Item | Value |
---|---|
geneid | 56852 |
ensemblid | ENSG00000070950.10 |
hgncid | 18278 |
symbol | RAD18 |
name | RAD18 E3 ubiquitin protein ligase |
refseq_nuc | NM_020165.4 |
refseq_prot | NP_064550.3 |
ensembl_nuc | ENST00000264926.7 |
ensembl_prot | ENSP00000264926.2 |
mane_status | MANE Select |
chr | chr3 |
start | 8877075 |
end | 8963472 |
strand | - |
ver | v1.2 |
region | chr3:8877075-8963472 |
region5000 | chr3:8872075-8968472 |
regionname0 | RAD18_chr3_8877075_8963472 |
regionname5000 | RAD18_chr3_8872075_8968472 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 495 | 175 | 59 | 38 | 53 | 2 | 22 | 41 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0002 | 1/0 | 495 | 149 | 22 | 19 | 97 | 4 | 6 | 79 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0003 | 0/0 | 495 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0004 | 0/0 | 495 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0005 | 0/0 | 495 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0006 | 0/0 | 495 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0007 | 0/0 | 495 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0008 | 0/0 | 495 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0009 | 0/0 | 495 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0010 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0011 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0012 | 0/0 | 495 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0013 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
a0014 | 0/0 | 495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | MDSLA others(490): Show |
chr3 | 8872075 | 8968472 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1485 | 173 | 59 | 38 | 52 | 2 | 21 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0001c0007 | 0/0 | 1485 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0001c0011 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0002c0002 | 1/0 | 1485 | 149 | 22 | 19 | 97 | 4 | 6 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0003c0003 | 0/0 | 1485 | 8 | 8 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0004c0004 | 0/0 | 1485 | 5 | 0 | 0 | 5 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0005c0005 | 0/0 | 1485 | 2 | 2 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0006c0008 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0007c0015 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0008c0010 | 0/0 | 1485 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0009c0013 | 0/0 | 1485 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0010c0016 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0011c0014 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0012c0012 | 0/0 | 1485 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0013c0009 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 | ||
a0014c0006 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | ATGGA others(1480): Show |
chr3 | 8872075 | 8968472 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5857 | 111 | 14 | 31 | 49 | 2 | 15 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0002 | 0/0 | 5857 | 9 | 9 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0005 | 0/0 | 5857 | 10 | 7 | 3 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0006 | 0/0 | 5857 | 9 | 9 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0008 | 0/0 | 5857 | 6 | 0 | 3 | 0 | 0 | 3 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0012 | 0/0 | 5857 | 4 | 4 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0013 | 0/0 | 5857 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0014 | 0/0 | 5856 | 2 | 2 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5851): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0015 | 0/0 | 5857 | 2 | 2 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0016 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0019 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0021 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5853): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0022 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0023 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0024 | 0/0 | 5856 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5851): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0026 | 0/0 | 5856 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5851): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0029 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0030 | 0/0 | 5857 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0031 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0032 | 0/1 | 5857 | 1 | 0 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0034 | 0/0 | 5858 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5853): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0037 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0038 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0042 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0043 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0045 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0048 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0001t0049 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5853): Show |
chr3 | 8872075 | 8968472 |
a0001c0007t0001 | 0/0 | 5857 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0001c0011t0001 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0002 | 1/0 | 5857 | 69 | 5 | 6 | 54 | 1 | 2 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0003 | 0/0 | 5857 | 30 | 2 | 0 | 28 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0004 | 0/0 | 5857 | 18 | 5 | 5 | 3 | 2 | 3 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0009 | 0/0 | 5857 | 6 | 0 | 6 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0010 | 0/0 | 5858 | 4 | 4 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5853): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0011 | 0/0 | 5857 | 4 | 0 | 0 | 4 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0013 | 0/0 | 5857 | 2 | 0 | 0 | 2 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0017 | 0/0 | 5857 | 2 | 0 | 0 | 2 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0018 | 0/0 | 5857 | 2 | 2 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0019 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0027 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0028 | 0/0 | 5857 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0035 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5853): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0036 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0039 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0040 | 0/0 | 5857 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0041 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0044 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0046 | 0/0 | 5857 | 1 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0047 | 0/0 | 5856 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5851): Show |
chr3 | 8872075 | 8968472 |
a0002c0002t0050 | 0/0 | 5857 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0003c0003t0007 | 0/0 | 5857 | 7 | 7 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0003c0003t0033 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0004c0004t0001 | 0/0 | 5857 | 5 | 0 | 0 | 5 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0005c0005t0020 | 0/0 | 5857 | 2 | 2 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0006c0008t0001 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0007c0015t0003 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0008c0010t0001 | 0/0 | 5857 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0009c0013t0001 | 0/0 | 5857 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0010c0016t0025 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0011c0014t0003 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0012c0012t0004 | 0/0 | 5857 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0013c0009t0016 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
a0014c0006t0002 | 0/0 | 5857 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | GTAAT others(5852): Show |
chr3 | 8872075 | 8968472 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0008g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0008g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0013g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0014g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0016g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0019g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0021g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0022g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0023g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0024g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0026g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0029g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0030g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0031g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0032g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0034g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0037g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0038g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0042g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0043g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0045g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0048g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0001t0049g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0007t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0001c0011t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0009g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0009g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0009g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0009g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0009g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0011g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0011g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0011g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0017g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0017g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0018g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0018g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0019g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0027g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0028g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0035g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0036g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0039g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0040g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0041g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0044g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0046g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0047g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0002c0002t0050g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0003c0003t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0003c0003t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0003c0003t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0003c0003t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0003c0003t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0003c0003t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0003c0003t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0003c0003t0033g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0004c0004t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0004c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0005c0005t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0005c0005t0020g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0006c0008t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0007c0015t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0008c0010t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0009c0013t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0010c0016t0025g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0011c0014t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0012c0012t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0013c0009t0016g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
a0014c0006t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00099 | hp2 | a0002 | c0002 | t0046 | g0321 | EUR | GBR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0307 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0308 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00438 | hp2 | a0002 | c0002 | t0011 | g0329 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0210 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00639 | hp2 | a0002 | c0002 | t0004 | g0053 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0285 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0317 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0310 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01081 | hp1 | a0002 | c0002 | t0040 | g0205 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01081 | hp2 | a0001 | c0001 | t0026 | g0063 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01106 | hp1 | a0001 | c0001 | t0008 | g0031 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01109 | hp2 | a0002 | c0002 | t0004 | g0042 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0288 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01168 | hp2 | a0002 | c0002 | t0004 | g0066 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01169 | hp2 | a0002 | c0002 | t0004 | g0067 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01243 | hp2 | a0002 | c0002 | t0009 | g0334 | AMR | PUR | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01257 | hp2 | a0001 | c0001 | t0008 | g0033 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01258 | hp1 | a0001 | c0001 | t0008 | g0032 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0323 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01358 | hp1 | a0002 | c0002 | t0009 | g0012 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01433 | hp1 | a0002 | c0002 | t0009 | g0012 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0264 | EUR | IBS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01516 | hp2 | a0002 | c0002 | t0004 | g0065 | EUR | IBS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01517 | hp2 | a0002 | c0002 | t0004 | g0054 | EUR | IBS | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01891 | hp1 | a0001 | c0001 | t0043 | g0197 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0280 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0301 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01981 | hp1 | a0002 | c0002 | t0004 | g0064 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01993 | hp1 | a0002 | c0002 | t0009 | g0330 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02004 | hp2 | a0002 | c0002 | t0009 | g0331 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02027 | hp1 | a0001 | c0011 | t0001 | g0092 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0294 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02055 | hp1 | a0002 | c0002 | t0018 | g0235 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02056 | hp1 | a0006 | c0008 | t0001 | g0151 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02056 | hp2 | a0002 | c0002 | t0003 | g0242 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02071 | hp2 | a0002 | c0002 | t0003 | g0214 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02083 | hp1 | a0002 | c0002 | t0003 | g0233 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0234 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0306 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02145 | hp1 | a0001 | c0001 | t0048 | g0244 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02145 | hp2 | a0001 | c0001 | t0023 | g0019 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02148 | hp1 | a0002 | c0002 | t0009 | g0333 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | CDX | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02155 | hp2 | a0007 | c0015 | t0003 | g0245 | EAS | CDX | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02165 | hp1 | a0002 | c0002 | t0003 | g0231 | EAS | CDX | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0258 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02300 | hp1 | a0008 | c0010 | t0001 | g0114 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02300 | hp2 | a0002 | c0002 | t0050 | g0332 | AMR | PEL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0194 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02572 | hp1 | a0001 | c0001 | t0045 | g0328 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02572 | hp2 | a0001 | c0001 | t0015 | g0023 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0292 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02615 | hp2 | a0002 | c0002 | t0003 | g0209 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0248 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02622 | hp2 | a0001 | c0001 | t0042 | g0247 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0249 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02647 | hp1 | a0003 | c0003 | t0007 | g0052 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02647 | hp2 | a0001 | c0001 | t0038 | g0193 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0325 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0035 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02717 | hp2 | a0002 | c0002 | t0004 | g0044 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02723 | hp1 | a0002 | c0002 | t0004 | g0059 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02738 | hp1 | a0009 | c0013 | t0001 | g0141 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02738 | hp2 | a0001 | c0001 | t0030 | g0079 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02809 | hp1 | a0002 | c0002 | t0018 | g0237 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02809 | hp2 | a0002 | c0002 | t0010 | g0189 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0199 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02886 | hp1 | a0001 | c0001 | t0024 | g0017 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0257 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02895 | hp2 | a0003 | c0003 | t0007 | g0046 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02896 | hp1 | a0005 | c0005 | t0020 | g0204 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02897 | hp1 | a0003 | c0003 | t0007 | g0049 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02897 | hp2 | a0005 | c0005 | t0020 | g0203 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02922 | hp1 | a0010 | c0016 | t0025 | g0192 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02922 | hp2 | a0001 | c0001 | t0015 | g0022 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02965 | hp1 | a0003 | c0003 | t0007 | g0051 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02970 | hp2 | a0003 | c0003 | t0007 | g0047 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02976 | hp1 | a0002 | c0002 | t0004 | g0045 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0250 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03041 | hp1 | a0002 | c0002 | t0004 | g0043 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0254 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03098 | hp1 | a0003 | c0003 | t0007 | g0048 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03098 | hp2 | a0002 | c0002 | t0010 | g0191 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03130 | hp2 | a0002 | c0002 | t0010 | g0190 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03225 | hp2 | a0003 | c0003 | t0033 | g0050 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03453 | hp1 | a0002 | c0002 | t0004 | g0069 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03453 | hp2 | a0001 | c0001 | t0037 | g0260 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0252 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03492 | hp2 | a0002 | c0002 | t0004 | g0062 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03516 | hp1 | a0001 | c0001 | t0022 | g0015 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03516 | hp2 | a0002 | c0002 | t0010 | g0188 | AFR | ESN | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0276 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03540 | hp2 | a0011 | c0014 | t0003 | g0253 | AFR | GWD | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03579 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03579 | hp2 | a0002 | c0002 | t0047 | g0327 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03688 | hp1 | a0012 | c0012 | t0004 | g0058 | SAS | STU | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03688 | hp2 | a0001 | c0001 | t0013 | g0085 | SAS | STU | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03704 | hp1 | a0002 | c0002 | t0004 | g0060 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03704 | hp2 | a0001 | c0007 | t0001 | g0124 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03942 | hp2 | a0002 | c0002 | t0028 | g0070 | SAS | BEB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG04115 | hp2 | a0001 | c0001 | t0008 | g0036 | SAS | STU | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG04184 | hp1 | a0001 | c0001 | t0034 | g0128 | SAS | BEB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG04184 | hp2 | a0002 | c0002 | t0004 | g0061 | SAS | BEB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | YRI | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18522 | hp2 | a0001 | c0001 | t0014 | g0013 | AFR | YRI | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0195 | AFR | YRI | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18906 | hp2 | a0002 | c0002 | t0027 | g0068 | AFR | YRI | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18939 | hp1 | a0002 | c0002 | t0041 | g0286 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18941 | hp1 | a0004 | c0004 | t0001 | g0187 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18941 | hp2 | a0002 | c0002 | t0011 | g0238 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18942 | hp2 | a0002 | c0002 | t0003 | g0228 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18944 | hp2 | a0002 | c0002 | t0017 | g0281 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0206 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18948 | hp2 | a0002 | c0002 | t0013 | g0075 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18949 | hp1 | a0001 | c0001 | t0019 | g0270 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18950 | hp1 | a0001 | c0001 | t0029 | g0148 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18951 | hp2 | a0002 | c0002 | t0003 | g0208 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18952 | hp1 | a0002 | c0002 | t0004 | g0057 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0217 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18961 | hp2 | a0002 | c0002 | t0044 | g0220 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18966 | hp1 | a0002 | c0002 | t0003 | g0241 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18967 | hp2 | a0002 | c0002 | t0003 | g0243 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0211 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18969 | hp1 | a0002 | c0002 | t0019 | g0326 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18969 | hp2 | a0002 | c0002 | t0011 | g0222 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18970 | hp1 | a0002 | c0002 | t0003 | g0227 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18973 | hp2 | a0002 | c0002 | t0039 | g0296 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18979 | hp1 | a0002 | c0002 | t0003 | g0232 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18980 | hp1 | a0002 | c0002 | t0003 | g0239 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18982 | hp1 | a0014 | c0006 | t0002 | g0267 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18984 | hp1 | a0002 | c0002 | t0004 | g0056 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18988 | hp2 | a0002 | c0002 | t0003 | g0218 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18993 | hp1 | a0002 | c0002 | t0003 | g0229 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18994 | hp1 | a0002 | c0002 | t0003 | g0213 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18997 | hp1 | a0002 | c0002 | t0003 | g0219 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19000 | hp1 | a0002 | c0002 | t0003 | g0230 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19000 | hp2 | a0002 | c0002 | t0017 | g0277 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19002 | hp1 | a0004 | c0004 | t0001 | g0186 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19002 | hp2 | a0002 | c0002 | t0003 | g0240 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19004 | hp1 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19006 | hp2 | a0002 | c0002 | t0011 | g0223 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0224 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19030 | hp1 | a0001 | c0001 | t0021 | g0016 | AFR | LWK | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19030 | hp2 | a0003 | c0003 | t0007 | g0055 | AFR | LWK | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0263 | AFR | LWK | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | LWK | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19060 | hp1 | a0002 | c0002 | t0013 | g0083 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19060 | hp2 | a0002 | c0002 | t0003 | g0212 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19065 | hp1 | a0001 | c0001 | t0031 | g0149 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19068 | hp2 | a0002 | c0002 | t0004 | g0039 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19072 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0319 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19077 | hp2 | a0002 | c0002 | t0003 | g0216 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19078 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19080 | hp1 | a0002 | c0002 | t0003 | g0207 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19081 | hp1 | a0002 | c0002 | t0003 | g0221 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19082 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19084 | hp2 | a0002 | c0002 | t0003 | g0226 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19090 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | YRI | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA20129 | hp2 | a0001 | c0001 | t0012 | g0200 | AFR | ASW | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA20905 | hp1 | a0001 | c0001 | t0008 | g0034 | SAS | GIH | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | GIH | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02559 | hp1 | a0002 | c0002 | t0003 | g0215 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG02559 | hp2 | a0002 | c0002 | t0035 | g0041 | AFR | ACB | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG03471 | hp2 | a0002 | c0002 | t0036 | g0236 | AFR | MSL | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | USA | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
HG06807 | hp2 | a0013 | c0009 | t0016 | g0262 | AFR | USA | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0300 | AFR | USA | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | LWK | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
NA21309 | hp2 | a0001 | c0001 | t0049 | g0261 | AFR | LWK | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0071 | REF | REF | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0271 | REF | REF | RAD18_chr3_8872075_8968472 | RAD18 | chr3 | 8872075 | 8968472 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:8881415 | C | T | 1 | a0006 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1430G>A | p.Arg477His | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 1517/5857 | 1430/1488 | 477/495 | chr3 | 8881415 | |||
chr3:8890447 | T | C | 1 | a0013 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1327A>G | p.Ser443Gly | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/13 | 1414/5857 | 1327/1488 | 443/495 | chr3 | 8890447 | |||
chr3:8899014 | T | C | 1 | a0008 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1202A>G | p.His401Arg | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/13 | 1289/5857 | 1202/1488 | 401/495 | chr3 | 8899014 | |||
chr3:8913691 | T | C | 2 | a0003 a0010 |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
missense_variant | MODERATE | c.919A>G | p.Ile307Val | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/13 | 1006/5857 | 919/1488 | 307/495 | chr3 | 8913691 | |||
chr3:8913705 | C | T | 7 | a0001 a0004 a0005 others(4): Show |
185 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(182): Show |
missense_variant | MODERATE | c.905G>A | p.Arg302Gln | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/13 | 992/5857 | 905/1488 | 302/495 | chr3 | 8913705 | |||
chr3:8936035 | G | A | 1 | a0012 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.725C>T | p.Pro242Leu | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/13 | 812/5857 | 725/1488 | 242/495 | chr3 | 8936035 | |||
chr3:8941583 | G | A | 1 | a0009 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.488C>T | p.Ala163Val | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/13 | 575/5857 | 488/1488 | 163/495 | chr3 | 8941583 | |||
chr3:8941592 | T | G | 1 | a0005 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.479A>C | p.Gln160Pro | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/13 | 566/5857 | 479/1488 | 160/495 | chr3 | 8941592 | |||
chr3:8941721 | T | C | 1 | a0004 | 5 | NA18941.hp1 NA19002.hp1 NA19004.hp1 others(2): Show |
missense_variant | MODERATE | c.350A>G | p.Tyr117Cys | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/13 | 437/5857 | 350/1488 | 117/495 | chr3 | 8941721 | |||
chr3:8941743 | T | C | 1 | a0011 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.328A>G | p.Lys110Glu | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/13 | 415/5857 | 328/1488 | 110/495 | chr3 | 8941743 | |||
chr3:8958935 | G | T | 1 | a0014 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.118C>A | p.Gln40Lys | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/13 | 205/5857 | 118/1488 | 40/495 | chr3 | 8958935 | |||
chr3:8958955 | T | C | 1 | a0007 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.98A>G | p.Asn33Ser | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/13 | 185/5857 | 98/1488 | 33/495 | chr3 | 8958955 | |||
chr3:8963369 | T | G | 1 | a0010 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.17A>C | p.Glu6Ala | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/13 | 104/5857 | 17/1488 | 6/495 | chr3 | 8963369 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:8898983 | C | T | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1233G>A | p.Glu411Glu | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/13 | 1320/5857 | 1233/1488 | 411/495 | chr3 | 8898983 | |||
chr3:8912349 | T | C | 1 | a0001c0011 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.990A>G | p.Gln330Gln | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/13 | 1077/5857 | 990/1488 | 330/495 | chr3 | 8912349 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:8877100 | T | G | 2 | a0002c0002t0018 a0002c0002t0036 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4257A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 4257 | chr3 | 8877100 | ||||||
chr3:8877115 | T | C | 47 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(44): Show |
248 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*4242A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 4242 | chr3 | 8877115 | ||||||
chr3:8877158 | T | C | 3 | a0003c0003t0007 a0003c0003t0033 a0010c0016t0025 |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4199A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 4199 | chr3 | 8877158 | ||||||
chr3:8877195 | C | A | 14 | a0001c0001t0001 a0001c0001t0019 a0001c0001t0029 others(11): Show |
128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*4162G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 4162 | chr3 | 8877195 | ||||||
chr3:8877351 | A | C | 1 | a0001c0001t0038 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4006T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 4006 | chr3 | 8877351 | ||||||
chr3:8877474 | T | C | 1 | a0001c0001t0049 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3883A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3883 | chr3 | 8877474 | ||||||
chr3:8877524 | T | C | 2 | a0002c0002t0011 a0002c0002t0044 |
5 | HG00438.hp2 NA18941.hp2 NA18961.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3833A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3833 | chr3 | 8877524 | ||||||
chr3:8877609 | T | C | 4 | a0001c0001t0021 a0001c0001t0049 a0002c0002t0010 others(1): Show |
7 | HG02559.hp2 HG02809.hp2 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3748A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3748 | chr3 | 8877609 | ||||||
chr3:8877742 | C | T | 6 | a0001c0001t0021 a0001c0001t0034 a0001c0001t0038 others(3): Show |
9 | HG02559.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3615G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3615 | chr3 | 8877742 | ||||||
chr3:8877754 | T | C | 2 | a0002c0002t0010 a0002c0002t0035 |
5 | HG02559.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3603A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3603 | chr3 | 8877754 | ||||||
chr3:8877777 | G | A | 1 | a0001c0001t0029 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3580C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3580 | chr3 | 8877777 | ||||||
chr3:8877821 | A | AG | 5 | a0001c0001t0021 a0001c0001t0034 a0001c0001t0049 others(2): Show |
8 | HG02559.hp2 HG02809.hp2 HG03098.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3535dupC | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3535 | chr3 | 8877821 | ||||||
chr3:8877856 | G | A | 2 | a0001c0001t0014 a0001c0001t0026 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3501C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3501 | chr3 | 8877856 | ||||||
chr3:8877888 | T | C | 6 | a0001c0001t0021 a0001c0001t0034 a0001c0001t0038 others(3): Show |
9 | HG02559.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3469A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3469 | chr3 | 8877888 | ||||||
chr3:8877895 | G | A | 1 | a0001c0001t0030 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3462C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3462 | chr3 | 8877895 | ||||||
chr3:8877899 | G | A | 1 | a0001c0001t0038 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3458C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3458 | chr3 | 8877899 | ||||||
chr3:8877954 | A | G | 1 | a0001c0001t0015 | 2 | HG02572.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3403T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3403 | chr3 | 8877954 | ||||||
chr3:8878008 | C | A | 1 | a0002c0002t0046 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3349G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3349 | chr3 | 8878008 | ||||||
chr3:8878068 | G | T | 1 | a0001c0001t0031 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3289C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3289 | chr3 | 8878068 | ||||||
chr3:8878069 | G | C | 1 | a0001c0001t0031 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3288C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3288 | chr3 | 8878069 | ||||||
chr3:8878070 | A | C | 1 | a0001c0001t0031 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3287T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3287 | chr3 | 8878070 | ||||||
chr3:8878073 | T | G | 1 | a0001c0001t0031 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3284A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3284 | chr3 | 8878073 | ||||||
chr3:8878074 | T | C | 3 | a0001c0001t0012 a0001c0001t0031 a0005c0005t0020 |
7 | HG02451.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3283A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3283 | chr3 | 8878074 | ||||||
chr3:8878075 | C | A | 1 | a0001c0001t0031 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3282G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3282 | chr3 | 8878075 | ||||||
chr3:8878133 | T | A | 1 | a0002c0002t0041 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3224A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 3224 | chr3 | 8878133 | ||||||
chr3:8878597 | G | A | 45 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(42): Show |
246 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*2760C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2760 | chr3 | 8878597 | ||||||
chr3:8878774 | C | G | 1 | a0001c0001t0049 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2583G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2583 | chr3 | 8878774 | ||||||
chr3:8878779 | C | G | 1 | a0001c0001t0022 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2578G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2578 | chr3 | 8878779 | ||||||
chr3:8878790 | C | A | 1 | a0001c0001t0021 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2567G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2567 | chr3 | 8878790 | ||||||
chr3:8878821 | T | C | 37 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(34): Show |
222 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*2536A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2536 | chr3 | 8878821 | ||||||
chr3:8878955 | A | C | 1 | a0002c0002t0040 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2402T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2402 | chr3 | 8878955 | ||||||
chr3:8878964 | C | A | 1 | a0001c0001t0042 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2393G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2393 | chr3 | 8878964 | ||||||
chr3:8879026 | T | A | 1 | a0001c0001t0043 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2331 | chr3 | 8879026 | ||||||
chr3:8879177 | C | T | 1 | a0002c0002t0039 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2180G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 2180 | chr3 | 8879177 | ||||||
chr3:8879452 | C | T | 3 | a0001c0001t0016 a0001c0001t0037 a0013c0009t0016 |
3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1905G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 1905 | chr3 | 8879452 | ||||||
chr3:8879609 | AC | A | 4 | a0001c0001t0014 a0001c0001t0024 a0001c0001t0026 others(1): Show |
5 | HG01081.hp2 HG02886.hp1 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1747delG | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 1747 | chr3 | 8879609 | ||||||
chr3:8879620 | C | G | 1 | a0002c0002t0027 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1737G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 1737 | chr3 | 8879620 | ||||||
chr3:8879666 | C | G | 1 | a0001c0001t0034 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1691G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 1691 | chr3 | 8879666 | ||||||
chr3:8879667 | A | G | 11 | a0001c0001t0014 a0001c0001t0021 a0001c0001t0024 others(8): Show |
15 | HG01081.hp2 HG02559.hp2 HG02647.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1690T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 1690 | chr3 | 8879667 | ||||||
chr3:8879818 | A | G | 7 | a0001c0001t0021 a0001c0001t0034 a0001c0001t0038 others(4): Show |
10 | HG02559.hp2 HG02647.hp2 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1539T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 1539 | chr3 | 8879818 | ||||||
chr3:8880079 | A | T | 2 | a0001c0001t0016 a0013c0009t0016 |
2 | HG06807.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1278T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 1278 | chr3 | 8880079 | ||||||
chr3:8880370 | T | C | 14 | a0001c0001t0001 a0001c0001t0019 a0001c0001t0029 others(11): Show |
128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*987A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 987 | chr3 | 8880370 | ||||||
chr3:8880409 | C | A | 1 | a0003c0003t0033 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 948 | chr3 | 8880409 | ||||||
chr3:8880437 | C | T | 2 | a0001c0001t0034 a0001c0001t0037 |
2 | HG03453.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*920G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 920 | chr3 | 8880437 | ||||||
chr3:8880483 | T | C | 1 | a0002c0002t0050 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*874A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 874 | chr3 | 8880483 | ||||||
chr3:8880558 | G | A | 1 | a0001c0001t0045 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*799C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 799 | chr3 | 8880558 | ||||||
chr3:8880558 | G | T | 1 | a0001c0001t0023 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 799 | chr3 | 8880558 | ||||||
chr3:8880648 | C | A | 1 | a0001c0001t0034 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 709 | chr3 | 8880648 | ||||||
chr3:8880774 | C | A | 1 | a0002c0002t0046 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 583 | chr3 | 8880774 | ||||||
chr3:8880815 | T | A | 1 | a0002c0002t0035 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 542 | chr3 | 8880815 | ||||||
chr3:8880822 | G | A | 4 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0023 others(1): Show |
15 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*535C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 535 | chr3 | 8880822 | ||||||
chr3:8880913 | G | A | 2 | a0001c0001t0024 a0002c0002t0047 |
2 | HG02886.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*444C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 444 | chr3 | 8880913 | ||||||
chr3:8881016 | C | T | 1 | a0002c0002t0036 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 341 | chr3 | 8881016 | ||||||
chr3:8881119 | T | C | 1 | a0001c0001t0048 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*238A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 238 | chr3 | 8881119 | ||||||
chr3:8881148 | T | G | 1 | a0001c0001t0049 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*209A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 13/13 | 209 | chr3 | 8881148 | ||||||
chr3:8963394 | C | T | 23 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0026 others(20): Show |
164 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(161): Show |
5_prime_UTR_variant | MODIFIER | c.-9G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/13 | 9 | chr3 | 8963394 | ||||||
chr3:8963401 | T | C | 2 | a0002c0002t0009 a0002c0002t0050 |
7 | HG01243.hp2 HG01358.hp1 HG01433.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-16A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/13 | 16 | chr3 | 8963401 | ||||||
chr3:8963418 | C | T | 8 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0014 others(5): Show |
24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-33G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/13 | 33 | chr3 | 8963418 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:8881624 | A | C | 49 | a0001c0001t0001g0126 a0001c0001t0001g0168 a0001c0001t0021g0016 others(46): Show |
49 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1386-165T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8881624 | |||||||
chr3:8881730 | G | A | 1 | a0002c0002t0009g0012 | 2 | HG01358.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1386-271C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8881730 | |||||||
chr3:8881807 | T | G | 5 | a0001c0001t0016g0263 a0001c0001t0021g0016 a0001c0001t0037g0260 others(2): Show |
5 | HG02145.hp1 HG03453.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386-348A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8881807 | |||||||
chr3:8881858 | A | T | 17 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(14): Show |
17 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1386-399T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8881858 | |||||||
chr3:8881889 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1386-430G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8881889 | |||||||
chr3:8882056 | C | T | 1 | a0007c0015t0003g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1386-597G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882056 | |||||||
chr3:8882071 | A | G | 16 | a0001c0001t0001g0164 a0001c0001t0012g0194 a0001c0001t0012g0195 others(13): Show |
16 | HG01081.hp2 HG01109.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1386-612T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882071 | |||||||
chr3:8882126 | G | A | 13 | a0001c0001t0002g0251 a0001c0001t0005g0018 a0001c0001t0005g0020 others(10): Show |
13 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1386-667C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882126 | |||||||
chr3:8882126 | G | C | 110 | a0001c0001t0001g0102 a0001c0001t0001g0107 a0001c0001t0001g0108 others(107): Show |
112 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1386-667C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882126 | |||||||
chr3:8882136 | GAAGTC | G | 185 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0072 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1386-682_1386-678d others(7): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882136 | |||||||
chr3:8882156 | C | T | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0040 others(142): Show |
154 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1386-697G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882156 | |||||||
chr3:8882166 | C | T | 1 | a0002c0002t0009g0012 | 2 | HG01358.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1386-707G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882166 | |||||||
chr3:8882291 | G | A | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1386-832C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882291 | |||||||
chr3:8882397 | C | G | 2 | a0001c0001t0005g0021 a0002c0002t0004g0059 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1386-938G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882397 | |||||||
chr3:8882641 | C | T | 10 | a0001c0001t0006g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386-1182G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882641 | |||||||
chr3:8882833 | A | T | 3 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0028 |
3 | HG01069.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1386-1374T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8882833 | |||||||
chr3:8883053 | A | G | 1 | a0001c0001t0014g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1386-1594T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883053 | |||||||
chr3:8883065 | A | G | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386-1606T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883065 | |||||||
chr3:8883110 | G | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0196 |
3 | HG02055.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1386-1651C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883110 | |||||||
chr3:8883111 | T | C | 2 | a0002c0002t0002g0274 a0002c0002t0002g0295 |
2 | NA18949.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1386-1652A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883111 | |||||||
chr3:8883133 | A | G | 10 | a0001c0001t0006g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386-1674T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883133 | |||||||
chr3:8883186 | A | G | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386-1727T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883186 | |||||||
chr3:8883191 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1386-1732T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883191 | |||||||
chr3:8883212 | A | G | 2 | a0002c0002t0002g0280 a0002c0002t0035g0041 |
2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1386-1753T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883212 | |||||||
chr3:8883220 | T | C | 1 | a0004c0004t0001g0186 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1386-1761A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883220 | |||||||
chr3:8883310 | T | C | 1 | a0002c0002t0013g0075 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1386-1851A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883310 | |||||||
chr3:8883357 | T | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
172 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.1386-1898A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883357 | |||||||
chr3:8883430 | T | C | 1 | a0001c0001t0037g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1386-1971A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883430 | |||||||
chr3:8883615 | C | T | 2 | a0001c0001t0024g0017 a0002c0002t0047g0327 |
2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1386-2156G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883615 | |||||||
chr3:8883704 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1386-2245A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883704 | |||||||
chr3:8883793 | A | T | 1 | a0001c0001t0034g0128 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1386-2334T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8883793 | |||||||
chr3:8884005 | G | A | 2 | a0003c0003t0007g0046 a0003c0003t0007g0049 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1386-2546C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884005 | |||||||
chr3:8884100 | C | T | 2 | a0002c0002t0017g0277 a0002c0002t0017g0281 |
2 | NA18944.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1386-2641G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884100 | |||||||
chr3:8884139 | C | T | 1 | a0007c0015t0003g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1386-2680G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884139 | |||||||
chr3:8884193 | G | C | 11 | a0001c0001t0045g0328 a0002c0002t0035g0041 a0003c0003t0007g0046 others(8): Show |
11 | HG02559.hp2 HG02572.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386-2734C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884193 | |||||||
chr3:8884401 | T | C | 12 | a0001c0001t0045g0328 a0002c0002t0004g0059 a0002c0002t0035g0041 others(9): Show |
12 | HG02559.hp2 HG02572.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1386-2942A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884401 | |||||||
chr3:8884628 | T | TA | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.1386-3170_1386-316 others(5): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884628 | |||||||
chr3:8884640 | T | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
142 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1386-3181A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884640 | |||||||
chr3:8884645 | C | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0156 others(1): Show |
4 | HG01256.hp2 HG01952.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386-3186G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884645 | |||||||
chr3:8884808 | G | A | 1 | a0001c0001t0022g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1386-3349C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884808 | |||||||
chr3:8884859 | C | T | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1386-3400G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884859 | |||||||
chr3:8884983 | C | T | 11 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(8): Show |
11 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386-3524G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8884983 | |||||||
chr3:8885049 | C | T | 18 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(15): Show |
18 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1386-3590G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8885049 | |||||||
chr3:8885249 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA18939.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1386-3790G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8885249 | |||||||
chr3:8885448 | T | C | 2 | a0001c0001t0008g0035 a0001c0001t0008g0036 |
2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1386-3989A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8885448 | |||||||
chr3:8885464 | C | A | 3 | a0002c0002t0002g0275 a0002c0002t0002g0282 a0002c0002t0002g0320 |
3 | NA18980.hp2 NA18998.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1386-4005G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8885464 | |||||||
chr3:8885569 | T | C | 15 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(12): Show |
16 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1386-4110A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8885569 | |||||||
chr3:8885610 | G | A | 1 | a0012c0012t0004g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1386-4151C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8885610 | |||||||
chr3:8885680 | G | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
174 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1386-4221C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8885680 | |||||||
chr3:8885687 | T | A | 1 | a0002c0002t0002g0317 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1386-4228A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8885687 | |||||||
chr3:8886046 | T | C | 1 | a0002c0002t0002g0309 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1385+4343A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886046 | |||||||
chr3:8886198 | T | C | 3 | a0002c0002t0002g0287 a0002c0002t0002g0290 a0002c0002t0002g0310 |
3 | HG00735.hp1 NA18975.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1385+4191A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886198 | |||||||
chr3:8886304 | G | C | 10 | a0001c0001t0045g0328 a0003c0003t0007g0046 a0003c0003t0007g0047 others(7): Show |
10 | HG02572.hp1 HG02647.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1385+4085C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886304 | |||||||
chr3:8886767 | G | A | 1 | a0002c0002t0002g0268 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1385+3622C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886767 | |||||||
chr3:8886772 | G | A | 15 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0056 others(12): Show |
15 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1385+3617C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886772 | |||||||
chr3:8886801 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1385+3588T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886801 | |||||||
chr3:8886920 | C | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
160 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1385+3469G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886920 | |||||||
chr3:8886941 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1385+3448C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886941 | |||||||
chr3:8886959 | AG | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1385+3429delC | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8886959 | |||||||
chr3:8887040 | G | T | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1385+3349C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887040 | |||||||
chr3:8887096 | T | A | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1385+3293A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887096 | |||||||
chr3:8887171 | T | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
239 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(236): Show |
intron_variant | MODIFIER | c.1385+3218A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887171 | |||||||
chr3:8887174 | A | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0196 |
3 | HG02055.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1385+3215T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887174 | |||||||
chr3:8887207 | A | C | 80 | a0001c0001t0005g0021 a0001c0001t0006g0246 a0001c0001t0006g0248 others(77): Show |
80 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.1385+3182T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887207 | |||||||
chr3:8887227 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1385+3162G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887227 | |||||||
chr3:8887232 | G | A | 30 | a0001c0001t0005g0021 a0001c0001t0045g0328 a0002c0002t0004g0053 others(27): Show |
30 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.1385+3157C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887232 | |||||||
chr3:8887380 | G | T | 2 | a0001c0001t0038g0193 a0010c0016t0025g0192 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1385+3009C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887380 | |||||||
chr3:8887449 | A | C | 1 | a0001c0001t0031g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1385+2940T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887449 | |||||||
chr3:8887456 | T | A | 10 | a0001c0001t0006g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1385+2933A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887456 | |||||||
chr3:8887595 | G | A | 9 | a0001c0001t0045g0328 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02572.hp1 HG02647.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1385+2794C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887595 | |||||||
chr3:8887646 | A | C | 11 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1385+2743T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887646 | |||||||
chr3:8887706 | G | C | 1 | a0002c0002t0004g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1385+2683C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887706 | |||||||
chr3:8887765 | G | C | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1385+2624C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8887765 | |||||||
chr3:8888122 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1385+2267C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888122 | |||||||
chr3:8888171 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
220 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.1385+2218G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888171 | |||||||
chr3:8888194 | C | T | 1 | a0002c0002t0002g0315 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1385+2195G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888194 | |||||||
chr3:8888195 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1385+2194C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888195 | |||||||
chr3:8888227 | G | A | 1 | a0001c0001t0031g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1385+2162C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888227 | |||||||
chr3:8888230 | T | C | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1385+2159A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888230 | |||||||
chr3:8888357 | C | T | 3 | a0001c0001t0006g0252 a0001c0001t0006g0257 a0001c0001t0006g0258 |
3 | HG02280.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1385+2032G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888357 | |||||||
chr3:8888457 | C | T | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1385+1932G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888457 | |||||||
chr3:8888532 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1385+1857C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888532 | |||||||
chr3:8888557 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1385+1832T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888557 | |||||||
chr3:8888589 | T | C | 1 | a0001c0001t0037g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1385+1800A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888589 | |||||||
chr3:8888624 | G | A | 5 | a0001c0001t0005g0020 a0001c0001t0005g0024 a0001c0001t0005g0025 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1385+1765C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8888624 | |||||||
chr3:8889051 | A | G | 11 | a0002c0002t0004g0059 a0002c0002t0035g0041 a0003c0003t0007g0046 others(8): Show |
11 | HG02559.hp2 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1385+1338T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889051 | |||||||
chr3:8889067 | C | T | 18 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(15): Show |
18 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1385+1322G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889067 | |||||||
chr3:8889114 | T | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1385+1275A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889114 | |||||||
chr3:8889177 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1385+1212G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889177 | |||||||
chr3:8889180 | A | G | 2 | a0002c0002t0004g0061 a0002c0002t0004g0062 |
2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1385+1209T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889180 | |||||||
chr3:8889354 | A | T | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1385+1035T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889354 | |||||||
chr3:8889363 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1385+1026T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889363 | |||||||
chr3:8889364 | T | C | 2 | a0001c0001t0024g0017 a0002c0002t0047g0327 |
2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1385+1025A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889364 | |||||||
chr3:8889468 | A | T | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1385+921T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889468 | |||||||
chr3:8889484 | A | T | 11 | a0001c0001t0045g0328 a0002c0002t0004g0059 a0002c0002t0035g0041 others(8): Show |
11 | HG02559.hp2 HG02572.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1385+905T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889484 | |||||||
chr3:8889519 | G | A | 1 | a0002c0002t0002g0284 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1385+870C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889519 | |||||||
chr3:8889598 | A | T | 44 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(41): Show |
44 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.1385+791T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889598 | |||||||
chr3:8889688 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1385+701C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889688 | |||||||
chr3:8889754 | C | G | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
259 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.1385+635G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889754 | |||||||
chr3:8889924 | C | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
159 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1385+465G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889924 | |||||||
chr3:8889972 | G | A | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1385+417C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8889972 | |||||||
chr3:8890023 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1385+366C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8890023 | |||||||
chr3:8890105 | T | C | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1385+284A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8890105 | |||||||
chr3:8890156 | T | C | 10 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(7): Show |
10 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1385+233A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8890156 | |||||||
chr3:8890196 | T | C | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1385+193A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8890196 | |||||||
chr3:8890266 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1385+123G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8890266 | |||||||
chr3:8890300 | A | C | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1385+89T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 12/12 | chr3 | 8890300 | |||||||
chr3:8890483 | C | A | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1323-32G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890483 | |||||||
chr3:8890501 | G | A | 1 | a0002c0002t0019g0326 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1323-50C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890501 | |||||||
chr3:8890505 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
141 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1323-54G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890505 | |||||||
chr3:8890615 | G | A | 3 | a0001c0001t0016g0263 a0001c0001t0037g0260 a0013c0009t0016g0262 |
3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1323-164C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890615 | |||||||
chr3:8890669 | A | G | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.1323-218T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890669 | |||||||
chr3:8890708 | C | G | 16 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0056 others(13): Show |
16 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1323-257G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890708 | |||||||
chr3:8890790 | C | G | 5 | a0001c0001t0005g0020 a0001c0001t0005g0024 a0001c0001t0005g0025 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323-339G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890790 | |||||||
chr3:8890905 | T | C | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1323-454A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890905 | |||||||
chr3:8890979 | C | T | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1323-528G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890979 | |||||||
chr3:8890986 | C | T | 11 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(8): Show |
11 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1323-535G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8890986 | |||||||
chr3:8891075 | A | AAT | 8 | a0002c0002t0002g0008 a0002c0002t0002g0268 a0002c0002t0002g0275 others(5): Show |
9 | HG01168.hp1 HG01496.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1323-626_1323-625d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891075 | |||||||
chr3:8891075 | A | AATATATA others(3): Show |
2 | a0005c0005t0020g0203 a0005c0005t0020g0204 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1323-634_1323-625d others(12): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891075 | |||||||
chr3:8891075 | A | AATATATA others(5): Show |
5 | a0001c0001t0005g0020 a0001c0001t0012g0194 a0001c0001t0012g0195 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323-636_1323-625d others(14): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891075 | |||||||
chr3:8891075 | A | AATATATA others(7): Show |
7 | a0001c0001t0005g0018 a0001c0001t0005g0021 a0001c0001t0005g0026 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323-638_1323-625d others(16): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891075 | |||||||
chr3:8891075 | A | AATATATA others(9): Show |
1 | a0001c0001t0005g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1323-640_1323-625d others(18): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891075 | |||||||
chr3:8891075 | AATAT | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
155 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1323-628_1323-625d others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891075 | |||||||
chr3:8891076 | ATAT | A | 87 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(84): Show |
88 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1323-628_1323-626d others(5): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891076 | |||||||
chr3:8891081 | T | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
155 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1323-630A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891081 | |||||||
chr3:8891094 | A | G | 97 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(94): Show |
98 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1323-643T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891094 | |||||||
chr3:8891114 | C | T | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
259 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.1323-663G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891114 | |||||||
chr3:8891190 | A | G | 21 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(18): Show |
22 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1323-739T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891190 | |||||||
chr3:8891234 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
161 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1323-783G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891234 | |||||||
chr3:8891305 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
142 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1323-854G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891305 | |||||||
chr3:8891364 | C | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1323-913G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891364 | |||||||
chr3:8891444 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1323-993G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891444 | |||||||
chr3:8891445 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1323-994T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891445 | |||||||
chr3:8891454 | G | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
229 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.1323-1003C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891454 | |||||||
chr3:8891486 | T | C | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1323-1035A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891486 | |||||||
chr3:8891748 | G | A | 1 | a0002c0002t0035g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1323-1297C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891748 | |||||||
chr3:8891750 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1323-1299A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891750 | |||||||
chr3:8891772 | G | A | 1 | a0002c0002t0002g0316 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1323-1321C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891772 | |||||||
chr3:8891776 | C | T | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323-1325G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891776 | |||||||
chr3:8891883 | G | A | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1323-1432C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891883 | |||||||
chr3:8891899 | C | T | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
259 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.1323-1448G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891899 | |||||||
chr3:8891900 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1323-1449T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891900 | |||||||
chr3:8891900 | A | G | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323-1449T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891900 | |||||||
chr3:8891906 | G | A | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1323-1455C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891906 | |||||||
chr3:8891936 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1323-1485A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8891936 | |||||||
chr3:8892171 | T | C | 1 | a0002c0002t0002g0304 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1323-1720A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892171 | |||||||
chr3:8892208 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1323-1757C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892208 | |||||||
chr3:8892262 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
142 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1323-1811G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892262 | |||||||
chr3:8892395 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
160 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1323-1944G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892395 | |||||||
chr3:8892396 | G | A | 43 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(40): Show |
43 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.1323-1945C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892396 | |||||||
chr3:8892429 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
142 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1323-1978C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892429 | |||||||
chr3:8892495 | C | A | 2 | a0002c0002t0002g0278 a0002c0002t0002g0316 |
2 | NA18995.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1323-2044G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892495 | |||||||
chr3:8892787 | A | AAATGTAT others(7): Show |
1 | a0002c0002t0003g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1323-2337_1323-233 others(18): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892787 | |||||||
chr3:8892799 | G | A | 84 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(81): Show |
85 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1323-2348C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892799 | |||||||
chr3:8892822 | C | A | 1 | a0002c0002t0003g0221 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1323-2371G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892822 | |||||||
chr3:8892834 | G | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
234 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.1323-2383C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892834 | |||||||
chr3:8892878 | T | A | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1323-2427A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8892878 | |||||||
chr3:8893323 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1323-2872C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893323 | |||||||
chr3:8893426 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1323-2975T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893426 | |||||||
chr3:8893530 | C | T | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1323-3079G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893530 | |||||||
chr3:8893543 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0143 |
2 | HG01069.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1323-3092A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893543 | |||||||
chr3:8893569 | G | C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1323-3118C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893569 | |||||||
chr3:8893619 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1323-3168C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893619 | |||||||
chr3:8893693 | A | AT | 44 | a0001c0001t0002g0201 a0001c0001t0005g0018 a0001c0001t0006g0246 others(41): Show |
44 | HG00639.hp2 HG01081.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.1323-3243dupA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893693 | |||||||
chr3:8893693 | AT | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
138 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1323-3243delA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893693 | |||||||
chr3:8893693 | ATT | A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0116 others(4): Show |
7 | HG01257.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323-3244_1323-324 others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893693 | |||||||
chr3:8893883 | T | C | 97 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(94): Show |
98 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1323-3432A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893883 | |||||||
chr3:8893927 | T | C | 1 | a0002c0002t0002g0323 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1323-3476A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8893927 | |||||||
chr3:8894213 | T | C | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1323-3762A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894213 | |||||||
chr3:8894280 | C | T | 96 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(93): Show |
97 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1323-3829G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894280 | |||||||
chr3:8894387 | G | A | 217 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(214): Show |
223 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.1323-3936C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894387 | |||||||
chr3:8894396 | A | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1323-3945T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894396 | |||||||
chr3:8894397 | C | T | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1323-3946G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894397 | |||||||
chr3:8894454 | T | C | 1 | a0002c0002t0009g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1323-4003A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894454 | |||||||
chr3:8894499 | A | G | 1 | a0002c0002t0002g0291 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1323-4048T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894499 | |||||||
chr3:8894584 | G | A | 114 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(111): Show |
115 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.1323-4133C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894584 | |||||||
chr3:8894633 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1323-4182G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894633 | |||||||
chr3:8894759 | C | CT | 25 | a0001c0001t0001g0103 a0001c0001t0001g0118 a0001c0001t0001g0161 others(22): Show |
25 | HG01106.hp1 HG01192.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1322+4134dupA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894759 | |||||||
chr3:8894759 | C | CTTTTT | 65 | a0001c0001t0002g0196 a0001c0001t0002g0198 a0001c0001t0002g0201 others(62): Show |
65 | HG00639.hp2 HG01081.hp1 HG01168.hp2 others(62): Show |
intron_variant | MODIFIER | c.1322+4130_1322+413 others(9): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894759 | |||||||
chr3:8894759 | C | CTTTTTT | 16 | a0001c0001t0002g0006 a0001c0001t0006g0246 a0001c0001t0006g0248 others(13): Show |
17 | HG00438.hp2 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1322+4129_1322+413 others(10): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894759 | |||||||
chr3:8894792 | G | A | 10 | a0002c0002t0004g0059 a0002c0002t0035g0041 a0003c0003t0007g0046 others(7): Show |
10 | HG02559.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1322+4102C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894792 | |||||||
chr3:8894824 | G | A | 1 | a0002c0002t0019g0326 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1322+4070C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894824 | |||||||
chr3:8894845 | C | T | 2 | a0002c0002t0002g0282 a0002c0002t0002g0320 |
2 | NA18998.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1322+4049G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894845 | |||||||
chr3:8894847 | G | A | 1 | a0002c0002t0011g0223 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1322+4047C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894847 | |||||||
chr3:8894861 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1322+4033T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894861 | |||||||
chr3:8894884 | C | T | 2 | a0002c0002t0004g0043 a0002c0002t0004g0045 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1322+4010G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894884 | |||||||
chr3:8894942 | G | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1322+3952C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8894942 | |||||||
chr3:8895000 | C | T | 1 | a0002c0002t0002g0295 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1322+3894G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895000 | |||||||
chr3:8895019 | T | A | 1 | a0002c0002t0003g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1322+3875A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895019 | |||||||
chr3:8895256 | T | A | 10 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(7): Show |
10 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1322+3638A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895256 | |||||||
chr3:8895319 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1322+3575G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895319 | |||||||
chr3:8895419 | G | C | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1322+3475C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895419 | |||||||
chr3:8895472 | T | C | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1322+3422A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895472 | |||||||
chr3:8895483 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322+3411G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895483 | |||||||
chr3:8895637 | CT | C | 94 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(91): Show |
95 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1322+3256delA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895637 | |||||||
chr3:8895637 | CTT | C | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1322+3255_1322+325 others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895637 | |||||||
chr3:8895644 | T | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1322+3250A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895644 | |||||||
chr3:8895744 | C | A | 1 | a0002c0002t0003g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1322+3150G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895744 | |||||||
chr3:8895770 | C | T | 2 | a0002c0002t0017g0277 a0002c0002t0017g0281 |
2 | NA18944.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1322+3124G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8895770 | |||||||
chr3:8896000 | A | G | 64 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(61): Show |
64 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1322+2894T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896000 | |||||||
chr3:8896334 | T | G | 1 | a0002c0002t0003g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1322+2560A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896334 | |||||||
chr3:8896335 | G | A | 40 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(37): Show |
41 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1322+2559C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896335 | |||||||
chr3:8896353 | G | A | 1 | a0002c0002t0011g0222 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1322+2541C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896353 | |||||||
chr3:8896425 | C | CA | 64 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(61): Show |
64 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1322+2468dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896425 | |||||||
chr3:8896470 | G | T | 63 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(60): Show |
63 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1322+2424C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896470 | |||||||
chr3:8896487 | G | T | 4 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(1): Show |
4 | HG02622.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1322+2407C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896487 | |||||||
chr3:8896712 | A | T | 1 | a0002c0002t0003g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1322+2182T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896712 | |||||||
chr3:8896774 | C | T | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1322+2120G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896774 | |||||||
chr3:8896775 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1322+2119C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896775 | |||||||
chr3:8896923 | T | C | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1322+1971A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896923 | |||||||
chr3:8896934 | C | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
189 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.1322+1960G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896934 | |||||||
chr3:8896953 | A | G | 5 | a0002c0002t0002g0269 a0002c0002t0002g0279 a0002c0002t0002g0322 others(2): Show |
5 | HG02135.hp1 NA18948.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1322+1941T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8896953 | |||||||
chr3:8897030 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1322+1864T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897030 | |||||||
chr3:8897054 | T | A | 1 | a0002c0002t0003g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1322+1840A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897054 | |||||||
chr3:8897234 | G | C | 2 | a0001c0001t0008g0032 a0001c0001t0008g0033 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1322+1660C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897234 | |||||||
chr3:8897255 | C | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.1322+1639G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897255 | |||||||
chr3:8897281 | G | A | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1322+1613C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897281 | |||||||
chr3:8897519 | G | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0037 others(82): Show |
89 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1322+1375C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897519 | |||||||
chr3:8897589 | G | C | 21 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(18): Show |
22 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1322+1305C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897589 | |||||||
chr3:8897674 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1322+1220G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897674 | |||||||
chr3:8897804 | G | A | 1 | a0002c0002t0002g0308 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1322+1090C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897804 | |||||||
chr3:8897896 | T | C | 2 | a0005c0005t0020g0203 a0005c0005t0020g0204 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1322+998A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897896 | |||||||
chr3:8897932 | C | T | 1 | a0001c0001t0015g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1322+962G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897932 | |||||||
chr3:8897939 | G | C | 1 | a0001c0001t0006g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1322+955C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897939 | |||||||
chr3:8897963 | T | C | 1 | a0002c0002t0002g0285 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1322+931A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8897963 | |||||||
chr3:8898019 | C | A | 1 | a0001c0001t0002g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1322+875G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898019 | |||||||
chr3:8898035 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1322+859C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898035 | |||||||
chr3:8898064 | T | C | 1 | a0002c0002t0041g0286 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1322+830A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898064 | |||||||
chr3:8898067 | G | C | 1 | a0002c0002t0050g0332 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1322+827C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898067 | |||||||
chr3:8898069 | C | T | 5 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 others(2): Show |
5 | HG01081.hp2 HG02300.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1322+825G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898069 | |||||||
chr3:8898094 | T | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1322+800A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898094 | |||||||
chr3:8898201 | G | A | 9 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1322+693C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898201 | |||||||
chr3:8898255 | G | A | 41 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(38): Show |
42 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.1322+639C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898255 | |||||||
chr3:8898381 | C | CGT | 22 | a0001c0001t0002g0251 a0001c0001t0012g0194 a0001c0001t0012g0195 others(19): Show |
22 | HG00408.hp2 HG01891.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.1322+511_1322+512d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898381 | C | CGTGT | 10 | a0001c0001t0002g0198 a0001c0001t0002g0201 a0001c0001t0002g0202 others(7): Show |
10 | HG02559.hp2 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1322+509_1322+512d others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898381 | C | CGTGTGT | 7 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0006g0249 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1322+507_1322+512d others(8): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898381 | C | CGTGTGTG others(1): Show |
4 | a0001c0001t0006g0248 a0001c0001t0006g0250 a0001c0001t0006g0252 others(1): Show |
4 | HG02280.hp1 HG02622.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1322+505_1322+512d others(10): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898381 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0006g0246 a0001c0001t0006g0257 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1322+503_1322+512d others(12): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898381 | C | T | 1 | a0002c0002t0002g0011 | 2 | NA19011.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1322+513G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898381 | CGT | C | 24 | a0001c0001t0001g0181 a0001c0001t0005g0018 a0001c0001t0005g0020 others(21): Show |
24 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1322+511_1322+512d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898381 | CGTGT | C | 19 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0117 others(16): Show |
19 | HG00558.hp1 HG00639.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1322+509_1322+512d others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898381 | CGTGTGT | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1322+507_1322+512d others(8): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898381 | |||||||
chr3:8898429 | T | A | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1322+465A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898429 | |||||||
chr3:8898542 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1322+352C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898542 | |||||||
chr3:8898701 | G | C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322+193C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898701 | |||||||
chr3:8898733 | G | C | 73 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(70): Show |
73 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1322+161C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898733 | |||||||
chr3:8898780 | A | G | 9 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1322+114T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 11/12 | chr3 | 8898780 | |||||||
chr3:8899081 | T | C | 74 | a0001c0001t0049g0261 a0002c0002t0002g0210 a0002c0002t0003g0206 others(71): Show |
74 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1169-34A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8899081 | |||||||
chr3:8899141 | A | ACT | 21 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(18): Show |
22 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1169-95_1169-94ins others(2): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8899141 | |||||||
chr3:8899187 | C | T | 15 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0056 others(12): Show |
15 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1169-140G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8899187 | |||||||
chr3:8899772 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1169-725G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8899772 | |||||||
chr3:8899775 | C | A | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169-728G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8899775 | |||||||
chr3:8899910 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1169-863C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8899910 | |||||||
chr3:8899992 | T | C | 21 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(18): Show |
21 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1169-945A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8899992 | |||||||
chr3:8900034 | T | C | 1 | a0002c0002t0010g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1169-987A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900034 | |||||||
chr3:8900150 | C | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
157 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1169-1103G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900150 | |||||||
chr3:8900324 | C | T | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169-1277G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900324 | |||||||
chr3:8900546 | C | T | 4 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(1): Show |
4 | HG02622.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169-1499G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900546 | |||||||
chr3:8900627 | C | G | 10 | a0001c0001t0006g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1169-1580G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900627 | |||||||
chr3:8900753 | C | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
158 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1168+1627G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900753 | |||||||
chr3:8900799 | C | A | 1 | a0002c0002t0003g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1168+1581G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900799 | |||||||
chr3:8900922 | G | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
158 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1168+1458C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900922 | |||||||
chr3:8900934 | A | T | 1 | a0002c0002t0013g0075 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1168+1446T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8900934 | |||||||
chr3:8901035 | G | A | 73 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(70): Show |
73 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1168+1345C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901035 | |||||||
chr3:8901152 | A | T | 1 | a0002c0002t0003g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1168+1228T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901152 | |||||||
chr3:8901181 | C | A | 2 | a0005c0005t0020g0203 a0005c0005t0020g0204 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1168+1199G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901181 | |||||||
chr3:8901261 | T | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+1119A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901261 | |||||||
chr3:8901509 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1168+871G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901509 | |||||||
chr3:8901692 | G | A | 8 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(5): Show |
8 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1168+688C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901692 | |||||||
chr3:8901705 | A | C | 1 | a0002c0002t0004g0064 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1168+675T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901705 | |||||||
chr3:8901841 | A | G | 2 | a0001c0001t0008g0032 a0001c0001t0008g0033 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1168+539T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901841 | |||||||
chr3:8901847 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1168+533T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901847 | |||||||
chr3:8901911 | T | C | 1 | a0002c0002t0002g0288 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1168+469A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901911 | |||||||
chr3:8901992 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1168+388T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8901992 | |||||||
chr3:8902095 | T | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
264 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1168+285A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8902095 | |||||||
chr3:8902241 | C | T | 8 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(5): Show |
8 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1168+139G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8902241 | |||||||
chr3:8902250 | T | C | 1 | a0006c0008t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1168+130A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8902250 | |||||||
chr3:8902304 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1168+76G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8902304 | |||||||
chr3:8902347 | G | A | 1 | a0002c0002t0004g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1168+33C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 10/12 | chr3 | 8902347 | |||||||
chr3:8902616 | G | A | 9 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1028-96C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8902616 | |||||||
chr3:8902714 | C | T | 1 | a0002c0002t0002g0210 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1028-194G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8902714 | |||||||
chr3:8902760 | C | T | 73 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(70): Show |
73 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1028-240G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8902760 | |||||||
chr3:8902982 | C | T | 73 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(70): Show |
73 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1028-462G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8902982 | |||||||
chr3:8903187 | C | G | 9 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1028-667G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903187 | |||||||
chr3:8903252 | A | G | 7 | a0001c0001t0006g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1028-732T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903252 | |||||||
chr3:8903370 | T | C | 3 | a0001c0001t0021g0016 a0001c0001t0048g0244 a0002c0002t0002g0307 |
3 | HG00408.hp2 HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1028-850A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903370 | |||||||
chr3:8903397 | C | A | 73 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(70): Show |
73 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1028-877G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903397 | |||||||
chr3:8903407 | GA | G | 93 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(90): Show |
94 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1028-888delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903407 | |||||||
chr3:8903415 | G | A | 1 | a0002c0002t0004g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1028-895C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903415 | |||||||
chr3:8903603 | T | C | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1028-1083A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903603 | |||||||
chr3:8903618 | T | C | 64 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(61): Show |
64 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1028-1098A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903618 | |||||||
chr3:8903873 | C | T | 73 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(70): Show |
73 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1028-1353G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903873 | |||||||
chr3:8903909 | T | A | 44 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(41): Show |
44 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.1028-1389A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8903909 | |||||||
chr3:8904194 | T | C | 1 | a0001c0001t0002g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1028-1674A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904194 | |||||||
chr3:8904207 | T | G | 1 | a0002c0002t0002g0312 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1028-1687A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904207 | |||||||
chr3:8904265 | A | G | 73 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(70): Show |
73 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1028-1745T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904265 | |||||||
chr3:8904339 | C | T | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1028-1819G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904339 | |||||||
chr3:8904474 | T | A | 1 | a0002c0002t0002g0301 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1028-1954A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904474 | |||||||
chr3:8904517 | A | G | 4 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(1): Show |
4 | HG02622.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-1997T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904517 | |||||||
chr3:8904539 | T | C | 2 | a0001c0001t0002g0198 a0001c0001t0043g0197 |
2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1028-2019A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904539 | |||||||
chr3:8904551 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0127 |
3 | HG01175.hp2 HG01257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1028-2031C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904551 | |||||||
chr3:8904606 | A | AC | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1028-2087dupG | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904606 | |||||||
chr3:8904617 | G | A | 1 | a0002c0002t0050g0332 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1028-2097C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904617 | |||||||
chr3:8904637 | T | C | 2 | a0001c0001t0021g0016 a0001c0001t0048g0244 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1028-2117A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904637 | |||||||
chr3:8904715 | C | T | 10 | a0001c0001t0006g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1028-2195G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904715 | |||||||
chr3:8904722 | T | C | 1 | a0001c0001t0002g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1028-2202A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904722 | |||||||
chr3:8904828 | G | T | 2 | a0002c0002t0004g0056 a0002c0002t0004g0057 |
2 | NA18952.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1028-2308C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8904828 | |||||||
chr3:8905005 | G | C | 4 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(1): Show |
4 | HG02622.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-2485C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905005 | |||||||
chr3:8905010 | C | A | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1028-2490G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905010 | |||||||
chr3:8905168 | T | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
230 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.1028-2648A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905168 | |||||||
chr3:8905200 | C | T | 1 | a0002c0002t0002g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1028-2680G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905200 | |||||||
chr3:8905416 | C | T | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1028-2896G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905416 | |||||||
chr3:8905593 | C | T | 1 | a0003c0003t0007g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1028-3073G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905593 | |||||||
chr3:8905635 | G | A | 1 | a0003c0003t0007g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1028-3115C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905635 | |||||||
chr3:8905812 | T | C | 1 | a0012c0012t0004g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1028-3292A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905812 | |||||||
chr3:8905858 | C | T | 14 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1028-3338G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905858 | |||||||
chr3:8905874 | A | G | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1028-3354T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905874 | |||||||
chr3:8905917 | A | G | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
186 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1028-3397T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905917 | |||||||
chr3:8905994 | C | A | 63 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(60): Show |
63 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1028-3474G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8905994 | |||||||
chr3:8906038 | CAG | C | 63 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(60): Show |
63 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1028-3520_1028-351 others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906038 | |||||||
chr3:8906087 | A | G | 1 | a0002c0002t0002g0323 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1028-3567T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906087 | |||||||
chr3:8906131 | G | T | 2 | a0002c0002t0002g0278 a0002c0002t0002g0316 |
2 | NA18995.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1028-3611C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906131 | |||||||
chr3:8906151 | C | T | 3 | a0003c0003t0007g0046 a0003c0003t0007g0048 a0003c0003t0007g0049 |
3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1028-3631G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906151 | |||||||
chr3:8906196 | TCAGTCAT others(11): Show |
T | 63 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(60): Show |
63 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1028-3694_1028-367 others(22): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906196 | |||||||
chr3:8906289 | T | C | 3 | a0004c0004t0001g0001 a0004c0004t0001g0186 a0004c0004t0001g0187 |
5 | NA18941.hp1 NA19002.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-3769A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906289 | |||||||
chr3:8906402 | ACCTCCCC others(31): Show |
A | 1 | a0014c0006t0002g0267 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1028-3920_1028-388 others(42): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906402 | |||||||
chr3:8906503 | C | T | 58 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(55): Show |
58 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1028-3983G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906503 | |||||||
chr3:8906537 | T | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
186 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1028-4017A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906537 | |||||||
chr3:8906643 | C | T | 3 | a0001c0001t0016g0263 a0001c0001t0037g0260 a0013c0009t0016g0262 |
3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1028-4123G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906643 | |||||||
chr3:8906683 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1028-4163G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906683 | |||||||
chr3:8906696 | ATT | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
143 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1028-4178_1028-417 others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906696 | |||||||
chr3:8906755 | T | C | 2 | a0001c0001t0021g0016 a0001c0001t0048g0244 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1028-4235A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906755 | |||||||
chr3:8906794 | G | GT | 78 | a0001c0001t0001g0164 a0001c0001t0014g0013 a0001c0001t0014g0014 others(75): Show |
78 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.1028-4275dupA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906794 | |||||||
chr3:8906794 | G | GTT | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0037 others(125): Show |
132 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1028-4276_1028-427 others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906794 | |||||||
chr3:8906794 | G | GTTT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0078 a0001c0001t0001g0080 others(3): Show |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1028-4277_1028-427 others(7): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906794 | |||||||
chr3:8906814 | AAT | A | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1028-4296_1028-429 others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906814 | |||||||
chr3:8906845 | T | A | 9 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1028-4325A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906845 | |||||||
chr3:8906893 | C | A | 15 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0056 others(12): Show |
15 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1028-4373G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906893 | |||||||
chr3:8906997 | G | A | 5 | a0002c0002t0002g0297 a0002c0002t0002g0299 a0002c0002t0002g0302 others(2): Show |
5 | HG02083.hp2 NA18957.hp2 NA19081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1028-4477C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8906997 | |||||||
chr3:8907059 | C | G | 1 | a0002c0002t0002g0324 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1028-4539G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907059 | |||||||
chr3:8907067 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.1028-4547T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907067 | |||||||
chr3:8907078 | A | G | 14 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1028-4558T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907078 | |||||||
chr3:8907220 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1028-4700G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907220 | |||||||
chr3:8907270 | T | A | 1 | a0002c0002t0003g0241 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1028-4750A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907270 | |||||||
chr3:8907308 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1028-4788T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907308 | |||||||
chr3:8907309 | T | TA | 41 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(38): Show |
42 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.1028-4790dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907309 | |||||||
chr3:8907586 | C | A | 1 | a0002c0002t0002g0306 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1027+4726G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907586 | |||||||
chr3:8907642 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1027+4670A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907642 | |||||||
chr3:8907659 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1027+4653T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907659 | |||||||
chr3:8907743 | G | A | 1 | a0002c0002t0040g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1027+4569C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907743 | |||||||
chr3:8907788 | T | TA | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
186 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1027+4523dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8907788 | |||||||
chr3:8908031 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1027+4281C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908031 | |||||||
chr3:8908119 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1027+4193A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908119 | |||||||
chr3:8908200 | T | C | 1 | a0002c0002t0002g0289 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1027+4112A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908200 | |||||||
chr3:8908257 | A | T | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1027+4055T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908257 | |||||||
chr3:8908272 | CA | C | 42 | a0001c0001t0001g0137 a0001c0001t0002g0006 a0001c0001t0002g0196 others(39): Show |
43 | HG00642.hp1 HG01106.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1027+4039delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908272 | |||||||
chr3:8908273 | A | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
152 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.1027+4039T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908273 | |||||||
chr3:8908273 | AT | A | 61 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(58): Show |
61 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1027+4038delA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908273 | |||||||
chr3:8908295 | TGAGA | T | 20 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(17): Show |
21 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1027+4013_1027+401 others(8): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908295 | |||||||
chr3:8908449 | C | T | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1027+3863G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908449 | |||||||
chr3:8908464 | T | C | 19 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0056 others(16): Show |
19 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1027+3848A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908464 | |||||||
chr3:8908585 | T | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
185 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.1027+3727A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908585 | |||||||
chr3:8908647 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1027+3665G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908647 | |||||||
chr3:8908736 | C | T | 1 | a0001c0001t0014g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1027+3576G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908736 | |||||||
chr3:8908875 | C | T | 20 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(17): Show |
21 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1027+3437G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908875 | |||||||
chr3:8908945 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.1027+3367G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8908945 | |||||||
chr3:8909109 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1027+3203T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909109 | |||||||
chr3:8909198 | G | C | 62 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(59): Show |
62 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1027+3114C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909198 | |||||||
chr3:8909211 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1027+3101C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909211 | |||||||
chr3:8909235 | T | C | 1 | a0002c0002t0002g0307 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1027+3077A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909235 | |||||||
chr3:8909285 | G | A | 15 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0056 others(12): Show |
15 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1027+3027C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909285 | |||||||
chr3:8909345 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1027+2967A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909345 | |||||||
chr3:8909409 | G | T | 1 | a0001c0007t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1027+2903C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909409 | |||||||
chr3:8909495 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.1027+2817C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909495 | |||||||
chr3:8909500 | G | A | 2 | a0002c0002t0004g0043 a0002c0002t0004g0045 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1027+2812C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909500 | |||||||
chr3:8909518 | T | TA | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
170 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1027+2793dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909518 | |||||||
chr3:8909518 | TA | T | 10 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(7): Show |
10 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027+2793delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909518 | |||||||
chr3:8909565 | C | A | 4 | a0001c0001t0012g0194 a0001c0001t0012g0195 a0001c0001t0012g0199 others(1): Show |
4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027+2747G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909565 | |||||||
chr3:8909751 | T | C | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1027+2561A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909751 | |||||||
chr3:8909770 | T | C | 1 | a0002c0002t0002g0316 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1027+2542A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909770 | |||||||
chr3:8909805 | A | G | 41 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(38): Show |
42 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.1027+2507T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909805 | |||||||
chr3:8909830 | T | C | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1027+2482A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909830 | |||||||
chr3:8909838 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1027+2474C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909838 | |||||||
chr3:8909868 | A | G | 9 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027+2444T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909868 | |||||||
chr3:8909931 | T | C | 2 | a0001c0001t0016g0263 a0013c0009t0016g0262 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1027+2381A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8909931 | |||||||
chr3:8910062 | T | C | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1027+2250A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910062 | |||||||
chr3:8910092 | A | G | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027+2220T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910092 | |||||||
chr3:8910093 | T | G | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
186 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1027+2219A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910093 | |||||||
chr3:8910256 | T | C | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027+2056A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910256 | |||||||
chr3:8910306 | A | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(1): Show |
5 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+2006T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910306 | |||||||
chr3:8910323 | A | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
187 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.1027+1989T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910323 | |||||||
chr3:8910395 | T | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
187 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.1027+1917A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910395 | |||||||
chr3:8910416 | C | T | 10 | a0001c0001t0006g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1027+1896G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910416 | |||||||
chr3:8910469 | A | G | 12 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(9): Show |
13 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1027+1843T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910469 | |||||||
chr3:8910490 | G | A | 1 | a0002c0002t0002g0268 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1027+1822C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910490 | |||||||
chr3:8910515 | G | A | 2 | a0002c0002t0003g0208 a0002c0002t0003g0212 |
2 | NA18951.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1027+1797C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910515 | |||||||
chr3:8910547 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1027+1765C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910547 | |||||||
chr3:8910577 | C | T | 3 | a0002c0002t0003g0209 a0002c0002t0003g0215 a0011c0014t0003g0253 |
3 | HG02559.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1027+1735G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910577 | |||||||
chr3:8910616 | A | G | 1 | a0002c0002t0002g0316 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1027+1696T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910616 | |||||||
chr3:8910813 | A | C | 1 | a0001c0001t0037g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1027+1499T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910813 | |||||||
chr3:8910893 | T | C | 9 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027+1419A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910893 | |||||||
chr3:8910927 | G | A | 9 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027+1385C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910927 | |||||||
chr3:8910930 | A | G | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
186 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1027+1382T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8910930 | |||||||
chr3:8911234 | A | C | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1027+1078T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911234 | |||||||
chr3:8911260 | A | T | 64 | a0001c0001t0005g0021 a0002c0002t0002g0210 a0002c0002t0003g0206 others(61): Show |
64 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1027+1052T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911260 | |||||||
chr3:8911496 | C | G | 1 | a0002c0002t0002g0314 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1027+816G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911496 | |||||||
chr3:8911548 | G | T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.1027+764C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911548 | |||||||
chr3:8911580 | T | G | 1 | a0002c0002t0003g0234 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1027+732A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911580 | |||||||
chr3:8911588 | ACATCCAG others(13): Show |
A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1027+704_1027+723d others(22): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911588 | |||||||
chr3:8911796 | A | G | 7 | a0002c0002t0003g0207 a0002c0002t0003g0226 a0002c0002t0003g0239 others(4): Show |
7 | HG01081.hp1 HG02155.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027+516T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911796 | |||||||
chr3:8911823 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1027+489C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911823 | |||||||
chr3:8911954 | T | C | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
8 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027+358A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911954 | |||||||
chr3:8911992 | G | A | 59 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(56): Show |
59 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1027+320C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911992 | |||||||
chr3:8911997 | C | T | 1 | a0001c0001t0005g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1027+315G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8911997 | |||||||
chr3:8912011 | G | A | 1 | a0002c0002t0004g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1027+301C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8912011 | |||||||
chr3:8912020 | C | T | 1 | a0002c0002t0003g0209 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1027+292G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8912020 | |||||||
chr3:8912109 | T | C | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1027+203A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8912109 | |||||||
chr3:8912147 | C | CA | 5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0173 others(2): Show |
5 | HG00558.hp2 HG02132.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+164dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8912147 | |||||||
chr3:8912182 | T | C | 48 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(45): Show |
49 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.1027+130A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 9/12 | chr3 | 8912182 | |||||||
chr3:8912522 | C | G | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.967-150G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912522 | |||||||
chr3:8912554 | T | C | 4 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-182A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912554 | |||||||
chr3:8912701 | G | A | 64 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(61): Show |
64 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.967-329C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912701 | |||||||
chr3:8912705 | C | T | 1 | a0001c0001t0005g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.967-333G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912705 | |||||||
chr3:8912709 | GCTGA | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
185 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.967-341_967-338del others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912709 | |||||||
chr3:8912788 | C | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
194 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.967-416G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912788 | |||||||
chr3:8912843 | C | T | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.967-471G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912843 | |||||||
chr3:8912854 | C | T | 1 | a0011c0014t0003g0253 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.967-482G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912854 | |||||||
chr3:8912886 | A | G | 2 | a0001c0001t0008g0032 a0001c0001t0008g0033 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.967-514T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912886 | |||||||
chr3:8912932 | T | C | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.967-560A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8912932 | |||||||
chr3:8913036 | GA | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
185 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.966+607delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8913036 | |||||||
chr3:8913275 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.966+369T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8913275 | |||||||
chr3:8913378 | A | G | 8 | a0002c0002t0003g0208 a0002c0002t0003g0212 a0002c0002t0003g0221 others(5): Show |
8 | HG00438.hp2 NA18941.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+266T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8913378 | |||||||
chr3:8913556 | T | C | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.966+88A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 8/12 | chr3 | 8913556 | |||||||
chr3:8913950 | C | T | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.890-230G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8913950 | |||||||
chr3:8913963 | G | GAGTCA | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
194 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.890-248_890-244dup others(5): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8913963 | |||||||
chr3:8913990 | G | A | 3 | a0004c0004t0001g0001 a0004c0004t0001g0186 a0004c0004t0001g0187 |
5 | NA18941.hp1 NA19002.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.890-270C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8913990 | |||||||
chr3:8914018 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-298C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914018 | |||||||
chr3:8914105 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG01192.hp1 HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.890-385C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914105 | |||||||
chr3:8914370 | T | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0183 |
2 | HG00597.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.890-650A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914370 | |||||||
chr3:8914447 | C | A | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
194 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.890-727G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914447 | |||||||
chr3:8914462 | T | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
186 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.890-742A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914462 | |||||||
chr3:8914513 | T | G | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.890-793A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914513 | |||||||
chr3:8914570 | G | A | 43 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(40): Show |
43 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.890-850C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914570 | |||||||
chr3:8914590 | A | T | 1 | a0002c0002t0002g0293 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.890-870T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914590 | |||||||
chr3:8914647 | T | G | 1 | a0002c0002t0002g0309 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.890-927A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914647 | |||||||
chr3:8914668 | T | C | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.890-948A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914668 | |||||||
chr3:8914687 | C | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
156 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.890-967G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914687 | |||||||
chr3:8914734 | A | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-1014T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914734 | |||||||
chr3:8914785 | A | G | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.890-1065T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914785 | |||||||
chr3:8914812 | CAG | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.890-1094_890-1093d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914812 | |||||||
chr3:8914865 | G | T | 8 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(5): Show |
8 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.890-1145C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914865 | |||||||
chr3:8914977 | A | C | 1 | a0002c0002t0002g0302 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.890-1257T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914977 | |||||||
chr3:8914989 | A | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
194 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.890-1269T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914989 | |||||||
chr3:8914993 | T | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-1273A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914993 | |||||||
chr3:8914994 | T | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-1274A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914994 | |||||||
chr3:8914995 | T | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.890-1275A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914995 | |||||||
chr3:8914996 | A | T | 9 | a0002c0002t0002g0007 a0002c0002t0002g0266 a0002c0002t0002g0318 others(6): Show |
10 | HG01109.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.890-1276T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8914996 | |||||||
chr3:8915021 | C | T | 1 | a0002c0002t0035g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.890-1301G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915021 | |||||||
chr3:8915074 | G | A | 2 | a0001c0001t0045g0328 a0002c0002t0002g0273 |
2 | HG00609.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.890-1354C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915074 | |||||||
chr3:8915081 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.890-1361C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915081 | |||||||
chr3:8915115 | C | T | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-1395G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915115 | |||||||
chr3:8915147 | C | CA | 20 | a0001c0001t0002g0006 a0001c0001t0002g0198 a0001c0001t0002g0201 others(17): Show |
22 | HG00423.hp1 HG01891.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.890-1428dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915147 | |||||||
chr3:8915147 | C | CAAAA | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
110 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.890-1431_890-1428d others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915147 | |||||||
chr3:8915147 | C | CAAAAA | 28 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0001g0088 others(25): Show |
28 | HG00423.hp2 HG00438.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.890-1432_890-1428d others(7): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915147 | |||||||
chr3:8915147 | C | CAAAAAA | 16 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.890-1433_890-1428d others(8): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915147 | |||||||
chr3:8915147 | CA | C | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.890-1428delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915147 | |||||||
chr3:8915193 | T | C | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.890-1473A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915193 | |||||||
chr3:8915265 | C | T | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.890-1545G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915265 | |||||||
chr3:8915278 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.890-1558G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915278 | |||||||
chr3:8915319 | G | C | 1 | a0002c0002t0002g0309 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.890-1599C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915319 | |||||||
chr3:8915377 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.890-1657C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915377 | |||||||
chr3:8915496 | A | G | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.890-1776T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915496 | |||||||
chr3:8915554 | C | T | 1 | a0013c0009t0016g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.890-1834G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915554 | |||||||
chr3:8915585 | C | CT | 13 | a0001c0001t0001g0086 a0001c0001t0001g0102 a0001c0001t0001g0116 others(10): Show |
13 | HG00673.hp2 HG01517.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.890-1866dupA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915585 | |||||||
chr3:8915607 | T | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
186 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.890-1887A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915607 | |||||||
chr3:8915646 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG02132.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.890-1926G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915646 | |||||||
chr3:8915709 | G | A | 1 | a0002c0002t0002g0291 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.890-1989C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915709 | |||||||
chr3:8915804 | C | T | 6 | a0001c0001t0012g0194 a0001c0001t0012g0195 a0001c0001t0012g0199 others(3): Show |
6 | HG01928.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-2084G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915804 | |||||||
chr3:8915819 | G | A | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.890-2099C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915819 | |||||||
chr3:8915851 | G | A | 1 | a0002c0002t0002g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.890-2131C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915851 | |||||||
chr3:8915912 | G | A | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.890-2192C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915912 | |||||||
chr3:8915966 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.890-2246A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8915966 | |||||||
chr3:8916013 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.890-2293G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916013 | |||||||
chr3:8916043 | T | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.890-2323A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916043 | |||||||
chr3:8916371 | T | C | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-2651A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916371 | |||||||
chr3:8916424 | A | C | 1 | a0002c0002t0010g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.890-2704T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916424 | |||||||
chr3:8916661 | A | G | 1 | a0002c0002t0002g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.890-2941T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916661 | |||||||
chr3:8916671 | A | G | 28 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(25): Show |
29 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.890-2951T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916671 | |||||||
chr3:8916678 | T | C | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.890-2958A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916678 | |||||||
chr3:8916703 | T | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
155 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.890-2983A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916703 | |||||||
chr3:8916758 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.890-3038G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916758 | |||||||
chr3:8916839 | G | C | 1 | a0002c0002t0002g0318 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.890-3119C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916839 | |||||||
chr3:8916908 | G | A | 1 | a0012c0012t0004g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.890-3188C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916908 | |||||||
chr3:8916922 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.890-3202C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916922 | |||||||
chr3:8916923 | T | C | 1 | a0012c0012t0004g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.890-3203A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916923 | |||||||
chr3:8916928 | G | T | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.890-3208C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8916928 | |||||||
chr3:8917069 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.890-3349T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917069 | |||||||
chr3:8917188 | C | T | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
185 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.890-3468G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917188 | |||||||
chr3:8917315 | T | C | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.890-3595A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917315 | |||||||
chr3:8917535 | T | A | 43 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(40): Show |
43 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.890-3815A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917535 | |||||||
chr3:8917586 | T | C | 1 | a0002c0002t0002g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.890-3866A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917586 | |||||||
chr3:8917597 | C | T | 64 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(61): Show |
64 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.890-3877G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917597 | |||||||
chr3:8917691 | A | C | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.890-3971T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917691 | |||||||
chr3:8917701 | AC | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.890-3982delG | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917701 | |||||||
chr3:8917729 | C | T | 83 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(80): Show |
84 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.890-4009G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917729 | |||||||
chr3:8917984 | G | A | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.890-4264C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917984 | |||||||
chr3:8917986 | A | G | 1 | a0001c0001t0008g0031 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.890-4266T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8917986 | |||||||
chr3:8918084 | G | A | 2 | a0001c0001t0001g0173 a0003c0003t0007g0052 |
2 | HG00558.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.890-4364C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918084 | |||||||
chr3:8918116 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.890-4396C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918116 | |||||||
chr3:8918135 | T | C | 1 | a0002c0002t0035g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.890-4415A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918135 | |||||||
chr3:8918163 | C | T | 1 | a0002c0002t0002g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.890-4443G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918163 | |||||||
chr3:8918173 | C | T | 2 | a0001c0001t0002g0251 a0001c0001t0002g0259 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.890-4453G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918173 | |||||||
chr3:8918175 | C | T | 5 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.890-4455G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918175 | |||||||
chr3:8918267 | G | C | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.890-4547C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918267 | |||||||
chr3:8918306 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.890-4586C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918306 | |||||||
chr3:8918318 | C | CA | 22 | a0001c0001t0002g0006 a0001c0001t0005g0025 a0001c0001t0048g0244 others(19): Show |
24 | HG00609.hp1 HG01175.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.890-4599dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918318 | |||||||
chr3:8918318 | CA | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
132 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.890-4599delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918318 | |||||||
chr3:8918355 | T | C | 28 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(25): Show |
29 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.890-4635A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918355 | |||||||
chr3:8918477 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.890-4757G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918477 | |||||||
chr3:8918518 | A | G | 1 | a0002c0002t0002g0310 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.890-4798T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918518 | |||||||
chr3:8918532 | G | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
185 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.890-4812C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918532 | |||||||
chr3:8918557 | G | A | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-4837C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918557 | |||||||
chr3:8918587 | CTG | C | 27 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(24): Show |
28 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.890-4869_890-4868d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918587 | |||||||
chr3:8918634 | T | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.890-4914A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918634 | |||||||
chr3:8918658 | C | T | 37 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(34): Show |
37 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.890-4938G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918658 | |||||||
chr3:8918744 | A | G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.890-5024T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8918744 | |||||||
chr3:8919132 | A | G | 4 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.890-5412T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919132 | |||||||
chr3:8919313 | A | G | 26 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(23): Show |
27 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.890-5593T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919313 | |||||||
chr3:8919469 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.890-5749C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919469 | |||||||
chr3:8919571 | C | T | 1 | a0002c0002t0002g0324 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.890-5851G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919571 | |||||||
chr3:8919603 | C | T | 1 | a0002c0002t0002g0300 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.890-5883G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919603 | |||||||
chr3:8919635 | C | T | 17 | a0001c0001t0005g0021 a0002c0002t0004g0053 a0002c0002t0004g0054 others(14): Show |
17 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.890-5915G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919635 | |||||||
chr3:8919668 | C | T | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.890-5948G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919668 | |||||||
chr3:8919679 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.890-5959C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919679 | |||||||
chr3:8919747 | C | T | 1 | a0002c0002t0002g0265 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.890-6027G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919747 | |||||||
chr3:8919851 | GGT | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
190 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.890-6133_890-6132d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919851 | |||||||
chr3:8919968 | T | C | 5 | a0002c0002t0003g0209 a0002c0002t0018g0235 a0002c0002t0018g0237 others(2): Show |
5 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.890-6248A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8919968 | |||||||
chr3:8920009 | G | A | 1 | a0001c0001t0005g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.890-6289C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920009 | |||||||
chr3:8920049 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-6329T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920049 | |||||||
chr3:8920065 | G | A | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.890-6345C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920065 | |||||||
chr3:8920152 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.890-6432C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920152 | |||||||
chr3:8920204 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.890-6484C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920204 | |||||||
chr3:8920210 | C | T | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.890-6490G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920210 | |||||||
chr3:8920227 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.890-6507G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920227 | |||||||
chr3:8920274 | G | A | 1 | a0002c0002t0035g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.890-6554C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920274 | |||||||
chr3:8920278 | C | CA | 70 | a0001c0001t0001g0121 a0001c0001t0001g0160 a0001c0001t0001g0178 others(67): Show |
70 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.890-6559dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920278 | |||||||
chr3:8920278 | C | CAA | 8 | a0002c0002t0003g0213 a0002c0002t0003g0214 a0002c0002t0003g0219 others(5): Show |
8 | HG02055.hp1 HG02071.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.890-6560_890-6559d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920278 | |||||||
chr3:8920278 | C | CAAA | 6 | a0001c0001t0045g0328 a0002c0002t0003g0224 a0002c0002t0010g0188 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.890-6561_890-6559d others(5): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920278 | |||||||
chr3:8920278 | CA | C | 37 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0001t0001g0097 others(34): Show |
38 | HG00609.hp2 HG01256.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.890-6559delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920278 | |||||||
chr3:8920379 | C | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-6659G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920379 | |||||||
chr3:8920541 | G | A | 1 | a0002c0002t0002g0312 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.890-6821C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920541 | |||||||
chr3:8920579 | C | A | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-6859G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920579 | |||||||
chr3:8920601 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.890-6881G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920601 | |||||||
chr3:8920648 | G | A | 2 | a0001c0001t0006g0254 a0001c0001t0006g0256 |
2 | HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.890-6928C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920648 | |||||||
chr3:8920665 | TA | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
155 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.890-6946delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920665 | |||||||
chr3:8920668 | A | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
155 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.890-6948T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920668 | |||||||
chr3:8920669 | T | C | 1 | a0002c0002t0003g0241 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.890-6949A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920669 | |||||||
chr3:8920773 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-7053G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920773 | |||||||
chr3:8920826 | T | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
155 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.890-7106A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920826 | |||||||
chr3:8920844 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-7124C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920844 | |||||||
chr3:8920881 | G | A | 26 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(23): Show |
27 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.890-7161C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920881 | |||||||
chr3:8920961 | T | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.890-7241A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8920961 | |||||||
chr3:8921007 | T | C | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-7287A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921007 | |||||||
chr3:8921040 | A | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.890-7320T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921040 | |||||||
chr3:8921041 | G | A | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.890-7321C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921041 | |||||||
chr3:8921077 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-7357C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921077 | |||||||
chr3:8921078 | C | G | 26 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(23): Show |
27 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.890-7358G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921078 | |||||||
chr3:8921103 | A | G | 68 | a0001c0001t0002g0198 a0001c0001t0005g0021 a0001c0001t0043g0197 others(65): Show |
68 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.890-7383T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921103 | |||||||
chr3:8921117 | A | G | 1 | a0013c0009t0016g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.890-7397T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921117 | |||||||
chr3:8921141 | A | T | 1 | a0002c0002t0002g0299 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.890-7421T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921141 | |||||||
chr3:8921259 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-7539G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921259 | |||||||
chr3:8921288 | G | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.890-7568C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921288 | |||||||
chr3:8921313 | A | G | 1 | a0002c0002t0002g0325 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.890-7593T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921313 | |||||||
chr3:8921364 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-7644A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921364 | |||||||
chr3:8921408 | T | C | 68 | a0001c0001t0002g0198 a0001c0001t0005g0021 a0001c0001t0043g0197 others(65): Show |
68 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.890-7688A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921408 | |||||||
chr3:8921433 | C | A | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.890-7713G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921433 | |||||||
chr3:8921440 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.890-7720G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921440 | |||||||
chr3:8921458 | C | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0201 others(1): Show |
5 | HG02055.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.890-7738G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921458 | |||||||
chr3:8921597 | G | A | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.890-7877C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921597 | |||||||
chr3:8921625 | G | C | 2 | a0001c0001t0006g0254 a0001c0001t0006g0256 |
2 | HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.890-7905C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921625 | |||||||
chr3:8921640 | T | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-7920A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921640 | |||||||
chr3:8921699 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.890-7979C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921699 | |||||||
chr3:8921709 | G | C | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.890-7989C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921709 | |||||||
chr3:8921874 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-8154A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921874 | |||||||
chr3:8921955 | G | A | 1 | a0001c0001t0012g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.890-8235C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8921955 | |||||||
chr3:8922015 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-8295C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922015 | |||||||
chr3:8922055 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-8335T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922055 | |||||||
chr3:8922057 | G | A | 1 | a0001c0001t0013g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.890-8337C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922057 | |||||||
chr3:8922079 | G | A | 6 | a0001c0001t0005g0021 a0001c0001t0014g0013 a0001c0001t0014g0014 others(3): Show |
6 | HG01081.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-8359C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922079 | |||||||
chr3:8922103 | A | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-8383T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922103 | |||||||
chr3:8922106 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-8386C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922106 | |||||||
chr3:8922112 | C | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-8392G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922112 | |||||||
chr3:8922114 | G | A | 25 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(22): Show |
26 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.890-8394C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922114 | |||||||
chr3:8922115 | G | A | 1 | a0001c0001t0005g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.890-8395C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922115 | |||||||
chr3:8922142 | C | T | 1 | a0003c0003t0007g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.890-8422G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922142 | |||||||
chr3:8922150 | C | G | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.890-8430G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922150 | |||||||
chr3:8922236 | C | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
156 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.890-8516G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922236 | |||||||
chr3:8922243 | A | G | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.890-8523T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922243 | |||||||
chr3:8922248 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.890-8528T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922248 | |||||||
chr3:8922295 | G | A | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-8575C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922295 | |||||||
chr3:8922425 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-8705T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922425 | |||||||
chr3:8922428 | C | A | 10 | a0002c0002t0004g0059 a0003c0003t0007g0046 a0003c0003t0007g0047 others(7): Show |
10 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.890-8708G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922428 | |||||||
chr3:8922456 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-8736C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922456 | |||||||
chr3:8922484 | C | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-8764G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922484 | |||||||
chr3:8922549 | G | A | 1 | a0003c0003t0007g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.890-8829C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922549 | |||||||
chr3:8922553 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.890-8833C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922553 | |||||||
chr3:8922645 | G | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-8925C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922645 | |||||||
chr3:8922663 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-8943A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922663 | |||||||
chr3:8922692 | C | T | 1 | a0002c0002t0003g0225 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.890-8972G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922692 | |||||||
chr3:8922703 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.890-8983G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922703 | |||||||
chr3:8922722 | C | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.890-9002G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922722 | |||||||
chr3:8922805 | G | A | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.890-9085C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922805 | |||||||
chr3:8922806 | G | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0143 |
2 | HG01069.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.890-9086C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922806 | |||||||
chr3:8922831 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-9111A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922831 | |||||||
chr3:8922962 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.890-9242C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8922962 | |||||||
chr3:8923035 | T | C | 5 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.890-9315A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923035 | |||||||
chr3:8923067 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0183 |
2 | HG00597.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.890-9347A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923067 | |||||||
chr3:8923074 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-9354C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923074 | |||||||
chr3:8923087 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-9367T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923087 | |||||||
chr3:8923092 | C | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-9372G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923092 | |||||||
chr3:8923256 | A | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0115 a0001c0001t0001g0130 others(2): Show |
5 | HG01243.hp1 HG01256.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.890-9536T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923256 | |||||||
chr3:8923275 | C | T | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.890-9555G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923275 | |||||||
chr3:8923283 | C | G | 1 | a0002c0002t0003g0224 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.890-9563G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923283 | |||||||
chr3:8923289 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.890-9569G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923289 | |||||||
chr3:8923314 | G | A | 12 | a0001c0001t0001g0100 a0001c0001t0001g0146 a0001c0001t0001g0147 others(9): Show |
12 | HG00408.hp1 HG02056.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.890-9594C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923314 | |||||||
chr3:8923326 | C | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.890-9606G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923326 | |||||||
chr3:8923431 | C | T | 17 | a0001c0001t0005g0021 a0002c0002t0004g0053 a0002c0002t0004g0054 others(14): Show |
17 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.890-9711G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923431 | |||||||
chr3:8923434 | C | A | 3 | a0002c0002t0018g0235 a0002c0002t0018g0237 a0002c0002t0036g0236 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.890-9714G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923434 | |||||||
chr3:8923438 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-9718G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923438 | |||||||
chr3:8923471 | C | G | 4 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 others(1): Show |
4 | HG01081.hp2 HG02738.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.890-9751G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923471 | |||||||
chr3:8923495 | A | G | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.890-9775T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923495 | |||||||
chr3:8923519 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9799C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923519 | |||||||
chr3:8923525 | C | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9805G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923525 | |||||||
chr3:8923530 | C | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9810G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923530 | |||||||
chr3:8923530 | C | T | 2 | a0001c0001t0002g0198 a0001c0001t0043g0197 |
2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.890-9810G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923530 | |||||||
chr3:8923533 | C | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-9813G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923533 | |||||||
chr3:8923544 | C | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9824G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923544 | |||||||
chr3:8923565 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9845C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923565 | |||||||
chr3:8923571 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.890-9851C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923571 | |||||||
chr3:8923582 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.890-9862G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923582 | |||||||
chr3:8923612 | A | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9892T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923612 | |||||||
chr3:8923622 | C | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9902G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923622 | |||||||
chr3:8923645 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9925G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923645 | |||||||
chr3:8923672 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9952C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923672 | |||||||
chr3:8923686 | G | C | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.890-9966C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923686 | |||||||
chr3:8923709 | T | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9989A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923709 | |||||||
chr3:8923716 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-9996G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923716 | |||||||
chr3:8923728 | T | C | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10008A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923728 | |||||||
chr3:8923743 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-10023T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923743 | |||||||
chr3:8923762 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10042C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923762 | |||||||
chr3:8923821 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10101C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923821 | |||||||
chr3:8923866 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10146C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923866 | |||||||
chr3:8923867 | G | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.890-10147C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923867 | |||||||
chr3:8923873 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10153G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923873 | |||||||
chr3:8923877 | T | C | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10157A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923877 | |||||||
chr3:8923882 | C | T | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.890-10162G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923882 | |||||||
chr3:8923887 | C | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.890-10167G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923887 | |||||||
chr3:8923915 | C | G | 65 | a0001c0001t0005g0021 a0002c0002t0002g0210 a0002c0002t0003g0206 others(62): Show |
65 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.890-10195G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923915 | |||||||
chr3:8923916 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.890-10196T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923916 | |||||||
chr3:8923922 | C | T | 1 | a0002c0002t0002g0272 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.890-10202G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923922 | |||||||
chr3:8923923 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10203C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923923 | |||||||
chr3:8923939 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10219T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923939 | |||||||
chr3:8923949 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10229T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923949 | |||||||
chr3:8923958 | A | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10238T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923958 | |||||||
chr3:8923961 | T | C | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.890-10241A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923961 | |||||||
chr3:8923968 | T | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10248A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923968 | |||||||
chr3:8923982 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10262T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923982 | |||||||
chr3:8923984 | G | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10264C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923984 | |||||||
chr3:8923997 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10277G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8923997 | |||||||
chr3:8924011 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10291T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924011 | |||||||
chr3:8924044 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10324T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924044 | |||||||
chr3:8924064 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.890-10344A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924064 | |||||||
chr3:8924073 | A | C | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10353T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924073 | |||||||
chr3:8924084 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10364C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924084 | |||||||
chr3:8924101 | A | C | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.890-10381T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924101 | |||||||
chr3:8924140 | C | A | 65 | a0001c0001t0005g0021 a0002c0002t0002g0210 a0002c0002t0003g0206 others(62): Show |
65 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.890-10420G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924140 | |||||||
chr3:8924142 | T | C | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10422A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924142 | |||||||
chr3:8924165 | T | C | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10445A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924165 | |||||||
chr3:8924173 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10453G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924173 | |||||||
chr3:8924174 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10454T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924174 | |||||||
chr3:8924201 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-10481T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924201 | |||||||
chr3:8924248 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.890-10528G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924248 | |||||||
chr3:8924291 | C | A | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
259 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.890-10571G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924291 | |||||||
chr3:8924292 | A | G | 3 | a0001c0001t0016g0263 a0001c0001t0037g0260 a0013c0009t0016g0262 |
3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.890-10572T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924292 | |||||||
chr3:8924314 | T | A | 6 | a0003c0003t0007g0046 a0003c0003t0007g0048 a0003c0003t0007g0049 others(3): Show |
6 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.890-10594A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924314 | |||||||
chr3:8924379 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-10659C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924379 | |||||||
chr3:8924442 | G | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-10722C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924442 | |||||||
chr3:8924446 | C | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.890-10726G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924446 | |||||||
chr3:8924503 | C | T | 1 | a0002c0002t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.890-10783G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924503 | |||||||
chr3:8924562 | C | T | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.890-10842G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924562 | |||||||
chr3:8924566 | T | C | 1 | a0001c0001t0022g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.890-10846A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924566 | |||||||
chr3:8924586 | C | T | 1 | a0002c0002t0027g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.890-10866G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924586 | |||||||
chr3:8924593 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | HG02280.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.890-10873T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924593 | |||||||
chr3:8924610 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-10890G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924610 | |||||||
chr3:8924660 | G | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-10940C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924660 | |||||||
chr3:8924671 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-10951A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924671 | |||||||
chr3:8924687 | G | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
174 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.890-10967C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924687 | |||||||
chr3:8924703 | A | T | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.890-10983T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924703 | |||||||
chr3:8924708 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.890-10988T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924708 | |||||||
chr3:8924768 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0006g0250 |
2 | HG02976.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.890-11048C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924768 | |||||||
chr3:8924890 | C | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.889+10981G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8924890 | |||||||
chr3:8925057 | G | A | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.889+10814C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925057 | |||||||
chr3:8925057 | G | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.889+10814C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925057 | |||||||
chr3:8925058 | A | G | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+10813T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925058 | |||||||
chr3:8925088 | C | CA | 43 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(40): Show |
43 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.889+10782dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925088 | |||||||
chr3:8925110 | A | G | 1 | a0001c0001t0013g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.889+10761T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925110 | |||||||
chr3:8925162 | A | G | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.889+10709T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925162 | |||||||
chr3:8925202 | G | C | 1 | a0002c0002t0018g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.889+10669C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925202 | |||||||
chr3:8925207 | A | C | 1 | a0001c0001t0022g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.889+10664T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925207 | |||||||
chr3:8925209 | T | TA | 64 | a0001c0001t0005g0021 a0002c0002t0002g0210 a0002c0002t0003g0206 others(61): Show |
64 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.889+10661dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925209 | |||||||
chr3:8925231 | C | G | 1 | a0001c0001t0042g0247 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.889+10640G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925231 | |||||||
chr3:8925238 | G | T | 43 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(40): Show |
43 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.889+10633C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925238 | |||||||
chr3:8925257 | T | C | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889+10614A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925257 | |||||||
chr3:8925331 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.889+10540C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925331 | |||||||
chr3:8925364 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.889+10507C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925364 | |||||||
chr3:8925390 | A | G | 1 | a0002c0002t0002g0298 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.889+10481T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925390 | |||||||
chr3:8925396 | C | T | 17 | a0001c0001t0005g0021 a0002c0002t0004g0053 a0002c0002t0004g0054 others(14): Show |
17 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.889+10475G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925396 | |||||||
chr3:8925448 | C | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.889+10423G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925448 | |||||||
chr3:8925451 | G | C | 64 | a0001c0001t0005g0021 a0002c0002t0002g0210 a0002c0002t0003g0206 others(61): Show |
64 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.889+10420C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925451 | |||||||
chr3:8925475 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+10396G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925475 | |||||||
chr3:8925490 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.889+10381C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925490 | |||||||
chr3:8925565 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.889+10306T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925565 | |||||||
chr3:8925613 | G | C | 1 | a0001c0001t0005g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.889+10258C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925613 | |||||||
chr3:8925667 | A | G | 1 | a0002c0002t0002g0319 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.889+10204T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925667 | |||||||
chr3:8925690 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+10181C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925690 | |||||||
chr3:8925801 | T | A | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889+10070A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925801 | |||||||
chr3:8925815 | T | A | 1 | a0001c0001t0002g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.889+10056A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925815 | |||||||
chr3:8925906 | G | A | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.889+9965C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925906 | |||||||
chr3:8925961 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.889+9910T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925961 | |||||||
chr3:8925996 | T | C | 3 | a0001c0001t0016g0263 a0001c0001t0037g0260 a0013c0009t0016g0262 |
3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.889+9875A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8925996 | |||||||
chr3:8926014 | C | A | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.889+9857G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926014 | |||||||
chr3:8926137 | T | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
155 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.889+9734A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926137 | |||||||
chr3:8926151 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.889+9720T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926151 | |||||||
chr3:8926212 | A | G | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
172 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.889+9659T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926212 | |||||||
chr3:8926309 | T | C | 74 | a0001c0001t0005g0021 a0002c0002t0002g0210 a0002c0002t0003g0206 others(71): Show |
74 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.889+9562A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926309 | |||||||
chr3:8926339 | C | T | 1 | a0002c0002t0002g0325 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.889+9532G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926339 | |||||||
chr3:8926363 | A | G | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.889+9508T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926363 | |||||||
chr3:8926392 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+9479G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926392 | |||||||
chr3:8926409 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+9462C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926409 | |||||||
chr3:8926410 | G | T | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889+9461C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926410 | |||||||
chr3:8926712 | T | G | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.889+9159A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926712 | |||||||
chr3:8926718 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+9153G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926718 | |||||||
chr3:8926756 | A | G | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+9115T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926756 | |||||||
chr3:8926975 | A | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.889+8896T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926975 | |||||||
chr3:8926990 | T | C | 1 | a0004c0004t0001g0187 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.889+8881A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8926990 | |||||||
chr3:8927004 | G | C | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+8867C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927004 | |||||||
chr3:8927063 | T | C | 5 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.889+8808A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927063 | |||||||
chr3:8927192 | T | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.889+8679A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927192 | |||||||
chr3:8927199 | C | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+8672G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927199 | |||||||
chr3:8927224 | A | T | 5 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.889+8647T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927224 | |||||||
chr3:8927366 | T | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.889+8505A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927366 | |||||||
chr3:8927503 | A | G | 1 | a0012c0012t0004g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.889+8368T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927503 | |||||||
chr3:8927611 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+8260T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927611 | |||||||
chr3:8927619 | A | G | 47 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(44): Show |
48 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.889+8252T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927619 | |||||||
chr3:8927629 | T | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0196 |
3 | HG02055.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.889+8242A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927629 | |||||||
chr3:8927702 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0143 |
2 | HG01069.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.889+8169G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927702 | |||||||
chr3:8927703 | G | A | 6 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0064 others(3): Show |
6 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.889+8168C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927703 | |||||||
chr3:8927773 | A | G | 1 | a0002c0002t0002g0274 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.889+8098T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927773 | |||||||
chr3:8927825 | C | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+8046G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927825 | |||||||
chr3:8927852 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
193 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.889+8019G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927852 | |||||||
chr3:8927889 | A | G | 54 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0074 others(51): Show |
56 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.889+7982T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927889 | |||||||
chr3:8927966 | G | A | 1 | a0001c0001t0042g0247 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.889+7905C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927966 | |||||||
chr3:8927969 | T | C | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.889+7902A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8927969 | |||||||
chr3:8928049 | T | TA | 24 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
24 | HG01081.hp2 HG02258.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.889+7821dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928049 | |||||||
chr3:8928049 | T | TAA | 11 | a0001c0001t0005g0020 a0001c0001t0005g0024 a0001c0001t0005g0025 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.889+7820_889+7821d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928049 | |||||||
chr3:8928049 | T | TAAA | 6 | a0001c0001t0005g0018 a0001c0001t0005g0026 a0001c0001t0005g0027 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.889+7819_889+7821d others(5): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928049 | |||||||
chr3:8928049 | T | TGA | 3 | a0001c0001t0002g0201 a0001c0001t0021g0016 a0001c0001t0048g0244 |
3 | HG02145.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.889+7821_889+7822i others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928049 | |||||||
chr3:8928049 | T | TGAA | 8 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+7821_889+7822i others(5): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928049 | |||||||
chr3:8928049 | TA | T | 28 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0101 others(25): Show |
28 | HG00099.hp2 HG00609.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.889+7821delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928049 | |||||||
chr3:8928049 | TAA | T | 9 | a0002c0002t0004g0043 a0003c0003t0007g0046 a0003c0003t0007g0047 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+7820_889+7821d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928049 | |||||||
chr3:8928114 | A | G | 8 | a0002c0002t0003g0208 a0002c0002t0003g0212 a0002c0002t0003g0221 others(5): Show |
8 | HG00438.hp2 NA18941.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.889+7757T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928114 | |||||||
chr3:8928117 | C | A | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889+7754G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928117 | |||||||
chr3:8928223 | A | C | 48 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(45): Show |
49 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.889+7648T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928223 | |||||||
chr3:8928254 | A | G | 201 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(198): Show |
210 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.889+7617T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928254 | |||||||
chr3:8928374 | T | C | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.889+7497A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928374 | |||||||
chr3:8928399 | T | A | 154 | a0001c0001t0005g0021 a0002c0002t0002g0002 a0002c0002t0002g0007 others(151): Show |
162 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.889+7472A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928399 | |||||||
chr3:8928418 | T | C | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.889+7453A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928418 | |||||||
chr3:8928465 | T | A | 1 | a0002c0002t0002g0319 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.889+7406A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928465 | |||||||
chr3:8928488 | A | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+7383T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928488 | |||||||
chr3:8928490 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+7381G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928490 | |||||||
chr3:8928587 | G | T | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+7284C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928587 | |||||||
chr3:8928693 | T | G | 50 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(47): Show |
51 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.889+7178A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928693 | |||||||
chr3:8928706 | C | A | 5 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.889+7165G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928706 | |||||||
chr3:8928717 | A | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
184 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.889+7154T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928717 | |||||||
chr3:8928757 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.889+7114A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928757 | |||||||
chr3:8928833 | GACCTAAC | G | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.889+7031_889+7037d others(9): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928833 | |||||||
chr3:8928902 | C | T | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+6969G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928902 | |||||||
chr3:8928911 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.889+6960T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928911 | |||||||
chr3:8928961 | CA | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.889+6909delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8928961 | |||||||
chr3:8929087 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.889+6784C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929087 | |||||||
chr3:8929314 | A | C | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.889+6557T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929314 | |||||||
chr3:8929319 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0037 others(86): Show |
93 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.889+6552G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929319 | |||||||
chr3:8929611 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.889+6260C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929611 | |||||||
chr3:8929623 | A | T | 1 | a0001c0001t0006g0256 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.889+6248T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929623 | |||||||
chr3:8929626 | T | A | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+6245A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929626 | |||||||
chr3:8929643 | AT | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
233 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.889+6227delA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929643 | |||||||
chr3:8929643 | ATT | A | 30 | a0001c0001t0001g0130 a0001c0001t0001g0170 a0001c0001t0005g0018 others(27): Show |
30 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.889+6226_889+6227d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929643 | |||||||
chr3:8929664 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.889+6207G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929664 | |||||||
chr3:8929679 | T | C | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+6192A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929679 | |||||||
chr3:8929703 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.889+6168T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929703 | |||||||
chr3:8929727 | C | T | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.889+6144G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929727 | |||||||
chr3:8929787 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
125 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.889+6084C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929787 | |||||||
chr3:8929831 | C | T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.889+6040G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929831 | |||||||
chr3:8929938 | C | T | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.889+5933G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929938 | |||||||
chr3:8929966 | C | T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.889+5905G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8929966 | |||||||
chr3:8930007 | A | T | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889+5864T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930007 | |||||||
chr3:8930026 | A | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.889+5845T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930026 | |||||||
chr3:8930049 | T | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.889+5822A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930049 | |||||||
chr3:8930060 | T | G | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889+5811A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930060 | |||||||
chr3:8930103 | G | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.889+5768C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930103 | |||||||
chr3:8930182 | T | G | 2 | a0001c0001t0005g0018 a0001c0001t0024g0017 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.889+5689A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930182 | |||||||
chr3:8930185 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
190 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.889+5686A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930185 | |||||||
chr3:8930215 | A | G | 13 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(10): Show |
13 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.889+5656T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930215 | |||||||
chr3:8930217 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.889+5654T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930217 | |||||||
chr3:8930230 | T | C | 5 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.889+5641A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930230 | |||||||
chr3:8930247 | G | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.889+5624C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930247 | |||||||
chr3:8930343 | A | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
126 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.889+5528T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930343 | |||||||
chr3:8930538 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.889+5333C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930538 | |||||||
chr3:8930591 | T | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.889+5280A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930591 | |||||||
chr3:8930617 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.889+5254T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930617 | |||||||
chr3:8930677 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.889+5194C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930677 | |||||||
chr3:8930679 | C | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.889+5192G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930679 | |||||||
chr3:8930816 | T | C | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.889+5055A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930816 | |||||||
chr3:8930919 | T | C | 1 | a0002c0002t0002g0314 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.889+4952A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930919 | |||||||
chr3:8930946 | T | C | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.889+4925A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8930946 | |||||||
chr3:8931001 | G | A | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889+4870C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931001 | |||||||
chr3:8931079 | CTG | C | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.889+4790_889+4791d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931079 | |||||||
chr3:8931264 | G | A | 3 | a0001c0001t0016g0263 a0001c0001t0037g0260 a0013c0009t0016g0262 |
3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.889+4607C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931264 | |||||||
chr3:8931387 | G | A | 2 | a0001c0001t0002g0198 a0001c0001t0043g0197 |
2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.889+4484C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931387 | |||||||
chr3:8931487 | C | G | 1 | a0001c0001t0002g0006 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.889+4384G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931487 | |||||||
chr3:8931527 | G | A | 1 | a0003c0003t0007g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.889+4344C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931527 | |||||||
chr3:8931587 | G | T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
132 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.889+4284C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931587 | |||||||
chr3:8931599 | C | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
263 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.889+4272G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931599 | |||||||
chr3:8931808 | A | G | 1 | a0010c0016t0025g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.889+4063T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931808 | |||||||
chr3:8931852 | T | C | 1 | a0001c0001t0002g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.889+4019A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931852 | |||||||
chr3:8931858 | T | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.889+4013A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8931858 | |||||||
chr3:8932033 | G | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
188 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.889+3838C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932033 | |||||||
chr3:8932093 | C | G | 1 | a0002c0002t0002g0272 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.889+3778G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932093 | |||||||
chr3:8932110 | T | A | 26 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(23): Show |
27 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.889+3761A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932110 | |||||||
chr3:8932120 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
190 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.889+3751A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932120 | |||||||
chr3:8932237 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.889+3634G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932237 | |||||||
chr3:8932343 | G | A | 1 | a0012c0012t0004g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.889+3528C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932343 | |||||||
chr3:8932409 | C | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.889+3462G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932409 | |||||||
chr3:8932582 | CTG | C | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.889+3287_889+3288d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932582 | |||||||
chr3:8932815 | T | C | 2 | a0002c0002t0004g0061 a0002c0002t0004g0062 |
2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.889+3056A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932815 | |||||||
chr3:8932835 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.889+3036A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932835 | |||||||
chr3:8932866 | G | A | 43 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(40): Show |
43 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.889+3005C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932866 | |||||||
chr3:8932904 | T | A | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.889+2967A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932904 | |||||||
chr3:8932960 | C | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
189 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.889+2911G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8932960 | |||||||
chr3:8933011 | G | A | 69 | a0001c0001t0005g0021 a0001c0001t0014g0013 a0001c0001t0014g0014 others(66): Show |
69 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.889+2860C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933011 | |||||||
chr3:8933109 | T | TAAATA | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
189 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.889+2757_889+2761d others(7): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933109 | |||||||
chr3:8933181 | T | C | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.889+2690A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933181 | |||||||
chr3:8933183 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.889+2688G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933183 | |||||||
chr3:8933196 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
189 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.889+2675T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933196 | |||||||
chr3:8933240 | C | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
192 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.889+2631G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933240 | |||||||
chr3:8933301 | G | C | 5 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.889+2570C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933301 | |||||||
chr3:8933369 | T | C | 10 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(7): Show |
11 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.889+2502A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933369 | |||||||
chr3:8933405 | A | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.889+2466T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933405 | |||||||
chr3:8933472 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
169 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.889+2399A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933472 | |||||||
chr3:8933516 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
189 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.889+2355T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933516 | |||||||
chr3:8933544 | G | T | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.889+2327C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933544 | |||||||
chr3:8933552 | G | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
190 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.889+2319C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933552 | |||||||
chr3:8933614 | A | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.889+2257T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933614 | |||||||
chr3:8933709 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
189 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.889+2162G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933709 | |||||||
chr3:8933790 | T | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0182 |
2 | HG02071.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.889+2081A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933790 | |||||||
chr3:8933854 | C | T | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.889+2017G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8933854 | |||||||
chr3:8934058 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
176 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.889+1813C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934058 | |||||||
chr3:8934060 | G | A | 2 | a0002c0002t0003g0233 a0002c0002t0003g0234 |
2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.889+1811C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934060 | |||||||
chr3:8934074 | A | AT | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+1796dupA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934074 | |||||||
chr3:8934077 | G | C | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+1794C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934077 | |||||||
chr3:8934078 | G | C | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+1793C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934078 | |||||||
chr3:8934079 | T | A | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+1792A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934079 | |||||||
chr3:8934088 | T | C | 1 | a0002c0002t0035g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.889+1783A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934088 | |||||||
chr3:8934202 | CAA | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.889+1667_889+1668d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934202 | |||||||
chr3:8934230 | AGGCT | A | 10 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(7): Show |
11 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.889+1637_889+1640d others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934230 | |||||||
chr3:8934335 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
188 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.889+1536T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934335 | |||||||
chr3:8934431 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
188 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.889+1440C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934431 | |||||||
chr3:8934503 | T | A | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889+1368A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934503 | |||||||
chr3:8934505 | A | G | 65 | a0001c0001t0005g0021 a0002c0002t0002g0210 a0002c0002t0003g0206 others(62): Show |
65 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.889+1366T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934505 | |||||||
chr3:8934507 | T | C | 11 | a0001c0001t0001g0076 a0001c0001t0001g0132 a0001c0001t0001g0133 others(8): Show |
11 | HG00099.hp1 HG00642.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.889+1364A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934507 | |||||||
chr3:8934543 | T | A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.889+1328A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934543 | |||||||
chr3:8934614 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.889+1257G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934614 | |||||||
chr3:8934795 | G | T | 1 | a0002c0002t0004g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.889+1076C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934795 | |||||||
chr3:8934901 | C | A | 4 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.889+970G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934901 | |||||||
chr3:8934922 | A | G | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.889+949T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8934922 | |||||||
chr3:8935095 | G | A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.889+776C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8935095 | |||||||
chr3:8935268 | T | C | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.889+603A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8935268 | |||||||
chr3:8935298 | C | T | 69 | a0001c0001t0005g0021 a0001c0001t0014g0013 a0001c0001t0014g0014 others(66): Show |
69 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.889+573G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8935298 | |||||||
chr3:8935474 | G | A | 70 | a0001c0001t0005g0021 a0001c0001t0014g0013 a0001c0001t0014g0014 others(67): Show |
70 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.889+397C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8935474 | |||||||
chr3:8935475 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
102 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.889+396C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8935475 | |||||||
chr3:8935479 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
188 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.889+392C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 7/12 | chr3 | 8935479 | |||||||
chr3:8936074 | A | C | 35 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(32): Show |
36 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(33): Show |
intron_variant | MODIFIER | c.705-19T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936074 | |||||||
chr3:8936078 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG02132.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.705-23C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936078 | |||||||
chr3:8936297 | G | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
142 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.705-242C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936297 | |||||||
chr3:8936335 | G | C | 71 | a0001c0001t0005g0021 a0001c0001t0014g0013 a0001c0001t0014g0014 others(68): Show |
71 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.705-280C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936335 | |||||||
chr3:8936443 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.705-388A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936443 | |||||||
chr3:8936491 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.705-436A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936491 | |||||||
chr3:8936585 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.705-530A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936585 | |||||||
chr3:8936792 | C | T | 65 | a0001c0001t0005g0021 a0001c0001t0045g0328 a0002c0002t0002g0210 others(62): Show |
65 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.705-737G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936792 | |||||||
chr3:8936905 | C | T | 1 | a0002c0002t0046g0321 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.705-850G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936905 | |||||||
chr3:8936921 | CAG | C | 10 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(7): Show |
11 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.705-868_705-867del others(2): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936921 | |||||||
chr3:8936944 | T | C | 6 | a0002c0002t0009g0012 a0002c0002t0009g0330 a0002c0002t0009g0331 others(3): Show |
7 | HG01243.hp2 HG01358.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.705-889A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8936944 | |||||||
chr3:8937022 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.705-967A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937022 | |||||||
chr3:8937027 | A | G | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.705-972T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937027 | |||||||
chr3:8937201 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.705-1146C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937201 | |||||||
chr3:8937288 | T | C | 21 | a0001c0001t0005g0021 a0002c0002t0004g0053 a0002c0002t0004g0054 others(18): Show |
21 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.705-1233A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937288 | |||||||
chr3:8937446 | G | A | 2 | a0001c0001t0002g0198 a0001c0001t0043g0197 |
2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.705-1391C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937446 | |||||||
chr3:8937514 | T | TTATATAT others(38): Show |
3 | a0002c0002t0004g0043 a0002c0002t0004g0044 a0002c0002t0004g0045 |
3 | HG02717.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.705-1460_705-1459i others(47): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937514 | |||||||
chr3:8937514 | T | TTATATAT others(40): Show |
1 | a0002c0002t0004g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.705-1460_705-1459i others(49): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937514 | |||||||
chr3:8937517 | AGG | A | 4 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-1464_705-1463d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937517 | |||||||
chr3:8937520 | G | T | 4 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-1465C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937520 | |||||||
chr3:8937534 | TC | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.705-1480delG | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937534 | |||||||
chr3:8937608 | C | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.705-1553G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937608 | |||||||
chr3:8937666 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0201 others(2): Show |
6 | HG02055.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.705-1611T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937666 | |||||||
chr3:8937714 | G | A | 15 | a0002c0002t0002g0010 a0002c0002t0002g0297 a0002c0002t0002g0298 others(12): Show |
16 | HG00408.hp2 HG00423.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.705-1659C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937714 | |||||||
chr3:8937721 | T | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.705-1666A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937721 | |||||||
chr3:8937762 | C | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0163 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.705-1707G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937762 | |||||||
chr3:8937800 | G | C | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.705-1745C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937800 | |||||||
chr3:8937923 | C | T | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(219): Show |
227 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.704+1631G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8937923 | |||||||
chr3:8938095 | T | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
235 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.704+1459A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8938095 | |||||||
chr3:8938206 | C | T | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.704+1348G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8938206 | |||||||
chr3:8938328 | G | T | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+1226C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8938328 | |||||||
chr3:8938468 | A | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.704+1086T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8938468 | |||||||
chr3:8938727 | A | AT | 4 | a0002c0002t0003g0216 a0002c0002t0003g0217 a0002c0002t0003g0218 others(1): Show |
4 | NA18956.hp1 NA18988.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+826dupA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8938727 | |||||||
chr3:8938960 | G | T | 4 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+594C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8938960 | |||||||
chr3:8938992 | T | C | 1 | a0002c0002t0002g0325 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.704+562A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8938992 | |||||||
chr3:8939032 | G | T | 1 | a0002c0002t0035g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.704+522C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8939032 | |||||||
chr3:8939033 | G | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.704+521C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8939033 | |||||||
chr3:8939190 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.704+364A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8939190 | |||||||
chr3:8939214 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
241 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.704+340G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8939214 | |||||||
chr3:8939239 | T | C | 5 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+315A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8939239 | |||||||
chr3:8939458 | G | A | 13 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(10): Show |
13 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.704+96C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 6/12 | chr3 | 8939458 | |||||||
chr3:8939657 | T | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | splice_region_variant&intron_variant | LOW | c.605-4A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8939657 | |||||||
chr3:8939686 | A | G | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.605-33T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8939686 | |||||||
chr3:8939706 | A | G | 7 | a0001c0001t0006g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.605-53T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8939706 | |||||||
chr3:8939780 | G | C | 1 | a0001c0001t0037g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.605-127C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8939780 | |||||||
chr3:8940079 | G | C | 2 | a0001c0001t0002g0198 a0001c0001t0043g0197 |
2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.605-426C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940079 | |||||||
chr3:8940105 | A | G | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.605-452T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940105 | |||||||
chr3:8940160 | T | C | 4 | a0002c0002t0003g0207 a0002c0002t0003g0239 a0002c0002t0003g0240 others(1): Show |
4 | NA18966.hp1 NA18980.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-507A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940160 | |||||||
chr3:8940221 | T | C | 13 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(10): Show |
13 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.605-568A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940221 | |||||||
chr3:8940233 | G | A | 63 | a0001c0001t0005g0021 a0002c0002t0002g0210 a0002c0002t0003g0206 others(60): Show |
63 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.605-580C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940233 | |||||||
chr3:8940312 | T | C | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.605-659A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940312 | |||||||
chr3:8940334 | A | G | 2 | a0001c0001t0021g0016 a0001c0001t0048g0244 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.605-681T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940334 | |||||||
chr3:8940414 | T | C | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.605-761A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940414 | |||||||
chr3:8940422 | C | G | 66 | a0001c0001t0005g0021 a0001c0001t0014g0013 a0001c0001t0014g0014 others(63): Show |
66 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.605-769G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940422 | |||||||
chr3:8940429 | T | C | 1 | a0010c0016t0025g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605-776A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940429 | |||||||
chr3:8940544 | C | T | 119 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(116): Show |
120 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.605-891G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940544 | |||||||
chr3:8940644 | T | C | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.604+823A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940644 | |||||||
chr3:8940797 | G | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
141 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.604+670C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940797 | |||||||
chr3:8940959 | G | A | 1 | a0003c0003t0007g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.604+508C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8940959 | |||||||
chr3:8941203 | T | C | 1 | a0010c0016t0025g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.604+264A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8941203 | |||||||
chr3:8941420 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.604+47A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 5/12 | chr3 | 8941420 | |||||||
chr3:8941976 | G | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
264 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.267-172C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8941976 | |||||||
chr3:8942137 | C | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.267-333G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8942137 | |||||||
chr3:8942393 | G | A | 4 | a0002c0002t0003g0207 a0002c0002t0003g0239 a0002c0002t0003g0240 others(1): Show |
4 | NA18966.hp1 NA18980.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.267-589C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8942393 | |||||||
chr3:8942491 | G | C | 2 | a0001c0001t0002g0198 a0001c0001t0043g0197 |
2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.267-687C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8942491 | |||||||
chr3:8942560 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.267-756G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8942560 | |||||||
chr3:8942780 | C | A | 200 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(197): Show |
209 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.267-976G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8942780 | |||||||
chr3:8942925 | G | A | 1 | a0002c0002t0002g0310 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.267-1121C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8942925 | |||||||
chr3:8942951 | G | T | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.267-1147C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8942951 | |||||||
chr3:8942967 | T | G | 2 | a0002c0002t0002g0311 a0002c0002t0002g0314 |
2 | HG00558.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.267-1163A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8942967 | |||||||
chr3:8943083 | AAAG | A | 40 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(37): Show |
40 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.267-1282_267-1280d others(5): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943083 | |||||||
chr3:8943261 | T | C | 1 | a0002c0002t0010g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.267-1457A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943261 | |||||||
chr3:8943296 | T | A | 1 | a0002c0002t0002g0323 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.267-1492A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943296 | |||||||
chr3:8943374 | G | A | 17 | a0001c0001t0005g0021 a0002c0002t0004g0053 a0002c0002t0004g0054 others(14): Show |
17 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.267-1570C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943374 | |||||||
chr3:8943430 | A | G | 1 | a0001c0001t0006g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.267-1626T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943430 | |||||||
chr3:8943556 | T | C | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.267-1752A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943556 | |||||||
chr3:8943576 | G | C | 80 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0008 others(77): Show |
88 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.267-1772C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943576 | |||||||
chr3:8943622 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.267-1818G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943622 | |||||||
chr3:8943641 | A | T | 1 | a0002c0002t0046g0321 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.267-1837T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943641 | |||||||
chr3:8943650 | G | A | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.267-1846C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943650 | |||||||
chr3:8943669 | T | C | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.267-1865A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943669 | |||||||
chr3:8943782 | T | C | 2 | a0001c0001t0016g0263 a0013c0009t0016g0262 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.267-1978A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943782 | |||||||
chr3:8943915 | A | G | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.267-2111T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8943915 | |||||||
chr3:8944002 | C | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.267-2198G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944002 | |||||||
chr3:8944023 | T | G | 1 | a0002c0002t0002g0312 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.267-2219A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944023 | |||||||
chr3:8944122 | G | A | 1 | a0002c0002t0002g0313 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.267-2318C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944122 | |||||||
chr3:8944190 | T | G | 37 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(34): Show |
37 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.267-2386A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944190 | |||||||
chr3:8944220 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
9 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.267-2416G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944220 | |||||||
chr3:8944243 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.267-2439C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944243 | |||||||
chr3:8944262 | G | A | 3 | a0002c0002t0018g0235 a0002c0002t0018g0237 a0002c0002t0036g0236 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.267-2458C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944262 | |||||||
chr3:8944275 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.267-2471C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944275 | |||||||
chr3:8944531 | G | T | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.266+2689C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944531 | |||||||
chr3:8944564 | G | A | 20 | a0001c0001t0005g0021 a0002c0002t0004g0053 a0002c0002t0004g0054 others(17): Show |
20 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.266+2656C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944564 | |||||||
chr3:8944631 | G | A | 1 | a0002c0002t0002g0314 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.266+2589C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944631 | |||||||
chr3:8944863 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.266+2357G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944863 | |||||||
chr3:8944918 | T | C | 22 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(19): Show |
22 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.266+2302A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944918 | |||||||
chr3:8944930 | G | A | 19 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0024 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.266+2290C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944930 | |||||||
chr3:8944979 | A | G | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266+2241T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944979 | |||||||
chr3:8944994 | A | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.266+2226T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8944994 | |||||||
chr3:8945041 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.266+2179G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945041 | |||||||
chr3:8945078 | T | A | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266+2142A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945078 | |||||||
chr3:8945361 | G | A | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.266+1859C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945361 | |||||||
chr3:8945468 | C | CTT | 42 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(39): Show |
43 | HG00408.hp1 HG00639.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.266+1750_266+1751d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945468 | |||||||
chr3:8945468 | C | CTTT | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0037 others(83): Show |
90 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.266+1749_266+1751d others(5): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945468 | |||||||
chr3:8945468 | CT | C | 36 | a0001c0001t0005g0018 a0001c0001t0005g0021 a0001c0001t0005g0028 others(33): Show |
36 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.266+1751delA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945468 | |||||||
chr3:8945512 | G | A | 1 | a0001c0001t0012g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.266+1708C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945512 | |||||||
chr3:8945559 | A | G | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG00597.hp2 HG00673.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.266+1661T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945559 | |||||||
chr3:8945674 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.266+1546C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945674 | |||||||
chr3:8945750 | G | A | 1 | a0002c0002t0004g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.266+1470C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945750 | |||||||
chr3:8945855 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.266+1365T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945855 | |||||||
chr3:8945871 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.266+1349T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945871 | |||||||
chr3:8945883 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.266+1337C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945883 | |||||||
chr3:8945914 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
137 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.266+1306T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8945914 | |||||||
chr3:8946021 | G | A | 21 | a0001c0001t0005g0021 a0002c0002t0004g0053 a0002c0002t0004g0054 others(18): Show |
21 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.266+1199C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946021 | |||||||
chr3:8946046 | G | A | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.266+1174C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946046 | |||||||
chr3:8946051 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.266+1169C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946051 | |||||||
chr3:8946064 | CT | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.266+1155delA | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946064 | |||||||
chr3:8946364 | C | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.266+856G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946364 | |||||||
chr3:8946505 | T | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
237 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.266+715A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946505 | |||||||
chr3:8946516 | T | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
155 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.266+704A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946516 | |||||||
chr3:8946544 | T | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(1): Show |
5 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.266+676A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946544 | |||||||
chr3:8946565 | C | T | 1 | a0002c0002t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.266+655G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946565 | |||||||
chr3:8946650 | C | T | 1 | a0003c0003t0007g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.266+570G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946650 | |||||||
chr3:8946713 | C | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.266+507G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946713 | |||||||
chr3:8946725 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.266+495A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946725 | |||||||
chr3:8946743 | A | C | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.266+477T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946743 | |||||||
chr3:8946789 | T | C | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.266+431A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946789 | |||||||
chr3:8946820 | G | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(46): Show |
50 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.266+400C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946820 | |||||||
chr3:8946850 | A | G | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266+370T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946850 | |||||||
chr3:8946928 | T | G | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG00423.hp2 NA18949.hp1 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.266+292A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946928 | |||||||
chr3:8946952 | G | A | 8 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(5): Show |
8 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.266+268C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946952 | |||||||
chr3:8946995 | G | A | 21 | a0001c0001t0005g0021 a0002c0002t0004g0053 a0002c0002t0004g0054 others(18): Show |
21 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.266+225C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8946995 | |||||||
chr3:8947112 | A | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.266+108T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8947112 | |||||||
chr3:8947125 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
131 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.266+95G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 4/12 | chr3 | 8947125 | |||||||
chr3:8947468 | A | C | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | HG02280.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.196-178T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8947468 | |||||||
chr3:8947549 | A | G | 1 | a0002c0002t0003g0213 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.196-259T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8947549 | |||||||
chr3:8947585 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.196-295A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8947585 | |||||||
chr3:8947606 | G | A | 37 | a0001c0001t0005g0021 a0001c0001t0008g0031 a0001c0001t0008g0032 others(34): Show |
37 | HG00639.hp2 HG01106.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.196-316C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8947606 | |||||||
chr3:8947683 | A | C | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-393T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8947683 | |||||||
chr3:8947969 | G | A | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+540C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8947969 | |||||||
chr3:8948102 | G | A | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+407C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8948102 | |||||||
chr3:8948122 | A | G | 37 | a0001c0001t0005g0021 a0001c0001t0008g0031 a0001c0001t0008g0032 others(34): Show |
37 | HG00639.hp2 HG01106.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.195+387T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8948122 | |||||||
chr3:8948129 | G | A | 1 | a0001c0001t0005g0029 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.195+380C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8948129 | |||||||
chr3:8948204 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.195+305T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8948204 | |||||||
chr3:8948355 | C | T | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+154G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8948355 | |||||||
chr3:8948425 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.195+84A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 3/12 | chr3 | 8948425 | |||||||
chr3:8948912 | A | G | 1 | a0003c0003t0007g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.134-342T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8948912 | |||||||
chr3:8949255 | A | C | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.134-685T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949255 | |||||||
chr3:8949351 | C | T | 20 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0056 others(17): Show |
20 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.134-781G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949351 | |||||||
chr3:8949358 | T | C | 3 | a0001c0001t0016g0263 a0001c0001t0037g0260 a0013c0009t0016g0262 |
3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.134-788A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949358 | |||||||
chr3:8949389 | T | C | 1 | a0002c0002t0002g0316 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.134-819A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949389 | |||||||
chr3:8949579 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG02132.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.134-1009T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949579 | |||||||
chr3:8949659 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.134-1089C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949659 | |||||||
chr3:8949674 | A | AGG | 23 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(20): Show |
23 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.134-1106_134-1105d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949674 | |||||||
chr3:8949677 | G | C | 10 | a0002c0002t0047g0327 a0003c0003t0007g0046 a0003c0003t0007g0047 others(7): Show |
10 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.134-1107C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949677 | |||||||
chr3:8949787 | T | C | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.134-1217A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949787 | |||||||
chr3:8949793 | G | A | 4 | a0002c0002t0003g0207 a0002c0002t0003g0239 a0002c0002t0003g0240 others(1): Show |
4 | NA18966.hp1 NA18980.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-1223C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949793 | |||||||
chr3:8949942 | T | C | 1 | a0002c0002t0004g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.134-1372A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949942 | |||||||
chr3:8949957 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01192.hp1 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-1387G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949957 | |||||||
chr3:8949999 | A | G | 1 | a0010c0016t0025g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.134-1429T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8949999 | |||||||
chr3:8950097 | C | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.134-1527G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950097 | |||||||
chr3:8950100 | G | A | 4 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1530C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950100 | |||||||
chr3:8950117 | G | A | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.134-1547C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950117 | |||||||
chr3:8950232 | C | T | 1 | a0002c0002t0028g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.134-1662G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950232 | |||||||
chr3:8950286 | C | G | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.134-1716G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950286 | |||||||
chr3:8950296 | G | A | 128 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(125): Show |
129 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.134-1726C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950296 | |||||||
chr3:8950370 | A | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 |
4 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1800T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950370 | |||||||
chr3:8950498 | G | A | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.134-1928C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950498 | |||||||
chr3:8950498 | G | T | 1 | a0001c0001t0016g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.134-1928C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950498 | |||||||
chr3:8950531 | G | A | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.134-1961C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950531 | |||||||
chr3:8950567 | C | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-1997G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950567 | |||||||
chr3:8950576 | C | A | 2 | a0002c0002t0004g0061 a0002c0002t0004g0062 |
2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.134-2006G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950576 | |||||||
chr3:8950797 | T | C | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.134-2227A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950797 | |||||||
chr3:8950842 | A | T | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-2272T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950842 | |||||||
chr3:8950853 | C | A | 1 | a0001c0001t0037g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.134-2283G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950853 | |||||||
chr3:8950866 | C | G | 1 | a0001c0001t0008g0031 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.134-2296G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950866 | |||||||
chr3:8950928 | A | G | 23 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(20): Show |
23 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.134-2358T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950928 | |||||||
chr3:8950956 | C | T | 1 | a0001c0011t0001g0092 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.134-2386G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8950956 | |||||||
chr3:8951015 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-2445A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951015 | |||||||
chr3:8951166 | A | G | 2 | a0005c0005t0020g0203 a0005c0005t0020g0204 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.134-2596T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951166 | |||||||
chr3:8951313 | A | C | 2 | a0001c0001t0005g0020 a0001c0001t0023g0019 |
2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.134-2743T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951313 | |||||||
chr3:8951437 | C | G | 1 | a0001c0001t0037g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.134-2867G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951437 | |||||||
chr3:8951472 | T | C | 4 | a0002c0002t0004g0042 a0002c0002t0004g0043 a0002c0002t0004g0044 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-2902A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951472 | |||||||
chr3:8951557 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.134-2987T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951557 | |||||||
chr3:8951655 | G | A | 1 | a0002c0002t0002g0007 | 2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.134-3085C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951655 | |||||||
chr3:8951675 | G | A | 1 | a0002c0002t0010g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.134-3105C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951675 | |||||||
chr3:8951688 | C | T | 126 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(123): Show |
127 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.134-3118G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951688 | |||||||
chr3:8951712 | T | G | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.134-3142A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951712 | |||||||
chr3:8951766 | G | C | 23 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(20): Show |
23 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.134-3196C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951766 | |||||||
chr3:8951826 | T | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | NA18951.hp1 NA18962.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-3256A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951826 | |||||||
chr3:8951924 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.134-3354C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951924 | |||||||
chr3:8951979 | G | A | 23 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 others(20): Show |
23 | HG00639.hp2 HG01081.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-3409C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8951979 | |||||||
chr3:8952051 | TC | T | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.134-3482delG | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8952051 | |||||||
chr3:8952085 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-3515C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8952085 | |||||||
chr3:8952089 | T | C | 1 | a0002c0002t0002g0011 | 2 | NA19011.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.134-3519A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8952089 | |||||||
chr3:8952100 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.134-3530C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8952100 | |||||||
chr3:8952387 | T | C | 2 | a0001c0001t0021g0016 a0001c0001t0048g0244 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.134-3817A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8952387 | |||||||
chr3:8952551 | C | T | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.134-3981G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8952551 | |||||||
chr3:8952738 | G | A | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-4168C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8952738 | |||||||
chr3:8952918 | T | C | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.134-4348A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8952918 | |||||||
chr3:8953099 | T | A | 3 | a0001c0001t0016g0263 a0001c0001t0037g0260 a0013c0009t0016g0262 |
3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.134-4529A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953099 | |||||||
chr3:8953229 | T | C | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.134-4659A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953229 | |||||||
chr3:8953255 | T | TTA | 6 | a0002c0002t0004g0053 a0002c0002t0004g0054 a0002c0002t0004g0064 others(3): Show |
6 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-4687_134-4686d others(4): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953255 | |||||||
chr3:8953286 | CATTT | C | 6 | a0003c0003t0007g0046 a0003c0003t0007g0048 a0003c0003t0007g0049 others(3): Show |
6 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-4720_134-4717d others(6): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953286 | |||||||
chr3:8953310 | A | G | 15 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(12): Show |
15 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.134-4740T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953310 | |||||||
chr3:8953417 | C | T | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.134-4847G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953417 | |||||||
chr3:8953435 | T | C | 1 | a0002c0002t0002g0317 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.134-4865A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953435 | |||||||
chr3:8953502 | T | C | 20 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.134-4932A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953502 | |||||||
chr3:8953519 | C | T | 2 | a0002c0002t0003g0208 a0002c0002t0003g0212 |
2 | NA18951.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.134-4949G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953519 | |||||||
chr3:8953602 | A | G | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.134-5032T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953602 | |||||||
chr3:8953603 | T | C | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-5033A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953603 | |||||||
chr3:8953925 | T | C | 15 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(12): Show |
15 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.133+4995A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953925 | |||||||
chr3:8953936 | C | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.133+4984G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8953936 | |||||||
chr3:8954101 | T | C | 9 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(6): Show |
9 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.133+4819A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8954101 | |||||||
chr3:8954238 | T | G | 23 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 others(20): Show |
23 | HG00639.hp2 HG01081.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.133+4682A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8954238 | |||||||
chr3:8954378 | T | C | 4 | a0001c0001t0006g0252 a0001c0001t0006g0257 a0001c0001t0006g0258 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+4542A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8954378 | |||||||
chr3:8954470 | G | A | 55 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(52): Show |
55 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.133+4450C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8954470 | |||||||
chr3:8954637 | G | T | 1 | a0013c0009t0016g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.133+4283C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8954637 | |||||||
chr3:8954657 | A | G | 42 | a0002c0002t0002g0210 a0002c0002t0003g0206 a0002c0002t0003g0207 others(39): Show |
42 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.133+4263T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8954657 | |||||||
chr3:8954956 | C | T | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+3964G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8954956 | |||||||
chr3:8955063 | G | A | 129 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(126): Show |
130 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.133+3857C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955063 | |||||||
chr3:8955066 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0026g0063 |
3 | HG01081.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.133+3854A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955066 | |||||||
chr3:8955412 | A | G | 2 | a0002c0002t0002g0269 a0002c0002t0002g0322 |
2 | NA18967.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.133+3508T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955412 | |||||||
chr3:8955418 | G | C | 21 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(18): Show |
21 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3502C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955418 | |||||||
chr3:8955453 | G | C | 117 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(114): Show |
118 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.133+3467C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955453 | |||||||
chr3:8955583 | A | G | 23 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(20): Show |
23 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.133+3337T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955583 | |||||||
chr3:8955616 | G | A | 3 | a0002c0002t0002g0266 a0002c0002t0002g0318 a0002c0002t0002g0319 |
3 | NA18956.hp2 NA19009.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.133+3304C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955616 | |||||||
chr3:8955676 | T | A | 1 | a0002c0002t0002g0320 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.133+3244A>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955676 | |||||||
chr3:8955722 | G | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.133+3198C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955722 | |||||||
chr3:8955808 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.133+3112G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955808 | |||||||
chr3:8955994 | C | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG01109.hp1 HG01928.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+2926G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8955994 | |||||||
chr3:8956007 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.133+2913A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956007 | |||||||
chr3:8956021 | A | G | 2 | a0002c0002t0002g0210 a0002c0002t0003g0211 |
2 | HG00609.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.133+2899T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956021 | |||||||
chr3:8956047 | A | G | 1 | a0001c0001t0049g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133+2873T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956047 | |||||||
chr3:8956048 | T | C | 1 | a0002c0002t0010g0191 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+2872A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956048 | |||||||
chr3:8956218 | G | A | 1 | a0002c0002t0046g0321 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.133+2702C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956218 | |||||||
chr3:8956317 | C | T | 107 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(104): Show |
108 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.133+2603G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956317 | |||||||
chr3:8956383 | A | G | 46 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0005g0018 others(43): Show |
46 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.133+2537T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956383 | |||||||
chr3:8956433 | C | T | 1 | a0001c0001t0013g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.133+2487G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956433 | |||||||
chr3:8956607 | T | G | 6 | a0001c0001t0002g0202 a0001c0001t0016g0263 a0001c0001t0026g0063 others(3): Show |
6 | HG01081.hp2 HG02922.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+2313A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956607 | |||||||
chr3:8956653 | C | T | 4 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(1): Show |
5 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+2267G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956653 | |||||||
chr3:8956745 | T | G | 7 | a0001c0001t0037g0260 a0002c0002t0004g0053 a0002c0002t0004g0054 others(4): Show |
7 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+2175A>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956745 | |||||||
chr3:8956750 | T | TAAAAAAA others(2): Show |
7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+2161_133+2169d others(11): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956750 | |||||||
chr3:8956750 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.133+2160_133+2169d others(12): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956750 | |||||||
chr3:8956750 | T | TAAAAAAA others(4): Show |
1 | a0002c0002t0004g0054 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.133+2159_133+2169d others(13): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956750 | |||||||
chr3:8956750 | T | TAAAAAAA others(5): Show |
14 | a0001c0001t0026g0063 a0002c0002t0004g0053 a0002c0002t0004g0056 others(11): Show |
14 | HG00639.hp2 HG01081.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.133+2169_133+2170i others(14): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956750 | |||||||
chr3:8956750 | T | TAAAAAAA others(6): Show |
45 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(42): Show |
46 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.133+2169_133+2170i others(15): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956750 | |||||||
chr3:8956750 | T | TAAAAAAA others(7): Show |
10 | a0001c0001t0002g0255 a0001c0001t0006g0254 a0001c0001t0006g0256 others(7): Show |
10 | HG01081.hp1 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+2169_133+2170i others(16): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956750 | |||||||
chr3:8956750 | T | TAAAAAAA others(8): Show |
48 | a0001c0001t0021g0016 a0001c0001t0022g0015 a0001c0001t0038g0193 others(45): Show |
48 | HG00438.hp2 HG00609.hp1 HG02055.hp1 others(45): Show |
intron_variant | MODIFIER | c.133+2169_133+2170i others(17): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956750 | |||||||
chr3:8956750 | T | TAAAAAAA others(9): Show |
4 | a0002c0002t0003g0242 a0002c0002t0003g0243 a0002c0002t0004g0039 others(1): Show |
4 | HG02056.hp2 HG02559.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+2169_133+2170i others(18): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956750 | |||||||
chr3:8956813 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.133+2107T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956813 | |||||||
chr3:8956916 | C | A | 59 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(56): Show |
60 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.133+2004G>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956916 | |||||||
chr3:8956995 | G | C | 3 | a0004c0004t0001g0001 a0004c0004t0001g0186 a0004c0004t0001g0187 |
5 | NA18941.hp1 NA19002.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+1925C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8956995 | |||||||
chr3:8957015 | T | C | 1 | a0001c0001t0048g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.133+1905A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957015 | |||||||
chr3:8957033 | T | C | 8 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0048 others(5): Show |
8 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+1887A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957033 | |||||||
chr3:8957212 | C | G | 1 | a0002c0002t0004g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.133+1708G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957212 | |||||||
chr3:8957241 | A | G | 1 | a0002c0002t0002g0268 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.133+1679T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957241 | |||||||
chr3:8957253 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.133+1667A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957253 | |||||||
chr3:8957258 | C | T | 12 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(9): Show |
13 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.133+1662G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957258 | |||||||
chr3:8957575 | A | G | 1 | a0001c0001t0021g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133+1345T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957575 | |||||||
chr3:8957785 | G | T | 2 | a0001c0001t0005g0018 a0001c0001t0024g0017 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.133+1135C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957785 | |||||||
chr3:8957834 | A | T | 73 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(70): Show |
74 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.133+1086T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8957834 | |||||||
chr3:8958083 | A | G | 14 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.133+837T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8958083 | |||||||
chr3:8958109 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+811G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8958109 | |||||||
chr3:8958363 | A | C | 56 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(53): Show |
56 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.133+557T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8958363 | |||||||
chr3:8958378 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.133+542G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8958378 | |||||||
chr3:8958379 | G | A | 78 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(75): Show |
78 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.133+541C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8958379 | |||||||
chr3:8958636 | A | G | 134 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(131): Show |
135 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.133+284T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 2/12 | chr3 | 8958636 | |||||||
chr3:8959431 | T | C | 1 | a0001c0001t0037g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.52-430A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8959431 | |||||||
chr3:8959625 | GGAAGGGA others(25): Show |
G | 1 | a0001c0001t0006g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52-656_52-625delAT others(30): Show |
RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8959625 | |||||||
chr3:8959813 | C | T | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-812G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8959813 | |||||||
chr3:8959879 | C | CA | 17 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0008g0031 others(14): Show |
19 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.52-879dupT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8959879 | |||||||
chr3:8959879 | CA | C | 18 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0006g0246 others(15): Show |
18 | HG00639.hp2 HG01081.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.52-879delT | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8959879 | |||||||
chr3:8959911 | A | T | 117 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(114): Show |
118 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.52-910T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8959911 | |||||||
chr3:8959988 | G | A | 1 | a0002c0002t0002g0325 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.52-987C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8959988 | |||||||
chr3:8959988 | G | C | 34 | a0001c0001t0026g0063 a0002c0002t0004g0042 a0002c0002t0004g0043 others(31): Show |
34 | HG00639.hp2 HG01081.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.52-987C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8959988 | |||||||
chr3:8960028 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.52-1027T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960028 | |||||||
chr3:8960240 | A | C | 1 | a0002c0002t0002g0264 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.52-1239T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960240 | |||||||
chr3:8960420 | C | G | 1 | a0001c0001t0037g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.52-1419G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960420 | |||||||
chr3:8960449 | A | T | 1 | a0002c0002t0002g0007 | 2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.52-1448T>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960449 | |||||||
chr3:8960538 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.52-1537G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960538 | |||||||
chr3:8960548 | A | C | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.52-1547T>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960548 | |||||||
chr3:8960572 | G | A | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0022g0015 |
3 | HG03516.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.52-1571C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960572 | |||||||
chr3:8960736 | A | G | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-1735T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960736 | |||||||
chr3:8960854 | C | T | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-1853G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960854 | |||||||
chr3:8960888 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.52-1887G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8960888 | |||||||
chr3:8961055 | G | A | 1 | a0002c0002t0019g0326 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.52-2054C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961055 | |||||||
chr3:8961151 | T | C | 17 | a0001c0001t0026g0063 a0002c0002t0004g0053 a0002c0002t0004g0054 others(14): Show |
17 | HG00639.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.52-2150A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961151 | |||||||
chr3:8961240 | C | T | 1 | a0002c0002t0035g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51+2095G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961240 | |||||||
chr3:8961295 | C | G | 1 | a0002c0002t0028g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.51+2040G>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961295 | |||||||
chr3:8961328 | G | A | 1 | a0001c0001t0002g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.51+2007C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961328 | |||||||
chr3:8961342 | T | C | 3 | a0001c0001t0016g0263 a0001c0001t0049g0261 a0013c0009t0016g0262 |
3 | HG06807.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.51+1993A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961342 | |||||||
chr3:8961362 | G | A | 75 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(72): Show |
75 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.51+1973C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961362 | |||||||
chr3:8961386 | A | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0014 a0001c0001t0022g0015 |
3 | HG03516.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.51+1949T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961386 | |||||||
chr3:8961440 | G | T | 75 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(72): Show |
75 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.51+1895C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961440 | |||||||
chr3:8961500 | T | C | 14 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.51+1835A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961500 | |||||||
chr3:8961802 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.51+1533C>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961802 | |||||||
chr3:8961826 | T | C | 2 | a0005c0005t0020g0203 a0005c0005t0020g0204 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.51+1509A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961826 | |||||||
chr3:8961837 | T | C | 1 | a0001c0001t0005g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.51+1498A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8961837 | |||||||
chr3:8962110 | A | G | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
264 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(261): Show |
intron_variant | MODIFIER | c.51+1225T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962110 | |||||||
chr3:8962159 | T | C | 6 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(3): Show |
6 | HG01106.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+1176A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962159 | |||||||
chr3:8962412 | G | A | 3 | a0001c0001t0016g0263 a0001c0001t0049g0261 a0013c0009t0016g0262 |
3 | HG06807.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.51+923C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962412 | |||||||
chr3:8962743 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
264 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(261): Show |
intron_variant | MODIFIER | c.51+592G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962743 | |||||||
chr3:8962766 | C | T | 44 | a0001c0001t0038g0193 a0001c0001t0048g0244 a0002c0002t0002g0210 others(41): Show |
44 | HG00438.hp2 HG00609.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.51+569G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962766 | |||||||
chr3:8962791 | G | C | 1 | a0002c0002t0047g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.51+544C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962791 | |||||||
chr3:8962877 | G | A | 1 | a0001c0001t0045g0328 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.51+458C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962877 | |||||||
chr3:8962900 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.51+435C>T | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962900 | |||||||
chr3:8962900 | G | C | 1 | a0002c0002t0011g0329 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.51+435C>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962900 | |||||||
chr3:8962908 | A | G | 12 | a0001c0001t0002g0006 a0001c0001t0002g0196 a0001c0001t0002g0198 others(9): Show |
13 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+427T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8962908 | |||||||
chr3:8963065 | T | C | 4 | a0002c0002t0010g0188 a0002c0002t0010g0189 a0002c0002t0010g0190 others(1): Show |
4 | HG02809.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+270A>G | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8963065 | |||||||
chr3:8963066 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.51+269G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8963066 | |||||||
chr3:8963110 | A | G | 1 | a0001c0001t0038g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.51+225T>C | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8963110 | |||||||
chr3:8963135 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.51+200G>A | RAD18 | ENSG00000070950.10 | transcript | ENST00000264926.7 | protein_coding | 1/12 | chr3 | 8963135 |