0149 a0001c0002t0001g0112 a0001c0004t0015g0017 others(2): Show |
5 | HG02258.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2778_489+2779d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808404 | ||||||
chr16:56808406 | T | A | 2 | a0001c0001t0001g0161 a0001c0002t0001g0098 |
2 | HG02280.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.489+2774T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808406 | |||||||
chr16:56808416 | T | C | 16 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0001t0007g0195 others(13): Show |
16 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+2784T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808416 | |||||||
chr16:56808417 | G | A | 148 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.489+2785G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808417 | |||||||
chr16:56808421 | CTA | C | 18 | a0001c0001t0001g0301 a0001c0001t0001g0309 a0001c0001t0001g0312 others(15): Show |
18 | HG00621.hp2 HG01123.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+2794_489+2795d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808421 | ||||||
chr16:56808421 | CTATATAA others(20): Show |
C | 18 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(15): Show |
18 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+2794_489+2820d others(29): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808421 | ||||||
chr16:56808423 | A | ATAAAATA others(187): Show |
1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.489+2793_489+2794i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808423 | ||||||
chr16:56808423 | A | ATAAAATA others(308): Show |
1 | a0001c0002t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.489+2793_489+2794i others(317): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808423 | ||||||
chr16:56808423 | A | ATATAAAA others(135): Show |
5 | a0001c0001t0001g0300 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG00140.hp2 NA18946.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2802_489+2803i others(144): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808423 | ||||||
chr16:56808423 | A | ATATAAAA others(137): Show |
1 | a0001c0001t0001g0335 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.489+2802_489+2803i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808423 | ||||||
chr16:56808441 | T | C | 14 | a0001c0001t0002g0290 a0001c0001t0007g0194 a0001c0001t0007g0195 others(11): Show |
14 | HG00642.hp2 HG02257.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+2809T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808441 | |||||||
chr16:56808442 | G | A | 103 | a0001c0001t0001g0054 a0001c0001t0001g0116 a0001c0001t0001g0122 others(100): Show |
104 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.489+2810G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808442 | |||||||
chr16:56808446 | CTA | C | 142 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(139): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.489+2819_489+2820d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808446 | ||||||
chr16:56808448 | A | ATAAAATA others(256): Show |
1 | a0001c0001t0001g0116 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.489+2818_489+2819i others(265): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATAAAATA others(235): Show |
1 | a0001c0001t0001g0132 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.489+2818_489+2819i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATAAAATA others(283): Show |
3 | a0001c0002t0001g0001 a0001c0002t0001g0073 a0001c0002t0001g0172 |
4 | HG00642.hp1 HG01361.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2818_489+2819i others(292): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATAAAATA others(306): Show |
1 | a0001c0002t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.489+2818_489+2819i others(315): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATAAAATA others(39): Show |
1 | a0001c0001t0027g0369 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.489+2818_489+2819i others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(185): Show |
9 | a0001c0002t0001g0046 a0001c0002t0001g0059 a0001c0002t0001g0060 others(6): Show |
9 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+2827_489+2828i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(158): Show |
1 | a0001c0001t0001g0125 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.489+2827_489+2828i others(167): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(231): Show |
1 | a0001c0001t0025g0310 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.489+2827_489+2828i others(240): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(158): Show |
10 | a0001c0001t0001g0302 a0001c0001t0001g0311 a0001c0001t0001g0319 others(7): Show |
10 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+2827_489+2828i others(167): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(181): Show |
1 | a0001c0001t0001g0314 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.489+2827_489+2828i others(190): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(158): Show |
1 | a0001c0001t0001g0333 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.489+2827_489+2828i others(167): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(137): Show |
1 | a0001c0016t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.489+2827_489+2828i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(160): Show |
1 | a0001c0001t0001g0124 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.489+2827_489+2828i others(169): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(112): Show |
1 | a0001c0001t0001g0146 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.489+2827_489+2828i others(121): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(135): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18946.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.489+2827_489+2828i others(144): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(110): Show |
2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02155.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.489+2827_489+2828i others(119): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(64): Show |
1 | a0001c0004t0005g0040 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.489+2827_489+2828i others(73): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(16): Show |
1 | a0001c0005t0007g0186 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.489+2833_489+2834i others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(64): Show |
1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489+2833_489+2834i others(73): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(260): Show |
4 | a0001c0001t0001g0054 a0001c0001t0001g0133 a0001c0001t0001g0159 others(1): Show |
4 | HG02257.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2834_489+2835i others(269): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(308): Show |
1 | a0001c0002t0010g0113 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(317): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(185): Show |
2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(135): Show |
1 | a0001c0001t0036g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(144): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(160): Show |
1 | a0001c0001t0001g0127 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(169): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(160): Show |
2 | a0001c0001t0001g0308 a0001c0001t0001g0328 |
2 | HG03654.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(169): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(183): Show |
2 | a0001c0001t0001g0307 a0001c0001t0001g0325 |
2 | NA19002.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(192): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(137): Show |
10 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(7): Show |
10 | HG00621.hp1 NA18943.hp2 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+2834_489+2835i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(112): Show |
1 | a0001c0001t0001g0151 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(121): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(89): Show |
1 | a0001c0004t0024g0041 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(98): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(285): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(294): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(356): Show |
1 | a0001c0002t0010g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(365): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(333): Show |
2 | a0001c0011t0001g0091 a0001c0011t0001g0092 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(342): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(208): Show |
1 | a0001c0001t0001g0315 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(217): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(114): Show |
12 | a0001c0004t0005g0022 a0001c0004t0005g0024 a0001c0004t0005g0025 others(9): Show |
12 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+2834_489+2835i others(123): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(139): Show |
7 | a0001c0004t0005g0027 a0001c0004t0005g0028 a0001c0004t0005g0030 others(4): Show |
7 | HG00741.hp2 HG01261.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2834_489+2835i others(148): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(260): Show |
1 | a0001c0002t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(269): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(189): Show |
1 | a0001c0004t0005g0033 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(198): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(285): Show |
1 | a0001c0002t0041g0115 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(294): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(110): Show |
1 | a0001c0001t0013g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(119): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(133): Show |
1 | a0001c0001t0013g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(142): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(16): Show |
1 | a0001c0001t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.489+2844_489+2866d others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(85): Show |
1 | a0001c0001t0013g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.489+2866_489+2867i others(94): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808448 | A | ATATAAAA others(66): Show |
7 | a0001c0001t0004g0198 a0001c0001t0004g0228 a0001c0001t0004g0236 others(4): Show |
7 | HG00597.hp2 NA18959.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+2843_489+2844i others(75): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | ||||||
chr16:56808450 | A | ATAAAATA others(137): Show |
1 | a0001c0007t0012g0346 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808450 | ||||||
chr16:56808450 | A | ATAAAATA others(162): Show |
2 | a0001c0007t0012g0067 a0001c0007t0012g0347 |
2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808450 | ||||||
chr16:56808456 | T | TATATAGT others(260): Show |
1 | a0001c0014t0001g0139 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(269): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808456 | ||||||
chr16:56808456 | T | TATATAGT others(14): Show |
2 | a0001c0004t0015g0017 a0001c0004t0015g0019 |
2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.489+2830_489+2850d others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808456 | ||||||
chr16:56808456 | T | TATATAGT others(216): Show |
1 | a0001c0001t0011g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(225): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808456 | ||||||
chr16:56808456 | T | TATATAGT others(241): Show |
1 | a0001c0001t0011g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(250): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808456 | ||||||
chr16:56808466 | T | C | 6 | a0001c0001t0001g0116 a0001c0001t0002g0290 a0001c0002t0001g0062 others(3): Show |
6 | HG02559.hp2 HG02717.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2834T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808466 | |||||||
chr16:56808467 | G | A | 4 | a0001c0001t0001g0123 a0001c0002t0010g0050 a0001c0002t0010g0051 others(1): Show |
4 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2835G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808467 | |||||||
chr16:56808471 | C | CTA | 15 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0011g0009 others(12): Show |
15 | HG00597.hp1 HG00673.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2842_489+2843d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATAAAA others(366): Show |
1 | a0001c0003t0032g0269 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.489+2866_489+2867i others(375): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATAAAA others(343): Show |
2 | a0001c0003t0002g0253 a0001c0003t0002g0287 |
2 | HG01109.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.489+2870_489+2871i others(352): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATAAAA others(368): Show |
2 | a0001c0003t0002g0264 a0001c0003t0002g0274 |
2 | HG01928.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.489+2870_489+2871i others(377): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(20): Show |
1 | a0001c0003t0002g0261 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(29): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(391): Show |
1 | a0001c0003t0002g0049 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(466): Show |
1 | a0002c0008t0002g0298 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(475): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(45): Show |
3 | a0001c0006t0009g0249 a0001c0006t0009g0250 a0001c0006t0009g0251 |
3 | HG02818.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(54): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(466): Show |
1 | a0001c0003t0002g0267 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(475): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(70): Show |
2 | a0001c0006t0009g0247 a0001c0006t0009g0248 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(79): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(91): Show |
7 | a0001c0001t0004g0223 a0001c0001t0004g0225 a0001c0001t0004g0229 others(4): Show |
7 | HG00408.hp2 HG00733.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2843_489+2844i others(100): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(116): Show |
6 | a0001c0001t0004g0003 a0001c0001t0004g0221 a0001c0001t0004g0222 others(3): Show |
6 | NA18941.hp1 NA18945.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2843_489+2844i others(125): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(116): Show |
2 | a0001c0001t0011g0011 a0001c0001t0046g0010 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(125): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(493): Show |
1 | a0001c0001t0002g0293 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(502): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(318): Show |
2 | a0001c0003t0020g0281 a0001c0003t0020g0295 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(327): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(370): Show |
1 | a0001c0003t0002g0268 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(379): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808471 | C | CTATATAA others(395): Show |
2 | a0001c0010t0022g0258 a0001c0010t0033g0259 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(404): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | ||||||
chr16:56808475 | A | AT | 4 | a0001c0001t0001g0125 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG03239.hp1 HG04199.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2843_489+2844i others(3): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808475 | |||||||
chr16:56808476 | A | T | 2 | a0001c0009t0018g0020 a0001c0009t0018g0021 |
2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2844A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808476 | |||||||
chr16:56808479 | T | A | 2 | a0001c0009t0018g0020 a0001c0009t0018g0021 |
2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2847T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808479 | |||||||
chr16:56808479 | T | TATAGTTA others(12): Show |
1 | a0001c0004t0015g0018 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.489+2850_489+2851i others(21): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808479 | ||||||
chr16:56808489 | T | C | 3 | a0001c0001t0001g0116 a0001c0001t0002g0290 a0009c0021t0001g0013 |
3 | HG02717.hp1 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489+2857T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808489 | |||||||
chr16:56808489 | T | TATAACTA others(331): Show |
1 | a0001c0001t0001g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.489+2857_489+2858i others(340): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808489 | |||||||
chr16:56808490 | G | A | 41 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(38): Show |
42 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.489+2858G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808490 | |||||||
chr16:56808498 | AT | A | 3 | a0001c0001t0004g0220 a0001c0001t0004g0227 a0001c0001t0004g0234 |
3 | HG01433.hp2 HG01496.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.489+2867delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808498 | |||||||
chr16:56808499 | T | TA | 6 | a0001c0001t0002g0290 a0001c0001t0011g0009 a0001c0009t0018g0020 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2870dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808499 | ||||||
chr16:56808499 | T | TAAAATAT others(17): Show |
1 | a0001c0003t0002g0276 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.489+2870_489+2871i others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808499 | ||||||
chr16:56808499 | T | TAAAATAT others(417): Show |
1 | a0002c0008t0002g0299 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.489+2870_489+2871i others(426): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808499 | ||||||
chr16:56808501 | A | AAATATAT others(392): Show |
2 | a0001c0003t0002g0266 a0001c0003t0002g0289 |
2 | HG02056.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.489+2870_489+2871i others(401): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808501 | ||||||
chr16:56808501 | A | AAATATAT others(293): Show |
1 | a0001c0003t0042g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.489+2870_489+2871i others(302): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808501 | ||||||
chr16:56808501 | A | AAATATAT others(18): Show |
1 | a0001c0003t0030g0272 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.489+2870_489+2871i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808501 | ||||||
chr16:56808501 | A | T | 45 | a0001c0002t0001g0046 a0001c0002t0001g0059 a0001c0002t0001g0060 others(42): Show |
45 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.489+2869A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808501 | |||||||
chr16:56808502 | AT | A | 3 | a0001c0002t0010g0050 a0001c0002t0010g0051 a0001c0002t0010g0052 |
3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.489+2871delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808502 | |||||||
chr16:56808503 | T | A | 49 | a0001c0002t0001g0046 a0001c0002t0001g0059 a0001c0002t0001g0060 others(46): Show |
49 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.489+2871T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808503 | |||||||
chr16:56808503 | T | TATATAGT others(17): Show |
10 | a0001c0003t0002g0253 a0001c0003t0002g0264 a0001c0003t0002g0268 others(7): Show |
10 | HG01109.hp2 HG01928.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+2882_489+2905d others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808503 | ||||||
chr16:56808513 | T | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG02717.hp1 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2881T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808513 | |||||||
chr16:56808514 | G | A | 3 | a0001c0002t0010g0050 a0001c0002t0010g0051 a0001c0002t0010g0052 |
3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.489+2882G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808514 | |||||||
chr16:56808524 | AT | A | 5 | a0001c0002t0010g0050 a0001c0002t0010g0051 a0001c0002t0010g0052 others(2): Show |
5 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+2893delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808524 | |||||||
chr16:56808525 | T | A | 28 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(25): Show |
28 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.489+2893T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808525 | |||||||
chr16:56808527 | A | T | 27 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(24): Show |
27 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.489+2895A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808527 | |||||||
chr16:56808537 | T | C | 1 | a0001c0001t0002g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.489+2905T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808537 | |||||||
chr16:56808538 | A | G | 106 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(103): Show |
106 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.489+2906A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808538 | |||||||
chr16:56808545 | T | TATA | 6 | a0001c0001t0011g0009 a0001c0002t0010g0050 a0001c0002t0010g0051 others(3): Show |
6 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+2914_489+2915i others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808545 | ||||||
chr16:56808552 | A | ATAGTTAT others(192): Show |
3 | a0001c0002t0010g0050 a0001c0002t0010g0051 a0001c0002t0010g0052 |
3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.489+2922_489+2923i others(201): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808552 | ||||||
chr16:56808552 | A | ATAGTTAT others(221): Show |
1 | a0001c0001t0011g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.489+2922_489+2923i others(230): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808552 | ||||||
chr16:56808554 | A | AGTTACGT others(50): Show |
1 | a0005c0024t0018g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489+2922_489+2923i others(59): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808554 | |||||||
chr16:56808554 | A | AGTTATGT others(50): Show |
1 | a0001c0009t0018g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+2922_489+2923i others(59): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808554 | |||||||
chr16:56808555 | A | AAAATATA others(25): Show |
11 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0003g0360 others(8): Show |
11 | HG00438.hp2 HG01884.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+2984_489+3015d others(34): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808555 | ||||||
chr16:56808555 | A | AAAATATA others(57): Show |
1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.489+2952_489+3015d others(66): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808555 | ||||||
chr16:56808555 | A | AAAATATA others(53): Show |
3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.489+2964_489+2965i others(62): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808555 | ||||||
chr16:56808555 | A | T | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2923A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808555 | |||||||
chr16:56808556 | A | C | 4 | a0001c0001t0011g0009 a0001c0002t0010g0050 a0001c0002t0010g0051 others(1): Show |
4 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2924A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808556 | |||||||
chr16:56808557 | A | T | 6 | a0001c0001t0011g0009 a0001c0002t0010g0050 a0001c0002t0010g0051 others(3): Show |
6 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+2925A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808557 | |||||||
chr16:56808558 | A | C | 1 | a0001c0009t0018g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2926A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808558 | |||||||
chr16:56808565 | A | G | 2 | a0001c0009t0018g0021 a0005c0024t0018g0012 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2933A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808565 | |||||||
chr16:56808565 | A | T | 1 | a0001c0009t0018g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2933A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808565 | |||||||
chr16:56808566 | A | T | 2 | a0001c0009t0018g0021 a0005c0024t0018g0012 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2934A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808566 | |||||||
chr16:56808569 | C | G | 1 | a0001c0009t0018g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2937C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808569 | |||||||
chr16:56808569 | C | T | 6 | a0001c0001t0011g0009 a0001c0002t0010g0050 a0001c0002t0010g0051 others(3): Show |
6 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+2937C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808569 | |||||||
chr16:56808570 | A | T | 1 | a0001c0009t0018g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2938A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808570 | |||||||
chr16:56808571 | T | G | 4 | a0001c0001t0011g0009 a0001c0002t0010g0050 a0001c0002t0010g0051 others(1): Show |
4 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2939T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808571 | |||||||
chr16:56808572 | T | A | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2940T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808572 | |||||||
chr16:56808573 | T | A | 2 | a0001c0009t0018g0021 a0005c0024t0018g0012 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2941T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808573 | |||||||
chr16:56808574 | A | ATATAAC | 4 | a0001c0001t0011g0009 a0001c0002t0010g0050 a0001c0002t0010g0051 others(1): Show |
4 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2947_489+2948i others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808574 | ||||||
chr16:56808574 | A | C | 2 | a0001c0009t0018g0021 a0005c0024t0018g0012 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2942A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808574 | |||||||
chr16:56808584 | T | A | 7 | a0001c0001t0011g0009 a0001c0002t0010g0050 a0001c0002t0010g0051 others(4): Show |
7 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2952T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808584 | |||||||
chr16:56808584 | T | TTATAAAT others(25): Show |
1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.489+2983_489+2984i others(34): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808584 | ||||||
chr16:56808587 | T | A | 7 | a0001c0001t0011g0009 a0001c0002t0010g0050 a0001c0002t0010g0051 others(4): Show |
7 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2955T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808587 | |||||||
chr16:56808590 | A | ATATATAA others(39): Show |
5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2969_489+3014d others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808590 | ||||||
chr16:56808623 | T | A | 4 | a0001c0002t0001g0078 a0001c0002t0001g0083 a0001c0002t0001g0169 others(1): Show |
4 | HG02071.hp2 HG02080.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2991T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808623 | |||||||
chr16:56808631 | T | TACATTTA others(15): Show |
6 | a0001c0001t0001g0315 a0001c0001t0001g0320 a0001c0001t0001g0321 others(3): Show |
6 | HG00609.hp1 NA18946.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+3001_489+3022d others(24): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808631 | ||||||
chr16:56808650 | AAAAATAC others(18): Show |
A | 2 | a0001c0004t0024g0041 a0001c0004t0024g0044 |
2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.489+3048_489+3072d others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808650 | ||||||
chr16:56808700 | TA | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(169): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.489+3073delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808700 | ||||||
chr16:56808724 | TAAATACA others(6): Show |
T | 1 | a0006c0020t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.489+3108_489+3120d others(15): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808724 | ||||||
chr16:56808736 | T | TA | 361 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(358): Show |
363 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.489+3108dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808736 | ||||||
chr16:56808847 | C | CAT | 3 | a0001c0001t0004g0228 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.489+3224_489+3225d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808847 | ||||||
chr16:56808871 | A | G | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.489+3239A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808871 | |||||||
chr16:56808997 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3365G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808997 | |||||||
chr16:56808999 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3367G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808999 | |||||||
chr16:56809002 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3370T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809002 | |||||||
chr16:56809003 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3371G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809003 | |||||||
chr16:56809004 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3372T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809004 | |||||||
chr16:56809005 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3373A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809005 | |||||||
chr16:56809006 | T | C | 3 | a0001c0006t0009g0248 a0001c0006t0009g0249 a0001c0006t0009g0251 |
3 | HG02615.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.489+3374T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809006 | |||||||
chr16:56809008 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3376T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809008 | |||||||
chr16:56809010 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3378C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809010 | |||||||
chr16:56809049 | A | C | 271 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(268): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.489+3417A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809049 | |||||||
chr16:56809086 | G | A | 23 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(20): Show |
23 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.489+3454G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809086 | |||||||
chr16:56809107 | A | G | 3 | a0001c0001t0003g0366 a0001c0001t0003g0367 a0001c0001t0003g0368 |
3 | NA18942.hp1 NA18952.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.489+3475A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809107 | |||||||
chr16:56809351 | A | G | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+3719A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809351 | |||||||
chr16:56809414 | T | TA | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.489+3786dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56809414 | ||||||
chr16:56809531 | G | A | 61 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(58): Show |
61 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.489+3899G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809531 | |||||||
chr16:56809613 | G | C | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+3981G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809613 | |||||||
chr16:56809651 | AC | A | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.489+4020delC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809651 | |||||||
chr16:56810111 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+4479C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810111 | |||||||
chr16:56810189 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.489+4557G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810189 | |||||||
chr16:56810252 | C | T | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.489+4620C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810252 | |||||||
chr16:56810331 | G | A | 3 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0001t0001g0318 |
3 | HG01358.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.489+4699G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810331 | |||||||
chr16:56810457 | C | T | 2 | a0001c0005t0007g0188 a0001c0005t0007g0197 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.489+4825C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810457 | |||||||
chr16:56810547 | G | A | 4 | a0001c0007t0012g0067 a0001c0007t0012g0345 a0001c0007t0012g0346 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+4915G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810547 | |||||||
chr16:56810659 | T | A | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+5027T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810659 | |||||||
chr16:56810727 | TACCAGCG others(33): Show |
T | 40 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(37): Show |
41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.489+5140_489+5179d others(42): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56810727 | ||||||
chr16:56810762 | C | A | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.489+5130C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810762 | |||||||
chr16:56811048 | T | C | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.489+5416T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811048 | |||||||
chr16:56811207 | A | C | 2 | a0001c0002t0001g0061 a0001c0002t0001g0064 |
2 | NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.489+5575A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811207 | |||||||
chr16:56811263 | C | A | 4 | a0001c0007t0012g0067 a0001c0007t0012g0345 a0001c0007t0012g0346 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+5631C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811263 | |||||||
chr16:56811388 | A | T | 13 | a0001c0001t0001g0054 a0001c0001t0001g0132 a0001c0001t0001g0133 others(10): Show |
13 | HG00099.hp1 HG00735.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+5756A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811388 | |||||||
chr16:56811478 | A | C | 2 | a0001c0001t0006g0210 a0001c0001t0006g0212 |
2 | HG01070.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.489+5846A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811478 | |||||||
chr16:56811517 | G | GT | 47 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0303 others(44): Show |
47 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.489+5896dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56811517 | ||||||
chr16:56811562 | G | C | 1 | a0001c0004t0005g0032 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.489+5930G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811562 | |||||||
chr16:56812118 | C | T | 2 | a0001c0002t0001g0001 a0001c0002t0001g0073 |
3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.489+6486C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812118 | |||||||
chr16:56812308 | A | G | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-6356A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812308 | |||||||
chr16:56812500 | C | T | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-6164C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812500 | |||||||
chr16:56812595 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-6069G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812595 | |||||||
chr16:56812624 | T | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(41): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.490-6040T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812624 | |||||||
chr16:56812644 | C | G | 1 | a0001c0017t0001g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.490-6020C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812644 | |||||||
chr16:56812852 | C | T | 12 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0072 others(9): Show |
13 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-5812C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812852 | |||||||
chr16:56812892 | C | T | 51 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(48): Show |
51 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.490-5772C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812892 | |||||||
chr16:56813003 | A | G | 5 | a0001c0002t0001g0096 a0001c0002t0001g0100 a0001c0002t0001g0101 others(2): Show |
5 | HG02886.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-5661A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813003 | |||||||
chr16:56813358 | G | A | 40 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(37): Show |
41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.490-5306G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813358 | |||||||
chr16:56813472 | G | A | 30 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.490-5192G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813472 | |||||||
chr16:56813655 | G | C | 1 | a0009c0021t0001g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.490-5009G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813655 | |||||||
chr16:56813676 | C | T | 1 | a0001c0002t0001g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.490-4988C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813676 | |||||||
chr16:56813838 | C | T | 2 | a0001c0001t0006g0201 a0001c0001t0006g0241 |
2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.490-4826C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813838 | |||||||
chr16:56814017 | C | A | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.490-4647C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814017 | |||||||
chr16:56814121 | A | T | 2 | a0001c0011t0001g0091 a0001c0011t0001g0092 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.490-4543A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814121 | |||||||
chr16:56814157 | G | A | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.490-4507G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814157 | |||||||
chr16:56814330 | C | T | 3 | a0001c0002t0010g0050 a0001c0002t0010g0051 a0001c0002t0010g0052 |
3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.490-4334C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814330 | |||||||
chr16:56814332 | C | T | 1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.490-4332C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814332 | |||||||
chr16:56814443 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490-4221G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814443 | |||||||
chr16:56814613 | C | T | 2 | a0001c0001t0006g0204 a0001c0001t0006g0206 |
2 | HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.490-4051C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814613 | |||||||
chr16:56814665 | C | T | 1 | a0001c0003t0002g0275 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.490-3999C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814665 | |||||||
chr16:56814731 | G | A | 1 | a0001c0004t0005g0037 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.490-3933G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814731 | |||||||
chr16:56814959 | G | A | 55 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(52): Show |
55 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.490-3705G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814959 | |||||||
chr16:56815074 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.490-3590A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815074 | |||||||
chr16:56815181 | TACA | T | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-3477_490-3475d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815181 | ||||||
chr16:56815202 | A | G | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-3462A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815202 | |||||||
chr16:56815206 | TG | T | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-3457delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815206 | |||||||
chr16:56815247 | C | G | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-3417C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815247 | |||||||
chr16:56815517 | T | C | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-3147T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815517 | |||||||
chr16:56815548 | CTGT | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-3109_490-3107d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815548 | ||||||
chr16:56815584 | G | A | 176 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(173): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.490-3080G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815584 | |||||||
chr16:56815678 | A | C | 2 | a0001c0004t0015g0017 a0001c0004t0015g0019 |
2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.490-2986A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815678 | |||||||
chr16:56815743 | A | G | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-2921A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815743 | |||||||
chr16:56815865 | A | ACTG | 93 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(90): Show |
94 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.490-2768_490-2766d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTG | 140 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0054 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.490-2771_490-2766d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(2): Show |
27 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0140 others(24): Show |
27 | HG00621.hp1 HG01346.hp2 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.490-2774_490-2766d others(11): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(11): Show |
2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02155.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.490-2788_490-2787i others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(5): Show |
3 | a0001c0001t0001g0151 a0001c0009t0018g0020 a0001c0009t0018g0021 |
3 | HG03209.hp1 HG03516.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.490-2777_490-2766d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(8): Show |
6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2780_490-2766d others(17): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(11): Show |
12 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0039 others(9): Show |
12 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-2783_490-2766d others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(14): Show |
2 | a0001c0004t0005g0038 a0005c0024t0018g0012 |
2 | HG02451.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.490-2786_490-2766d others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(17): Show |
1 | a0001c0004t0005g0029 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.490-2789_490-2766d others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(29): Show |
1 | a0001c0004t0005g0036 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.490-2766_490-2765i others(38): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(32): Show |
6 | a0001c0004t0005g0025 a0001c0004t0005g0027 a0001c0004t0005g0028 others(3): Show |
6 | HG01261.hp1 HG01993.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2766_490-2765i others(41): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | A | ACTGCTGC others(35): Show |
3 | a0001c0004t0005g0024 a0001c0004t0005g0032 a0001c0004t0005g0035 |
3 | HG01099.hp2 HG01346.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.490-2766_490-2765i others(44): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | ACTGCTG | A | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.490-2771_490-2766d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | ACTGCTGC others(5): Show |
A | 2 | a0001c0001t0036g0150 a0001c0003t0002g0287 |
2 | HG02300.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.490-2777_490-2766d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815865 | ACTGCTGC others(8): Show |
A | 10 | a0001c0003t0002g0267 a0001c0006t0009g0247 a0001c0006t0009g0248 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-2780_490-2766d others(17): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | ||||||
chr16:56815881 | C | CTGCTGCT others(17): Show |
1 | a0001c0002t0041g0115 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.490-2766_490-2765i others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815881 | ||||||
chr16:56815881 | C | CTGCTGCT others(14): Show |
11 | a0001c0001t0003g0353 a0001c0001t0003g0354 a0001c0001t0003g0355 others(8): Show |
11 | HG00323.hp1 HG00639.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-2766_490-2765i others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815881 | ||||||
chr16:56815881 | CTGCTGCT others(11): Show |
C | 6 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0072 others(3): Show |
7 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-2751_490-2734d others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815881 | ||||||
chr16:56815896 | C | CTGG | 4 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2765_490-2763d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815896 | ||||||
chr16:56815899 | G | C | 4 | a0001c0004t0005g0031 a0001c0009t0018g0020 a0001c0009t0018g0021 others(1): Show |
4 | HG02451.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2765G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815899 | |||||||
chr16:56815899 | G | GTGC | 11 | a0001c0001t0003g0353 a0001c0001t0003g0354 a0001c0001t0003g0355 others(8): Show |
11 | HG00323.hp1 HG00639.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-2750_490-2748d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815899 | ||||||
chr16:56815899 | G | GTGCTGCT others(14): Show |
33 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(30): Show |
34 | HG00642.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.490-2754_490-2734d others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815899 | ||||||
chr16:56815899 | GTGC | G | 26 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(23): Show |
26 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-2750_490-2748d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815899 | ||||||
chr16:56815902 | C | CTGCTGCT others(32): Show |
1 | a0001c0004t0005g0031 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.490-2748_490-2747i others(41): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815902 | ||||||
chr16:56815922 | G | A | 1 | a0001c0001t0031g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.490-2742G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815922 | |||||||
chr16:56815947 | C | T | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-2717C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815947 | |||||||
chr16:56815968 | A | C | 1 | a0001c0001t0011g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-2696A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815968 | |||||||
chr16:56815973 | T | A | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.490-2691T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815973 | |||||||
chr16:56816087 | T | C | 2 | a0001c0010t0022g0258 a0001c0010t0033g0259 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.490-2577T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816087 | |||||||
chr16:56816448 | A | T | 2 | a0001c0011t0001g0091 a0001c0011t0001g0092 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.490-2216A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816448 | |||||||
chr16:56816548 | T | C | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2116T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816548 | |||||||
chr16:56816611 | A | G | 58 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
58 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.490-2053A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816611 | |||||||
chr16:56816690 | A | G | 174 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(171): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.490-1974A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816690 | |||||||
chr16:56816939 | G | A | 1 | a0001c0004t0005g0039 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.490-1725G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816939 | |||||||
chr16:56817000 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490-1664A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817000 | |||||||
chr16:56817075 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.490-1589G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817075 | |||||||
chr16:56817175 | A | C | 2 | a0001c0010t0022g0258 a0001c0010t0033g0259 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.490-1489A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817175 | |||||||
chr16:56817180 | A | T | 1 | a0001c0003t0002g0262 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.490-1484A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817180 | |||||||
chr16:56817352 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.490-1312C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817352 | |||||||
chr16:56817504 | T | C | 14 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0072 others(11): Show |
15 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-1160T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817504 | |||||||
chr16:56817534 | C | T | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-1130C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817534 | |||||||
chr16:56817655 | CTG | C | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-1008_490-1007d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817655 | |||||||
chr16:56817723 | G | A | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-941G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817723 | |||||||
chr16:56817893 | T | A | 4 | a0001c0001t0003g0349 a0001c0001t0003g0350 a0001c0001t0003g0353 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-771T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817893 | |||||||
chr16:56817921 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.490-743C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817921 | |||||||
chr16:56818399 | A | C | 333 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(330): Show |
335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.490-265A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818399 | |||||||
chr16:56818427 | G | T | 1 | a0001c0003t0002g0280 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490-237G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818427 | |||||||
chr16:56818430 | G | A | 1 | a0008c0023t0026g0370 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.490-234G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818430 | |||||||
chr16:56818456 | A | G | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.490-208A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818456 | |||||||
chr16:56818477 | T | C | 92 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(89): Show |
93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.490-187T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818477 | |||||||
chr16:56818853 | AT | A | 3 | a0001c0005t0007g0183 a0001c0005t0007g0184 a0001c0005t0007g0185 |
3 | HG02257.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.564+118delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr16 | 56818853 | ||||||
chr16:56818910 | G | T | 171 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(168): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.564+172G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56818910 | |||||||
chr16:56819530 | G | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.564+792G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56819530 | |||||||
chr16:56819572 | A | G | 1 | a0001c0003t0002g0289 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.564+834A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56819572 | |||||||
chr16:56819644 | A | G | 2 | a0001c0002t0001g0001 a0001c0002t0001g0073 |
3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.564+906A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56819644 | |||||||
chr16:56819845 | C | T | 1 | a0001c0002t0001g0344 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.564+1107C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56819845 | |||||||
chr16:56820090 | C | A | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.564+1352C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820090 | |||||||
chr16:56820093 | T | G | 1 | a0001c0005t0007g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.564+1355T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820093 | |||||||
chr16:56820184 | C | T | 1 | a0001c0004t0005g0039 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.565-1320C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820184 | |||||||
chr16:56820240 | A | C | 1 | a0001c0014t0001g0139 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.565-1264A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820240 | |||||||
chr16:56820372 | C | T | 92 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(89): Show |
93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.565-1132C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820372 | |||||||
chr16:56820508 | G | A | 2 | a0001c0003t0002g0254 a0001c0003t0002g0279 |
2 | HG01175.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.565-996G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820508 | |||||||
chr16:56820615 | C | T | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.565-889C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820615 | |||||||
chr16:56820837 | A | G | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.565-667A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820837 | |||||||
chr16:56820953 | C | T | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(1): Show |
4 | HG00735.hp2 HG01081.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-551C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820953 | |||||||
chr16:56821112 | C | T | 2 | a0001c0005t0007g0183 a0001c0005t0007g0184 |
2 | HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.565-392C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56821112 | |||||||
chr16:56821280 | C | T | 51 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(48): Show |
51 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.565-224C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56821280 | |||||||
chr16:56821399 | A | G | 1 | a0001c0003t0002g0277 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.565-105A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56821399 | |||||||
chr16:56821637 | TC | T | 56 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(53): Show |
56 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.654+46delC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56821637 | ||||||
chr16:56822098 | C | CA | 18 | a0001c0001t0001g0163 a0001c0001t0001g0343 a0001c0001t0003g0363 others(15): Show |
18 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.654+523dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56822098 | ||||||
chr16:56822116 | A | G | 5 | a0001c0003t0002g0271 a0001c0007t0012g0067 a0001c0007t0012g0346 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.654+523A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822116 | |||||||
chr16:56822442 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.654+849G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822442 | |||||||
chr16:56822446 | C | A | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.654+853C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822446 | |||||||
chr16:56822564 | C | CT | 157 | a0001c0001t0001g0335 a0001c0001t0002g0282 a0001c0001t0002g0290 others(154): Show |
158 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.654+984dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56822564 | ||||||
chr16:56822564 | C | CTT | 171 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(168): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.654+983_654+984dup others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56822564 | ||||||
chr16:56822564 | CT | C | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.654+984delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56822564 | ||||||
chr16:56822660 | A | G | 72 | a0001c0002t0001g0001 a0001c0002t0001g0046 a0001c0002t0001g0053 others(69): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.655-1047A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822660 | |||||||
chr16:56822933 | C | T | 1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.655-774C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822933 | |||||||
chr16:56822936 | G | T | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.655-771G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822936 | |||||||
chr16:56822998 | C | T | 1 | a0001c0004t0005g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.655-709C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822998 | |||||||
chr16:56823043 | G | A | 51 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(48): Show |
51 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.655-664G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823043 | |||||||
chr16:56823059 | C | A | 365 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(362): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.655-648C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823059 | |||||||
chr16:56823059 | C | G | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-648C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823059 | |||||||
chr16:56823155 | T | C | 1 | a0001c0001t0004g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.655-552T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823155 | |||||||
chr16:56823318 | A | G | 3 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0001t0001g0318 |
3 | HG01358.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.655-389A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823318 | |||||||
chr16:56823319 | T | C | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.655-388T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823319 | |||||||
chr16:56824042 | G | A | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.794+196G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824042 | |||||||
chr16:56824098 | C | G | 2 | a0001c0001t0003g0352 a0001c0001t0003g0372 |
2 | NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.794+252C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824098 | |||||||
chr16:56824257 | G | A | 1 | a0001c0003t0002g0275 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.794+411G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824257 | |||||||
chr16:56824298 | CA | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+453delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824298 | |||||||
chr16:56824436 | G | A | 1 | a0001c0001t0003g0354 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.794+590G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824436 | |||||||
chr16:56824782 | TGA | T | 40 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(37): Show |
40 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.794+940_794+941del others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56824782 | ||||||
chr16:56825205 | C | CT | 40 | a0001c0001t0003g0362 a0001c0001t0004g0232 a0001c0001t0004g0235 others(37): Show |
40 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.794+1382dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56825205 | ||||||
chr16:56825205 | CT | C | 207 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0055 others(204): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.794+1382delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56825205 | ||||||
chr16:56825205 | CTT | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+1381_794+1382d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56825205 | ||||||
chr16:56825304 | C | T | 67 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(64): Show |
68 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.794+1458C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825304 | |||||||
chr16:56825475 | G | A | 13 | a0001c0003t0002g0253 a0001c0003t0002g0264 a0001c0003t0002g0266 others(10): Show |
13 | HG00597.hp1 HG00673.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.794+1629G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825475 | |||||||
chr16:56825509 | AT | A | 24 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.794+1671delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56825509 | ||||||
chr16:56825598 | T | C | 1 | a0001c0002t0001g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.794+1752T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825598 | |||||||
chr16:56825683 | G | A | 172 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(169): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.794+1837G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825683 | |||||||
chr16:56825985 | A | G | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.794+2139A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825985 | |||||||
chr16:56826021 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794+2175G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826021 | |||||||
chr16:56826141 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.794+2295T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826141 | |||||||
chr16:56826311 | A | G | 27 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.794+2465A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826311 | |||||||
chr16:56826350 | A | G | 5 | a0001c0006t0009g0247 a0001c0006t0009g0248 a0001c0006t0009g0249 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+2504A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826350 | |||||||
chr16:56826467 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.795-2510G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826467 | |||||||
chr16:56826514 | TA | T | 238 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(235): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.795-2445delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56826514 | ||||||
chr16:56826514 | TAA | T | 24 | a0001c0001t0003g0350 a0001c0001t0006g0199 a0001c0001t0006g0200 others(21): Show |
24 | HG01070.hp1 HG01070.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.795-2446_795-2445d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56826514 | ||||||
chr16:56826827 | C | T | 1 | a0001c0001t0003g0363 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.795-2150C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826827 | |||||||
chr16:56826882 | C | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.795-2095C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826882 | |||||||
chr16:56827039 | C | T | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.795-1938C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827039 | |||||||
chr16:56827040 | G | A | 1 | a0006c0020t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.795-1937G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827040 | |||||||
chr16:56827044 | C | CAAAAA | 30 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0303 others(27): Show |
30 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.795-1912_795-1908d others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAA | 16 | a0001c0001t0001g0057 a0001c0001t0001g0302 a0001c0001t0001g0304 others(13): Show |
16 | HG00438.hp1 HG00735.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.795-1913_795-1908d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA | 34 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0054 others(31): Show |
34 | HG00099.hp1 HG00735.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.795-1914_795-1908d others(9): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(1): Show |
20 | a0001c0001t0001g0058 a0001c0001t0001g0122 a0001c0001t0001g0128 others(17): Show |
20 | HG01070.hp2 HG01515.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-1915_795-1908d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0146 others(20): Show |
24 | HG00642.hp1 HG01069.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.795-1916_795-1908d others(11): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(3): Show |
28 | a0001c0001t0001g0118 a0001c0001t0001g0126 a0001c0001t0001g0149 others(25): Show |
28 | HG00323.hp2 HG00544.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.795-1917_795-1908d others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(4): Show |
27 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0153 others(24): Show |
27 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.795-1918_795-1908d others(13): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(5): Show |
10 | a0001c0001t0001g0168 a0001c0002t0001g0076 a0001c0002t0001g0084 others(7): Show |
10 | HG01258.hp1 HG01981.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.795-1919_795-1908d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(6): Show |
8 | a0001c0001t0029g0243 a0001c0002t0001g0062 a0001c0002t0001g0088 others(5): Show |
8 | HG00408.hp1 HG02132.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.795-1920_795-1908d others(15): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(11): Show |
1 | a0001c0010t0033g0259 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.795-1925_795-1908d others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.795-1928_795-1908d others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.795-1930_795-1908d others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(17): Show |
4 | a0001c0005t0007g0183 a0001c0005t0007g0184 a0001c0005t0007g0186 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-1931_795-1908d others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(19): Show |
1 | a0001c0005t0007g0185 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.795-1908_795-1907i others(28): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(21): Show |
2 | a0001c0001t0007g0195 a0001c0001t0016g0192 |
2 | HG00642.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(30): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0016g0193 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.795-1908_795-1907i others(34): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | CAA | C | 8 | a0001c0001t0011g0007 a0001c0001t0011g0008 a0001c0001t0011g0009 others(5): Show |
8 | HG00423.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.795-1909_795-1908d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | CAAA | C | 27 | a0001c0001t0011g0011 a0001c0004t0005g0022 a0001c0004t0005g0023 others(24): Show |
27 | HG00438.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.795-1910_795-1908d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827044 | CAAAAAA | C | 54 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(51): Show |
54 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.795-1913_795-1908d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | ||||||
chr16:56827064 | AAAAAAT | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.795-1912_795-1907d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827064 | |||||||
chr16:56827069 | A | AAAAAAAA others(26): Show |
1 | a0001c0001t0003g0366 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.795-1908_795-1907i others(35): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0003g0368 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.795-1908_795-1907i others(28): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0003g0365 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.795-1908_795-1907i others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0003g0351 a0001c0001t0003g0355 |
2 | NA19005.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(24): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0003g0356 a0001c0001t0003g0372 |
2 | NA18979.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0003g0352 a0001c0001t0003g0371 |
2 | NA18961.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(22): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0003g0004 a0001c0001t0003g0360 |
2 | HG01981.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(21): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(11): Show |
9 | a0001c0001t0003g0004 a0001c0001t0003g0349 a0001c0001t0003g0350 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-1908_795-1907i others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(10): Show |
4 | a0001c0001t0003g0348 a0001c0001t0003g0363 a0001c0001t0027g0369 others(1): Show |
4 | HG00639.hp1 HG01361.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-1908_795-1907i others(19): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0003g0364 a0001c0001t0003g0373 |
2 | HG01081.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(18): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0003g0374 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.795-1908_795-1907i others(17): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827069 | A | T | 2 | a0001c0001t0028g0358 a0001c0007t0012g0345 |
2 | HG02027.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.795-1908A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | |||||||
chr16:56827070 | T | A | 7 | a0001c0002t0001g0066 a0001c0002t0001g0068 a0001c0002t0001g0069 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-1907T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827070 | |||||||
chr16:56827071 | T | A | 3 | a0001c0002t0001g0068 a0001c0002t0001g0070 a0001c0002t0001g0071 |
3 | HG02622.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.795-1906T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827071 | |||||||
chr16:56827171 | C | T | 1 | a0001c0001t0011g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.795-1806C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827171 | |||||||
chr16:56827246 | C | G | 1 | a0001c0001t0006g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.795-1731C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827246 | |||||||
chr16:56827389 | T | C | 1 | a0001c0003t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.795-1588T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827389 | |||||||
chr16:56827532 | G | C | 20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-1445G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827532 | |||||||
chr16:56827533 | T | G | 2 | a0001c0001t0006g0203 a0001c0001t0006g0208 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.795-1444T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827533 | |||||||
chr16:56827614 | A | G | 1 | a0001c0010t0033g0259 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.795-1363A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827614 | |||||||
chr16:56827631 | G | T | 3 | a0001c0004t0008g0002 a0001c0004t0008g0176 a0001c0004t0044g0179 |
4 | HG00099.hp2 HG00741.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-1346G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827631 | |||||||
chr16:56827660 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.795-1317T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827660 | |||||||
chr16:56827763 | A | C | 1 | a0001c0006t0009g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.795-1214A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827763 | |||||||
chr16:56827805 | T | G | 1 | a0008c0023t0026g0370 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.795-1172T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827805 | |||||||
chr16:56827881 | A | C | 20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-1096A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827881 | |||||||
chr16:56827969 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.795-1008A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827969 | |||||||
chr16:56827981 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.795-996G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827981 | |||||||
chr16:56828083 | C | G | 175 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(172): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.795-894C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828083 | |||||||
chr16:56828117 | C | T | 1 | a0001c0004t0005g0030 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.795-860C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828117 | |||||||
chr16:56828184 | C | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.795-793C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828184 | |||||||
chr16:56828194 | T | TA | 16 | a0001c0001t0001g0122 a0001c0001t0001g0159 a0001c0001t0011g0006 others(13): Show |
16 | HG00323.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.795-763dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56828194 | ||||||
chr16:56828194 | T | TAA | 219 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(216): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.795-764_795-763dup others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56828194 | ||||||
chr16:56828194 | TA | T | 7 | a0001c0001t0003g0350 a0001c0001t0003g0357 a0001c0001t0003g0374 others(4): Show |
7 | HG01070.hp1 HG01167.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.795-763delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56828194 | ||||||
chr16:56828210 | A | T | 20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-767A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828210 | |||||||
chr16:56828231 | GA | G | 175 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(172): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.795-745delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828231 | |||||||
chr16:56828854 | G | T | 16 | a0001c0001t0006g0202 a0001c0001t0006g0203 a0001c0001t0006g0204 others(13): Show |
16 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.795-123G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828854 | |||||||
chr16:56829115 | G | A | 21 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(18): Show |
21 | HG00621.hp1 HG02071.hp1 HG03239.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.927+6G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829115 | |||||||
chr16:56829160 | C | T | 20 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(17): Show |
20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.927+51C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829160 | |||||||
chr16:56829303 | C | T | 42 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(39): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.927+194C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829303 | |||||||
chr16:56829317 | T | C | 58 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(55): Show |
58 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.927+208T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829317 | |||||||
chr16:56829555 | A | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.927+446A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829555 | |||||||
chr16:56829584 | T | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+475T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829584 | |||||||
chr16:56829708 | A | G | 4 | a0001c0007t0012g0067 a0001c0007t0012g0345 a0001c0007t0012g0346 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+599A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829708 | |||||||
chr16:56829770 | C | T | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.927+661C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829770 | |||||||
chr16:56830089 | G | A | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.928-439G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830089 | |||||||
chr16:56830146 | C | T | 1 | a0001c0001t0011g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.928-382C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830146 | |||||||
chr16:56830178 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.928-350G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830178 | |||||||
chr16:56830202 | C | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.928-326C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830202 | |||||||
chr16:56830382 | G | A | 5 | a0001c0002t0001g0096 a0001c0002t0001g0100 a0001c0002t0001g0101 others(2): Show |
5 | HG02886.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-146G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830382 | |||||||
chr16:56830486 | C | T | 271 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(268): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.928-42C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830486 | |||||||
chr16:56830487 | T | C | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-41T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830487 | |||||||
chr16:56830706 | C | T | 204 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(201): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1085+21C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56830706 | |||||||
chr16:56830775 | G | T | 1 | a0001c0002t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1085+90G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56830775 | |||||||
chr16:56830900 | C | T | 1 | a0001c0001t0036g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1085+215C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56830900 | |||||||
chr16:56830938 | G | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(21): Show |
24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1085+253G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56830938 | |||||||
chr16:56831259 | A | G | 3 | a0001c0001t0006g0204 a0001c0001t0006g0206 a0001c0001t0006g0242 |
3 | HG02083.hp1 NA18747.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1085+574A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831259 | |||||||
chr16:56831337 | C | A | 203 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(200): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1086-505C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831337 | |||||||
chr16:56831345 | A | G | 1 | a0001c0010t0033g0259 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1086-497A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831345 | |||||||
chr16:56831462 | G | A | 58 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(55): Show |
58 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1086-380G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831462 | |||||||
chr16:56831506 | G | A | 1 | a0001c0004t0019g0180 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1086-336G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831506 | |||||||
chr16:56831633 | G | A | 1 | a0004c0022t0022g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1086-209G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831633 | |||||||
chr16:56831793 | G | T | 2 | a0001c0001t0011g0011 a0001c0001t0046g0010 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1086-49G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831793 | |||||||
chr16:56831816 | A | G | 1 | a0001c0002t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1086-26A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831816 | |||||||
chr16:56832142 | A | AT | 58 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(55): Show |
58 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1251+141dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr16 | 56832142 | ||||||
chr16:56832284 | T | C | 58 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(55): Show |
58 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1252-11T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 11/21 | chr16 | 56832284 | |||||||
chr16:56832590 | T | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(41): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1345+202T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832590 | |||||||
chr16:56832591 | A | G | 1 | a0001c0004t0005g0032 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1345+203A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832591 | |||||||
chr16:56832638 | A | G | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1345+250A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832638 | |||||||
chr16:56832737 | CCTTT | C | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1345+353_1345+356d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr16 | 56832737 | ||||||
chr16:56832848 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1346-367C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832848 | |||||||
chr16:56832889 | G | T | 44 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(41): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1346-326G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832889 | |||||||
chr16:56833501 | G | A | 2 | a0001c0001t0004g0237 a0001c0001t0004g0239 |
2 | NA19083.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1537+95G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/21 | chr16 | 56833501 | |||||||
chr16:56833865 | A | C | 10 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(7): Show |
10 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1538-263A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/21 | chr16 | 56833865 | |||||||
chr16:56833892 | C | T | 362 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(359): Show |
364 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1538-236C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/21 | chr16 | 56833892 | |||||||
chr16:56833977 | A | G | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1538-151A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/21 | chr16 | 56833977 | |||||||
chr16:56834558 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0133 a0001c0001t0001g0162 |
3 | HG03130.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1737+116T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 15/21 | chr16 | 56834558 | |||||||
chr16:56834653 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1738-81C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 15/21 | chr16 | 56834653 | |||||||
chr16:56834687 | T | G | 1 | a0001c0003t0002g0245 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1738-47T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 15/21 | chr16 | 56834687 | |||||||
chr16:56834788 | A | G | 201 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(198): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1782+10A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56834788 | |||||||
chr16:56834821 | G | A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1782+43G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56834821 | |||||||
chr16:56835107 | G | T | 6 | a0001c0001t0011g0006 a0001c0001t0011g0007 a0001c0001t0011g0008 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+329G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835107 | |||||||
chr16:56835485 | T | C | 2 | a0001c0004t0005g0032 a0001c0004t0005g0034 |
2 | HG01099.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1782+707T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835485 | |||||||
chr16:56835517 | G | A | 2 | a0001c0002t0001g0085 a0001c0002t0001g0344 |
2 | HG02015.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1782+739G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835517 | |||||||
chr16:56835518 | T | C | 362 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(359): Show |
364 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1782+740T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835518 | |||||||
chr16:56835544 | G | T | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1782+766G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835544 | |||||||
chr16:56835635 | G | T | 4 | a0001c0002t0001g0098 a0001c0004t0015g0017 a0001c0004t0015g0018 others(1): Show |
4 | HG02280.hp1 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1782+857G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835635 | |||||||
chr16:56835704 | G | A | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1783-897G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835704 | |||||||
chr16:56835803 | T | A | 74 | a0001c0002t0001g0001 a0001c0002t0001g0046 a0001c0002t0001g0053 others(71): Show |
75 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1783-798T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835803 | |||||||
chr16:56835850 | C | T | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1783-751C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835850 | |||||||
chr16:56835902 | G | T | 2 | a0001c0001t0016g0192 a0001c0001t0016g0193 |
2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1783-699G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835902 | |||||||
chr16:56836128 | C | CAAA | 48 | a0001c0001t0002g0282 a0001c0001t0002g0293 a0001c0003t0002g0049 others(45): Show |
48 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1783-460_1783-458d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 56836128 | ||||||
chr16:56836171 | G | GT | 40 | a0001c0001t0003g0004 a0001c0001t0003g0348 a0001c0001t0003g0349 others(37): Show |
41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1783-424dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 56836171 | ||||||
chr16:56836233 | A | G | 1 | a0001c0017t0001g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1783-368A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56836233 | |||||||
chr16:56836526 | G | T | 1 | a0001c0001t0002g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1783-75G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56836526 | |||||||
chr16:56836541 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1783-60A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56836541 | |||||||
chr16:56836863 | G | T | 1 | a0001c0001t0001g0337 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1899+146G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56836863 | |||||||
chr16:56836955 | A | C | 1 | a0001c0002t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1899+238A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56836955 | |||||||
chr16:56837004 | G | T | 16 | a0001c0001t0006g0202 a0001c0001t0006g0203 a0001c0001t0006g0204 others(13): Show |
16 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1899+287G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56837004 | |||||||
chr16:56837260 | G | A | 3 | a0001c0001t0014g0217 a0001c0001t0014g0218 a0001c0001t0014g0219 |
3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1900-348G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56837260 | |||||||
chr16:56837489 | G | C | 1 | a0001c0001t0003g0372 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1900-119G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56837489 | |||||||
chr16:56837557 | TTTTATTG others(5): Show |
T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
58 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1900-40_1900-29del others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 56837557 | ||||||
chr16:56837574 | T | C | 1 | a0002c0008t0002g0297 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1900-34T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56837574 | |||||||
chr16:56837764 | C | A | 2 | a0001c0001t0006g0199 a0001c0001t0006g0200 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2018+38C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56837764 | |||||||
chr16:56837784 | C | T | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2018+58C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56837784 | |||||||
chr16:56837893 | C | T | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2018+167C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56837893 | |||||||
chr16:56838014 | G | A | 3 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 |
3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2018+288G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838014 | |||||||
chr16:56838030 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2018+304A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838030 | |||||||
chr16:56838347 | C | T | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2019-605C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838347 | |||||||
chr16:56838804 | A | G | 1 | a0001c0004t0005g0038 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2019-148A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838804 | |||||||
chr16:56838810 | C | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(54): Show |
57 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.2019-142C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838810 | |||||||
chr16:56838866 | T | G | 3 | a0001c0001t0013g0014 a0001c0001t0013g0015 a0001c0001t0013g0016 |
3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2019-86T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838866 | |||||||
chr16:56838912 | G | A | 58 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(55): Show |
58 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2019-40G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838912 | |||||||
chr16:56839233 | C | CT | 60 | a0001c0001t0001g0163 a0001c0001t0001g0300 a0001c0001t0001g0304 others(57): Show |
61 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2136+191dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839233 | ||||||
chr16:56839233 | C | CTT | 12 | a0001c0001t0003g0361 a0001c0001t0003g0362 a0001c0001t0003g0364 others(9): Show |
12 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2136+190_2136+191d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839233 | ||||||
chr16:56839233 | CT | C | 162 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0054 others(159): Show |
163 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.2136+191delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839233 | ||||||
chr16:56839233 | CTT | C | 8 | a0001c0002t0001g0098 a0001c0006t0009g0247 a0001c0006t0009g0249 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2136+190_2136+191d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839233 | ||||||
chr16:56839260 | T | G | 19 | a0001c0001t0004g0003 a0001c0001t0004g0198 a0001c0001t0004g0220 others(16): Show |
19 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2136+191T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | chr16 | 56839260 | |||||||
chr16:56839260 | T | TG | 5 | a0001c0001t0004g0223 a0001c0001t0004g0228 a0001c0001t0004g0230 others(2): Show |
5 | HG01175.hp1 HG01978.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+192dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839260 | ||||||
chr16:56839622 | G | A | 1 | a0001c0001t0003g0348 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2220+18G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839622 | |||||||
chr16:56839701 | T | TA | 53 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(50): Show |
53 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2220+98dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 56839701 | ||||||
chr16:56839703 | C | T | 1 | a0001c0001t0046g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2220+99C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839703 | |||||||
chr16:56839877 | T | C | 58 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(55): Show |
58 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2220+273T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839877 | |||||||
chr16:56839902 | A | G | 5 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2220+298A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839902 | |||||||
chr16:56839928 | G | A | 72 | a0001c0002t0001g0001 a0001c0002t0001g0046 a0001c0002t0001g0053 others(69): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2220+324G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839928 | |||||||
chr16:56839961 | T | C | 8 | a0001c0001t0003g0351 a0001c0001t0003g0352 a0001c0001t0003g0354 others(5): Show |
8 | NA18961.hp1 NA18969.hp2 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.2220+357T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839961 | |||||||
chr16:56840060 | A | G | 368 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(365): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.2220+456A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840060 | |||||||
chr16:56840109 | C | G | 3 | a0001c0003t0002g0265 a0001c0003t0002g0273 a0001c0003t0002g0294 |
3 | NA18942.hp2 NA18981.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2220+505C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840109 | |||||||
chr16:56840178 | G | T | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2220+574G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840178 | |||||||
chr16:56840179 | C | T | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2220+575C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840179 | |||||||
chr16:56840272 | G | A | 72 | a0001c0002t0001g0001 a0001c0002t0001g0046 a0001c0002t0001g0053 others(69): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2220+668G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840272 | |||||||
chr16:56840285 | G | A | 172 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(169): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2220+681G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840285 | |||||||
chr16:56840299 | C | T | 1 | a0001c0001t0003g0362 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2220+695C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840299 | |||||||
chr16:56840356 | C | T | 3 | a0001c0002t0001g0075 a0001c0002t0001g0104 a0001c0019t0001g0080 |
3 | NA18954.hp2 NA19011.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2220+752C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840356 | |||||||
chr16:56840360 | G | C | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.2220+756G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840360 | |||||||
chr16:56840564 | A | G | 25 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(22): Show |
25 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.2220+960A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840564 | |||||||
chr16:56840681 | T | C | 1 | a0007c0013t0007g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2221-1024T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840681 | |||||||
chr16:56840788 | G | A | 1 | a0001c0003t0002g0049 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2221-917G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840788 | |||||||
chr16:56840945 | C | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(169): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2221-760C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840945 | |||||||
chr16:56840976 | G | A | 3 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 |
3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2221-729G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840976 | |||||||
chr16:56840991 | T | C | 363 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(360): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.2221-714T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840991 | |||||||
chr16:56840996 | C | CA | 49 | a0001c0001t0001g0047 a0001c0001t0001g0155 a0001c0001t0001g0171 others(46): Show |
49 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.2221-692dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 56840996 | ||||||
chr16:56840996 | CA | C | 11 | a0001c0001t0001g0145 a0001c0001t0004g0231 a0001c0003t0002g0244 others(8): Show |
11 | HG00597.hp1 HG00673.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.2221-692delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 56840996 | ||||||
chr16:56841018 | C | T | 28 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(25): Show |
28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2221-687C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841018 | |||||||
chr16:56841041 | C | T | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2221-664C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841041 | |||||||
chr16:56841060 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18946.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2221-645G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841060 | |||||||
chr16:56841222 | C | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2221-483C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841222 | |||||||
chr16:56841223 | G | A | 1 | a0001c0007t0012g0347 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2221-482G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841223 | |||||||
chr16:56841291 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2221-414G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841291 | |||||||
chr16:56841323 | C | T | 4 | a0001c0003t0002g0278 a0001c0003t0002g0279 a0001c0003t0020g0281 others(1): Show |
4 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2221-382C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841323 | |||||||
chr16:56841360 | A | AT | 172 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(169): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2221-343dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 56841360 | ||||||
chr16:56841367 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2221-338T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841367 | |||||||
chr16:56841370 | A | T | 1 | a0001c0002t0001g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2221-335A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841370 | |||||||
chr16:56841371 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2221-334A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841371 | |||||||
chr16:56841383 | G | A | 25 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(22): Show |
25 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.2221-322G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841383 | |||||||
chr16:56841390 | C | A | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2221-315C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841390 | |||||||
chr16:56841472 | A | T | 1 | a0001c0002t0001g0110 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2221-233A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841472 | |||||||
chr16:56841664 | G | A | 1 | a0001c0003t0002g0261 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2221-41G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841664 | |||||||
chr16:56842086 | CTAATTTC others(39): Show |
C | 1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2349+257_2349+302d others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 56842086 | ||||||
chr16:56842141 | T | TTTTGGGG others(39): Show |
1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2349+312_2349+313i others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 56842141 | ||||||
chr16:56842332 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2349+499C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842332 | |||||||
chr16:56842417 | C | T | 1 | a0001c0001t0006g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2349+584C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842417 | |||||||
chr16:56842448 | A | G | 3 | a0001c0009t0018g0020 a0001c0009t0018g0021 a0005c0024t0018g0012 |
3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2349+615A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842448 | |||||||
chr16:56842488 | C | T | 1 | a0001c0001t0029g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2349+655C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842488 | |||||||
chr16:56842555 | CT | C | 261 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(258): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.2349+737delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 56842555 | ||||||
chr16:56842616 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2349+783G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842616 | |||||||
chr16:56842699 | C | T | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2349+866C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842699 | |||||||
chr16:56842933 | T | G | 58 | a0001c0001t0002g0282 a0001c0001t0002g0290 a0001c0001t0002g0293 others(55): Show |
58 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2349+1100T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842933 | |||||||
chr16:56842963 | A | G | 1 | a0001c0002t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2349+1130A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842963 | |||||||
chr16:56842983 | C | T | 2 | a0001c0004t0015g0017 a0001c0004t0015g0019 |
2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2349+1150C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842983 | |||||||
chr16:56843173 | C | T | 28 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(25): Show |
28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2350-1326C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843173 | |||||||
chr16:56843240 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2350-1259A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843240 | |||||||
chr16:56843565 | C | T | 28 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(25): Show |
28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2350-934C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843565 | |||||||
chr16:56843742 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2350-757G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843742 | |||||||
chr16:56843906 | A | G | 3 | a0001c0001t0003g0364 a0001c0001t0003g0373 a0001c0001t0003g0374 |
3 | HG01081.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2350-593A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843906 | |||||||
chr16:56843909 | C | A | 3 | a0001c0001t0016g0191 a0001c0001t0016g0192 a0001c0001t0016g0193 |
3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2350-590C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843909 | |||||||
chr16:56843938 | G | A | 1 | a0001c0001t0011g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2350-561G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843938 | |||||||
chr16:56844161 | T | A | 25 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(22): Show |
25 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.2350-338T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844161 | |||||||
chr16:56844196 | A | G | 6 | a0001c0001t0006g0202 a0001c0001t0006g0204 a0001c0001t0006g0205 others(3): Show |
6 | HG02015.hp1 HG02083.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.2350-303A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844196 | |||||||
chr16:56844302 | C | T | 1 | a0001c0001t0013g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2350-197C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844302 | |||||||
chr16:56844303 | G | A | 3 | a0001c0007t0012g0067 a0001c0007t0012g0346 a0001c0007t0012g0347 |
3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2350-196G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844303 | |||||||
chr16:56844438 | G | A | 2 | a0001c0010t0022g0258 a0001c0010t0033g0259 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2350-61G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844438 | |||||||
chr16:56844466 | C | T | 28 | a0001c0004t0005g0022 a0001c0004t0005g0023 a0001c0004t0005g0024 others(25): Show |
28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2350-33C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844466 |