Item | Value |
---|---|
geneid | 5884 |
ensemblid | ENSG00000152942.19 |
hgncid | 9807 |
symbol | RAD17 |
name | RAD17 checkpoint clamp loader component |
refseq_nuc | NM_133338.3 |
refseq_prot | NP_579916.1 |
ensembl_nuc | ENST00000354868.10 |
ensembl_prot | ENSP00000346938.5 |
mane_status | MANE Select |
chr | chr5 |
start | 69369818 |
end | 69414801 |
strand | + |
ver | v1.2 |
region | chr5:69369818-69414801 |
region5000 | chr5:69364818-69419801 |
regionname0 | RAD17_chr5_69369818_69414801 |
regionname5000 | RAD17_chr5_69364818_69419801 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 670 | 264 | 68 | 48 | 118 | 6 | 23 | 93 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0002 | 0/0 | 670 | 76 | 2 | 19 | 45 | 2 | 8 | 34 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0003 | 0/0 | 670 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0004 | 0/0 | 670 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0005 | 0/0 | 670 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0006 | 0/0 | 670 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0007 | 0/0 | 670 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0008 | 0/0 | 670 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0009 | 0/0 | 670 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0010 | 0/0 | 670 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
a0011 | 0/0 | 670 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | MNQVT others(665): Show |
chr5 | 69364818 | 69419801 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2010 | 262 | 67 | 48 | 118 | 6 | 22 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0001c0007 | 0/0 | 2010 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0001c0009 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0002c0002 | 0/0 | 2010 | 76 | 2 | 19 | 45 | 2 | 8 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0003c0003 | 0/0 | 2010 | 8 | 8 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0004c0004 | 0/0 | 2010 | 3 | 0 | 2 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0005c0005 | 0/0 | 2010 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0006c0013 | 0/0 | 2010 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0007c0010 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0008c0008 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0009c0006 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0010c0011 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 | ||
a0011c0012 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | ATGAA others(2005): Show |
chr5 | 69364818 | 69419801 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3054 | 176 | 38 | 33 | 87 | 5 | 12 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0001c0001t0002 | 0/0 | 3054 | 80 | 28 | 12 | 29 | 1 | 10 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0001c0001t0003 | 0/0 | 3054 | 3 | 0 | 3 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0001c0001t0005 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0001c0001t0006 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0001c0001t0007 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0001c0007t0001 | 0/0 | 3054 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0001c0009t0001 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0002c0002t0001 | 0/0 | 3054 | 76 | 2 | 19 | 45 | 2 | 8 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0003c0003t0001 | 0/0 | 3054 | 8 | 8 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0004c0004t0001 | 0/0 | 3054 | 3 | 0 | 2 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0005c0005t0002 | 0/0 | 3054 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0006c0013t0001 | 0/0 | 3054 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0007c0010t0002 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0008c0008t0001 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0009c0006t0004 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0010c0011t0002 | 0/0 | 3054 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
a0011c0012t0001 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | GTACC others(3049): Show |
chr5 | 69364818 | 69419801 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0007t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0001c0009t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0003c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0004c0004t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0004c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0004c0004t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0005c0005t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0005c0005t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0006c0013t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0007c0010t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0008c0008t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0009c0006t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0010c0011t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
a0011c0012t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0171 | EUR | GBR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0182 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01168 | hp2 | a0004 | c0004 | t0001 | g0164 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0168 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01256 | hp1 | a0006 | c0013 | t0001 | g0254 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0265 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01952 | hp2 | a0004 | c0004 | t0001 | g0162 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0266 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | CDX | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | CDX | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | CDX | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02896 | hp1 | a0005 | c0005 | t0002 | g0317 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0031 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02897 | hp2 | a0005 | c0005 | t0002 | g0316 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03453 | hp1 | a0007 | c0010 | t0002 | g0314 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03453 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03490 | hp1 | a0004 | c0004 | t0001 | g0163 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | ESN | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0343 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0344 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG04204 | hp2 | a0001 | c0007 | t0001 | g0219 | SAS | STU | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18522 | hp1 | a0001 | c0009 | t0001 | g0128 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | CHB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18940 | hp2 | a0008 | c0008 | t0001 | g0180 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18977 | hp1 | a0009 | c0006 | t0004 | g0076 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | LWK | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19078 | hp1 | a0010 | c0011 | t0002 | g0332 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0028 | AFR | YRI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ASW | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20129 | hp2 | a0011 | c0012 | t0001 | g0245 | AFR | ASW | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0176 | EUR | TSI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0310 | EUR | TSI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | GIH | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | GIH | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0200 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | USA | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | USA | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0215 | REF | REF | RAD17_chr5_69364818_69419801 | RAD17 | chr5 | 69364818 | 69419801 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:69373887 | A | G | 1 | a0006 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.67A>G | p.Thr23Ala | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/19 | 599/3054 | 67/2013 | 23/670 | chr5 | 69373887 | |||
chr5:69373909 | G | T | 1 | a0011 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.89G>T | p.Gly30Val | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/19 | 621/3054 | 89/2013 | 30/670 | chr5 | 69373909 | |||
chr5:69386200 | G | A | 1 | a0009 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.719G>A | p.Arg240Gln | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 10/19 | 1251/3054 | 719/2013 | 240/670 | chr5 | 69386200 | |||
chr5:69386217 | A | T | 1 | a0010 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.736A>T | p.Ile246Leu | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 10/19 | 1268/3054 | 736/2013 | 246/670 | chr5 | 69386217 | |||
chr5:69386218 | T | A | 1 | a0010 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.737T>A | p.Ile246Lys | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 10/19 | 1269/3054 | 737/2013 | 246/670 | chr5 | 69386218 | |||
chr5:69391965 | G | A | 1 | a0003 | 8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
missense_variant | MODERATE | c.1141G>A | p.Val381Ile | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/19 | 1673/3054 | 1141/2013 | 381/670 | chr5 | 69391965 | |||
chr5:69393445 | T | C | 1 | a0008 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.1367T>C | p.Ile456Thr | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/19 | 1899/3054 | 1367/2013 | 456/670 | chr5 | 69393445 | |||
chr5:69396401 | G | T | 1 | a0005 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.1427G>T | p.Arg476Leu | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/19 | 1959/3054 | 1427/2013 | 476/670 | chr5 | 69396401 | |||
chr5:69400113 | T | G | 2 | a0002 a0008 |
77 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(74): Show |
missense_variant | MODERATE | c.1637T>G | p.Leu546Arg | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/19 | 2169/3054 | 1637/2013 | 546/670 | chr5 | 69400113 | |||
chr5:69414045 | C | T | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1766C>T | p.Ala589Val | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 2298/3054 | 1766/2013 | 589/670 | chr5 | 69414045 | |||
chr5:69414057 | G | A | 1 | a0004 | 3 | HG01168.hp2 HG01952.hp2 HG03490.hp1 |
missense_variant | MODERATE | c.1778G>A | p.Arg593Lys | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 2310/3054 | 1778/2013 | 593/670 | chr5 | 69414057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:69386219 | A | T | 1 | a0010c0011 | 1 | NA19078.hp1 | synonymous_variant | LOW | c.738A>T | p.Ile246Ile | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 10/19 | 1270/3054 | 738/2013 | 246/670 | chr5 | 69386219 | |||
chr5:69389135 | T | G | 1 | a0001c0007 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.996T>G | p.Ser332Ser | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/19 | 1528/3054 | 996/2013 | 332/670 | chr5 | 69389135 | |||
chr5:69414052 | T | G | 1 | a0001c0009 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1773T>G | p.Thr591Thr | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 2305/3054 | 1773/2013 | 591/670 | chr5 | 69414052 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:69369909 | T | C | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(11): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
5_prime_UTR_variant | MODIFIER | c.-441T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/19 | 2300 | chr5 | 69369909 | ||||||
chr5:69371085 | C | T | 1 | a0001c0001t0003 | 3 | HG01433.hp2 HG01496.hp2 HG01952.hp1 |
5_prime_UTR_variant | MODIFIER | c.-366C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/19 | 1124 | chr5 | 69371085 | ||||||
chr5:69372154 | T | A | 1 | a0009c0006t0004 | 1 | NA18977.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/19 | 55 | chr5 | 69372154 | ||||||
chr5:69414380 | A | G | 1 | a0001c0001t0007 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 88 | chr5 | 69414380 | ||||||
chr5:69414636 | A | G | 1 | a0001c0001t0006 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*344A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 344 | chr5 | 69414636 | ||||||
chr5:69414768 | A | C | 1 | a0001c0001t0005 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*476A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 19/19 | 476 | chr5 | 69414768 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:69369982 | T | C | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.-417+49T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69369982 | |||||||
chr5:69370145 | C | T | 1 | a0001c0001t0002g0346 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-417+212C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370145 | |||||||
chr5:69370156 | G | A | 3 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-417+223G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370156 | |||||||
chr5:69370655 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-416-380T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370655 | |||||||
chr5:69370802 | G | C | 9 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0015 others(6): Show |
9 | HG01975.hp2 HG02071.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-416-233G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370802 | |||||||
chr5:69370855 | G | C | 4 | a0002c0002t0001g0001 a0002c0002t0001g0022 a0002c0002t0001g0023 others(1): Show |
7 | HG00558.hp2 HG02155.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-416-180G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370855 | |||||||
chr5:69370938 | C | G | 1 | a0002c0002t0001g0269 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-416-97C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370938 | |||||||
chr5:69370958 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-416-77A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 1/18 | chr5 | 69370958 | |||||||
chr5:69371436 | T | TC | 28 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0002g0320 others(25): Show |
28 | HG00609.hp1 HG00642.hp1 HG01243.hp1 others(25): Show |
splice_acceptor_variant&intron_variant | HIGH | c.-279-3dupC | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 69371436 | ||||||
chr5:69371436 | TCC | T | 31 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0246 others(28): Show |
32 | HG00423.hp1 HG00733.hp1 HG00741.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.-279-4_-279-3delCC | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 69371436 | ||||||
chr5:69371436 | TCCC | T | 231 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
splice_region_variant&intron_variant | LOW | c.-279-5_-279-3delCC others(1): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 69371436 | ||||||
chr5:69371448 | C | A | 8 | a0002c0002t0001g0025 a0003c0003t0001g0002 a0003c0003t0001g0026 others(5): Show |
9 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.-279-6C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 2/18 | chr5 | 69371448 | |||||||
chr5:69371576 | G | A | 7 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-176+19G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 3/18 | chr5 | 69371576 | |||||||
chr5:69371796 | G | A | 9 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0015 others(6): Show |
9 | HG01975.hp2 HG02071.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-175-238G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 3/18 | chr5 | 69371796 | |||||||
chr5:69371979 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-175-55C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 3/18 | chr5 | 69371979 | |||||||
chr5:69372377 | C | T | 2 | a0005c0005t0002g0316 a0005c0005t0002g0317 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.9+160C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372377 | |||||||
chr5:69372395 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9+178C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372395 | |||||||
chr5:69372559 | A | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0216 a0001c0001t0001g0217 others(25): Show |
29 | HG00438.hp1 HG00621.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.9+342A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372559 | |||||||
chr5:69372704 | C | T | 1 | a0003c0003t0001g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.9+487C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372704 | |||||||
chr5:69372840 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.9+623G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372840 | |||||||
chr5:69372944 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.9+727T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69372944 | |||||||
chr5:69373165 | T | C | 2 | a0002c0002t0001g0032 a0002c0002t0001g0033 |
2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.10-665T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373165 | |||||||
chr5:69373422 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.10-408G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373422 | |||||||
chr5:69373431 | G | C | 1 | a0003c0003t0001g0002 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.10-399G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373431 | |||||||
chr5:69373443 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.10-387T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373443 | |||||||
chr5:69373628 | T | G | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10-202T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373628 | |||||||
chr5:69373663 | G | A | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.10-167G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373663 | |||||||
chr5:69373684 | AAATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10-145_10-134delAA others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373684 | |||||||
chr5:69373685 | AATTTT | A | 18 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0243 others(15): Show |
18 | HG00423.hp1 HG00733.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.10-144_10-140delAT others(3): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373685 | |||||||
chr5:69373685 | AATTTTT | A | 134 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(131): Show |
139 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.10-144_10-139delAT others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373685 | |||||||
chr5:69373685 | AATTTTTT | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0146 others(13): Show |
16 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.10-144_10-138delAT others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373685 | |||||||
chr5:69373686 | A | AT | 13 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0273 others(10): Show |
13 | HG01243.hp1 HG02148.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.10-114dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | ||||||
chr5:69373686 | AT | A | 14 | a0001c0001t0001g0277 a0001c0001t0002g0010 a0001c0001t0002g0011 others(11): Show |
15 | HG00741.hp1 HG01256.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.10-114delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | ||||||
chr5:69373686 | ATT | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0078 a0001c0001t0001g0092 others(5): Show |
8 | HG00621.hp1 HG02071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-115_10-114delTT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | ||||||
chr5:69373686 | ATTT | A | 82 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(79): Show |
82 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.10-116_10-114delTT others(1): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | ||||||
chr5:69373686 | ATTTT | A | 8 | a0001c0001t0001g0039 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
8 | HG00323.hp1 HG01168.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.10-117_10-114delTT others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 69373686 | ||||||
chr5:69373717 | A | T | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.10-113A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 4/18 | chr5 | 69373717 | |||||||
chr5:69374108 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.267+21A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374108 | |||||||
chr5:69374112 | C | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.267+25C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374112 | |||||||
chr5:69374223 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.267+136T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374223 | |||||||
chr5:69374274 | A | G | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.267+187A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374274 | |||||||
chr5:69374312 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.267+225G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374312 | |||||||
chr5:69374530 | A | C | 1 | a0001c0001t0005g0240 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.268-98A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374530 | |||||||
chr5:69374586 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.268-42C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 5/18 | chr5 | 69374586 | |||||||
chr5:69375033 | C | G | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+322C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375033 | |||||||
chr5:69375157 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0210 others(6): Show |
10 | HG01074.hp2 HG02647.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+446A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375157 | |||||||
chr5:69375215 | A | T | 1 | a0001c0001t0002g0315 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.351+504A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375215 | |||||||
chr5:69375626 | G | GTC | 264 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.351+917_351+918dup others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69375626 | ||||||
chr5:69375630 | G | C | 1 | a0002c0002t0001g0209 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.351+919G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375630 | |||||||
chr5:69375638 | A | T | 1 | a0002c0002t0001g0209 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.351+927A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375638 | |||||||
chr5:69375759 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.351+1048T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375759 | |||||||
chr5:69375855 | T | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | NA18956.hp2 NA18963.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+1144T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69375855 | |||||||
chr5:69376088 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0238 a0001c0001t0001g0239 |
4 | HG02083.hp1 HG03669.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1377C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376088 | |||||||
chr5:69376089 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.351+1378G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376089 | |||||||
chr5:69376142 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.351+1431A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376142 | |||||||
chr5:69376332 | G | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.351+1621G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376332 | |||||||
chr5:69376334 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351+1623C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376334 | |||||||
chr5:69376486 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.351+1775A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376486 | |||||||
chr5:69376569 | A | G | 1 | a0007c0010t0002g0314 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+1858A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376569 | |||||||
chr5:69376685 | G | C | 1 | a0002c0002t0001g0123 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.351+1974G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376685 | |||||||
chr5:69376762 | C | CT | 264 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.351+2061dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69376762 | ||||||
chr5:69376913 | G | T | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351+2202G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376913 | |||||||
chr5:69376916 | G | C | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.351+2205G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376916 | |||||||
chr5:69376985 | C | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2274C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376985 | |||||||
chr5:69376999 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.351+2288C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69376999 | |||||||
chr5:69377122 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.351+2411A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377122 | |||||||
chr5:69377288 | A | G | 1 | a0002c0002t0001g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.351+2577A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377288 | |||||||
chr5:69377339 | T | C | 163 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
171 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.351+2628T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377339 | |||||||
chr5:69377343 | A | G | 4 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 others(1): Show |
4 | HG02165.hp2 NA18994.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2632A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377343 | |||||||
chr5:69377415 | G | GTA | 14 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0243 others(11): Show |
15 | HG00558.hp1 HG00733.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.351+2708_351+2709d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377415 | ||||||
chr5:69377419 | A | ATATG | 7 | a0001c0001t0001g0127 a0001c0001t0001g0218 a0001c0001t0001g0253 others(4): Show |
7 | HG01496.hp2 HG01975.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2709_351+2710i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377419 | ||||||
chr5:69377419 | ATG | A | 9 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0284 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2728_351+2729d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377419 | ||||||
chr5:69377421 | G | A | 145 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(142): Show |
152 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.351+2710G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377421 | |||||||
chr5:69377437 | G | GTATA | 3 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0288 |
3 | HG02895.hp2 HG02897.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.351+2727_351+2728i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377437 | G | GTATATAT others(13): Show |
12 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.351+2727_351+2728i others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377437 | G | GTATATAT others(19): Show |
1 | a0001c0001t0002g0309 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.351+2727_351+2728i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377437 | G | GTATATAT others(21): Show |
1 | a0001c0001t0002g0310 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.351+2727_351+2728i others(30): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377437 | GTGTA | G | 3 | a0001c0001t0001g0268 a0001c0001t0002g0281 a0001c0001t0002g0320 |
3 | HG02572.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.351+2728_351+2731d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377437 | GTGTATA | G | 5 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0279 others(2): Show |
5 | HG01243.hp1 HG01261.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2728_351+2733d others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377437 | GTGTATAT others(5): Show |
G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.351+2728_351+2739d others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377437 | GTGTATAT others(9): Show |
G | 1 | a0001c0001t0001g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.351+2728_351+2743d others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377437 | GTGTATAT others(11): Show |
G | 1 | a0001c0001t0002g0318 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.351+2728_351+2745d others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377437 | ||||||
chr5:69377439 | G | A | 46 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(43): Show |
50 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(47): Show |
intron_variant | MODIFIER | c.351+2728G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377439 | |||||||
chr5:69377439 | GTATATAT others(11): Show |
G | 1 | a0001c0001t0001g0246 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.351+2747_351+2764d others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377439 | ||||||
chr5:69377441 | A | ATATATAT others(11): Show |
14 | a0001c0001t0002g0011 a0001c0001t0002g0296 a0001c0001t0002g0297 others(11): Show |
15 | HG01256.hp2 HG01258.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.351+2747_351+2748i others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377441 | ||||||
chr5:69377441 | A | G | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
153 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.351+2730A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377441 | |||||||
chr5:69377443 | A | ATATATAT others(9): Show |
6 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 others(3): Show |
6 | HG01943.hp2 HG02155.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2747_351+2748i others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377443 | ||||||
chr5:69377443 | A | G | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+2732A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377443 | |||||||
chr5:69377445 | A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0328 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.351+2749_351+2750i others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377445 | ||||||
chr5:69377445 | A | ATATATAT others(7): Show |
6 | a0001c0001t0002g0010 a0001c0001t0002g0275 a0001c0001t0002g0276 others(3): Show |
7 | HG01109.hp2 HG03579.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2747_351+2748i others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377445 | ||||||
chr5:69377450 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0253 a0001c0001t0003g0265 a0002c0002t0001g0013 others(1): Show |
4 | HG01496.hp2 HG01975.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2740_351+2741i others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377450 | ||||||
chr5:69377450 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0127 |
2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.351+2740_351+2741i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377450 | ||||||
chr5:69377450 | T | TATACACA others(3): Show |
3 | a0002c0002t0001g0022 a0002c0002t0001g0025 a0002c0002t0001g0125 |
3 | HG02155.hp2 NA18948.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.351+2742_351+2743i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377450 | ||||||
chr5:69377450 | T | TATATATA others(21): Show |
1 | a0001c0001t0002g0290 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.351+2747_351+2748i others(30): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377450 | ||||||
chr5:69377452 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2741T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377452 | |||||||
chr5:69377452 | T | TATATATG others(19): Show |
1 | a0001c0001t0002g0009 | 2 | HG02148.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.351+2747_351+2748i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377452 | ||||||
chr5:69377453 | A | ACACACAC others(65): Show |
5 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(2): Show |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+2742_351+2743i others(74): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377453 | |||||||
chr5:69377453 | A | ACACACAC others(63): Show |
1 | a0003c0003t0001g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.351+2742_351+2743i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377453 | |||||||
chr5:69377453 | A | ACACACAC others(21): Show |
2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2742_351+2743i others(30): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377453 | |||||||
chr5:69377453 | A | ACACACAC others(63): Show |
3 | a0001c0001t0001g0218 a0001c0009t0001g0128 a0002c0002t0001g0129 |
3 | NA18522.hp1 NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.351+2742_351+2743i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377453 | |||||||
chr5:69377453 | A | ATACACAC others(65): Show |
1 | a0006c0013t0001g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.351+2744_351+2745i others(74): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377453 | ||||||
chr5:69377453 | A | ATATATGT others(65): Show |
1 | a0001c0001t0002g0346 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.351+2747_351+2748i others(74): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377453 | ||||||
chr5:69377454 | T | TACACAC | 6 | a0001c0001t0001g0203 a0001c0001t0001g0259 a0002c0002t0001g0199 others(3): Show |
6 | HG00609.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2744_351+2745i others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377454 | ||||||
chr5:69377454 | T | TATATGTA others(17): Show |
1 | a0001c0001t0002g0289 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.351+2747_351+2748i others(26): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377454 | ||||||
chr5:69377455 | A | ACACACAC others(33): Show |
1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2744_351+2745i others(42): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | |||||||
chr5:69377455 | A | ACACACAC others(63): Show |
1 | a0002c0002t0001g0023 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.351+2744_351+2745i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | |||||||
chr5:69377455 | A | ACACACAC others(63): Show |
1 | a0002c0002t0001g0015 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.351+2744_351+2745i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | |||||||
chr5:69377455 | A | ACACACAC others(63): Show |
133 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
140 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.351+2744_351+2745i others(72): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | |||||||
chr5:69377455 | A | ACACACAC others(117): Show |
1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351+2744_351+2745i others(126): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | |||||||
chr5:69377455 | A | ACACACAC others(65): Show |
1 | a0002c0002t0001g0021 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.351+2744_351+2745i others(74): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377455 | |||||||
chr5:69377456 | T | C | 6 | a0001c0001t0001g0203 a0001c0001t0001g0259 a0002c0002t0001g0199 others(3): Show |
6 | HG00609.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2745T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377456 | |||||||
chr5:69377456 | TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0045 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.351+2747_351+2766d others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377456 | ||||||
chr5:69377458 | T | TAC | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2748_351+2749i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377458 | ||||||
chr5:69377458 | TATATATA others(11): Show |
T | 79 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(76): Show |
79 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.351+2749_351+2766d others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377458 | ||||||
chr5:69377459 | A | ACG | 9 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0253 others(6): Show |
9 | HG01496.hp2 HG01975.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2748_351+2749i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377459 | |||||||
chr5:69377460 | T | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2749T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377460 | |||||||
chr5:69377460 | TATATATA others(9): Show |
T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2751_351+2766d others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377460 | ||||||
chr5:69377460 | TATATATA others(11): Show |
T | 1 | a0001c0001t0001g0036 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.351+2751_351+2768d others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377460 | ||||||
chr5:69377462 | T | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2751T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377462 | |||||||
chr5:69377463 | A | G | 14 | a0001c0001t0001g0218 a0001c0001t0001g0243 a0001c0001t0001g0244 others(11): Show |
15 | HG00733.hp1 HG01256.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.351+2752A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377463 | |||||||
chr5:69377464 | T | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2753T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377464 | |||||||
chr5:69377464 | TATATATA others(195): Show |
T | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2764_351+2965d others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377464 | ||||||
chr5:69377465 | A | G | 147 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
155 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.351+2754A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377465 | |||||||
chr5:69377466 | T | C | 16 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00609.hp2 HG01099.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+2755T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377466 | |||||||
chr5:69377467 | A | G | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
151 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.351+2756A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377467 | |||||||
chr5:69377468 | T | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01099.hp2 HG03704.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2757T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377468 | |||||||
chr5:69377469 | A | G | 9 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0253 others(6): Show |
9 | HG01496.hp2 HG01975.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2758A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377469 | |||||||
chr5:69377470 | T | C | 6 | a0001c0001t0001g0268 a0001c0001t0002g0283 a0001c0001t0002g0285 others(3): Show |
6 | HG02258.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+2759T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377470 | |||||||
chr5:69377472 | T | C | 10 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0268 others(7): Show |
10 | HG02258.hp1 HG02572.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+2761T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377472 | |||||||
chr5:69377473 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2762A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377473 | |||||||
chr5:69377474 | T | C | 14 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0268 others(11): Show |
14 | HG00642.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.351+2763T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377474 | |||||||
chr5:69377474 | T | TATAC | 6 | a0001c0001t0002g0008 a0001c0001t0002g0270 a0001c0001t0002g0278 others(3): Show |
6 | HG02559.hp2 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2764_351+2765i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377474 | ||||||
chr5:69377475 | A | G | 3 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG00733.hp1 HG02895.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.351+2764A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377475 | |||||||
chr5:69377476 | C | T | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.351+2765C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377476 | |||||||
chr5:69377477 | A | G | 27 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(24): Show |
28 | HG00609.hp2 HG01099.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.351+2766A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377477 | |||||||
chr5:69377478 | C | T | 39 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(36): Show |
40 | HG00609.hp2 HG00733.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.351+2767C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377478 | |||||||
chr5:69377479 | A | G | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
151 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.351+2768A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377479 | |||||||
chr5:69377480 | C | T | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
182 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.351+2769C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377480 | |||||||
chr5:69377482 | C | T | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
182 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.351+2771C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377482 | |||||||
chr5:69377483 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351+2772A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377483 | |||||||
chr5:69377484 | C | T | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
182 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.351+2773C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377484 | |||||||
chr5:69377485 | A | ATGTG | 9 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0253 others(6): Show |
9 | HG01496.hp2 HG01975.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2774_351+2775i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377485 | |||||||
chr5:69377485 | A | G | 2 | a0001c0001t0001g0241 a0003c0003t0001g0030 |
2 | HG01884.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.351+2774A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377485 | |||||||
chr5:69377486 | C | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
180 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.351+2775C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377486 | |||||||
chr5:69377487 | A | G | 28 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(25): Show |
29 | HG00609.hp2 HG00733.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.351+2776A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377487 | |||||||
chr5:69377488 | T | C | 86 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(83): Show |
86 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.351+2777T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377488 | |||||||
chr5:69377489 | A | G | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
142 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.351+2778A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377489 | |||||||
chr5:69377495 | A | G | 18 | a0001c0001t0001g0203 a0001c0001t0001g0218 a0001c0001t0001g0259 others(15): Show |
19 | HG00609.hp2 HG01256.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.351+2784A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377495 | |||||||
chr5:69377496 | C | T | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
164 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.351+2785C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377496 | |||||||
chr5:69377499 | A | G | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
142 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.351+2788A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377499 | |||||||
chr5:69377499 | ATATATAT others(155): Show |
A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2793_351+2954d others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377499 | ||||||
chr5:69377505 | A | ATG | 3 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG01099.hp2 HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.351+2796_351+2797d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377505 | ||||||
chr5:69377505 | A | G | 4 | a0001c0001t0001g0218 a0001c0009t0001g0128 a0002c0002t0001g0021 others(1): Show |
4 | NA18522.hp1 NA18946.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2794A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377505 | |||||||
chr5:69377506 | T | C | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+2795T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377506 | |||||||
chr5:69377506 | T | TAC | 7 | a0001c0001t0001g0203 a0001c0001t0001g0259 a0002c0002t0001g0199 others(4): Show |
7 | HG00609.hp2 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2795_351+2796i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377506 | |||||||
chr5:69377507 | G | GTA | 4 | a0001c0001t0001g0218 a0001c0009t0001g0128 a0002c0002t0001g0021 others(1): Show |
4 | NA18522.hp1 NA18946.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2803_351+2804d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377507 | ||||||
chr5:69377507 | G | GTGTA | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
152 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.351+2797_351+2798i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377507 | ||||||
chr5:69377509 | A | ATATATAT others(57): Show |
6 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0253 others(3): Show |
6 | HG01496.hp2 HG01975.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+2804_351+2805i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377509 | ||||||
chr5:69377509 | A | ATATATAT others(59): Show |
1 | a0002c0002t0001g0125 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.351+2804_351+2805i others(68): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377509 | ||||||
chr5:69377509 | A | ATATATAT others(55): Show |
2 | a0002c0002t0001g0022 a0002c0002t0001g0025 |
2 | HG02155.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.351+2804_351+2805i others(64): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377509 | ||||||
chr5:69377516 | C | T | 18 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0203 others(15): Show |
18 | HG00609.hp2 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.351+2805C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377516 | |||||||
chr5:69377519 | A | ATATATG | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
147 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.351+2813_351+2814i others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377519 | ||||||
chr5:69377525 | A | ATGTATAT others(3): Show |
6 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(3): Show |
7 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2817_351+2818i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377525 | ||||||
chr5:69377525 | A | G | 11 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0241 others(8): Show |
11 | HG01496.hp2 HG01884.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.351+2814A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377525 | |||||||
chr5:69377527 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2817_351+2818i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377527 | ||||||
chr5:69377528 | T | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG01099.hp2 HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.351+2817T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377528 | |||||||
chr5:69377529 | G | A | 22 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 others(19): Show |
23 | HG00733.hp1 HG01099.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.351+2818G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377529 | |||||||
chr5:69377529 | G | GTA | 145 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(142): Show |
152 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.351+2825_351+2826d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377529 | ||||||
chr5:69377538 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG01099.hp2 HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.351+2827C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377538 | |||||||
chr5:69377540 | T | TATAC | 3 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG01099.hp2 HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.351+2832_351+2833i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377540 | ||||||
chr5:69377540 | T | TATATATA others(97): Show |
1 | a0001c0001t0001g0050 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.351+2837_351+2838i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377540 | ||||||
chr5:69377540 | T | TATATATA others(95): Show |
8 | a0001c0001t0001g0049 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG01168.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2847_351+2848i others(104): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377540 | ||||||
chr5:69377550 | C | CAT | 108 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0036 others(105): Show |
110 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.351+2846_351+2847d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377550 | ||||||
chr5:69377550 | C | T | 7 | a0001c0001t0001g0203 a0001c0001t0001g0259 a0002c0002t0001g0199 others(4): Show |
7 | HG00609.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2839C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377550 | |||||||
chr5:69377554 | T | C | 2 | a0001c0001t0001g0210 a0002c0002t0001g0130 |
2 | NA18952.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.351+2843T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377554 | |||||||
chr5:69377555 | A | ATGTGTAT others(107): Show |
1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+2845_351+2846i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377555 | ||||||
chr5:69377557 | A | G | 6 | a0001c0001t0001g0203 a0001c0001t0001g0259 a0002c0002t0001g0199 others(3): Show |
6 | HG00609.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2846A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377557 | |||||||
chr5:69377558 | T | C | 2 | a0001c0001t0002g0288 a0001c0001t0002g0310 |
2 | HG03834.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.351+2847T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377558 | |||||||
chr5:69377559 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
7 | HG01243.hp2 NA18956.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2848G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377559 | |||||||
chr5:69377559 | GTA | G | 9 | a0001c0001t0002g0283 a0001c0001t0002g0284 a0001c0001t0002g0285 others(6): Show |
9 | HG02258.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2858_351+2859d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377559 | ||||||
chr5:69377560 | T | C | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+2849T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377560 | |||||||
chr5:69377560 | T | TATAC | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0243 others(3): Show |
6 | HG00733.hp1 HG01099.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2852_351+2853i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377560 | ||||||
chr5:69377560 | T | TATATATG others(121): Show |
1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.351+2855_351+2856i others(130): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377560 | ||||||
chr5:69377562 | T | TAC | 240 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(237): Show |
248 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.351+2852_351+2853i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377562 | ||||||
chr5:69377562 | T | TATATGTG others(103): Show |
2 | a0002c0002t0001g0199 a0002c0002t0001g0200 |
2 | HG02559.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.351+2855_351+2856i others(112): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377562 | ||||||
chr5:69377562 | T | TATATGTG others(101): Show |
3 | a0001c0001t0001g0203 a0002c0002t0001g0201 a0002c0002t0001g0202 |
3 | HG00609.hp2 NA18980.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.351+2855_351+2856i others(110): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377562 | ||||||
chr5:69377562 | T | TGTATAC | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | NA18956.hp2 NA18963.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2851_351+2852i others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377562 | |||||||
chr5:69377572 | C | CAT | 4 | a0001c0001t0001g0050 a0001c0001t0001g0107 a0001c0001t0001g0259 others(1): Show |
4 | HG02155.hp2 HG02280.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2868_351+2869d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377572 | ||||||
chr5:69377572 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351+2861C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377572 | |||||||
chr5:69377585 | A | ACATATAT others(31): Show |
1 | a0001c0001t0002g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.351+2883_351+2884i others(40): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377585 | ||||||
chr5:69377585 | A | G | 12 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(9): Show |
12 | HG00609.hp2 HG00733.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.351+2874A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377585 | |||||||
chr5:69377586 | C | CAT | 8 | a0001c0001t0001g0049 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG01168.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2884_351+2885d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | ||||||
chr5:69377586 | C | CATATATA others(99): Show |
1 | a0001c0001t0001g0051 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.351+2885_351+2886i others(108): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | ||||||
chr5:69377586 | C | CATATATA others(97): Show |
21 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0068 others(18): Show |
21 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | ||||||
chr5:69377586 | C | CATATATA others(99): Show |
1 | a0001c0001t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.351+2883_351+2884i others(108): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | ||||||
chr5:69377586 | C | CATATATA others(95): Show |
2 | a0001c0001t0001g0109 a0001c0001t0001g0121 |
2 | HG04204.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.351+2883_351+2884i others(104): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | ||||||
chr5:69377586 | CAT | C | 8 | a0001c0001t0001g0111 a0001c0001t0001g0124 a0001c0001t0001g0131 others(5): Show |
8 | HG01099.hp2 HG01243.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+2884_351+2885d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | ||||||
chr5:69377586 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351+2879_351+2902d others(26): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377586 | ||||||
chr5:69377587 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377587 | ||||||
chr5:69377587 | A | C | 1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2876A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377587 | |||||||
chr5:69377588 | T | TATATATA others(95): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02572.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.351+2895_351+2896i others(104): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | ||||||
chr5:69377588 | T | TATATATA others(67): Show |
1 | a0001c0001t0001g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(76): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | ||||||
chr5:69377588 | T | TATATATA others(93): Show |
2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00741.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.351+2895_351+2896i others(102): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | ||||||
chr5:69377588 | T | TATATATG others(87): Show |
1 | a0002c0002t0001g0191 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.351+2883_351+2884i others(96): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | ||||||
chr5:69377588 | T | TATATATG others(85): Show |
1 | a0002c0002t0001g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.351+2883_351+2884i others(94): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377588 | ||||||
chr5:69377593 | A | ATATGCAT others(97): Show |
1 | a0001c0001t0001g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377593 | ||||||
chr5:69377593 | A | ATGCATAT others(5): Show |
2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.351+2883_351+2884i others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377593 | ||||||
chr5:69377594 | T | TATGCATA others(59): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0210 others(5): Show |
9 | HG01074.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(68): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(87): Show |
1 | a0001c0001t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(96): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(95): Show |
1 | a0002c0002t0001g0024 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(104): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(237): Show |
1 | a0002c0002t0001g0167 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(246): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(131): Show |
1 | a0002c0002t0001g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(140): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(143): Show |
1 | a0001c0001t0001g0195 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(152): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(143): Show |
33 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(30): Show |
38 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(152): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(185): Show |
1 | a0002c0002t0001g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(194): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(171): Show |
5 | a0002c0002t0001g0021 a0002c0002t0001g0168 a0002c0002t0001g0169 others(2): Show |
5 | HG00099.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(180): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(129): Show |
1 | a0002c0002t0001g0182 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(138): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(195): Show |
1 | a0002c0002t0001g0183 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(204): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(227): Show |
1 | a0002c0002t0001g0023 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(236): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(169): Show |
2 | a0002c0002t0001g0184 a0002c0002t0001g0185 |
2 | NA18981.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.351+2895_351+2896i others(178): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(121): Show |
1 | a0001c0001t0001g0186 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(130): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(141): Show |
1 | a0001c0001t0001g0187 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(150): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(169): Show |
1 | a0001c0001t0003g0188 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(178): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TATGCATA others(143): Show |
1 | a0002c0002t0001g0013 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.351+2893_351+2894i others(152): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377594 | ||||||
chr5:69377594 | T | TGCATATA others(141): Show |
2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.351+2883_351+2884i others(150): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377594 | |||||||
chr5:69377594 | T | TGCATATA others(207): Show |
1 | a0002c0002t0001g0192 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.351+2883_351+2884i others(216): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377594 | |||||||
chr5:69377594 | T | TGCATATA others(141): Show |
3 | a0001c0001t0001g0193 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG01346.hp1 HG01358.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.351+2883_351+2884i others(150): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377594 | |||||||
chr5:69377598 | CAT | C | 65 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0037 others(62): Show |
66 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.351+2896_351+2897d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377598 | ||||||
chr5:69377600 | T | TATATATG others(1): Show |
33 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0126 others(30): Show |
33 | HG00323.hp2 HG00558.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | ||||||
chr5:69377600 | T | TATATATG others(27): Show |
1 | a0002c0002t0001g0130 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.351+2895_351+2896i others(36): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | ||||||
chr5:69377600 | T | TATATATG others(51): Show |
12 | a0002c0002t0001g0016 a0002c0002t0001g0022 a0002c0002t0001g0135 others(9): Show |
12 | HG00423.hp1 HG01928.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.351+2895_351+2896i others(60): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | ||||||
chr5:69377600 | T | TATATATG others(43): Show |
1 | a0001c0001t0001g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(52): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | ||||||
chr5:69377600 | T | TATATATG others(41): Show |
2 | a0001c0001t0001g0046 a0001c0001t0001g0053 |
2 | HG00735.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.351+2895_351+2896i others(50): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | ||||||
chr5:69377600 | T | TATATATG others(133): Show |
1 | a0001c0001t0001g0036 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(142): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377600 | ||||||
chr5:69377604 | T | TATGTATA others(107): Show |
1 | a0001c0001t0001g0042 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.351+2895_351+2896i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377604 | ||||||
chr5:69377607 | A | G | 10 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(7): Show |
10 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+2896A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377607 | |||||||
chr5:69377609 | G | A | 11 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
11 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.351+2898G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377609 | |||||||
chr5:69377610 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0187 others(60): Show |
69 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.351+2899T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377610 | |||||||
chr5:69377612 | T | C | 10 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(7): Show |
10 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+2901T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377612 | |||||||
chr5:69377613 | A | G | 33 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0042 others(30): Show |
33 | HG00323.hp2 HG00558.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.351+2902A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377613 | |||||||
chr5:69377614 | C | CAT | 9 | a0001c0001t0001g0036 a0001c0001t0001g0124 a0001c0001t0001g0131 others(6): Show |
9 | HG00741.hp1 HG01243.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+2910_351+2911d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(37): Show |
1 | a0001c0001t0001g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.351+2911_351+2912i others(46): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(115): Show |
1 | a0001c0001t0001g0047 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.351+2911_351+2912i others(124): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(97): Show |
1 | a0001c0001t0001g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.351+2911_351+2912i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(83): Show |
4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | NA18956.hp2 NA18963.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2911_351+2912i others(92): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(113): Show |
1 | a0001c0001t0001g0063 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.351+2911_351+2912i others(122): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(111): Show |
18 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0065 others(15): Show |
18 | HG00099.hp2 HG00438.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.351+2911_351+2912i others(120): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(109): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02132.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.351+2911_351+2912i others(118): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(109): Show |
1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.351+2911_351+2912i others(118): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(107): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0120 |
3 | HG03139.hp2 NA19058.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.351+2911_351+2912i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(5): Show |
38 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0049 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.351+2910_351+2921d others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(57): Show |
1 | a0001c0001t0002g0345 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | CATATATA others(81): Show |
1 | a0001c0001t0001g0041 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(90): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377614 | ||||||
chr5:69377614 | C | T | 11 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(8): Show |
11 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.351+2903C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377614 | |||||||
chr5:69377619 | A | ATG | 4 | a0001c0001t0001g0211 a0001c0001t0003g0188 a0002c0002t0001g0021 others(1): Show |
4 | HG01433.hp2 HG03834.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2909_351+2910i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377619 | ||||||
chr5:69377620 | T | TATATGCA others(249): Show |
2 | a0001c0001t0001g0127 a0001c0009t0001g0128 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.351+2911_351+2912i others(258): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377620 | ||||||
chr5:69377620 | T | TGC | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0186 others(60): Show |
69 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.351+2909_351+2910i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377620 | |||||||
chr5:69377623 | G | GCATATAT others(75): Show |
1 | a0001c0001t0002g0282 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.351+2921_351+2922i others(84): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377623 | ||||||
chr5:69377623 | G | GCATATAT others(73): Show |
1 | a0001c0001t0002g0312 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(82): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377623 | ||||||
chr5:69377623 | GCATATAT others(7): Show |
G | 1 | a0001c0001t0002g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.351+2922_351+2935d others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377623 | ||||||
chr5:69377624 | C | CAT | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0052 others(67): Show |
76 | HG00099.hp1 HG00558.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.351+2920_351+2921d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377624 | ||||||
chr5:69377624 | C | CATATATA others(201): Show |
1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.351+2922_351+2923i others(210): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377624 | ||||||
chr5:69377624 | C | CATATATA others(97): Show |
4 | a0001c0001t0002g0337 a0001c0001t0002g0338 a0001c0001t0002g0339 others(1): Show |
4 | NA18960.hp2 NA18997.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(106): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377624 | ||||||
chr5:69377624 | C | CATATATA others(89): Show |
1 | a0001c0001t0001g0134 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.351+2925_351+2926i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377624 | ||||||
chr5:69377626 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.351+2921_351+2922i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377626 | ||||||
chr5:69377628 | T | TATATATA others(67): Show |
2 | a0001c0001t0002g0275 a0001c0001t0002g0276 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.351+2921_351+2922i others(76): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377628 | ||||||
chr5:69377628 | T | TATATATG others(17): Show |
2 | a0001c0001t0001g0277 a0001c0001t0002g0320 |
2 | HG00741.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.351+2921_351+2922i others(26): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377628 | ||||||
chr5:69377632 | T | TGCATACA others(5): Show |
1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2922_351+2923i others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377632 | ||||||
chr5:69377633 | G | A | 4 | a0001c0001t0001g0277 a0001c0001t0002g0275 a0001c0001t0002g0276 others(1): Show |
4 | HG00741.hp1 HG01109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2922G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377633 | |||||||
chr5:69377634 | T | C | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0193 others(2): Show |
5 | HG01346.hp1 HG01358.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2923T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377634 | |||||||
chr5:69377637 | A | ACATATAT others(5): Show |
2 | a0001c0001t0001g0268 a0001c0001t0002g0345 |
2 | HG00642.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.351+2939_351+2950d others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(71): Show |
1 | a0001c0001t0002g0279 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.351+2977_351+2978i others(80): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(57): Show |
1 | a0001c0001t0002g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.351+2975_351+2976i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(121): Show |
1 | a0007c0010t0002g0314 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+2963_351+2964i others(130): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(71): Show |
2 | a0001c0001t0002g0318 a0001c0001t0002g0325 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(80): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(69): Show |
1 | a0001c0001t0002g0344 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(78): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(57): Show |
2 | a0001c0001t0002g0283 a0001c0001t0002g0323 |
2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(69): Show |
38 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(35): Show |
41 | HG00609.hp1 HG01256.hp2 HG01258.hp1 others(38): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(78): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(29): Show |
3 | a0001c0001t0002g0291 a0001c0001t0002g0294 a0001c0001t0002g0330 |
3 | HG04184.hp1 NA18977.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(38): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(119): Show |
11 | a0001c0001t0002g0008 a0001c0001t0002g0271 a0001c0001t0002g0272 others(8): Show |
12 | HG01243.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(128): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(145): Show |
1 | a0001c0001t0002g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(154): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(67): Show |
5 | a0001c0001t0002g0280 a0001c0001t0002g0286 a0001c0001t0002g0295 others(2): Show |
5 | HG02965.hp2 HG03540.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(76): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(107): Show |
1 | a0001c0001t0002g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(159): Show |
1 | a0001c0001t0001g0095 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(168): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(81): Show |
1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(90): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | ACATATAT others(117): Show |
1 | a0001c0001t0002g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.351+2933_351+2934i others(126): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377637 | ||||||
chr5:69377637 | A | G | 4 | a0001c0001t0001g0277 a0001c0001t0002g0275 a0001c0001t0002g0276 others(1): Show |
4 | HG00741.hp1 HG01109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2926A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377637 | |||||||
chr5:69377639 | A | G | 1 | a0003c0003t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.351+2928A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377639 | |||||||
chr5:69377640 | T | TATATATA others(149): Show |
1 | a0001c0001t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.351+2937_351+2938i others(158): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377640 | ||||||
chr5:69377640 | T | TATATATA others(177): Show |
1 | a0001c0001t0001g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2937_351+2938i others(186): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377640 | ||||||
chr5:69377640 | T | TATATATA others(59): Show |
1 | a0001c0001t0002g0311 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.351+2977_351+2978i others(68): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377640 | ||||||
chr5:69377645 | A | ATGCATAT others(91): Show |
1 | a0001c0001t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(100): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(89): Show |
1 | a0002c0002t0001g0022 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(89): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | HG00323.hp2 HG01070.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(75): Show |
1 | a0002c0002t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(84): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(113): Show |
2 | a0002c0002t0001g0199 a0002c0002t0001g0200 |
2 | HG02559.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(122): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(137): Show |
1 | a0006c0013t0001g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(137): Show |
1 | a0001c0001t0001g0152 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(165): Show |
3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0002c0002t0001g0151 |
3 | HG03927.hp2 NA18955.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(174): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(137): Show |
11 | a0001c0001t0001g0034 a0001c0001t0001g0155 a0001c0001t0001g0156 others(8): Show |
11 | HG01167.hp1 HG02074.hp2 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(135): Show |
3 | a0004c0004t0001g0162 a0004c0004t0001g0163 a0004c0004t0001g0164 |
3 | HG01168.hp2 HG01952.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(144): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(137): Show |
1 | a0001c0001t0001g0165 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | ATGCATAT others(137): Show |
3 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0002c0002t0001g0166 |
3 | HG01496.hp2 HG01952.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377645 | ||||||
chr5:69377645 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0127 others(69): Show |
78 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.351+2934A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377645 | |||||||
chr5:69377646 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.351+2935T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TATGCATA others(239): Show |
1 | a0001c0001t0001g0220 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(248): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(267): Show |
1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(276): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(267): Show |
1 | a0001c0001t0001g0221 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(276): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(239): Show |
2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18954.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(248): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(267): Show |
1 | a0001c0001t0001g0235 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(276): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(263): Show |
1 | a0001c0001t0001g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(272): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(263): Show |
7 | a0001c0001t0001g0218 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
7 | NA18949.hp2 NA18955.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2947_351+2948i others(272): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(261): Show |
1 | a0001c0001t0001g0237 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(270): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(239): Show |
2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(248): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(293): Show |
1 | a0001c0001t0001g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(302): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(211): Show |
1 | a0001c0001t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(220): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(239): Show |
1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(248): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(267): Show |
1 | a0001c0001t0005g0240 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(276): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(263): Show |
1 | a0001c0001t0001g0133 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(272): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TATGCATA others(237): Show |
1 | a0001c0001t0001g0236 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(246): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377646 | ||||||
chr5:69377646 | T | TGCATATA others(89): Show |
3 | a0002c0002t0001g0137 a0002c0002t0001g0191 a0002c0002t0001g0194 |
3 | HG01074.hp1 HG03688.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(117): Show |
1 | a0002c0002t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(126): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(117): Show |
1 | a0002c0002t0001g0136 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(126): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(89): Show |
6 | a0001c0001t0001g0143 a0002c0002t0001g0138 a0002c0002t0001g0139 others(3): Show |
6 | HG00423.hp1 HG01978.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(98): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(101): Show |
1 | a0002c0002t0001g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(110): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(125): Show |
1 | a0002c0002t0001g0016 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(134): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(113): Show |
1 | a0002c0002t0001g0130 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(122): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(237): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0238 a0001c0001t0001g0239 |
4 | HG02083.hp1 HG03669.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2935_351+2936i others(246): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(261): Show |
1 | a0001c0001t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(270): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(237): Show |
1 | a0001c0001t0001g0233 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(246): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(235): Show |
1 | a0001c0001t0001g0234 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(244): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(113): Show |
2 | a0002c0002t0001g0201 a0002c0002t0001g0202 |
2 | HG00609.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.351+2935_351+2936i others(122): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(111): Show |
1 | a0001c0001t0001g0203 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(120): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(137): Show |
1 | a0001c0001t0001g0148 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377646 | T | TGCATATA others(137): Show |
1 | a0001c0001t0001g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.351+2935_351+2936i others(146): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377646 | |||||||
chr5:69377650 | C | CAT | 79 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(76): Show |
79 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.351+2948_351+2949d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377650 | ||||||
chr5:69377650 | C | CATATATA others(111): Show |
1 | a0001c0001t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.351+2947_351+2948i others(120): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377650 | ||||||
chr5:69377650 | CAT | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0111 others(1): Show |
4 | HG01099.hp2 HG01978.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2948_351+2949d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377650 | ||||||
chr5:69377652 | T | TATATATA others(29): Show |
2 | a0001c0001t0001g0046 a0001c0001t0001g0053 |
2 | HG00735.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.351+2963_351+2964i others(38): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377652 | ||||||
chr5:69377652 | T | TATATATG others(83): Show |
1 | a0001c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.351+2947_351+2948i others(92): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377652 | ||||||
chr5:69377652 | T | TATATATG others(81): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG00642.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(90): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377652 | ||||||
chr5:69377652 | T | TATATATG others(107): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0247 |
2 | HG02080.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.351+2947_351+2948i others(116): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377652 | ||||||
chr5:69377654 | T | C | 2 | a0001c0001t0002g0328 a0003c0003t0001g0030 |
2 | HG01884.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.351+2943T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377654 | |||||||
chr5:69377660 | T | C | 1 | a0003c0003t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.351+2949T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377660 | |||||||
chr5:69377660 | T | G | 1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2949T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377660 | |||||||
chr5:69377661 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2950G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377661 | |||||||
chr5:69377662 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.351+2951T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377662 | |||||||
chr5:69377663 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2952A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377663 | |||||||
chr5:69377665 | A | G | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0007t0001g0219 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2954A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377665 | |||||||
chr5:69377666 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2955C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377666 | |||||||
chr5:69377667 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2956A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377667 | |||||||
chr5:69377668 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.351+2957T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377668 | |||||||
chr5:69377668 | T | TATATATG others(19): Show |
1 | a0001c0001t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.351+2963_351+2964i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377668 | ||||||
chr5:69377670 | T | TATATGCA others(249): Show |
1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.351+2963_351+2964i others(258): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377670 | ||||||
chr5:69377671 | A | ATATGTAT others(101): Show |
1 | a0003c0003t0001g0002 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.351+2963_351+2964i others(110): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377671 | ||||||
chr5:69377671 | A | G | 2 | a0001c0001t0001g0044 a0006c0013t0001g0254 |
2 | HG01256.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.351+2960A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377671 | |||||||
chr5:69377673 | A | G | 154 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
161 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.351+2962A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377673 | |||||||
chr5:69377674 | T | C | 1 | a0002c0002t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.351+2963T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377674 | |||||||
chr5:69377675 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2964A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377675 | |||||||
chr5:69377677 | GCATA | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2967_351+2970d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377677 | |||||||
chr5:69377678 | C | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0124 a0003c0003t0001g0002 others(5): Show |
9 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2967C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377678 | |||||||
chr5:69377678 | CAT | C | 161 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.351+2978_351+2979d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377678 | ||||||
chr5:69377678 | CATAT | C | 64 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(61): Show |
64 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.351+2976_351+2979d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377678 | ||||||
chr5:69377680 | T | TACATATA others(35): Show |
1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2970_351+2971i others(44): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | ||||||
chr5:69377680 | T | TACATATA others(105): Show |
4 | a0003c0003t0001g0027 a0003c0003t0001g0028 a0003c0003t0001g0029 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+2970_351+2971i others(114): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | ||||||
chr5:69377680 | T | TACATATA others(105): Show |
1 | a0003c0003t0001g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+2970_351+2971i others(114): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | ||||||
chr5:69377680 | T | TATATATA others(21): Show |
3 | a0001c0001t0001g0053 a0001c0001t0001g0057 a0001c0001t0001g0097 |
3 | HG00735.hp1 HG01346.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.351+2996_351+2997i others(30): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | ||||||
chr5:69377680 | T | TATATATA others(85): Show |
1 | a0001c0001t0001g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.351+2977_351+2978i others(94): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | ||||||
chr5:69377680 | T | TATATATA others(19): Show |
2 | a0002c0002t0001g0191 a0002c0002t0001g0194 |
2 | HG01074.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.351+2977_351+2978i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | ||||||
chr5:69377680 | T | TATATATG others(281): Show |
1 | a0001c0001t0001g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(290): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | ||||||
chr5:69377680 | T | TATATATG others(227): Show |
1 | a0001c0007t0001g0219 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(236): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377680 | ||||||
chr5:69377680 | T | TGC | 2 | a0001c0001t0001g0124 a0003c0003t0001g0002 |
3 | HG02258.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.351+2969_351+2970i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377680 | |||||||
chr5:69377681 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2970A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377681 | |||||||
chr5:69377682 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+2971T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377682 | |||||||
chr5:69377682 | T | TATATATA others(19): Show |
6 | a0001c0001t0001g0046 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | HG00642.hp2 HG01934.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+2996_351+2997i others(28): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | ||||||
chr5:69377682 | T | TATATATG others(57): Show |
1 | a0001c0001t0001g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.351+2977_351+2978i others(66): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | ||||||
chr5:69377682 | T | TATATATG others(83): Show |
1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.351+2977_351+2978i others(92): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | ||||||
chr5:69377682 | T | TATATGTA others(15): Show |
1 | a0001c0001t0001g0090 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.351+2975_351+2976i others(24): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | ||||||
chr5:69377682 | T | TATATGTA others(41): Show |
1 | a0001c0001t0001g0112 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(50): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | ||||||
chr5:69377682 | T | TATATGTA others(157): Show |
1 | a0001c0001t0001g0111 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(166): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | ||||||
chr5:69377682 | T | TATATGTA others(155): Show |
1 | a0001c0001t0001g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.351+2975_351+2976i others(164): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | ||||||
chr5:69377682 | T | TATATGTA others(15): Show |
3 | a0002c0002t0001g0205 a0002c0002t0001g0206 a0002c0002t0001g0207 |
3 | NA18994.hp1 NA19004.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.351+2975_351+2976i others(24): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377682 | ||||||
chr5:69377684 | T | C | 1 | a0002c0002t0001g0172 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.351+2973T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377684 | |||||||
chr5:69377688 | T | C | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2977T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377688 | |||||||
chr5:69377689 | A | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2978A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377689 | |||||||
chr5:69377692 | T | C | 1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+2981T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377692 | |||||||
chr5:69377697 | A | C | 7 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2986A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377697 | |||||||
chr5:69377721 | ATTTTC | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.351+3014_351+3018d others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69377721 | ||||||
chr5:69377747 | C | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0131 a0001c0001t0001g0259 |
3 | HG01243.hp2 HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.351+3036C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377747 | |||||||
chr5:69377826 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | NA18979.hp2 NA19058.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.351+3115C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377826 | |||||||
chr5:69377970 | A | T | 1 | a0003c0003t0001g0002 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.351+3259A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69377970 | |||||||
chr5:69378086 | C | T | 1 | a0003c0003t0001g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+3375C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378086 | |||||||
chr5:69378233 | A | G | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.351+3522A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378233 | |||||||
chr5:69378359 | G | C | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.352-3542G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378359 | |||||||
chr5:69378594 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.352-3307C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378594 | |||||||
chr5:69378732 | G | T | 2 | a0001c0001t0002g0319 a0001c0001t0002g0322 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.352-3169G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378732 | |||||||
chr5:69378814 | G | A | 1 | a0001c0001t0002g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.352-3087G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69378814 | |||||||
chr5:69379015 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-2886G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379015 | |||||||
chr5:69379111 | G | A | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.352-2790G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379111 | |||||||
chr5:69379189 | T | C | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.352-2712T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379189 | |||||||
chr5:69379316 | C | T | 17 | a0002c0002t0001g0004 a0002c0002t0001g0125 a0002c0002t0001g0129 others(14): Show |
18 | HG00423.hp1 HG02056.hp2 NA18939.hp1 others(15): Show |
intron_variant | MODIFIER | c.352-2585C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379316 | |||||||
chr5:69379335 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.352-2566T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379335 | |||||||
chr5:69379622 | TTATTCTA others(50): Show |
T | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-2278_352-2222d others(59): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379622 | |||||||
chr5:69379623 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.352-2278T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379623 | |||||||
chr5:69379656 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.352-2245A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379656 | |||||||
chr5:69379657 | T | A | 1 | a0002c0002t0001g0001 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.352-2244T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379657 | |||||||
chr5:69379920 | G | C | 1 | a0002c0002t0001g0204 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.352-1981G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379920 | |||||||
chr5:69379983 | C | G | 1 | a0001c0001t0002g0330 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.352-1918C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379983 | |||||||
chr5:69379989 | T | C | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1912T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379989 | |||||||
chr5:69379990 | C | T | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1911C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379990 | |||||||
chr5:69379992 | T | G | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1909T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69379992 | |||||||
chr5:69380038 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.352-1863G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380038 | |||||||
chr5:69380068 | A | T | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1833A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380068 | |||||||
chr5:69380069 | T | G | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1832T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380069 | |||||||
chr5:69380073 | G | C | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.352-1828G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380073 | |||||||
chr5:69380193 | T | A | 1 | a0002c0002t0001g0139 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.352-1708T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380193 | |||||||
chr5:69380434 | A | G | 1 | a0002c0002t0001g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.352-1467A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380434 | |||||||
chr5:69380528 | C | A | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1373C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380528 | |||||||
chr5:69380563 | C | G | 1 | a0001c0001t0001g0277 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.352-1338C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380563 | |||||||
chr5:69380727 | T | C | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-1174T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380727 | |||||||
chr5:69380744 | C | T | 36 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0044 others(33): Show |
36 | HG00423.hp2 HG00621.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.352-1157C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380744 | |||||||
chr5:69380771 | CT | C | 8 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(5): Show |
9 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.352-1118delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69380771 | ||||||
chr5:69380807 | G | A | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.352-1094G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380807 | |||||||
chr5:69380972 | T | A | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352-929T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69380972 | |||||||
chr5:69381012 | G | A | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.352-889G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69381012 | |||||||
chr5:69381337 | C | T | 1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.352-564C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69381337 | |||||||
chr5:69381355 | CCTGTAGT others(125): Show |
C | 1 | a0001c0001t0002g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.352-545_352-414del | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69381355 | |||||||
chr5:69381479 | CA | C | 14 | a0001c0001t0001g0155 a0001c0001t0001g0165 a0001c0001t0001g0263 others(11): Show |
15 | HG01123.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.352-409delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 69381479 | ||||||
chr5:69381521 | C | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.352-380C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 6/18 | chr5 | 69381521 | |||||||
chr5:69382304 | G | A | 2 | a0001c0001t0003g0265 a0001c0001t0003g0267 |
2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.508+247G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382304 | |||||||
chr5:69382357 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.508+300A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382357 | |||||||
chr5:69382504 | A | G | 2 | a0001c0001t0002g0291 a0001c0001t0002g0294 |
2 | HG04184.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.508+447A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382504 | |||||||
chr5:69382534 | T | C | 1 | a0004c0004t0001g0162 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.508+477T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382534 | |||||||
chr5:69382544 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.508+487G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382544 | |||||||
chr5:69382721 | A | G | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508+664A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382721 | |||||||
chr5:69382764 | G | A | 1 | a0003c0003t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508+707G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382764 | |||||||
chr5:69382784 | A | C | 1 | a0001c0001t0002g0336 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.508+727A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382784 | |||||||
chr5:69382838 | C | T | 1 | a0002c0002t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.508+781C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382838 | |||||||
chr5:69382890 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.508+833T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382890 | |||||||
chr5:69382959 | T | C | 50 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(47): Show |
53 | HG00609.hp1 HG00642.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.508+902T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382959 | |||||||
chr5:69382983 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.508+926C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69382983 | |||||||
chr5:69383003 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.508+946C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383003 | |||||||
chr5:69383038 | C | T | 1 | a0006c0013t0001g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.508+981C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383038 | |||||||
chr5:69383046 | A | T | 1 | a0001c0001t0002g0336 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.508+989A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383046 | |||||||
chr5:69383140 | T | G | 1 | a0001c0001t0002g0010 | 2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+1083T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383140 | |||||||
chr5:69383144 | C | G | 1 | a0002c0002t0001g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.508+1087C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383144 | |||||||
chr5:69383323 | A | G | 1 | a0002c0002t0001g0200 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.508+1266A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383323 | |||||||
chr5:69383540 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.509-1257G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383540 | |||||||
chr5:69383660 | G | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02572.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.509-1137G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383660 | |||||||
chr5:69383719 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.509-1078A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383719 | |||||||
chr5:69383735 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.509-1062A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383735 | |||||||
chr5:69383766 | C | T | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.509-1031C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383766 | |||||||
chr5:69383796 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.509-1001G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383796 | |||||||
chr5:69383969 | C | G | 1 | a0002c0002t0001g0151 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.509-828C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383969 | |||||||
chr5:69383995 | G | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.509-802G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69383995 | |||||||
chr5:69384005 | A | AAAATTCA others(72): Show |
3 | a0001c0001t0002g0291 a0001c0001t0002g0294 a0001c0001t0002g0330 |
3 | HG04184.hp1 NA18977.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.509-715_509-714ins others(79): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 69384005 | ||||||
chr5:69384030 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.509-767G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384030 | |||||||
chr5:69384090 | T | G | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.509-707T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384090 | |||||||
chr5:69384207 | T | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.509-590T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384207 | |||||||
chr5:69384505 | C | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.509-292C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384505 | |||||||
chr5:69384516 | A | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.509-281A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 7/18 | chr5 | 69384516 | |||||||
chr5:69384954 | C | CT | 10 | a0001c0001t0001g0078 a0001c0001t0001g0089 a0002c0002t0001g0161 others(7): Show |
11 | HG01884.hp1 HG01884.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.645+38dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 69384954 | ||||||
chr5:69384982 | C | A | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.645+49C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69384982 | |||||||
chr5:69385033 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.645+100C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385033 | |||||||
chr5:69385045 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.645+112T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385045 | |||||||
chr5:69385050 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.645+117C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385050 | |||||||
chr5:69385120 | C | T | 2 | a0001c0001t0002g0302 a0001c0001t0002g0303 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.645+187C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385120 | |||||||
chr5:69385150 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0124 a0001c0001t0001g0127 others(44): Show |
49 | HG00438.hp1 HG00621.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.645+217C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385150 | |||||||
chr5:69385192 | C | A | 1 | a0002c0002t0001g0181 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.645+259C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385192 | |||||||
chr5:69385266 | C | CT | 101 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(98): Show |
101 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.645+353dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 69385266 | ||||||
chr5:69385266 | C | CTT | 9 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0049 others(6): Show |
9 | HG01358.hp2 HG01934.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+352_645+353dup others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 69385266 | ||||||
chr5:69385266 | CT | C | 9 | a0001c0001t0001g0145 a0001c0001t0001g0223 a0001c0001t0001g0238 others(6): Show |
9 | HG00323.hp2 HG00733.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.645+353delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 69385266 | ||||||
chr5:69385329 | T | C | 2 | a0001c0001t0003g0265 a0001c0001t0003g0267 |
2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.645+396T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385329 | |||||||
chr5:69385354 | C | T | 2 | a0001c0001t0001g0261 a0011c0012t0001g0245 |
2 | NA18612.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.645+421C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385354 | |||||||
chr5:69385796 | T | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.646-247T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385796 | |||||||
chr5:69385812 | A | T | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.646-231A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385812 | |||||||
chr5:69385817 | A | G | 1 | a0002c0002t0001g0019 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.646-226A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385817 | |||||||
chr5:69385848 | A | C | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.646-195A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385848 | |||||||
chr5:69385869 | C | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.646-174C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385869 | |||||||
chr5:69385878 | T | A | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.646-165T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69385878 | |||||||
chr5:69386023 | T | A | 1 | a0010c0011t0002g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.646-20T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 8/18 | chr5 | 69386023 | |||||||
chr5:69386646 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.894+181T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69386646 | |||||||
chr5:69386709 | A | C | 4 | a0002c0002t0001g0123 a0002c0002t0001g0140 a0002c0002t0001g0182 others(1): Show |
4 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+244A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69386709 | |||||||
chr5:69386771 | C | G | 3 | a0001c0001t0002g0009 a0001c0001t0002g0289 a0001c0001t0002g0290 |
4 | HG01261.hp2 HG02148.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+306C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69386771 | |||||||
chr5:69386926 | C | CT | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
166 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.894+476dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 69386926 | ||||||
chr5:69387220 | G | A | 4 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG01167.hp2 HG02486.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+755G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387220 | |||||||
chr5:69387230 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.894+765C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387230 | |||||||
chr5:69387242 | G | T | 2 | a0002c0002t0001g0169 a0002c0002t0001g0183 |
2 | HG02738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.894+777G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387242 | |||||||
chr5:69387390 | C | T | 3 | a0002c0002t0001g0168 a0002c0002t0001g0170 a0002c0002t0001g0171 |
3 | HG00099.hp1 HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.894+925C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387390 | |||||||
chr5:69387417 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.894+952G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387417 | |||||||
chr5:69387544 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.894+1079T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387544 | |||||||
chr5:69387610 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.894+1145C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387610 | |||||||
chr5:69387641 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.894+1176T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387641 | |||||||
chr5:69387718 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.894+1253G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387718 | |||||||
chr5:69387719 | T | G | 1 | a0001c0001t0002g0292 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.894+1254T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387719 | |||||||
chr5:69387723 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.894+1258G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387723 | |||||||
chr5:69387758 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.895-1276G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387758 | |||||||
chr5:69387786 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.895-1248G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69387786 | |||||||
chr5:69388011 | A | G | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.895-1023A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388011 | |||||||
chr5:69388081 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.895-953A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388081 | |||||||
chr5:69388134 | C | T | 1 | a0002c0002t0001g0200 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.895-900C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388134 | |||||||
chr5:69388191 | A | AT | 104 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(101): Show |
105 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.895-833dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 69388191 | ||||||
chr5:69388228 | T | C | 1 | a0003c0003t0001g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.895-806T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388228 | |||||||
chr5:69388233 | T | C | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.895-801T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388233 | |||||||
chr5:69388387 | ATTTTGAG others(5): Show |
A | 1 | a0009c0006t0004g0076 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.895-641_895-630del others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 69388387 | ||||||
chr5:69388396 | G | GT | 4 | a0001c0001t0002g0342 a0002c0002t0001g0141 a0002c0002t0001g0167 others(1): Show |
4 | HG01192.hp2 HG02056.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-631dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 69388396 | ||||||
chr5:69388492 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.895-542A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388492 | |||||||
chr5:69388611 | C | T | 341 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(338): Show |
353 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.895-423C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388611 | |||||||
chr5:69388643 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.895-391A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388643 | |||||||
chr5:69388645 | T | A | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.895-389T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 11/18 | chr5 | 69388645 | |||||||
chr5:69389210 | A | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01070.hp2 HG01071.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1006+65A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389210 | |||||||
chr5:69389240 | T | G | 1 | a0001c0009t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1006+95T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389240 | |||||||
chr5:69389457 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1006+312C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389457 | |||||||
chr5:69389457 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1006+312C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389457 | |||||||
chr5:69389458 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1006+313T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389458 | |||||||
chr5:69389528 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1006+383G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389528 | |||||||
chr5:69389580 | C | CA | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1006+436dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69389580 | ||||||
chr5:69389616 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1006+471G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389616 | |||||||
chr5:69389620 | C | A | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(116): Show |
125 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1006+475C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389620 | |||||||
chr5:69389683 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1006+538C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389683 | |||||||
chr5:69389798 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1006+653G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389798 | |||||||
chr5:69389858 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1006+713G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389858 | |||||||
chr5:69389858 | G | T | 154 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
161 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1006+713G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389858 | |||||||
chr5:69389887 | C | T | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1006+742C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389887 | |||||||
chr5:69389957 | T | G | 1 | a0001c0001t0002g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1006+812T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69389957 | |||||||
chr5:69390398 | G | A | 2 | a0001c0001t0003g0265 a0001c0001t0003g0267 |
2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1006+1253G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390398 | |||||||
chr5:69390434 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1006+1289G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390434 | |||||||
chr5:69390695 | C | G | 154 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
161 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1007-1136C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390695 | |||||||
chr5:69390699 | T | G | 1 | a0001c0001t0001g0235 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1007-1132T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390699 | |||||||
chr5:69390797 | AAT | A | 93 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(90): Show |
93 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1007-1020_1007-101 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69390797 | ||||||
chr5:69390838 | C | T | 7 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-993C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390838 | |||||||
chr5:69390916 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1007-915G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390916 | |||||||
chr5:69390952 | C | CA | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1007-866dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69390952 | ||||||
chr5:69390952 | C | CAA | 10 | a0001c0001t0001g0234 a0001c0007t0001g0219 a0002c0002t0001g0125 others(7): Show |
11 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-867_1007-866d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69390952 | ||||||
chr5:69390952 | CA | C | 95 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(92): Show |
95 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1007-866delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69390952 | ||||||
chr5:69390976 | G | A | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1007-855G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69390976 | |||||||
chr5:69391055 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007-776G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391055 | |||||||
chr5:69391094 | C | T | 7 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-737C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391094 | |||||||
chr5:69391120 | C | T | 1 | a0001c0001t0002g0345 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1007-711C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391120 | |||||||
chr5:69391122 | C | T | 10 | a0001c0001t0001g0218 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
10 | HG01433.hp1 NA18949.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.1007-709C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391122 | |||||||
chr5:69391229 | CA | C | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1007-584delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 69391229 | ||||||
chr5:69391687 | A | C | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1007-144A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 12/18 | chr5 | 69391687 | |||||||
chr5:69392199 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1189+186G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392199 | |||||||
chr5:69392358 | T | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1189+345T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392358 | |||||||
chr5:69392582 | G | T | 1 | a0002c0002t0001g0013 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1189+569G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392582 | |||||||
chr5:69392616 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1190-539A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392616 | |||||||
chr5:69392781 | T | C | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1190-374T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69392781 | |||||||
chr5:69393057 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1190-98G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 13/18 | chr5 | 69393057 | |||||||
chr5:69393710 | C | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1422+210C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69393710 | |||||||
chr5:69393908 | G | GT | 7 | a0001c0001t0002g0276 a0001c0001t0002g0282 a0001c0001t0002g0302 others(4): Show |
7 | HG01256.hp1 HG01256.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1422+431dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | ||||||
chr5:69393908 | G | GTT | 7 | a0001c0001t0001g0142 a0001c0001t0001g0187 a0002c0002t0001g0015 others(4): Show |
8 | HG02258.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1422+430_1422+431d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | ||||||
chr5:69393908 | G | GTTT | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
145 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.1422+429_1422+431d others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | ||||||
chr5:69393908 | G | GTTTT | 16 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0190 others(13): Show |
16 | HG00438.hp1 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1422+428_1422+431d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | ||||||
chr5:69393908 | G | T | 1 | a0003c0003t0001g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1422+408G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69393908 | |||||||
chr5:69393908 | GT | G | 89 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(86): Show |
89 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1422+431delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69393908 | ||||||
chr5:69393945 | A | G | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1422+445A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69393945 | |||||||
chr5:69394059 | T | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG00438.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1422+559T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394059 | |||||||
chr5:69394077 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1422+577C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394077 | |||||||
chr5:69394142 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1422+642C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394142 | |||||||
chr5:69394184 | T | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1422+684T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394184 | |||||||
chr5:69394192 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1422+692C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394192 | |||||||
chr5:69394442 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1422+942T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394442 | |||||||
chr5:69394598 | T | TTTAA | 266 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(263): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1422+1099_1422+110 others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 69394598 | ||||||
chr5:69394667 | C | A | 1 | a0003c0003t0001g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1422+1167C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394667 | |||||||
chr5:69394782 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0132 a0001c0001t0001g0133 others(27): Show |
31 | HG00438.hp1 HG00621.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.1422+1282C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69394782 | |||||||
chr5:69395065 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0075 others(4): Show |
7 | NA18994.hp2 NA18995.hp2 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.1423-1332A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395065 | |||||||
chr5:69395111 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1423-1286C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395111 | |||||||
chr5:69395498 | T | C | 1 | a0006c0013t0001g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1423-899T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395498 | |||||||
chr5:69395847 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1423-550G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395847 | |||||||
chr5:69395934 | A | G | 6 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(3): Show |
7 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1423-463A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69395934 | |||||||
chr5:69396091 | C | G | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1423-306C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69396091 | |||||||
chr5:69396217 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0131 a0001c0001t0001g0259 |
3 | HG01243.hp2 HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1423-180A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69396217 | |||||||
chr5:69396353 | C | A | 1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1423-44C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 15/18 | chr5 | 69396353 | |||||||
chr5:69396548 | T | TA | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
259 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.1572+19dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69396548 | ||||||
chr5:69396548 | T | TAA | 93 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(90): Show |
93 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1572+18_1572+19dup others(2): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69396548 | ||||||
chr5:69396645 | GA | G | 7 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+105delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69396645 | ||||||
chr5:69396707 | A | T | 1 | a0002c0002t0001g0205 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1572+161A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396707 | |||||||
chr5:69396708 | T | A | 1 | a0002c0002t0001g0205 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1572+162T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396708 | |||||||
chr5:69396709 | A | T | 1 | a0002c0002t0001g0205 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1572+163A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396709 | |||||||
chr5:69396809 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1572+263C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396809 | |||||||
chr5:69396981 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1572+435A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69396981 | |||||||
chr5:69397076 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1572+530C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397076 | |||||||
chr5:69397228 | A | T | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1572+682A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397228 | |||||||
chr5:69397501 | C | T | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1572+955C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397501 | |||||||
chr5:69397520 | G | A | 1 | a0001c0001t0002g0310 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1572+974G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397520 | |||||||
chr5:69397636 | A | C | 2 | a0001c0001t0002g0301 a0001c0001t0002g0335 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1572+1090A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397636 | |||||||
chr5:69397709 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1572+1163A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397709 | |||||||
chr5:69397737 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1572+1191G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397737 | |||||||
chr5:69397740 | G | C | 7 | a0001c0001t0002g0283 a0001c0001t0002g0285 a0001c0001t0002g0320 others(4): Show |
7 | HG02258.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572+1194G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397740 | |||||||
chr5:69397784 | T | G | 1 | a0006c0013t0001g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1572+1238T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397784 | |||||||
chr5:69397851 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1572+1305C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397851 | |||||||
chr5:69397855 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1572+1309C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69397855 | |||||||
chr5:69398040 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1572+1494C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398040 | |||||||
chr5:69398073 | C | T | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1572+1527C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398073 | |||||||
chr5:69398098 | C | T | 1 | a0001c0001t0002g0313 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1572+1552C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398098 | |||||||
chr5:69398115 | T | TA | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0210 others(9): Show |
13 | HG00733.hp1 HG01074.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1572+1582dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398115 | ||||||
chr5:69398144 | G | A | 1 | a0002c0002t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+1598G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398144 | |||||||
chr5:69398306 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1573-1743A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398306 | |||||||
chr5:69398314 | A | G | 1 | a0001c0001t0002g0331 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1573-1735A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398314 | |||||||
chr5:69398342 | A | G | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1573-1707A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398342 | |||||||
chr5:69398344 | A | G | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
166 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1573-1705A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398344 | |||||||
chr5:69398604 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1573-1445G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398604 | |||||||
chr5:69398707 | G | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0066 a0001c0001t0001g0074 others(7): Show |
10 | HG02129.hp2 HG03834.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.1573-1342G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398707 | |||||||
chr5:69398723 | G | A | 1 | a0001c0001t0002g0344 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1573-1326G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69398723 | |||||||
chr5:69398811 | GA | G | 18 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(15): Show |
18 | HG00438.hp2 HG01167.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1573-1227delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398811 | ||||||
chr5:69398868 | T | TA | 84 | a0001c0001t0001g0034 a0001c0001t0001g0159 a0001c0001t0001g0195 others(81): Show |
88 | HG00609.hp1 HG00642.hp1 HG01109.hp2 others(85): Show |
intron_variant | MODIFIER | c.1573-1161dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | ||||||
chr5:69398868 | T | TAA | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
152 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1573-1162_1573-116 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | ||||||
chr5:69398868 | T | TAAA | 18 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0071 others(15): Show |
18 | HG00099.hp2 HG00733.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1573-1163_1573-116 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | ||||||
chr5:69398868 | T | TAAAA | 77 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(74): Show |
77 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1573-1164_1573-116 others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | ||||||
chr5:69398868 | T | TAAAAA | 10 | a0001c0001t0001g0053 a0001c0001t0001g0057 a0001c0001t0001g0068 others(7): Show |
10 | HG00735.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1573-1165_1573-116 others(9): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69398868 | ||||||
chr5:69399009 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1573-1040T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399009 | |||||||
chr5:69399018 | A | T | 31 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0126 others(28): Show |
31 | HG00323.hp2 HG00558.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1573-1031A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399018 | |||||||
chr5:69399282 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1573-767A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399282 | |||||||
chr5:69399347 | A | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0148 a0001c0001t0001g0149 others(5): Show |
8 | HG00558.hp1 NA18955.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-702A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399347 | |||||||
chr5:69399580 | C | T | 30 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0126 others(27): Show |
30 | HG00323.hp2 HG00558.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1573-469C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69399580 | |||||||
chr5:69399685 | C | CGTT | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1573-362_1573-361i others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 69399685 | ||||||
chr5:69400010 | C | A | 1 | a0001c0001t0002g0335 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1573-39C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69400010 | |||||||
chr5:69400045 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18970.hp1 | splice_region_variant&intron_variant | LOW | c.1573-4A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 16/18 | chr5 | 69400045 | |||||||
chr5:69400208 | G | GTTTATTT others(1): Show |
262 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1693+55_1693+62dup others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69400208 | ||||||
chr5:69400208 | G | GTTTATTT others(5): Show |
1 | a0001c0001t0001g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1693+51_1693+62dup others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69400208 | ||||||
chr5:69400208 | G | GTTTATTT others(9): Show |
1 | a0003c0003t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1693+47_1693+62dup others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69400208 | ||||||
chr5:69400232 | T | A | 1 | a0002c0002t0001g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1693+63T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400232 | |||||||
chr5:69400244 | G | A | 6 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0296 others(3): Show |
6 | HG02080.hp1 HG02155.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693+75G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400244 | |||||||
chr5:69400273 | G | A | 1 | a0003c0003t0001g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1693+104G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400273 | |||||||
chr5:69400280 | C | T | 1 | a0002c0002t0001g0172 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1693+111C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400280 | |||||||
chr5:69400467 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1693+298C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400467 | |||||||
chr5:69400510 | A | G | 262 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1693+341A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400510 | |||||||
chr5:69400579 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1693+410C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400579 | |||||||
chr5:69400596 | T | A | 1 | a0002c0002t0001g0014 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1693+427T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69400596 | |||||||
chr5:69400626 | G | GT | 260 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1693+467dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69400626 | ||||||
chr5:69401023 | A | G | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(117): Show |
126 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1693+854A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401023 | |||||||
chr5:69401102 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1693+933C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401102 | |||||||
chr5:69401133 | C | T | 1 | a0001c0001t0002g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1693+964C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401133 | |||||||
chr5:69401321 | A | G | 1 | a0002c0002t0001g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1693+1152A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401321 | |||||||
chr5:69401499 | T | TA | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1693+1330_1693+133 others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401499 | |||||||
chr5:69401760 | G | A | 8 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0193 others(5): Show |
8 | HG01167.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1693+1591G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401760 | |||||||
chr5:69401783 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1693+1614C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401783 | |||||||
chr5:69401831 | C | CA | 7 | a0001c0001t0001g0058 a0001c0001t0001g0090 a0001c0001t0001g0114 others(4): Show |
7 | HG01192.hp1 HG01496.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+1670dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69401831 | ||||||
chr5:69401839 | A | C | 12 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(9): Show |
12 | HG01167.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1693+1670A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69401839 | |||||||
chr5:69401851 | C | CA | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1693+1689dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69401851 | ||||||
chr5:69402003 | C | CA | 88 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0038 others(85): Show |
91 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1693+1858dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69402003 | ||||||
chr5:69402003 | C | CAA | 87 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(84): Show |
91 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1693+1857_1693+185 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69402003 | ||||||
chr5:69402003 | C | CAAA | 13 | a0001c0001t0001g0126 a0001c0001t0001g0149 a0001c0001t0001g0155 others(10): Show |
14 | HG00558.hp1 HG00735.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1693+1856_1693+185 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69402003 | ||||||
chr5:69402271 | G | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1693+2102G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402271 | |||||||
chr5:69402273 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1693+2104A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402273 | |||||||
chr5:69402340 | G | A | 2 | a0001c0001t0001g0234 a0001c0007t0001g0219 |
2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1693+2171G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402340 | |||||||
chr5:69402341 | C | T | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1693+2172C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402341 | |||||||
chr5:69402346 | G | A | 1 | a0003c0003t0001g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1693+2177G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402346 | |||||||
chr5:69402483 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0056 |
2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1693+2314G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402483 | |||||||
chr5:69402654 | C | CA | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1693+2500dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69402654 | ||||||
chr5:69402939 | C | CA | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1693+2770_1693+277 others(5): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69402939 | |||||||
chr5:69403004 | T | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1693+2835T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403004 | |||||||
chr5:69403019 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1693+2850A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403019 | |||||||
chr5:69403229 | G | A | 1 | a0002c0002t0001g0017 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1693+3060G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403229 | |||||||
chr5:69403568 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1693+3399A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403568 | |||||||
chr5:69403579 | T | G | 1 | a0001c0001t0002g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1693+3410T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403579 | |||||||
chr5:69403621 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1693+3452T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403621 | |||||||
chr5:69403682 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1693+3513G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403682 | |||||||
chr5:69403737 | C | A | 1 | a0001c0001t0002g0340 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1693+3568C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403737 | |||||||
chr5:69403745 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1693+3576C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403745 | |||||||
chr5:69403937 | AAAAAT | A | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1693+3779_1693+378 others(9): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69403937 | ||||||
chr5:69403963 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1693+3794T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69403963 | |||||||
chr5:69404011 | ATTCTGTT | A | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1693+3852_1693+385 others(11): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69404011 | ||||||
chr5:69404399 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1693+4230A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404399 | |||||||
chr5:69404566 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02615.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1693+4397G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404566 | |||||||
chr5:69404625 | T | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
172 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1693+4456T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404625 | |||||||
chr5:69404641 | CG | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(1): Show |
4 | NA18956.hp2 NA18989.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693+4473delG | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404641 | |||||||
chr5:69404643 | C | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(1): Show |
4 | NA18956.hp2 NA18989.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693+4474C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404643 | |||||||
chr5:69404769 | C | CA | 10 | a0001c0001t0001g0042 a0001c0001t0001g0066 a0001c0001t0001g0074 others(7): Show |
10 | HG00741.hp2 HG02071.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1693+4614dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69404769 | ||||||
chr5:69404769 | CA | C | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
170 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1693+4614delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69404769 | ||||||
chr5:69404810 | C | G | 1 | a0002c0002t0001g0151 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1693+4641C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404810 | |||||||
chr5:69404922 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1693+4753A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69404922 | |||||||
chr5:69405043 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1693+4874C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405043 | |||||||
chr5:69405226 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1693+5057G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405226 | |||||||
chr5:69405256 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1693+5087C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405256 | |||||||
chr5:69405279 | G | A | 9 | a0002c0002t0001g0025 a0002c0002t0001g0154 a0002c0002t0001g0161 others(6): Show |
9 | HG02896.hp2 HG03453.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.1693+5110G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405279 | |||||||
chr5:69405352 | C | A | 1 | a0001c0001t0002g0311 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1694-5141C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405352 | |||||||
chr5:69405352 | C | CA | 11 | a0001c0001t0001g0127 a0001c0001t0001g0165 a0001c0001t0001g0260 others(8): Show |
11 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694-5129dupA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69405352 | ||||||
chr5:69405354 | A | C | 95 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(92): Show |
95 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1694-5139A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405354 | |||||||
chr5:69405433 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1694-5060G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405433 | |||||||
chr5:69405503 | C | A | 8 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0193 others(5): Show |
8 | HG01167.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1694-4990C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405503 | |||||||
chr5:69405527 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1694-4966C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405527 | |||||||
chr5:69405551 | C | T | 44 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(41): Show |
47 | HG00609.hp1 HG00642.hp1 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1694-4942C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405551 | |||||||
chr5:69405623 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-4870C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405623 | |||||||
chr5:69405677 | CA | C | 47 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(44): Show |
50 | HG00609.hp1 HG00642.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.1694-4806delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69405677 | ||||||
chr5:69405681 | A | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0216 |
2 | HG02109.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1694-4812A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405681 | |||||||
chr5:69405806 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-4687C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405806 | |||||||
chr5:69405866 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1694-4627C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405866 | |||||||
chr5:69405913 | A | T | 1 | a0001c0001t0002g0283 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1694-4580A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405913 | |||||||
chr5:69405950 | G | C | 1 | a0001c0001t0002g0313 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1694-4543G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405950 | |||||||
chr5:69405974 | A | G | 264 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1694-4519A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69405974 | |||||||
chr5:69406041 | CA | C | 257 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.1694-4436delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406041 | ||||||
chr5:69406300 | A | G | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1694-4193A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406300 | |||||||
chr5:69406368 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1694-4125A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406368 | |||||||
chr5:69406461 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1694-4032A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406461 | |||||||
chr5:69406487 | T | TTG | 36 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0044 others(33): Show |
36 | HG00423.hp2 HG00621.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.1694-3993_1694-399 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406487 | ||||||
chr5:69406621 | C | T | 154 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
161 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1694-3872C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406621 | |||||||
chr5:69406747 | T | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-3746T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406747 | |||||||
chr5:69406802 | G | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
172 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1694-3691G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69406802 | |||||||
chr5:69406999 | A | AT | 7 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0277 others(4): Show |
7 | HG00741.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1694-3473dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406999 | ||||||
chr5:69406999 | AT | A | 250 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1694-3473delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406999 | ||||||
chr5:69406999 | ATT | A | 6 | a0001c0001t0001g0045 a0003c0003t0001g0027 a0003c0003t0001g0028 others(3): Show |
6 | HG01256.hp1 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1694-3474_1694-347 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69406999 | ||||||
chr5:69407362 | G | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
160 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1694-3131G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407362 | |||||||
chr5:69407395 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-3098C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407395 | |||||||
chr5:69407562 | G | GT | 6 | a0001c0001t0001g0241 a0001c0001t0001g0277 a0001c0001t0002g0344 others(3): Show |
6 | HG00741.hp1 HG01175.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1694-2900dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | G | GTT | 20 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0040 others(17): Show |
20 | HG00733.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1694-2901_1694-290 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | G | GTTT | 36 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0045 others(33): Show |
36 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1694-2902_1694-290 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | G | GTTTT | 26 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0043 others(23): Show |
26 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1694-2903_1694-290 others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | G | GTTTTT | 7 | a0001c0001t0001g0050 a0001c0001t0001g0092 a0001c0001t0001g0095 others(4): Show |
7 | HG00621.hp1 HG01071.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1694-2904_1694-290 others(9): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | GT | G | 87 | a0001c0001t0001g0217 a0001c0001t0002g0008 a0001c0001t0002g0009 others(84): Show |
95 | HG00735.hp2 HG00738.hp1 HG01106.hp1 others(92): Show |
intron_variant | MODIFIER | c.1694-2900delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | GTT | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0143 others(20): Show |
24 | HG00558.hp2 HG01074.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1694-2901_1694-290 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | GTTT | G | 49 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0126 others(46): Show |
50 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1694-2902_1694-290 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | GTTTT | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0124 a0001c0001t0001g0131 others(23): Show |
27 | HG00438.hp1 HG01243.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1694-2903_1694-290 others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0002g0342 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1694-2916_1694-290 others(21): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407562 | GTTTTTTT others(11): Show |
G | 8 | a0001c0001t0002g0011 a0001c0001t0002g0298 a0001c0001t0002g0302 others(5): Show |
9 | HG01256.hp2 HG01258.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1694-2917_1694-290 others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69407562 | ||||||
chr5:69407599 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0238 a0001c0001t0001g0239 |
4 | HG02083.hp1 HG03669.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1694-2894C>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407599 | |||||||
chr5:69407737 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-2756C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407737 | |||||||
chr5:69407741 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1694-2752G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407741 | |||||||
chr5:69407809 | C | T | 1 | a0002c0002t0001g0024 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1694-2684C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407809 | |||||||
chr5:69407827 | C | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0216 a0001c0001t0001g0218 others(23): Show |
27 | HG00438.hp1 HG00621.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.1694-2666C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407827 | |||||||
chr5:69407925 | A | G | 1 | a0006c0013t0001g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1694-2568A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69407925 | |||||||
chr5:69408119 | C | T | 44 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(41): Show |
47 | HG00609.hp1 HG00642.hp1 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1694-2374C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408119 | |||||||
chr5:69408153 | G | T | 1 | a0001c0001t0002g0310 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1694-2340G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408153 | |||||||
chr5:69408179 | T | C | 2 | a0001c0001t0002g0295 a0001c0001t0002g0331 |
2 | NA18950.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1694-2314T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408179 | |||||||
chr5:69408191 | ATTTTTTG others(30): Show |
A | 5 | a0002c0002t0001g0138 a0002c0002t0001g0167 a0002c0002t0001g0191 others(2): Show |
5 | HG01071.hp2 HG01074.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694-2301_1694-226 others(41): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408191 | |||||||
chr5:69408274 | TTTA | T | 3 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0266 |
3 | HG01081.hp1 HG01978.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1694-2216_1694-221 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408274 | ||||||
chr5:69408376 | C | T | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
160 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1694-2117C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408376 | |||||||
chr5:69408485 | C | T | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1694-2008C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408485 | |||||||
chr5:69408506 | C | CT | 20 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0106 others(17): Show |
20 | HG00609.hp1 HG01243.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1694-1963dupT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408506 | ||||||
chr5:69408506 | C | CTT | 133 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
140 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1694-1964_1694-196 others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408506 | ||||||
chr5:69408506 | C | CTTT | 17 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0155 others(14): Show |
17 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1694-1965_1694-196 others(7): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408506 | ||||||
chr5:69408506 | CT | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0088 a0001c0001t0001g0103 others(3): Show |
6 | HG01109.hp2 HG01168.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1694-1963delT | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 69408506 | ||||||
chr5:69408710 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0147 |
2 | HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1694-1783C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408710 | |||||||
chr5:69408754 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1694-1739A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408754 | |||||||
chr5:69408829 | A | G | 7 | a0003c0003t0001g0002 a0003c0003t0001g0026 a0003c0003t0001g0027 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1694-1664A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408829 | |||||||
chr5:69408847 | A | T | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1694-1646A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408847 | |||||||
chr5:69408885 | G | A | 264 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1694-1608G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69408885 | |||||||
chr5:69409022 | G | A | 9 | a0001c0001t0002g0291 a0001c0001t0002g0294 a0001c0001t0002g0295 others(6): Show |
9 | HG04184.hp1 NA18950.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1694-1471G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409022 | |||||||
chr5:69409103 | T | G | 2 | a0002c0002t0001g0173 a0002c0002t0001g0199 |
2 | NA18970.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1694-1390T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409103 | |||||||
chr5:69409149 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1694-1344T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409149 | |||||||
chr5:69409321 | A | G | 340 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(337): Show |
352 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.1694-1172A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409321 | |||||||
chr5:69409377 | T | A | 164 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
172 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1694-1116T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409377 | |||||||
chr5:69409553 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0001g0066 others(7): Show |
10 | HG02129.hp2 NA18959.hp1 NA18994.hp2 others(7): Show |
intron_variant | MODIFIER | c.1694-940T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409553 | |||||||
chr5:69409573 | A | C | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1694-920A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409573 | |||||||
chr5:69409583 | C | T | 1 | a0002c0002t0001g0137 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1694-910C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409583 | |||||||
chr5:69409603 | A | T | 1 | a0006c0013t0001g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1694-890A>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69409603 | |||||||
chr5:69410349 | A | G | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1694-144A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69410349 | |||||||
chr5:69410425 | G | T | 263 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1694-68G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 17/18 | chr5 | 69410425 | |||||||
chr5:69410574 | A | G | 2 | a0001c0001t0001g0127 a0001c0009t0001g0128 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1751+24A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410574 | |||||||
chr5:69410581 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1751+31T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410581 | |||||||
chr5:69410582 | G | C | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+32G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410582 | |||||||
chr5:69410611 | G | A | 263 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1751+61G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410611 | |||||||
chr5:69410959 | G | GTCTA | 14 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0084 others(11): Show |
15 | HG00738.hp2 HG01258.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.1751+412_1751+413i others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410959 | ||||||
chr5:69410963 | G | A | 248 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0034 others(245): Show |
255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.1751+413G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410963 | |||||||
chr5:69410965 | C | CTA | 3 | a0001c0001t0001g0241 a0001c0001t0002g0284 a0001c0001t0002g0288 |
3 | HG03516.hp2 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1751+446_1751+447d others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTATA | 21 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(18): Show |
22 | HG01081.hp2 HG01256.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1751+444_1751+447d others(6): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTATATA | 25 | a0001c0001t0001g0277 a0001c0001t0002g0008 a0001c0001t0002g0009 others(22): Show |
25 | HG00642.hp1 HG00741.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1751+442_1751+447d others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTATATAT others(1): Show |
14 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0275 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1751+440_1751+447d others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTATATAT others(3): Show |
14 | a0001c0001t0002g0008 a0001c0001t0002g0281 a0001c0001t0002g0283 others(11): Show |
14 | HG00609.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1751+438_1751+447d others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTATATAT others(5): Show |
1 | a0001c0001t0002g0335 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1751+436_1751+447d others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTATATAT others(7): Show |
5 | a0001c0001t0001g0217 a0001c0001t0002g0278 a0001c0001t0002g0292 others(2): Show |
5 | HG02155.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1751+434_1751+447d others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTATATAT others(9): Show |
3 | a0001c0001t0002g0301 a0001c0001t0002g0324 a0001c0001t0002g0327 |
3 | HG02647.hp1 HG03130.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1751+432_1751+447d others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTG | 4 | a0002c0002t0001g0122 a0003c0003t0001g0028 a0003c0003t0001g0029 others(1): Show |
4 | HG02004.hp1 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(4): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCCAT others(1): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0055 others(6): Show |
9 | HG00423.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCCAT others(3): Show |
9 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0057 others(6): Show |
9 | HG00733.hp2 HG01346.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCCAT others(5): Show |
30 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(27): Show |
30 | HG00323.hp1 HG00642.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCCAT others(7): Show |
21 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0044 others(18): Show |
21 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCCAT others(9): Show |
16 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0042 others(13): Show |
16 | HG00735.hp1 HG02071.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCCAT others(11): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0085 a0001c0001t0001g0105 others(1): Show |
4 | NA18944.hp2 NA18946.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCCAT others(13): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0088 a0001c0001t0001g0115 |
3 | NA18989.hp1 NA19054.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1751+416_1751+417i others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCCAT others(15): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0082 |
2 | NA18959.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1751+416_1751+417i others(24): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCTA | 45 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0144 others(42): Show |
47 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(8): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCTAT others(1): Show |
42 | a0001c0001t0001g0006 a0001c0001t0001g0124 a0001c0001t0001g0126 others(39): Show |
44 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(10): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCTAT others(3): Show |
14 | a0001c0001t0001g0142 a0001c0001t0001g0187 a0001c0001t0001g0190 others(11): Show |
14 | HG00558.hp2 HG00733.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(12): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCTAT others(5): Show |
16 | a0001c0001t0001g0132 a0001c0001t0001g0155 a0001c0001t0001g0165 others(13): Show |
18 | HG00423.hp1 HG00738.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(14): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCTAT others(7): Show |
16 | a0001c0001t0001g0034 a0001c0001t0001g0073 a0001c0001t0001g0127 others(13): Show |
16 | HG01106.hp1 HG01167.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(16): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCTAT others(9): Show |
9 | a0001c0001t0001g0133 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
9 | HG01109.hp1 HG03486.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(18): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCTAT others(11): Show |
3 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0264 |
3 | NA18522.hp2 NA18970.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1751+416_1751+417i others(20): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410965 | C | CTGTCTAT others(13): Show |
4 | a0001c0001t0001g0197 a0001c0001t0001g0232 a0001c0001t0001g0263 others(1): Show |
4 | HG01433.hp1 HG02486.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+416_1751+417i others(22): Show |
RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69410965 | ||||||
chr5:69410966 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1751+416T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410966 | |||||||
chr5:69410967 | A | C | 4 | a0002c0002t0001g0122 a0003c0003t0001g0028 a0003c0003t0001g0029 others(1): Show |
4 | HG02004.hp1 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+417A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410967 | |||||||
chr5:69410967 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+417A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410967 | |||||||
chr5:69410969 | A | C | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+419A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410969 | |||||||
chr5:69410971 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1751+421A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410971 | |||||||
chr5:69410973 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1751+423A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410973 | |||||||
chr5:69410975 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1751+425A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410975 | |||||||
chr5:69410998 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1751+448C>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410998 | |||||||
chr5:69410998 | C | T | 95 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(92): Show |
95 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1751+448C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69410998 | |||||||
chr5:69411262 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1751+712T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411262 | |||||||
chr5:69411267 | T | C | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1751+717T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411267 | |||||||
chr5:69411270 | G | T | 2 | a0002c0002t0001g0135 a0002c0002t0001g0153 |
2 | HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1751+720G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411270 | |||||||
chr5:69411333 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0210 others(6): Show |
10 | HG01074.hp2 HG02647.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1751+783C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411333 | |||||||
chr5:69411336 | A | G | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
160 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1751+786A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411336 | |||||||
chr5:69411474 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1751+924G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411474 | |||||||
chr5:69411545 | T | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
160 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1751+995T>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411545 | |||||||
chr5:69411605 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1751+1055G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411605 | |||||||
chr5:69411644 | G | C | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1751+1094G>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411644 | |||||||
chr5:69411690 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1751+1140A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411690 | |||||||
chr5:69411980 | G | A | 1 | a0006c0013t0001g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1751+1430G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69411980 | |||||||
chr5:69412039 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+1489C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412039 | |||||||
chr5:69412133 | T | G | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1751+1583T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412133 | |||||||
chr5:69412181 | C | T | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1751+1631C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412181 | |||||||
chr5:69412446 | A | C | 1 | a0001c0001t0002g0309 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1752-1585A>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412446 | |||||||
chr5:69412452 | T | C | 4 | a0003c0003t0001g0027 a0003c0003t0001g0028 a0003c0003t0001g0029 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-1579T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412452 | |||||||
chr5:69412481 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1752-1550A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412481 | |||||||
chr5:69412496 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1752-1535T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412496 | |||||||
chr5:69412510 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1752-1521G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412510 | |||||||
chr5:69412659 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00733.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1752-1372C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412659 | |||||||
chr5:69412746 | T | G | 2 | a0002c0002t0001g0125 a0002c0002t0001g0137 |
2 | NA18948.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1752-1285T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412746 | |||||||
chr5:69412781 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1752-1250G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412781 | |||||||
chr5:69412784 | T | C | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1752-1247T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412784 | |||||||
chr5:69412861 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1752-1170C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69412861 | |||||||
chr5:69412984 | CA | C | 259 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1752-1034delA | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 69412984 | ||||||
chr5:69413196 | T | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1752-835T>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413196 | |||||||
chr5:69413421 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1752-610A>G | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413421 | |||||||
chr5:69413597 | C | T | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | NA18954.hp1 NA18964.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752-434C>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413597 | |||||||
chr5:69413682 | G | A | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1752-349G>A | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413682 | |||||||
chr5:69413823 | T | C | 263 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1752-208T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413823 | |||||||
chr5:69413874 | T | C | 1 | a0011c0012t0001g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1752-157T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413874 | |||||||
chr5:69413877 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1752-154T>C | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69413877 | |||||||
chr5:69414013 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1752-18G>T | RAD17 | ENSG00000152942.19 | transcript | ENST00000354868.10 | protein_coding | 18/18 | chr5 | 69414013 |