Item | Value |
---|---|
geneid | 79902 |
ensemblid | ENSG00000125450.11 |
hgncid | 8734 |
symbol | NUP85 |
name | nucleoporin 85 |
refseq_nuc | NM_024844.5 |
refseq_prot | NP_079120.1 |
ensembl_nuc | ENST00000245544.9 |
ensembl_prot | ENSP00000245544.4 |
mane_status | MANE Select |
chr | chr17 |
start | 75205679 |
end | 75235758 |
strand | + |
ver | v1.2 |
region | chr17:75205679-75235758 |
region5000 | chr17:75200679-75240758 |
regionname0 | NUP85_chr17_75205679_75235758 |
regionname5000 | NUP85_chr17_75200679_75240758 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 656 | 271 | 91 | 61 | 64 | 13 | 40 | 38 | NUP85_chr17_75200679_75240758 | NUP85 | MEELD others(651): Show |
chr17 | 75200679 | 75240758 |
a0002 | 0/0 | 656 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | MEELD others(651): Show |
chr17 | 75200679 | 75240758 |
a0003 | 0/0 | 656 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | MEELD others(651): Show |
chr17 | 75200679 | 75240758 |
a0004 | 0/0 | 656 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | MEELD others(651): Show |
chr17 | 75200679 | 75240758 |
a0005 | 0/0 | 656 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | MEELD others(651): Show |
chr17 | 75200679 | 75240758 |
a0006 | 0/0 | 656 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | MEELD others(651): Show |
chr17 | 75200679 | 75240758 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1968 | 180 | 62 | 40 | 43 | 8 | 26 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0001c0002 | 0/0 | 1968 | 45 | 17 | 9 | 11 | 0 | 8 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0001c0003 | 0/0 | 1968 | 24 | 0 | 6 | 10 | 4 | 4 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0001c0004 | 1/0 | 1968 | 9 | 8 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0001c0005 | 0/0 | 1968 | 8 | 1 | 5 | 0 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0001c0006 | 0/0 | 1968 | 3 | 3 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0001c0008 | 0/0 | 1968 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0001c0010 | 0/0 | 1968 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0002c0009 | 0/0 | 1968 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0003c0012 | 0/0 | 1968 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0004c0007 | 0/0 | 1968 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0005c0011 | 0/0 | 1968 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 | ||
a0006c0013 | 0/0 | 1968 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | ATGGA others(1963): Show |
chr17 | 75200679 | 75240758 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2132 | 179 | 62 | 39 | 43 | 8 | 26 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0001c0001t0003 | 0/0 | 2132 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0001c0002t0001 | 0/0 | 2132 | 45 | 17 | 9 | 11 | 0 | 8 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0001c0003t0002 | 0/0 | 2133 | 24 | 0 | 6 | 10 | 4 | 4 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2128): Show |
chr17 | 75200679 | 75240758 |
a0001c0004t0002 | 1/0 | 2133 | 9 | 8 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2128): Show |
chr17 | 75200679 | 75240758 |
a0001c0005t0002 | 0/0 | 2133 | 8 | 1 | 5 | 0 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2128): Show |
chr17 | 75200679 | 75240758 |
a0001c0006t0001 | 0/0 | 2132 | 3 | 3 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0001c0008t0001 | 0/0 | 2132 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0001c0010t0001 | 0/0 | 2132 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0002c0009t0001 | 0/0 | 2132 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0003c0012t0001 | 0/0 | 2132 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0004c0007t0001 | 0/0 | 2132 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0005c0011t0001 | 0/0 | 2132 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
a0006c0013t0001 | 0/0 | 2132 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | GTCTC others(2127): Show |
chr17 | 75200679 | 75240758 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0003t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0008 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0004t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0005t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0006t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0006t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0006t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0008t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0001c0010t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0002c0009t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0003c0012t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0004c0007t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0005c0011t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
a0006c0013t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0005 | t0002 | g0172 | EUR | GBR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00544 | hp1 | a0001 | c0003 | t0002 | g0181 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00597 | hp1 | a0001 | c0003 | t0002 | g0180 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00735 | hp1 | a0001 | c0005 | t0002 | g0187 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01069 | hp1 | a0001 | c0005 | t0002 | g0207 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01070 | hp1 | a0001 | c0003 | t0002 | g0195 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01071 | hp2 | a0001 | c0005 | t0002 | g0208 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01074 | hp1 | a0001 | c0005 | t0002 | g0169 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01109 | hp2 | a0001 | c0008 | t0001 | g0188 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0017 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0017 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01361 | hp1 | a0001 | c0005 | t0002 | g0171 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01361 | hp2 | a0002 | c0009 | t0001 | g0036 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01433 | hp1 | a0001 | c0003 | t0002 | g0185 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0194 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0196 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0192 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0197 | EUR | IBS | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01891 | hp1 | a0001 | c0005 | t0002 | g0167 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01891 | hp2 | a0003 | c0012 | t0001 | g0168 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01928 | hp2 | a0001 | c0003 | t0002 | g0199 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02015 | hp2 | a0001 | c0003 | t0002 | g0176 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02129 | hp1 | a0001 | c0003 | t0002 | g0174 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02135 | hp1 | a0001 | c0003 | t0002 | g0186 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CDX | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02451 | hp1 | a0001 | c0004 | t0002 | g0007 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02572 | hp1 | a0001 | c0004 | t0002 | g0029 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02698 | hp2 | a0001 | c0003 | t0002 | g0173 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02723 | hp1 | a0001 | c0004 | t0002 | g0025 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02886 | hp2 | a0001 | c0006 | t0001 | g0190 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02922 | hp2 | a0001 | c0004 | t0002 | g0027 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03139 | hp1 | a0001 | c0006 | t0001 | g0189 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03486 | hp1 | a0001 | c0006 | t0001 | g0191 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0231 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03516 | hp1 | a0001 | c0004 | t0002 | g0007 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | GWD | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03710 | hp1 | a0004 | c0007 | t0001 | g0227 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03710 | hp2 | a0001 | c0005 | t0002 | g0170 | SAS | PJL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03834 | hp1 | a0005 | c0011 | t0001 | g0065 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0183 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03942 | hp2 | a0001 | c0010 | t0001 | g0078 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04204 | hp2 | a0001 | c0003 | t0002 | g0198 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0184 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18982 | hp1 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18989 | hp1 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA18990 | hp2 | a0001 | c0003 | t0002 | g0182 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19068 | hp2 | a0001 | c0003 | t0002 | g0177 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19090 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | JPT | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | YRI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ASW | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | ASW | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20752 | hp1 | a0006 | c0013 | t0001 | g0031 | EUR | TSI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0193 | EUR | TSI | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | GIH | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA20300 | hp2 | a0001 | c0004 | t0002 | g0028 | AFR | USA | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0116 | REF | REF | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
homoSapiens | grch38p0 | a0001 | c0004 | t0002 | g0008 | REF | REF | NUP85_chr17_75200679_75240758 | NUP85 | chr17 | 75200679 | 75240758 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75208539 | G | A | 1 | a0004 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.46G>A | p.Val16Met | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/19 | 129/2133 | 46/1971 | 16/656 | chr17 | 75208539 | |||
chr17:75225351 | A | G | 1 | a0006 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.742A>G | p.Thr248Ala | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 9/19 | 825/2133 | 742/1971 | 248/656 | chr17 | 75225351 | |||
chr17:75225432 | G | A | 1 | a0002 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.823G>A | p.Ala275Thr | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 9/19 | 906/2133 | 823/1971 | 275/656 | chr17 | 75225432 | |||
chr17:75234684 | G | A | 1 | a0005 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1663G>A | p.Asp555Asn | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/19 | 1746/2133 | 1663/1971 | 555/656 | chr17 | 75234684 | |||
chr17:75234721 | G | A | 1 | a0003 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1700G>A | p.Arg567Gln | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/19 | 1783/2133 | 1700/1971 | 567/656 | chr17 | 75234721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75209881 | T | C | 1 | a0001c0003 | 24 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(21): Show |
synonymous_variant | LOW | c.186T>C | p.Asp62Asp | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/19 | 269/2133 | 186/1971 | 62/656 | chr17 | 75209881 | |||
chr17:75225344 | C | T | 8 | a0001c0001 a0001c0003 a0001c0005 others(5): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
splice_region_variant&synonymous_variant | LOW | c.735C>T | p.Pro245Pro | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 9/19 | 818/2133 | 735/1971 | 245/656 | chr17 | 75225344 | |||
chr17:75231840 | G | A | 1 | a0001c0010 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.1257G>A | p.Leu419Leu | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/19 | 1340/2133 | 1257/1971 | 419/656 | chr17 | 75231840 | |||
chr17:75232942 | C | T | 1 | a0001c0008 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1488C>T | p.Ala496Ala | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 15/19 | 1571/2133 | 1488/1971 | 496/656 | chr17 | 75232942 | |||
chr17:75234701 | T | C | 2 | a0001c0002 a0004c0007 |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
synonymous_variant | LOW | c.1680T>C | p.Leu560Leu | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/19 | 1763/2133 | 1680/1971 | 560/656 | chr17 | 75234701 | |||
chr17:75234761 | C | T | 10 | a0001c0001 a0001c0002 a0001c0006 others(7): Show |
234 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
synonymous_variant | LOW | c.1740C>T | p.Asp580Asp | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/19 | 1823/2133 | 1740/1971 | 580/656 | chr17 | 75234761 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75205738 | T | C | 1 | a0001c0001t0003 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/19 | 24 | chr17 | 75205738 | ||||||
chr17:75235722 | AT | A | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0001 others(8): Show |
234 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*50delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 19/19 | 50 | INFO_REALIGN_3_PRIME | chr17 | 75235722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75205874 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.33+80T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75205874 | |||||||
chr17:75205897 | G | C | 1 | a0001c0001t0001g0021 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.33+103G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75205897 | |||||||
chr17:75205905 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02486.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.33+111C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75205905 | |||||||
chr17:75206136 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.33+342G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206136 | |||||||
chr17:75206467 | A | G | 42 | a0001c0001t0001g0215 a0001c0001t0001g0247 a0001c0002t0001g0001 others(39): Show |
48 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.33+673A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206467 | |||||||
chr17:75206526 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.33+732G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206526 | |||||||
chr17:75206604 | G | A | 42 | a0001c0001t0001g0215 a0001c0001t0001g0247 a0001c0002t0001g0001 others(39): Show |
48 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.33+810G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206604 | |||||||
chr17:75206851 | C | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.33+1057C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75206851 | |||||||
chr17:75207105 | C | G | 2 | a0001c0005t0002g0207 a0001c0005t0002g0208 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.33+1311C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207105 | |||||||
chr17:75207173 | A | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0201 others(5): Show |
10 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.34-1354A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207173 | |||||||
chr17:75207254 | G | A | 7 | a0001c0002t0001g0018 a0001c0002t0001g0209 a0001c0002t0001g0210 others(4): Show |
8 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-1273G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207254 | |||||||
chr17:75207314 | G | T | 9 | a0001c0003t0002g0017 a0001c0003t0002g0192 a0001c0003t0002g0193 others(6): Show |
10 | HG01070.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.34-1213G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207314 | |||||||
chr17:75207558 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.34-969C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207558 | |||||||
chr17:75207693 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.34-834T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207693 | |||||||
chr17:75207769 | C | T | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.34-758C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207769 | |||||||
chr17:75207934 | G | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.34-593G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207934 | |||||||
chr17:75207937 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.34-590T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75207937 | |||||||
chr17:75208042 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.34-485C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75208042 | |||||||
chr17:75208157 | C | T | 30 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.34-370C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75208157 | |||||||
chr17:75208179 | T | C | 1 | a0006c0013t0001g0031 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.34-348T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75208179 | |||||||
chr17:75208280 | G | GA | 35 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(32): Show |
37 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.34-231dupA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208280 | ||||||
chr17:75208280 | GA | G | 58 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(55): Show |
65 | HG00733.hp1 HG00738.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.34-231delA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208280 | ||||||
chr17:75208435 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.34-92T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | chr17 | 75208435 | |||||||
chr17:75208440 | C | CA | 38 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0018 others(35): Show |
44 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.34-65dupA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208440 | ||||||
chr17:75208440 | CA | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0035 others(34): Show |
40 | HG00738.hp2 HG01261.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.34-65delA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208440 | ||||||
chr17:75208440 | CAA | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.34-66_34-65delAA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208440 | ||||||
chr17:75208440 | CAAA | C | 37 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(34): Show |
38 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.34-67_34-65delAAA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr17 | 75208440 | ||||||
chr17:75208829 | A | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.127+209A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75208829 | |||||||
chr17:75208964 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.127+344G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75208964 | |||||||
chr17:75208992 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127+372C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75208992 | |||||||
chr17:75209150 | A | G | 1 | a0006c0013t0001g0031 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.127+530A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209150 | |||||||
chr17:75209270 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.128-553G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209270 | |||||||
chr17:75209445 | C | CT | 7 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0004t0002g0029 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-359dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr17 | 75209445 | ||||||
chr17:75209445 | CT | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG00639.hp1 HG01074.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-359delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr17 | 75209445 | ||||||
chr17:75209445 | CTT | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.128-360_128-359del others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr17 | 75209445 | ||||||
chr17:75209470 | G | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0048 others(5): Show |
8 | HG01069.hp2 HG01074.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-353G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209470 | |||||||
chr17:75209517 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.128-306C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209517 | |||||||
chr17:75209644 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.128-179A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209644 | |||||||
chr17:75209782 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.128-41T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209782 | |||||||
chr17:75209804 | T | C | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.128-19T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 2/18 | chr17 | 75209804 | |||||||
chr17:75210140 | G | A | 1 | a0002c0009t0001g0036 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.290+155G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210140 | |||||||
chr17:75210226 | G | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.290+241G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210226 | |||||||
chr17:75210368 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.290+383C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210368 | |||||||
chr17:75210384 | C | T | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.290+399C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210384 | |||||||
chr17:75210482 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+497C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210482 | |||||||
chr17:75210683 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.290+698G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210683 | |||||||
chr17:75210762 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.290+777C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210762 | |||||||
chr17:75210784 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0131 |
3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.290+799C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210784 | |||||||
chr17:75210812 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290+827C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210812 | |||||||
chr17:75210850 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.290+865T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210850 | |||||||
chr17:75210981 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.290+996G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75210981 | |||||||
chr17:75211003 | G | GT | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.291-972dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr17 | 75211003 | ||||||
chr17:75211003 | G | GTT | 18 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0117 others(15): Show |
18 | HG00639.hp2 HG01175.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.291-973_291-972dup others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr17 | 75211003 | ||||||
chr17:75211055 | T | G | 1 | a0006c0013t0001g0031 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.291-937T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211055 | |||||||
chr17:75211064 | G | A | 41 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0018 others(38): Show |
47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.291-928G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211064 | |||||||
chr17:75211097 | G | C | 1 | a0001c0003t0002g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.291-895G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211097 | |||||||
chr17:75211112 | C | T | 41 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0018 others(38): Show |
47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.291-880C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211112 | |||||||
chr17:75211168 | A | G | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.291-824A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211168 | |||||||
chr17:75211222 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.291-770T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211222 | |||||||
chr17:75211224 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.291-768A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211224 | |||||||
chr17:75211379 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0003c0012t0001g0168 |
4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-613A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211379 | |||||||
chr17:75211411 | A | T | 1 | a0001c0003t0002g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291-581A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211411 | |||||||
chr17:75211429 | CT | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.291-548delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr17 | 75211429 | ||||||
chr17:75211638 | C | T | 41 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0018 others(38): Show |
47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.291-354C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211638 | |||||||
chr17:75211675 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.291-317G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211675 | |||||||
chr17:75211705 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.291-287C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211705 | |||||||
chr17:75211824 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.291-168G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 3/18 | chr17 | 75211824 | |||||||
chr17:75212081 | T | TGC | 31 | a0001c0001t0001g0205 a0001c0003t0002g0017 a0001c0003t0002g0173 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.361+25_361+26dupCG | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212081 | ||||||
chr17:75212083 | CGCGCGTG others(5): Show |
C | 8 | a0001c0002t0001g0018 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
9 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.361+23_361+34delCG others(10): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212083 | ||||||
chr17:75212087 | C | CGT | 3 | a0001c0004t0002g0007 a0001c0004t0002g0025 a0001c0004t0002g0026 |
3 | HG02723.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.361+47_361+48dupTG | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212087 | ||||||
chr17:75212087 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.361+25C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212087 | |||||||
chr17:75212087 | CGT | C | 33 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0019 others(30): Show |
38 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+47_361+48delTG | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212087 | ||||||
chr17:75212087 | CGTGTGTG others(3): Show |
C | 1 | a0001c0008t0001g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.361+39_361+48delTG others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212087 | ||||||
chr17:75212089 | T | C | 8 | a0001c0001t0001g0205 a0001c0005t0002g0169 a0001c0005t0002g0170 others(5): Show |
8 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+27T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212089 | |||||||
chr17:75212091 | T | C | 33 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0019 others(30): Show |
38 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+29T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212091 | |||||||
chr17:75212093 | T | C | 3 | a0001c0002t0001g0001 a0001c0002t0001g0219 a0001c0002t0001g0220 |
3 | NA18945.hp1 NA18947.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.361+31T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212093 | |||||||
chr17:75212110 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.361+48_361+49insTG others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | |||||||
chr17:75212110 | G | GTGTGTT | 30 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0020 others(27): Show |
32 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.361+48_361+49insTG others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | |||||||
chr17:75212110 | G | GTGTT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
132 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.361+48_361+49insTG others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | |||||||
chr17:75212110 | G | GTT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0146 a0001c0001t0001g0147 others(10): Show |
15 | HG00639.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.361+48_361+49insTT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | |||||||
chr17:75212110 | G | T | 33 | a0001c0001t0001g0115 a0001c0001t0001g0205 a0001c0003t0002g0017 others(30): Show |
34 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.361+48G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212110 | |||||||
chr17:75212187 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.361+125T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212187 | |||||||
chr17:75212228 | GGTTTTTT others(23): Show |
G | 1 | a0001c0001t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.361+167_361+196del others(30): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | |||||||
chr17:75212228 | GGTTTTTT others(24): Show |
G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0114 a0001c0001t0001g0140 others(7): Show |
10 | HG00140.hp1 HG01928.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+167_361+197del others(31): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | |||||||
chr17:75212228 | GGTTTTTT others(25): Show |
G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0020 others(60): Show |
67 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.361+167_361+198del others(32): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | |||||||
chr17:75212228 | GGTTTTTT others(26): Show |
G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.361+167_361+199del others(33): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | |||||||
chr17:75212228 | GGTTTTTT others(27): Show |
G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0142 |
2 | HG01256.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.361+167_361+200del others(34): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | |||||||
chr17:75212228 | GGTTTTTT others(39): Show |
G | 1 | a0001c0003t0002g0195 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.361+167_361+212del others(46): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | |||||||
chr17:75212228 | GGTTTTTT others(41): Show |
G | 1 | a0001c0001t0001g0061 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.361+167_361+214del others(48): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212228 | |||||||
chr17:75212247 | G | GTTGTTGT | 4 | a0001c0002t0001g0001 a0001c0002t0001g0224 a0001c0002t0001g0226 others(1): Show |
5 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+187_361+188ins others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(1): Show |
8 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0216 others(5): Show |
9 | HG01358.hp1 HG01975.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.361+187_361+188ins others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(3): Show |
2 | a0001c0002t0001g0019 a0001c0002t0001g0234 |
2 | HG01106.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.361+187_361+188ins others(10): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(4): Show |
1 | a0001c0002t0001g0223 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.361+187_361+188ins others(11): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(2): Show |
9 | a0001c0002t0001g0018 a0001c0002t0001g0221 a0001c0002t0001g0222 others(6): Show |
9 | HG01243.hp2 HG02071.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.361+187_361+188ins others(9): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(3): Show |
5 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0211 others(2): Show |
5 | HG02559.hp2 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.361+187_361+188ins others(10): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(4): Show |
3 | a0001c0002t0001g0209 a0001c0002t0001g0210 a0001c0002t0001g0233 |
3 | HG03471.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.361+187_361+188ins others(11): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(5): Show |
1 | a0001c0002t0001g0212 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.361+187_361+188ins others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(7): Show |
1 | a0004c0007t0001g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.361+187_361+188ins others(14): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(9): Show |
2 | a0001c0002t0001g0213 a0001c0002t0001g0246 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.361+187_361+188ins others(16): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | G | GTTGTTGT others(10): Show |
1 | a0001c0002t0001g0019 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361+187_361+188ins others(17): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | GTTTTTTT others(7): Show |
G | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.361+211_361+224del others(14): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | GTTTTTTT others(8): Show |
G | 2 | a0001c0002t0001g0219 a0001c0002t0001g0220 |
2 | NA18945.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.361+210_361+224del others(15): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212247 | GTTTTTTT others(10): Show |
G | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.361+208_361+224del others(17): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212247 | ||||||
chr17:75212250 | T | G | 1 | a0001c0002t0001g0238 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.361+188T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212250 | |||||||
chr17:75212251 | T | G | 2 | a0001c0002t0001g0240 a0001c0002t0001g0243 |
2 | HG02886.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.361+189T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212251 | |||||||
chr17:75212254 | T | G | 1 | a0001c0002t0001g0240 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361+192T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212254 | |||||||
chr17:75212256 | T | TG | 7 | a0001c0004t0002g0007 a0001c0004t0002g0025 a0001c0004t0002g0026 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.361+194_361+195ins others(1): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212256 | |||||||
chr17:75212264 | T | G | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.361+202T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212264 | |||||||
chr17:75212265 | T | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0001c0002t0001g0219 others(2): Show |
6 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+203T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212265 | |||||||
chr17:75212267 | T | G | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.361+205T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212267 | |||||||
chr17:75212268 | T | G | 2 | a0001c0002t0001g0219 a0001c0002t0001g0220 |
2 | NA18945.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.361+206T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212268 | |||||||
chr17:75212270 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.361+208T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212270 | |||||||
chr17:75212307 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG00639.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+245C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212307 | |||||||
chr17:75212406 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.361+344C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212406 | |||||||
chr17:75212469 | GTT | G | 39 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0018 others(36): Show |
45 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.361+433_361+434del others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212469 | ||||||
chr17:75212469 | GTTTTT | G | 56 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(53): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.361+430_361+434del others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212469 | ||||||
chr17:75212469 | GTTTTTT | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.361+429_361+434del others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212469 | ||||||
chr17:75212469 | GTTTTTTT | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.361+428_361+434del others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr17 | 75212469 | ||||||
chr17:75212476 | T | G | 3 | a0001c0003t0002g0186 a0001c0003t0002g0193 a0001c0005t0002g0167 |
3 | HG01891.hp1 HG02135.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.361+414T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212476 | |||||||
chr17:75212477 | T | G | 28 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(25): Show |
29 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.361+415T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212477 | |||||||
chr17:75212562 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
8 | HG00621.hp2 HG00673.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+500G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212562 | |||||||
chr17:75212629 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.362-447T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212629 | |||||||
chr17:75212677 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.362-399T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75212677 | |||||||
chr17:75213030 | G | A | 1 | a0001c0002t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.362-46G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 4/18 | chr17 | 75213030 | |||||||
chr17:75213125 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG01255.hp1 | splice_region_variant&intron_variant | LOW | c.405+6G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213125 | |||||||
chr17:75213270 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.405+151C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213270 | |||||||
chr17:75213375 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.405+256G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213375 | |||||||
chr17:75213559 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.405+440G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213559 | |||||||
chr17:75213649 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.405+530G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213649 | |||||||
chr17:75213725 | A | AT | 42 | a0001c0001t0001g0133 a0001c0001t0001g0247 a0001c0002t0001g0001 others(39): Show |
48 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.405+616dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75213725 | ||||||
chr17:75213862 | G | GT | 6 | a0001c0002t0001g0237 a0001c0002t0001g0238 a0001c0002t0001g0241 others(3): Show |
6 | HG02074.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+770dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75213862 | ||||||
chr17:75213862 | GT | G | 35 | a0001c0001t0001g0038 a0001c0001t0001g0098 a0001c0001t0001g0249 others(32): Show |
40 | HG00597.hp1 HG00733.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.405+770delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75213862 | ||||||
chr17:75213862 | GTT | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.405+769_405+770del others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75213862 | ||||||
chr17:75213863 | T | G | 1 | a0001c0003t0002g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.405+744T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213863 | |||||||
chr17:75213864 | T | G | 7 | a0001c0003t0002g0180 a0001c0003t0002g0183 a0001c0003t0002g0184 others(4): Show |
7 | HG00597.hp1 HG01074.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+745T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213864 | |||||||
chr17:75213865 | T | G | 23 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(20): Show |
24 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.405+746T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213865 | |||||||
chr17:75213870 | T | G | 1 | a0001c0002t0001g0222 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.405+751T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213870 | |||||||
chr17:75213873 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.405+754T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213873 | |||||||
chr17:75213874 | T | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.405+755T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213874 | |||||||
chr17:75213877 | T | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0098 |
2 | HG04115.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.405+758T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213877 | |||||||
chr17:75213878 | T | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
181 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.405+759T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213878 | |||||||
chr17:75213883 | T | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0118 others(3): Show |
8 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.405+764T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213883 | |||||||
chr17:75213902 | C | T | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.405+783C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213902 | |||||||
chr17:75213903 | T | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.405+784T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75213903 | |||||||
chr17:75214046 | G | A | 14 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.405+927G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214046 | |||||||
chr17:75214080 | G | A | 2 | a0001c0002t0001g0224 a0001c0002t0001g0241 |
2 | HG00733.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.405+961G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214080 | |||||||
chr17:75214245 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.405+1126C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214245 | |||||||
chr17:75214393 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0166 |
3 | HG02622.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.405+1274G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214393 | |||||||
chr17:75214482 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.406-1272C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214482 | |||||||
chr17:75214610 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0001c0001t0001g0215 others(1): Show |
5 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.406-1144G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214610 | |||||||
chr17:75214856 | CAAAA | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.406-890_406-887del others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr17 | 75214856 | ||||||
chr17:75214866 | A | C | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.406-888A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214866 | |||||||
chr17:75214948 | T | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.406-806T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75214948 | |||||||
chr17:75215062 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0149 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.406-692T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215062 | |||||||
chr17:75215225 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.406-529T>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215225 | |||||||
chr17:75215324 | C | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0145 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.406-430C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215324 | |||||||
chr17:75215451 | C | T | 12 | a0001c0002t0001g0001 a0001c0002t0001g0219 a0001c0002t0001g0220 others(9): Show |
16 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.406-303C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215451 | |||||||
chr17:75215489 | A | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.406-265A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215489 | |||||||
chr17:75215490 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.406-264A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215490 | |||||||
chr17:75215530 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.406-224A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215530 | |||||||
chr17:75215547 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.406-207A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215547 | |||||||
chr17:75215576 | A | G | 1 | a0001c0002t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.406-178A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215576 | |||||||
chr17:75215651 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.406-103A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215651 | |||||||
chr17:75215673 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.406-81C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 5/18 | chr17 | 75215673 | |||||||
chr17:75215855 | A | C | 1 | a0001c0002t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.475+32A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75215855 | |||||||
chr17:75216269 | C | CT | 5 | a0001c0001t0001g0035 a0001c0001t0001g0135 a0001c0006t0001g0189 others(2): Show |
5 | HG01074.hp2 HG01261.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+459dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr17 | 75216269 | ||||||
chr17:75216329 | G | A | 41 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0018 others(38): Show |
47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.475+506G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216329 | |||||||
chr17:75216332 | C | G | 1 | a0001c0002t0001g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.475+509C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216332 | |||||||
chr17:75216342 | C | T | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.475+519C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216342 | |||||||
chr17:75216354 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.475+531C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216354 | |||||||
chr17:75216384 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.475+561A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216384 | |||||||
chr17:75216395 | A | G | 41 | a0001c0001t0001g0247 a0001c0002t0001g0001 a0001c0002t0001g0018 others(38): Show |
47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.475+572A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216395 | |||||||
chr17:75216558 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.475+735C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75216558 | |||||||
chr17:75217033 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.476-1152G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217033 | |||||||
chr17:75217123 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0003c0012t0001g0168 |
4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-1062C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217123 | |||||||
chr17:75217373 | A | AT | 15 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(12): Show |
16 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.476-803dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr17 | 75217373 | ||||||
chr17:75217373 | A | ATT | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.476-804_476-803dup others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr17 | 75217373 | ||||||
chr17:75217377 | T | TTA | 11 | a0001c0001t0001g0006 a0001c0001t0001g0146 a0001c0001t0001g0147 others(8): Show |
13 | HG00639.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.476-807_476-806ins others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr17 | 75217377 | ||||||
chr17:75217604 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.476-581G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217604 | |||||||
chr17:75217790 | C | G | 1 | a0001c0005t0002g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.476-395C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217790 | |||||||
chr17:75217924 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.476-261T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75217924 | |||||||
chr17:75218050 | A | G | 1 | a0001c0005t0002g0187 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.476-135A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75218050 | |||||||
chr17:75218173 | C | G | 1 | a0004c0007t0001g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.476-12C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 6/18 | chr17 | 75218173 | |||||||
chr17:75218588 | G | GTT | 25 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0209 others(22): Show |
30 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.597+300_597+301dup others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | ||||||
chr17:75218588 | G | GTTT | 19 | a0001c0001t0001g0022 a0001c0001t0001g0205 a0001c0002t0001g0019 others(16): Show |
20 | HG01106.hp1 HG01255.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.597+299_597+301dup others(3): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | ||||||
chr17:75218588 | G | GTTTT | 30 | a0001c0001t0001g0038 a0001c0001t0001g0099 a0001c0001t0001g0119 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.597+298_597+301dup others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | ||||||
chr17:75218588 | G | GTTTTT | 98 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(95): Show |
106 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.597+297_597+301dup others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | ||||||
chr17:75218588 | G | GTTTTTT | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
72 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.597+296_597+301dup others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | ||||||
chr17:75218588 | G | GTTTTTTT | 6 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0056 others(3): Show |
6 | HG01123.hp1 HG02055.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+295_597+301dup others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75218588 | ||||||
chr17:75218839 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.597+533C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75218839 | |||||||
chr17:75218911 | G | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.597+605G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75218911 | |||||||
chr17:75218977 | C | T | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.597+671C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75218977 | |||||||
chr17:75218978 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.597+672A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75218978 | |||||||
chr17:75219045 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0064 a0001c0001t0001g0093 others(3): Show |
6 | HG00741.hp1 HG01123.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+739G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219045 | |||||||
chr17:75219143 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.597+837A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219143 | |||||||
chr17:75219173 | G | A | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.597+867G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219173 | |||||||
chr17:75219241 | G | A | 1 | a0005c0011t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.597+935G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219241 | |||||||
chr17:75219318 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.597+1012C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219318 | |||||||
chr17:75219324 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.597+1018G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219324 | |||||||
chr17:75219511 | C | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+1205C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219511 | |||||||
chr17:75219655 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+1349C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219655 | |||||||
chr17:75219896 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0105 |
2 | HG01993.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.597+1590T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75219896 | |||||||
chr17:75220210 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.597+1904T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220210 | |||||||
chr17:75220261 | ACTACAGG others(10): Show |
A | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.597+1957_597+1973d others(19): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75220261 | ||||||
chr17:75220270 | G | A | 1 | a0001c0006t0001g0191 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.597+1964G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220270 | |||||||
chr17:75220290 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.597+1984A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220290 | |||||||
chr17:75220422 | C | CT | 13 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0057 others(10): Show |
13 | HG00597.hp2 HG00673.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.597+2131dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75220422 | ||||||
chr17:75220437 | T | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0106 |
2 | HG00673.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.597+2131T>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220437 | |||||||
chr17:75220484 | G | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.597+2178G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220484 | |||||||
chr17:75220734 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0003c0012t0001g0168 |
4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+2428G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220734 | |||||||
chr17:75220752 | TTTTTG | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0089 a0001c0001t0001g0248 others(1): Show |
5 | HG01081.hp1 HG01081.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2466_597+2470d others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75220752 | ||||||
chr17:75220878 | A | AT | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.597+2594dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75220878 | ||||||
chr17:75220893 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.597+2587T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220893 | |||||||
chr17:75220918 | A | G | 1 | a0003c0012t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.597+2612A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220918 | |||||||
chr17:75220944 | C | T | 1 | a0001c0002t0001g0240 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.597+2638C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220944 | |||||||
chr17:75220955 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.597+2649C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220955 | |||||||
chr17:75220968 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.597+2662G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75220968 | |||||||
chr17:75221039 | G | A | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.597+2733G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221039 | |||||||
chr17:75221054 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0003c0012t0001g0168 |
4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+2748T>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221054 | |||||||
chr17:75221102 | C | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0050 |
2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.597+2796C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221102 | |||||||
chr17:75221166 | C | T | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.597+2860C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221166 | |||||||
chr17:75221171 | C | T | 2 | a0001c0005t0002g0207 a0001c0005t0002g0208 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.597+2865C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221171 | |||||||
chr17:75221176 | G | A | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.597+2870G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221176 | |||||||
chr17:75221247 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.597+2941A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221247 | |||||||
chr17:75221535 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.597+3229C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221535 | |||||||
chr17:75221678 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.597+3372C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221678 | |||||||
chr17:75221734 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0083 |
2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.598-3369G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221734 | |||||||
chr17:75221812 | A | G | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.598-3291A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221812 | |||||||
chr17:75221910 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.598-3193G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75221910 | |||||||
chr17:75222022 | CGTGT | C | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.598-3070_598-3067d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222022 | ||||||
chr17:75222041 | TTTTG | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.598-3042_598-3039d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222041 | ||||||
chr17:75222062 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.598-3041T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222062 | |||||||
chr17:75222161 | A | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.598-2942A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222161 | |||||||
chr17:75222234 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-2869G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222234 | |||||||
chr17:75222388 | A | G | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.598-2715A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222388 | |||||||
chr17:75222478 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-2625A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222478 | |||||||
chr17:75222495 | ATTT | A | 6 | a0001c0002t0001g0237 a0001c0002t0001g0238 a0001c0002t0001g0246 others(3): Show |
6 | HG02055.hp2 HG02074.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-2581_598-2579d others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | ||||||
chr17:75222495 | ATTTT | A | 42 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0001c0002t0001g0001 others(39): Show |
49 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.598-2582_598-2579d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | ||||||
chr17:75222495 | ATTTTT | A | 30 | a0001c0001t0001g0051 a0001c0001t0001g0215 a0001c0002t0001g0209 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.598-2583_598-2579d others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | ||||||
chr17:75222495 | ATTTTTT | A | 21 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0037 others(18): Show |
21 | HG00140.hp2 HG00733.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.598-2584_598-2579d others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | ||||||
chr17:75222495 | ATTTTTTT | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
155 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.598-2585_598-2579d others(9): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75222495 | ||||||
chr17:75222658 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.598-2445A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222658 | |||||||
chr17:75222843 | G | A | 17 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0037 others(14): Show |
17 | HG01069.hp2 HG01074.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.598-2260G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222843 | |||||||
chr17:75222928 | G | A | 1 | a0001c0003t0002g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.598-2175G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222928 | |||||||
chr17:75222976 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.598-2127A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75222976 | |||||||
chr17:75223032 | C | CA | 40 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0043 others(37): Show |
44 | HG00597.hp1 HG00639.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.598-2049dupA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75223032 | ||||||
chr17:75223032 | C | CAA | 20 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0035 others(17): Show |
20 | HG00738.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.598-2050_598-2049d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75223032 | ||||||
chr17:75223044 | A | AC | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.598-2059_598-2058i others(3): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223044 | |||||||
chr17:75223044 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.598-2059A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223044 | |||||||
chr17:75223130 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-1973A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223130 | |||||||
chr17:75223157 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.598-1946G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223157 | |||||||
chr17:75223369 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.598-1734A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223369 | |||||||
chr17:75223382 | TTTATG | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0157 a0001c0001t0001g0201 others(2): Show |
7 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-1706_598-1702d others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75223382 | ||||||
chr17:75223511 | C | T | 1 | a0001c0004t0002g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.598-1592C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223511 | |||||||
chr17:75223513 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0041 others(7): Show |
13 | HG00735.hp2 HG01123.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.598-1590G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223513 | |||||||
chr17:75223549 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.598-1554G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223549 | |||||||
chr17:75223959 | G | A | 1 | a0001c0003t0002g0182 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.598-1144G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223959 | |||||||
chr17:75223992 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.598-1111C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75223992 | |||||||
chr17:75224031 | A | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.598-1072A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224031 | |||||||
chr17:75224086 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.598-1017T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224086 | |||||||
chr17:75224127 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0048 others(5): Show |
8 | HG01069.hp2 HG01074.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-976C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224127 | |||||||
chr17:75224202 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.598-901C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224202 | |||||||
chr17:75224261 | G | A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG00639.hp2 HG01175.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-842G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224261 | |||||||
chr17:75224288 | G | C | 1 | a0001c0003t0002g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.598-815G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224288 | |||||||
chr17:75224337 | G | A | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG00639.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-766G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224337 | |||||||
chr17:75224719 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598-384C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224719 | |||||||
chr17:75224729 | G | T | 23 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(20): Show |
24 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.598-374G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224729 | |||||||
chr17:75224756 | C | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0154 others(6): Show |
10 | HG00738.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-347C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224756 | |||||||
chr17:75224814 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-289A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224814 | |||||||
chr17:75224829 | G | GA | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.598-258dupA | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75224829 | ||||||
chr17:75224829 | G | GAA | 6 | a0001c0001t0001g0039 a0001c0001t0001g0056 a0001c0001t0001g0110 others(3): Show |
6 | HG00140.hp1 HG02148.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-259_598-258dup others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr17 | 75224829 | ||||||
chr17:75224904 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.598-199C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224904 | |||||||
chr17:75224979 | T | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.598-124T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 7/18 | chr17 | 75224979 | |||||||
chr17:75225557 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0003c0012t0001g0168 |
4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.855+93A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 9/18 | chr17 | 75225557 | |||||||
chr17:75225975 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.988-76C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 10/18 | chr17 | 75225975 | |||||||
chr17:75225992 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.988-59G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 10/18 | chr17 | 75225992 | |||||||
chr17:75226178 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1094+21C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226178 | |||||||
chr17:75226285 | C | T | 1 | a0001c0002t0001g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1094+128C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226285 | |||||||
chr17:75226293 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1094+136T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226293 | |||||||
chr17:75226357 | C | T | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1094+200C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226357 | |||||||
chr17:75226724 | A | G | 4 | a0001c0001t0001g0056 a0001c0006t0001g0189 a0001c0006t0001g0190 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+567A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226724 | |||||||
chr17:75226752 | C | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1094+595C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226752 | |||||||
chr17:75226770 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1094+613G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226770 | |||||||
chr17:75226931 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1094+774C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75226931 | |||||||
chr17:75227002 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1094+845A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227002 | |||||||
chr17:75227003 | TAATC | T | 7 | a0001c0001t0001g0125 a0001c0003t0002g0174 a0001c0003t0002g0175 others(4): Show |
7 | HG00597.hp1 HG02015.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1094+853_1094+856d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227003 | ||||||
chr17:75227073 | G | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1094+916G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227073 | |||||||
chr17:75227299 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1094+1142A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227299 | |||||||
chr17:75227326 | G | GTTT | 14 | a0001c0003t0002g0173 a0001c0003t0002g0174 a0001c0003t0002g0175 others(11): Show |
14 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.1094+1193_1094+119 others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227326 | ||||||
chr17:75227326 | G | GTTTT | 7 | a0001c0003t0002g0177 a0001c0003t0002g0178 a0001c0003t0002g0179 others(4): Show |
7 | HG01361.hp1 HG02135.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1094+1192_1094+119 others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227326 | ||||||
chr17:75227326 | GT | G | 31 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(28): Show |
33 | HG01070.hp1 HG01099.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.1094+1195delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227326 | ||||||
chr17:75227326 | GTT | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1094+1194_1094+119 others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75227326 | ||||||
chr17:75227334 | T | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
13 | HG01361.hp2 HG01496.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1094+1177T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227334 | |||||||
chr17:75227335 | T | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1094+1178T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227335 | |||||||
chr17:75227336 | T | G | 4 | a0001c0001t0001g0056 a0001c0006t0001g0189 a0001c0006t0001g0190 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+1179T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227336 | |||||||
chr17:75227340 | T | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0141 |
2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1094+1183T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227340 | |||||||
chr17:75227422 | A | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1094+1265A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227422 | |||||||
chr17:75227429 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1094+1272G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227429 | |||||||
chr17:75227579 | C | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1094+1422C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227579 | |||||||
chr17:75227662 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1094+1505G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227662 | |||||||
chr17:75227750 | G | A | 4 | a0001c0001t0001g0056 a0001c0006t0001g0189 a0001c0006t0001g0190 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+1593G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227750 | |||||||
chr17:75227771 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1094+1614A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227771 | |||||||
chr17:75227772 | G | A | 1 | a0003c0012t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1094+1615G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227772 | |||||||
chr17:75227779 | A | C | 1 | a0001c0002t0001g0223 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1094+1622A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227779 | |||||||
chr17:75227810 | A | T | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1094+1653A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227810 | |||||||
chr17:75227887 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1094+1730T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227887 | |||||||
chr17:75227937 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0067 a0001c0001t0001g0143 |
3 | HG02895.hp1 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1094+1780G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75227937 | |||||||
chr17:75228107 | A | T | 1 | a0001c0006t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1094+1950A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228107 | |||||||
chr17:75228130 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1094+1973C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228130 | |||||||
chr17:75228284 | A | T | 8 | a0001c0002t0001g0018 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
9 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1094+2127A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228284 | |||||||
chr17:75228292 | C | T | 4 | a0001c0001t0001g0056 a0001c0006t0001g0189 a0001c0006t0001g0190 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+2135C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228292 | |||||||
chr17:75228544 | G | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1094+2387G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228544 | |||||||
chr17:75228558 | T | G | 3 | a0001c0005t0002g0170 a0001c0005t0002g0171 a0001c0005t0002g0172 |
3 | HG00140.hp1 HG01361.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1094+2401T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228558 | |||||||
chr17:75228646 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1094+2489C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228646 | |||||||
chr17:75228700 | A | C | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1094+2543A>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228700 | |||||||
chr17:75228984 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1095-2356C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75228984 | |||||||
chr17:75229043 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1095-2297A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229043 | |||||||
chr17:75229154 | C | T | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG00639.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095-2186C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229154 | |||||||
chr17:75229224 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1095-2116A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229224 | |||||||
chr17:75229277 | A | T | 3 | a0001c0003t0002g0174 a0001c0003t0002g0176 a0001c0003t0002g0178 |
3 | HG02015.hp2 HG02129.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1095-2063A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229277 | |||||||
chr17:75229278 | T | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1095-2062T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229278 | |||||||
chr17:75229441 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1095-1899C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229441 | |||||||
chr17:75229527 | G | A | 1 | a0003c0012t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1095-1813G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229527 | |||||||
chr17:75229664 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1095-1676G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229664 | |||||||
chr17:75229679 | A | G | 5 | a0001c0002t0001g0018 a0001c0002t0001g0210 a0001c0002t0001g0212 others(2): Show |
6 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095-1661A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229679 | |||||||
chr17:75229778 | C | T | 1 | a0001c0002t0001g0209 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1095-1562C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229778 | |||||||
chr17:75229820 | C | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1095-1520C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229820 | |||||||
chr17:75229861 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1095-1479A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75229861 | |||||||
chr17:75230044 | A | AT | 17 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0097 others(14): Show |
19 | HG00639.hp1 HG01516.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1095-1280dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230044 | ||||||
chr17:75230044 | A | ATT | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1095-1281_1095-128 others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230044 | ||||||
chr17:75230044 | A | ATTT | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0041 others(10): Show |
16 | HG00735.hp2 HG01123.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095-1282_1095-128 others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230044 | ||||||
chr17:75230105 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1095-1235A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230105 | |||||||
chr17:75230124 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1095-1216G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230124 | |||||||
chr17:75230285 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0108 others(2): Show |
5 | HG01256.hp2 HG01981.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095-1055C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230285 | |||||||
chr17:75230306 | G | A | 1 | a0001c0002t0001g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1095-1034G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230306 | |||||||
chr17:75230362 | G | GT | 60 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(57): Show |
67 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1095-963dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230362 | ||||||
chr17:75230362 | G | GTT | 36 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0001c0001t0001g0202 others(33): Show |
40 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1095-964_1095-963d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230362 | ||||||
chr17:75230362 | G | T | 3 | a0001c0003t0002g0177 a0001c0003t0002g0179 a0001c0003t0002g0182 |
3 | NA18990.hp2 NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1095-978G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230362 | |||||||
chr17:75230364 | T | TG | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1095-976_1095-975i others(3): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230364 | |||||||
chr17:75230382 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1095-958T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230382 | |||||||
chr17:75230520 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1095-820C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230520 | |||||||
chr17:75230705 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0076 |
2 | HG01109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1095-635A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230705 | |||||||
chr17:75230722 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1095-618T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230722 | |||||||
chr17:75230722 | T | G | 31 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1095-618T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230722 | |||||||
chr17:75230742 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1095-598G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230742 | |||||||
chr17:75230903 | G | A | 1 | a0001c0002t0001g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1095-437G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230903 | |||||||
chr17:75230936 | A | ATTT | 34 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0166 others(31): Show |
36 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.1095-393_1095-391d others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230936 | ||||||
chr17:75230936 | A | ATTTT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1095-394_1095-391d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230936 | ||||||
chr17:75230936 | A | ATTTTT | 10 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0057 others(7): Show |
10 | HG00544.hp2 HG00673.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1095-395_1095-391d others(7): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr17 | 75230936 | ||||||
chr17:75230959 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1095-381T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230959 | |||||||
chr17:75230987 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1095-353G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75230987 | |||||||
chr17:75231057 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1095-283G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75231057 | |||||||
chr17:75231315 | C | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0001c0001t0001g0215 others(1): Show |
5 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095-25C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 11/18 | chr17 | 75231315 | |||||||
chr17:75231434 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1178+11G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 12/18 | chr17 | 75231434 | |||||||
chr17:75231473 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1178+50G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 12/18 | chr17 | 75231473 | |||||||
chr17:75231665 | TATGCGGG others(11): Show |
T | 33 | a0001c0001t0001g0215 a0001c0002t0001g0001 a0001c0002t0001g0019 others(30): Show |
38 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1244+38_1244+55del others(18): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr17 | 75231665 | ||||||
chr17:75231666 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0056 |
2 | HG01255.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1244+28A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | chr17 | 75231666 | |||||||
chr17:75231671 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1244+33G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | chr17 | 75231671 | |||||||
chr17:75231732 | G | GT | 7 | a0001c0001t0001g0012 a0001c0001t0001g0064 a0001c0001t0001g0093 others(4): Show |
7 | HG00741.hp1 HG01123.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1244+94_1244+95ins others(1): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | chr17 | 75231732 | |||||||
chr17:75231779 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1245-49C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 13/18 | chr17 | 75231779 | |||||||
chr17:75232004 | A | G | 6 | a0001c0001t0001g0056 a0001c0002t0001g0217 a0001c0002t0001g0218 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+25A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232004 | |||||||
chr17:75232006 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1396+27T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232006 | |||||||
chr17:75232049 | T | C | 37 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0049 others(34): Show |
38 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1396+70T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232049 | |||||||
chr17:75232078 | C | T | 34 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0001c0001t0001g0215 others(31): Show |
36 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.1396+99C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232078 | |||||||
chr17:75232141 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1396+162C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232141 | |||||||
chr17:75232216 | C | T | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1396+237C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232216 | |||||||
chr17:75232290 | G | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0041 others(7): Show |
13 | HG00735.hp2 HG01123.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.1396+311G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232290 | |||||||
chr17:75232383 | C | T | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1396+404C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232383 | |||||||
chr17:75232458 | C | T | 3 | a0001c0006t0001g0189 a0001c0006t0001g0190 a0001c0006t0001g0191 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1397-393C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232458 | |||||||
chr17:75232472 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1397-379A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232472 | |||||||
chr17:75232544 | G | A | 32 | a0001c0002t0001g0001 a0001c0002t0001g0019 a0001c0002t0001g0216 others(29): Show |
37 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1397-307G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232544 | |||||||
chr17:75232564 | A | G | 41 | a0001c0001t0001g0147 a0001c0002t0001g0001 a0001c0002t0001g0018 others(38): Show |
47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1397-287A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232564 | |||||||
chr17:75232609 | C | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1397-242C>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 14/18 | chr17 | 75232609 | |||||||
chr17:75232983 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1514+15T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 15/18 | chr17 | 75232983 | |||||||
chr17:75232997 | G | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0037 others(10): Show |
15 | HG00738.hp2 HG01069.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1514+29G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 15/18 | chr17 | 75232997 | |||||||
chr17:75233002 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1514+34G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 15/18 | chr17 | 75233002 | |||||||
chr17:75233294 | G | A | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG00639.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615+136G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233294 | |||||||
chr17:75233315 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1615+157T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233315 | |||||||
chr17:75233343 | A | ATGTT | 7 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
9 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1615+207_1615+210d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233343 | ||||||
chr17:75233363 | T | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
8 | HG00621.hp2 HG00673.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615+205T>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233363 | |||||||
chr17:75233367 | TTTTC | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0113 others(1): Show |
4 | HG01099.hp2 HG01496.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615+219_1615+222d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233367 | ||||||
chr17:75233373 | T | TTC | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615+217_1615+218d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233373 | ||||||
chr17:75233377 | T | C | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615+219T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233377 | |||||||
chr17:75233377 | T | TTCTC | 6 | a0001c0001t0001g0056 a0001c0005t0002g0167 a0001c0006t0001g0189 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1615+223_1615+226d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233377 | ||||||
chr17:75233377 | TTCTC | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0151 a0001c0001t0001g0166 others(1): Show |
5 | HG00738.hp2 HG01891.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615+223_1615+226d others(6): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233377 | ||||||
chr17:75233379 | CTCTCTTT others(3): Show |
C | 1 | a0005c0011t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1615+231_1615+240d others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233379 | ||||||
chr17:75233385 | TTCTTTC | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
145 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.1615+247_1615+252d others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233385 | ||||||
chr17:75233386 | T | G | 4 | a0001c0001t0001g0056 a0001c0006t0001g0189 a0001c0006t0001g0190 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615+228T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233386 | |||||||
chr17:75233393 | C | CTTTCTCT others(1): Show |
41 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(38): Show |
47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1615+237_1615+244d others(10): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233393 | ||||||
chr17:75233396 | T | TCTCTTTT others(3): Show |
1 | a0001c0002t0001g0222 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1615+244_1615+245i others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233396 | ||||||
chr17:75233397 | CTCTTTCT others(3): Show |
C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0120 |
2 | HG00639.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1615+247_1615+256d others(12): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233397 | ||||||
chr17:75233399 | C | CTT | 4 | a0001c0001t0001g0056 a0001c0006t0001g0189 a0001c0006t0001g0190 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615+243_1615+244d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233399 | ||||||
chr17:75233420 | C | CT | 46 | a0001c0001t0001g0056 a0001c0002t0001g0001 a0001c0002t0001g0018 others(43): Show |
52 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1615+266dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233420 | ||||||
chr17:75233424 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0003c0012t0001g0168 |
4 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615+266T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233424 | |||||||
chr17:75233426 | TTTTATTT others(4): Show |
T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG00639.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1615+272_1615+282d others(13): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233426 | ||||||
chr17:75233430 | A | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.1615+272A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233430 | |||||||
chr17:75233436 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0205 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1615+278T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233436 | |||||||
chr17:75233437 | C | CT | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1615+294dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233437 | ||||||
chr17:75233437 | C | CTT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0056 others(3): Show |
6 | HG01070.hp2 HG01109.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615+293_1615+294d others(4): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233437 | ||||||
chr17:75233437 | C | CTTT | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
45 | HG00733.hp1 HG01071.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1615+292_1615+294d others(5): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75233437 | ||||||
chr17:75233437 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0205 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1615+279C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233437 | |||||||
chr17:75233469 | C | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1615+311C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233469 | |||||||
chr17:75233512 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1615+354C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233512 | |||||||
chr17:75233532 | G | A | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615+374G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233532 | |||||||
chr17:75233565 | G | A | 6 | a0001c0004t0002g0007 a0001c0004t0002g0025 a0001c0004t0002g0026 others(3): Show |
7 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615+407G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233565 | |||||||
chr17:75233569 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0089 others(1): Show |
4 | HG00544.hp2 HG00597.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615+411G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233569 | |||||||
chr17:75233677 | C | T | 1 | a0001c0005t0002g0187 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1615+519C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233677 | |||||||
chr17:75233721 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1615+563C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233721 | |||||||
chr17:75233761 | G | C | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615+603G>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233761 | |||||||
chr17:75233825 | C | G | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1615+667C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233825 | |||||||
chr17:75233889 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1615+731C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233889 | |||||||
chr17:75233894 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0166 a0001c0003t0002g0185 others(1): Show |
5 | HG01433.hp1 HG01891.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615+736C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233894 | |||||||
chr17:75233986 | G | A | 14 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
15 | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1616-651G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75233986 | |||||||
chr17:75234049 | CTTCTTT | C | 41 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(38): Show |
47 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1616-585_1616-580d others(8): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75234049 | ||||||
chr17:75234052 | C | CT | 27 | a0001c0003t0002g0017 a0001c0003t0002g0173 a0001c0003t0002g0174 others(24): Show |
28 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1616-568dupT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75234052 | ||||||
chr17:75234052 | CT | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1616-568delT | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr17 | 75234052 | ||||||
chr17:75234058 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0074 others(2): Show |
5 | HG02071.hp2 HG02080.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1616-579T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234058 | |||||||
chr17:75234063 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0131 |
3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1616-574T>C | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234063 | |||||||
chr17:75234096 | C | G | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1616-541C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234096 | |||||||
chr17:75234115 | A | G | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1616-522A>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234115 | |||||||
chr17:75234133 | C | T | 1 | a0001c0003t0002g0196 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1616-504C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234133 | |||||||
chr17:75234134 | C | T | 1 | a0001c0005t0002g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1616-503C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234134 | |||||||
chr17:75234286 | A | T | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1616-351A>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234286 | |||||||
chr17:75234360 | G | T | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1616-277G>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 16/18 | chr17 | 75234360 | |||||||
chr17:75234841 | TTA | T | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1767+54_1767+55del others(2): Show |
NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75234841 | |||||||
chr17:75234865 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1767+77T>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75234865 | |||||||
chr17:75234868 | G | A | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1767+80G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75234868 | |||||||
chr17:75234899 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1767+111C>T | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75234899 | |||||||
chr17:75235001 | G | A | 4 | a0001c0001t0001g0056 a0001c0006t0001g0189 a0001c0006t0001g0190 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1768-99G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75235001 | |||||||
chr17:75235053 | C | G | 40 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
46 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1768-47C>G | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 17/18 | chr17 | 75235053 | |||||||
chr17:75235543 | G | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0069 others(8): Show |
12 | HG00280.hp1 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1870-35G>A | NUP85 | ENSG00000125450.11 | transcript | ENST00000245544.9 | protein_coding | 18/18 | chr17 | 75235543 |