Item | Value |
---|---|
geneid | 7347 |
ensemblid | ENSG00000118939.19 |
hgncid | 12515 |
symbol | UCHL3 |
name | ubiquitin C-terminal hydrolase L3 |
refseq_nuc | NM_006002.5 |
refseq_prot | NP_005993.1 |
ensembl_nuc | ENST00000377595.8 |
ensembl_prot | ENSP00000366819.3 |
mane_status | MANE Select |
chr | chr13 |
start | 75549791 |
end | 75606020 |
strand | + |
ver | v1.2 |
region | chr13:75549791-75606020 |
region5000 | chr13:75544791-75611020 |
regionname0 | UCHL3_chr13_75549791_75606020 |
regionname5000 | UCHL3_chr13_75544791_75611020 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 230 | 325 | 92 | 66 | 119 | 8 | 38 | 90 | UCHL3_chr13_75544791_75611020 | UCHL3 | MEGQR others(225): Show |
chr13 | 75544791 | 75611020 |
a0002 | 0/0 | 230 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | MEGQR others(225): Show |
chr13 | 75544791 | 75611020 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 690 | 325 | 92 | 66 | 119 | 8 | 38 | UCHL3_chr13_75544791_75611020 | UCHL3 | ATGGA others(685): Show |
chr13 | 75544791 | 75611020 | ||
a0002c0002 | 0/0 | 690 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | ATGGA others(685): Show |
chr13 | 75544791 | 75611020 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 931 | 259 | 65 | 56 | 108 | 6 | 22 | UCHL3_chr13_75544791_75611020 | UCHL3 | GTCAG others(926): Show |
chr13 | 75544791 | 75611020 |
a0001c0001t0002 | 0/0 | 931 | 41 | 5 | 7 | 11 | 2 | 16 | UCHL3_chr13_75544791_75611020 | UCHL3 | GTCAG others(926): Show |
chr13 | 75544791 | 75611020 |
a0001c0001t0003 | 0/0 | 931 | 19 | 17 | 2 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | GTCAG others(926): Show |
chr13 | 75544791 | 75611020 |
a0001c0001t0004 | 0/0 | 931 | 4 | 4 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | GTCAG others(926): Show |
chr13 | 75544791 | 75611020 |
a0001c0001t0005 | 0/0 | 931 | 2 | 1 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | GTCAG others(926): Show |
chr13 | 75544791 | 75611020 |
a0002c0002t0001 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | GTCAG others(926): Show |
chr13 | 75544791 | 75611020 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0109 | EUR | GBR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0204 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | IBS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | BEB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | BEB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | STU | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | STU | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | STU | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | STU | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | LWK | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ASW | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ASW | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | GIH | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | GIH | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | USA | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | USA | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | LWK | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0276 | REF | REF | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0131 | REF | REF | UCHL3_chr13_75544791_75611020 | UCHL3 | chr13 | 75544791 | 75611020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:75549855 | A | G | 1 | a0002 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.35A>G | p.Asn12Ser | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 1/9 | 65/931 | 35/693 | 12/230 | chr13 | 75549855 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:75549811 | C | T | 1 | a0001c0001t0003 | 19 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-10C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 1/9 | 10 | chr13 | 75549811 | ||||||
chr13:75549815 | G | A | 1 | a0001c0001t0005 | 2 | HG00735.hp1 HG02818.hp2 |
5_prime_UTR_variant | MODIFIER | c.-6G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 1/9 | 6 | chr13 | 75549815 | ||||||
chr13:75549819 | C | T | 1 | a0001c0001t0004 | 4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-2C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 1/9 | 2 | chr13 | 75549819 | ||||||
chr13:75605906 | T | G | 1 | a0001c0001t0002 | 41 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*94T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 9/9 | 94 | chr13 | 75605906 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:75550015 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(104): Show |
117 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.54+28C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550015 | |||||||
chr13:75550059 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54+72C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550059 | |||||||
chr13:75550185 | A | G | 3 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 |
3 | HG01261.hp1 HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.54+198A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550185 | |||||||
chr13:75550492 | T | G | 19 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(16): Show |
19 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.54+505T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550492 | |||||||
chr13:75550511 | A | C | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.54+524A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550511 | |||||||
chr13:75550638 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.54+651G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550638 | |||||||
chr13:75550720 | G | GT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(85): Show |
93 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.54+749dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75550720 | ||||||
chr13:75550720 | GT | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
138 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.54+749delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75550720 | ||||||
chr13:75550720 | GTT | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(38): Show |
42 | HG00735.hp1 HG01099.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.54+748_54+749delTT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75550720 | ||||||
chr13:75550725 | T | G | 1 | a0001c0001t0004g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.54+738T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550725 | |||||||
chr13:75550737 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.54+750C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550737 | |||||||
chr13:75550982 | G | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+995G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75550982 | |||||||
chr13:75551056 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.54+1069G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75551056 | |||||||
chr13:75551239 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.54+1252C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75551239 | |||||||
chr13:75551250 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.54+1263G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75551250 | |||||||
chr13:75551430 | C | CA | 14 | a0001c0001t0001g0094 a0001c0001t0001g0136 a0001c0001t0001g0207 others(11): Show |
15 | HG00733.hp2 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.54+1459dupA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75551430 | ||||||
chr13:75551430 | CA | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
13 | HG01993.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.54+1459delA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75551430 | ||||||
chr13:75551441 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.54+1454A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75551441 | |||||||
chr13:75551513 | A | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+1526A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75551513 | |||||||
chr13:75551875 | G | C | 1 | a0001c0001t0001g0213 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.54+1888G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75551875 | |||||||
chr13:75552032 | ATAG | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.54+2047_54+2049del others(3): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75552032 | ||||||
chr13:75552101 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.54+2114T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75552101 | |||||||
chr13:75552225 | T | C | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+2238T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75552225 | |||||||
chr13:75552402 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.54+2415C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75552402 | |||||||
chr13:75552435 | G | A | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+2448G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75552435 | |||||||
chr13:75552689 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54+2702T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75552689 | |||||||
chr13:75552764 | A | G | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.54+2777A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75552764 | |||||||
chr13:75552823 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18985.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.54+2836G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75552823 | |||||||
chr13:75553314 | T | C | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.54+3327T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75553314 | |||||||
chr13:75553446 | A | G | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.54+3459A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75553446 | |||||||
chr13:75553578 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0197 a0001c0001t0001g0198 others(1): Show |
5 | NA18954.hp2 NA18982.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+3591C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75553578 | |||||||
chr13:75553644 | CT | C | 25 | a0001c0001t0001g0099 a0001c0001t0001g0119 a0001c0001t0002g0007 others(22): Show |
27 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.54+3658delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75553644 | |||||||
chr13:75553649 | G | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0200 |
2 | NA18967.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.54+3662G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75553649 | |||||||
chr13:75553669 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.54+3682A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75553669 | |||||||
chr13:75553777 | A | G | 36 | a0001c0001t0001g0119 a0001c0001t0002g0006 a0001c0001t0002g0007 others(33): Show |
39 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.54+3790A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75553777 | |||||||
chr13:75554173 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.54+4186A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75554173 | |||||||
chr13:75554328 | C | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG01106.hp1 HG01256.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.54+4341C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75554328 | |||||||
chr13:75554423 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.54+4436C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75554423 | |||||||
chr13:75554512 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.54+4525C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75554512 | |||||||
chr13:75554512 | CGGCTATT others(8): Show |
C | 1 | a0001c0001t0001g0297 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.54+4536_54+4550del others(15): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75554512 | ||||||
chr13:75554749 | C | CT | 46 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(43): Show |
49 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.54+4768dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75554749 | ||||||
chr13:75554998 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.54+5011G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75554998 | |||||||
chr13:75555497 | T | A | 1 | a0001c0001t0001g0216 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.55-5256T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75555497 | |||||||
chr13:75555617 | T | TATA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(178): Show |
195 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.55-5129_55-5127dup others(3): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75555617 | ||||||
chr13:75555784 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55-4969G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75555784 | |||||||
chr13:75555793 | A | G | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-4960A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75555793 | |||||||
chr13:75555793 | A | T | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.55-4960A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75555793 | |||||||
chr13:75556070 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG01109.hp2 HG02145.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-4683C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556070 | |||||||
chr13:75556418 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55-4335G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556418 | |||||||
chr13:75556467 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.55-4286G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556467 | |||||||
chr13:75556625 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
135 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.55-4128T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556625 | |||||||
chr13:75556709 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA19012.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.55-4044T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556709 | |||||||
chr13:75556775 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.55-3978A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556775 | |||||||
chr13:75556862 | G | A | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.55-3891G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556862 | |||||||
chr13:75556903 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-3850C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556903 | |||||||
chr13:75556993 | G | T | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-3760G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75556993 | |||||||
chr13:75557188 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.55-3565C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75557188 | |||||||
chr13:75557193 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(9): Show |
13 | HG01109.hp2 HG01891.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.55-3560G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75557193 | |||||||
chr13:75557291 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.55-3462C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75557291 | |||||||
chr13:75557487 | G | C | 1 | a0001c0001t0001g0217 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.55-3266G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75557487 | |||||||
chr13:75557596 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-3157C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75557596 | |||||||
chr13:75557643 | A | G | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.55-3110A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75557643 | |||||||
chr13:75557849 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
122 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.55-2904A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75557849 | |||||||
chr13:75557961 | A | AT | 13 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0082 others(10): Show |
13 | HG01192.hp2 HG01891.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-2778dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75557961 | ||||||
chr13:75557961 | ATT | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(125): Show |
139 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.55-2779_55-2778del others(2): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75557961 | ||||||
chr13:75558030 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.55-2723G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75558030 | |||||||
chr13:75558104 | A | C | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02074.hp1 NA18948.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.55-2649A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75558104 | |||||||
chr13:75558348 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-2405A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75558348 | |||||||
chr13:75558474 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.55-2279C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75558474 | |||||||
chr13:75558490 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.55-2263A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75558490 | |||||||
chr13:75558617 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.55-2136T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75558617 | |||||||
chr13:75558707 | G | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-2046G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75558707 | |||||||
chr13:75558757 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.55-1996C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75558757 | |||||||
chr13:75559029 | T | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.55-1724T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559029 | |||||||
chr13:75559030 | C | CT | 34 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(31): Show |
36 | HG01109.hp2 HG01978.hp1 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-1696dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559030 | ||||||
chr13:75559030 | C | CTT | 7 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0068 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-1697_55-1696dup others(2): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559030 | ||||||
chr13:75559030 | C | CTTTT | 14 | a0001c0001t0003g0018 a0001c0001t0003g0023 a0001c0001t0003g0024 others(11): Show |
14 | HG00735.hp2 HG01496.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.55-1699_55-1696dup others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559030 | ||||||
chr13:75559030 | CT | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
113 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.55-1696delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559030 | ||||||
chr13:75559030 | CTT | C | 20 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0075 others(17): Show |
20 | HG00621.hp2 HG01517.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.55-1697_55-1696del others(2): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559030 | ||||||
chr13:75559030 | CTTT | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
9 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.55-1698_55-1696del others(3): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559030 | ||||||
chr13:75559030 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.55-1705_55-1696del others(10): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559030 | ||||||
chr13:75559030 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0218 |
3 | HG00621.hp1 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.55-1706_55-1696del others(11): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559030 | ||||||
chr13:75559088 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.55-1665G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559088 | |||||||
chr13:75559120 | A | C | 1 | a0001c0001t0002g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.55-1633A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559120 | |||||||
chr13:75559178 | T | A | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-1575T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559178 | |||||||
chr13:75559205 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.55-1548A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559205 | |||||||
chr13:75559283 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.55-1470A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559283 | |||||||
chr13:75559348 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.55-1405C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559348 | |||||||
chr13:75559406 | AT | A | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.55-1345delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 75559406 | ||||||
chr13:75559462 | C | G | 19 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0100 others(16): Show |
21 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.55-1291C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559462 | |||||||
chr13:75559677 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.55-1076G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559677 | |||||||
chr13:75559774 | T | C | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-979T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559774 | |||||||
chr13:75559787 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.55-966T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559787 | |||||||
chr13:75559823 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.55-930A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75559823 | |||||||
chr13:75560144 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.55-609T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75560144 | |||||||
chr13:75560183 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-570T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75560183 | |||||||
chr13:75560539 | C | T | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.55-214C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75560539 | |||||||
chr13:75560695 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.55-58A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 2/8 | chr13 | 75560695 | |||||||
chr13:75560892 | T | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.183+11T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75560892 | |||||||
chr13:75561084 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.183+203C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561084 | |||||||
chr13:75561134 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.183+253C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561134 | |||||||
chr13:75561213 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.183+332A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561213 | |||||||
chr13:75561511 | T | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+630T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561511 | |||||||
chr13:75561541 | A | AATAT | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+672_183+675dup others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75561541 | ||||||
chr13:75561558 | G | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+677G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561558 | |||||||
chr13:75561559 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+678G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561559 | |||||||
chr13:75561611 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.183+730C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561611 | |||||||
chr13:75561747 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
133 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.183+866C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561747 | |||||||
chr13:75561764 | T | C | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+883T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561764 | |||||||
chr13:75561769 | G | C | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+888G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561769 | |||||||
chr13:75561788 | T | TGTATATA others(35): Show |
1 | a0001c0001t0001g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.183+937_183+938ins others(42): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75561788 | ||||||
chr13:75561796 | T | TGTATACG others(35): Show |
1 | a0001c0001t0002g0007 | 2 | HG03491.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.183+937_183+938ins others(42): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75561796 | ||||||
chr13:75561796 | TGTATACG others(35): Show |
T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.183+938_183+979del others(42): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75561796 | ||||||
chr13:75561808 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA19012.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.183+927C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561808 | |||||||
chr13:75561819 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(160): Show |
172 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.183+938G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561819 | |||||||
chr13:75561827 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(163): Show |
175 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.183+946G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561827 | |||||||
chr13:75561838 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
101 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.183+957C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561838 | |||||||
chr13:75561881 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0056 others(40): Show |
44 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.183+1000G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561881 | |||||||
chr13:75561961 | A | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0056 others(20): Show |
24 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.183+1080A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75561961 | |||||||
chr13:75562005 | G | A | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1124G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562005 | |||||||
chr13:75562118 | G | A | 20 | a0001c0001t0001g0214 a0001c0001t0003g0017 a0001c0001t0003g0018 others(17): Show |
20 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.183+1237G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562118 | |||||||
chr13:75562290 | T | C | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0193 others(1): Show |
4 | HG02132.hp2 HG02523.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+1409T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562290 | |||||||
chr13:75562388 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.183+1507A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562388 | |||||||
chr13:75562411 | A | G | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1530A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562411 | |||||||
chr13:75562512 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(176): Show |
193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.183+1631G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562512 | |||||||
chr13:75562798 | T | A | 1 | a0001c0001t0002g0096 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.183+1917T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562798 | |||||||
chr13:75562838 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+1957G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562838 | |||||||
chr13:75562840 | A | G | 23 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0100 others(20): Show |
25 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.183+1959A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75562840 | |||||||
chr13:75563125 | C | CTGTA | 8 | a0001c0001t0001g0050 a0001c0001t0001g0121 a0001c0001t0001g0122 others(5): Show |
8 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+2245_183+2246i others(6): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563125 | ||||||
chr13:75563125 | CTTTA | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0277 others(1): Show |
4 | HG01106.hp2 HG01192.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+2246_183+2249d others(6): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563125 | ||||||
chr13:75563125 | CTTTATGT others(1): Show |
C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
125 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.183+2246_183+2253d others(10): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563125 | ||||||
chr13:75563125 | CTTTATGT others(9): Show |
C | 7 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG00733.hp2 HG00738.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+2246_183+2261d others(18): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563125 | ||||||
chr13:75563127 | T | G | 11 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
11 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.183+2246T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75563127 | |||||||
chr13:75563127 | T | TTATG | 34 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0143 others(31): Show |
36 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+2282_183+2285d others(6): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563127 | ||||||
chr13:75563127 | T | TTATGTAT others(1): Show |
4 | a0001c0001t0002g0006 a0001c0001t0002g0090 a0001c0001t0002g0095 others(1): Show |
4 | HG04184.hp2 NA18964.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+2278_183+2285d others(10): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563127 | ||||||
chr13:75563127 | TTATGTAT others(1): Show |
T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0178 a0001c0001t0001g0182 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+2278_183+2285d others(10): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563127 | ||||||
chr13:75563138 | T | A | 1 | a0001c0001t0001g0219 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.183+2257T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75563138 | |||||||
chr13:75563229 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.183+2348G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75563229 | |||||||
chr13:75563570 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.183+2689C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75563570 | |||||||
chr13:75563628 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.183+2747G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75563628 | |||||||
chr13:75563822 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.184-2873C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75563822 | |||||||
chr13:75563908 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.184-2787C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75563908 | |||||||
chr13:75563920 | C | CTG | 23 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(20): Show |
23 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.184-2753_184-2752d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563920 | ||||||
chr13:75563920 | C | CTGTGTG | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(125): Show |
138 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.184-2757_184-2752d others(8): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563920 | ||||||
chr13:75563920 | C | CTGTGTGT others(1): Show |
5 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
6 | HG00558.hp2 HG02970.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-2759_184-2752d others(10): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75563920 | ||||||
chr13:75564133 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA19012.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.184-2562G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564133 | |||||||
chr13:75564153 | A | G | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-2542A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564153 | |||||||
chr13:75564155 | C | CT | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(9): Show |
12 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.184-2527dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75564155 | ||||||
chr13:75564173 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.184-2522T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564173 | |||||||
chr13:75564236 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.184-2459C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564236 | |||||||
chr13:75564250 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.184-2445G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564250 | |||||||
chr13:75564252 | G | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0283 |
3 | NA18950.hp1 NA18967.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.184-2443G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564252 | |||||||
chr13:75564273 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0113 a0001c0001t0002g0114 others(1): Show |
5 | HG02055.hp1 HG03491.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-2422C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564273 | |||||||
chr13:75564298 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.184-2397C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564298 | |||||||
chr13:75564318 | T | C | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.184-2377T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564318 | |||||||
chr13:75564396 | C | T | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-2299C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564396 | |||||||
chr13:75564487 | C | T | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0135 |
3 | HG00741.hp2 HG02004.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.184-2208C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564487 | |||||||
chr13:75564684 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.184-2011T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564684 | |||||||
chr13:75564694 | G | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
217 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.184-2001G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564694 | |||||||
chr13:75564773 | G | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-1922G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564773 | |||||||
chr13:75564929 | CAGATGAT others(27): Show |
C | 1 | a0001c0001t0001g0291 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.184-1765_184-1732d others(36): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75564929 | |||||||
chr13:75565303 | C | T | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.184-1392C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565303 | |||||||
chr13:75565312 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0074 others(1): Show |
7 | HG01081.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.184-1383A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565312 | |||||||
chr13:75565493 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0057 others(17): Show |
21 | HG01109.hp2 HG01891.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.184-1202G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565493 | |||||||
chr13:75565499 | T | C | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01099.hp2 HG01106.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.184-1196T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565499 | |||||||
chr13:75565500 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-1195A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565500 | |||||||
chr13:75565553 | A | AGGACTAG others(25): Show |
1 | a0001c0001t0001g0291 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.184-1140_184-1109d others(34): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75565553 | ||||||
chr13:75565625 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.184-1070T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565625 | |||||||
chr13:75565673 | C | G | 7 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG00733.hp2 HG00738.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.184-1022C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565673 | |||||||
chr13:75565715 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-980C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565715 | |||||||
chr13:75565853 | G | A | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.184-842G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565853 | |||||||
chr13:75565905 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0150 |
2 | HG02135.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.184-790G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565905 | |||||||
chr13:75565933 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
134 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.184-762C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565933 | |||||||
chr13:75565955 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.184-740A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75565955 | |||||||
chr13:75566163 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.184-532C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75566163 | |||||||
chr13:75566325 | T | C | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.184-370T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75566325 | |||||||
chr13:75566338 | C | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0298 |
2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.184-357C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75566338 | |||||||
chr13:75566361 | A | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.184-334A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75566361 | |||||||
chr13:75566423 | A | C | 3 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0002g0130 |
3 | NA18946.hp1 NA19060.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.184-272A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75566423 | |||||||
chr13:75566498 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.184-197A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75566498 | |||||||
chr13:75566632 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.184-63C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | chr13 | 75566632 | |||||||
chr13:75566678 | CT | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
splice_region_variant&intron_variant | LOW | c.184-6delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 75566678 | ||||||
chr13:75566955 | G | A | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.340+104G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 4/8 | chr13 | 75566955 | |||||||
chr13:75567120 | A | G | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.341-107A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 4/8 | chr13 | 75567120 | |||||||
chr13:75567396 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.426+84C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75567396 | |||||||
chr13:75567551 | AT | A | 34 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(31): Show |
37 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.426+253delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 75567551 | ||||||
chr13:75567585 | C | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.426+273C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75567585 | |||||||
chr13:75567586 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.426+274C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75567586 | |||||||
chr13:75567741 | T | G | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.426+429T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75567741 | |||||||
chr13:75567825 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.426+513A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75567825 | |||||||
chr13:75568003 | T | C | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.426+691T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75568003 | |||||||
chr13:75568454 | C | T | 4 | a0001c0001t0002g0006 a0001c0001t0002g0095 a0001c0001t0002g0097 others(1): Show |
5 | NA18612.hp1 NA18940.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1006C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75568454 | |||||||
chr13:75568475 | G | GTA | 4 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0198 others(1): Show |
4 | HG01884.hp1 NA18906.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-974_427-973dup others(2): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 75568475 | ||||||
chr13:75568945 | G | GT | 6 | a0001c0001t0001g0073 a0001c0001t0001g0199 a0001c0001t0001g0277 others(3): Show |
6 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.427-506dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 75568945 | ||||||
chr13:75569436 | T | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.427-24T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75569436 | |||||||
chr13:75569440 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.427-20T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 5/8 | chr13 | 75569440 | |||||||
chr13:75570056 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.474+549T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570056 | |||||||
chr13:75570097 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.474+590A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570097 | |||||||
chr13:75570247 | G | GT | 14 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(11): Show |
14 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.474+748dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75570247 | ||||||
chr13:75570479 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.474+972A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570479 | |||||||
chr13:75570689 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.474+1182G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570689 | |||||||
chr13:75570766 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
140 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.474+1259C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570766 | |||||||
chr13:75570817 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.474+1310T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570817 | |||||||
chr13:75570822 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.474+1315G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570822 | |||||||
chr13:75570917 | A | AAT | 5 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+1423_474+1424d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75570917 | ||||||
chr13:75570917 | A | T | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+1410A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570917 | |||||||
chr13:75570945 | C | T | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+1438C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75570945 | |||||||
chr13:75571281 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0056 others(20): Show |
24 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.474+1774G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75571281 | |||||||
chr13:75571489 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.474+1982G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75571489 | |||||||
chr13:75571535 | A | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0056 others(20): Show |
24 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.474+2028A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75571535 | |||||||
chr13:75571698 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
140 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.474+2191T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75571698 | |||||||
chr13:75571801 | T | C | 1 | a0001c0001t0003g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474+2294T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75571801 | |||||||
chr13:75571974 | C | CCTGTCTG others(16): Show |
1 | a0001c0001t0001g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474+2468_474+2469i others(25): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571974 | ||||||
chr13:75571976 | C | CTGTCT | 15 | a0001c0001t0001g0046 a0001c0001t0001g0078 a0001c0001t0001g0081 others(12): Show |
16 | HG01243.hp2 HG01433.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.474+2516_474+2520d others(7): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75571976 | C | CTGTCTTG others(3): Show |
101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(98): Show |
109 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.474+2511_474+2520d others(12): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75571976 | C | CTGTCTTG others(8): Show |
40 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0041 others(37): Show |
41 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.474+2506_474+2520d others(17): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75571976 | C | CTGTCTTG others(13): Show |
7 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0067 others(4): Show |
7 | HG02886.hp1 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+2501_474+2520d others(22): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75571976 | C | CTGTCTTG others(18): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0064 others(8): Show |
12 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+2496_474+2520d others(27): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75571976 | C | CTGTCTTG others(23): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0070 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.474+2491_474+2520d others(32): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75571976 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474+2469C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75571976 | |||||||
chr13:75571976 | CTGTCTTG others(3): Show |
C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
60 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.474+2511_474+2520d others(12): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75571976 | CTGTCTTG others(8): Show |
C | 17 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0173 others(14): Show |
17 | HG01099.hp1 HG01123.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+2506_474+2520d others(17): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75571976 | CTGTCTTG others(18): Show |
C | 1 | a0001c0001t0001g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.474+2496_474+2520d others(27): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75571976 | ||||||
chr13:75572026 | T | TTGTCTTG others(5): Show |
1 | a0001c0001t0001g0235 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.474+2520_474+2521i others(14): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75572026 | ||||||
chr13:75572028 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.474+2521T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572028 | |||||||
chr13:75572028 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.474+2521T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572028 | |||||||
chr13:75572029 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.474+2522A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572029 | |||||||
chr13:75572031 | T | TTGTCTTG others(17): Show |
1 | a0001c0001t0001g0063 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.474+2525_474+2526i others(26): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75572031 | ||||||
chr13:75572035 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.474+2528C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572035 | |||||||
chr13:75572414 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.474+2907G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572414 | |||||||
chr13:75572596 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.474+3089A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572596 | |||||||
chr13:75572721 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.474+3214A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572721 | |||||||
chr13:75572986 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.474+3479C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572986 | |||||||
chr13:75572987 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474+3480G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75572987 | |||||||
chr13:75573169 | C | T | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+3662C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75573169 | |||||||
chr13:75573266 | GA | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
302 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.474+3777delA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75573266 | ||||||
chr13:75573266 | GAA | G | 6 | a0001c0001t0001g0065 a0001c0001t0001g0079 a0001c0001t0001g0171 others(3): Show |
6 | HG01070.hp1 HG01884.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+3776_474+3777d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75573266 | ||||||
chr13:75573273 | A | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+3766A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75573273 | |||||||
chr13:75573319 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.474+3812G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75573319 | |||||||
chr13:75573590 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA19012.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.474+4083G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75573590 | |||||||
chr13:75573676 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00140.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.474+4169G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75573676 | |||||||
chr13:75573767 | G | T | 45 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(42): Show |
48 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.474+4260G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75573767 | |||||||
chr13:75573798 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.474+4291G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75573798 | |||||||
chr13:75573872 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0266 |
3 | HG02027.hp1 HG02083.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.474+4365C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75573872 | |||||||
chr13:75574044 | C | T | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+4537C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574044 | |||||||
chr13:75574075 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.474+4568A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574075 | |||||||
chr13:75574184 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+4677C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574184 | |||||||
chr13:75574291 | T | A | 24 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(21): Show |
24 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.474+4784T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574291 | |||||||
chr13:75574348 | T | G | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+4841T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574348 | |||||||
chr13:75574634 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.474+5127C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574634 | |||||||
chr13:75574681 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.474+5174G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574681 | |||||||
chr13:75574738 | C | T | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+5231C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574738 | |||||||
chr13:75574753 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.474+5246G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574753 | |||||||
chr13:75574858 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474+5351G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75574858 | |||||||
chr13:75575044 | T | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
140 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.474+5537T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575044 | |||||||
chr13:75575079 | C | A | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.474+5572C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575079 | |||||||
chr13:75575240 | C | T | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0295 |
3 | HG01081.hp2 HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.474+5733C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575240 | |||||||
chr13:75575295 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
140 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.474+5788C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575295 | |||||||
chr13:75575424 | T | C | 1 | a0001c0001t0002g0097 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.474+5917T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575424 | |||||||
chr13:75575526 | T | A | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.474+6019T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575526 | |||||||
chr13:75575820 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.474+6313C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575820 | |||||||
chr13:75575854 | C | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.474+6347C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575854 | |||||||
chr13:75575855 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.474+6348G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575855 | |||||||
chr13:75575940 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.474+6433C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75575940 | |||||||
chr13:75576038 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.474+6531C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576038 | |||||||
chr13:75576115 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.474+6608A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576115 | |||||||
chr13:75576260 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.474+6753C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576260 | |||||||
chr13:75576269 | T | G | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.474+6762T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576269 | |||||||
chr13:75576405 | A | G | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.474+6898A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576405 | |||||||
chr13:75576501 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.474+6994C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576501 | |||||||
chr13:75576530 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.474+7023G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576530 | |||||||
chr13:75576644 | G | A | 4 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0106 others(1): Show |
4 | HG01168.hp2 HG01496.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+7137G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576644 | |||||||
chr13:75576674 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.474+7167G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576674 | |||||||
chr13:75576686 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.474+7179T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576686 | |||||||
chr13:75576795 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
168 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.474+7288T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576795 | |||||||
chr13:75576802 | C | T | 38 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0233 others(35): Show |
41 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.474+7295C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576802 | |||||||
chr13:75576828 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.474+7321G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75576828 | |||||||
chr13:75577245 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.474+7738C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577245 | |||||||
chr13:75577377 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.474+7870A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577377 | |||||||
chr13:75577379 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.474+7872T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577379 | |||||||
chr13:75577401 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
219 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(216): Show |
intron_variant | MODIFIER | c.474+7894G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577401 | |||||||
chr13:75577401 | GA | G | 11 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0177 others(8): Show |
11 | HG01099.hp1 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+7895delA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577401 | |||||||
chr13:75577498 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | NA18957.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.474+7991C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577498 | |||||||
chr13:75577764 | T | C | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0135 |
3 | HG00741.hp2 HG02004.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.474+8257T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577764 | |||||||
chr13:75577771 | C | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
142 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.474+8264C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577771 | |||||||
chr13:75577850 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.474+8343A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577850 | |||||||
chr13:75577890 | CCA | C | 21 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0214 others(18): Show |
21 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+8384_474+8385d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577890 | |||||||
chr13:75577895 | C | T | 21 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0214 others(18): Show |
21 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+8388C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577895 | |||||||
chr13:75577896 | CAGA | C | 21 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0214 others(18): Show |
21 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+8390_474+8392d others(5): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577896 | |||||||
chr13:75577983 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.474+8476A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75577983 | |||||||
chr13:75578014 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+8507T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578014 | |||||||
chr13:75578035 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.474+8528C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578035 | |||||||
chr13:75578104 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.474+8597C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578104 | |||||||
chr13:75578129 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0223 others(2): Show |
7 | HG00408.hp2 HG01928.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+8622C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578129 | |||||||
chr13:75578239 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.474+8732C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578239 | |||||||
chr13:75578243 | AATTT | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
119 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.474+8741_474+8744d others(6): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75578243 | ||||||
chr13:75578465 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.474+8958C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578465 | |||||||
chr13:75578740 | A | C | 1 | a0001c0001t0001g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.474+9233A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578740 | |||||||
chr13:75578795 | G | C | 1 | a0001c0001t0003g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.474+9288G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578795 | |||||||
chr13:75578918 | G | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
140 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.474+9411G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578918 | |||||||
chr13:75578966 | A | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
119 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.474+9459A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75578966 | |||||||
chr13:75579107 | G | A | 11 | a0001c0001t0001g0213 a0001c0001t0001g0221 a0001c0001t0001g0235 others(8): Show |
11 | HG02074.hp1 NA18940.hp2 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.474+9600G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579107 | |||||||
chr13:75579209 | C | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.474+9702C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579209 | |||||||
chr13:75579268 | C | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0057 others(17): Show |
21 | HG01109.hp2 HG01891.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+9761C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579268 | |||||||
chr13:75579279 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
119 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.474+9772C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579279 | |||||||
chr13:75579539 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0299 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.474+10032G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579539 | |||||||
chr13:75579612 | A | G | 33 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0233 others(30): Show |
35 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.474+10105A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579612 | |||||||
chr13:75579665 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.474+10158T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579665 | |||||||
chr13:75579919 | G | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.474+10412G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579919 | |||||||
chr13:75579950 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474+10443A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579950 | |||||||
chr13:75579962 | G | C | 7 | a0001c0001t0002g0007 a0001c0001t0002g0111 a0001c0001t0002g0112 others(4): Show |
8 | HG00741.hp2 HG02004.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+10455G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75579962 | |||||||
chr13:75580065 | A | C | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+10558A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580065 | |||||||
chr13:75580214 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
129 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.474+10707C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580214 | |||||||
chr13:75580339 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.474+10832C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580339 | |||||||
chr13:75580507 | T | C | 12 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.474+11000T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580507 | |||||||
chr13:75580513 | T | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.474+11006T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580513 | |||||||
chr13:75580560 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474+11053C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580560 | |||||||
chr13:75580560 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.474+11053C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580560 | |||||||
chr13:75580707 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.474+11200G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580707 | |||||||
chr13:75580742 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG01109.hp2 HG02145.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+11235C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75580742 | |||||||
chr13:75581031 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474+11524G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581031 | |||||||
chr13:75581154 | TA | T | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+11648delA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581154 | |||||||
chr13:75581156 | T | G | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+11649T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581156 | |||||||
chr13:75581157 | C | A | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+11650C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581157 | |||||||
chr13:75581347 | CT | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
166 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.474+11856delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75581347 | ||||||
chr13:75581401 | G | A | 24 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(21): Show |
24 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.474+11894G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581401 | |||||||
chr13:75581412 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+11905C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581412 | |||||||
chr13:75581425 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474+11918C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581425 | |||||||
chr13:75581428 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
217 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.474+11921T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581428 | |||||||
chr13:75581516 | A | AT | 6 | a0001c0001t0001g0170 a0001c0001t0001g0214 a0001c0001t0003g0017 others(3): Show |
6 | HG02055.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+12031dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75581516 | ||||||
chr13:75581516 | AT | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
180 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.474+12031delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75581516 | ||||||
chr13:75581516 | ATT | A | 19 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(16): Show |
19 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.474+12030_474+1203 others(6): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75581516 | ||||||
chr13:75581694 | A | ATTTTTTT others(835): Show |
7 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(4): Show |
7 | HG02647.hp2 HG02723.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+12203_474+1220 others(846): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75581694 | ||||||
chr13:75581694 | A | ATTTTTTT others(835): Show |
1 | a0001c0001t0001g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.474+12203_474+1220 others(846): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75581694 | ||||||
chr13:75581694 | AT | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
134 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.474+12203delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75581694 | ||||||
chr13:75581805 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.474+12298G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75581805 | |||||||
chr13:75582000 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
119 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.474+12493G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75582000 | |||||||
chr13:75582191 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.474+12684G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75582191 | |||||||
chr13:75582191 | G | T | 12 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
12 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+12684G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75582191 | |||||||
chr13:75582356 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.475-12559T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75582356 | |||||||
chr13:75582523 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.475-12392G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75582523 | |||||||
chr13:75582957 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-11958G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75582957 | |||||||
chr13:75582965 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.475-11950A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75582965 | |||||||
chr13:75582990 | A | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-11925A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75582990 | |||||||
chr13:75583091 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-11824G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583091 | |||||||
chr13:75583203 | C | A | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-11712C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583203 | |||||||
chr13:75583230 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.475-11685T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583230 | |||||||
chr13:75583233 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.475-11682C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583233 | |||||||
chr13:75583253 | C | A | 1 | a0001c0001t0003g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.475-11662C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583253 | |||||||
chr13:75583381 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0193 others(1): Show |
4 | HG02132.hp2 HG02523.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-11534A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583381 | |||||||
chr13:75583672 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.475-11243G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583672 | |||||||
chr13:75583780 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.475-11135T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583780 | |||||||
chr13:75583806 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.475-11109T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583806 | |||||||
chr13:75583919 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-10996A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583919 | |||||||
chr13:75583945 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.475-10970C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75583945 | |||||||
chr13:75584029 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.475-10886G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75584029 | |||||||
chr13:75584546 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.475-10369C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75584546 | |||||||
chr13:75584563 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.475-10352A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75584563 | |||||||
chr13:75584643 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.475-10272A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75584643 | |||||||
chr13:75584689 | A | T | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.475-10226A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75584689 | |||||||
chr13:75584968 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.475-9947A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75584968 | |||||||
chr13:75585061 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.475-9854G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75585061 | |||||||
chr13:75585153 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.475-9762A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75585153 | |||||||
chr13:75585297 | G | T | 10 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(7): Show |
10 | HG00735.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-9618G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75585297 | |||||||
chr13:75585338 | A | C | 2 | a0001c0001t0001g0214 a0001c0001t0003g0017 |
2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.475-9577A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75585338 | |||||||
chr13:75585788 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0170 |
2 | NA19078.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.475-9127C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75585788 | |||||||
chr13:75585853 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(125): Show |
139 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.475-9062A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75585853 | |||||||
chr13:75585945 | A | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0069 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.475-8970A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75585945 | |||||||
chr13:75585974 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.475-8941G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75585974 | |||||||
chr13:75586030 | C | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-8885C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586030 | |||||||
chr13:75586264 | T | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.475-8651T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586264 | |||||||
chr13:75586381 | A | G | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.475-8534A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586381 | |||||||
chr13:75586458 | A | ACAAAT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.475-8457_475-8456i others(7): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586458 | |||||||
chr13:75586562 | T | C | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-8353T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586562 | |||||||
chr13:75586648 | T | A | 5 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0024 others(2): Show |
5 | HG01496.hp1 HG02895.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.475-8267T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586648 | |||||||
chr13:75586666 | C | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-8249C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586666 | |||||||
chr13:75586755 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.475-8160A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586755 | |||||||
chr13:75586758 | G | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0057 others(19): Show |
23 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.475-8157G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586758 | |||||||
chr13:75586798 | A | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-8117A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586798 | |||||||
chr13:75586880 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.475-8035G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586880 | |||||||
chr13:75586910 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.475-8005A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586910 | |||||||
chr13:75586944 | A | G | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-7971A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75586944 | |||||||
chr13:75587000 | T | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0106 |
3 | HG01168.hp2 HG01496.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.475-7915T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587000 | |||||||
chr13:75587017 | C | CA | 44 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(41): Show |
45 | HG00735.hp1 HG01081.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.475-7880dupA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75587017 | ||||||
chr13:75587017 | C | CAA | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
119 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.475-7881_475-7880d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75587017 | ||||||
chr13:75587036 | G | T | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.475-7879G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587036 | |||||||
chr13:75587047 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.475-7868A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587047 | |||||||
chr13:75587064 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.475-7851G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587064 | |||||||
chr13:75587324 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.475-7591T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587324 | |||||||
chr13:75587325 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.475-7590G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587325 | |||||||
chr13:75587330 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.475-7585A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587330 | |||||||
chr13:75587331 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.475-7584T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587331 | |||||||
chr13:75587332 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.475-7583A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587332 | |||||||
chr13:75587333 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.475-7582A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587333 | |||||||
chr13:75587334 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.475-7581A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587334 | |||||||
chr13:75587342 | T | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0063 others(10): Show |
14 | HG01109.hp2 HG01891.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-7573T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587342 | |||||||
chr13:75587360 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0215 a0001c0001t0001g0222 others(5): Show |
11 | HG00621.hp2 HG02071.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.475-7555C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587360 | |||||||
chr13:75587511 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.475-7404T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587511 | |||||||
chr13:75587628 | G | T | 1 | a0001c0001t0001g0228 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.475-7287G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587628 | |||||||
chr13:75587638 | A | G | 38 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(35): Show |
41 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.475-7277A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587638 | |||||||
chr13:75587828 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.475-7087A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587828 | |||||||
chr13:75587858 | T | C | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-7057T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587858 | |||||||
chr13:75587890 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.475-7025C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587890 | |||||||
chr13:75587903 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
214 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.475-7012A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75587903 | |||||||
chr13:75588025 | AT | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0172 a0001c0001t0002g0116 others(4): Show |
7 | HG01978.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-6879delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75588025 | ||||||
chr13:75588297 | A | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
150 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.475-6618A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75588297 | |||||||
chr13:75588335 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.475-6580A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75588335 | |||||||
chr13:75588363 | C | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0055 others(19): Show |
23 | HG01109.hp2 HG01891.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.475-6552C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75588363 | |||||||
chr13:75588666 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.475-6249G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75588666 | |||||||
chr13:75588684 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.475-6231G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75588684 | |||||||
chr13:75588744 | A | G | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-6171A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75588744 | |||||||
chr13:75588809 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.475-6106T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75588809 | |||||||
chr13:75589170 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-5745T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75589170 | |||||||
chr13:75589374 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-5541G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75589374 | |||||||
chr13:75589434 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-5481C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75589434 | |||||||
chr13:75589538 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.475-5377C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75589538 | |||||||
chr13:75589660 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
214 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.475-5255A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75589660 | |||||||
chr13:75589825 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.475-5090A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75589825 | |||||||
chr13:75589937 | GTCC | G | 48 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(45): Show |
51 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.475-4972_475-4970d others(5): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75589937 | ||||||
chr13:75589943 | C | G | 7 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-4972C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75589943 | |||||||
chr13:75590177 | C | CT | 33 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(30): Show |
34 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.475-4722dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75590177 | ||||||
chr13:75590385 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-4530C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75590385 | |||||||
chr13:75590521 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02027.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.475-4394A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75590521 | |||||||
chr13:75590690 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.475-4225T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75590690 | |||||||
chr13:75590709 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
202 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.475-4206T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75590709 | |||||||
chr13:75590802 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
213 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.475-4113C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75590802 | |||||||
chr13:75590873 | T | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-4042T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75590873 | |||||||
chr13:75590978 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.475-3937G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75590978 | |||||||
chr13:75591079 | C | G | 9 | a0001c0001t0001g0217 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG00438.hp2 HG02155.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-3836C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591079 | |||||||
chr13:75591112 | G | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-3803G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591112 | |||||||
chr13:75591146 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
213 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.475-3769T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591146 | |||||||
chr13:75591186 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-3729G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591186 | |||||||
chr13:75591285 | A | G | 49 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(46): Show |
52 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.475-3630A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591285 | |||||||
chr13:75591431 | C | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0055 others(18): Show |
22 | HG01109.hp2 HG01891.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.475-3484C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591431 | |||||||
chr13:75591466 | G | A | 21 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0214 others(18): Show |
21 | HG00735.hp2 HG01496.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-3449G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591466 | |||||||
chr13:75591510 | T | C | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.475-3405T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591510 | |||||||
chr13:75591523 | A | C | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.475-3392A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591523 | |||||||
chr13:75591888 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.475-3027T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591888 | |||||||
chr13:75591943 | T | G | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-2972T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591943 | |||||||
chr13:75591989 | T | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2926T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591989 | |||||||
chr13:75591994 | A | T | 1 | a0001c0001t0002g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.475-2921A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75591994 | |||||||
chr13:75592084 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.475-2831G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592084 | |||||||
chr13:75592172 | T | A | 2 | a0001c0001t0001g0214 a0001c0001t0003g0017 |
2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.475-2743T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592172 | |||||||
chr13:75592266 | G | T | 35 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(32): Show |
38 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.475-2649G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592266 | |||||||
chr13:75592330 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.475-2585C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592330 | |||||||
chr13:75592368 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.475-2547A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592368 | |||||||
chr13:75592386 | G | C | 49 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(46): Show |
52 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.475-2529G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592386 | |||||||
chr13:75592414 | T | TCATATAT others(9): Show |
1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.475-2500_475-2485d others(18): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592414 | ||||||
chr13:75592415 | C | CAT | 7 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0140 others(4): Show |
7 | HG02280.hp1 HG03017.hp2 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-2449_475-2448d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.475-2461_475-2448d others(16): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | C | CATATATA others(51): Show |
1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.475-2486_475-2485i others(60): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CAT | C | 16 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0133 others(13): Show |
16 | HG01257.hp1 HG01891.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.475-2449_475-2448d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CATAT | C | 17 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0120 others(14): Show |
17 | HG00438.hp1 HG00544.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.475-2451_475-2448d others(6): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CATATAT | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0086 others(20): Show |
25 | HG01099.hp1 HG01884.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.475-2453_475-2448d others(8): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CATATATA others(1): Show |
C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0080 others(18): Show |
23 | HG00408.hp1 HG01070.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.475-2455_475-2448d others(10): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CATATATA others(3): Show |
C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0175 a0001c0001t0001g0183 others(3): Show |
6 | HG00558.hp1 HG02273.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-2457_475-2448d others(12): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.475-2459_475-2448d others(14): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0009 a0001c0001t0005g0204 |
3 | HG00735.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.475-2461_475-2448d others(16): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CATATATA others(17): Show |
C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.475-2471_475-2448d others(26): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592415 | CATATATA others(33): Show |
C | 1 | a0001c0001t0001g0239 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.475-2487_475-2448d others(42): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592415 | ||||||
chr13:75592417 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.475-2486_475-2485i others(22): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592417 | ||||||
chr13:75592417 | T | TATATATA others(19): Show |
1 | a0001c0001t0004g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.475-2488_475-2487i others(28): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592417 | ||||||
chr13:75592419 | T | TATATATA others(11): Show |
1 | a0001c0001t0001g0072 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.475-2486_475-2485i others(20): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592419 | ||||||
chr13:75592419 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0048 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.475-2486_475-2485i others(28): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592419 | ||||||
chr13:75592421 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.475-2486_475-2485i others(18): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592421 | ||||||
chr13:75592421 | T | TATATATA others(17): Show |
4 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0123 others(1): Show |
4 | HG02886.hp1 HG03453.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-2486_475-2485i others(26): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592421 | ||||||
chr13:75592421 | T | TATATATA others(49): Show |
1 | a0001c0001t0002g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.475-2486_475-2485i others(58): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592421 | ||||||
chr13:75592421 | T | TATATATG others(15): Show |
1 | a0001c0001t0004g0052 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.475-2488_475-2487i others(24): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592421 | ||||||
chr13:75592423 | T | TATATATG others(7): Show |
9 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0071 others(6): Show |
10 | HG01952.hp2 HG03669.hp1 HG06807.hp2 others(7): Show |
intron_variant | MODIFIER | c.475-2486_475-2485i others(16): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592423 | ||||||
chr13:75592423 | T | TATATATG others(15): Show |
12 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0055 others(9): Show |
12 | HG02723.hp2 HG03041.hp1 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.475-2486_475-2485i others(24): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592423 | ||||||
chr13:75592423 | T | TATATATG others(45): Show |
4 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG01099.hp2 HG01257.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-2486_475-2485i others(54): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592423 | ||||||
chr13:75592423 | T | TATATATG others(81): Show |
1 | a0001c0001t0001g0037 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.475-2486_475-2485i others(90): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592423 | ||||||
chr13:75592423 | T | TATATGTA others(13): Show |
2 | a0001c0001t0004g0036 a0001c0001t0004g0053 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.475-2488_475-2487i others(22): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592423 | ||||||
chr13:75592424 | A | ATATATGT others(41): Show |
1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.475-2486_475-2485i others(50): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592424 | ||||||
chr13:75592425 | T | TATATGTA others(5): Show |
9 | a0001c0001t0001g0050 a0001c0001t0002g0100 a0001c0001t0002g0102 others(6): Show |
9 | HG00733.hp1 HG00738.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-2486_475-2485i others(14): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592425 | ||||||
chr13:75592425 | T | TATATGTA others(13): Show |
7 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0064 others(4): Show |
8 | HG01978.hp2 HG02735.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-2486_475-2485i others(22): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592425 | ||||||
chr13:75592425 | T | TATATGTA others(51): Show |
1 | a0001c0001t0001g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.475-2486_475-2485i others(60): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592425 | ||||||
chr13:75592427 | T | TATGTATA others(3): Show |
9 | a0001c0001t0001g0059 a0001c0001t0002g0007 a0001c0001t0002g0101 others(6): Show |
10 | HG00741.hp2 HG01516.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-2486_475-2485i others(12): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592427 | ||||||
chr13:75592427 | T | TATGTATA others(11): Show |
6 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0062 others(3): Show |
6 | HG00140.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-2486_475-2485i others(20): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592427 | ||||||
chr13:75592427 | T | TATGTATA others(49): Show |
1 | a0001c0001t0001g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.475-2486_475-2485i others(58): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592427 | ||||||
chr13:75592428 | A | ATGTATAT others(44): Show |
1 | a0001c0001t0002g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-2486_475-2485i others(53): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592428 | ||||||
chr13:75592429 | T | TGTATATA others(9): Show |
2 | a0001c0001t0001g0004 a0001c0001t0002g0096 |
3 | HG02976.hp2 HG03139.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.475-2486_475-2485i others(18): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592429 | |||||||
chr13:75592429 | T | TGTATATA others(41): Show |
1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.475-2486_475-2485i others(50): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592429 | |||||||
chr13:75592429 | T | TGTATATA others(47): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0045 |
2 | HG02293.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.475-2486_475-2485i others(56): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592429 | |||||||
chr13:75592429 | T | TGTATATA others(83): Show |
1 | a0001c0001t0001g0039 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.475-2486_475-2485i others(92): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592429 | |||||||
chr13:75592431 | T | C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0042 others(11): Show |
15 | HG01099.hp2 HG01106.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.475-2484T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592431 | |||||||
chr13:75592433 | T | C | 9 | a0001c0001t0001g0050 a0001c0001t0002g0100 a0001c0001t0002g0102 others(6): Show |
9 | HG00733.hp1 HG00738.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-2482T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592433 | |||||||
chr13:75592435 | T | C | 9 | a0001c0001t0001g0059 a0001c0001t0002g0007 a0001c0001t0002g0101 others(6): Show |
10 | HG00741.hp2 HG01516.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-2480T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592435 | |||||||
chr13:75592436 | A | ATATATAC others(23): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-2473_475-2472i others(32): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592436 | ||||||
chr13:75592436 | A | ATATATAC others(23): Show |
4 | a0001c0001t0001g0244 a0001c0001t0001g0252 a0001c0001t0001g0268 others(1): Show |
4 | HG03942.hp1 HG04204.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-2473_475-2472i others(32): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592436 | ||||||
chr13:75592437 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0078 |
2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.475-2478T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592437 | |||||||
chr13:75592438 | A | ATATACAT others(49): Show |
1 | a0001c0001t0001g0254 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.475-2473_475-2472i others(58): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592438 | ||||||
chr13:75592438 | A | ATATACAT others(21): Show |
64 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(61): Show |
70 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.475-2473_475-2472i others(30): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592438 | ||||||
chr13:75592438 | A | ATATACAT others(19): Show |
2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.475-2473_475-2472i others(28): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592438 | ||||||
chr13:75592438 | A | ATATACAT others(13): Show |
1 | a0001c0001t0001g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.475-2473_475-2472i others(22): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592438 | ||||||
chr13:75592438 | A | ATATATAC others(23): Show |
9 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0219 others(6): Show |
9 | HG00738.hp1 HG01255.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-2471_475-2470i others(32): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592438 | ||||||
chr13:75592438 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.475-2477A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592438 | |||||||
chr13:75592440 | A | ATATATAC others(23): Show |
1 | a0001c0001t0001g0279 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.475-2469_475-2468i others(32): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592440 | ||||||
chr13:75592443 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-2472T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592443 | |||||||
chr13:75592444 | A | ACACATAT others(25): Show |
1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.475-2471_475-2470i others(34): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592444 | |||||||
chr13:75592444 | A | ACATATAT others(25): Show |
3 | a0001c0001t0001g0243 a0001c0001t0001g0253 a0001c0001t0001g0299 |
3 | HG03491.hp1 HG03492.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.475-2471_475-2470i others(34): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592444 | |||||||
chr13:75592444 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(5): Show |
9 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-2471A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592444 | |||||||
chr13:75592445 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.475-2470T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592445 | |||||||
chr13:75592446 | A | ACATATAT others(25): Show |
2 | a0001c0001t0001g0289 a0001c0001t0001g0304 |
2 | HG00741.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.475-2469_475-2468i others(34): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592446 | |||||||
chr13:75592446 | A | ACATATAT others(23): Show |
3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG00733.hp2 HG02004.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.475-2469_475-2468i others(32): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592446 | |||||||
chr13:75592446 | A | ATACATAT others(27): Show |
7 | a0001c0001t0001g0003 a0001c0001t0001g0216 a0001c0001t0001g0247 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-2467_475-2466i others(36): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592446 | ||||||
chr13:75592446 | A | ATATACAT others(29): Show |
7 | a0001c0001t0001g0014 a0001c0001t0001g0206 a0001c0001t0001g0234 others(4): Show |
8 | HG01109.hp1 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-2465_475-2464i others(38): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592446 | ||||||
chr13:75592446 | A | ATATATAC others(31): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0273 |
3 | HG01070.hp2 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.475-2463_475-2462i others(40): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592446 | ||||||
chr13:75592446 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(74): Show |
83 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.475-2469A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592446 | |||||||
chr13:75592448 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0279 |
2 | HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.475-2467A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592448 | |||||||
chr13:75592452 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0079 |
3 | HG01099.hp2 HG01257.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.475-2463A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592452 | |||||||
chr13:75592453 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.475-2462T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592453 | |||||||
chr13:75592455 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.475-2460T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592455 | |||||||
chr13:75592494 | C | CT | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0136 others(11): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.475-2407dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592494 | ||||||
chr13:75592494 | CT | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
135 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.475-2407delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75592494 | ||||||
chr13:75592505 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.475-2410T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592505 | |||||||
chr13:75592666 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
222 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.475-2249G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592666 | |||||||
chr13:75592806 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.475-2109C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75592806 | |||||||
chr13:75593005 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.475-1910G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593005 | |||||||
chr13:75593158 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.475-1757C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593158 | |||||||
chr13:75593297 | T | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.475-1618T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593297 | |||||||
chr13:75593401 | C | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
210 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(207): Show |
intron_variant | MODIFIER | c.475-1514C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593401 | |||||||
chr13:75593401 | C | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02004.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.475-1514C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593401 | |||||||
chr13:75593732 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00140.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.475-1183C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593732 | |||||||
chr13:75593768 | A | G | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-1147A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593768 | |||||||
chr13:75593876 | A | T | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.475-1039A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593876 | |||||||
chr13:75593949 | C | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-966C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75593949 | |||||||
chr13:75594142 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.475-773A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594142 | |||||||
chr13:75594230 | ATTGT | A | 37 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(34): Show |
40 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.475-679_475-676del others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 75594230 | ||||||
chr13:75594409 | A | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0170 |
2 | NA19078.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.475-506A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594409 | |||||||
chr13:75594410 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-505C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594410 | |||||||
chr13:75594417 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.475-498C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594417 | |||||||
chr13:75594555 | C | T | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.475-360C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594555 | |||||||
chr13:75594573 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0055 others(22): Show |
26 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.475-342T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594573 | |||||||
chr13:75594590 | G | GA | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
150 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.475-325_475-324ins others(1): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594590 | |||||||
chr13:75594591 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
150 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.475-324T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594591 | |||||||
chr13:75594613 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.475-302T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594613 | |||||||
chr13:75594623 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.475-292G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594623 | |||||||
chr13:75594724 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.475-191G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 6/8 | chr13 | 75594724 | |||||||
chr13:75595083 | T | G | 38 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(35): Show |
41 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.550+93T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595083 | |||||||
chr13:75595098 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.550+108G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595098 | |||||||
chr13:75595121 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.550+131A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595121 | |||||||
chr13:75595211 | C | G | 37 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(34): Show |
40 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.550+221C>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595211 | |||||||
chr13:75595242 | A | G | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.550+252A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595242 | |||||||
chr13:75595384 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+394G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595384 | |||||||
chr13:75595512 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.550+522G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595512 | |||||||
chr13:75595597 | C | CA | 70 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
75 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.550+637dupA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | C | CAA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0055 others(33): Show |
37 | HG01167.hp1 HG01175.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.550+636_550+637dup others(2): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | C | CAAA | 67 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(64): Show |
74 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.550+635_550+637dup others(3): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | C | CAAAA | 37 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0057 others(34): Show |
41 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.550+634_550+637dup others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | C | CAAAAA | 19 | a0001c0001t0001g0119 a0001c0001t0001g0215 a0001c0001t0001g0217 others(16): Show |
19 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.550+633_550+637dup others(5): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0087 |
2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.550+628_550+637dup others(10): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0124 |
3 | HG02723.hp1 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.550+627_550+637dup others(11): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0123 |
3 | HG02647.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.550+626_550+637dup others(12): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | CA | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
9 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.550+637delA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | CAAAAAAA others(3): Show |
C | 22 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0100 others(19): Show |
24 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.550+628_550+637del others(10): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | CAAAAAAA others(4): Show |
C | 13 | a0001c0001t0002g0006 a0001c0001t0002g0090 a0001c0001t0002g0095 others(10): Show |
14 | HG03453.hp2 HG04204.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.550+627_550+637del others(11): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595597 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG03490.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.550+621_550+637del others(17): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595597 | ||||||
chr13:75595632 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0079 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.550+642G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595632 | |||||||
chr13:75595641 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.550+651G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595641 | |||||||
chr13:75595649 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.550+659T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595649 | |||||||
chr13:75595787 | CT | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
214 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.550+810delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75595787 | ||||||
chr13:75595842 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02027.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.550+852A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595842 | |||||||
chr13:75595957 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.550+967A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595957 | |||||||
chr13:75595980 | AGAG | A | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.550+991_550+993del others(3): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75595980 | |||||||
chr13:75596031 | C | T | 37 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(34): Show |
40 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.550+1041C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596031 | |||||||
chr13:75596048 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1058T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596048 | |||||||
chr13:75596132 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.550+1142A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596132 | |||||||
chr13:75596174 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.550+1184A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596174 | |||||||
chr13:75596264 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0055 others(21): Show |
25 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.550+1274G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596264 | |||||||
chr13:75596332 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
150 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.550+1342A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596332 | |||||||
chr13:75596346 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.550+1356C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596346 | |||||||
chr13:75596377 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
150 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.550+1387A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596377 | |||||||
chr13:75596409 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.550+1419A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596409 | |||||||
chr13:75596450 | G | A | 2 | a0001c0001t0003g0022 a0001c0001t0003g0031 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.550+1460G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596450 | |||||||
chr13:75596558 | G | T | 8 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(5): Show |
8 | HG00733.hp2 HG00738.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.550+1568G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596558 | |||||||
chr13:75596576 | A | G | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+1586A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596576 | |||||||
chr13:75596734 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.550+1744G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596734 | |||||||
chr13:75596750 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.550+1760G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596750 | |||||||
chr13:75596814 | A | G | 4 | a0001c0001t0004g0036 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+1824A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75596814 | |||||||
chr13:75597086 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.550+2096A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75597086 | |||||||
chr13:75597195 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.550+2205A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75597195 | |||||||
chr13:75597222 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.550+2232G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75597222 | |||||||
chr13:75597361 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(110): Show |
124 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.550+2371C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75597361 | |||||||
chr13:75597371 | TAAAA | T | 48 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(45): Show |
51 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.550+2388_550+2391d others(6): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75597371 | ||||||
chr13:75597784 | A | T | 1 | a0001c0001t0001g0262 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.550+2794A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75597784 | |||||||
chr13:75597863 | T | G | 38 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(35): Show |
41 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.550+2873T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75597863 | |||||||
chr13:75597925 | T | G | 1 | a0001c0001t0002g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.550+2935T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75597925 | |||||||
chr13:75598278 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.550+3288C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598278 | |||||||
chr13:75598298 | G | C | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.550+3308G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598298 | |||||||
chr13:75598298 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
209 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.550+3308G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598298 | |||||||
chr13:75598337 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.550+3347T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598337 | |||||||
chr13:75598407 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.550+3417C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598407 | |||||||
chr13:75598498 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
321 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.550+3508T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598498 | |||||||
chr13:75598593 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.550+3603C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598593 | |||||||
chr13:75598608 | T | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.550+3618T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598608 | |||||||
chr13:75598873 | A | T | 2 | a0001c0001t0002g0110 a0001c0001t0002g0139 |
2 | HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.550+3883A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75598873 | |||||||
chr13:75599134 | A | AT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(104): Show |
115 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.550+4162dupT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75599134 | ||||||
chr13:75599134 | AT | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(182): Show |
194 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.550+4162delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75599134 | ||||||
chr13:75599152 | T | TG | 5 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0251 others(2): Show |
8 | HG01109.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.550+4163dupG | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75599152 | ||||||
chr13:75599272 | A | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.550+4282A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75599272 | |||||||
chr13:75599314 | A | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.550+4324A>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75599314 | |||||||
chr13:75599316 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.550+4326A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75599316 | |||||||
chr13:75599525 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.550+4535G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75599525 | |||||||
chr13:75599583 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
99 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.550+4593G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75599583 | |||||||
chr13:75599611 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
222 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.550+4621G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75599611 | |||||||
chr13:75599797 | G | C | 1 | a0001c0001t0001g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.550+4807G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75599797 | |||||||
chr13:75599916 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.551-4853A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75599916 | |||||||
chr13:75600015 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.551-4754G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600015 | |||||||
chr13:75600123 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.551-4646G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600123 | |||||||
chr13:75600340 | T | G | 10 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(7): Show |
10 | HG00735.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.551-4429T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600340 | |||||||
chr13:75600441 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.551-4328C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600441 | |||||||
chr13:75600525 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.551-4244T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600525 | |||||||
chr13:75600570 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0267 |
2 | NA19010.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.551-4199A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600570 | |||||||
chr13:75600687 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0215 a0001c0001t0001g0217 others(21): Show |
27 | HG00438.hp2 HG00621.hp2 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.551-4082C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600687 | |||||||
chr13:75600870 | C | T | 48 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(45): Show |
51 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.551-3899C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600870 | |||||||
chr13:75600938 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
222 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.551-3831G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600938 | |||||||
chr13:75600977 | A | G | 1 | a0001c0001t0003g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.551-3792A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75600977 | |||||||
chr13:75601096 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.551-3673G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601096 | |||||||
chr13:75601192 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.551-3577G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601192 | |||||||
chr13:75601252 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.551-3517T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601252 | |||||||
chr13:75601390 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.551-3379C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601390 | |||||||
chr13:75601397 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.551-3372A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601397 | |||||||
chr13:75601446 | G | A | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.551-3323G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601446 | |||||||
chr13:75601493 | A | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-3276A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601493 | |||||||
chr13:75601496 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.551-3273A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601496 | |||||||
chr13:75601634 | A | G | 11 | a0001c0001t0001g0217 a0001c0001t0001g0227 a0001c0001t0001g0228 others(8): Show |
11 | HG00438.hp2 HG02155.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.551-3135A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601634 | |||||||
chr13:75601729 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
160 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.551-3040G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601729 | |||||||
chr13:75601762 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.551-3007A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601762 | |||||||
chr13:75601809 | A | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(110): Show |
124 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.551-2960A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601809 | |||||||
chr13:75601867 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.551-2902T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601867 | |||||||
chr13:75601970 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.551-2799G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75601970 | |||||||
chr13:75602065 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.551-2704T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75602065 | |||||||
chr13:75602099 | ACT | A | 11 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0177 others(8): Show |
11 | HG01099.hp1 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.551-2667_551-2666d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75602099 | ||||||
chr13:75602108 | C | CA | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
122 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.551-2653dupA | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75602108 | ||||||
chr13:75602108 | C | CAA | 25 | a0001c0001t0001g0001 a0001c0001t0001g0073 a0001c0001t0001g0215 others(22): Show |
28 | HG00438.hp2 HG00621.hp2 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.551-2654_551-2653d others(4): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75602108 | ||||||
chr13:75602222 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.551-2547A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75602222 | |||||||
chr13:75602544 | A | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
222 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.551-2225A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75602544 | |||||||
chr13:75602763 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
150 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.551-2006A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75602763 | |||||||
chr13:75602829 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0298 |
2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.551-1940A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75602829 | |||||||
chr13:75602944 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.551-1825A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75602944 | |||||||
chr13:75602999 | AT | A | 10 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(7): Show |
10 | HG00735.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.551-1763delT | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75602999 | ||||||
chr13:75603043 | G | A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG00558.hp1 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.551-1726G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603043 | |||||||
chr13:75603196 | C | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.551-1573C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603196 | |||||||
chr13:75603263 | CAGCCATA others(12): Show |
C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.551-1502_551-1484d others(21): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75603263 | ||||||
chr13:75603297 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.551-1472A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603297 | |||||||
chr13:75603305 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.551-1464C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603305 | |||||||
chr13:75603350 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-1419C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603350 | |||||||
chr13:75603420 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.551-1349A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603420 | |||||||
chr13:75603518 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.551-1251T>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603518 | |||||||
chr13:75603579 | A | G | 38 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(35): Show |
41 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.551-1190A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603579 | |||||||
chr13:75603682 | TAAG | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.551-1082_551-1080d others(5): Show |
UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 75603682 | ||||||
chr13:75603693 | T | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-1076T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603693 | |||||||
chr13:75603822 | C | T | 11 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.551-947C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603822 | |||||||
chr13:75603967 | G | T | 1 | a0001c0001t0002g0113 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.551-802G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603967 | |||||||
chr13:75603999 | A | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0161 |
2 | HG00438.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.551-770A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75603999 | |||||||
chr13:75604174 | G | T | 1 | a0001c0001t0005g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.551-595G>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75604174 | |||||||
chr13:75604304 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.551-465C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75604304 | |||||||
chr13:75604366 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0160 |
3 | HG01516.hp1 HG01517.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.551-403T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75604366 | |||||||
chr13:75604545 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.551-224T>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75604545 | |||||||
chr13:75604715 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.551-54C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 7/8 | chr13 | 75604715 | |||||||
chr13:75604949 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.609+122G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75604949 | |||||||
chr13:75605034 | A | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
222 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.609+207A>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605034 | |||||||
chr13:75605042 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.609+215G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605042 | |||||||
chr13:75605079 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.609+252G>C | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605079 | |||||||
chr13:75605178 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.609+351G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605178 | |||||||
chr13:75605305 | C | T | 11 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.610-424C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605305 | |||||||
chr13:75605419 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0215 a0001c0001t0001g0222 others(6): Show |
12 | HG00621.hp2 HG02071.hp1 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.610-310A>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605419 | |||||||
chr13:75605433 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.610-296G>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605433 | |||||||
chr13:75605503 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.610-226C>A | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605503 | |||||||
chr13:75605583 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.610-146C>T | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605583 | |||||||
chr13:75605675 | T | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.610-54T>G | UCHL3 | ENSG00000118939.19 | transcript | ENST00000377595.8 | protein_coding | 8/8 | chr13 | 75605675 |