Item | Value |
---|---|
geneid | 254048 |
ensemblid | ENSG00000157741.15 |
hgncid | 21931 |
symbol | UBN2 |
name | ubinuclein 2 |
refseq_nuc | NM_173569.4 |
refseq_prot | NP_775840.3 |
ensembl_nuc | ENST00000473989.8 |
ensembl_prot | ENSP00000418648.2 |
mane_status | MANE Select |
chr | chr7 |
start | 139231237 |
end | 139308236 |
strand | + |
ver | v1.2 |
region | chr7:139231237-139308236 |
region5000 | chr7:139226237-139313236 |
regionname0 | UBN2_chr7_139231237_139308236 |
regionname5000 | UBN2_chr7_139226237_139313236 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1347 | 245 | 86 | 38 | 83 | 7 | 31 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0002 | 0/0 | 1347 | 6 | 0 | 1 | 5 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0003 | 0/0 | 1347 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0004 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0005 | 0/0 | 1347 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0006 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0007 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0008 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0009 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
a0010 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | MAEPR others(1342): Show |
chr7 | 139226237 | 139313236 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4041 | 182 | 65 | 25 | 60 | 6 | 26 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0001c0002 | 0/0 | 4041 | 49 | 12 | 9 | 23 | 1 | 4 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0001c0004 | 0/0 | 4041 | 5 | 5 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0001c0005 | 0/0 | 4041 | 3 | 0 | 2 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0001c0007 | 0/0 | 4041 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0001c0011 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0001c0012 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0001c0014 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0001c0015 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0002c0003 | 0/0 | 4041 | 6 | 0 | 1 | 5 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0003c0006 | 0/0 | 4041 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0004c0010 | 0/0 | 4041 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0005c0016 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0006c0018 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0007c0017 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0008c0008 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0009c0009 | 0/0 | 4041 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 | ||
a0010c0013 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | ATGGC others(4036): Show |
chr7 | 139226237 | 139313236 |
acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 14694 | 28 | 4 | 4 | 12 | 2 | 6 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0002 | 0/0 | 14694 | 22 | 1 | 7 | 7 | 0 | 7 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0003 | 0/0 | 14696 | 20 | 0 | 3 | 14 | 2 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0005 | 0/0 | 14693 | 7 | 7 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0006 | 0/0 | 14693 | 7 | 1 | 0 | 3 | 0 | 3 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0009 | 0/0 | 14694 | 5 | 5 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0012 | 0/0 | 14696 | 4 | 1 | 0 | 3 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0013 | 0/0 | 14695 | 4 | 4 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0014 | 0/0 | 14693 | 4 | 4 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0015 | 0/0 | 14695 | 4 | 1 | 0 | 0 | 0 | 3 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0020 | 0/0 | 14694 | 3 | 3 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0021 | 0/0 | 14694 | 3 | 1 | 2 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0024 | 0/0 | 14697 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14692): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0025 | 0/0 | 14708 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14703): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0026 | 0/0 | 14698 | 2 | 0 | 1 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14693): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0027 | 0/0 | 14696 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0028 | 0/0 | 14698 | 2 | 0 | 1 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14693): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0029 | 0/0 | 14694 | 2 | 0 | 0 | 0 | 0 | 2 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0030 | 0/0 | 14694 | 2 | 0 | 2 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0031 | 0/0 | 14694 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0032 | 0/0 | 14694 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0033 | 0/0 | 14692 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14687): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0034 | 0/0 | 14697 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14692): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0035 | 0/0 | 14695 | 2 | 1 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0036 | 0/0 | 14697 | 2 | 0 | 0 | 0 | 0 | 2 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14692): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0037 | 0/0 | 14698 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14693): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0038 | 0/0 | 14697 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14692): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0039 | 0/0 | 14694 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0040 | 0/0 | 14694 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0042 | 0/0 | 14708 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14703): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0043 | 0/0 | 14718 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14713): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0044 | 0/0 | 14696 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0062 | 0/0 | 14696 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0064 | 0/0 | 14700 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14695): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0066 | 0/0 | 14720 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14715): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0068 | 0/0 | 14695 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0069 | 0/0 | 14695 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0070 | 0/0 | 14698 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14693): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0071 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14706): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0072 | 0/0 | 14695 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0075 | 0/0 | 14694 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0076 | 0/0 | 14693 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0077 | 0/0 | 14694 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0078 | 0/0 | 14692 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14687): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0079 | 0/0 | 14694 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0080 | 0/0 | 14694 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0081 | 0/0 | 14694 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0082 | 0/0 | 14696 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0083 | 0/0 | 14696 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0084 | 0/0 | 14697 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14692): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0085 | 0/0 | 14698 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14693): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0086 | 0/0 | 14700 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14695): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0087 | 0/0 | 14694 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0088 | 0/0 | 14692 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14687): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0092 | 0/0 | 14695 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0095 | 0/0 | 14698 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14693): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0096 | 0/0 | 14692 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14687): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0098 | 0/0 | 14696 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0099 | 0/0 | 14700 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14695): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0100 | 0/0 | 14693 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0101 | 0/0 | 14695 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0102 | 0/0 | 14693 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0103 | 0/0 | 14694 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0104 | 0/0 | 14696 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0106 | 0/0 | 14698 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14693): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0107 | 0/0 | 14691 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14686): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0108 | 0/0 | 14694 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0109 | 0/0 | 14696 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0110 | 0/0 | 14695 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14690): Show |
chr7 | 139226237 | 139313236 |
a0001c0001t0111 | 0/0 | 14693 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0004 | 0/0 | 14711 | 7 | 0 | 4 | 2 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14706): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0007 | 0/0 | 14709 | 3 | 0 | 1 | 2 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14704): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0008 | 0/0 | 14721 | 5 | 0 | 0 | 5 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14716): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0011 | 0/0 | 14723 | 4 | 0 | 0 | 4 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14718): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0016 | 0/0 | 14697 | 3 | 1 | 1 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14692): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0017 | 0/0 | 14713 | 2 | 0 | 1 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14708): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0018 | 0/0 | 14715 | 2 | 0 | 0 | 2 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14710): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0019 | 0/0 | 14717 | 2 | 0 | 0 | 2 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14712): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0022 | 0/0 | 14719 | 2 | 0 | 0 | 2 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14714): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0023 | 0/0 | 14719 | 2 | 1 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14714): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0045 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14706): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0046 | 0/0 | 14728 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14723): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0047 | 0/0 | 14705 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14700): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0048 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14705): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0049 | 0/0 | 14712 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14707): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0050 | 0/0 | 14719 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14714): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0051 | 0/0 | 14725 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14720): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0053 | 0/0 | 14712 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14707): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0054 | 0/0 | 14721 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14716): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0055 | 0/0 | 14713 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14708): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0056 | 0/0 | 14714 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14709): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0057 | 0/0 | 14715 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14710): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0058 | 0/0 | 14716 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14711): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0059 | 0/0 | 14717 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14712): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0060 | 0/0 | 14715 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14710): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0061 | 0/0 | 14704 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14699): Show |
chr7 | 139226237 | 139313236 |
a0001c0002t0105 | 0/0 | 14713 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14708): Show |
chr7 | 139226237 | 139313236 |
a0001c0004t0010 | 0/0 | 14691 | 3 | 3 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14686): Show |
chr7 | 139226237 | 139313236 |
a0001c0004t0093 | 0/0 | 14697 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14692): Show |
chr7 | 139226237 | 139313236 |
a0001c0004t0094 | 0/0 | 14696 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0001c0005t0067 | 0/0 | 14694 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0005t0073 | 0/0 | 14692 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14687): Show |
chr7 | 139226237 | 139313236 |
a0001c0005t0074 | 0/0 | 14693 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0001c0007t0010 | 0/0 | 14691 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14686): Show |
chr7 | 139226237 | 139313236 |
a0001c0011t0002 | 0/0 | 14694 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0012t0001 | 0/0 | 14694 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0001c0014t0065 | 0/0 | 14691 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14686): Show |
chr7 | 139226237 | 139313236 |
a0001c0015t0032 | 0/0 | 14694 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0002c0003t0007 | 0/0 | 14709 | 2 | 0 | 0 | 2 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14704): Show |
chr7 | 139226237 | 139313236 |
a0002c0003t0017 | 0/0 | 14713 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14708): Show |
chr7 | 139226237 | 139313236 |
a0002c0003t0018 | 0/0 | 14715 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14710): Show |
chr7 | 139226237 | 139313236 |
a0002c0003t0019 | 0/0 | 14717 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14712): Show |
chr7 | 139226237 | 139313236 |
a0002c0003t0052 | 0/0 | 14712 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14707): Show |
chr7 | 139226237 | 139313236 |
a0003c0006t0089 | 0/0 | 14691 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14686): Show |
chr7 | 139226237 | 139313236 |
a0003c0006t0091 | 0/0 | 14691 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14686): Show |
chr7 | 139226237 | 139313236 |
a0004c0010t0001 | 0/0 | 14694 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
a0005c0016t0041 | 0/0 | 14708 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14703): Show |
chr7 | 139226237 | 139313236 |
a0006c0018t0004 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14706): Show |
chr7 | 139226237 | 139313236 |
a0007c0017t0090 | 0/0 | 14690 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14685): Show |
chr7 | 139226237 | 139313236 |
a0008c0008t0063 | 0/0 | 14693 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14688): Show |
chr7 | 139226237 | 139313236 |
a0009c0009t0003 | 0/0 | 14696 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14691): Show |
chr7 | 139226237 | 139313236 |
a0010c0013t0001 | 0/0 | 14694 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | CTGCT others(14689): Show |
chr7 | 139226237 | 139313236 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0012g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0012g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0012g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0015g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0015g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0015g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0020g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0020g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0021g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0021g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0021g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0024g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0024g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0025g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0025g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0026g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0026g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0027g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0027g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0028g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0028g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0029g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0029g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0030g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0030g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0031g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0031g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0032g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0033g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0034g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0034g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0035g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0035g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0036g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0036g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0037g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0037g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0038g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0039g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0040g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0042g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0043g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0044g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0062g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0064g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0066g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0068g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0069g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0070g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0071g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0072g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0075g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0076g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0077g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0078g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0079g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0080g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0081g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0082g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0083g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0084g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0085g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0086g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0087g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0088g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0092g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0095g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0096g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0098g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0099g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0100g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0101g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0102g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0103g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0104g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0106g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0107g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0108g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0109g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0110g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0001t0111g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0008g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0011g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0011g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0016g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0016g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0017g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0017g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0018g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0018g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0019g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0022g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0022g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0023g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0023g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0045g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0046g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0047g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0048g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0049g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0050g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0051g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0053g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0054g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0055g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0056g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0057g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0058g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0059g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0060g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0061g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0002t0105g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0004t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0004t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0004t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0004t0093g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0004t0094g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0005t0067g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0005t0073g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0005t0074g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0007t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0007t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0011t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0012t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0014t0065g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0001c0015t0032g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0002c0003t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0002c0003t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0002c0003t0017g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0002c0003t0018g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0002c0003t0019g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0002c0003t0052g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0003c0006t0089g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0003c0006t0091g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0004c0010t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0005c0016t0041g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0006c0018t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0007c0017t0090g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0008c0008t0063g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0009c0009t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
a0010c0013t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0055 | EUR | GBR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00099 | hp2 | a0001 | c0001 | t0032 | g0227 | EUR | GBR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00140 | hp1 | a0004 | c0010 | t0001 | g0200 | EUR | GBR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00140 | hp2 | a0001 | c0002 | t0046 | g0112 | EUR | GBR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00280 | hp1 | a0001 | c0001 | t0028 | g0056 | EUR | FIN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | FIN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0043 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00609 | hp1 | a0001 | c0001 | t0071 | g0061 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00609 | hp2 | a0001 | c0001 | t0012 | g0226 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00621 | hp1 | a0001 | c0001 | t0012 | g0221 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00621 | hp2 | a0001 | c0001 | t0088 | g0075 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00639 | hp1 | a0001 | c0001 | t0030 | g0168 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00639 | hp2 | a0001 | c0001 | t0064 | g0013 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0042 | EAS | CHS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00741 | hp1 | a0001 | c0015 | t0032 | g0154 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG00741 | hp2 | a0001 | c0012 | t0001 | g0208 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01074 | hp1 | a0001 | c0001 | t0085 | g0178 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01074 | hp2 | a0001 | c0001 | t0021 | g0136 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01081 | hp1 | a0001 | c0001 | t0087 | g0009 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01081 | hp2 | a0001 | c0002 | t0004 | g0101 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01109 | hp1 | a0001 | c0001 | t0021 | g0138 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01109 | hp2 | a0001 | c0002 | t0016 | g0110 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01167 | hp1 | a0001 | c0002 | t0007 | g0098 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01167 | hp2 | a0001 | c0001 | t0069 | g0058 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01243 | hp1 | a0001 | c0005 | t0074 | g0211 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01243 | hp2 | a0005 | c0016 | t0041 | g0137 | AMR | PUR | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01255 | hp1 | a0001 | c0001 | t0030 | g0009 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01256 | hp2 | a0001 | c0002 | t0004 | g0106 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01258 | hp2 | a0001 | c0002 | t0004 | g0115 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01361 | hp2 | a0001 | c0005 | t0073 | g0149 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0052 | EUR | IBS | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01891 | hp1 | a0001 | c0001 | t0038 | g0008 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01891 | hp2 | a0001 | c0001 | t0009 | g0237 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01928 | hp1 | a0001 | c0002 | t0004 | g0116 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01928 | hp2 | a0001 | c0001 | t0026 | g0001 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01943 | hp1 | a0001 | c0001 | t0035 | g0119 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01943 | hp2 | a0001 | c0002 | t0048 | g0104 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01993 | hp2 | a0001 | c0002 | t0017 | g0105 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02015 | hp1 | a0006 | c0018 | t0004 | g0081 | EAS | KHV | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02027 | hp1 | a0001 | c0002 | t0019 | g0113 | EAS | KHV | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0239 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02074 | hp1 | a0001 | c0001 | t0102 | g0014 | EAS | KHV | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02145 | hp2 | a0001 | c0001 | t0034 | g0120 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02257 | hp1 | a0001 | c0001 | t0078 | g0148 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02258 | hp1 | a0003 | c0006 | t0091 | g0032 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0238 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02280 | hp1 | a0001 | c0001 | t0043 | g0079 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02280 | hp2 | a0001 | c0002 | t0016 | g0114 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02300 | hp1 | a0001 | c0001 | t0028 | g0053 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02300 | hp2 | a0002 | c0003 | t0019 | g0087 | AMR | PEL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02451 | hp1 | a0001 | c0002 | t0055 | g0147 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02451 | hp2 | a0007 | c0017 | t0090 | g0080 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02572 | hp1 | a0001 | c0004 | t0010 | g0016 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02572 | hp2 | a0001 | c0001 | t0110 | g0144 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0046 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02615 | hp1 | a0001 | c0001 | t0096 | g0140 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02615 | hp2 | a0001 | c0001 | t0031 | g0164 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02622 | hp1 | a0001 | c0002 | t0049 | g0126 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02622 | hp2 | a0001 | c0001 | t0107 | g0025 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02630 | hp2 | a0001 | c0001 | t0015 | g0026 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02647 | hp2 | a0001 | c0001 | t0092 | g0004 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02683 | hp1 | a0001 | c0001 | t0080 | g0171 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02698 | hp1 | a0001 | c0001 | t0077 | g0172 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02723 | hp1 | a0001 | c0001 | t0027 | g0060 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02738 | hp1 | a0001 | c0001 | t0015 | g0048 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02809 | hp1 | a0001 | c0001 | t0013 | g0175 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02809 | hp2 | a0001 | c0002 | t0060 | g0129 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02818 | hp1 | a0001 | c0004 | t0093 | g0021 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02818 | hp2 | a0001 | c0001 | t0024 | g0223 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02886 | hp1 | a0001 | c0001 | t0099 | g0029 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02895 | hp2 | a0001 | c0001 | t0020 | g0007 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02896 | hp1 | a0001 | c0001 | t0037 | g0027 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02897 | hp1 | a0001 | c0001 | t0020 | g0007 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02897 | hp2 | a0001 | c0001 | t0037 | g0028 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02922 | hp1 | a0001 | c0001 | t0024 | g0222 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02922 | hp2 | a0001 | c0001 | t0072 | g0177 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02965 | hp1 | a0001 | c0004 | t0010 | g0017 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02965 | hp2 | a0001 | c0002 | t0058 | g0130 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02976 | hp1 | a0001 | c0001 | t0013 | g0173 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02976 | hp2 | a0001 | c0001 | t0025 | g0134 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03017 | hp2 | a0001 | c0001 | t0015 | g0040 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03041 | hp1 | a0001 | c0004 | t0010 | g0018 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03041 | hp2 | a0001 | c0001 | t0076 | g0201 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03098 | hp1 | a0001 | c0004 | t0094 | g0022 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03098 | hp2 | a0001 | c0001 | t0042 | g0125 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03139 | hp1 | a0001 | c0002 | t0105 | g0145 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03139 | hp2 | a0001 | c0001 | t0106 | g0127 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03195 | hp1 | a0001 | c0001 | t0044 | g0024 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03195 | hp2 | a0001 | c0001 | t0021 | g0141 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03209 | hp1 | a0001 | c0001 | t0034 | g0122 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0039 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03225 | hp1 | a0001 | c0001 | t0086 | g0203 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03225 | hp2 | a0001 | c0001 | t0020 | g0142 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03453 | hp2 | a0001 | c0011 | t0002 | g0155 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0235 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03486 | hp2 | a0001 | c0001 | t0075 | g0217 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03491 | hp2 | a0001 | c0001 | t0029 | g0184 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03516 | hp1 | a0001 | c0002 | t0059 | g0133 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0174 | AFR | ESN | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03540 | hp1 | a0001 | c0001 | t0104 | g0139 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03579 | hp1 | a0001 | c0001 | t0027 | g0068 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03579 | hp2 | a0001 | c0014 | t0065 | g0035 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03654 | hp1 | a0001 | c0002 | t0004 | g0100 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03654 | hp2 | a0009 | c0009 | t0003 | g0069 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0047 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03704 | hp1 | a0001 | c0001 | t0015 | g0002 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03831 | hp1 | a0001 | c0001 | t0029 | g0228 | SAS | BEB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03831 | hp2 | a0001 | c0002 | t0016 | g0102 | SAS | BEB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03834 | hp2 | a0001 | c0002 | t0017 | g0103 | SAS | BEB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03927 | hp2 | a0001 | c0001 | t0036 | g0002 | SAS | BEB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG04184 | hp1 | a0001 | c0002 | t0050 | g0089 | SAS | BEB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG04204 | hp1 | a0001 | c0001 | t0036 | g0041 | SAS | STU | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG04204 | hp2 | a0001 | c0005 | t0067 | g0213 | SAS | STU | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18522 | hp1 | a0001 | c0001 | t0014 | g0005 | AFR | YRI | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18522 | hp2 | a0001 | c0001 | t0038 | g0008 | AFR | YRI | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18612 | hp1 | a0001 | c0002 | t0008 | g0093 | EAS | CHB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18612 | hp2 | a0001 | c0001 | t0070 | g0224 | EAS | CHB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18906 | hp1 | a0001 | c0001 | t0101 | g0005 | AFR | YRI | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18906 | hp2 | a0001 | c0001 | t0084 | g0204 | AFR | YRI | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18939 | hp1 | a0001 | c0002 | t0022 | g0109 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18940 | hp1 | a0001 | c0002 | t0004 | g0097 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18946 | hp2 | a0001 | c0002 | t0004 | g0092 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18949 | hp1 | a0001 | c0002 | t0023 | g0090 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18951 | hp1 | a0001 | c0002 | t0018 | g0099 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18951 | hp2 | a0001 | c0001 | t0068 | g0062 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18954 | hp2 | a0001 | c0002 | t0051 | g0003 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18957 | hp1 | a0001 | c0001 | t0108 | g0198 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18957 | hp2 | a0002 | c0003 | t0018 | g0083 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18962 | hp1 | a0001 | c0002 | t0011 | g0188 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18964 | hp1 | a0002 | c0003 | t0007 | g0082 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18964 | hp2 | a0001 | c0001 | t0033 | g0202 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18966 | hp1 | a0001 | c0001 | t0095 | g0063 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18966 | hp2 | a0001 | c0002 | t0008 | g0189 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18968 | hp1 | a0001 | c0001 | t0026 | g0023 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18968 | hp2 | a0002 | c0003 | t0052 | g0086 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18970 | hp1 | a0001 | c0001 | t0100 | g0044 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18972 | hp1 | a0001 | c0001 | t0082 | g0159 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18972 | hp2 | a0001 | c0001 | t0083 | g0242 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18975 | hp2 | a0001 | c0002 | t0008 | g0095 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18977 | hp2 | a0001 | c0002 | t0054 | g0094 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18979 | hp1 | a0001 | c0002 | t0007 | g0108 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18980 | hp1 | a0001 | c0001 | t0081 | g0214 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18980 | hp2 | a0001 | c0002 | t0007 | g0107 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18983 | hp2 | a0001 | c0002 | t0008 | g0088 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18984 | hp1 | a0001 | c0001 | t0039 | g0160 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18984 | hp2 | a0002 | c0003 | t0007 | g0084 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18986 | hp1 | a0002 | c0003 | t0017 | g0085 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18986 | hp2 | a0001 | c0001 | t0079 | g0245 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18989 | hp2 | a0001 | c0001 | t0012 | g0220 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18990 | hp1 | a0001 | c0002 | t0019 | g0003 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18993 | hp2 | a0001 | c0002 | t0011 | g0091 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18999 | hp1 | a0001 | c0001 | t0066 | g0059 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA18999 | hp2 | a0001 | c0002 | t0022 | g0118 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19001 | hp1 | a0010 | c0013 | t0001 | g0241 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19004 | hp1 | a0001 | c0002 | t0011 | g0096 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19004 | hp2 | a0001 | c0001 | t0062 | g0065 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19006 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19030 | hp1 | a0001 | c0002 | t0057 | g0131 | AFR | LWK | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19030 | hp2 | a0001 | c0001 | t0031 | g0234 | AFR | LWK | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19043 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | LWK | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0236 | AFR | LWK | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19054 | hp2 | a0001 | c0002 | t0045 | g0117 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19056 | hp1 | a0001 | c0001 | t0040 | g0215 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19056 | hp2 | a0001 | c0002 | t0008 | g0003 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19060 | hp2 | a0001 | c0001 | t0098 | g0225 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19062 | hp2 | a0001 | c0002 | t0018 | g0146 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19066 | hp1 | a0001 | c0001 | t0103 | g0158 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19066 | hp2 | a0001 | c0002 | t0011 | g0193 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19068 | hp1 | a0001 | c0001 | t0109 | g0076 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19240 | hp1 | a0001 | c0007 | t0010 | g0019 | AFR | YRI | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0176 | AFR | YRI | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA20129 | hp1 | a0001 | c0002 | t0061 | g0124 | AFR | ASW | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA20129 | hp2 | a0001 | c0002 | t0056 | g0132 | AFR | ASW | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01123 | hp1 | a0001 | c0002 | t0053 | g0111 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02109 | hp1 | a0001 | c0001 | t0014 | g0038 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02109 | hp2 | a0001 | c0001 | t0025 | g0135 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02486 | hp1 | a0003 | c0006 | t0089 | g0049 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG02486 | hp2 | a0008 | c0008 | t0063 | g0015 | AFR | ACB | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0205 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG03471 | hp2 | a0001 | c0001 | t0014 | g0037 | AFR | MSL | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG06807 | hp1 | a0001 | c0001 | t0035 | g0121 | AFR | USA | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
HG06807 | hp2 | a0001 | c0002 | t0023 | g0128 | AFR | USA | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | USA | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA20300 | hp2 | a0001 | c0007 | t0010 | g0020 | AFR | USA | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA21309 | hp1 | a0001 | c0002 | t0047 | g0123 | AFR | LWK | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
NA21309 | hp2 | a0001 | c0001 | t0111 | g0143 | AFR | LWK | UBN2_chr7_139226237_139313236 | UBN2 | chr7 | 139226237 | 139313236 |
view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:139231586 | G | C | 1 | a0009 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.102G>C | p.Glu34Asp | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/18 | 350/14692 | 102/4044 | 34/1347 | chr7 | 139231586 | |||
chr7:139231842 | C | T | 1 | a0008 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.358C>T | p.Pro120Ser | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/18 | 606/14692 | 358/4044 | 120/1347 | chr7 | 139231842 | |||
chr7:139231908 | G | T | 2 | a0002a0006 | 7 | HG02015.hp1 HG02300.hp2 NA18957.hp2 others(4): Show |
missense_variant | MODERATE | c.424G>T | p.Val142Leu | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/18 | 672/14692 | 424/4044 | 142/1347 | chr7 | 139231908 | |||
chr7:139231951 | G | C | 1 | a0004 | 1 | HG00140.hp1 | missense_variant&splice_region_variant | MODERATE | c.467G>C | p.Arg156Pro | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/18 | 715/14692 | 467/4044 | 156/1347 | chr7 | 139231951 | |||
chr7:139261418 | C | A | 1 | a0010 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.1072C>A | p.Pro358Thr | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/18 | 1320/14692 | 1072/4044 | 358/1347 | chr7 | 139261418 | |||
chr7:139261550 | A | G | 2 | a0002a0006 | 7 | HG02015.hp1 HG02300.hp2 NA18957.hp2 others(4): Show |
missense_variant | MODERATE | c.1204A>G | p.Met402Val | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/18 | 1452/14692 | 1204/4044 | 402/1347 | chr7 | 139261550 | |||
chr7:139261617 | C | T | 1 | a0007 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1271C>T | p.Ser424Leu | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/18 | 1519/14692 | 1271/4044 | 424/1347 | chr7 | 139261617 | |||
chr7:139283078 | A | G | 1 | a0003 | 2 | HG02258.hp1 HG02486.hp1 |
missense_variant | MODERATE | c.2173A>G | p.Ser725Gly | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/18 | 2421/14692 | 2173/4044 | 725/1347 | chr7 | 139283078 | |||
chr7:139283229 | C | T | 1 | a0007 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.2324C>T | p.Ala775Val | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/18 | 2572/14692 | 2324/4044 | 775/1347 | chr7 | 139283229 | |||
chr7:139283834 | C | T | 1 | a0005 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.2929C>T | p.Pro977Ser | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/18 | 3177/14692 | 2929/4044 | 977/1347 | chr7 | 139283834 | |||
chr7:139284385 | G | C | 1 | a0005 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.3480G>C | p.Lys1160Asn | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/18 | 3728/14692 | 3480/4044 | 1160/1347 | chr7 | 139284385 | |||
chr7:139293933 | A | G | 1 | a0008 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.3946A>G | p.Thr1316Ala | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/18 | 4194/14692 | 3946/4044 | 1316/1347 | chr7 | 139293933 | |||
chr7:139293961 | A | G | 1 | a0006 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.3974A>G | p.His1325Arg | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/18 | 4222/14692 | 3974/4044 | 1325/1347 | chr7 | 139293961 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:139231547 | G | A | 1 | a0008c0008 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.63G>A | p.Glu21Glu | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/18 | 311/14692 | 63/4044 | 21/1347 | chr7 | 139231547 | |||
chr7:139231935 | C | T | 2 | a0001c0004a0001c0007 | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
synonymous_variant | LOW | c.451C>T | p.Leu151Leu | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/18 | 699/14692 | 451/4044 | 151/1347 | chr7 | 139231935 | |||
chr7:139252054 | G | A | 1 | a0001c0011 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.660G>A | p.Glu220Glu | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/18 | 908/14692 | 660/4044 | 220/1347 | chr7 | 139252054 | |||
chr7:139259314 | G | A | 1 | a0001c0012 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.849G>A | p.Arg283Arg | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/18 | 1097/14692 | 849/4044 | 283/1347 | chr7 | 139259314 | |||
chr7:139261456 | G | A | 1 | a0001c0014 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1110G>A | p.Pro370Pro | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/18 | 1358/14692 | 1110/4044 | 370/1347 | chr7 | 139261456 | |||
chr7:139269454 | T | G | 1 | a0001c0015 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.1527T>G | p.Leu509Leu | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/18 | 1775/14692 | 1527/4044 | 509/1347 | chr7 | 139269454 | |||
chr7:139283068 | G | A | 4 | a0001c0002a0002c0003a0005c0016others(1): Show | 57 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(54): Show |
synonymous_variant | LOW | c.2163G>A | p.Val721Val | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/18 | 2411/14692 | 2163/4044 | 721/1347 | chr7 | 139283068 | |||
chr7:139284067 | G | A | 1 | a0001c0005 | 3 | HG01243.hp1 HG01361.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.3162G>A | p.Ser1054Ser | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/18 | 3410/14692 | 3162/4044 | 1054/1347 | chr7 | 139284067 | |||
chr7:139293947 | A | G | 1 | a0001c0007 | 2 | NA19240.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.3960A>G | p.Ser1320Ser | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/18 | 4208/14692 | 3960/4044 | 1320/1347 | chr7 | 139293947 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:139297950 | G | A | 2 | a0001c0001t0039a0001c0001t0040 | 2 | NA18984.hp1 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*114G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 114 | chr7 | 139297950 | ||||||
chr7:139298298 | G | A | 37 | a0001c0001t0042a0001c0001t0043a0001c0001t0044others(34): Show | 60 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*462G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 462 | chr7 | 139298298 | ||||||
chr7:139298325 | G | A | 37 | a0001c0001t0042a0001c0001t0043a0001c0001t0044others(34): Show | 60 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*489G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 489 | chr7 | 139298325 | ||||||
chr7:139298512 | A | C | 3 | a0001c0001t0038a0001c0001t0110a0001c0001t0111 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*676A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 676 | chr7 | 139298512 | ||||||
chr7:139298638 | T | C | 1 | a0008c0008t0063 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 802 | chr7 | 139298638 | ||||||
chr7:139298738 | G | C | 1 | a0001c0001t0024 | 2 | HG02818.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*902G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 902 | chr7 | 139298738 | ||||||
chr7:139298901 | G | A | 1 | a0001c0001t0064 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1065G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 1065 | chr7 | 139298901 | ||||||
chr7:139299152 | T | G | 1 | a0001c0001t0025 | 2 | HG02109.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1316T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 1316 | chr7 | 139299152 | ||||||
chr7:139299197 | G | A | 36 | a0001c0001t0042a0001c0001t0043a0001c0001t0044others(33): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1361G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 1361 | chr7 | 139299197 | ||||||
chr7:139299199 | A | G | 1 | a0001c0001t0109 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1363A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 1363 | chr7 | 139299199 | ||||||
chr7:139299486 | A | G | 1 | a0001c0001t0108 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1650A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 1650 | chr7 | 139299486 | ||||||
chr7:139299819 | T | C | 1 | a0001c0014t0065 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1983T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 1983 | chr7 | 139299819 | ||||||
chr7:139300121 | A | G | 1 | a0001c0001t0107 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2285A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 2285 | chr7 | 139300121 | ||||||
chr7:139300298 | A | G | 39 | a0001c0001t0042a0001c0001t0043a0001c0001t0044others(36): Show | 62 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2462A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 2462 | chr7 | 139300298 | ||||||
chr7:139300653 | C | T | 2 | a0001c0001t0021a0001c0001t0104 | 4 | HG01074.hp2 HG01109.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2817C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 2817 | chr7 | 139300653 | ||||||
chr7:139301131 | A | G | 1 | a0001c0001t0103 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3295A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 3295 | chr7 | 139301131 | ||||||
chr7:139301341 | C | T | 10 | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(7): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3505C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 3505 | chr7 | 139301341 | ||||||
chr7:139301403 | C | T | 1 | a0001c0001t0098 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3567C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 3567 | chr7 | 139301403 | ||||||
chr7:139301747 | G | C | 1 | a0008c0008t0063 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3911G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 3911 | chr7 | 139301747 | ||||||
chr7:139301927 | C | CAGT | 3 | a0001c0001t0038a0001c0001t0110a0001c0001t0111 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4097_*4099dupTAG | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4100 | INFO_REALIGN_3_PRIME | chr7 | 139301927 | |||||
chr7:139302404 | G | T | 1 | a0001c0001t0097 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4568G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4568 | chr7 | 139302404 | ||||||
chr7:139302413 | C | T | 1 | a0001c0001t0096 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4577C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4577 | chr7 | 139302413 | ||||||
chr7:139302424 | G | A | 1 | a0005c0016t0041 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4588G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4588 | chr7 | 139302424 | ||||||
chr7:139302561 | T | C | 1 | a0001c0001t0042 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4725T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4725 | chr7 | 139302561 | ||||||
chr7:139302737 | C | T | 1 | a0005c0016t0041 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4901C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4901 | chr7 | 139302737 | ||||||
chr7:139302768 | C | T | 1 | a0001c0001t0095 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4932C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4932 | chr7 | 139302768 | ||||||
chr7:139302775 | A | AAC | 72 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(69): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*4964_*4965dupAC | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4966 | INFO_REALIGN_3_PRIME | chr7 | 139302775 | |||||
chr7:139302775 | A | AACAC | 22 | a0001c0001t0003a0001c0001t0012a0001c0001t0025others(19): Show | 48 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*4962_*4965dupACAC | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4966 | INFO_REALIGN_3_PRIME | chr7 | 139302775 | |||||
chr7:139302775 | A | AACACAC | 1 | a0001c0001t0026 | 2 | HG01928.hp2 NA18968.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4960_*4965dupACAC others(2): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4966 | INFO_REALIGN_3_PRIME | chr7 | 139302775 | |||||
chr7:139302775 | A | AACACACA others(5): Show |
1 | a0001c0001t0043 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4954_*4965dupACAC others(8): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4966 | INFO_REALIGN_3_PRIME | chr7 | 139302775 | |||||
chr7:139302775 | AACACACA others(3): Show |
A | 4 | a0001c0004t0010a0001c0004t0093a0001c0004t0094others(1): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4956_*4965delACAC others(6): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 4956 | INFO_REALIGN_3_PRIME | chr7 | 139302775 | |||||
chr7:139302965 | T | C | 6 | a0001c0002t0055a0001c0002t0056a0001c0002t0057others(3): Show | 6 | HG02451.hp1 HG02809.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5129T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 5129 | chr7 | 139302965 | ||||||
chr7:139303089 | T | A | 1 | a0001c0001t0072 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5253T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 5253 | chr7 | 139303089 | ||||||
chr7:139303094 | A | G | 1 | a0001c0002t0054 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5258A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 5258 | chr7 | 139303094 | ||||||
chr7:139303140 | G | A | 1 | a0001c0001t0100 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5304G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 5304 | chr7 | 139303140 | ||||||
chr7:139303268 | A | T | 7 | a0001c0001t0006a0001c0001t0015a0001c0001t0036others(4): Show | 18 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5432A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 5432 | chr7 | 139303268 | ||||||
chr7:139303504 | C | G | 8 | a0001c0001t0005a0001c0001t0024a0001c0001t0034others(5): Show | 17 | HG01943.hp1 HG02055.hp1 HG02145.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5668C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 5668 | chr7 | 139303504 | ||||||
chr7:139303933 | C | T | 2 | a0001c0001t0032a0001c0015t0032 | 2 | HG00099.hp2 HG00741.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6097C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6097 | chr7 | 139303933 | ||||||
chr7:139304052 | C | T | 2 | a0001c0001t0031a0001c0001t0087 | 3 | HG01081.hp1 HG02615.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6216C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6216 | chr7 | 139304052 | ||||||
chr7:139304255 | C | T | 1 | a0008c0008t0063 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6419C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6419 | chr7 | 139304255 | ||||||
chr7:139304315 | G | GGTC | 2 | a0001c0001t0037a0001c0001t0099 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6481_*6483dupTCG | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6484 | INFO_REALIGN_3_PRIME | chr7 | 139304315 | |||||
chr7:139304422 | C | G | 2 | a0001c0004t0093a0001c0004t0094 | 2 | HG02818.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6586C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6586 | chr7 | 139304422 | ||||||
chr7:139304448 | G | A | 1 | a0001c0001t0034 | 2 | HG02145.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6612G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6612 | chr7 | 139304448 | ||||||
chr7:139304461 | G | A | 1 | a0003c0006t0089 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6625G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6625 | chr7 | 139304461 | ||||||
chr7:139304631 | G | A | 2 | a0001c0002t0047a0001c0002t0061 | 2 | NA20129.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6795G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6795 | chr7 | 139304631 | ||||||
chr7:139304706 | G | GGGGTGTG others(3): Show |
1 | a0001c0002t0061 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6871_*6872insGGTG others(6): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6872 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGGGTGTG others(17): Show |
2 | a0001c0001t0066a0001c0002t0022 | 3 | NA18939.hp1 NA18999.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6871_*6872insGGTG others(20): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6872 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGT | 18 | a0001c0001t0005a0001c0001t0015a0001c0001t0020others(15): Show | 37 | HG00280.hp1 HG01074.hp2 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*6903_*6904dupGT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGT | 6 | a0001c0001t0024a0001c0001t0035a0001c0001t0064others(3): Show | 8 | HG00639.hp2 HG01074.hp1 HG01943.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6901_*6904dupGTGT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGT | 2 | a0001c0001t0034a0001c0001t0086 | 3 | HG02145.hp2 HG03209.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6899_*6904dupGTGT others(2): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(3): Show |
3 | a0001c0002t0047a0001c0004t0010a0001c0007t0010 | 6 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6895_*6904dupGTGT others(6): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0025 | 2 | HG02109.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6893_*6904dupGTGT others(8): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(11): Show |
1 | a0001c0002t0105 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6883_*6884insGGTG others(14): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6884 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(7): Show |
5 | a0001c0001t0043a0001c0002t0007a0001c0002t0045others(2): Show | 8 | HG01167.hp1 HG01243.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6891_*6904dupGTGT others(10): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(9): Show |
6 | a0001c0001t0042a0001c0002t0004a0001c0002t0048others(3): Show | 12 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6889_*6904dupGTGT others(12): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(11): Show |
2 | a0001c0002t0017a0002c0003t0017 | 3 | HG01993.hp2 HG03834.hp2 NA18986.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6887_*6904dupGTGT others(14): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(13): Show |
3 | a0001c0002t0018a0001c0002t0055a0002c0003t0018 | 4 | HG02451.hp1 NA18951.hp1 NA18957.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6885_*6904dupGTGT others(16): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(15): Show |
4 | a0001c0002t0019a0001c0002t0056a0001c0002t0057others(1): Show | 5 | HG02027.hp1 HG02300.hp2 NA18990.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6883_*6904dupGTGT others(18): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(17): Show |
4 | a0001c0002t0023a0001c0002t0050a0001c0002t0058others(1): Show | 5 | HG02965.hp2 HG03516.hp1 HG04184.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6881_*6904dupGTGT others(20): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(19): Show |
2 | a0001c0002t0008a0001c0002t0054 | 6 | NA18612.hp1 NA18966.hp2 NA18975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6879_*6904dupGTGT others(22): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(21): Show |
1 | a0001c0002t0011 | 4 | NA18962.hp1 NA18993.hp2 NA19004.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6877_*6904dupGTGT others(24): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(23): Show |
1 | a0001c0002t0051 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6875_*6904dupGTGT others(26): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GGTGTGTG others(25): Show |
1 | a0001c0002t0046 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6873_*6904dupGTGT others(28): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304706 | G | GTGTGTGT others(8): Show |
2 | a0001c0001t0071a0001c0004t0094 | 2 | HG00609.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6870_*6871insTGTG others(11): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6871 | chr7 | 139304706 | ||||||
chr7:139304706 | G | GTGTGTGT others(10): Show |
1 | a0001c0002t0053 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6870_*6871insTGTG others(13): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6871 | chr7 | 139304706 | ||||||
chr7:139304706 | G | GTGTGTGT others(16): Show |
1 | a0001c0002t0060 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6870_*6871insTGTG others(19): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6871 | chr7 | 139304706 | ||||||
chr7:139304706 | GGT | G | 4 | a0001c0005t0067a0001c0005t0073a0001c0005t0074others(1): Show | 4 | HG01243.hp1 HG01361.hp2 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6903_*6904delGT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6903 | INFO_REALIGN_3_PRIME | chr7 | 139304706 | |||||
chr7:139304735 | G | GTGTGTGT others(10): Show |
1 | a0002c0003t0052 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6904_*6905insGTGT others(13): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 6905 | INFO_REALIGN_3_PRIME | chr7 | 139304735 | |||||
chr7:139304872 | A | G | 1 | a0001c0001t0081 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7036A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 7036 | chr7 | 139304872 | ||||||
chr7:139305054 | A | G | 1 | a0001c0001t0080 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7218A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 7218 | chr7 | 139305054 | ||||||
chr7:139305133 | T | C | 1 | a0001c0001t0108 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7297T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 7297 | chr7 | 139305133 | ||||||
chr7:139305202 | A | C | 1 | a0001c0002t0050 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7366A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 7366 | chr7 | 139305202 | ||||||
chr7:139305695 | G | T | 1 | a0001c0001t0030 | 2 | HG00639.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7859G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 7859 | chr7 | 139305695 | ||||||
chr7:139305806 | C | T | 1 | a0007c0017t0090 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7970C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 7970 | chr7 | 139305806 | ||||||
chr7:139306065 | C | T | 102 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(99): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*8229C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 8229 | chr7 | 139306065 | ||||||
chr7:139306167 | A | C | 1 | a0001c0001t0069 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8331A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 8331 | chr7 | 139306167 | ||||||
chr7:139306530 | T | A | 1 | a0001c0001t0075 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8694T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 8694 | chr7 | 139306530 | ||||||
chr7:139306612 | A | G | 2 | a0001c0002t0016a0001c0002t0046 | 4 | HG00140.hp2 HG01109.hp2 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8776A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 8776 | chr7 | 139306612 | ||||||
chr7:139306654 | T | G | 4 | a0001c0001t0005a0001c0001t0092a0003c0006t0089others(1): Show | 10 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8818T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 8818 | chr7 | 139306654 | ||||||
chr7:139306770 | C | G | 1 | a0001c0002t0105 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8934C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 8934 | chr7 | 139306770 | ||||||
chr7:139307107 | C | T | 1 | a0001c0001t0079 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9271C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 9271 | chr7 | 139307107 | ||||||
chr7:139307116 | C | T | 1 | a0001c0001t0009 | 5 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9280C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 9280 | chr7 | 139307116 | ||||||
chr7:139307481 | T | TA | 32 | a0001c0001t0025a0001c0001t0106a0001c0002t0004others(29): Show | 56 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*9660dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 9661 | INFO_REALIGN_3_PRIME | chr7 | 139307481 | |||||
chr7:139307481 | TA | T | 8 | a0001c0001t0020a0001c0001t0021a0001c0001t0038others(5): Show | 13 | HG01074.hp2 HG01109.hp1 HG01891.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*9660delA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 9660 | INFO_REALIGN_3_PRIME | chr7 | 139307481 | |||||
chr7:139307494 | A | T | 3 | a0001c0001t0009a0001c0001t0077a0001c0001t0108 | 7 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9658A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 9658 | chr7 | 139307494 | ||||||
chr7:139307900 | C | A | 1 | a0008c0008t0063 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10064C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 10064 | chr7 | 139307900 | ||||||
chr7:139308025 | G | GT | 11 | a0001c0001t0013a0001c0001t0024a0001c0001t0072others(8): Show | 15 | HG01243.hp1 HG02486.hp2 HG02622.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*10205dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 10206 | INFO_REALIGN_3_PRIME | chr7 | 139308025 | |||||
chr7:139308025 | GT | G | 37 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(34): Show | 68 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*10205delT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 10205 | INFO_REALIGN_3_PRIME | chr7 | 139308025 | |||||
chr7:139308070 | T | G | 1 | a0001c0001t0027 | 2 | HG02723.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10234T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 10234 | chr7 | 139308070 | ||||||
chr7:139308154 | C | T | 1 | a0001c0001t0029 | 2 | HG03491.hp2 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10318C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 18/18 | 10318 | chr7 | 139308154 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:139232061 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.468+109C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232061 | |||||||
chr7:139232208 | T | C | 150 | a0001c0001t0001g0072a0001c0001t0003g0006a0001c0001t0003g0050others(147): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.468+256T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232208 | |||||||
chr7:139232209 | C | T | 150 | a0001c0001t0001g0072a0001c0001t0003g0006a0001c0001t0003g0050others(147): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.468+257C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232209 | |||||||
chr7:139232225 | T | C | 1 | a0001c0001t0005g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.468+273T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232225 | |||||||
chr7:139232485 | C | G | 1 | a0001c0001t0079g0245 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.468+533C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232485 | |||||||
chr7:139232493 | A | G | 1 | a0001c0001t0078g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.468+541A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232493 | |||||||
chr7:139232530 | A | G | 1 | a0001c0002t0055g0147 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.468+578A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232530 | |||||||
chr7:139232861 | G | A | 1 | a0001c0001t0064g0013 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.468+909G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232861 | |||||||
chr7:139232861 | G | T | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0083g0242others(1): Show | 4 | HG00673.hp1 NA18949.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+909G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232861 | |||||||
chr7:139232922 | A | G | 1 | a0001c0002t0018g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.468+970A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139232922 | |||||||
chr7:139233089 | A | C | 13 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(10): Show | 15 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.468+1137A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139233089 | |||||||
chr7:139233136 | C | A | 1 | a0001c0001t0102g0014 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.468+1184C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139233136 | |||||||
chr7:139233175 | A | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.468+1223A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139233175 | |||||||
chr7:139233187 | C | A | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.468+1235C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139233187 | |||||||
chr7:139233392 | G | A | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1440G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139233392 | |||||||
chr7:139233511 | C | G | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1559C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139233511 | |||||||
chr7:139233778 | T | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.468+1826T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139233778 | |||||||
chr7:139233809 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.468+1857A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139233809 | |||||||
chr7:139234039 | A | C | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.468+2087A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139234039 | |||||||
chr7:139234244 | A | G | 60 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(57): Show | 60 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.468+2292A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139234244 | |||||||
chr7:139234544 | G | T | 1 | a0001c0001t0003g0006 | 2 | NA18989.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.469-2461G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139234544 | |||||||
chr7:139234838 | C | T | 1 | a0007c0017t0090g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.469-2167C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139234838 | |||||||
chr7:139234956 | T | C | 1 | a0001c0005t0073g0149 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.469-2049T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139234956 | |||||||
chr7:139234985 | C | G | 1 | a0001c0001t0043g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.469-2020C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139234985 | |||||||
chr7:139235064 | CAA | C | 3 | a0001c0004t0093g0021a0001c0004t0094g0022a0008c0008t0063g0015 | 3 | HG02486.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.469-1940_469-1939d others(4): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235064 | |||||||
chr7:139235129 | T | A | 1 | a0001c0001t0002g0150 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.469-1876T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235129 | |||||||
chr7:139235309 | C | G | 1 | a0001c0001t0005g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.469-1696C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235309 | |||||||
chr7:139235365 | T | A | 1 | a0001c0001t0043g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.469-1640T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235365 | |||||||
chr7:139235509 | C | A | 7 | a0002c0003t0007g0082a0002c0003t0007g0084a0002c0003t0017g0085others(4): Show | 7 | HG02015.hp1 HG02300.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-1496C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235509 | |||||||
chr7:139235525 | G | A | 35 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0004g0100others(32): Show | 35 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.469-1480G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235525 | |||||||
chr7:139235585 | T | G | 10 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(7): Show | 11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.469-1420T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235585 | |||||||
chr7:139235595 | C | T | 54 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(51): Show | 54 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.469-1410C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235595 | |||||||
chr7:139235615 | T | C | 1 | a0001c0001t0026g0023 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.469-1390T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235615 | |||||||
chr7:139235767 | T | C | 1 | a0001c0002t0008g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.469-1238T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235767 | |||||||
chr7:139235818 | C | T | 5 | a0001c0001t0009g0235a0001c0001t0009g0236a0001c0001t0009g0237others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-1187C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235818 | |||||||
chr7:139235847 | G | A | 1 | a0001c0004t0093g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.469-1158G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235847 | |||||||
chr7:139235894 | T | C | 2 | a0001c0002t0047g0123a0001c0002t0061g0124 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.469-1111T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235894 | |||||||
chr7:139235991 | G | A | 119 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(116): Show | 121 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(118): Show |
intron_variant | MODIFIER | c.469-1014G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235991 | |||||||
chr7:139235997 | A | G | 1 | a0001c0001t0003g0006 | 2 | NA18989.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.469-1008A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139235997 | |||||||
chr7:139236047 | C | T | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-958C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139236047 | |||||||
chr7:139236203 | C | G | 1 | a0001c0001t0031g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.469-802C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139236203 | |||||||
chr7:139236219 | G | T | 253 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0072others(250): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.469-786G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139236219 | |||||||
chr7:139236310 | G | C | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.469-695G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139236310 | |||||||
chr7:139236670 | A | G | 1 | a0001c0001t0001g0011 | 2 | NA18939.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.469-335A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139236670 | |||||||
chr7:139236730 | C | A | 1 | a0001c0001t0044g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.469-275C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139236730 | |||||||
chr7:139236895 | A | T | 1 | a0003c0006t0089g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.469-110A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 1/17 | chr7 | 139236895 | |||||||
chr7:139237183 | T | C | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+86T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237183 | |||||||
chr7:139237213 | A | T | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+116A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237213 | |||||||
chr7:139237257 | C | T | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.561+160C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237257 | |||||||
chr7:139237451 | C | T | 55 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(52): Show | 55 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.561+354C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237451 | |||||||
chr7:139237592 | G | A | 1 | a0001c0002t0050g0089 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.561+495G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237592 | |||||||
chr7:139237686 | C | T | 55 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(52): Show | 55 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.561+589C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237686 | |||||||
chr7:139237920 | G | A | 10 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0052others(7): Show | 10 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+823G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237920 | |||||||
chr7:139237930 | A | G | 1 | a0001c0001t0069g0058 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.561+833A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237930 | |||||||
chr7:139237941 | T | C | 10 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(7): Show | 11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.561+844T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237941 | |||||||
chr7:139237967 | T | G | 1 | a0001c0001t0107g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561+870T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139237967 | |||||||
chr7:139238282 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.561+1185C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139238282 | |||||||
chr7:139238318 | A | G | 14 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(11): Show | 14 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.561+1221A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139238318 | |||||||
chr7:139238434 | C | G | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.561+1337C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139238434 | |||||||
chr7:139238454 | GTC | G | 55 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(52): Show | 55 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.561+1361_561+1362d others(4): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139238454 | ||||||
chr7:139238589 | A | C | 1 | a0001c0002t0105g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.561+1492A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139238589 | |||||||
chr7:139238760 | G | C | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.561+1663G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139238760 | |||||||
chr7:139238914 | T | TA | 12 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0008g0003others(9): Show | 12 | NA18612.hp1 NA18940.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.561+1821dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139238914 | ||||||
chr7:139238984 | A | T | 6 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(3): Show | 6 | HG02109.hp1 HG02622.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+1887A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139238984 | |||||||
chr7:139239048 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.561+1951C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139239048 | |||||||
chr7:139239106 | G | A | 18 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(15): Show | 18 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.561+2009G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139239106 | |||||||
chr7:139239182 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.561+2085C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139239182 | |||||||
chr7:139239188 | A | T | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.561+2091A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139239188 | |||||||
chr7:139239320 | A | G | 1 | a0001c0001t0109g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.561+2223A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139239320 | |||||||
chr7:139239551 | C | CT | 81 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.561+2477dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139239551 | ||||||
chr7:139239551 | C | CTT | 19 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0138others(16): Show | 21 | HG01109.hp1 HG01258.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.561+2476_561+2477d others(4): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139239551 | ||||||
chr7:139239562 | T | G | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.561+2465T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139239562 | |||||||
chr7:139239772 | G | T | 10 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(7): Show | 11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.561+2675G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139239772 | |||||||
chr7:139239929 | A | G | 5 | a0001c0001t0001g0216a0001c0001t0001g0218a0001c0001t0001g0219others(2): Show | 5 | HG00280.hp2 HG01257.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+2832A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139239929 | |||||||
chr7:139240161 | A | G | 2 | a0001c0001t0040g0215a0001c0001t0081g0214 | 2 | NA18980.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.561+3064A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240161 | |||||||
chr7:139240429 | A | AAT | 10 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(7): Show | 10 | HG00621.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+3357_561+3358d others(4): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240429 | ||||||
chr7:139240429 | AAT | A | 15 | a0001c0001t0015g0026a0001c0001t0020g0007a0001c0001t0020g0142others(12): Show | 16 | HG01074.hp2 HG01109.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.561+3357_561+3358d others(4): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240429 | ||||||
chr7:139240429 | AATAT | A | 45 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0004g0100others(42): Show | 45 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.561+3355_561+3358d others(6): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240429 | ||||||
chr7:139240449 | TA | T | 3 | a0001c0001t0006g0047a0001c0001t0015g0048a0001c0007t0010g0020 | 3 | HG02738.hp1 HG03669.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.561+3353delA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240449 | |||||||
chr7:139240450 | A | AT | 9 | a0001c0001t0001g0212a0001c0001t0001g0232a0001c0001t0034g0120others(6): Show | 9 | HG01243.hp1 HG01361.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.561+3354dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240450 | ||||||
chr7:139240451 | TA | T | 10 | a0001c0001t0006g0002a0001c0001t0006g0042a0001c0001t0006g0043others(7): Show | 10 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.561+3355delA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240451 | |||||||
chr7:139240452 | A | AT | 18 | a0001c0001t0001g0210a0001c0001t0001g0231a0001c0001t0002g0206others(15): Show | 18 | HG00140.hp1 HG00741.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+3356dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240452 | ||||||
chr7:139240452 | A | T | 29 | a0001c0001t0001g0212a0001c0001t0001g0232a0001c0001t0006g0047others(26): Show | 30 | HG00140.hp2 HG01123.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.561+3355A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240452 | |||||||
chr7:139240453 | TA | T | 5 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(2): Show | 5 | HG03017.hp2 HG03471.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+3357delA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240453 | |||||||
chr7:139240454 | A | AT | 57 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0072others(54): Show | 62 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.561+3368dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240454 | ||||||
chr7:139240454 | A | ATAT | 6 | a0001c0001t0001g0216a0001c0001t0001g0240a0001c0001t0002g0161others(3): Show | 6 | HG00621.hp2 HG01257.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+3358_561+3359i others(5): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240454 | ||||||
chr7:139240454 | A | ATTT | 5 | a0001c0001t0001g0196a0001c0001t0001g0230a0001c0001t0002g0197others(2): Show | 5 | HG00597.hp1 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+3366_561+3368d others(5): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240454 | ||||||
chr7:139240454 | A | T | 100 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0212others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.561+3357A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240454 | |||||||
chr7:139240454 | AT | A | 7 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0038g0008others(4): Show | 8 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+3368delT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139240454 | ||||||
chr7:139240455 | T | TA | 27 | a0001c0001t0003g0006a0001c0001t0003g0050a0001c0001t0003g0051others(24): Show | 28 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.561+3358_561+3359i others(3): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240455 | |||||||
chr7:139240455 | T | TATA | 8 | a0001c0001t0001g0152a0001c0001t0027g0060a0001c0001t0064g0013others(5): Show | 8 | HG00609.hp1 HG00639.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+3358_561+3359i others(5): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240455 | |||||||
chr7:139240457 | T | A | 4 | a0001c0001t0003g0006a0001c0001t0027g0060a0001c0001t0031g0234others(1): Show | 5 | HG02723.hp1 NA18989.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+3360T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240457 | |||||||
chr7:139240465 | T | A | 1 | a0001c0001t0014g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.561+3368T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240465 | |||||||
chr7:139240543 | G | A | 1 | a0001c0001t0035g0119 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.561+3446G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240543 | |||||||
chr7:139240684 | C | T | 1 | a0001c0001t0079g0245 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.561+3587C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240684 | |||||||
chr7:139240936 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.561+3839C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139240936 | |||||||
chr7:139241207 | A | C | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.561+4110A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139241207 | |||||||
chr7:139241253 | T | C | 1 | a0002c0003t0007g0084 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.561+4156T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139241253 | |||||||
chr7:139241565 | G | T | 13 | a0001c0001t0006g0002a0001c0001t0006g0042a0001c0001t0006g0043others(10): Show | 13 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.561+4468G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139241565 | |||||||
chr7:139241690 | TAATAAG | T | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+4605_561+4610d others(8): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139241690 | ||||||
chr7:139241958 | G | A | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.561+4861G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139241958 | |||||||
chr7:139241963 | A | T | 2 | a0001c0001t0024g0222a0001c0001t0024g0223 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.561+4866A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139241963 | |||||||
chr7:139241975 | C | A | 54 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(51): Show | 54 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.561+4878C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139241975 | |||||||
chr7:139241985 | G | A | 8 | a0001c0001t0003g0006a0001c0001t0003g0064a0001c0001t0003g0077others(5): Show | 9 | HG00408.hp2 HG00609.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.561+4888G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139241985 | |||||||
chr7:139242000 | C | CG | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+4903_561+4904i others(3): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242000 | |||||||
chr7:139242002 | C | G | 2 | a0001c0001t0015g0026a0008c0008t0063g0015 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.561+4905C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242002 | |||||||
chr7:139242006 | A | C | 24 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(21): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.561+4909A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242006 | |||||||
chr7:139242019 | A | T | 3 | a0001c0001t0037g0027a0001c0001t0037g0028a0001c0001t0099g0029 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.561+4922A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242019 | |||||||
chr7:139242033 | A | G | 119 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(116): Show | 121 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(118): Show |
intron_variant | MODIFIER | c.561+4936A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242033 | |||||||
chr7:139242173 | T | G | 1 | a0006c0018t0004g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.561+5076T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242173 | |||||||
chr7:139242182 | T | A | 1 | a0001c0002t0019g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.561+5085T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242182 | |||||||
chr7:139242237 | C | T | 7 | a0002c0003t0007g0082a0002c0003t0007g0084a0002c0003t0017g0085others(4): Show | 7 | HG02015.hp1 HG02300.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+5140C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242237 | |||||||
chr7:139242331 | C | T | 5 | a0001c0001t0009g0235a0001c0001t0009g0236a0001c0001t0009g0237others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+5234C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242331 | |||||||
chr7:139242351 | G | A | 1 | a0001c0001t0006g0042 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.561+5254G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242351 | |||||||
chr7:139242471 | C | G | 1 | a0001c0001t0107g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561+5374C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242471 | |||||||
chr7:139242574 | T | TTAAA | 59 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.561+5478_561+5481d others(6): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139242574 | ||||||
chr7:139242614 | C | A | 3 | a0001c0001t0038g0008a0001c0001t0110g0144a0001c0001t0111g0143 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+5517C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242614 | |||||||
chr7:139242623 | A | C | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.561+5526A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242623 | |||||||
chr7:139242904 | A | G | 1 | a0001c0001t0102g0014 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.561+5807A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139242904 | |||||||
chr7:139243028 | A | G | 1 | a0006c0018t0004g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.561+5931A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139243028 | |||||||
chr7:139243087 | G | A | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+5990G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139243087 | |||||||
chr7:139243292 | G | GT | 8 | a0001c0001t0001g0194a0001c0001t0002g0195a0001c0001t0002g0229others(5): Show | 8 | HG01256.hp1 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+6204dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139243292 | ||||||
chr7:139243973 | TG | T | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+6879delG | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139243973 | ||||||
chr7:139244164 | A | G | 2 | a0001c0001t0024g0222a0001c0001t0024g0223 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.561+7067A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244164 | |||||||
chr7:139244277 | A | C | 1 | a0001c0001t0003g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.561+7180A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244277 | |||||||
chr7:139244280 | C | T | 1 | a0001c0002t0016g0110 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.561+7183C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244280 | |||||||
chr7:139244347 | G | A | 119 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(116): Show | 121 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(118): Show |
intron_variant | MODIFIER | c.561+7250G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244347 | |||||||
chr7:139244562 | A | G | 1 | a0001c0002t0047g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.562-7394A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244562 | |||||||
chr7:139244622 | C | G | 1 | a0001c0001t0006g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.562-7334C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244622 | |||||||
chr7:139244642 | C | G | 1 | a0001c0001t0001g0010 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.562-7314C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244642 | |||||||
chr7:139244788 | A | G | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-7168A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244788 | |||||||
chr7:139244942 | A | G | 4 | a0001c0001t0021g0136a0001c0001t0021g0138a0001c0001t0021g0141others(1): Show | 4 | HG01074.hp2 HG01109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-7014A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139244942 | |||||||
chr7:139245073 | A | G | 1 | a0001c0002t0023g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.562-6883A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139245073 | |||||||
chr7:139245097 | C | CT | 32 | a0001c0001t0001g0191a0001c0001t0001g0210a0001c0001t0002g0192others(29): Show | 32 | HG00597.hp2 HG01433.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.562-6835dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139245097 | ||||||
chr7:139245097 | C | CTT | 50 | a0001c0001t0002g0161a0001c0001t0005g0031a0001c0001t0014g0005others(47): Show | 50 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.562-6836_562-6835d others(4): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139245097 | ||||||
chr7:139245097 | C | CTTT | 13 | a0001c0001t0034g0122a0001c0001t0035g0119a0001c0001t0035g0121others(10): Show | 13 | HG01943.hp1 HG02300.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.562-6837_562-6835d others(5): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139245097 | ||||||
chr7:139245411 | T | A | 9 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(6): Show | 10 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-6545T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139245411 | |||||||
chr7:139245424 | C | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.562-6532C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139245424 | |||||||
chr7:139245593 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.562-6363A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139245593 | |||||||
chr7:139245859 | G | C | 18 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(15): Show | 18 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.562-6097G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139245859 | |||||||
chr7:139245936 | T | A | 1 | a0001c0001t0044g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.562-6020T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139245936 | |||||||
chr7:139246042 | T | C | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.562-5914T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246042 | |||||||
chr7:139246220 | C | T | 2 | a0001c0002t0007g0107a0001c0002t0007g0108 | 2 | NA18979.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.562-5736C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246220 | |||||||
chr7:139246297 | A | G | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.562-5659A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246297 | |||||||
chr7:139246479 | T | C | 2 | a0001c0001t0042g0125a0001c0002t0105g0145 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.562-5477T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246479 | |||||||
chr7:139246584 | T | C | 1 | a0001c0001t0015g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.562-5372T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246584 | |||||||
chr7:139246591 | G | A | 1 | a0001c0001t0035g0121 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.562-5365G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246591 | |||||||
chr7:139246809 | G | C | 1 | a0001c0001t0036g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.562-5147G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246809 | |||||||
chr7:139246895 | T | C | 19 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(16): Show | 19 | HG01943.hp1 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-5061T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246895 | |||||||
chr7:139246972 | G | A | 1 | a0007c0017t0090g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.562-4984G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139246972 | |||||||
chr7:139247177 | A | G | 53 | a0001c0001t0106g0127a0001c0002t0004g0092a0001c0002t0004g0097others(50): Show | 53 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.562-4779A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139247177 | |||||||
chr7:139247529 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.562-4427C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139247529 | |||||||
chr7:139247678 | A | G | 1 | a0001c0001t0043g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.562-4278A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139247678 | |||||||
chr7:139248145 | G | A | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-3811G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139248145 | |||||||
chr7:139248159 | T | C | 1 | a0001c0001t0062g0065 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.562-3797T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139248159 | |||||||
chr7:139248326 | A | G | 1 | a0001c0002t0047g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.562-3630A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139248326 | |||||||
chr7:139248496 | A | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.562-3460A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139248496 | |||||||
chr7:139248631 | C | T | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-3325C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139248631 | |||||||
chr7:139249010 | C | CTG | 18 | a0001c0001t0001g0231a0001c0001t0014g0038a0001c0001t0015g0048others(15): Show | 19 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.562-2922_562-2921d others(4): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139249010 | ||||||
chr7:139249010 | C | CTGTG | 9 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(6): Show | 10 | HG01891.hp1 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-2924_562-2921d others(6): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139249010 | ||||||
chr7:139249010 | C | CTGTGTG | 6 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-2926_562-2921d others(8): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139249010 | ||||||
chr7:139249010 | C | CTGTGTGT others(1): Show |
48 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0004g0100others(45): Show | 48 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.562-2928_562-2921d others(10): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139249010 | ||||||
chr7:139249010 | C | CTGTGTGT others(3): Show |
3 | a0001c0001t0106g0127a0001c0002t0023g0128a0001c0002t0049g0126 | 3 | HG02622.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.562-2930_562-2921d others(12): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139249010 | ||||||
chr7:139249131 | A | C | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.562-2825A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139249131 | |||||||
chr7:139249214 | G | A | 1 | a0004c0010t0001g0200 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.562-2742G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139249214 | |||||||
chr7:139249737 | G | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.562-2219G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139249737 | |||||||
chr7:139249898 | A | T | 59 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.562-2058A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139249898 | |||||||
chr7:139249937 | G | A | 8 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0070others(5): Show | 8 | NA18940.hp2 NA18969.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-2019G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139249937 | |||||||
chr7:139250481 | G | T | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-1475G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139250481 | |||||||
chr7:139250546 | C | CA | 59 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.562-1397dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139250546 | ||||||
chr7:139250548 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.562-1408A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139250548 | |||||||
chr7:139250566 | C | G | 41 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0150others(38): Show | 44 | HG00099.hp2 HG00597.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.562-1390C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139250566 | |||||||
chr7:139250592 | A | C | 1 | a0001c0002t0055g0147 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.562-1364A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139250592 | |||||||
chr7:139250597 | A | G | 1 | a0001c0001t0088g0075 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.562-1359A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139250597 | |||||||
chr7:139250665 | G | A | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-1291G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139250665 | |||||||
chr7:139250748 | A | G | 1 | a0001c0001t0038g0008 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.562-1208A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139250748 | |||||||
chr7:139250888 | C | G | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-1068C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139250888 | |||||||
chr7:139251028 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.562-928C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251028 | |||||||
chr7:139251066 | C | A | 3 | a0001c0001t0038g0008a0001c0001t0110g0144a0001c0001t0111g0143 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-890C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251066 | |||||||
chr7:139251134 | A | G | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.562-822A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251134 | |||||||
chr7:139251187 | T | A | 14 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(11): Show | 14 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.562-769T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251187 | |||||||
chr7:139251226 | A | G | 6 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(3): Show | 6 | HG02109.hp1 HG02622.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.562-730A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251226 | |||||||
chr7:139251247 | A | G | 1 | a0001c0001t0028g0056 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.562-709A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251247 | |||||||
chr7:139251315 | C | T | 7 | a0002c0003t0007g0082a0002c0003t0007g0084a0002c0003t0017g0085others(4): Show | 7 | HG02015.hp1 HG02300.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-641C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251315 | |||||||
chr7:139251344 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.562-612C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251344 | |||||||
chr7:139251596 | C | T | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-360C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251596 | |||||||
chr7:139251685 | G | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.562-271G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251685 | |||||||
chr7:139251743 | G | T | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-213G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 2/17 | chr7 | 139251743 | |||||||
chr7:139252116 | T | A | 1 | a0001c0001t0076g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.663+59T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139252116 | |||||||
chr7:139252203 | C | CT | 10 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0003g0054others(7): Show | 10 | HG00099.hp1 HG00673.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.663+160dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 139252203 | ||||||
chr7:139252309 | C | G | 7 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0071others(4): Show | 7 | NA18940.hp2 NA18983.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+252C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139252309 | |||||||
chr7:139252431 | A | G | 1 | a0001c0001t0085g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.663+374A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139252431 | |||||||
chr7:139252618 | A | T | 2 | a0001c0002t0047g0123a0001c0002t0061g0124 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.663+561A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139252618 | |||||||
chr7:139252671 | C | T | 4 | a0001c0001t0042g0125a0001c0002t0047g0123a0001c0002t0061g0124others(1): Show | 4 | HG02486.hp2 HG03098.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+614C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139252671 | |||||||
chr7:139252690 | T | C | 4 | a0001c0001t0006g0042a0001c0001t0006g0043a0001c0001t0006g0045others(1): Show | 4 | HG00408.hp1 HG00673.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+633T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139252690 | |||||||
chr7:139253229 | CATCTGGG others(32): Show |
C | 122 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(119): Show | 124 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(121): Show |
intron_variant | MODIFIER | c.663+1212_663+1250d others(41): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 139253229 | ||||||
chr7:139253390 | G | A | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.663+1333G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139253390 | |||||||
chr7:139253796 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.663+1739C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139253796 | |||||||
chr7:139253983 | T | C | 10 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(7): Show | 10 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.663+1926T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139253983 | |||||||
chr7:139254022 | G | A | 18 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(15): Show | 18 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.663+1965G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254022 | |||||||
chr7:139254126 | T | A | 1 | a0001c0002t0004g0101 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.663+2069T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254126 | |||||||
chr7:139254170 | G | A | 47 | a0001c0001t0106g0127a0001c0002t0004g0092a0001c0002t0004g0097others(44): Show | 47 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+2113G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254170 | |||||||
chr7:139254225 | G | A | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.663+2168G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254225 | |||||||
chr7:139254266 | C | T | 1 | a0001c0001t0012g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.663+2209C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254266 | |||||||
chr7:139254386 | C | T | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.663+2329C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254386 | |||||||
chr7:139254472 | G | A | 5 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.663+2415G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254472 | |||||||
chr7:139254698 | A | G | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.663+2641A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254698 | |||||||
chr7:139254753 | C | G | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.663+2696C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254753 | |||||||
chr7:139254761 | A | C | 1 | a0001c0001t0001g0010 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.663+2704A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254761 | |||||||
chr7:139254879 | C | T | 1 | a0001c0001t0078g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.663+2822C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254879 | |||||||
chr7:139254919 | G | C | 8 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(5): Show | 8 | HG01943.hp1 HG02145.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+2862G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254919 | |||||||
chr7:139254958 | C | T | 14 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(11): Show | 14 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.663+2901C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139254958 | |||||||
chr7:139255037 | T | C | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.663+2980T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139255037 | |||||||
chr7:139255084 | A | G | 9 | a0001c0002t0004g0101a0001c0002t0004g0106a0001c0002t0004g0115others(6): Show | 9 | HG01081.hp2 HG01123.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.663+3027A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139255084 | |||||||
chr7:139255121 | C | G | 1 | a0001c0001t0003g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.663+3064C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139255121 | |||||||
chr7:139255175 | A | G | 1 | a0001c0001t0003g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.663+3118A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139255175 | |||||||
chr7:139255709 | A | G | 1 | a0003c0006t0089g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.664-2779A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139255709 | |||||||
chr7:139255945 | A | C | 2 | a0001c0001t0003g0064a0001c0001t0109g0076 | 2 | NA19062.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.664-2543A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139255945 | |||||||
chr7:139256018 | G | A | 1 | a0003c0006t0091g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.664-2470G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139256018 | |||||||
chr7:139256043 | A | G | 1 | a0001c0002t0023g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.664-2445A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139256043 | |||||||
chr7:139256248 | C | T | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.664-2240C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139256248 | |||||||
chr7:139256357 | C | G | 1 | a0001c0002t0050g0089 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.664-2131C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139256357 | |||||||
chr7:139256546 | G | A | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.664-1942G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139256546 | |||||||
chr7:139256559 | C | G | 1 | a0001c0001t0062g0065 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.664-1929C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139256559 | |||||||
chr7:139257077 | A | G | 124 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(121): Show | 126 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(123): Show |
intron_variant | MODIFIER | c.664-1411A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139257077 | |||||||
chr7:139257201 | A | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.664-1287A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139257201 | |||||||
chr7:139257401 | T | C | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-1087T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139257401 | |||||||
chr7:139257568 | G | A | 5 | a0001c0001t0001g0196a0001c0001t0034g0120a0001c0001t0034g0122others(2): Show | 5 | HG01943.hp1 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-920G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139257568 | |||||||
chr7:139257577 | A | G | 59 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.664-911A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139257577 | |||||||
chr7:139258032 | C | G | 1 | a0002c0003t0018g0083 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.664-456C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139258032 | |||||||
chr7:139258095 | C | T | 6 | a0001c0002t0055g0147a0001c0002t0056g0132a0001c0002t0057g0131others(3): Show | 6 | HG02451.hp1 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-393C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139258095 | |||||||
chr7:139258461 | C | G | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.664-27C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 3/17 | chr7 | 139258461 | |||||||
chr7:139258721 | G | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.801+96G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 4/17 | chr7 | 139258721 | |||||||
chr7:139258905 | T | A | 24 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(21): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.801+280T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 4/17 | chr7 | 139258905 | |||||||
chr7:139259404 | G | A | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905+34G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139259404 | |||||||
chr7:139259521 | G | A | 1 | a0001c0002t0061g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.905+151G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139259521 | |||||||
chr7:139259631 | T | C | 8 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(5): Show | 8 | HG01943.hp1 HG02145.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.905+261T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139259631 | |||||||
chr7:139259730 | G | A | 1 | a0004c0010t0001g0200 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.905+360G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139259730 | |||||||
chr7:139259832 | C | T | 204 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0150others(201): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.905+462C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139259832 | |||||||
chr7:139259910 | G | A | 1 | a0003c0006t0091g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.905+540G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139259910 | |||||||
chr7:139260118 | A | G | 1 | a0001c0001t0005g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.905+748A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139260118 | |||||||
chr7:139260271 | A | G | 1 | a0001c0002t0105g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.905+901A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139260271 | |||||||
chr7:139260310 | C | A | 1 | a0001c0001t0025g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.905+940C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139260310 | |||||||
chr7:139260317 | C | G | 1 | a0003c0006t0089g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.906-935C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139260317 | |||||||
chr7:139260337 | A | AT | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.906-913dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139260337 | ||||||
chr7:139260380 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.906-872G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139260380 | |||||||
chr7:139260731 | C | G | 59 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.906-521C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139260731 | |||||||
chr7:139260983 | G | C | 57 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(54): Show | 57 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.906-269G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139260983 | |||||||
chr7:139261242 | G | A | 1 | a0001c0001t0034g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-10G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 5/17 | chr7 | 139261242 | |||||||
chr7:139261905 | T | G | 58 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(55): Show | 58 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.1395+164T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139261905 | |||||||
chr7:139261948 | CT | C | 54 | a0001c0001t0037g0027a0001c0001t0042g0125a0001c0001t0106g0127others(51): Show | 54 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1395+223delT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 139261948 | ||||||
chr7:139261985 | G | A | 14 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(11): Show | 14 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395+244G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139261985 | |||||||
chr7:139262025 | C | T | 1 | a0001c0001t0028g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1395+284C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262025 | |||||||
chr7:139262134 | C | T | 4 | a0001c0001t0006g0042a0001c0001t0006g0043a0001c0001t0006g0045others(1): Show | 4 | HG00408.hp1 HG00673.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395+393C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262134 | |||||||
chr7:139262193 | A | G | 59 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1395+452A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262193 | |||||||
chr7:139262222 | C | G | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1395+481C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262222 | |||||||
chr7:139262225 | A | G | 59 | a0001c0001t0042g0125a0001c0001t0106g0127a0001c0002t0004g0092others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1395+484A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262225 | |||||||
chr7:139262539 | T | C | 1 | a0001c0002t0019g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1395+798T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262539 | |||||||
chr7:139262583 | C | T | 1 | a0001c0002t0023g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395+842C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262583 | |||||||
chr7:139262646 | A | G | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1395+905A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262646 | |||||||
chr7:139262671 | G | A | 3 | a0001c0001t0037g0027a0001c0001t0037g0028a0001c0001t0099g0029 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1395+930G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262671 | |||||||
chr7:139262713 | C | CA | 24 | a0001c0001t0001g0233a0001c0001t0002g0001a0001c0001t0002g0179others(21): Show | 27 | HG00099.hp2 HG00741.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1395+988dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 139262713 | ||||||
chr7:139262732 | C | A | 1 | a0002c0003t0017g0085 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1395+991C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262732 | |||||||
chr7:139262753 | C | T | 4 | a0001c0001t0021g0136a0001c0001t0021g0138a0001c0001t0021g0141others(1): Show | 4 | HG01074.hp2 HG01109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+1012C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139262753 | |||||||
chr7:139263191 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1395+1450T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139263191 | |||||||
chr7:139263432 | G | A | 204 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0150others(201): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1395+1691G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139263432 | |||||||
chr7:139263516 | G | A | 2 | a0001c0004t0093g0021a0001c0004t0094g0022 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1395+1775G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139263516 | |||||||
chr7:139263681 | G | A | 1 | a0001c0002t0061g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1395+1940G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139263681 | |||||||
chr7:139263730 | G | A | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1395+1989G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139263730 | |||||||
chr7:139263752 | G | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1395+2011G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139263752 | |||||||
chr7:139263760 | C | T | 5 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(2): Show | 5 | HG02109.hp1 HG03471.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+2019C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139263760 | |||||||
chr7:139263766 | C | CA | 55 | a0001c0001t0001g0243a0001c0001t0003g0153a0001c0001t0081g0214others(52): Show | 55 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.1395+2043dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 139263766 | ||||||
chr7:139263852 | A | G | 38 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0150others(35): Show | 41 | HG00099.hp2 HG00597.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1395+2111A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139263852 | |||||||
chr7:139264074 | T | C | 8 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(5): Show | 8 | HG01943.hp1 HG02145.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396-2259T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264074 | |||||||
chr7:139264139 | C | T | 1 | a0001c0004t0010g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1396-2194C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264139 | |||||||
chr7:139264175 | C | T | 12 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(9): Show | 14 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396-2158C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264175 | |||||||
chr7:139264227 | A | G | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-2106A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264227 | |||||||
chr7:139264404 | A | G | 1 | a0001c0001t0029g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1396-1929A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264404 | |||||||
chr7:139264420 | T | C | 7 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0071others(4): Show | 7 | NA18940.hp2 NA18983.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-1913T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264420 | |||||||
chr7:139264517 | A | G | 6 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(3): Show | 6 | HG02109.hp1 HG02622.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-1816A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264517 | |||||||
chr7:139264532 | T | C | 3 | a0001c0001t0038g0008a0001c0001t0110g0144a0001c0001t0111g0143 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1801T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264532 | |||||||
chr7:139264697 | T | C | 2 | a0001c0001t0001g0191a0001c0001t0085g0178 | 2 | HG01074.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1396-1636T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264697 | |||||||
chr7:139264865 | T | G | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1396-1468T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139264865 | |||||||
chr7:139265027 | A | G | 1 | a0007c0017t0090g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1396-1306A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139265027 | |||||||
chr7:139265193 | T | C | 1 | a0001c0001t0070g0224 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1396-1140T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139265193 | |||||||
chr7:139265388 | G | A | 5 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-945G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139265388 | |||||||
chr7:139265473 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1396-860G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139265473 | |||||||
chr7:139265546 | A | C | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1396-787A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139265546 | |||||||
chr7:139266177 | G | A | 1 | a0001c0015t0032g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1396-156G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139266177 | |||||||
chr7:139266195 | C | T | 1 | a0001c0002t0057g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1396-138C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139266195 | |||||||
chr7:139266226 | C | CA | 24 | a0001c0001t0001g0167a0001c0001t0001g0233a0001c0001t0003g0074others(21): Show | 25 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1396-88dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 139266226 | ||||||
chr7:139266226 | CA | C | 5 | a0001c0001t0001g0165a0001c0001t0024g0222a0001c0001t0037g0027others(2): Show | 5 | HG02698.hp1 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-88delA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 139266226 | ||||||
chr7:139266242 | A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0165 | 2 | NA18946.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1396-91A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139266242 | |||||||
chr7:139266246 | G | A | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-87G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139266246 | |||||||
chr7:139266310 | T | G | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1396-23T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 6/17 | chr7 | 139266310 | |||||||
chr7:139266621 | C | G | 3 | a0001c0002t0008g0189a0001c0002t0011g0188a0001c0002t0011g0193 | 3 | NA18962.hp1 NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1466+218C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139266621 | |||||||
chr7:139266627 | C | T | 3 | a0001c0001t0038g0008a0001c0001t0110g0144a0001c0001t0111g0143 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466+224C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139266627 | |||||||
chr7:139266699 | A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0165 | 2 | NA18946.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1466+296A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139266699 | |||||||
chr7:139267028 | C | T | 1 | a0001c0012t0001g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1466+625C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139267028 | |||||||
chr7:139267408 | C | T | 13 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(10): Show | 13 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1466+1005C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139267408 | |||||||
chr7:139267453 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1466+1050T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139267453 | |||||||
chr7:139267536 | C | CA | 8 | a0001c0001t0001g0231a0001c0001t0042g0125a0001c0001t0043g0079others(5): Show | 8 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1466+1146dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139267536 | ||||||
chr7:139267550 | G | A | 4 | a0001c0001t0042g0125a0001c0002t0047g0123a0001c0002t0061g0124others(1): Show | 4 | HG01243.hp2 HG03098.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1466+1147G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139267550 | |||||||
chr7:139267608 | C | T | 5 | a0001c0001t0042g0125a0001c0002t0047g0123a0001c0002t0061g0124others(2): Show | 5 | HG01243.hp2 HG02486.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1466+1205C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139267608 | |||||||
chr7:139267954 | C | A | 41 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0161others(38): Show | 45 | HG00099.hp2 HG00597.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1467-1440C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139267954 | |||||||
chr7:139268549 | G | A | 1 | a0001c0001t0040g0215 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1467-845G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139268549 | |||||||
chr7:139268586 | C | T | 45 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0150others(42): Show | 50 | HG00099.hp2 HG00597.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.1467-808C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139268586 | |||||||
chr7:139268778 | C | G | 2 | a0001c0004t0010g0016a0001c0004t0010g0017 | 2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1467-616C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139268778 | |||||||
chr7:139269077 | C | T | 1 | a0001c0001t0035g0119 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1467-317C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139269077 | |||||||
chr7:139269157 | C | T | 1 | a0003c0006t0091g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1467-237C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139269157 | |||||||
chr7:139269264 | C | T | 1 | a0001c0001t0003g0067 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1467-130C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 7/17 | chr7 | 139269264 | |||||||
chr7:139269700 | A | G | 5 | a0001c0001t0031g0164a0001c0001t0031g0234a0001c0001t0040g0215others(2): Show | 5 | HG02615.hp2 HG03139.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+177A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139269700 | |||||||
chr7:139269711 | T | G | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+188T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139269711 | |||||||
chr7:139269729 | T | A | 4 | a0001c0001t0002g0001a0001c0001t0002g0195a0001c0001t0002g0206others(1): Show | 7 | HG01255.hp2 HG01256.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+206T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139269729 | |||||||
chr7:139269742 | G | A | 1 | a0001c0001t0005g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1596+219G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139269742 | |||||||
chr7:139269742 | G | T | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+219G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139269742 | |||||||
chr7:139269908 | G | C | 3 | a0001c0005t0067g0213a0001c0005t0073g0149a0001c0005t0074g0211 | 3 | HG01243.hp1 HG01361.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1596+385G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139269908 | |||||||
chr7:139269965 | C | G | 2 | a0001c0001t0042g0125a0008c0008t0063g0015 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1596+442C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139269965 | |||||||
chr7:139269971 | C | G | 1 | a0001c0001t0006g0045 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1596+448C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139269971 | |||||||
chr7:139270249 | T | C | 40 | a0001c0001t0001g0010a0001c0001t0003g0070a0001c0002t0004g0092others(37): Show | 41 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1596+726T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270249 | |||||||
chr7:139270270 | C | CT | 5 | a0001c0001t0001g0210a0001c0001t0034g0120a0001c0001t0040g0215others(2): Show | 5 | HG02145.hp2 HG02738.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+766dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 139270270 | ||||||
chr7:139270273 | T | C | 1 | a0001c0001t0003g0157 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1596+750T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270273 | |||||||
chr7:139270289 | T | G | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+766T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270289 | |||||||
chr7:139270349 | A | G | 5 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(2): Show | 5 | HG02109.hp1 HG03471.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+826A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270349 | |||||||
chr7:139270401 | T | C | 1 | a0001c0001t0003g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1596+878T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270401 | |||||||
chr7:139270539 | G | A | 1 | a0006c0018t0004g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+1016G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270539 | |||||||
chr7:139270692 | A | C | 1 | a0005c0016t0041g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1596+1169A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270692 | |||||||
chr7:139270710 | A | C | 54 | a0001c0001t0095g0063a0001c0002t0004g0092a0001c0002t0004g0097others(51): Show | 54 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1596+1187A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270710 | |||||||
chr7:139270727 | G | A | 24 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(21): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596+1204G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270727 | |||||||
chr7:139270779 | C | T | 66 | a0001c0001t0003g0070a0001c0001t0042g0125a0001c0001t0095g0063others(63): Show | 66 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.1596+1256C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139270779 | |||||||
chr7:139271137 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1597-1185A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271137 | |||||||
chr7:139271236 | A | G | 1 | a0001c0001t0080g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1597-1086A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271236 | |||||||
chr7:139271307 | T | G | 1 | a0001c0001t0044g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1597-1015T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271307 | |||||||
chr7:139271351 | C | T | 1 | a0009c0009t0003g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1597-971C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271351 | |||||||
chr7:139271506 | A | G | 1 | a0005c0016t0041g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1597-816A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271506 | |||||||
chr7:139271563 | G | C | 54 | a0001c0001t0106g0127a0001c0002t0004g0092a0001c0002t0004g0097others(51): Show | 54 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1597-759G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271563 | |||||||
chr7:139271603 | G | A | 6 | a0001c0001t0021g0136a0001c0001t0021g0138a0001c0001t0021g0141others(3): Show | 6 | HG01074.hp2 HG01109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-719G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271603 | |||||||
chr7:139271802 | T | C | 1 | a0006c0018t0004g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1597-520T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271802 | |||||||
chr7:139271898 | A | G | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-424A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271898 | |||||||
chr7:139271936 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1597-386A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139271936 | |||||||
chr7:139272090 | C | T | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-232C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139272090 | |||||||
chr7:139272216 | A | C | 2 | a0001c0001t0042g0125a0008c0008t0063g0015 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1597-106A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139272216 | |||||||
chr7:139272289 | T | G | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1597-33T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 8/17 | chr7 | 139272289 | |||||||
chr7:139272483 | G | GTGTATGT others(6): Show |
1 | a0001c0001t0085g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1715+52_1715+64dup others(13): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139272483 | ||||||
chr7:139272494 | T | TTATG | 24 | a0001c0001t0001g0010a0001c0001t0001g0240a0001c0001t0002g0179others(21): Show | 26 | HG00741.hp1 HG01261.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.1715+98_1715+101du others(5): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139272494 | ||||||
chr7:139272494 | T | TTATGTAT others(1): Show |
37 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(34): Show | 37 | HG01167.hp1 HG01243.hp2 HG01943.hp1 others(34): Show |
intron_variant | MODIFIER | c.1715+94_1715+101du others(9): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139272494 | ||||||
chr7:139272494 | T | TTATGTAT others(5): Show |
43 | a0001c0001t0015g0026a0001c0001t0020g0007a0001c0001t0020g0142others(40): Show | 44 | HG00140.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1715+90_1715+101du others(13): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139272494 | ||||||
chr7:139272494 | T | TTATGTAT others(9): Show |
6 | a0001c0001t0021g0141a0001c0001t0078g0148a0001c0002t0004g0092others(3): Show | 6 | HG02257.hp1 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1715+86_1715+101du others(17): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139272494 | ||||||
chr7:139272494 | T | TTATGTAT others(13): Show |
1 | a0001c0002t0105g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1715+82_1715+101du others(21): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139272494 | ||||||
chr7:139272494 | TTATG | T | 25 | a0001c0001t0001g0232a0001c0001t0005g0004a0001c0001t0005g0012others(22): Show | 25 | HG00408.hp1 HG00673.hp2 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.1715+98_1715+101de others(5): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139272494 | ||||||
chr7:139272514 | G | A | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1715+74G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | chr7 | 139272514 | |||||||
chr7:139272519 | T | TATGTATG others(5): Show |
1 | a0001c0002t0011g0091 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1715+90_1715+91ins others(12): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139272519 | ||||||
chr7:139272673 | C | T | 1 | a0001c0001t0029g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1715+233C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | chr7 | 139272673 | |||||||
chr7:139272787 | A | G | 1 | a0001c0001t0107g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1715+347A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | chr7 | 139272787 | |||||||
chr7:139272807 | G | A | 3 | a0001c0001t0038g0008a0001c0001t0110g0144a0001c0001t0111g0143 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1715+367G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 9/17 | chr7 | 139272807 | |||||||
chr7:139273442 | A | G | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1829+32A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 10/17 | chr7 | 139273442 | |||||||
chr7:139273461 | C | G | 1 | a0001c0001t0015g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1829+51C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 10/17 | chr7 | 139273461 | |||||||
chr7:139273718 | C | T | 3 | a0001c0002t0055g0147a0001c0002t0058g0130a0001c0002t0059g0133 | 3 | HG02451.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1830-213C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 10/17 | chr7 | 139273718 | |||||||
chr7:139274160 | A | G | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1973+86A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139274160 | |||||||
chr7:139274265 | A | G | 19 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(16): Show | 19 | HG00408.hp1 HG00673.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1973+191A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139274265 | |||||||
chr7:139274450 | C | T | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973+376C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139274450 | |||||||
chr7:139274601 | A | G | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1973+527A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139274601 | |||||||
chr7:139274884 | A | G | 62 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(59): Show | 62 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.1973+810A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139274884 | |||||||
chr7:139275069 | G | T | 2 | a0001c0001t0024g0222a0001c0001t0024g0223 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1973+995G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139275069 | |||||||
chr7:139275134 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1974-963T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139275134 | |||||||
chr7:139275277 | C | CA | 20 | a0001c0001t0001g0194a0001c0001t0001g0243a0001c0001t0002g0186others(17): Show | 21 | HG00673.hp2 HG01261.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.1974-798dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 139275277 | ||||||
chr7:139275277 | CA | C | 6 | a0001c0001t0001g0011a0001c0001t0037g0028a0001c0001t0097g0183others(3): Show | 7 | HG02897.hp2 HG03041.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.1974-798delA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 139275277 | ||||||
chr7:139275366 | G | A | 1 | a0001c0002t0047g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1974-731G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139275366 | |||||||
chr7:139275582 | C | CA | 9 | a0001c0001t0001g0243a0001c0001t0003g0064a0001c0001t0006g0045others(6): Show | 9 | HG01167.hp2 HG02109.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1974-503dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 139275582 | ||||||
chr7:139275835 | C | T | 12 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(9): Show | 14 | HG01074.hp2 HG01109.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1974-262C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139275835 | |||||||
chr7:139276015 | T | C | 54 | a0001c0001t0106g0127a0001c0002t0004g0092a0001c0002t0004g0097others(51): Show | 54 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1974-82T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139276015 | |||||||
chr7:139276033 | TAAAAC | T | 9 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(6): Show | 10 | HG01074.hp2 HG01109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1974-61_1974-57del others(5): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 139276033 | ||||||
chr7:139276047 | T | C | 63 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(60): Show | 63 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.1974-50T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139276047 | |||||||
chr7:139276051 | A | G | 1 | a0001c0004t0093g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1974-46A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 11/17 | chr7 | 139276051 | |||||||
chr7:139276445 | C | T | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2024+298C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139276445 | |||||||
chr7:139276544 | G | A | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2024+397G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139276544 | |||||||
chr7:139276553 | C | T | 12 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0008g0003others(9): Show | 12 | NA18612.hp1 NA18940.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.2024+406C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139276553 | |||||||
chr7:139276710 | A | G | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0192 | 3 | HG03017.hp1 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2024+563A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139276710 | |||||||
chr7:139276777 | A | G | 7 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0071others(4): Show | 7 | NA18940.hp2 NA18983.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.2024+630A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139276777 | |||||||
chr7:139276989 | A | G | 123 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(120): Show | 125 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.2024+842A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139276989 | |||||||
chr7:139277070 | A | G | 1 | a0007c0017t0090g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2024+923A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139277070 | |||||||
chr7:139277206 | C | T | 1 | a0001c0001t0024g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2024+1059C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139277206 | |||||||
chr7:139277254 | C | T | 56 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0004g0100others(53): Show | 56 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.2024+1107C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139277254 | |||||||
chr7:139277293 | C | T | 1 | a0001c0001t0106g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2024+1146C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139277293 | |||||||
chr7:139277391 | A | T | 1 | a0001c0001t0064g0013 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2024+1244A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139277391 | |||||||
chr7:139277515 | T | C | 1 | a0003c0006t0091g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2024+1368T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139277515 | |||||||
chr7:139277576 | G | C | 1 | a0001c0001t0088g0075 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2024+1429G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139277576 | |||||||
chr7:139277900 | A | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2025-1418A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139277900 | |||||||
chr7:139278042 | G | A | 58 | a0001c0001t0042g0125a0001c0002t0004g0092a0001c0002t0004g0097others(55): Show | 58 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.2025-1276G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139278042 | |||||||
chr7:139278181 | C | CT | 17 | a0001c0001t0001g0210a0001c0001t0001g0243a0001c0001t0002g0163others(14): Show | 17 | HG01123.hp1 HG01167.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2025-1119dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139278181 | ||||||
chr7:139278506 | A | C | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2025-812A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139278506 | |||||||
chr7:139278506 | A | G | 6 | a0001c0001t0005g0004a0001c0001t0005g0031a0001c0001t0005g0033others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2025-812A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139278506 | |||||||
chr7:139278617 | T | TC | 3 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0026g0023 | 3 | HG02109.hp2 HG02976.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2025-701_2025-700i others(3): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139278617 | |||||||
chr7:139278618 | A | C | 206 | a0001c0001t0001g0152a0001c0001t0001g0212a0001c0001t0001g0216others(203): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2025-700A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139278618 | |||||||
chr7:139278955 | T | G | 1 | a0001c0002t0048g0104 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2025-363T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139278955 | |||||||
chr7:139279050 | C | T | 123 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(120): Show | 125 | HG00140.hp2 HG00408.hp1 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.2025-268C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139279050 | |||||||
chr7:139279191 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2025-127C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 12/17 | chr7 | 139279191 | |||||||
chr7:139279410 | A | T | 2 | a0001c0001t0042g0125a0008c0008t0063g0015 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2067+50A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139279410 | |||||||
chr7:139279561 | T | C | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2067+201T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139279561 | |||||||
chr7:139280119 | T | C | 1 | a0001c0001t0075g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2067+759T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280119 | |||||||
chr7:139280174 | T | C | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2067+814T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280174 | |||||||
chr7:139280260 | A | G | 4 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(1): Show | 4 | HG03471.hp2 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2067+900A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280260 | |||||||
chr7:139280276 | T | C | 1 | a0001c0001t0107g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2067+916T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280276 | |||||||
chr7:139280419 | A | C | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2067+1059A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280419 | |||||||
chr7:139280450 | C | T | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2067+1090C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280450 | |||||||
chr7:139280682 | A | G | 11 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(8): Show | 11 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2067+1322A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280682 | |||||||
chr7:139280727 | C | T | 7 | a0001c0004t0010g0016a0001c0004t0010g0017a0001c0004t0010g0018others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2068-1278C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280727 | |||||||
chr7:139280928 | G | C | 3 | a0001c0002t0008g0189a0001c0002t0011g0188a0001c0002t0011g0193 | 3 | NA18962.hp1 NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2068-1077G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280928 | |||||||
chr7:139280935 | T | G | 1 | a0001c0001t0014g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2068-1070T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139280935 | |||||||
chr7:139281193 | T | C | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068-812T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139281193 | |||||||
chr7:139281198 | G | A | 60 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(57): Show | 62 | HG00408.hp1 HG00673.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.2068-807G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139281198 | |||||||
chr7:139281223 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2068-782C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139281223 | |||||||
chr7:139281284 | T | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2068-721T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139281284 | |||||||
chr7:139281508 | G | A | 62 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(59): Show | 64 | HG00408.hp1 HG00673.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.2068-497G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139281508 | |||||||
chr7:139281597 | T | C | 1 | a0001c0001t0005g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2068-408T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139281597 | |||||||
chr7:139281707 | G | A | 1 | a0001c0001t0043g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2068-298G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 13/17 | chr7 | 139281707 | |||||||
chr7:139282320 | C | T | 3 | a0001c0001t0038g0008a0001c0001t0110g0144a0001c0001t0111g0143 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2118+265C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282320 | |||||||
chr7:139282380 | G | A | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2118+325G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282380 | |||||||
chr7:139282406 | T | C | 2 | a0001c0001t0042g0125a0008c0008t0063g0015 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2118+351T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282406 | |||||||
chr7:139282482 | T | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2118+427T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282482 | |||||||
chr7:139282489 | G | A | 16 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(13): Show | 16 | HG01943.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.2118+434G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282489 | |||||||
chr7:139282503 | G | A | 1 | a0001c0002t0017g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2118+448G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282503 | |||||||
chr7:139282539 | G | A | 56 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0004g0100others(53): Show | 56 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.2118+484G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282539 | |||||||
chr7:139282632 | C | T | 24 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(21): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2119-392C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282632 | |||||||
chr7:139282707 | A | C | 1 | a0007c0017t0090g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2119-317A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282707 | |||||||
chr7:139282874 | C | T | 1 | a0001c0001t0078g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2119-150C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 14/17 | chr7 | 139282874 | |||||||
chr7:139284591 | C | T | 1 | a0001c0001t0072g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3669+17C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139284591 | |||||||
chr7:139284735 | A | T | 1 | a0001c0001t0028g0056 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3669+161A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139284735 | |||||||
chr7:139284958 | C | T | 2 | a0001c0001t0024g0222a0001c0001t0024g0223 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3669+384C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139284958 | |||||||
chr7:139284966 | C | T | 24 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(21): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.3669+392C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139284966 | |||||||
chr7:139285088 | A | G | 1 | a0007c0017t0090g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3669+514A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285088 | |||||||
chr7:139285183 | A | G | 1 | a0001c0001t0009g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3669+609A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285183 | |||||||
chr7:139285208 | A | G | 2 | a0003c0006t0089g0049a0003c0006t0091g0032 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3669+634A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285208 | |||||||
chr7:139285382 | T | C | 1 | a0001c0001t0044g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3669+808T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285382 | |||||||
chr7:139285427 | G | A | 58 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0002t0004g0092others(55): Show | 58 | HG01081.hp2 HG01109.hp2 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.3669+853G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285427 | |||||||
chr7:139285578 | T | C | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3669+1004T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285578 | |||||||
chr7:139285788 | G | A | 3 | a0001c0001t0037g0027a0001c0001t0037g0028a0001c0001t0099g0029 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3669+1214G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285788 | |||||||
chr7:139285803 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3669+1229C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285803 | |||||||
chr7:139285939 | A | T | 3 | a0001c0001t0037g0027a0001c0001t0037g0028a0001c0001t0099g0029 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3669+1365A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285939 | |||||||
chr7:139285964 | G | T | 1 | a0001c0001t0027g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3669+1390G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139285964 | |||||||
chr7:139286325 | A | G | 1 | a0001c0001t0107g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3669+1751A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139286325 | |||||||
chr7:139286631 | G | A | 1 | a0001c0004t0094g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3669+2057G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139286631 | |||||||
chr7:139286952 | C | T | 2 | a0001c0001t0001g0191a0001c0001t0085g0178 | 2 | HG01074.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.3669+2378C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139286952 | |||||||
chr7:139287022 | G | A | 1 | a0001c0001t0015g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3669+2448G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139287022 | |||||||
chr7:139287113 | A | C | 14 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(11): Show | 14 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.3669+2539A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139287113 | |||||||
chr7:139287199 | G | A | 8 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3669+2625G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139287199 | |||||||
chr7:139287278 | A | C | 1 | a0005c0016t0041g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3669+2704A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139287278 | |||||||
chr7:139287669 | CT | C | 76 | a0001c0001t0001g0166a0001c0001t0003g0050a0001c0001t0003g0051others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.3669+3111delT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139287669 | ||||||
chr7:139287746 | T | C | 1 | a0001c0001t0042g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3669+3172T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139287746 | |||||||
chr7:139287776 | A | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3669+3202A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139287776 | |||||||
chr7:139287829 | A | G | 2 | a0001c0001t0043g0079a0001c0001t0044g0024 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3669+3255A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139287829 | |||||||
chr7:139287840 | AC | A | 12 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(9): Show | 14 | HG01074.hp2 HG01109.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3669+3267delC | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139287840 | |||||||
chr7:139288188 | G | C | 1 | a0001c0002t0046g0112 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3669+3614G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288188 | |||||||
chr7:139288205 | G | A | 1 | a0001c0001t0044g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3669+3631G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288205 | |||||||
chr7:139288373 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3669+3799A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288373 | |||||||
chr7:139288445 | A | C | 1 | a0001c0001t0107g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3669+3871A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288445 | |||||||
chr7:139288505 | A | C | 2 | a0001c0001t0043g0079a0001c0001t0044g0024 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3669+3931A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288505 | |||||||
chr7:139288648 | T | C | 1 | a0001c0004t0010g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3669+4074T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288648 | |||||||
chr7:139288653 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3669+4079G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288653 | |||||||
chr7:139288697 | G | C | 1 | a0001c0001t0012g0220 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3669+4123G>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288697 | |||||||
chr7:139288791 | C | G | 1 | a0005c0016t0041g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3669+4217C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288791 | |||||||
chr7:139288838 | C | A | 7 | a0001c0001t0021g0136a0001c0001t0021g0138a0001c0001t0021g0141others(4): Show | 7 | HG01074.hp2 HG01109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3669+4264C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139288838 | |||||||
chr7:139289000 | C | CA | 29 | a0001c0001t0001g0152a0001c0001t0001g0243a0001c0001t0002g0185others(26): Show | 30 | HG00609.hp1 HG01074.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.3670-4212dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289000 | ||||||
chr7:139289000 | C | CAA | 32 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(29): Show | 33 | HG00408.hp1 HG00673.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.3670-4213_3670-421 others(6): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289000 | ||||||
chr7:139289015 | A | G | 1 | a0001c0001t0003g0071 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3670-4217A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289015 | |||||||
chr7:139289414 | C | CT | 10 | a0001c0001t0001g0210a0001c0001t0001g0233a0001c0001t0002g0161others(7): Show | 10 | HG01943.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.3670-3802dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(3): Show |
4 | a0001c0002t0049g0126a0001c0004t0010g0016a0001c0004t0010g0018others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3670-3811_3670-380 others(14): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(4): Show |
5 | a0001c0004t0010g0017a0001c0004t0093g0021a0001c0004t0094g0022others(2): Show | 5 | HG02818.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3670-3812_3670-380 others(15): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0025g0134 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3670-3814_3670-380 others(17): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0025g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3670-3815_3670-380 others(18): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(9): Show |
4 | a0001c0002t0023g0128a0002c0003t0007g0084a0002c0003t0017g0085others(1): Show | 4 | HG06807.hp2 NA18968.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.3670-3817_3670-380 others(20): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(10): Show |
11 | a0001c0002t0004g0115a0001c0002t0007g0098a0001c0002t0008g0189others(8): Show | 11 | HG00140.hp2 HG01167.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3670-3802_3670-380 others(21): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(11): Show |
23 | a0001c0002t0004g0100a0001c0002t0004g0101a0001c0002t0004g0106others(20): Show | 23 | HG01081.hp2 HG01109.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.3670-3802_3670-380 others(22): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(12): Show |
6 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0008g0088others(3): Show | 6 | HG02027.hp1 NA18940.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.3670-3802_3670-380 others(23): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(13): Show |
4 | a0001c0002t0023g0090a0001c0002t0055g0147a0001c0002t0056g0132others(1): Show | 4 | HG02451.hp1 HG02965.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.3670-3802_3670-380 others(24): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(14): Show |
2 | a0001c0002t0008g0095a0001c0002t0059g0133 | 2 | HG03516.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.3670-3802_3670-380 others(25): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(15): Show |
1 | a0001c0002t0057g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3670-3802_3670-380 others(26): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0043g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3670-3802_3670-380 others(28): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(19): Show |
1 | a0001c0002t0060g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3670-3802_3670-380 others(30): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289414 | C | CTTTTTTT others(20): Show |
1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3670-3802_3670-380 others(31): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139289414 | ||||||
chr7:139289447 | C | G | 1 | a0001c0001t0009g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3670-3785C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289447 | |||||||
chr7:139289609 | A | G | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3670-3623A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289609 | |||||||
chr7:139289622 | G | T | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3670-3610G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289622 | |||||||
chr7:139289643 | C | G | 1 | a0001c0001t0003g0071 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3670-3589C>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289643 | |||||||
chr7:139289701 | C | T | 1 | a0001c0001t0006g0042 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3670-3531C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289701 | |||||||
chr7:139289722 | A | G | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3670-3510A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289722 | |||||||
chr7:139289800 | C | T | 1 | a0001c0001t0020g0007 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3670-3432C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289800 | |||||||
chr7:139289815 | A | G | 24 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(21): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.3670-3417A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289815 | |||||||
chr7:139289896 | A | T | 2 | a0001c0001t0024g0222a0001c0001t0024g0223 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3670-3336A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139289896 | |||||||
chr7:139290043 | G | A | 1 | a0001c0001t0006g0046 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3670-3189G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290043 | |||||||
chr7:139290083 | T | A | 10 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(7): Show | 11 | HG01074.hp2 HG01109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3670-3149T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290083 | |||||||
chr7:139290205 | A | T | 59 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.3670-3027A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290205 | |||||||
chr7:139290226 | G | T | 1 | a0001c0001t0015g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3670-3006G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290226 | |||||||
chr7:139290312 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3670-2920A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290312 | |||||||
chr7:139290402 | A | C | 59 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(56): Show | 59 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.3670-2830A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290402 | |||||||
chr7:139290403 | T | C | 5 | a0001c0001t0001g0212a0001c0001t0001g0231a0001c0001t0012g0205others(2): Show | 5 | HG02647.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3670-2829T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290403 | |||||||
chr7:139290423 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3670-2809C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290423 | |||||||
chr7:139290446 | G | A | 8 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3670-2786G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290446 | |||||||
chr7:139290660 | A | T | 1 | a0001c0001t0001g0010 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3670-2572A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290660 | |||||||
chr7:139290698 | T | C | 74 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0120others(71): Show | 74 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(71): Show |
intron_variant | MODIFIER | c.3670-2534T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290698 | |||||||
chr7:139290699 | G | A | 60 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(57): Show | 60 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.3670-2533G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290699 | |||||||
chr7:139290797 | G | A | 1 | a0005c0016t0041g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3670-2435G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290797 | |||||||
chr7:139290873 | T | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3670-2359T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290873 | |||||||
chr7:139290924 | C | T | 1 | a0001c0001t0006g0046 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3670-2308C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139290924 | |||||||
chr7:139291008 | A | T | 1 | a0001c0004t0094g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3670-2224A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139291008 | |||||||
chr7:139291098 | C | T | 1 | a0001c0014t0065g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3670-2134C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139291098 | |||||||
chr7:139291109 | C | T | 6 | a0001c0001t0014g0005a0001c0001t0014g0036a0001c0001t0014g0037others(3): Show | 6 | HG02109.hp1 HG02622.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.3670-2123C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139291109 | |||||||
chr7:139291229 | T | C | 54 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(51): Show | 54 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.3670-2003T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139291229 | |||||||
chr7:139291360 | C | CA | 83 | a0001c0001t0001g0210a0001c0001t0002g0163a0001c0001t0002g0181others(80): Show | 83 | HG01081.hp2 HG01109.hp2 HG01123.hp1 others(80): Show |
intron_variant | MODIFIER | c.3670-1850dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139291360 | ||||||
chr7:139291360 | C | CAA | 10 | a0001c0001t0024g0223a0001c0001t0099g0029a0001c0002t0004g0106others(7): Show | 10 | HG00140.hp2 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.3670-1851_3670-185 others(6): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139291360 | ||||||
chr7:139291360 | CA | C | 11 | a0001c0001t0001g0072a0001c0001t0001g0165a0001c0001t0001g0170others(8): Show | 11 | HG00597.hp1 HG00673.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.3670-1850delA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139291360 | ||||||
chr7:139291538 | T | C | 1 | a0010c0013t0001g0241 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3670-1694T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139291538 | |||||||
chr7:139291863 | T | A | 1 | a0001c0001t0012g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3670-1369T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139291863 | |||||||
chr7:139291873 | T | A | 70 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0042g0125others(67): Show | 70 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.3670-1359T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139291873 | |||||||
chr7:139291990 | A | G | 61 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(58): Show | 61 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.3670-1242A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139291990 | |||||||
chr7:139292057 | C | T | 24 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(21): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.3670-1175C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292057 | |||||||
chr7:139292127 | G | A | 11 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(8): Show | 11 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3670-1105G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292127 | |||||||
chr7:139292131 | G | A | 1 | a0001c0001t0015g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3670-1101G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292131 | |||||||
chr7:139292266 | C | T | 53 | a0001c0002t0004g0092a0001c0002t0004g0097a0001c0002t0004g0100others(50): Show | 53 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.3670-966C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292266 | |||||||
chr7:139292267 | G | A | 3 | a0001c0001t0031g0164a0001c0001t0031g0234a0001c0001t0106g0127 | 3 | HG02615.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3670-965G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292267 | |||||||
chr7:139292320 | A | G | 1 | a0001c0002t0004g0092 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3670-912A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292320 | |||||||
chr7:139292460 | G | A | 71 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0042g0125others(68): Show | 71 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.3670-772G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292460 | |||||||
chr7:139292489 | A | C | 24 | a0001c0001t0006g0002a0001c0001t0006g0039a0001c0001t0006g0042others(21): Show | 24 | HG00408.hp1 HG00673.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.3670-743A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292489 | |||||||
chr7:139292615 | T | A | 3 | a0001c0001t0037g0027a0001c0001t0037g0028a0001c0001t0099g0029 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3670-617T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292615 | |||||||
chr7:139292616 | A | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3670-616A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292616 | |||||||
chr7:139292682 | A | G | 1 | a0001c0001t0038g0008 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3670-550A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292682 | |||||||
chr7:139292707 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3670-525C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292707 | |||||||
chr7:139292930 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3670-302G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139292930 | |||||||
chr7:139293089 | C | T | 8 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(5): Show | 9 | HG01074.hp2 HG01109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3670-143C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139293089 | |||||||
chr7:139293185 | T | A | 1 | a0001c0001t0013g0173 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3670-47T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 15/17 | chr7 | 139293185 | |||||||
chr7:139293572 | G | GT | 6 | a0001c0001t0006g0042a0001c0001t0012g0205a0001c0001t0037g0027others(3): Show | 6 | HG00673.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3901+126dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139293572 | ||||||
chr7:139293572 | GT | G | 72 | a0001c0001t0001g0072a0001c0001t0001g0165a0001c0001t0003g0054others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.3901+126delT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139293572 | ||||||
chr7:139293753 | C | T | 68 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0042g0125others(65): Show | 68 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.3902-136C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 16/17 | chr7 | 139293753 | |||||||
chr7:139293756 | A | T | 1 | a0001c0001t0002g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3902-133A>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 16/17 | chr7 | 139293756 | |||||||
chr7:139293766 | T | C | 1 | a0001c0001t0014g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3902-123T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 16/17 | chr7 | 139293766 | |||||||
chr7:139294175 | A | C | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3994+194A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139294175 | |||||||
chr7:139294217 | C | T | 2 | a0001c0004t0010g0016a0001c0004t0010g0017 | 2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3994+236C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139294217 | |||||||
chr7:139294253 | A | G | 1 | a0001c0001t0077g0172 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3994+272A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139294253 | |||||||
chr7:139294541 | A | G | 1 | a0001c0001t0110g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3994+560A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139294541 | |||||||
chr7:139294757 | C | T | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3994+776C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139294757 | |||||||
chr7:139294771 | G | T | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3994+790G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139294771 | |||||||
chr7:139294887 | A | G | 10 | a0001c0001t0001g0072a0001c0001t0001g0165a0001c0001t0001g0170others(7): Show | 10 | HG00597.hp1 HG00673.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.3994+906A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139294887 | |||||||
chr7:139294966 | C | T | 9 | a0001c0001t0020g0007a0001c0001t0020g0142a0001c0001t0021g0136others(6): Show | 10 | HG01074.hp2 HG01109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3994+985C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139294966 | |||||||
chr7:139295000 | A | C | 60 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(57): Show | 60 | HG00140.hp2 HG01081.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.3994+1019A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295000 | |||||||
chr7:139295082 | G | T | 2 | a0001c0001t0014g0005a0001c0001t0101g0005 | 2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3994+1101G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295082 | |||||||
chr7:139295088 | C | CT | 11 | a0001c0001t0002g0229a0001c0001t0020g0007a0001c0001t0020g0142others(8): Show | 12 | HG01361.hp1 HG02015.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.3994+1123dupT | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 139295088 | ||||||
chr7:139295118 | AAAATG | A | 4 | a0001c0001t0034g0120a0001c0001t0034g0122a0001c0001t0035g0119others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3994+1139_3994+114 others(9): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 139295118 | ||||||
chr7:139295375 | A | AG | 8 | a0001c0001t0005g0004a0001c0001t0005g0012a0001c0001t0005g0030others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3994+1395dupG | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 139295375 | ||||||
chr7:139295393 | T | A | 2 | a0003c0006t0089g0049a0003c0006t0091g0032 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3994+1412T>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295393 | |||||||
chr7:139295421 | C | T | 1 | a0001c0001t0015g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3994+1440C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295421 | |||||||
chr7:139295446 | C | A | 1 | a0008c0008t0063g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3994+1465C>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295446 | |||||||
chr7:139295695 | G | A | 1 | a0001c0004t0094g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3994+1714G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295695 | |||||||
chr7:139295879 | C | T | 1 | a0001c0001t0012g0226 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3994+1898C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295879 | |||||||
chr7:139295883 | C | T | 1 | a0001c0001t0001g0011 | 2 | NA18939.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.3994+1902C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295883 | |||||||
chr7:139295884 | G | A | 1 | a0001c0001t0006g0043 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3994+1903G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295884 | |||||||
chr7:139295925 | A | C | 1 | a0001c0001t0072g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3995-1862A>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139295925 | |||||||
chr7:139296045 | C | T | 1 | a0001c0001t0075g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3995-1742C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296045 | |||||||
chr7:139296165 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3995-1622G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296165 | |||||||
chr7:139296252 | G | T | 3 | a0001c0001t0037g0027a0001c0001t0037g0028a0001c0001t0099g0029 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3995-1535G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296252 | |||||||
chr7:139296338 | G | A | 4 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(1): Show | 4 | HG02280.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3995-1449G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296338 | |||||||
chr7:139296410 | C | T | 1 | a0002c0003t0018g0083 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3995-1377C>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296410 | |||||||
chr7:139296431 | T | G | 5 | a0001c0001t0009g0235a0001c0001t0009g0236a0001c0001t0009g0237others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3995-1356T>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296431 | |||||||
chr7:139296511 | G | A | 1 | a0001c0002t0018g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3995-1276G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296511 | |||||||
chr7:139296748 | T | C | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3995-1039T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296748 | |||||||
chr7:139296757 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3995-1030G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296757 | |||||||
chr7:139296914 | G | A | 4 | a0001c0001t0042g0125a0001c0001t0043g0079a0001c0001t0044g0024others(1): Show | 4 | HG02280.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3995-873G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296914 | |||||||
chr7:139296919 | G | T | 1 | a0001c0001t0003g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3995-868G>T | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139296919 | |||||||
chr7:139297142 | T | C | 1 | a0001c0002t0105g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3995-645T>C | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139297142 | |||||||
chr7:139297183 | G | A | 3 | a0001c0001t0038g0008a0001c0001t0110g0144a0001c0001t0111g0143 | 4 | HG01891.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3995-604G>A | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139297183 | |||||||
chr7:139297193 | C | CA | 7 | a0001c0001t0002g0197a0001c0001t0003g0064a0001c0001t0003g0156others(4): Show | 7 | HG00741.hp1 HG02027.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.3995-576dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 139297193 | ||||||
chr7:139297201 | AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0105g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3995-585_3995-575d others(13): Show |
UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139297201 | |||||||
chr7:139297385 | C | CA | 11 | a0001c0001t0031g0164a0001c0001t0031g0234a0001c0001t0106g0127others(8): Show | 11 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.3995-389dupA | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 139297385 | ||||||
chr7:139297633 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3995-154A>G | UBN2 | ENSG00000157741.15 | transcript | ENST00000473989.8 | protein_coding | 17/17 | chr7 | 139297633 |