Item | Value |
---|---|
geneid | 6185 |
ensemblid | ENSG00000118705.18 |
hgncid | 10382 |
symbol | RPN2 |
name | ribophorin II |
refseq_nuc | NM_002951.5 |
refseq_prot | NP_002942.2 |
ensembl_nuc | ENST00000237530.11 |
ensembl_prot | ENSP00000237530.6 |
mane_status | MANE Select |
chr | chr20 |
start | 37179330 |
end | 37241619 |
strand | + |
ver | v1.2 |
region | chr20:37179330-37241619 |
region5000 | chr20:37174330-37246619 |
regionname0 | RPN2_chr20_37179330_37241619 |
regionname5000 | RPN2_chr20_37174330_37246619 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 631 | 331 | 75 | 63 | 144 | 12 | 35 | 112 | RPN2_chr20_37174330_37246619 | RPN2 | MAPPG others(626): Show |
chr20 | 37174330 | 37246619 |
a0002 | 0/0 | 631 | 4 | 0 | 0 | 1 | 0 | 3 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | MAPPG others(626): Show |
chr20 | 37174330 | 37246619 |
a0003 | 0/0 | 631 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | MAPPG others(626): Show |
chr20 | 37174330 | 37246619 |
a0004 | 0/0 | 631 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | MAPPG others(626): Show |
chr20 | 37174330 | 37246619 |
a0005 | 0/0 | 631 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | MAPPG others(626): Show |
chr20 | 37174330 | 37246619 |
a0006 | 0/0 | 631 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | MAPPG others(626): Show |
chr20 | 37174330 | 37246619 |
a0007 | 0/0 | 631 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | MAPPG others(626): Show |
chr20 | 37174330 | 37246619 |
a0008 | 0/0 | 631 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | MAPPG others(626): Show |
chr20 | 37174330 | 37246619 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1893 | 199 | 56 | 38 | 71 | 8 | 25 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0001c0002 | 1/0 | 1893 | 129 | 19 | 25 | 70 | 4 | 10 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0001c0004 | 0/0 | 1893 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0002c0003 | 0/0 | 1893 | 4 | 0 | 0 | 1 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0003c0008 | 0/0 | 1893 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0003c0010 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0004c0005 | 0/0 | 1893 | 2 | 0 | 1 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0005c0007 | 0/0 | 1893 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0006c0006 | 0/0 | 1893 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0007c0009 | 0/0 | 1893 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 | ||
a0008c0011 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | ATGGC others(1888): Show |
chr20 | 37174330 | 37246619 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2227 | 198 | 56 | 38 | 71 | 7 | 25 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0001c0001t0002 | 0/0 | 2227 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0001c0002t0001 | 1/0 | 2227 | 129 | 19 | 25 | 70 | 4 | 10 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0001c0004t0001 | 0/0 | 2227 | 3 | 0 | 0 | 3 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0002c0003t0001 | 0/0 | 2227 | 4 | 0 | 0 | 1 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0003c0008t0001 | 0/0 | 2227 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0003c0010t0001 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0004c0005t0001 | 0/0 | 2227 | 2 | 0 | 1 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0005c0007t0001 | 0/0 | 2227 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0006c0006t0001 | 0/0 | 2227 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0007c0009t0001 | 0/0 | 2227 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
a0008c0011t0001 | 0/0 | 2227 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | GGACT others(2222): Show |
chr20 | 37174330 | 37246619 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 21 | 0 | 6 | 12 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0020 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0002 | 0/0 | 17 | 1 | 6 | 7 | 0 | 3 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0003 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0003c0008t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0003c0008t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0003c0010t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0004c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0004c0005t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0005c0007t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0005c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0006c0006t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0007c0009t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
a0008c0011t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0226 | EUR | FIN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0096 | EUR | FIN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00639 | hp2 | a0004 | c0005 | t0001 | g0220 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0045 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0043 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02080 | hp1 | a0001 | c0004 | t0001 | g0156 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | CDX | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02523 | hp2 | a0002 | c0003 | t0001 | g0141 | EAS | KHV | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02615 | hp2 | a0005 | c0007 | t0001 | g0193 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02622 | hp1 | a0003 | c0010 | t0001 | g0131 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0143 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03492 | hp1 | a0002 | c0003 | t0001 | g0128 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03579 | hp2 | a0005 | c0007 | t0001 | g0194 | AFR | MSL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04184 | hp1 | a0007 | c0009 | t0001 | g0227 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04204 | hp1 | a0002 | c0003 | t0001 | g0129 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18747 | hp2 | a0003 | c0008 | t0001 | g0052 | EAS | CHB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18954 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19003 | hp2 | a0003 | c0008 | t0001 | g0084 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19012 | hp1 | a0008 | c0011 | t0001 | g0176 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19067 | hp1 | a0006 | c0006 | t0001 | g0009 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19076 | hp1 | a0001 | c0004 | t0001 | g0173 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19088 | hp2 | a0006 | c0006 | t0001 | g0009 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | TSI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0076 | EUR | TSI | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA20905 | hp1 | a0004 | c0005 | t0001 | g0219 | SAS | GIH | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | USA | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | LWK | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0098 | REF | REF | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0171 | REF | REF | RPN2_chr20_37174330_37246619 | RPN2 | chr20 | 37174330 | 37246619 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:37184332 | G | A | 1 | a0007 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.166G>A | p.Val56Met | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/17 | 193/2227 | 166/1896 | 56/631 | chr20 | 37184332 | |||
chr20:37199103 | C | G | 1 | a0008 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.357C>G | p.Asp119Glu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/17 | 384/2227 | 357/1896 | 119/631 | chr20 | 37199103 | |||
chr20:37207423 | G | A | 1 | a0004 | 2 | HG00639.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.841G>A | p.Asp281Asn | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/17 | 868/2227 | 841/1896 | 281/631 | chr20 | 37207423 | |||
chr20:37223906 | G | A | 1 | a0002 | 4 | HG02523.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
missense_variant | MODERATE | c.1121G>A | p.Gly374Asp | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/17 | 1148/2227 | 1121/1896 | 374/631 | chr20 | 37223906 | |||
chr20:37228577 | A | T | 1 | a0006 | 2 | NA19067.hp1 NA19088.hp2 |
missense_variant | MODERATE | c.1327A>T | p.Thr443Ser | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/17 | 1354/2227 | 1327/1896 | 443/631 | chr20 | 37228577 | |||
chr20:37228622 | G | A | 1 | a0003 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1372G>A | p.Val458Met | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/17 | 1399/2227 | 1372/1896 | 458/631 | chr20 | 37228622 | |||
chr20:37228622 | G | T | 1 | a0003 | 2 | NA18747.hp2 NA19003.hp2 |
missense_variant | MODERATE | c.1372G>T | p.Val458Leu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/17 | 1399/2227 | 1372/1896 | 458/631 | chr20 | 37228622 | |||
chr20:37229979 | G | T | 1 | a0005 | 2 | HG02615.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.1501G>T | p.Val501Leu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/17 | 1528/2227 | 1501/1896 | 501/631 | chr20 | 37229979 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:37228576 | G | A | 1 | a0006c0006 | 2 | NA19067.hp1 NA19088.hp2 |
synonymous_variant | LOW | c.1326G>A | p.Lys442Lys | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/17 | 1353/2227 | 1326/1896 | 442/631 | chr20 | 37228576 | |||
chr20:37232377 | C | T | 1 | a0001c0004 | 3 | HG02080.hp1 NA18954.hp2 NA19076.hp1 |
synonymous_variant | LOW | c.1663C>T | p.Leu555Leu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/17 | 1690/2227 | 1663/1896 | 555/631 | chr20 | 37232377 | |||
chr20:37236651 | C | T | 9 | a0001c0001 a0001c0004 a0002c0003 others(6): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
synonymous_variant | LOW | c.1825C>T | p.Leu609Leu | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/17 | 1852/2227 | 1825/1896 | 609/631 | chr20 | 37236651 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:37241413 | A | G | 1 | a0001c0001t0002 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 17/17 | 98 | chr20 | 37241413 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:37179387 | G | GCTTACAG others(22): Show |
61 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0004 others(58): Show |
96 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.13+21_13+22insACAG others(25): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37179387 | ||||||
chr20:37179394 | GGA | G | 4 | a0001c0002t0001g0012 a0001c0002t0001g0042 a0001c0002t0001g0244 others(1): Show |
7 | HG00609.hp2 HG02738.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+29_13+30delAG | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37179394 | ||||||
chr20:37179449 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.13+80C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179449 | |||||||
chr20:37179610 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(8): Show |
18 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+241C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179610 | |||||||
chr20:37179804 | C | T | 67 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(64): Show |
84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.13+435C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179804 | |||||||
chr20:37179821 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.13+452G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179821 | |||||||
chr20:37179882 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
28 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.13+513A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37179882 | |||||||
chr20:37180031 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.13+662G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180031 | |||||||
chr20:37180151 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.13+782C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180151 | |||||||
chr20:37180173 | C | T | 8 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
8 | HG00609.hp1 HG00738.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.13+804C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180173 | |||||||
chr20:37180220 | C | G | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(66): Show |
86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.13+851C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180220 | |||||||
chr20:37180410 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
10 | HG01361.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.13+1041T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180410 | |||||||
chr20:37180576 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.13+1207G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180576 | |||||||
chr20:37180614 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13+1245C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180614 | |||||||
chr20:37180819 | T | G | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.13+1450T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180819 | |||||||
chr20:37180893 | T | C | 3 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 |
3 | HG01074.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.13+1524T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180893 | |||||||
chr20:37180920 | C | T | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.13+1551C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37180920 | |||||||
chr20:37181005 | C | T | 67 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(64): Show |
84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.13+1636C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181005 | |||||||
chr20:37181047 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.13+1678G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181047 | |||||||
chr20:37181076 | A | C | 1 | a0008c0011t0001g0176 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.13+1707A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181076 | |||||||
chr20:37181099 | C | T | 63 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(60): Show |
80 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.13+1730C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181099 | |||||||
chr20:37181178 | G | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(64): Show |
84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.13+1809G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181178 | |||||||
chr20:37181209 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.13+1840C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181209 | |||||||
chr20:37181226 | TA | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(6): Show |
11 | HG01361.hp2 HG01934.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.13+1871delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181226 | ||||||
chr20:37181380 | T | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(66): Show |
86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.13+2011T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181380 | |||||||
chr20:37181421 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13+2052T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181421 | |||||||
chr20:37181431 | C | CT | 9 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0104 others(6): Show |
11 | HG00323.hp2 HG02280.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.13+2080dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181431 | ||||||
chr20:37181431 | CT | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): Show |
61 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.13+2080delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181431 | ||||||
chr20:37181431 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.13+2069_13+2080del others(12): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181431 | ||||||
chr20:37181577 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.13+2208G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181577 | |||||||
chr20:37181769 | T | C | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.13+2400T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181769 | |||||||
chr20:37181882 | T | C | 2 | a0004c0005t0001g0219 a0004c0005t0001g0220 |
2 | HG00639.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.14-2298T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181882 | |||||||
chr20:37181912 | G | GTTC | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.14-2266_14-2265ins others(3): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37181912 | ||||||
chr20:37181943 | A | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
146 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.14-2237A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181943 | |||||||
chr20:37181969 | T | C | 77 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0016 others(74): Show |
96 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.14-2211T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37181969 | |||||||
chr20:37182159 | T | A | 3 | a0001c0002t0001g0015 a0001c0002t0001g0101 a0001c0002t0001g0102 |
4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-2021T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182159 | |||||||
chr20:37182160 | C | A | 3 | a0001c0002t0001g0015 a0001c0002t0001g0101 a0001c0002t0001g0102 |
4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-2020C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182160 | |||||||
chr20:37182178 | C | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0103 others(7): Show |
12 | HG01361.hp2 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.14-2002C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182178 | |||||||
chr20:37182362 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.14-1818G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182362 | |||||||
chr20:37182550 | C | T | 2 | a0001c0002t0001g0046 a0001c0002t0001g0094 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.14-1630C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182550 | |||||||
chr20:37182638 | G | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(64): Show |
84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.14-1542G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182638 | |||||||
chr20:37182664 | G | A | 63 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(60): Show |
80 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.14-1516G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182664 | |||||||
chr20:37182686 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.14-1494C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182686 | |||||||
chr20:37182773 | G | A | 6 | a0001c0002t0001g0028 a0001c0002t0001g0047 a0001c0002t0001g0167 others(3): Show |
7 | HG00741.hp2 HG01167.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.14-1407G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182773 | |||||||
chr20:37182971 | T | C | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.14-1209T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37182971 | |||||||
chr20:37183083 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.14-1097G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183083 | |||||||
chr20:37183219 | A | AT | 77 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0016 others(74): Show |
96 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.14-948dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr20 | 37183219 | ||||||
chr20:37183405 | G | A | 77 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0016 others(74): Show |
96 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.14-775G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183405 | |||||||
chr20:37183490 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.14-690C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183490 | |||||||
chr20:37183558 | T | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.14-622T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183558 | |||||||
chr20:37183767 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.14-413G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183767 | |||||||
chr20:37183769 | A | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.14-411A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183769 | |||||||
chr20:37183805 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-375G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183805 | |||||||
chr20:37183845 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.14-335C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37183845 | |||||||
chr20:37184071 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0158 a0001c0001t0001g0159 others(8): Show |
14 | HG00408.hp2 HG00621.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.14-109C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37184071 | |||||||
chr20:37184123 | C | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(64): Show |
84 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.14-57C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 1/16 | chr20 | 37184123 | |||||||
chr20:37184424 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.207+51C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184424 | |||||||
chr20:37184508 | T | A | 1 | a0001c0002t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.207+135T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184508 | |||||||
chr20:37184526 | C | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0108 a0001c0001t0001g0155 others(4): Show |
8 | HG02080.hp1 NA18954.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+153C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184526 | |||||||
chr20:37184626 | G | A | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(66): Show |
86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.207+253G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184626 | |||||||
chr20:37184967 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.207+594T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184967 | |||||||
chr20:37184971 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+598C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37184971 | |||||||
chr20:37185111 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.207+738T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185111 | |||||||
chr20:37185144 | CT | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(68): Show |
86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.207+788delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37185144 | ||||||
chr20:37185240 | A | G | 1 | a0001c0002t0001g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.207+867A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185240 | |||||||
chr20:37185576 | T | G | 7 | a0001c0002t0001g0015 a0001c0002t0001g0018 a0001c0002t0001g0019 others(4): Show |
10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+1203T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185576 | |||||||
chr20:37185599 | C | T | 69 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(66): Show |
86 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.207+1226C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185599 | |||||||
chr20:37185642 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.207+1269G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185642 | |||||||
chr20:37185822 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.207+1449C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185822 | |||||||
chr20:37185948 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.207+1575A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37185948 | |||||||
chr20:37186098 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.207+1725A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186098 | |||||||
chr20:37186318 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+1945T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186318 | |||||||
chr20:37186567 | C | G | 1 | a0005c0007t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.207+2194C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186567 | |||||||
chr20:37186765 | C | T | 2 | a0004c0005t0001g0219 a0004c0005t0001g0220 |
2 | HG00639.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.207+2392C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186765 | |||||||
chr20:37186768 | C | T | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.207+2395C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186768 | |||||||
chr20:37186895 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.207+2522A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37186895 | |||||||
chr20:37187089 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.207+2716A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187089 | |||||||
chr20:37187206 | TAAGATCA others(305): Show |
T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.207+2848_207+3159d others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187206 | ||||||
chr20:37187285 | G | A | 2 | a0001c0002t0001g0002 a0001c0002t0001g0073 |
3 | NA18948.hp2 NA18995.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.207+2912G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187285 | |||||||
chr20:37187394 | T | C | 1 | a0001c0002t0001g0070 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.207+3021T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187394 | |||||||
chr20:37187501 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0001g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.207+3137_207+3147d others(13): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | ||||||
chr20:37187501 | C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.207+3134_207+3147d others(16): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | ||||||
chr20:37187501 | C | CAAAAAAA others(10): Show |
1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.207+3131_207+3147d others(19): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | ||||||
chr20:37187501 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.207+3129_207+3147d others(21): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | ||||||
chr20:37187501 | C | CAAAAAAA others(17): Show |
1 | a0001c0002t0001g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.207+3147_207+3148i others(26): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | ||||||
chr20:37187501 | C | CAAAAAAA others(18): Show |
1 | a0001c0002t0001g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.207+3147_207+3148i others(27): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | ||||||
chr20:37187501 | C | CAAAAAAA others(29): Show |
1 | a0001c0002t0001g0018 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.207+3147_207+3148i others(38): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | ||||||
chr20:37187501 | CAA | C | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+3146_207+3147d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37187501 | ||||||
chr20:37187635 | A | T | 1 | a0001c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.207+3262A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187635 | |||||||
chr20:37187669 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.207+3296T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187669 | |||||||
chr20:37187921 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.207+3548G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187921 | |||||||
chr20:37187976 | T | G | 1 | a0001c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.207+3603T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37187976 | |||||||
chr20:37188208 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.207+3835T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188208 | |||||||
chr20:37188209 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG00408.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.207+3836G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188209 | |||||||
chr20:37188271 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3898C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188271 | |||||||
chr20:37188303 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.207+3930C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188303 | |||||||
chr20:37188320 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.207+3947G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188320 | |||||||
chr20:37188331 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+3958T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188331 | |||||||
chr20:37188414 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0182 |
2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.207+4041A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188414 | |||||||
chr20:37188420 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.207+4047T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188420 | |||||||
chr20:37188448 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.207+4075C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188448 | |||||||
chr20:37188574 | T | C | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+4201T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188574 | |||||||
chr20:37188594 | G | A | 4 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0110 others(1): Show |
6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+4221G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188594 | |||||||
chr20:37188620 | C | CT | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.207+4260dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37188620 | ||||||
chr20:37188620 | CT | C | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+4260delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37188620 | ||||||
chr20:37188663 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0239 |
3 | HG02622.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.207+4290G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188663 | |||||||
chr20:37188784 | A | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.207+4411A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188784 | |||||||
chr20:37188798 | T | A | 29 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(26): Show |
34 | HG00741.hp1 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.207+4425T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37188798 | |||||||
chr20:37189025 | G | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.207+4652G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189025 | |||||||
chr20:37189114 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.207+4741T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189114 | |||||||
chr20:37189209 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.207+4836A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189209 | |||||||
chr20:37189311 | CTGTGTGT others(5): Show |
C | 6 | a0001c0001t0001g0100 a0001c0001t0001g0109 a0001c0001t0001g0152 others(3): Show |
6 | HG00438.hp1 HG01099.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+4950_207+4961d others(14): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189311 | ||||||
chr20:37189311 | CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02040.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.207+4950_207+4963d others(16): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189311 | ||||||
chr20:37189311 | CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0001g0114 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.207+4950_207+4967d others(20): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189311 | ||||||
chr20:37189311 | CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0001g0213 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.207+4950_207+4971d others(24): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189311 | ||||||
chr20:37189313 | GTGTGTGT others(3): Show |
G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0022 others(25): Show |
32 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.207+4950_207+4959d others(12): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189313 | ||||||
chr20:37189315 | GTGTGTGT others(1): Show |
G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0020 others(25): Show |
38 | HG00639.hp1 HG00741.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.207+4950_207+4957d others(10): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189315 | ||||||
chr20:37189317 | GTGTGTA | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(41): Show |
57 | HG00099.hp1 HG00408.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.207+4950_207+4955d others(8): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189317 | ||||||
chr20:37189319 | GTGTA | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(15): Show |
23 | HG01943.hp1 HG02055.hp1 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.207+4950_207+4953d others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189319 | ||||||
chr20:37189321 | GTA | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0041 others(5): Show |
10 | HG01943.hp2 HG02027.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+4950_207+4951d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189321 | ||||||
chr20:37189323 | A | ATG | 8 | a0001c0001t0001g0191 a0001c0002t0001g0002 a0001c0002t0001g0056 others(5): Show |
12 | HG02602.hp1 HG02698.hp2 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+4987_207+4988d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | ||||||
chr20:37189323 | A | ATGTG | 13 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(10): Show |
30 | HG00408.hp1 HG00621.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.207+4985_207+4988d others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | ||||||
chr20:37189323 | A | ATGTGTG | 2 | a0001c0002t0001g0003 a0003c0008t0001g0084 |
3 | HG01952.hp1 NA18953.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.207+4983_207+4988d others(8): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | ||||||
chr20:37189323 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0041 others(6): Show |
12 | HG01515.hp1 HG02080.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.207+4950A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189323 | |||||||
chr20:37189323 | ATG | A | 18 | a0001c0001t0001g0103 a0001c0001t0001g0192 a0001c0002t0001g0028 others(15): Show |
19 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.207+4987_207+4988d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | ||||||
chr20:37189323 | ATGTG | A | 5 | a0001c0001t0001g0228 a0001c0002t0001g0002 a0001c0002t0001g0018 others(2): Show |
6 | HG01346.hp1 HG01358.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+4985_207+4988d others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | ||||||
chr20:37189323 | ATGTGTG | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(14): Show |
22 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.207+4983_207+4988d others(8): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | ||||||
chr20:37189323 | ATGTGTGT others(1): Show |
A | 5 | a0001c0001t0001g0233 a0001c0001t0001g0236 a0001c0002t0001g0015 others(2): Show |
5 | HG01109.hp2 HG01361.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+4981_207+4988d others(10): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | ||||||
chr20:37189323 | ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0001g0222 a0001c0002t0001g0015 |
2 | HG02976.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.207+4979_207+4988d others(12): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37189323 | ||||||
chr20:37189432 | C | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01074.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.207+5059C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189432 | |||||||
chr20:37189491 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG00738.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.207+5118G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189491 | |||||||
chr20:37189554 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+5181A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189554 | |||||||
chr20:37189595 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.207+5222G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189595 | |||||||
chr20:37189672 | G | A | 7 | a0001c0002t0001g0015 a0001c0002t0001g0018 a0001c0002t0001g0019 others(4): Show |
10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+5299G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189672 | |||||||
chr20:37189838 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.207+5465T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189838 | |||||||
chr20:37189922 | C | G | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+5549C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37189922 | |||||||
chr20:37190005 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.207+5632T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190005 | |||||||
chr20:37190104 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.207+5731T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190104 | |||||||
chr20:37190119 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
28 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.207+5746C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190119 | |||||||
chr20:37190547 | T | C | 1 | a0001c0002t0001g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.207+6174T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190547 | |||||||
chr20:37190572 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.207+6199C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190572 | |||||||
chr20:37190726 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6353A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190726 | |||||||
chr20:37190752 | T | G | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+6379T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190752 | |||||||
chr20:37190834 | T | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0182 |
2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.207+6461T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37190834 | |||||||
chr20:37191184 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.207+6811G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191184 | |||||||
chr20:37191184 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.207+6811G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191184 | |||||||
chr20:37191205 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6832G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191205 | |||||||
chr20:37191258 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.207+6885C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191258 | |||||||
chr20:37191295 | G | A | 1 | a0003c0008t0001g0052 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.207+6922G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191295 | |||||||
chr20:37191341 | G | T | 1 | a0001c0002t0001g0092 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.207+6968G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191341 | |||||||
chr20:37191658 | CT | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
7 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-6726delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37191658 | ||||||
chr20:37191806 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.208-6591G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37191806 | |||||||
chr20:37192014 | A | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6383A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192014 | |||||||
chr20:37192073 | G | T | 1 | a0001c0002t0001g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.208-6324G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192073 | |||||||
chr20:37192103 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.208-6294A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192103 | |||||||
chr20:37192143 | G | T | 1 | a0001c0001t0001g0113 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.208-6254G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192143 | |||||||
chr20:37192154 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208-6243A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192154 | |||||||
chr20:37192291 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.208-6106C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192291 | |||||||
chr20:37192339 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.208-6058A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192339 | |||||||
chr20:37192472 | T | C | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208-5925T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192472 | |||||||
chr20:37192580 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.208-5817G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192580 | |||||||
chr20:37192698 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.208-5699T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37192698 | |||||||
chr20:37193067 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.208-5330G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193067 | |||||||
chr20:37193165 | A | G | 5 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG01109.hp2 HG03225.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-5232A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193165 | |||||||
chr20:37193340 | C | A | 3 | a0001c0002t0001g0015 a0001c0002t0001g0101 a0001c0002t0001g0102 |
4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-5057C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193340 | |||||||
chr20:37193341 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-5056G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193341 | |||||||
chr20:37193662 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
27 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.208-4735C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193662 | |||||||
chr20:37193692 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-4705G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193692 | |||||||
chr20:37193706 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-4691T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193706 | |||||||
chr20:37193848 | G | T | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.208-4549G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193848 | |||||||
chr20:37193880 | A | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.208-4517A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37193880 | |||||||
chr20:37194032 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208-4365A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194032 | |||||||
chr20:37194085 | A | T | 1 | a0001c0002t0001g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.208-4312A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194085 | |||||||
chr20:37194153 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.208-4244G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194153 | |||||||
chr20:37194203 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.208-4194C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194203 | |||||||
chr20:37194218 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.208-4179G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194218 | |||||||
chr20:37194255 | ATTG | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.208-4118_208-4116d others(5): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr20 | 37194255 | ||||||
chr20:37194408 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.208-3989C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194408 | |||||||
chr20:37194418 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.208-3979C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194418 | |||||||
chr20:37194493 | C | T | 1 | a0001c0002t0001g0245 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.208-3904C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194493 | |||||||
chr20:37194509 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.208-3888G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194509 | |||||||
chr20:37194621 | A | G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 |
3 | HG02572.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.208-3776A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194621 | |||||||
chr20:37194779 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-3618G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194779 | |||||||
chr20:37194797 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0240 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-3600G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194797 | |||||||
chr20:37194891 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.208-3506G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194891 | |||||||
chr20:37194985 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-3412G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37194985 | |||||||
chr20:37195035 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.208-3362C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195035 | |||||||
chr20:37195066 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.208-3331C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195066 | |||||||
chr20:37195085 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.208-3312G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195085 | |||||||
chr20:37195172 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-3225A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195172 | |||||||
chr20:37195186 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-3211C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195186 | |||||||
chr20:37195265 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.208-3132C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195265 | |||||||
chr20:37195287 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.208-3110G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195287 | |||||||
chr20:37195317 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-3080C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195317 | |||||||
chr20:37195388 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.208-3009T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195388 | |||||||
chr20:37195518 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.208-2879A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195518 | |||||||
chr20:37195519 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.208-2878T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195519 | |||||||
chr20:37195551 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.208-2846G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195551 | |||||||
chr20:37195693 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-2704G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195693 | |||||||
chr20:37195694 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-2703G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195694 | |||||||
chr20:37195802 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.208-2595T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195802 | |||||||
chr20:37195827 | A | T | 1 | a0001c0002t0001g0102 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.208-2570A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195827 | |||||||
chr20:37195968 | A | G | 1 | a0001c0002t0001g0089 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.208-2429A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37195968 | |||||||
chr20:37196186 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
176 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.208-2211A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196186 | |||||||
chr20:37196235 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.208-2162C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196235 | |||||||
chr20:37196239 | T | G | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208-2158T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196239 | |||||||
chr20:37196267 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.208-2130C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196267 | |||||||
chr20:37196275 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-2122C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196275 | |||||||
chr20:37196314 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.208-2083T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196314 | |||||||
chr20:37196321 | C | T | 1 | a0001c0002t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.208-2076C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196321 | |||||||
chr20:37196343 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.208-2054C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196343 | |||||||
chr20:37196354 | C | G | 4 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0110 others(1): Show |
6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-2043C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196354 | |||||||
chr20:37196416 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.208-1981G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196416 | |||||||
chr20:37196434 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.208-1963C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196434 | |||||||
chr20:37196437 | G | C | 1 | a0001c0002t0001g0042 | 2 | NA18942.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.208-1960G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196437 | |||||||
chr20:37196477 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0196 |
3 | HG02257.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.208-1920C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196477 | |||||||
chr20:37196484 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.208-1913T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196484 | |||||||
chr20:37196709 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1688A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37196709 | |||||||
chr20:37197001 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
123 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.208-1396C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197001 | |||||||
chr20:37197090 | C | T | 1 | a0001c0002t0001g0086 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.208-1307C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197090 | |||||||
chr20:37197107 | G | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1290G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197107 | |||||||
chr20:37197190 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.208-1207G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197190 | |||||||
chr20:37197557 | G | A | 1 | a0005c0007t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.208-840G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197557 | |||||||
chr20:37197638 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.208-759G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197638 | |||||||
chr20:37197863 | G | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-534G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197863 | |||||||
chr20:37197917 | A | C | 1 | a0001c0002t0001g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.208-480A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197917 | |||||||
chr20:37197984 | A | G | 3 | a0001c0002t0001g0015 a0001c0002t0001g0101 a0001c0002t0001g0102 |
4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-413A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37197984 | |||||||
chr20:37198011 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.208-386G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37198011 | |||||||
chr20:37198027 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.208-370G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37198027 | |||||||
chr20:37198244 | C | T | 4 | a0001c0002t0001g0012 a0001c0002t0001g0042 a0001c0002t0001g0244 others(1): Show |
7 | HG00609.hp2 HG02738.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-153C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37198244 | |||||||
chr20:37198280 | T | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
176 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.208-117T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 2/16 | chr20 | 37198280 | |||||||
chr20:37198506 | C | T | 4 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0110 others(1): Show |
6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+14C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | chr20 | 37198506 | |||||||
chr20:37198561 | A | T | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.303+69A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | chr20 | 37198561 | |||||||
chr20:37198625 | A | AT | 12 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(9): Show |
17 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.303+143dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr20 | 37198625 | ||||||
chr20:37198625 | A | ATT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.303+142_303+143dup others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr20 | 37198625 | ||||||
chr20:37198663 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.303+171C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | chr20 | 37198663 | |||||||
chr20:37199017 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0113 |
5 | NA18986.hp1 NA19058.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-33T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 3/16 | chr20 | 37199017 | |||||||
chr20:37199279 | G | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.479+54G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199279 | |||||||
chr20:37199439 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.479+214A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199439 | |||||||
chr20:37199445 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.479+220C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199445 | |||||||
chr20:37199725 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.479+500G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199725 | |||||||
chr20:37199825 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.479+600A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37199825 | |||||||
chr20:37199997 | AT | A | 12 | a0001c0001t0001g0160 a0001c0001t0001g0191 a0001c0001t0001g0192 others(9): Show |
27 | HG00408.hp1 HG00621.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.479+787delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37199997 | ||||||
chr20:37200081 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.479+856G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200081 | |||||||
chr20:37200199 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.479+974G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200199 | |||||||
chr20:37200293 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.479+1068A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200293 | |||||||
chr20:37200328 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.479+1103T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200328 | |||||||
chr20:37200354 | A | AT | 10 | a0001c0002t0001g0028 a0001c0002t0001g0047 a0001c0002t0001g0049 others(7): Show |
11 | HG00741.hp2 HG01167.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+1142dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37200354 | ||||||
chr20:37200354 | ATT | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.479+1141_479+1142d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37200354 | ||||||
chr20:37200463 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.479+1238G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200463 | |||||||
chr20:37200535 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.479+1310T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200535 | |||||||
chr20:37200734 | C | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.479+1509C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200734 | |||||||
chr20:37200846 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+1621C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200846 | |||||||
chr20:37200848 | G | A | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG00438.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.479+1623G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37200848 | |||||||
chr20:37201014 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.479+1789C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201014 | |||||||
chr20:37201136 | C | T | 4 | a0001c0002t0001g0004 a0001c0002t0001g0013 a0001c0002t0001g0058 others(1): Show |
8 | NA18951.hp1 NA18960.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.479+1911C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201136 | |||||||
chr20:37201137 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.479+1912G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201137 | |||||||
chr20:37201251 | G | A | 1 | a0001c0002t0001g0057 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.479+2026G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201251 | |||||||
chr20:37201281 | C | CT | 133 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.479+2074dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37201281 | ||||||
chr20:37201281 | C | CTT | 11 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0120 others(8): Show |
13 | HG00544.hp1 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.479+2073_479+2074d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37201281 | ||||||
chr20:37201316 | G | C | 1 | a0001c0002t0001g0062 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.479+2091G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201316 | |||||||
chr20:37201376 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.479+2151T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201376 | |||||||
chr20:37201391 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.479+2166T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201391 | |||||||
chr20:37201452 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.479+2227A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201452 | |||||||
chr20:37201541 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.479+2316T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201541 | |||||||
chr20:37201578 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0152 |
2 | HG01099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.480-2307G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201578 | |||||||
chr20:37201685 | C | G | 1 | a0001c0002t0001g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.480-2200C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201685 | |||||||
chr20:37201698 | C | T | 1 | a0001c0002t0001g0081 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.480-2187C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201698 | |||||||
chr20:37201898 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-1987G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37201898 | |||||||
chr20:37202222 | G | A | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.480-1663G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37202222 | |||||||
chr20:37202357 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480-1528G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37202357 | |||||||
chr20:37202738 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-1147A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37202738 | |||||||
chr20:37202909 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0104 a0001c0001t0001g0105 |
4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-976A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37202909 | |||||||
chr20:37203130 | G | A | 1 | a0001c0002t0001g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.480-755G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203130 | |||||||
chr20:37203287 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.480-598A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203287 | |||||||
chr20:37203361 | CT | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(13): Show |
21 | HG01070.hp2 HG01361.hp2 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.480-501delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37203361 | ||||||
chr20:37203361 | CTT | C | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.480-502_480-501del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37203361 | ||||||
chr20:37203361 | CTTTTTTT others(3): Show |
C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.480-510_480-501del others(10): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37203361 | ||||||
chr20:37203361 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0160 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.480-511_480-501del others(11): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr20 | 37203361 | ||||||
chr20:37203411 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.480-474C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203411 | |||||||
chr20:37203461 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.480-424C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203461 | |||||||
chr20:37203529 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.480-356G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203529 | |||||||
chr20:37203538 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.480-347C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203538 | |||||||
chr20:37203549 | C | T | 29 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(26): Show |
34 | HG00741.hp1 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.480-336C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203549 | |||||||
chr20:37203808 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.480-77A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 4/16 | chr20 | 37203808 | |||||||
chr20:37204055 | G | T | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.555+95G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 5/16 | chr20 | 37204055 | |||||||
chr20:37204078 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0228 |
2 | HG01346.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.555+118G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 5/16 | chr20 | 37204078 | |||||||
chr20:37204500 | A | G | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.556-267A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 5/16 | chr20 | 37204500 | |||||||
chr20:37204550 | C | T | 3 | a0001c0002t0001g0015 a0001c0002t0001g0101 a0001c0002t0001g0102 |
4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-217C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 5/16 | chr20 | 37204550 | |||||||
chr20:37205047 | A | G | 4 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0110 others(1): Show |
6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+146A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205047 | |||||||
chr20:37205074 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+173G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205074 | |||||||
chr20:37205265 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0239 |
3 | HG02622.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.690+364T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205265 | |||||||
chr20:37205380 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.690+479C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205380 | |||||||
chr20:37205505 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.690+604A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205505 | |||||||
chr20:37205590 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.690+689A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205590 | |||||||
chr20:37205621 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.690+720G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37205621 | |||||||
chr20:37206048 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.690+1147A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37206048 | |||||||
chr20:37206200 | C | T | 1 | a0002c0003t0001g0143 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.691-1073C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37206200 | |||||||
chr20:37206285 | G | A | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.691-988G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37206285 | |||||||
chr20:37206919 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.691-354C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37206919 | |||||||
chr20:37207095 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.691-178A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37207095 | |||||||
chr20:37207254 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.691-19C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 6/16 | chr20 | 37207254 | |||||||
chr20:37207486 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.867+37A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37207486 | |||||||
chr20:37207705 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+256A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37207705 | |||||||
chr20:37208059 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.867+610G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208059 | |||||||
chr20:37208185 | G | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(9): Show |
19 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.867+736G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208185 | |||||||
chr20:37208267 | T | TAA | 9 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(6): Show |
14 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.867+836_867+837dup others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr20 | 37208267 | ||||||
chr20:37208267 | TAA | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0103 others(7): Show |
11 | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.867+836_867+837del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr20 | 37208267 | ||||||
chr20:37208267 | TAAA | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.867+835_867+837del others(3): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr20 | 37208267 | ||||||
chr20:37208444 | A | G | 1 | a0001c0002t0001g0083 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.867+995A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208444 | |||||||
chr20:37208448 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.867+999C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208448 | |||||||
chr20:37208449 | G | T | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.867+1000G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208449 | |||||||
chr20:37208477 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.867+1028A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208477 | |||||||
chr20:37208548 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.867+1099T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208548 | |||||||
chr20:37208557 | A | G | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+1108A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208557 | |||||||
chr20:37208609 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.867+1160G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208609 | |||||||
chr20:37208626 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.867+1177C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208626 | |||||||
chr20:37208689 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.867+1240G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208689 | |||||||
chr20:37208723 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.867+1274C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208723 | |||||||
chr20:37208807 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.868-1240T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208807 | |||||||
chr20:37208814 | A | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.868-1233A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208814 | |||||||
chr20:37208863 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.868-1184A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208863 | |||||||
chr20:37208902 | G | A | 2 | a0001c0002t0001g0046 a0001c0002t0001g0094 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.868-1145G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208902 | |||||||
chr20:37208919 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0166 |
3 | HG02155.hp2 NA18960.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.868-1128A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37208919 | |||||||
chr20:37209118 | C | T | 3 | a0001c0001t0001g0157 a0001c0004t0001g0156 a0001c0004t0001g0173 |
3 | HG02080.hp1 NA18954.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.868-929C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209118 | |||||||
chr20:37209469 | A | AT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.868-567dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr20 | 37209469 | ||||||
chr20:37209519 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0104 a0001c0001t0001g0105 |
4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.868-528G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209519 | |||||||
chr20:37209527 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.868-520G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209527 | |||||||
chr20:37209626 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.868-421G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209626 | |||||||
chr20:37209879 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG00544.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.868-168A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209879 | |||||||
chr20:37209969 | T | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.868-78T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 7/16 | chr20 | 37209969 | |||||||
chr20:37210188 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
341 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.986+23T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210188 | |||||||
chr20:37210353 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.986+188G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210353 | |||||||
chr20:37210377 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.986+212A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210377 | |||||||
chr20:37210528 | CT | C | 33 | a0001c0001t0001g0157 a0001c0001t0001g0238 a0001c0002t0001g0010 others(30): Show |
43 | HG00609.hp2 HG00741.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.986+382delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37210528 | ||||||
chr20:37210528 | CTT | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.986+381_986+382del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37210528 | ||||||
chr20:37210634 | G | A | 1 | a0005c0007t0001g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.986+469G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210634 | |||||||
chr20:37210771 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.986+606G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210771 | |||||||
chr20:37210925 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.986+760T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37210925 | |||||||
chr20:37211064 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.986+899T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211064 | |||||||
chr20:37211125 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.986+960C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211125 | |||||||
chr20:37211313 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.986+1148G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211313 | |||||||
chr20:37211397 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+1232G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211397 | |||||||
chr20:37211455 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.986+1290A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211455 | |||||||
chr20:37211628 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.986+1463C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211628 | |||||||
chr20:37211645 | TA | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.986+1497delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37211645 | ||||||
chr20:37211679 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.986+1514A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211679 | |||||||
chr20:37211714 | T | C | 1 | a0001c0002t0001g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.986+1549T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211714 | |||||||
chr20:37211731 | AT | A | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.986+1577delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37211731 | ||||||
chr20:37211881 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.986+1716G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211881 | |||||||
chr20:37211898 | C | T | 1 | a0001c0002t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.986+1733C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211898 | |||||||
chr20:37211918 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.986+1753G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211918 | |||||||
chr20:37211994 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.987-1766C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37211994 | |||||||
chr20:37212025 | C | T | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.987-1735C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212025 | |||||||
chr20:37212131 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.987-1629A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212131 | |||||||
chr20:37212132 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.987-1628G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212132 | |||||||
chr20:37212193 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-1567C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212193 | |||||||
chr20:37212320 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.987-1440A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212320 | |||||||
chr20:37212391 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.987-1369A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212391 | |||||||
chr20:37212485 | AT | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.987-1260delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37212485 | ||||||
chr20:37212512 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.987-1248G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212512 | |||||||
chr20:37212541 | C | T | 3 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 |
4 | HG02886.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-1219C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212541 | |||||||
chr20:37212701 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.987-1059G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212701 | |||||||
chr20:37212745 | G | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.987-1015G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212745 | |||||||
chr20:37212840 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.987-920T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212840 | |||||||
chr20:37212854 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.987-906G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212854 | |||||||
chr20:37212917 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.987-843G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37212917 | |||||||
chr20:37213027 | GAT | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-730_987-729del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr20 | 37213027 | ||||||
chr20:37213028 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0103 others(3): Show |
7 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.987-732A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213028 | |||||||
chr20:37213252 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.987-508G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213252 | |||||||
chr20:37213349 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.987-411A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213349 | |||||||
chr20:37213456 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0152 |
2 | HG01099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.987-304G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213456 | |||||||
chr20:37213712 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.987-48T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 8/16 | chr20 | 37213712 | |||||||
chr20:37213930 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1092+65C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37213930 | |||||||
chr20:37214173 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+308G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214173 | |||||||
chr20:37214237 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1092+372C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214237 | |||||||
chr20:37214431 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1092+566G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214431 | |||||||
chr20:37214520 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
176 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1092+655A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214520 | |||||||
chr20:37214598 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1092+733C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37214598 | |||||||
chr20:37215281 | C | T | 2 | a0001c0002t0001g0051 a0001c0002t0001g0077 |
2 | HG00597.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1092+1416C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215281 | |||||||
chr20:37215324 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1092+1459G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215324 | |||||||
chr20:37215401 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1092+1536G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215401 | |||||||
chr20:37215426 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1092+1561A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215426 | |||||||
chr20:37215462 | T | C | 5 | a0001c0002t0001g0028 a0001c0002t0001g0167 a0001c0002t0001g0168 others(2): Show |
6 | HG00741.hp2 HG01167.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+1597T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215462 | |||||||
chr20:37215531 | CTTTTCTT others(3): Show |
C | 4 | a0001c0002t0001g0028 a0001c0002t0001g0167 a0001c0002t0001g0168 others(1): Show |
5 | HG00741.hp2 HG02145.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+1674_1092+168 others(14): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37215531 | ||||||
chr20:37215644 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1092+1779T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215644 | |||||||
chr20:37215654 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0103 others(3): Show |
7 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092+1789C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215654 | |||||||
chr20:37215718 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1092+1853A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215718 | |||||||
chr20:37215791 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1092+1926G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215791 | |||||||
chr20:37215844 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1092+1979A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215844 | |||||||
chr20:37215978 | C | T | 2 | a0001c0002t0001g0076 a0001c0002t0001g0085 |
2 | HG03834.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1092+2113C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37215978 | |||||||
chr20:37216002 | T | C | 16 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(13): Show |
35 | HG00408.hp1 HG00621.hp1 HG01952.hp1 others(32): Show |
intron_variant | MODIFIER | c.1092+2137T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216002 | |||||||
chr20:37216229 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | HG01070.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1092+2364C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216229 | |||||||
chr20:37216231 | C | T | 1 | a0005c0007t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1092+2366C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216231 | |||||||
chr20:37216308 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1092+2443C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216308 | |||||||
chr20:37216393 | A | G | 4 | a0001c0002t0001g0064 a0001c0002t0001g0067 a0001c0002t0001g0078 others(1): Show |
4 | NA18946.hp2 NA18998.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+2528A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216393 | |||||||
chr20:37216425 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+2560A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216425 | |||||||
chr20:37216465 | T | TTTATTTT others(316): Show |
1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1092+2614_1092+261 others(327): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37216465 | ||||||
chr20:37216507 | G | C | 1 | a0001c0001t0001g0036 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1092+2642G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216507 | |||||||
chr20:37216544 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1092+2679C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216544 | |||||||
chr20:37216564 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+2699C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216564 | |||||||
chr20:37216627 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1092+2762A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216627 | |||||||
chr20:37216704 | C | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1092+2839C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216704 | |||||||
chr20:37216808 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1092+2943T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216808 | |||||||
chr20:37216907 | A | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0138 a0001c0001t0001g0144 |
3 | HG00642.hp2 HG01516.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1092+3042A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37216907 | |||||||
chr20:37216939 | C | CT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1092+3083dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37216939 | ||||||
chr20:37217147 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1092+3282C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217147 | |||||||
chr20:37217272 | A | ATAT | 7 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0103 others(4): Show |
8 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1092+3433_1092+343 others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217272 | ||||||
chr20:37217272 | A | ATATTATT others(5): Show |
1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+3424_1092+343 others(16): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217272 | ||||||
chr20:37217272 | ATAT | A | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0002t0001g0010 others(26): Show |
39 | HG00609.hp2 HG00741.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1092+3433_1092+343 others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217272 | ||||||
chr20:37217286 | A | ATTG | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1092+3423_1092+342 others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217286 | ||||||
chr20:37217289 | A | G | 1 | a0001c0001t0001g0024 | 2 | NA18981.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1092+3424A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217289 | |||||||
chr20:37217301 | C | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0103 others(3): Show |
8 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+3436C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217301 | |||||||
chr20:37217304 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+3439T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217304 | |||||||
chr20:37217328 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1092+3463C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217328 | |||||||
chr20:37217347 | C | T | 1 | a0007c0009t0001g0227 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1092+3482C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217347 | |||||||
chr20:37217395 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1092+3530T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217395 | |||||||
chr20:37217399 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1092+3534T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217399 | |||||||
chr20:37217759 | TTGC | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1092+3897_1092+389 others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37217759 | ||||||
chr20:37217966 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0103 others(3): Show |
7 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092+4101C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37217966 | |||||||
chr20:37218033 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1092+4168C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218033 | |||||||
chr20:37218034 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1092+4169G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218034 | |||||||
chr20:37218337 | CA | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1092+4473delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218337 | |||||||
chr20:37218341 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1092+4476A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218341 | |||||||
chr20:37218464 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1092+4599T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218464 | |||||||
chr20:37218545 | T | TA | 153 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.1092+4691dupA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37218545 | ||||||
chr20:37218556 | A | AAC | 5 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+4691_1092+469 others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218556 | |||||||
chr20:37218557 | C | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
10 | HG02280.hp2 HG02723.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1092+4692C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218557 | |||||||
chr20:37218567 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1092+4702A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218567 | |||||||
chr20:37218573 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1092+4708A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218573 | |||||||
chr20:37218615 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+4750C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218615 | |||||||
chr20:37218661 | A | T | 2 | a0001c0002t0001g0168 a0001c0002t0001g0170 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1092+4796A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218661 | |||||||
chr20:37218668 | T | A | 7 | a0001c0002t0001g0015 a0001c0002t0001g0018 a0001c0002t0001g0019 others(4): Show |
10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1092+4803T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218668 | |||||||
chr20:37218739 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+4874G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218739 | |||||||
chr20:37218821 | A | T | 1 | a0001c0001t0001g0235 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1092+4956A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37218821 | |||||||
chr20:37219057 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1093-4821G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37219057 | |||||||
chr20:37219311 | C | G | 1 | a0001c0002t0001g0075 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1093-4567C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37219311 | |||||||
chr20:37219814 | T | C | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1093-4064T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37219814 | |||||||
chr20:37219939 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-3939G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37219939 | |||||||
chr20:37220183 | T | TTG | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0103 others(13): Show |
23 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.1093-3674_1093-367 others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37220183 | ||||||
chr20:37220193 | G | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0104 a0001c0001t0001g0105 |
4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1093-3685G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220193 | |||||||
chr20:37220297 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-3581A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220297 | |||||||
chr20:37220404 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1093-3474G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220404 | |||||||
chr20:37220496 | A | G | 9 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(6): Show |
14 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1093-3382A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220496 | |||||||
chr20:37220608 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1093-3270T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220608 | |||||||
chr20:37220643 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0207 |
4 | HG01358.hp1 HG01993.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-3235A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220643 | |||||||
chr20:37220908 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0113 others(10): Show |
19 | HG00408.hp2 HG00621.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1093-2970G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220908 | |||||||
chr20:37220980 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1093-2898G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37220980 | |||||||
chr20:37221035 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-2843T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221035 | |||||||
chr20:37221059 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1093-2819G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221059 | |||||||
chr20:37221195 | C | CT | 38 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(35): Show |
43 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1093-2665dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37221195 | ||||||
chr20:37221195 | CT | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0103 others(5): Show |
9 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1093-2665delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37221195 | ||||||
chr20:37221219 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
18 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1093-2659G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221219 | |||||||
chr20:37221224 | C | G | 1 | a0001c0002t0001g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1093-2654C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221224 | |||||||
chr20:37221341 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1093-2537G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221341 | |||||||
chr20:37221449 | C | T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(21): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1093-2429C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221449 | |||||||
chr20:37221478 | G | A | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1093-2400G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221478 | |||||||
chr20:37221542 | T | C | 2 | a0001c0002t0001g0046 a0001c0002t0001g0094 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1093-2336T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221542 | |||||||
chr20:37221842 | G | A | 1 | a0008c0011t0001g0176 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1093-2036G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37221842 | |||||||
chr20:37222005 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1093-1873C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222005 | |||||||
chr20:37222155 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1093-1723C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222155 | |||||||
chr20:37222273 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1093-1605C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222273 | |||||||
chr20:37222397 | GT | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1093-1470delT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37222397 | ||||||
chr20:37222490 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1093-1388C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222490 | |||||||
chr20:37222593 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1093-1285G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222593 | |||||||
chr20:37222693 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1093-1185C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222693 | |||||||
chr20:37222881 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1093-997C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222881 | |||||||
chr20:37222936 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093-942A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37222936 | |||||||
chr20:37223025 | T | C | 7 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(4): Show |
7 | HG01109.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-853T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223025 | |||||||
chr20:37223063 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1093-815C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223063 | |||||||
chr20:37223324 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-554G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223324 | |||||||
chr20:37223528 | C | G | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1093-350C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223528 | |||||||
chr20:37223603 | G | T | 1 | a0001c0001t0001g0023 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1093-275G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | chr20 | 37223603 | |||||||
chr20:37223635 | C | CT | 81 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0030 others(78): Show |
107 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1093-230dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr20 | 37223635 | ||||||
chr20:37223985 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1184+16C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37223985 | |||||||
chr20:37223992 | A | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1184+23A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37223992 | |||||||
chr20:37224035 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG00408.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1184+66G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224035 | |||||||
chr20:37224047 | G | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1184+78G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224047 | |||||||
chr20:37224083 | A | G | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1184+114A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224083 | |||||||
chr20:37224157 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+188G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224157 | |||||||
chr20:37224201 | TA | T | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1184+234delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr20 | 37224201 | ||||||
chr20:37224357 | G | A | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1184+388G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224357 | |||||||
chr20:37224440 | T | G | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1184+471T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224440 | |||||||
chr20:37224562 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1184+593C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224562 | |||||||
chr20:37224625 | A | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1184+656A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224625 | |||||||
chr20:37224693 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(8): Show |
18 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1184+724C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224693 | |||||||
chr20:37224816 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1184+847G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224816 | |||||||
chr20:37224833 | T | G | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1185-855T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224833 | |||||||
chr20:37224875 | G | C | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1185-813G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224875 | |||||||
chr20:37224903 | A | G | 1 | a0001c0002t0001g0067 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1185-785A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37224903 | |||||||
chr20:37225060 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1185-628T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37225060 | |||||||
chr20:37225209 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1185-479T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37225209 | |||||||
chr20:37225606 | A | G | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1185-82A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 10/16 | chr20 | 37225606 | |||||||
chr20:37225846 | T | A | 1 | a0001c0001t0001g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1299+44T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37225846 | |||||||
chr20:37225921 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0234 |
3 | HG00738.hp1 HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1299+119C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37225921 | |||||||
chr20:37226028 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1299+226T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226028 | |||||||
chr20:37226218 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1299+416A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226218 | |||||||
chr20:37226254 | G | A | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1299+452G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226254 | |||||||
chr20:37226284 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+482G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226284 | |||||||
chr20:37226386 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0136 |
3 | NA18971.hp1 NA18995.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1299+584T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226386 | |||||||
chr20:37226423 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1299+621C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226423 | |||||||
chr20:37226496 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1299+694G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226496 | |||||||
chr20:37226621 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1299+819T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37226621 | |||||||
chr20:37227019 | C | G | 2 | a0001c0001t0001g0225 a0001c0001t0002g0226 |
2 | HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1299+1217C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227019 | |||||||
chr20:37227084 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1299+1282A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227084 | |||||||
chr20:37227269 | G | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1300-1281G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227269 | |||||||
chr20:37227359 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0104 a0001c0001t0001g0105 |
4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-1191T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227359 | |||||||
chr20:37227378 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1300-1172C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227378 | |||||||
chr20:37227504 | G | A | 7 | a0001c0002t0001g0015 a0001c0002t0001g0018 a0001c0002t0001g0019 others(4): Show |
10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1300-1046G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227504 | |||||||
chr20:37227562 | T | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-988T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227562 | |||||||
chr20:37227610 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1300-940A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227610 | |||||||
chr20:37227868 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-682T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227868 | |||||||
chr20:37227898 | A | G | 7 | a0001c0002t0001g0028 a0001c0002t0001g0047 a0001c0002t0001g0099 others(4): Show |
8 | HG00741.hp2 HG01167.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-652A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37227898 | |||||||
chr20:37228091 | C | G | 1 | a0001c0001t0001g0022 | 2 | HG01261.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1300-459C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228091 | |||||||
chr20:37228091 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1300-459C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228091 | |||||||
chr20:37228102 | A | G | 4 | a0001c0002t0001g0064 a0001c0002t0001g0067 a0001c0002t0001g0078 others(1): Show |
4 | NA18946.hp2 NA18998.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-448A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228102 | |||||||
chr20:37228132 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1300-418G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228132 | |||||||
chr20:37228266 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1300-284G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228266 | |||||||
chr20:37228393 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-157G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228393 | |||||||
chr20:37228444 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1300-106C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228444 | |||||||
chr20:37228530 | T | G | 1 | a0001c0002t0001g0017 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1300-20T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 11/16 | chr20 | 37228530 | |||||||
chr20:37228881 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+137T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37228881 | |||||||
chr20:37228976 | A | ACTTAC | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1494+235_1494+236i others(7): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr20 | 37228976 | ||||||
chr20:37229012 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1494+268C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229012 | |||||||
chr20:37229013 | A | G | 8 | a0001c0002t0001g0048 a0001c0002t0001g0054 a0001c0002t0001g0060 others(5): Show |
8 | HG00438.hp2 HG02027.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1494+269A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229013 | |||||||
chr20:37229029 | G | A | 7 | a0001c0002t0001g0015 a0001c0002t0001g0018 a0001c0002t0001g0019 others(4): Show |
10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1494+285G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229029 | |||||||
chr20:37229054 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1494+310T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229054 | |||||||
chr20:37229063 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1494+319G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229063 | |||||||
chr20:37229259 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0221 others(5): Show |
12 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1494+515G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229259 | |||||||
chr20:37229317 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1494+573G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229317 | |||||||
chr20:37229546 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1495-427C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229546 | |||||||
chr20:37229613 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1495-360C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229613 | |||||||
chr20:37229710 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0166 |
3 | HG02155.hp2 NA18960.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1495-263G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | chr20 | 37229710 | |||||||
chr20:37229899 | CAG | C | 3 | a0001c0002t0001g0063 a0001c0002t0001g0069 a0001c0002t0001g0087 |
3 | HG01975.hp1 HG02004.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1495-70_1495-69del others(2): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr20 | 37229899 | ||||||
chr20:37230099 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1581+40A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230099 | |||||||
chr20:37230149 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1581+90G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230149 | |||||||
chr20:37230205 | C | A | 1 | a0001c0001t0001g0038 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1581+146C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230205 | |||||||
chr20:37230242 | C | A | 1 | a0001c0002t0001g0101 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1581+183C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230242 | |||||||
chr20:37230346 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1581+287C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230346 | |||||||
chr20:37230585 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1581+526A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230585 | |||||||
chr20:37230673 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1581+614C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37230673 | |||||||
chr20:37231075 | T | A | 4 | a0002c0003t0001g0128 a0002c0003t0001g0129 a0002c0003t0001g0141 others(1): Show |
4 | HG02523.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1581+1016T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231075 | |||||||
chr20:37231220 | G | C | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1582-1076G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231220 | |||||||
chr20:37231249 | C | T | 1 | a0002c0003t0001g0129 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1582-1047C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231249 | |||||||
chr20:37231333 | G | A | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1582-963G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231333 | |||||||
chr20:37231370 | A | G | 1 | a0001c0002t0001g0070 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1582-926A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231370 | |||||||
chr20:37231383 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1582-913A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231383 | |||||||
chr20:37231386 | A | C | 1 | a0001c0002t0001g0014 | 2 | NA18992.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1582-910A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231386 | |||||||
chr20:37231387 | C | A | 8 | a0001c0002t0001g0015 a0001c0002t0001g0017 a0001c0002t0001g0018 others(5): Show |
12 | HG01361.hp2 HG02055.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1582-909C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231387 | |||||||
chr20:37231397 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1582-899C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231397 | |||||||
chr20:37231599 | C | G | 1 | a0001c0001t0001g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1582-697C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231599 | |||||||
chr20:37231711 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1582-585C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231711 | |||||||
chr20:37231714 | T | TAAAA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0039 others(8): Show |
17 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1582-577_1582-574d others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr20 | 37231714 | ||||||
chr20:37231714 | T | TAAAAAAA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
158 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1582-580_1582-574d others(9): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr20 | 37231714 | ||||||
chr20:37231714 | T | TAAAAAAA others(1): Show |
22 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
27 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1582-581_1582-574d others(10): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr20 | 37231714 | ||||||
chr20:37231723 | G | A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0039 others(8): Show |
17 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1582-573G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231723 | |||||||
chr20:37231734 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1582-562G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231734 | |||||||
chr20:37231800 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1582-496G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231800 | |||||||
chr20:37231816 | G | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1582-480G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231816 | |||||||
chr20:37231841 | G | T | 1 | a0001c0002t0001g0048 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1582-455G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231841 | |||||||
chr20:37231885 | T | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1582-411T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37231885 | |||||||
chr20:37232027 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1582-269G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37232027 | |||||||
chr20:37232211 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1582-85C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37232211 | |||||||
chr20:37232237 | A | C | 1 | a0008c0011t0001g0176 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1582-59A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 13/16 | chr20 | 37232237 | |||||||
chr20:37232704 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1677+313G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37232704 | |||||||
chr20:37232921 | G | C | 1 | a0001c0002t0001g0244 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1677+530G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37232921 | |||||||
chr20:37233002 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0100 a0001c0001t0001g0103 others(3): Show |
7 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1677+611G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233002 | |||||||
chr20:37233070 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1677+679A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233070 | |||||||
chr20:37233097 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1677+706C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233097 | |||||||
chr20:37233240 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1678-780C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233240 | |||||||
chr20:37233261 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678-759A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233261 | |||||||
chr20:37233273 | T | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1678-747T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233273 | |||||||
chr20:37233287 | A | G | 7 | a0001c0002t0001g0015 a0001c0002t0001g0018 a0001c0002t0001g0019 others(4): Show |
10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1678-733A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233287 | |||||||
chr20:37233374 | A | G | 1 | a0001c0002t0001g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1678-646A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233374 | |||||||
chr20:37233563 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1678-457C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233563 | |||||||
chr20:37233570 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1678-450C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233570 | |||||||
chr20:37233599 | T | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1678-421T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233599 | |||||||
chr20:37233602 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1678-418C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233602 | |||||||
chr20:37233641 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1678-379C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233641 | |||||||
chr20:37233654 | T | C | 18 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(15): Show |
27 | HG00609.hp2 HG01361.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1678-366T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233654 | |||||||
chr20:37233816 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678-204T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233816 | |||||||
chr20:37233866 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1678-154T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233866 | |||||||
chr20:37233964 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1678-56G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 14/16 | chr20 | 37233964 | |||||||
chr20:37234141 | T | A | 3 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 |
4 | HG02886.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+46T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234141 | |||||||
chr20:37234305 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1753+210T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234305 | |||||||
chr20:37234461 | G | T | 1 | a0001c0002t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1753+366G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234461 | |||||||
chr20:37234647 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1753+552G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234647 | |||||||
chr20:37234685 | G | GT | 27 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
32 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1753+603dupT | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37234685 | ||||||
chr20:37234685 | G | GTT | 132 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
181 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.1753+602_1753+603d others(4): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37234685 | ||||||
chr20:37234902 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1753+807C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234902 | |||||||
chr20:37234969 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1753+874C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37234969 | |||||||
chr20:37235008 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1753+913C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235008 | |||||||
chr20:37235068 | T | TAAGTCTC others(3): Show |
1 | a0001c0002t0001g0048 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1753+976_1753+985d others(12): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37235068 | ||||||
chr20:37235113 | AAG | A | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+1025_1753+102 others(6): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37235113 | ||||||
chr20:37235149 | G | A | 1 | a0001c0002t0001g0067 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1753+1054G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235149 | |||||||
chr20:37235303 | A | G | 3 | a0001c0002t0001g0015 a0001c0002t0001g0101 a0001c0002t0001g0102 |
4 | HG01361.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+1208A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235303 | |||||||
chr20:37235354 | G | A | 1 | a0003c0010t0001g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1754-1226G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235354 | |||||||
chr20:37235658 | T | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
180 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1754-922T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235658 | |||||||
chr20:37235691 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1754-889C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235691 | |||||||
chr20:37235811 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1754-769T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235811 | |||||||
chr20:37235875 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1754-705C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235875 | |||||||
chr20:37235951 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0005c0007t0001g0193 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1754-629A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37235951 | |||||||
chr20:37236042 | T | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1754-538T>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236042 | |||||||
chr20:37236086 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
27 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1754-494C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236086 | |||||||
chr20:37236093 | T | TTGTGGGT others(5): Show |
160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1754-482_1754-471d others(14): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr20 | 37236093 | ||||||
chr20:37236192 | A | T | 1 | a0001c0002t0001g0048 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1754-388A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236192 | |||||||
chr20:37236322 | A | T | 1 | a0001c0002t0001g0048 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1754-258A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236322 | |||||||
chr20:37236326 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1754-254A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236326 | |||||||
chr20:37236379 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1754-201G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 15/16 | chr20 | 37236379 | |||||||
chr20:37236867 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1883+158A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37236867 | |||||||
chr20:37236948 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
27 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1883+239G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37236948 | |||||||
chr20:37236958 | TA | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1883+250delA | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37236958 | |||||||
chr20:37237124 | C | T | 7 | a0001c0002t0001g0015 a0001c0002t0001g0018 a0001c0002t0001g0019 others(4): Show |
10 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+415C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237124 | |||||||
chr20:37237138 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1883+429C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237138 | |||||||
chr20:37237146 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1883+437T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237146 | |||||||
chr20:37237389 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1883+680G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237389 | |||||||
chr20:37237550 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1883+841G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237550 | |||||||
chr20:37237588 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1883+879G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237588 | |||||||
chr20:37237808 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1883+1099C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237808 | |||||||
chr20:37237843 | G | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+1134G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237843 | |||||||
chr20:37237864 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1883+1155A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237864 | |||||||
chr20:37237884 | G | A | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG00438.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1883+1175G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237884 | |||||||
chr20:37237915 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0146 |
2 | HG00735.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1883+1206G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37237915 | |||||||
chr20:37238337 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1883+1628T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37238337 | |||||||
chr20:37238662 | A | G | 4 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0110 others(1): Show |
6 | HG02818.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1883+1953A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37238662 | |||||||
chr20:37238731 | G | T | 1 | a0001c0002t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1883+2022G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37238731 | |||||||
chr20:37238981 | C | G | 1 | a0001c0001t0001g0011 | 3 | HG02055.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1883+2272C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37238981 | |||||||
chr20:37239137 | G | A | 1 | a0001c0002t0001g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1884-2166G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239137 | |||||||
chr20:37239307 | G | T | 1 | a0001c0002t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1884-1996G>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239307 | |||||||
chr20:37239573 | ATTTG | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
244 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.1884-1698_1884-169 others(8): Show |
RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr20 | 37239573 | ||||||
chr20:37239593 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1884-1710G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239593 | |||||||
chr20:37239643 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
109 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1884-1660A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239643 | |||||||
chr20:37239660 | T | C | 1 | a0001c0002t0001g0077 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1884-1643T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239660 | |||||||
chr20:37239816 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1884-1487C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239816 | |||||||
chr20:37239834 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(12): Show |
20 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1884-1469C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239834 | |||||||
chr20:37239907 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0221 others(5): Show |
12 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1884-1396G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239907 | |||||||
chr20:37239998 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1884-1305A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37239998 | |||||||
chr20:37240038 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1884-1265C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240038 | |||||||
chr20:37240092 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1211T>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240092 | |||||||
chr20:37240113 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1190A>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240113 | |||||||
chr20:37240115 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1188G>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240115 | |||||||
chr20:37240118 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1185G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240118 | |||||||
chr20:37240119 | A | C | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1184A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240119 | |||||||
chr20:37240123 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1180T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240123 | |||||||
chr20:37240126 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1177C>A | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240126 | |||||||
chr20:37240127 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1176T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240127 | |||||||
chr20:37240129 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1174G>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240129 | |||||||
chr20:37240131 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1172T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240131 | |||||||
chr20:37240132 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1171C>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240132 | |||||||
chr20:37240135 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1884-1168T>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240135 | |||||||
chr20:37240939 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1884-364A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37240939 | |||||||
chr20:37241012 | A | C | 10 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0042 others(7): Show |
15 | HG00609.hp2 HG01934.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1884-291A>C | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37241012 | |||||||
chr20:37241135 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
28 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1884-168A>G | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37241135 | |||||||
chr20:37241216 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1884-87C>T | RPN2 | ENSG00000118705.18 | transcript | ENST00000237530.11 | protein_coding | 16/16 | chr20 | 37241216 |