Item | Value |
---|---|
geneid | 285671 |
ensemblid | ENSG00000164197.12 |
hgncid | 27752 |
symbol | RNF180 |
name | ring finger protein 180 |
refseq_nuc | NM_001113561.2 |
refseq_prot | NP_001107033.1 |
ensembl_nuc | ENST00000389100.9 |
ensembl_prot | ENSP00000373752.4 |
mane_status | MANE Select |
chr | chr5 |
start | 64165843 |
end | 64372869 |
strand | + |
ver | v1.2 |
region | chr5:64165843-64372869 |
region5000 | chr5:64160843-64377869 |
regionname0 | RNF180_chr5_64165843_64372869 |
regionname5000 | RNF180_chr5_64160843_64377869 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 592 | 227 | 66 | 51 | 69 | 11 | 28 | 57 | RNF180_chr5_64160843_64377869 | RNF180 | MKRSK others(587): Show |
chr5 | 64160843 | 64377869 |
a0002 | 0/0 | 592 | 19 | 6 | 10 | 0 | 1 | 2 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | MKRSK others(587): Show |
chr5 | 64160843 | 64377869 |
a0003 | 0/0 | 592 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | MKRSK others(587): Show |
chr5 | 64160843 | 64377869 |
a0004 | 0/0 | 428 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | MKRSK others(423): Show |
chr5 | 64160843 | 64377869 |
a0005 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | MKRSK others(587): Show |
chr5 | 64160843 | 64377869 |
a0006 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | MKRSK others(587): Show |
chr5 | 64160843 | 64377869 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1776 | 226 | 66 | 51 | 68 | 11 | 28 | RNF180_chr5_64160843_64377869 | RNF180 | ATGAA others(1771): Show |
chr5 | 64160843 | 64377869 | ||
a0001c0003 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | ATGAA others(1771): Show |
chr5 | 64160843 | 64377869 | ||
a0002c0002 | 0/0 | 1776 | 19 | 6 | 10 | 0 | 1 | 2 | RNF180_chr5_64160843_64377869 | RNF180 | ATGAA others(1771): Show |
chr5 | 64160843 | 64377869 | ||
a0003c0006 | 0/0 | 1776 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | ATGAA others(1771): Show |
chr5 | 64160843 | 64377869 | ||
a0004c0004 | 0/0 | 1604 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | ATGAA others(1599): Show |
chr5 | 64160843 | 64377869 | ||
a0005c0005 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | ATGAA others(1771): Show |
chr5 | 64160843 | 64377869 | ||
a0006c0007 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | ATGAA others(1771): Show |
chr5 | 64160843 | 64377869 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4945 | 56 | 16 | 17 | 9 | 5 | 9 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0002 | 0/0 | 4945 | 42 | 3 | 12 | 20 | 1 | 6 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0003 | 1/1 | 4945 | 39 | 9 | 6 | 12 | 3 | 7 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0004 | 0/0 | 4945 | 27 | 7 | 7 | 12 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0005 | 0/0 | 4945 | 26 | 14 | 0 | 12 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0007 | 0/0 | 4945 | 9 | 1 | 5 | 1 | 0 | 2 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0009 | 0/0 | 4945 | 4 | 1 | 1 | 0 | 1 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0011 | 0/0 | 4946 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4941): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0012 | 0/0 | 4945 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0013 | 0/0 | 4945 | 2 | 0 | 1 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0014 | 0/0 | 4946 | 2 | 2 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4941): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0015 | 0/0 | 4945 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0017 | 0/0 | 4945 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0019 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0020 | 0/0 | 4945 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0021 | 0/0 | 4945 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0022 | 0/0 | 4945 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0023 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0024 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0025 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0026 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0027 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0028 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0001t0029 | 0/0 | 4945 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0001c0003t0002 | 0/0 | 4945 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0002c0002t0006 | 0/0 | 4945 | 10 | 0 | 8 | 0 | 1 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0002c0002t0008 | 0/0 | 4945 | 4 | 2 | 2 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0002c0002t0010 | 0/0 | 4945 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0002c0002t0016 | 0/0 | 4945 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0002c0002t0018 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0003c0006t0002 | 0/0 | 4945 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0004c0004t0004 | 0/0 | 4773 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4768): Show |
chr5 | 64160843 | 64377869 |
a0005c0005t0001 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
a0006c0007t0002 | 0/0 | 4945 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | GAACC others(4940): Show |
chr5 | 64160843 | 64377869 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0008 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0009g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0013g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0013g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0014g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0015g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0017g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0019g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0020g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0021g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0022g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0023g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0024g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0025g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0026g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0027g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0028g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0001t0029g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0016g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0002c0002t0018g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0003c0006t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0004c0004t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0005c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
a0006c0007t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | GBR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00323 | hp2 | a0001 | c0001 | t0009 | g0037 | EUR | FIN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0237 | EAS | CHS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00642 | hp2 | a0001 | c0001 | t0021 | g0047 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG00741 | hp2 | a0002 | c0002 | t0008 | g0062 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01074 | hp2 | a0002 | c0002 | t0006 | g0068 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01081 | hp1 | a0002 | c0002 | t0006 | g0069 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01168 | hp2 | a0001 | c0001 | t0020 | g0024 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01175 | hp1 | a0002 | c0002 | t0006 | g0072 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01175 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01255 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0108 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01257 | hp1 | a0002 | c0002 | t0006 | g0074 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01257 | hp2 | a0002 | c0002 | t0008 | g0063 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01258 | hp1 | a0002 | c0002 | t0006 | g0075 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0109 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01261 | hp2 | a0001 | c0001 | t0013 | g0009 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01516 | hp2 | a0001 | c0001 | t0013 | g0013 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01943 | hp2 | a0001 | c0001 | t0007 | g0032 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01952 | hp1 | a0001 | c0001 | t0007 | g0034 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01952 | hp2 | a0003 | c0006 | t0002 | g0175 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01975 | hp2 | a0002 | c0002 | t0006 | g0071 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01978 | hp1 | a0002 | c0002 | t0006 | g0065 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01993 | hp1 | a0002 | c0002 | t0006 | g0070 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02040 | hp2 | a0001 | c0003 | t0002 | g0246 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0036 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02280 | hp1 | a0002 | c0002 | t0008 | g0061 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02622 | hp2 | a0002 | c0002 | t0010 | g0057 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02647 | hp2 | a0004 | c0004 | t0004 | g0093 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02735 | hp1 | a0002 | c0002 | t0016 | g0067 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02818 | hp1 | a0001 | c0001 | t0026 | g0247 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02886 | hp2 | a0001 | c0001 | t0019 | g0166 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02896 | hp2 | a0001 | c0001 | t0028 | g0193 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03041 | hp2 | a0001 | c0001 | t0025 | g0105 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0191 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0053 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03195 | hp1 | a0005 | c0005 | t0001 | g0140 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03225 | hp1 | a0002 | c0002 | t0010 | g0076 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0196 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03453 | hp2 | a0002 | c0002 | t0010 | g0058 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03516 | hp1 | a0001 | c0001 | t0027 | g0060 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03540 | hp2 | a0001 | c0001 | t0011 | g0052 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0051 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0106 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04115 | hp2 | a0001 | c0001 | t0017 | g0020 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04184 | hp1 | a0001 | c0001 | t0022 | g0019 | SAS | BEB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04199 | hp2 | a0001 | c0001 | t0009 | g0182 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04228 | hp1 | a0002 | c0002 | t0006 | g0066 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0197 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | CHB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18943 | hp2 | a0001 | c0001 | t0015 | g0033 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0238 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18950 | hp2 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18966 | hp1 | a0001 | c0001 | t0029 | g0236 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | LWK | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19076 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19076 | hp2 | a0006 | c0007 | t0002 | g0205 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19240 | hp1 | a0001 | c0001 | t0014 | g0056 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ASW | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ASW | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA20752 | hp1 | a0002 | c0002 | t0006 | g0073 | EUR | TSI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | TSI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0035 | SAS | GIH | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | GIH | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0030 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0195 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02109 | hp2 | a0002 | c0002 | t0018 | g0059 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02559 | hp1 | a0001 | c0001 | t0024 | g0192 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG06807 | hp1 | a0002 | c0002 | t0008 | g0064 | AFR | USA | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | USA | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA20300 | hp1 | a0001 | c0001 | t0014 | g0055 | AFR | USA | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
NA20300 | hp2 | a0001 | c0001 | t0023 | g0165 | AFR | USA | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0008 | REF | REF | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0029 | REF | REF | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:64165951 | C | A | 1 | a0002 | 1 | HG02735.hp1 | splice_region_variant | LOW | c.-3C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/8 | chr5 | 64165951 | |||||||
chr5:64212109 | G | T | 1 | a0006 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.180G>T | p.Trp60Cys | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/8 | 291/4945 | 180/1779 | 60/592 | chr5 | 64212109 | |||
chr5:64213964 | A | G | 1 | a0003 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.638A>G | p.Gln213Arg | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/8 | 749/4945 | 638/1779 | 213/592 | chr5 | 64213964 | |||
chr5:64214071 | C | T | 1 | a0005 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.745C>T | p.His249Tyr | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/8 | 856/4945 | 745/1779 | 249/592 | chr5 | 64214071 | |||
chr5:64324627 | TCCCATAA others(723): Show |
T | 1 | a0004 | 1 | HG02647.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1228-558_1399del | p.Thr410fs | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/8 | 1228/1779 | 410/592 | chr5 | 64324627 | ||||
chr5:64369621 | G | A | 1 | a0002 | 19 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(16): Show |
missense_variant | MODERATE | c.1586G>A | p.Arg529His | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1697/4945 | 1586/1779 | 529/592 | chr5 | 64369621 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:64214199 | G | C | 1 | a0001c0003 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.873G>C | p.Leu291Leu | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/8 | 984/4945 | 873/1779 | 291/592 | chr5 | 64214199 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:64165874 | G | C | 1 | a0001c0001t0015 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/8 | 34934 | chr5 | 64165874 | ||||||
chr5:64369836 | T | C | 1 | a0002c0002t0008 | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*22T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 22 | chr5 | 64369836 | ||||||
chr5:64370030 | A | G | 1 | a0001c0001t0012 | 3 | HG02109.hp1 HG03225.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*216A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 216 | chr5 | 64370030 | ||||||
chr5:64370034 | A | G | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(9): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*220A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 220 | chr5 | 64370034 | ||||||
chr5:64370090 | T | C | 1 | a0001c0001t0017 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 276 | chr5 | 64370090 | ||||||
chr5:64370119 | A | C | 1 | a0001c0001t0029 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 305 | chr5 | 64370119 | ||||||
chr5:64370136 | C | T | 1 | a0001c0001t0028 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 322 | chr5 | 64370136 | ||||||
chr5:64370289 | A | G | 2 | a0001c0001t0011 a0001c0001t0014 |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*475A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 475 | chr5 | 64370289 | ||||||
chr5:64370452 | C | A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(22): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*638C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 638 | chr5 | 64370452 | ||||||
chr5:64370453 | T | G | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(22): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*639T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 639 | chr5 | 64370453 | ||||||
chr5:64370457 | T | C | 2 | a0001c0001t0013 a0001c0001t0021 |
3 | HG00642.hp2 HG01261.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 643 | chr5 | 64370457 | ||||||
chr5:64370488 | A | G | 1 | a0001c0001t0022 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 674 | chr5 | 64370488 | ||||||
chr5:64370643 | A | C | 1 | a0001c0001t0027 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*829A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 829 | chr5 | 64370643 | ||||||
chr5:64370862 | G | A | 1 | a0001c0001t0009 | 4 | HG00323.hp2 HG01175.hp2 HG02257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1048G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1048 | chr5 | 64370862 | ||||||
chr5:64371361 | T | C | 5 | a0002c0002t0006 a0002c0002t0008 a0002c0002t0010 others(2): Show |
19 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1547T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1547 | chr5 | 64371361 | ||||||
chr5:64371369 | G | C | 1 | a0001c0001t0019 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1555G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1555 | chr5 | 64371369 | ||||||
chr5:64371471 | A | T | 3 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0015 |
14 | HG00323.hp2 HG01123.hp2 HG01175.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1657A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1657 | chr5 | 64371471 | ||||||
chr5:64371695 | C | T | 1 | a0001c0001t0011 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1881C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1881 | chr5 | 64371695 | ||||||
chr5:64371834 | T | C | 1 | a0001c0001t0020 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2020 | chr5 | 64371834 | ||||||
chr5:64371944 | T | A | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2130T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2130 | chr5 | 64371944 | ||||||
chr5:64372189 | T | TA | 2 | a0001c0001t0011 a0001c0001t0014 |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2382dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2383 | INFO_REALIGN_3_PRIME | chr5 | 64372189 | |||||
chr5:64372190 | A | T | 2 | a0001c0001t0026 a0002c0002t0018 |
2 | HG02109.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2376A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2376 | chr5 | 64372190 | ||||||
chr5:64372196 | A | G | 2 | a0002c0002t0006 a0002c0002t0016 |
11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2382A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2382 | chr5 | 64372196 | ||||||
chr5:64372212 | A | G | 4 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0025 others(1): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2398A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2398 | chr5 | 64372212 | ||||||
chr5:64372466 | C | T | 1 | a0001c0001t0025 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2652C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2652 | chr5 | 64372466 | ||||||
chr5:64372543 | A | C | 1 | a0001c0001t0021 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2729A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2729 | chr5 | 64372543 | ||||||
chr5:64372556 | A | G | 7 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0024 others(4): Show |
32 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2742A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2742 | chr5 | 64372556 | ||||||
chr5:64372774 | C | A | 1 | a0001c0001t0024 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2960C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2960 | chr5 | 64372774 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:64166002 | T | A | 1 | a0001c0001t0002g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-1+49T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166002 | |||||||
chr5:64166149 | C | G | 199 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-1+196C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166149 | |||||||
chr5:64166243 | T | C | 1 | a0001c0001t0011g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-1+290T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166243 | |||||||
chr5:64166283 | A | T | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-1+330A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166283 | |||||||
chr5:64166738 | C | T | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-1+785C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166738 | |||||||
chr5:64166800 | T | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+847T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166800 | |||||||
chr5:64166851 | G | A | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-1+898G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166851 | |||||||
chr5:64166915 | A | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+962A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166915 | |||||||
chr5:64167316 | G | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+1363G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167316 | |||||||
chr5:64167544 | G | C | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-1+1591G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167544 | |||||||
chr5:64167623 | T | A | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1+1670T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167623 | |||||||
chr5:64167694 | A | G | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1+1741A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167694 | |||||||
chr5:64167745 | G | T | 1 | a0001c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-1+1792G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167745 | |||||||
chr5:64168030 | G | T | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-1+2077G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168030 | |||||||
chr5:64168055 | G | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+2102G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168055 | |||||||
chr5:64168120 | A | G | 13 | a0001c0001t0005g0232 a0001c0001t0005g0233 a0001c0001t0005g0234 others(10): Show |
13 | HG00597.hp1 NA18942.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+2167A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168120 | |||||||
chr5:64168412 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-1+2459G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168412 | |||||||
chr5:64168466 | G | C | 1 | a0001c0001t0004g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-1+2513G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168466 | |||||||
chr5:64168695 | A | G | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-1+2742A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168695 | |||||||
chr5:64168726 | C | T | 1 | a0001c0001t0005g0244 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-1+2773C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168726 | |||||||
chr5:64168799 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+2846T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168799 | |||||||
chr5:64169022 | T | C | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+3069T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64169022 | |||||||
chr5:64169859 | G | C | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-1+3906G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64169859 | |||||||
chr5:64169887 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0006 |
3 | HG00741.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-1+3934G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64169887 | |||||||
chr5:64170063 | C | T | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-1+4110C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170063 | |||||||
chr5:64170078 | G | C | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-1+4125G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170078 | |||||||
chr5:64170092 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1+4139G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170092 | |||||||
chr5:64170240 | G | T | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1+4287G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170240 | |||||||
chr5:64170429 | G | A | 111 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(108): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-1+4476G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170429 | |||||||
chr5:64170965 | T | C | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+5012T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170965 | |||||||
chr5:64171079 | A | C | 1 | a0001c0001t0023g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-1+5126A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171079 | |||||||
chr5:64171195 | G | T | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-1+5242G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171195 | |||||||
chr5:64171386 | A | G | 4 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0010g0076 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5433A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171386 | |||||||
chr5:64171411 | C | T | 10 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(7): Show |
10 | HG02040.hp1 NA18950.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+5458C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171411 | |||||||
chr5:64171593 | T | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-1+5640T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171593 | |||||||
chr5:64171712 | A | G | 2 | a0002c0002t0006g0074 a0002c0002t0006g0075 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-1+5759A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171712 | |||||||
chr5:64171827 | G | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1+5874G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171827 | |||||||
chr5:64171836 | C | T | 21 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0204 others(18): Show |
21 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1+5883C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171836 | |||||||
chr5:64171849 | C | G | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-1+5896C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171849 | |||||||
chr5:64171990 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+6037C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171990 | |||||||
chr5:64172058 | C | T | 12 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(9): Show |
12 | HG00408.hp1 HG02074.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+6105C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172058 | |||||||
chr5:64172192 | G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+6239G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172192 | |||||||
chr5:64172300 | T | C | 92 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(89): Show |
93 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1+6347T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172300 | |||||||
chr5:64172398 | G | T | 1 | a0001c0001t0014g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-1+6445G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172398 | |||||||
chr5:64172419 | G | T | 1 | a0001c0001t0002g0231 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-1+6466G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172419 | |||||||
chr5:64172458 | G | A | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+6505G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172458 | |||||||
chr5:64172780 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-1+6827G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172780 | |||||||
chr5:64172858 | A | G | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+6905A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172858 | |||||||
chr5:64172943 | A | G | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+6990A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172943 | |||||||
chr5:64173383 | G | T | 2 | a0001c0001t0003g0046 a0001c0001t0021g0047 |
2 | HG00642.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-1+7430G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173383 | |||||||
chr5:64173578 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+7625C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173578 | |||||||
chr5:64173595 | A | G | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-1+7642A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173595 | |||||||
chr5:64173697 | C | G | 11 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(8): Show |
11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1+7744C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173697 | |||||||
chr5:64173703 | T | C | 2 | a0001c0001t0019g0166 a0001c0001t0026g0247 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-1+7750T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173703 | |||||||
chr5:64173712 | A | G | 147 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(144): Show |
148 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-1+7759A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173712 | |||||||
chr5:64173717 | C | CT | 25 | a0001c0001t0003g0045 a0001c0001t0003g0198 a0001c0001t0003g0199 others(22): Show |
25 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1+7780dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64173717 | ||||||
chr5:64173717 | CT | C | 32 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0002g0222 others(29): Show |
33 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.-1+7780delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64173717 | ||||||
chr5:64173802 | G | A | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7849G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173802 | |||||||
chr5:64174107 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+8154C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174107 | |||||||
chr5:64174555 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-1+8602A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174555 | |||||||
chr5:64174589 | A | G | 26 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(23): Show |
26 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+8636A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174589 | |||||||
chr5:64174909 | T | C | 1 | a0001c0001t0013g0009 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-1+8956T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174909 | |||||||
chr5:64174959 | C | CT | 92 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0083 others(89): Show |
93 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1+9032dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | ||||||
chr5:64174959 | C | CTT | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(4): Show |
7 | HG01109.hp2 HG01928.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+9031_-1+9032dup others(2): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | ||||||
chr5:64174959 | C | CTTTTT | 20 | a0001c0001t0005g0168 a0001c0001t0005g0169 a0001c0001t0005g0170 others(17): Show |
20 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+9028_-1+9032dup others(5): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | ||||||
chr5:64174959 | CT | C | 8 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
8 | HG00597.hp2 HG01943.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+9032delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | ||||||
chr5:64174959 | CTTTTTTT others(4): Show |
C | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+9022_-1+9032del others(11): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | ||||||
chr5:64174959 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0003g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-1+9019_-1+9032del others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | ||||||
chr5:64175012 | G | T | 1 | a0001c0001t0002g0231 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-1+9059G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175012 | |||||||
chr5:64175037 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-1+9084G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175037 | |||||||
chr5:64175060 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-1+9107C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175060 | |||||||
chr5:64175088 | C | T | 2 | a0002c0002t0006g0074 a0002c0002t0006g0075 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-1+9135C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175088 | |||||||
chr5:64175213 | C | T | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-1+9260C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175213 | |||||||
chr5:64175263 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-1+9310C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175263 | |||||||
chr5:64175264 | G | A | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+9311G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175264 | |||||||
chr5:64175302 | T | C | 1 | a0001c0001t0013g0013 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-1+9349T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175302 | |||||||
chr5:64175517 | A | C | 5 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0191 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+9564A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175517 | |||||||
chr5:64175785 | G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+9832G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175785 | |||||||
chr5:64175805 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1+9852A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175805 | |||||||
chr5:64175861 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+9908G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175861 | |||||||
chr5:64175875 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+9922G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175875 | |||||||
chr5:64175997 | T | G | 140 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(137): Show |
141 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-1+10044T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175997 | |||||||
chr5:64176208 | G | A | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+10255G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176208 | |||||||
chr5:64176276 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+10323A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176276 | |||||||
chr5:64176599 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+10646A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176599 | |||||||
chr5:64176665 | T | G | 1 | a0001c0001t0002g0208 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-1+10712T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176665 | |||||||
chr5:64176785 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-1+10832C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176785 | |||||||
chr5:64176946 | C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+10993C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176946 | |||||||
chr5:64176957 | T | C | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+11004T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176957 | |||||||
chr5:64177049 | G | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+11096G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177049 | |||||||
chr5:64177237 | A | G | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+11284A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177237 | |||||||
chr5:64177241 | A | T | 140 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(137): Show |
141 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-1+11288A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177241 | |||||||
chr5:64177247 | G | A | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+11294G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177247 | |||||||
chr5:64177466 | A | G | 2 | a0001c0001t0004g0108 a0001c0001t0004g0109 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-1+11513A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177466 | |||||||
chr5:64177485 | T | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG02055.hp2 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+11532T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177485 | |||||||
chr5:64177526 | C | CAT | 18 | a0001c0001t0002g0027 a0001c0001t0002g0178 a0001c0001t0002g0215 others(15): Show |
18 | HG00741.hp1 HG01168.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1+11612_-1+11613d others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | C | CATAT | 28 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0183 others(25): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+11610_-1+11613d others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | C | CATATAT | 8 | a0001c0001t0002g0211 a0001c0001t0002g0220 a0001c0001t0002g0224 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+11608_-1+11613d others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | C | CATATATA others(1): Show |
4 | a0001c0001t0002g0187 a0001c0001t0003g0015 a0001c0001t0003g0016 others(1): Show |
4 | HG00408.hp1 HG02572.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+11606_-1+11613d others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | C | CATATATA others(3): Show |
3 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0223 |
3 | HG00099.hp2 NA18954.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-1+11604_-1+11613d others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | C | CATATATA others(5): Show |
3 | a0001c0001t0002g0174 a0001c0001t0002g0230 a0001c0001t0003g0014 |
3 | HG00738.hp2 HG02602.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-1+11602_-1+11613d others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | C | CATATATA others(7): Show |
4 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0228 others(1): Show |
4 | HG00597.hp2 HG01943.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+11600_-1+11613d others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CAT | C | 5 | a0001c0001t0002g0080 a0001c0001t0002g0207 a0001c0001t0002g0218 others(2): Show |
5 | HG03471.hp2 HG03927.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+11612_-1+11613d others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(1): Show |
C | 7 | a0001c0001t0005g0172 a0001c0001t0005g0189 a0001c0001t0005g0232 others(4): Show |
7 | HG00597.hp1 HG01175.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+11606_-1+11613d others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(3): Show |
C | 19 | a0001c0001t0002g0039 a0001c0001t0005g0167 a0001c0001t0005g0168 others(16): Show |
20 | HG00323.hp2 HG01255.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+11604_-1+11613d others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(5): Show |
C | 5 | a0001c0001t0005g0234 a0001c0001t0005g0240 a0001c0001t0005g0241 others(2): Show |
5 | NA18954.hp2 NA18977.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+11602_-1+11613d others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(7): Show |
C | 6 | a0001c0001t0002g0219 a0001c0001t0005g0173 a0001c0001t0011g0052 others(3): Show |
6 | HG02280.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+11600_-1+11613d others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(9): Show |
C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+11598_-1+11613d others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(11): Show |
C | 5 | a0001c0001t0003g0044 a0002c0002t0010g0057 a0002c0002t0010g0058 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+11596_-1+11613d others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(13): Show |
C | 16 | a0001c0001t0004g0248 a0001c0001t0027g0060 a0002c0002t0006g0065 others(13): Show |
16 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1+11594_-1+11613d others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(15): Show |
C | 91 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(88): Show |
92 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-1+11592_-1+11613d others(24): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177526 | CATATATA others(17): Show |
C | 3 | a0001c0001t0003g0040 a0001c0001t0005g0185 a0001c0001t0005g0186 |
3 | HG03098.hp2 NA18906.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-1+11590_-1+11613d others(26): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | ||||||
chr5:64177561 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1+11608A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177561 | |||||||
chr5:64177563 | A | G | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-1+11610A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177563 | |||||||
chr5:64177565 | A | G | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+11612A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177565 | |||||||
chr5:64177932 | G | A | 2 | a0001c0001t0005g0235 a0001c0001t0029g0236 |
2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-1+11979G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177932 | |||||||
chr5:64178014 | A | G | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+12061A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178014 | |||||||
chr5:64178184 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-1+12231C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178184 | |||||||
chr5:64178202 | CA | C | 196 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(193): Show |
198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-1+12269delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64178202 | ||||||
chr5:64178218 | A | G | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-1+12265A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178218 | |||||||
chr5:64178307 | C | T | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+12354C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178307 | |||||||
chr5:64178326 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1+12373T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178326 | |||||||
chr5:64178363 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-1+12410G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178363 | |||||||
chr5:64178422 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+12469G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178422 | |||||||
chr5:64178532 | T | G | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1+12579T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178532 | |||||||
chr5:64178556 | G | A | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+12603G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178556 | |||||||
chr5:64178632 | G | A | 1 | a0001c0001t0007g0023 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-1+12679G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178632 | |||||||
chr5:64178939 | G | A | 1 | a0003c0006t0002g0175 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-1+12986G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178939 | |||||||
chr5:64179019 | C | G | 1 | a0001c0001t0002g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-1+13066C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179019 | |||||||
chr5:64179156 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-1+13203A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179156 | |||||||
chr5:64179238 | C | T | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+13285C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179238 | |||||||
chr5:64179280 | A | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG01433.hp2 HG01928.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+13327A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179280 | |||||||
chr5:64179322 | T | C | 2 | a0001c0001t0003g0041 a0001c0001t0013g0013 |
2 | HG01261.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-1+13369T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179322 | |||||||
chr5:64179431 | TTTGCTAC others(7): Show |
T | 61 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-1+13480_-1+13493d others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64179431 | ||||||
chr5:64180143 | G | T | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+14190G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64180143 | |||||||
chr5:64180785 | G | A | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+14832G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64180785 | |||||||
chr5:64180983 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+15030C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64180983 | |||||||
chr5:64181054 | G | A | 1 | a0001c0001t0022g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-1+15101G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181054 | |||||||
chr5:64181222 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-1+15269T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181222 | |||||||
chr5:64181391 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-1+15438A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181391 | |||||||
chr5:64181686 | T | C | 5 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+15733T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181686 | |||||||
chr5:64181720 | G | A | 111 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(108): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-1+15767G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181720 | |||||||
chr5:64181802 | A | G | 1 | a0001c0001t0003g0018 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-1+15849A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181802 | |||||||
chr5:64181986 | C | CT | 19 | a0001c0001t0002g0039 a0001c0001t0002g0203 a0001c0001t0002g0204 others(16): Show |
19 | HG00323.hp2 HG00597.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1+16056dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64181986 | ||||||
chr5:64181986 | CT | C | 55 | a0001c0001t0001g0153 a0001c0001t0003g0005 a0001c0001t0004g0002 others(52): Show |
56 | HG01074.hp2 HG01081.hp1 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.-1+16056delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64181986 | ||||||
chr5:64181986 | CTT | C | 80 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-1+16055_-1+16056d others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64181986 | ||||||
chr5:64181986 | CTTT | C | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0005g0188 others(5): Show |
8 | HG00738.hp1 HG01515.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+16054_-1+16056d others(5): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64181986 | ||||||
chr5:64182076 | C | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1+16123C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182076 | |||||||
chr5:64182147 | C | T | 27 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(24): Show |
27 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.-1+16194C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182147 | |||||||
chr5:64182156 | A | G | 1 | a0001c0001t0004g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-1+16203A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182156 | |||||||
chr5:64182184 | A | G | 1 | a0002c0002t0006g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-1+16231A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182184 | |||||||
chr5:64182240 | T | C | 214 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+16287T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182240 | |||||||
chr5:64182351 | A | T | 2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-1+16398A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182351 | |||||||
chr5:64182728 | G | C | 2 | a0001c0001t0004g0089 a0001c0001t0004g0090 |
2 | NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-1+16775G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182728 | |||||||
chr5:64182911 | C | T | 2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-1+16958C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182911 | |||||||
chr5:64182928 | A | T | 1 | a0001c0001t0002g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-1+16975A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182928 | |||||||
chr5:64183441 | C | CT | 60 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(57): Show |
60 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1-17341dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64183441 | ||||||
chr5:64183441 | C | CTT | 22 | a0001c0001t0001g0088 a0001c0001t0001g0116 a0001c0001t0001g0117 others(19): Show |
22 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1-17342_1-17341dup others(2): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64183441 | ||||||
chr5:64183441 | C | CTTT | 12 | a0001c0001t0001g0119 a0001c0001t0001g0162 a0001c0001t0027g0060 others(9): Show |
12 | HG01081.hp1 HG01175.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1-17343_1-17341dup others(3): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64183441 | ||||||
chr5:64183441 | CT | C | 5 | a0001c0001t0002g0209 a0001c0001t0002g0215 a0001c0001t0003g0198 others(2): Show |
5 | HG01993.hp2 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-17341delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64183441 | ||||||
chr5:64184056 | T | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-16752T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184056 | |||||||
chr5:64184085 | G | T | 1 | a0001c0001t0009g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1-16723G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184085 | |||||||
chr5:64184108 | T | G | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-16700T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184108 | |||||||
chr5:64184210 | C | A | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1-16598C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184210 | |||||||
chr5:64184362 | GTACTT | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-16443_1-16439del others(5): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64184362 | ||||||
chr5:64184404 | A | T | 1 | a0001c0001t0004g0090 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1-16404A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184404 | |||||||
chr5:64184672 | G | C | 53 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(50): Show |
53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1-16136G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184672 | |||||||
chr5:64184749 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-16059G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184749 | |||||||
chr5:64184799 | A | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-16009A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184799 | |||||||
chr5:64185177 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1-15631T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64185177 | |||||||
chr5:64185207 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-15601A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64185207 | |||||||
chr5:64186000 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1-14808G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186000 | |||||||
chr5:64186061 | T | C | 1 | a0001c0001t0012g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1-14747T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186061 | |||||||
chr5:64186136 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1-14672A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186136 | |||||||
chr5:64186288 | C | T | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1-14520C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186288 | |||||||
chr5:64186376 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1-14432G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186376 | |||||||
chr5:64186765 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0006 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1-14043A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186765 | |||||||
chr5:64187436 | G | T | 10 | a0001c0001t0002g0039 a0001c0001t0003g0017 a0001c0001t0007g0001 others(7): Show |
11 | HG00323.hp2 HG01175.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1-13372G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187436 | |||||||
chr5:64187528 | G | C | 1 | a0001c0001t0004g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1-13280G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187528 | |||||||
chr5:64187567 | A | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1-13241A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187567 | |||||||
chr5:64187621 | T | C | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-13187T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187621 | |||||||
chr5:64187839 | T | G | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1-12969T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187839 | |||||||
chr5:64188029 | C | T | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1-12779C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64188029 | |||||||
chr5:64188134 | A | G | 2 | a0001c0001t0002g0183 a0001c0001t0003g0179 |
2 | HG02735.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1-12674A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64188134 | |||||||
chr5:64188253 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1-12555A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64188253 | |||||||
chr5:64188838 | T | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-11970T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64188838 | |||||||
chr5:64189081 | A | G | 3 | a0001c0001t0005g0240 a0001c0001t0005g0241 a0001c0001t0005g0242 |
3 | NA18954.hp2 NA19056.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1-11727A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189081 | |||||||
chr5:64189268 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1-11540A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189268 | |||||||
chr5:64189288 | T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1-11520T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189288 | |||||||
chr5:64189354 | C | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-11454C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189354 | |||||||
chr5:64189529 | G | A | 2 | a0001c0001t0005g0237 a0001c0001t0005g0244 |
2 | HG00597.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1-11279G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189529 | |||||||
chr5:64190051 | C | G | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1-10757C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190051 | |||||||
chr5:64190076 | T | C | 11 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(8): Show |
11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1-10732T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190076 | |||||||
chr5:64190350 | A | G | 2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1-10458A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190350 | |||||||
chr5:64190433 | C | T | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-10375C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190433 | |||||||
chr5:64190576 | T | C | 1 | a0001c0001t0004g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1-10232T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190576 | |||||||
chr5:64190713 | G | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1-10095G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190713 | |||||||
chr5:64190776 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1-10032G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190776 | |||||||
chr5:64190784 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0040 |
2 | NA18946.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1-10024G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190784 | |||||||
chr5:64190811 | G | A | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1-9997G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190811 | |||||||
chr5:64190821 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-9987A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190821 | |||||||
chr5:64190994 | C | T | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1-9814C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190994 | |||||||
chr5:64190995 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1-9813G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190995 | |||||||
chr5:64191091 | G | T | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-9717G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191091 | |||||||
chr5:64191405 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1-9403C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191405 | |||||||
chr5:64191418 | C | T | 1 | a0001c0001t0007g0032 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1-9390C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191418 | |||||||
chr5:64191693 | T | G | 4 | a0002c0002t0006g0065 a0002c0002t0006g0069 a0002c0002t0006g0070 others(1): Show |
4 | HG01081.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-9115T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191693 | |||||||
chr5:64191953 | G | A | 1 | a0001c0001t0003g0018 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1-8855G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191953 | |||||||
chr5:64192155 | G | T | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1-8653G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192155 | |||||||
chr5:64192179 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-8629G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192179 | |||||||
chr5:64192187 | A | G | 90 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(87): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1-8621A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192187 | |||||||
chr5:64192205 | C | T | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1-8603C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192205 | |||||||
chr5:64192245 | C | T | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-8563C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192245 | |||||||
chr5:64192285 | G | C | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-8523G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192285 | |||||||
chr5:64192286 | G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1-8522G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192286 | |||||||
chr5:64192335 | G | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1-8473G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192335 | |||||||
chr5:64192399 | C | T | 1 | a0001c0001t0003g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1-8409C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192399 | |||||||
chr5:64192449 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1-8359G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192449 | |||||||
chr5:64192541 | G | A | 90 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(87): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1-8267G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192541 | |||||||
chr5:64192542 | C | T | 3 | a0001c0001t0002g0027 a0001c0001t0003g0031 a0001c0001t0007g0030 |
3 | HG01123.hp2 HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1-8266C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192542 | |||||||
chr5:64192575 | G | A | 1 | a0001c0001t0003g0040 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1-8233G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192575 | |||||||
chr5:64192628 | C | T | 5 | a0001c0001t0001g0158 a0001c0001t0003g0144 a0001c0001t0003g0145 others(2): Show |
5 | HG02886.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-8180C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192628 | |||||||
chr5:64192791 | A | G | 2 | a0001c0001t0004g0102 a0001c0001t0004g0103 |
2 | NA18943.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1-8017A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192791 | |||||||
chr5:64192900 | C | CATGTATA others(49): Show |
1 | a0001c0001t0011g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1-7869_1-7868insTA others(54): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192900 | ||||||
chr5:64192900 | C | CATGTATA others(47): Show |
1 | a0001c0001t0011g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1-7869_1-7868insTA others(52): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192900 | ||||||
chr5:64192900 | C | CATGTATA others(45): Show |
1 | a0001c0001t0011g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1-7869_1-7868insTA others(50): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192900 | ||||||
chr5:64192903 | G | GTA | 14 | a0001c0001t0002g0183 a0001c0001t0002g0220 a0001c0001t0003g0007 others(11): Show |
14 | HG00408.hp1 HG00639.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1-7870_1-7869dupTA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATA | 30 | a0001c0001t0002g0080 a0001c0001t0002g0181 a0001c0001t0002g0203 others(27): Show |
31 | HG00099.hp2 HG00597.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1-7872_1-7869dupTA others(2): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATA | 12 | a0001c0001t0002g0039 a0001c0001t0002g0211 a0001c0001t0002g0213 others(9): Show |
12 | HG00323.hp2 HG00642.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1-7874_1-7869dupTA others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(1): Show |
7 | a0001c0001t0002g0202 a0001c0001t0002g0230 a0001c0001t0003g0041 others(4): Show |
7 | HG01261.hp1 HG01943.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-7876_1-7869dupTA others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(3): Show |
6 | a0001c0001t0002g0226 a0001c0001t0002g0229 a0001c0001t0003g0124 others(3): Show |
6 | HG00597.hp1 HG01168.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-7878_1-7869dupTA others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(5): Show |
11 | a0001c0001t0002g0003 a0001c0001t0002g0177 a0001c0001t0002g0227 others(8): Show |
11 | HG00741.hp1 HG01109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1-7880_1-7869dupTA others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(7): Show |
1 | a0001c0001t0029g0236 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1-7882_1-7869dupTA others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(9): Show |
8 | a0001c0001t0002g0223 a0001c0001t0005g0171 a0001c0001t0005g0232 others(5): Show |
8 | HG02630.hp2 HG02818.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-7884_1-7869dupTA others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(11): Show |
9 | a0001c0001t0002g0027 a0001c0001t0002g0174 a0001c0001t0002g0209 others(6): Show |
9 | HG00738.hp2 HG01516.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-7886_1-7869dupTA others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(13): Show |
3 | a0001c0001t0005g0173 a0001c0001t0007g0030 a0001c0001t0014g0056 |
3 | HG01123.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1-7888_1-7869dupTA others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(15): Show |
3 | a0001c0001t0002g0176 a0001c0001t0003g0199 a0001c0001t0012g0195 |
3 | HG01496.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1-7890_1-7869dupTA others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(17): Show |
5 | a0001c0001t0002g0178 a0001c0001t0002g0206 a0001c0001t0003g0194 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-7892_1-7869dupTA others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(19): Show |
2 | a0001c0001t0005g0235 a0001c0001t0014g0055 |
2 | NA19068.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-7894_1-7869dupTA others(24): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(21): Show |
2 | a0001c0001t0003g0077 a0001c0001t0012g0196 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1-7896_1-7869dupTA others(26): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATATAT others(23): Show |
2 | a0001c0001t0003g0005 a0001c0001t0003g0006 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1-7898_1-7869dupTA others(28): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTATGTAT others(21): Show |
1 | a0001c0001t0021g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1-7902_1-7901insGT others(26): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTGTATAT others(9): Show |
1 | a0001c0001t0002g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1-7904_1-7903insGT others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTGTATAT others(11): Show |
1 | a0001c0001t0002g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-7904_1-7903insGT others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTGTATAT others(17): Show |
2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1-7904_1-7903insGT others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTGTGTAT others(5): Show |
1 | a0002c0002t0008g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1-7904_1-7903insGT others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTGTGTAT others(11): Show |
2 | a0002c0002t0008g0062 a0002c0002t0008g0064 |
2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1-7904_1-7903insGT others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | G | GTGTGTGT others(25): Show |
1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1-7904_1-7903insGT others(30): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | GTATATA | G | 12 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(9): Show |
12 | HG01074.hp1 HG01074.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1-7874_1-7869delTA others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | GTATATAT others(1): Show |
G | 13 | a0001c0001t0001g0079 a0001c0001t0001g0111 a0001c0001t0001g0153 others(10): Show |
13 | HG00639.hp2 HG01081.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-7876_1-7869delTA others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | GTATATAT others(3): Show |
G | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0142 others(5): Show |
8 | HG00738.hp1 HG01515.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-7878_1-7869delTA others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | GTATATAT others(5): Show |
G | 46 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(43): Show |
46 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.1-7880_1-7869delTA others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192903 | GTATATAT others(7): Show |
G | 25 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(22): Show |
26 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1-7882_1-7869delTA others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | ||||||
chr5:64192911 | A | G | 6 | a0002c0002t0006g0068 a0002c0002t0006g0072 a0002c0002t0010g0057 others(3): Show |
6 | HG01074.hp2 HG01175.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-7897A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192911 | |||||||
chr5:64192913 | A | G | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1-7895A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192913 | |||||||
chr5:64192915 | A | G | 10 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(7): Show |
10 | HG01081.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1-7893A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192915 | |||||||
chr5:64192928 | TATATATA others(5): Show |
T | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1-7878_1-7867delTA others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192928 | ||||||
chr5:64192939 | A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1-7869_1-7868insTA others(19): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192939 | |||||||
chr5:64192940 | A | T | 19 | a0001c0001t0003g0041 a0001c0001t0005g0167 a0001c0001t0005g0168 others(16): Show |
19 | HG00597.hp1 HG01261.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1-7868A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192940 | |||||||
chr5:64192941 | A | T | 1 | a0001c0001t0013g0009 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1-7867A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192941 | |||||||
chr5:64193049 | C | A | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1-7759C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193049 | |||||||
chr5:64193058 | A | T | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-7750A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193058 | |||||||
chr5:64193446 | G | A | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1-7362G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193446 | |||||||
chr5:64193460 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-7348C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193460 | |||||||
chr5:64193518 | C | G | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1-7290C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193518 | |||||||
chr5:64193565 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1-7243C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193565 | |||||||
chr5:64193574 | A | T | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1-7234A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193574 | |||||||
chr5:64193773 | G | A | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1-7035G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193773 | |||||||
chr5:64193900 | A | G | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-6908A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193900 | |||||||
chr5:64194036 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1-6772G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194036 | |||||||
chr5:64194111 | G | A | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1-6697G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194111 | |||||||
chr5:64194341 | T | G | 3 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 |
3 | HG02109.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1-6467T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194341 | |||||||
chr5:64194354 | A | G | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-6454A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194354 | |||||||
chr5:64194396 | A | G | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1-6412A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194396 | |||||||
chr5:64194407 | T | A | 1 | a0001c0001t0003g0015 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1-6401T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194407 | |||||||
chr5:64194433 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0142 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1-6375T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194433 | |||||||
chr5:64194603 | T | G | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1-6205T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194603 | |||||||
chr5:64194728 | T | C | 2 | a0001c0001t0003g0011 a0001c0001t0007g0051 |
2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1-6080T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194728 | |||||||
chr5:64194912 | G | T | 199 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1-5896G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194912 | |||||||
chr5:64195231 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1-5577C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195231 | |||||||
chr5:64195273 | T | C | 139 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(136): Show |
140 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1-5535T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195273 | |||||||
chr5:64195275 | A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-5533A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195275 | |||||||
chr5:64195396 | C | T | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1-5412C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195396 | |||||||
chr5:64195439 | T | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-5369T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195439 | |||||||
chr5:64195516 | A | C | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1-5292A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195516 | |||||||
chr5:64195603 | A | G | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-5205A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195603 | |||||||
chr5:64195899 | T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1-4909T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195899 | |||||||
chr5:64195903 | A | G | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-4905A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195903 | |||||||
chr5:64196084 | A | C | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-4724A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196084 | |||||||
chr5:64196103 | T | C | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-4705T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196103 | |||||||
chr5:64196123 | T | C | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1-4685T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196123 | |||||||
chr5:64196190 | G | GT | 15 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0232 others(12): Show |
15 | HG00597.hp1 HG02922.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1-4605dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64196190 | ||||||
chr5:64196190 | GT | G | 108 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(105): Show |
109 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1-4605delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64196190 | ||||||
chr5:64196203 | T | C | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1-4605T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196203 | |||||||
chr5:64196203 | T | TC | 5 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-4602dupC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64196203 | ||||||
chr5:64196295 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0142 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1-4513T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196295 | |||||||
chr5:64196733 | C | G | 2 | a0001c0001t0002g0027 a0001c0001t0003g0031 |
2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1-4075C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196733 | |||||||
chr5:64197186 | A | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-3622A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197186 | |||||||
chr5:64197285 | A | G | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-3523A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197285 | |||||||
chr5:64197376 | G | A | 54 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(51): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1-3432G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197376 | |||||||
chr5:64197381 | C | T | 2 | a0002c0002t0008g0062 a0002c0002t0008g0064 |
2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1-3427C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197381 | |||||||
chr5:64197753 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-3055C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197753 | |||||||
chr5:64197843 | A | T | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1-2965A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197843 | |||||||
chr5:64197893 | A | G | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-2915A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197893 | |||||||
chr5:64197932 | G | A | 1 | a0001c0001t0020g0024 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1-2876G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197932 | |||||||
chr5:64197944 | A | G | 4 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(1): Show |
4 | HG02559.hp2 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2864A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197944 | |||||||
chr5:64198150 | A | G | 33 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0087 others(30): Show |
33 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1-2658A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198150 | |||||||
chr5:64198159 | T | C | 1 | a0001c0001t0003g0042 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1-2649T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198159 | |||||||
chr5:64198456 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-2352G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198456 | |||||||
chr5:64198818 | A | AT | 27 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(24): Show |
27 | HG00597.hp1 HG00741.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1-1976dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64198818 | ||||||
chr5:64198818 | A | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-1990A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198818 | |||||||
chr5:64198849 | C | T | 62 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(59): Show |
62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1-1959C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198849 | |||||||
chr5:64198884 | C | T | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-1924C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198884 | |||||||
chr5:64198897 | C | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1-1911C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198897 | |||||||
chr5:64198955 | A | G | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1-1853A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198955 | |||||||
chr5:64199043 | C | G | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1-1765C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64199043 | |||||||
chr5:64199059 | C | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-1749C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64199059 | |||||||
chr5:64199097 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0023g0165 |
3 | HG01081.hp2 HG01346.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1-1711C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64199097 | |||||||
chr5:64200208 | A | G | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1-600A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200208 | |||||||
chr5:64200319 | G | A | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1-489G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200319 | |||||||
chr5:64200332 | A | G | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-476A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200332 | |||||||
chr5:64200371 | C | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-437C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200371 | |||||||
chr5:64200623 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1-185G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200623 | |||||||
chr5:64200717 | G | A | 7 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-91G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200717 | |||||||
chr5:64200981 | A | G | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+39A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64200981 | |||||||
chr5:64200998 | A | G | 22 | a0001c0001t0002g0208 a0001c0001t0002g0212 a0001c0001t0002g0213 others(19): Show |
22 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.135+56A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64200998 | |||||||
chr5:64201030 | CTTA | C | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.135+92_135+94delTT others(1): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 64201030 | ||||||
chr5:64201040 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.135+98A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201040 | |||||||
chr5:64201251 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.135+309A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201251 | |||||||
chr5:64201319 | A | G | 4 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(1): Show |
4 | HG02559.hp2 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+377A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201319 | |||||||
chr5:64201324 | T | C | 1 | a0006c0007t0002g0205 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.135+382T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201324 | |||||||
chr5:64201353 | A | G | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.135+411A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201353 | |||||||
chr5:64201435 | A | C | 1 | a0001c0001t0003g0006 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.135+493A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201435 | |||||||
chr5:64201961 | G | A | 2 | a0001c0001t0003g0011 a0001c0001t0007g0051 |
2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.135+1019G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201961 | |||||||
chr5:64201994 | T | A | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.135+1052T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201994 | |||||||
chr5:64202009 | T | A | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.135+1067T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64202009 | |||||||
chr5:64202384 | A | G | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.135+1442A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64202384 | |||||||
chr5:64203205 | G | A | 1 | a0001c0001t0013g0013 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.135+2263G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64203205 | |||||||
chr5:64203410 | C | A | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+2468C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64203410 | |||||||
chr5:64204134 | T | C | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.135+3192T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64204134 | |||||||
chr5:64204396 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.135+3454T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64204396 | |||||||
chr5:64204730 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135+3788T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64204730 | |||||||
chr5:64204919 | G | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.135+3977G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64204919 | |||||||
chr5:64205055 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+4113C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205055 | |||||||
chr5:64205139 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.135+4197C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205139 | |||||||
chr5:64205344 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+4402A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205344 | |||||||
chr5:64205349 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+4407G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205349 | |||||||
chr5:64205706 | T | C | 139 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(136): Show |
140 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.135+4764T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205706 | |||||||
chr5:64205896 | A | T | 1 | a0001c0001t0003g0025 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.135+4954A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205896 | |||||||
chr5:64206191 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.135+5249C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64206191 | |||||||
chr5:64206569 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.136-5496C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64206569 | |||||||
chr5:64207022 | G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.136-5043G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207022 | |||||||
chr5:64207081 | T | C | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.136-4984T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207081 | |||||||
chr5:64207422 | T | C | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.136-4643T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207422 | |||||||
chr5:64207440 | T | G | 1 | a0001c0001t0003g0017 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136-4625T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207440 | |||||||
chr5:64207465 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.136-4600A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207465 | |||||||
chr5:64207502 | G | A | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.136-4563G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207502 | |||||||
chr5:64207678 | T | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.136-4387T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207678 | |||||||
chr5:64207950 | A | G | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.136-4115A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207950 | |||||||
chr5:64208155 | TTAAAA | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0027 |
2 | HG02698.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.136-3906_136-3902d others(7): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 64208155 | ||||||
chr5:64208403 | A | G | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-3662A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208403 | |||||||
chr5:64208553 | TCTTTA | T | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-3508_136-3504d others(7): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 64208553 | ||||||
chr5:64208710 | C | T | 1 | a0002c0002t0006g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.136-3355C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208710 | |||||||
chr5:64208759 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.136-3306A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208759 | |||||||
chr5:64208796 | T | G | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-3269T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208796 | |||||||
chr5:64208836 | AT | A | 10 | a0001c0001t0001g0111 a0001c0001t0001g0116 a0001c0001t0001g0117 others(7): Show |
10 | HG02055.hp2 HG02622.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-3228delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208836 | |||||||
chr5:64208995 | A | T | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.136-3070A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208995 | |||||||
chr5:64209031 | G | A | 6 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
6 | HG00738.hp1 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-3034G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209031 | |||||||
chr5:64209093 | C | T | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-2972C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209093 | |||||||
chr5:64209536 | GT | G | 45 | a0001c0001t0002g0003 a0001c0001t0002g0080 a0001c0001t0002g0174 others(42): Show |
45 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.136-2526delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 64209536 | ||||||
chr5:64209603 | A | G | 2 | a0001c0001t0012g0195 a0001c0001t0012g0196 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-2462A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209603 | |||||||
chr5:64209745 | T | C | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.136-2320T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209745 | |||||||
chr5:64209768 | G | A | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-2297G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209768 | |||||||
chr5:64209772 | T | G | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.136-2293T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209772 | |||||||
chr5:64209809 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG03491.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.136-2256G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209809 | |||||||
chr5:64210001 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.136-2064G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210001 | |||||||
chr5:64210131 | G | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-1934G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210131 | |||||||
chr5:64210187 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136-1878G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210187 | |||||||
chr5:64210320 | C | A | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.136-1745C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210320 | |||||||
chr5:64210553 | C | T | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-1512C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210553 | |||||||
chr5:64210801 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.136-1264A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210801 | |||||||
chr5:64210913 | A | G | 1 | a0001c0001t0003g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136-1152A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210913 | |||||||
chr5:64211053 | C | T | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-1012C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211053 | |||||||
chr5:64211171 | T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-894T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211171 | |||||||
chr5:64211180 | G | A | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.136-885G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211180 | |||||||
chr5:64211832 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.136-233A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211832 | |||||||
chr5:64211866 | C | G | 1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.136-199C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211866 | |||||||
chr5:64211880 | G | T | 1 | a0001c0001t0005g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.136-185G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211880 | |||||||
chr5:64211889 | A | T | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-176A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211889 | |||||||
chr5:64211994 | A | G | 9 | a0001c0001t0003g0077 a0001c0001t0003g0194 a0001c0001t0003g0198 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-71A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211994 | |||||||
chr5:64212044 | T | A | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-21T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64212044 | |||||||
chr5:64212053 | T | G | 1 | a0001c0001t0013g0009 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.136-12T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64212053 | |||||||
chr5:64212344 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.231+184G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212344 | |||||||
chr5:64212353 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.231+193C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212353 | |||||||
chr5:64212371 | CAT | C | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.231+213_231+214del others(2): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 64212371 | ||||||
chr5:64212377 | A | G | 1 | a0001c0001t0017g0020 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.231+217A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212377 | |||||||
chr5:64212418 | T | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+258T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212418 | |||||||
chr5:64212797 | T | C | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+637T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212797 | |||||||
chr5:64213089 | A | G | 1 | a0001c0001t0003g0017 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.232-469A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213089 | |||||||
chr5:64213132 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.232-426G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213132 | |||||||
chr5:64213258 | G | A | 1 | a0002c0002t0006g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.232-300G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213258 | |||||||
chr5:64213323 | T | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.232-235T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213323 | |||||||
chr5:64213353 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232-205A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213353 | |||||||
chr5:64213522 | G | A | 15 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(12): Show |
15 | HG01081.hp1 HG01175.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.232-36G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213522 | |||||||
chr5:64214947 | CATTT | C | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1191+433_1191+436d others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 64214947 | ||||||
chr5:64215280 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1191+763T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64215280 | |||||||
chr5:64215297 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1191+780A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64215297 | |||||||
chr5:64215758 | A | C | 1 | a0001c0001t0003g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1191+1241A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64215758 | |||||||
chr5:64215989 | G | GT | 17 | a0001c0001t0002g0183 a0001c0001t0003g0179 a0001c0001t0003g0198 others(14): Show |
17 | HG00597.hp1 HG02735.hp2 HG03492.hp2 others(14): Show |
intron_variant | MODIFIER | c.1192-1362dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 64215989 | ||||||
chr5:64215989 | G | GTT | 7 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1192-1363_1192-136 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 64215989 | ||||||
chr5:64215989 | GT | G | 28 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(25): Show |
29 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1192-1362delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 64215989 | ||||||
chr5:64216002 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1192-1359A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216002 | |||||||
chr5:64216044 | G | A | 7 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1192-1317G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216044 | |||||||
chr5:64216076 | C | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1192-1285C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216076 | |||||||
chr5:64216609 | A | G | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1192-752A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216609 | |||||||
chr5:64216712 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1192-649C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216712 | |||||||
chr5:64216735 | G | A | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-626G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216735 | |||||||
chr5:64216903 | G | A | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-458G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216903 | |||||||
chr5:64217040 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1192-321A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64217040 | |||||||
chr5:64217042 | T | A | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1192-319T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64217042 | |||||||
chr5:64217272 | A | G | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1192-89A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64217272 | |||||||
chr5:64217417 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+21A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217417 | |||||||
chr5:64217442 | A | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1227+46A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217442 | |||||||
chr5:64217768 | A | G | 1 | a0001c0001t0002g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1227+372A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217768 | |||||||
chr5:64217923 | C | T | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+527C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217923 | |||||||
chr5:64217942 | A | C | 61 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1227+546A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217942 | |||||||
chr5:64217958 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1227+562T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217958 | |||||||
chr5:64218044 | T | C | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+648T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218044 | |||||||
chr5:64218100 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1227+704T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218100 | |||||||
chr5:64218129 | C | T | 124 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(121): Show |
125 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1227+733C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218129 | |||||||
chr5:64218203 | G | A | 44 | a0001c0001t0002g0003 a0001c0001t0002g0080 a0001c0001t0002g0174 others(41): Show |
44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+807G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218203 | |||||||
chr5:64218229 | C | T | 119 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(116): Show |
120 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1227+833C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218229 | |||||||
chr5:64218325 | A | G | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+929A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218325 | |||||||
chr5:64218498 | A | AC | 6 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0002g0208 others(3): Show |
6 | HG00733.hp1 HG01361.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+1106dupC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64218498 | ||||||
chr5:64218558 | T | C | 4 | a0002c0002t0006g0065 a0002c0002t0006g0069 a0002c0002t0006g0070 others(1): Show |
4 | HG01081.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+1162T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218558 | |||||||
chr5:64218689 | C | T | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1227+1293C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218689 | |||||||
chr5:64218921 | A | T | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1227+1525A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218921 | |||||||
chr5:64218924 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1227+1528C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218924 | |||||||
chr5:64219187 | G | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+1791G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219187 | |||||||
chr5:64219201 | G | A | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+1805G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219201 | |||||||
chr5:64219223 | GT | G | 146 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(143): Show |
147 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1227+1830delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64219223 | ||||||
chr5:64219368 | A | AT | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+1978dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64219368 | ||||||
chr5:64219531 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1227+2135A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219531 | |||||||
chr5:64219575 | C | T | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+2179C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219575 | |||||||
chr5:64219643 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1227+2247A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219643 | |||||||
chr5:64219680 | AT | A | 119 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(116): Show |
120 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1227+2296delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64219680 | ||||||
chr5:64219768 | C | A | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+2372C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219768 | |||||||
chr5:64219811 | G | A | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1227+2415G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219811 | |||||||
chr5:64220092 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1227+2696C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220092 | |||||||
chr5:64220181 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1227+2785A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220181 | |||||||
chr5:64220257 | T | C | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+2861T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220257 | |||||||
chr5:64220286 | AATTT | A | 5 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+2895_1227+289 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64220286 | ||||||
chr5:64220420 | G | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+3024G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220420 | |||||||
chr5:64220622 | A | T | 1 | a0001c0001t0003g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+3226A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220622 | |||||||
chr5:64220737 | C | G | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+3341C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220737 | |||||||
chr5:64220863 | A | T | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+3467A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220863 | |||||||
chr5:64220869 | A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+3473A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220869 | |||||||
chr5:64220934 | A | T | 8 | a0001c0001t0002g0204 a0001c0001t0002g0208 a0001c0001t0002g0212 others(5): Show |
8 | HG01243.hp1 HG01928.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+3538A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220934 | |||||||
chr5:64222211 | G | C | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1227+4815G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222211 | |||||||
chr5:64222250 | G | A | 1 | a0001c0001t0005g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1227+4854G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222250 | |||||||
chr5:64222289 | G | GT | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+4902dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64222289 | ||||||
chr5:64222326 | G | A | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1227+4930G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222326 | |||||||
chr5:64222350 | A | G | 1 | a0001c0001t0003g0042 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1227+4954A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222350 | |||||||
chr5:64222395 | T | A | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+4999T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222395 | |||||||
chr5:64222438 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1227+5042G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222438 | |||||||
chr5:64222441 | A | G | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+5045A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222441 | |||||||
chr5:64222492 | G | A | 2 | a0001c0001t0019g0166 a0001c0001t0026g0247 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1227+5096G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222492 | |||||||
chr5:64222526 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1227+5130C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222526 | |||||||
chr5:64222548 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1227+5152A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222548 | |||||||
chr5:64222810 | A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+5414A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222810 | |||||||
chr5:64222941 | CAG | C | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+5548_1227+554 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64222941 | ||||||
chr5:64223363 | T | G | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+5967T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223363 | |||||||
chr5:64223556 | C | CAGAG | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+6160_1227+616 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223556 | |||||||
chr5:64223643 | C | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+6247C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223643 | |||||||
chr5:64223644 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+6248A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223644 | |||||||
chr5:64223684 | C | CT | 5 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+6297dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64223684 | ||||||
chr5:64223801 | CAAGTATT others(3): Show |
C | 1 | a0001c0001t0005g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1227+6406_1227+641 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223801 | |||||||
chr5:64223835 | A | G | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+6439A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223835 | |||||||
chr5:64223837 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1227+6441C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223837 | |||||||
chr5:64223861 | G | A | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+6465G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223861 | |||||||
chr5:64223977 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+6581G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223977 | |||||||
chr5:64223990 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1227+6594G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223990 | |||||||
chr5:64224062 | G | GGT | 75 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0111 others(72): Show |
75 | HG00099.hp2 HG00408.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.1227+6707_1227+670 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | ||||||
chr5:64224062 | G | GGTGT | 28 | a0001c0001t0001g0079 a0001c0001t0001g0113 a0001c0001t0001g0115 others(25): Show |
29 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227+6705_1227+670 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | ||||||
chr5:64224062 | G | GGTGTGT | 3 | a0001c0001t0001g0133 a0001c0001t0001g0160 a0001c0001t0004g0091 |
3 | HG01109.hp2 HG03927.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1227+6703_1227+670 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | ||||||
chr5:64224062 | GGT | G | 42 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0085 others(39): Show |
42 | HG00323.hp1 HG00597.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1227+6707_1227+670 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | ||||||
chr5:64224062 | GGTGT | G | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0009g0036 others(1): Show |
4 | HG02257.hp1 HG03492.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+6705_1227+670 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | ||||||
chr5:64224062 | GGTGTGT | G | 4 | a0001c0001t0002g0229 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+6703_1227+670 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | ||||||
chr5:64224062 | GGTGTGTG others(5): Show |
G | 2 | a0001c0001t0002g0208 a0006c0007t0002g0205 |
2 | HG02004.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1227+6697_1227+670 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | ||||||
chr5:64224065 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1227+6669G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224065 | |||||||
chr5:64224270 | G | A | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1227+6874G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224270 | |||||||
chr5:64224478 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1227+7082C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224478 | |||||||
chr5:64224678 | A | G | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1227+7282A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224678 | |||||||
chr5:64224722 | T | C | 1 | a0001c0001t0002g0229 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1227+7326T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224722 | |||||||
chr5:64224886 | GCTTGCTC others(16): Show |
G | 1 | a0001c0001t0002g0207 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1227+7491_1227+751 others(27): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224886 | |||||||
chr5:64225078 | T | A | 61 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1227+7682T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225078 | |||||||
chr5:64225121 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+7725C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225121 | |||||||
chr5:64225164 | A | T | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1227+7768A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225164 | |||||||
chr5:64225252 | A | G | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+7856A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225252 | |||||||
chr5:64225345 | A | AGTGAGGA others(147): Show |
1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+7972_1227+797 others(158): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225345 | ||||||
chr5:64225369 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+7973G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225369 | |||||||
chr5:64225369 | G | GCCCTGTC others(147): Show |
86 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(83): Show |
87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1227+8126_1227+812 others(158): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225369 | ||||||
chr5:64225369 | G | GCCCTGTC others(147): Show |
1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1227+8044_1227+804 others(158): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225369 | ||||||
chr5:64225428 | A | G | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+8032A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225428 | |||||||
chr5:64225430 | C | CGCCTCTG others(147): Show |
1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1227+8126_1227+812 others(158): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225430 | ||||||
chr5:64225441 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1227+8045A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225441 | |||||||
chr5:64225445 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1227+8049G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225445 | |||||||
chr5:64225452 | G | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+8056G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225452 | |||||||
chr5:64225489 | CCGTCTGG others(32): Show |
C | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1227+8122_1227+816 others(43): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225489 | ||||||
chr5:64225491 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1227+8095G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225491 | |||||||
chr5:64225567 | G | A | 3 | a0001c0001t0002g0003 a0001c0001t0002g0177 a0001c0001t0009g0182 |
3 | HG01109.hp1 HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1227+8171G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225567 | |||||||
chr5:64225640 | C | T | 29 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0004g0002 others(26): Show |
30 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+8244C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225640 | |||||||
chr5:64225672 | T | TGCCCCGT others(30): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1227+8314_1227+835 others(41): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225672 | ||||||
chr5:64225696 | G | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+8300G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225696 | |||||||
chr5:64225774 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+8378C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225774 | |||||||
chr5:64225775 | T | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+8379T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225775 | |||||||
chr5:64225825 | G | A | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+8429G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225825 | |||||||
chr5:64225829 | C | T | 1 | a0002c0002t0006g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1227+8433C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225829 | |||||||
chr5:64225844 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1227+8448G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225844 | |||||||
chr5:64225884 | T | G | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+8488T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225884 | |||||||
chr5:64225895 | G | A | 4 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0010g0076 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+8499G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225895 | |||||||
chr5:64225935 | G | A | 1 | a0001c0001t0004g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1227+8539G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225935 | |||||||
chr5:64225948 | T | TGCCCCGT others(67): Show |
1 | a0001c0001t0003g0016 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1227+8585_1227+865 others(78): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225948 | ||||||
chr5:64225972 | G | A | 1 | a0001c0001t0003g0022 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1227+8576G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225972 | |||||||
chr5:64225981 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1227+8585C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225981 | |||||||
chr5:64226055 | T | C | 2 | a0001c0001t0002g0222 a0001c0003t0002g0246 |
2 | HG02040.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1227+8659T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226055 | |||||||
chr5:64226065 | A | G | 1 | a0001c0001t0007g0023 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227+8669A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226065 | |||||||
chr5:64226074 | G | A | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+8678G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226074 | |||||||
chr5:64226203 | A | G | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+8807A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226203 | |||||||
chr5:64226460 | G | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+9064G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226460 | |||||||
chr5:64226471 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1227+9075G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226471 | |||||||
chr5:64226540 | C | A | 53 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(50): Show |
53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1227+9144C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226540 | |||||||
chr5:64226626 | C | G | 1 | a0001c0001t0003g0042 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1227+9230C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226626 | |||||||
chr5:64226665 | TA | T | 5 | a0001c0001t0001g0162 a0001c0001t0002g0222 a0001c0001t0003g0016 others(2): Show |
5 | HG01168.hp1 HG02040.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227+9282delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64226665 | ||||||
chr5:64226678 | A | G | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+9282A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226678 | |||||||
chr5:64226746 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+9350G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226746 | |||||||
chr5:64226768 | C | T | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+9372C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226768 | |||||||
chr5:64226892 | G | A | 1 | a0001c0001t0003g0016 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1227+9496G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226892 | |||||||
chr5:64226901 | C | T | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+9505C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226901 | |||||||
chr5:64227089 | C | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+9693C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227089 | |||||||
chr5:64227130 | G | A | 8 | a0001c0001t0004g0002 a0001c0001t0004g0086 a0001c0001t0004g0092 others(5): Show |
9 | HG01243.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1227+9734G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227130 | |||||||
chr5:64227207 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1227+9811G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227207 | |||||||
chr5:64227368 | C | T | 1 | a0002c0002t0008g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1227+9972C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227368 | |||||||
chr5:64227459 | G | A | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1227+10063G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227459 | |||||||
chr5:64227539 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0142 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1227+10143C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227539 | |||||||
chr5:64227587 | A | G | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+10191A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227587 | |||||||
chr5:64227611 | C | T | 3 | a0001c0001t0005g0235 a0001c0001t0005g0239 a0001c0001t0029g0236 |
3 | NA18966.hp1 NA19068.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1227+10215C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227611 | |||||||
chr5:64227708 | T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+10312T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227708 | |||||||
chr5:64227732 | T | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+10336T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227732 | |||||||
chr5:64227856 | C | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+10460C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227856 | |||||||
chr5:64228283 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0003g0144 a0001c0001t0003g0145 |
3 | HG02886.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1227+10887G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64228283 | |||||||
chr5:64228871 | A | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+11475A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64228871 | |||||||
chr5:64228915 | C | CT | 15 | a0001c0001t0001g0112 a0001c0001t0001g0132 a0001c0001t0001g0142 others(12): Show |
15 | HG00597.hp2 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1227+11543dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64228915 | ||||||
chr5:64228915 | CT | C | 40 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(37): Show |
40 | HG00597.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1227+11543delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64228915 | ||||||
chr5:64228915 | CTT | C | 30 | a0001c0001t0004g0002 a0001c0001t0004g0086 a0001c0001t0004g0092 others(27): Show |
31 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1227+11542_1227+11 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64228915 | ||||||
chr5:64228915 | CTTT | C | 16 | a0001c0001t0019g0166 a0001c0001t0027g0060 a0002c0002t0006g0065 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1227+11541_1227+11 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64228915 | ||||||
chr5:64229216 | C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+11820C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229216 | |||||||
chr5:64229244 | A | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+11848A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229244 | |||||||
chr5:64229345 | A | T | 1 | a0001c0001t0003g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1227+11949A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229345 | |||||||
chr5:64229878 | G | T | 9 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0134 others(6): Show |
9 | HG00408.hp2 HG02074.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1227+12482G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229878 | |||||||
chr5:64229968 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1227+12572G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229968 | |||||||
chr5:64230051 | ATTTTTCT others(2): Show |
A | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+12660_1227+12 others(15): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64230051 | ||||||
chr5:64230298 | A | C | 1 | a0001c0001t0002g0231 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1227+12902A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230298 | |||||||
chr5:64230347 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1227+12951G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230347 | |||||||
chr5:64230348 | G | GACATAAC others(39): Show |
1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1227+12952_1227+12 others(52): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230348 | |||||||
chr5:64230415 | A | G | 3 | a0001c0001t0003g0012 a0001c0001t0003g0022 a0001c0001t0003g0045 |
3 | NA18964.hp1 NA18983.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1227+13019A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230415 | |||||||
chr5:64230680 | GGCCTCTT others(4): Show |
G | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1227+13286_1227+13 others(17): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64230680 | ||||||
chr5:64230734 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+13338G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230734 | |||||||
chr5:64230965 | G | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+13569G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230965 | |||||||
chr5:64231016 | C | G | 10 | a0001c0001t0001g0111 a0001c0001t0001g0116 a0001c0001t0001g0117 others(7): Show |
10 | HG02055.hp2 HG02622.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+13620C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64231016 | |||||||
chr5:64231138 | A | T | 1 | a0001c0001t0002g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1227+13742A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64231138 | |||||||
chr5:64231219 | A | C | 1 | a0001c0001t0007g0034 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1227+13823A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64231219 | |||||||
chr5:64231298 | G | A | 2 | a0002c0002t0006g0074 a0002c0002t0006g0075 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1227+13902G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64231298 | |||||||
chr5:64232001 | T | G | 236 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1227+14605T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232001 | |||||||
chr5:64232031 | T | G | 1 | a0001c0001t0003g0022 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1227+14635T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232031 | |||||||
chr5:64232748 | A | G | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+15352A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232748 | |||||||
chr5:64232829 | A | T | 1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1227+15433A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232829 | |||||||
chr5:64232912 | A | T | 3 | a0001c0001t0002g0027 a0001c0001t0003g0031 a0001c0001t0007g0030 |
3 | HG01123.hp2 HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1227+15516A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232912 | |||||||
chr5:64233216 | G | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+15820G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233216 | |||||||
chr5:64233447 | C | T | 90 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(87): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1227+16051C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233447 | |||||||
chr5:64233535 | T | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+16139T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233535 | |||||||
chr5:64233615 | A | G | 6 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
6 | HG00738.hp1 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+16219A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233615 | |||||||
chr5:64233618 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1227+16222A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233618 | |||||||
chr5:64233634 | T | C | 1 | a0001c0001t0003g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1227+16238T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233634 | |||||||
chr5:64233947 | A | G | 5 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0191 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+16551A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233947 | |||||||
chr5:64234021 | T | C | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+16625T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234021 | |||||||
chr5:64234123 | C | T | 7 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+16727C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234123 | |||||||
chr5:64234269 | T | C | 1 | a0001c0001t0003g0015 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1227+16873T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234269 | |||||||
chr5:64234427 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1227+17031G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234427 | |||||||
chr5:64234467 | AAAATAAA others(3): Show |
A | 1 | a0002c0002t0006g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1227+17079_1227+17 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234467 | ||||||
chr5:64234524 | C | G | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1227+17128C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234524 | |||||||
chr5:64234575 | GTTCTTTT others(8): Show |
G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+17182_1227+17 others(21): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234575 | ||||||
chr5:64234578 | C | CT | 28 | a0001c0001t0002g0003 a0001c0001t0002g0027 a0001c0001t0002g0039 others(25): Show |
28 | HG00642.hp1 HG00733.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+17221dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | C | CTT | 8 | a0001c0001t0002g0177 a0001c0001t0002g0226 a0001c0001t0002g0230 others(5): Show |
8 | HG00741.hp1 HG01109.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1227+17220_1227+17 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | C | CTTT | 12 | a0001c0001t0003g0010 a0001c0001t0003g0026 a0001c0001t0003g0048 others(9): Show |
12 | HG00408.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1227+17219_1227+17 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | C | CTTTT | 10 | a0001c0001t0002g0183 a0001c0001t0003g0012 a0001c0001t0003g0045 others(7): Show |
10 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+17218_1227+17 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | C | CTTTTTTT others(3): Show |
1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1227+17212_1227+17 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | C | CTTTTTTT others(4): Show |
2 | a0002c0002t0010g0058 a0002c0002t0018g0059 |
2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1227+17211_1227+17 others(17): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | C | CTTTTTTT others(5): Show |
1 | a0002c0002t0006g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1227+17210_1227+17 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CT | C | 10 | a0001c0001t0002g0206 a0001c0001t0002g0210 a0001c0001t0002g0212 others(7): Show |
10 | HG00099.hp2 HG00741.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1227+17221delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTT | C | 14 | a0001c0001t0002g0187 a0001c0001t0002g0202 a0001c0001t0002g0203 others(11): Show |
14 | HG00597.hp2 HG01243.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1227+17220_1227+17 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0005g0234 a0001c0001t0005g0239 a0001c0001t0005g0244 |
3 | NA18942.hp2 NA19063.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1227+17212_1227+17 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTTTTTTT others(4): Show |
C | 16 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(13): Show |
16 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1227+17211_1227+17 others(17): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTTTTTTT others(5): Show |
C | 11 | a0001c0001t0002g0227 a0001c0001t0005g0172 a0001c0001t0005g0185 others(8): Show |
11 | HG01891.hp2 HG02559.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+17210_1227+17 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0003g0077 a0001c0001t0028g0193 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1227+17209_1227+17 others(19): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0160 a0001c0001t0004g0107 |
2 | HG01109.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1227+17207_1227+17 others(21): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTTTTTTT others(9): Show |
C | 83 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(80): Show |
84 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1227+17206_1227+17 others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTTTTTTT others(10): Show |
C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0138 others(3): Show |
6 | HG00099.hp1 HG01517.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+17205_1227+17 others(23): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234578 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0002g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1227+17199_1227+17 others(29): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | ||||||
chr5:64234599 | T | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+17203T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234599 | |||||||
chr5:64234603 | T | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+17207T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234603 | |||||||
chr5:64234745 | G | A | 11 | a0001c0001t0002g0027 a0001c0001t0003g0004 a0001c0001t0003g0005 others(8): Show |
11 | HG00642.hp2 HG00741.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+17349G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234745 | |||||||
chr5:64234760 | T | G | 1 | a0001c0001t0007g0023 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227+17364T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234760 | |||||||
chr5:64234800 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+17404C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234800 | |||||||
chr5:64234859 | G | A | 125 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(122): Show |
126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1227+17463G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234859 | |||||||
chr5:64234948 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1227+17552T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234948 | |||||||
chr5:64235316 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1227+17920T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64235316 | |||||||
chr5:64235532 | T | A | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+18136T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64235532 | |||||||
chr5:64235594 | A | G | 1 | a0001c0001t0007g0023 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227+18198A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64235594 | |||||||
chr5:64235605 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0162 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1227+18209C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64235605 | |||||||
chr5:64236004 | G | A | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1227+18608G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236004 | |||||||
chr5:64236372 | C | A | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1227+18976C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236372 | |||||||
chr5:64236435 | C | G | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1227+19039C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236435 | |||||||
chr5:64236716 | C | T | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+19320C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236716 | |||||||
chr5:64236744 | A | G | 2 | a0001c0001t0005g0188 a0001c0001t0024g0192 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1227+19348A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236744 | |||||||
chr5:64236792 | A | C | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1227+19396A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236792 | |||||||
chr5:64236902 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1227+19506C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236902 | |||||||
chr5:64236958 | A | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+19562A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236958 | |||||||
chr5:64237265 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+19869G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237265 | |||||||
chr5:64237569 | G | C | 1 | a0001c0001t0005g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1227+20173G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237569 | |||||||
chr5:64237639 | T | G | 4 | a0001c0001t0004g0078 a0001c0001t0004g0094 a0001c0001t0004g0101 others(1): Show |
4 | NA18960.hp1 NA18964.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+20243T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237639 | |||||||
chr5:64237851 | C | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+20455C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237851 | |||||||
chr5:64237901 | C | T | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+20505C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237901 | |||||||
chr5:64238210 | T | A | 190 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1227+20814T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238210 | |||||||
chr5:64238357 | G | T | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1227+20961G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238357 | |||||||
chr5:64238370 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1227+20974G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238370 | |||||||
chr5:64238734 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1227+21338C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238734 | |||||||
chr5:64238794 | G | A | 2 | a0001c0001t0013g0009 a0001c0001t0020g0024 |
2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1227+21398G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238794 | |||||||
chr5:64238797 | G | A | 1 | a0001c0001t0017g0020 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1227+21401G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238797 | |||||||
chr5:64238838 | A | G | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1227+21442A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238838 | |||||||
chr5:64238953 | C | T | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+21557C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238953 | |||||||
chr5:64239018 | A | G | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+21622A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239018 | |||||||
chr5:64239137 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1227+21741T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239137 | |||||||
chr5:64239447 | T | C | 44 | a0001c0001t0002g0003 a0001c0001t0002g0080 a0001c0001t0002g0174 others(41): Show |
44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+22051T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239447 | |||||||
chr5:64239515 | G | A | 5 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0097 others(2): Show |
5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+22119G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239515 | |||||||
chr5:64239532 | A | G | 4 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0010g0076 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+22136A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239532 | |||||||
chr5:64239806 | C | T | 3 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 |
3 | HG02109.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1227+22410C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239806 | |||||||
chr5:64239874 | A | G | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+22478A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239874 | |||||||
chr5:64240036 | T | G | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1227+22640T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240036 | |||||||
chr5:64240109 | T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1227+22713T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240109 | |||||||
chr5:64240419 | A | T | 5 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+23023A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240419 | |||||||
chr5:64240466 | A | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+23070A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240466 | |||||||
chr5:64240660 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1227+23264C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240660 | |||||||
chr5:64240764 | A | G | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+23368A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240764 | |||||||
chr5:64240810 | T | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+23414T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240810 | |||||||
chr5:64240927 | A | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+23531A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240927 | |||||||
chr5:64240965 | T | C | 245 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1227+23569T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240965 | |||||||
chr5:64241046 | T | C | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1227+23650T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241046 | |||||||
chr5:64241100 | C | T | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1227+23704C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241100 | |||||||
chr5:64241487 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0161 |
2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1227+24091G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241487 | |||||||
chr5:64241608 | T | C | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+24212T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241608 | |||||||
chr5:64241611 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1227+24215C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241611 | |||||||
chr5:64241846 | G | T | 6 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+24450G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241846 | |||||||
chr5:64241855 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+24459G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241855 | |||||||
chr5:64242016 | T | G | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+24620T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64242016 | |||||||
chr5:64242106 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1227+24710C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64242106 | |||||||
chr5:64242325 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1227+24929G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64242325 | |||||||
chr5:64242434 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+25038A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64242434 | |||||||
chr5:64243251 | C | T | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1227+25855C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64243251 | |||||||
chr5:64243306 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1227+25910C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64243306 | |||||||
chr5:64243435 | G | A | 1 | a0001c0001t0003g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1227+26039G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64243435 | |||||||
chr5:64243626 | A | T | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1227+26230A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64243626 | |||||||
chr5:64244062 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1227+26666G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244062 | |||||||
chr5:64244067 | C | T | 5 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+26671C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244067 | |||||||
chr5:64244322 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+26926C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244322 | |||||||
chr5:64244361 | T | A | 1 | a0001c0001t0007g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1227+26965T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244361 | |||||||
chr5:64244397 | AC | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+27003delC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64244397 | ||||||
chr5:64244410 | G | GA | 62 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(59): Show |
62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1227+27022dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64244410 | ||||||
chr5:64244719 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+27323A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244719 | |||||||
chr5:64244821 | G | T | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1227+27425G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244821 | |||||||
chr5:64244858 | A | G | 19 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(16): Show |
19 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1227+27462A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244858 | |||||||
chr5:64244906 | C | T | 11 | a0001c0001t0003g0077 a0001c0001t0003g0144 a0001c0001t0003g0145 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27510C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244906 | |||||||
chr5:64244907 | A | T | 11 | a0001c0001t0003g0077 a0001c0001t0003g0144 a0001c0001t0003g0145 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27511A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244907 | |||||||
chr5:64244908 | A | T | 11 | a0001c0001t0003g0077 a0001c0001t0003g0144 a0001c0001t0003g0145 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27512A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244908 | |||||||
chr5:64244910 | CCAGAAGA others(3): Show |
C | 11 | a0001c0001t0003g0077 a0001c0001t0003g0144 a0001c0001t0003g0145 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27515_1227+27 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244910 | |||||||
chr5:64244921 | T | A | 11 | a0001c0001t0003g0077 a0001c0001t0003g0144 a0001c0001t0003g0145 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27525T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244921 | |||||||
chr5:64245071 | C | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1227+27675C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245071 | |||||||
chr5:64245407 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1227+28011C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245407 | |||||||
chr5:64245601 | A | C | 5 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0097 others(2): Show |
5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+28205A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245601 | |||||||
chr5:64245625 | T | C | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00323.hp1 HG01106.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1227+28229T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245625 | |||||||
chr5:64245659 | A | G | 1 | a0001c0001t0015g0033 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1227+28263A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245659 | |||||||
chr5:64245798 | G | A | 245 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1227+28402G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245798 | |||||||
chr5:64245799 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1227+28403A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245799 | |||||||
chr5:64246292 | C | T | 21 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0204 others(18): Show |
21 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1227+28896C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246292 | |||||||
chr5:64246487 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1227+29091A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246487 | |||||||
chr5:64246653 | T | C | 210 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(207): Show |
211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1227+29257T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246653 | |||||||
chr5:64246738 | G | A | 1 | a0001c0001t0004g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1227+29342G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246738 | |||||||
chr5:64246741 | T | A | 1 | a0001c0001t0004g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1227+29345T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246741 | |||||||
chr5:64246837 | G | T | 1 | a0001c0001t0002g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1227+29441G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246837 | |||||||
chr5:64247101 | T | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+29705T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247101 | |||||||
chr5:64247239 | T | C | 146 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(143): Show |
147 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1227+29843T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247239 | |||||||
chr5:64247375 | G | A | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+29979G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247375 | |||||||
chr5:64247418 | C | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+30022C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247418 | |||||||
chr5:64247705 | A | C | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+30309A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247705 | |||||||
chr5:64247710 | A | G | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+30314A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247710 | |||||||
chr5:64247813 | C | T | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+30417C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247813 | |||||||
chr5:64247830 | G | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+30434G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247830 | |||||||
chr5:64247897 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0023g0165 |
3 | HG01081.hp2 HG01346.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1227+30501G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247897 | |||||||
chr5:64247946 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+30550A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247946 | |||||||
chr5:64247954 | A | T | 6 | a0001c0001t0002g0208 a0001c0001t0002g0212 a0001c0001t0002g0213 others(3): Show |
6 | HG01243.hp1 HG01928.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+30558A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247954 | |||||||
chr5:64248056 | C | T | 3 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 |
3 | HG00408.hp1 HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1227+30660C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248056 | |||||||
chr5:64248061 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+30665A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248061 | |||||||
chr5:64248201 | A | G | 1 | a0001c0001t0005g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1227+30805A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248201 | |||||||
chr5:64248260 | G | A | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+30864G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248260 | |||||||
chr5:64248353 | A | G | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+30957A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248353 | |||||||
chr5:64248445 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+31049C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248445 | |||||||
chr5:64248582 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1227+31186C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248582 | |||||||
chr5:64248861 | C | G | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1227+31465C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248861 | |||||||
chr5:64248968 | G | C | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+31572G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248968 | |||||||
chr5:64249184 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0003g0010 |
2 | HG00639.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1227+31788G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249184 | |||||||
chr5:64249187 | G | T | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+31791G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249187 | |||||||
chr5:64249252 | T | TA | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+31863dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64249252 | ||||||
chr5:64249276 | T | C | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1227+31880T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249276 | |||||||
chr5:64249375 | C | T | 1 | a0001c0001t0002g0217 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1227+31979C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249375 | |||||||
chr5:64249437 | C | T | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1227+32041C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249437 | |||||||
chr5:64249492 | G | A | 3 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 |
3 | HG00408.hp1 HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1227+32096G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249492 | |||||||
chr5:64249543 | T | TAAGAAAT others(311): Show |
1 | a0001c0001t0005g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1227+32158_1227+32 others(324): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64249543 | ||||||
chr5:64249543 | T | TAAGAAAT others(312): Show |
1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1227+32158_1227+32 others(325): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64249543 | ||||||
chr5:64249655 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1227+32259A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249655 | |||||||
chr5:64249698 | T | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+32302T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249698 | |||||||
chr5:64250034 | G | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+32638G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250034 | |||||||
chr5:64250111 | A | C | 1 | a0001c0001t0004g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1227+32715A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250111 | |||||||
chr5:64250255 | T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1227+32859T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250255 | |||||||
chr5:64250265 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1227+32869A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250265 | |||||||
chr5:64250485 | G | T | 60 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(57): Show |
60 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1227+33089G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250485 | |||||||
chr5:64250538 | G | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+33142G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250538 | |||||||
chr5:64250670 | A | C | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+33274A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250670 | |||||||
chr5:64250780 | A | T | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+33384A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250780 | |||||||
chr5:64250820 | A | G | 7 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+33424A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250820 | |||||||
chr5:64250957 | C | A | 2 | a0001c0001t0003g0011 a0001c0001t0007g0051 |
2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1227+33561C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250957 | |||||||
chr5:64251044 | G | A | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+33648G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251044 | |||||||
chr5:64251056 | A | G | 1 | a0002c0002t0006g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1227+33660A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251056 | |||||||
chr5:64251386 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1227+33990C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251386 | |||||||
chr5:64251522 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1227+34126G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251522 | |||||||
chr5:64251596 | T | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+34200T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251596 | |||||||
chr5:64251634 | C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+34238C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251634 | |||||||
chr5:64251638 | A | T | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1227+34242A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251638 | |||||||
chr5:64251663 | C | T | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1227+34267C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251663 | |||||||
chr5:64251684 | G | A | 119 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(116): Show |
120 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1227+34288G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251684 | |||||||
chr5:64251733 | C | G | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0198 others(3): Show |
6 | HG02559.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+34337C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251733 | |||||||
chr5:64251746 | T | A | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+34350T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251746 | |||||||
chr5:64251973 | A | G | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+34577A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251973 | |||||||
chr5:64251978 | T | C | 8 | a0001c0001t0004g0002 a0001c0001t0004g0086 a0001c0001t0004g0092 others(5): Show |
9 | HG01243.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1227+34582T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251978 | |||||||
chr5:64252029 | A | G | 1 | a0001c0001t0007g0023 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227+34633A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252029 | |||||||
chr5:64252511 | A | G | 1 | a0001c0001t0020g0024 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1227+35115A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252511 | |||||||
chr5:64252554 | T | C | 44 | a0001c0001t0002g0003 a0001c0001t0002g0080 a0001c0001t0002g0174 others(41): Show |
44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+35158T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252554 | |||||||
chr5:64252562 | C | T | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+35166C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252562 | |||||||
chr5:64252839 | G | A | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1227+35443G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252839 | |||||||
chr5:64252982 | G | A | 1 | a0001c0001t0003g0042 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1227+35586G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252982 | |||||||
chr5:64253244 | A | G | 1 | a0001c0001t0022g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1227+35848A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253244 | |||||||
chr5:64253264 | A | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+35868A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253264 | |||||||
chr5:64253370 | GT | G | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+35975delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253370 | |||||||
chr5:64253502 | C | A | 1 | a0001c0001t0002g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1227+36106C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253502 | |||||||
chr5:64253593 | T | A | 1 | a0001c0001t0003g0045 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1227+36197T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253593 | |||||||
chr5:64253951 | A | G | 44 | a0001c0001t0002g0003 a0001c0001t0002g0080 a0001c0001t0002g0174 others(41): Show |
44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+36555A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253951 | |||||||
chr5:64253982 | A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+36586A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253982 | |||||||
chr5:64254187 | T | C | 9 | a0001c0001t0002g0039 a0001c0001t0007g0001 a0001c0001t0007g0032 others(6): Show |
10 | HG00323.hp2 HG01175.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1227+36791T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254187 | |||||||
chr5:64254202 | G | A | 1 | a0001c0001t0003g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1227+36806G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254202 | |||||||
chr5:64254360 | T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+36964T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254360 | |||||||
chr5:64254686 | T | C | 1 | a0001c0001t0003g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1227+37290T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254686 | |||||||
chr5:64254766 | G | A | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1227+37370G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254766 | |||||||
chr5:64255059 | A | AT | 44 | a0001c0001t0002g0003 a0001c0001t0002g0080 a0001c0001t0002g0174 others(41): Show |
44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+37669dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64255059 | ||||||
chr5:64255106 | A | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+37710A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255106 | |||||||
chr5:64255187 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1227+37791C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255187 | |||||||
chr5:64255267 | A | T | 2 | a0001c0001t0002g0228 a0001c0001t0002g0231 |
2 | NA18955.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1227+37871A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255267 | |||||||
chr5:64255350 | C | T | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1227+37954C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255350 | |||||||
chr5:64255427 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+38031C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255427 | |||||||
chr5:64255547 | G | A | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+38151G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255547 | |||||||
chr5:64255549 | A | G | 8 | a0001c0001t0001g0111 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
8 | HG02055.hp2 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+38153A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255549 | |||||||
chr5:64255644 | G | A | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+38248G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255644 | |||||||
chr5:64255767 | A | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+38371A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255767 | |||||||
chr5:64255827 | G | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+38431G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255827 | |||||||
chr5:64255835 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1227+38439A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255835 | |||||||
chr5:64255885 | T | C | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+38489T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255885 | |||||||
chr5:64255886 | G | A | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+38490G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255886 | |||||||
chr5:64255953 | A | C | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1227+38557A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255953 | |||||||
chr5:64256003 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+38607G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256003 | |||||||
chr5:64256019 | T | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+38623T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256019 | |||||||
chr5:64256026 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1227+38630C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256026 | |||||||
chr5:64256035 | G | T | 1 | a0002c0002t0010g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1227+38639G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256035 | |||||||
chr5:64256186 | C | A | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+38790C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256186 | |||||||
chr5:64256228 | G | T | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+38832G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256228 | |||||||
chr5:64256238 | C | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+38842C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256238 | |||||||
chr5:64256276 | G | A | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1227+38880G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256276 | |||||||
chr5:64256318 | G | T | 2 | a0001c0001t0002g0203 a0001c0001t0002g0207 |
2 | HG00597.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1227+38922G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256318 | |||||||
chr5:64256367 | G | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0162 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1227+38971G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256367 | |||||||
chr5:64256384 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+38988G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256384 | |||||||
chr5:64256586 | G | T | 1 | a0001c0001t0003g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1227+39190G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256586 | |||||||
chr5:64256595 | T | G | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+39199T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256595 | |||||||
chr5:64256768 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+39372A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256768 | |||||||
chr5:64256964 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1227+39568A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256964 | |||||||
chr5:64257065 | T | C | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+39669T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257065 | |||||||
chr5:64257127 | A | C | 3 | a0001c0001t0001g0158 a0001c0001t0003g0144 a0001c0001t0003g0145 |
3 | HG02886.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1227+39731A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257127 | |||||||
chr5:64257147 | A | G | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+39751A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257147 | |||||||
chr5:64257166 | C | A | 1 | a0001c0001t0005g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1227+39770C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257166 | |||||||
chr5:64257169 | A | C | 7 | a0001c0001t0001g0112 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
7 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+39773A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257169 | |||||||
chr5:64257238 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+39842C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257238 | |||||||
chr5:64257269 | T | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+39873T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257269 | |||||||
chr5:64257410 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1227+40014G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257410 | |||||||
chr5:64257414 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1227+40018G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257414 | |||||||
chr5:64257517 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+40121G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257517 | |||||||
chr5:64257563 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+40167A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257563 | |||||||
chr5:64257740 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1227+40344C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257740 | |||||||
chr5:64257819 | T | A | 1 | a0001c0001t0003g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1227+40423T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257819 | |||||||
chr5:64257915 | C | T | 1 | a0001c0001t0015g0033 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1227+40519C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257915 | |||||||
chr5:64258017 | A | G | 61 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1227+40621A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258017 | |||||||
chr5:64258269 | T | C | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+40873T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258269 | |||||||
chr5:64258389 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1227+40993T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258389 | |||||||
chr5:64258566 | C | T | 1 | a0004c0004t0004g0093 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1227+41170C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258566 | |||||||
chr5:64258833 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+41437G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258833 | |||||||
chr5:64258985 | C | A | 1 | a0001c0001t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1227+41589C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258985 | |||||||
chr5:64259030 | ATTGT | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+41657_1227+41 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64259030 | ||||||
chr5:64259157 | T | G | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1227+41761T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259157 | |||||||
chr5:64259480 | T | C | 1 | a0001c0001t0003g0040 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1227+42084T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259480 | |||||||
chr5:64259514 | C | G | 1 | a0001c0001t0003g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+42118C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259514 | |||||||
chr5:64259621 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1227+42225A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259621 | |||||||
chr5:64259704 | C | T | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+42308C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259704 | |||||||
chr5:64259824 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1227+42428G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259824 | |||||||
chr5:64259845 | C | T | 1 | a0001c0001t0003g0044 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1227+42449C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259845 | |||||||
chr5:64259933 | C | A | 4 | a0002c0002t0006g0065 a0002c0002t0006g0069 a0002c0002t0006g0070 others(1): Show |
4 | HG01081.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+42537C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259933 | |||||||
chr5:64259943 | A | T | 1 | a0001c0001t0003g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1227+42547A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259943 | |||||||
chr5:64259979 | T | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+42583T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259979 | |||||||
chr5:64260144 | A | G | 1 | a0004c0004t0004g0093 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1227+42748A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260144 | |||||||
chr5:64260167 | G | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1227+42771G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260167 | |||||||
chr5:64260207 | T | TC | 32 | a0001c0001t0002g0204 a0001c0001t0005g0167 a0001c0001t0005g0168 others(29): Show |
32 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1227+42816dupC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64260207 | ||||||
chr5:64260443 | T | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+43047T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260443 | |||||||
chr5:64260500 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1227+43104A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260500 | |||||||
chr5:64260583 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1227+43187C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260583 | |||||||
chr5:64260752 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1227+43356A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260752 | |||||||
chr5:64260866 | A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+43470A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260866 | |||||||
chr5:64260880 | T | C | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+43484T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260880 | |||||||
chr5:64260910 | A | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+43514A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260910 | |||||||
chr5:64260940 | C | CT | 13 | a0001c0001t0002g0184 a0001c0001t0002g0187 a0001c0001t0003g0016 others(10): Show |
13 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1227+43558dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64260940 | ||||||
chr5:64260940 | CT | C | 26 | a0001c0001t0003g0018 a0001c0001t0004g0002 a0001c0001t0004g0078 others(23): Show |
27 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1227+43558delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64260940 | ||||||
chr5:64260941 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1227+43545T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260941 | |||||||
chr5:64261151 | A | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+43755A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64261151 | |||||||
chr5:64261426 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+44030G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64261426 | |||||||
chr5:64261911 | G | A | 61 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1227+44515G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64261911 | |||||||
chr5:64262417 | G | A | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | NA18966.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1227+45021G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64262417 | |||||||
chr5:64262524 | G | A | 1 | a0001c0001t0015g0033 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1227+45128G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64262524 | |||||||
chr5:64262574 | G | GA | 21 | a0001c0001t0002g0204 a0001c0001t0005g0167 a0001c0001t0005g0168 others(18): Show |
21 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1227+45184dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64262574 | ||||||
chr5:64262605 | C | T | 2 | a0001c0001t0002g0222 a0001c0003t0002g0246 |
2 | HG02040.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1227+45209C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64262605 | |||||||
chr5:64263093 | T | G | 1 | a0001c0001t0002g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1227+45697T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263093 | |||||||
chr5:64263101 | G | A | 2 | a0001c0001t0003g0046 a0001c0001t0021g0047 |
2 | HG00642.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1227+45705G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263101 | |||||||
chr5:64263404 | G | T | 244 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(241): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1227+46008G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263404 | |||||||
chr5:64263810 | G | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1227+46414G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263810 | |||||||
chr5:64263861 | T | A | 1 | a0001c0001t0003g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+46465T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263861 | |||||||
chr5:64263939 | C | G | 1 | a0001c0001t0002g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1227+46543C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263939 | |||||||
chr5:64264463 | G | T | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1227+47067G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264463 | |||||||
chr5:64264469 | G | A | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1227+47073G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264469 | |||||||
chr5:64264537 | A | G | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+47141A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264537 | |||||||
chr5:64264837 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1227+47441A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264837 | |||||||
chr5:64264985 | T | A | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1227+47589T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264985 | |||||||
chr5:64265284 | G | A | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+47888G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64265284 | |||||||
chr5:64265308 | A | G | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+47912A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64265308 | |||||||
chr5:64265367 | G | A | 88 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(85): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1227+47971G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64265367 | |||||||
chr5:64265782 | G | A | 88 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(85): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1227+48386G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64265782 | |||||||
chr5:64266048 | T | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+48652T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266048 | |||||||
chr5:64266105 | T | C | 1 | a0001c0001t0004g0090 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1227+48709T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266105 | |||||||
chr5:64266108 | A | T | 1 | a0001c0001t0012g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1227+48712A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266108 | |||||||
chr5:64266147 | A | C | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1227+48751A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266147 | |||||||
chr5:64266204 | C | T | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1227+48808C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266204 | |||||||
chr5:64266402 | TTATAA | T | 58 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(55): Show |
58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1227+49011_1227+49 others(11): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64266402 | ||||||
chr5:64266465 | T | A | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+49069T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266465 | |||||||
chr5:64266610 | G | A | 1 | a0001c0001t0003g0022 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1227+49214G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266610 | |||||||
chr5:64266645 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1227+49249A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266645 | |||||||
chr5:64266870 | A | G | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1227+49474A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266870 | |||||||
chr5:64267391 | G | C | 2 | a0001c0001t0003g0012 a0001c0001t0003g0045 |
2 | NA18964.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1227+49995G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267391 | |||||||
chr5:64267409 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1227+50013A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267409 | |||||||
chr5:64267486 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1227+50090A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267486 | |||||||
chr5:64267560 | A | G | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+50164A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267560 | |||||||
chr5:64267904 | C | A | 1 | a0001c0001t0023g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1227+50508C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267904 | |||||||
chr5:64267926 | T | C | 1 | a0001c0001t0003g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+50530T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267926 | |||||||
chr5:64268210 | G | T | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+50814G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268210 | |||||||
chr5:64268454 | A | G | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+51058A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268454 | |||||||
chr5:64268463 | G | C | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+51067G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268463 | |||||||
chr5:64268578 | C | G | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+51182C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268578 | |||||||
chr5:64268712 | C | G | 22 | a0001c0001t0002g0003 a0001c0001t0002g0174 a0001c0001t0002g0176 others(19): Show |
22 | HG00733.hp2 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1227+51316C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268712 | |||||||
chr5:64268827 | T | C | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+51431T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268827 | |||||||
chr5:64268943 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1227+51547C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268943 | |||||||
chr5:64268968 | CTAA | C | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+51574_1227+51 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64268968 | ||||||
chr5:64269120 | G | T | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+51724G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269120 | |||||||
chr5:64269265 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1227+51869C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269265 | |||||||
chr5:64269568 | T | C | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1227+52172T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269568 | |||||||
chr5:64269592 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+52196C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269592 | |||||||
chr5:64269701 | A | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+52305A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269701 | |||||||
chr5:64269743 | T | C | 89 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(86): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+52347T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269743 | |||||||
chr5:64269766 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+52370A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269766 | |||||||
chr5:64269785 | G | T | 10 | a0001c0001t0002g0039 a0001c0001t0003g0017 a0001c0001t0007g0001 others(7): Show |
11 | HG00323.hp2 HG01175.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+52389G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269785 | |||||||
chr5:64269846 | G | A | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1227+52450G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269846 | |||||||
chr5:64269982 | A | C | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+52586A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269982 | |||||||
chr5:64270026 | A | AAC | 22 | a0001c0001t0002g0206 a0001c0001t0002g0229 a0001c0001t0004g0090 others(19): Show |
22 | HG00741.hp2 HG01257.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1227+52652_1227+52 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270026 | ||||||
chr5:64270026 | A | AACAC | 23 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(20): Show |
23 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1227+52650_1227+52 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270026 | ||||||
chr5:64270026 | AAC | A | 58 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(55): Show |
58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1227+52652_1227+52 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270026 | ||||||
chr5:64270048 | C | CAA | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+52655_1227+52 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270048 | ||||||
chr5:64270055 | C | T | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+52659C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270055 | |||||||
chr5:64270212 | T | TA | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+52818dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270212 | ||||||
chr5:64270303 | T | C | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1227+52907T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270303 | |||||||
chr5:64270367 | A | G | 9 | a0001c0001t0004g0002 a0001c0001t0004g0086 a0001c0001t0004g0092 others(6): Show |
10 | HG01243.hp2 HG01978.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+52971A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270367 | |||||||
chr5:64270368 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1227+52972T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270368 | |||||||
chr5:64270443 | T | C | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+53047T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270443 | |||||||
chr5:64270795 | A | T | 2 | a0001c0001t0004g0078 a0001c0001t0004g0101 |
2 | NA18960.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1227+53399A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270795 | |||||||
chr5:64270957 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+53561C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270957 | |||||||
chr5:64271267 | A | C | 62 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(59): Show |
62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1227+53871A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271267 | |||||||
chr5:64271390 | G | A | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1228-53796G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271390 | |||||||
chr5:64271598 | C | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-53588C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271598 | |||||||
chr5:64271726 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1228-53460C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271726 | |||||||
chr5:64271769 | G | GAAAC | 101 | a0001c0001t0002g0003 a0001c0001t0002g0080 a0001c0001t0002g0174 others(98): Show |
101 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.1228-53414_1228-53 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64271769 | ||||||
chr5:64271865 | C | T | 60 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(57): Show |
60 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1228-53321C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271865 | |||||||
chr5:64272647 | C | G | 62 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(59): Show |
62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1228-52539C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64272647 | |||||||
chr5:64273037 | T | C | 1 | a0001c0001t0005g0237 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1228-52149T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64273037 | |||||||
chr5:64273213 | C | T | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-51973C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64273213 | |||||||
chr5:64273572 | T | C | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-51614T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64273572 | |||||||
chr5:64273810 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1228-51376A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64273810 | |||||||
chr5:64274163 | G | A | 10 | a0001c0001t0002g0027 a0001c0001t0003g0004 a0001c0001t0003g0005 others(7): Show |
10 | HG00642.hp2 HG00741.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1228-51023G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274163 | |||||||
chr5:64274410 | A | G | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-50776A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274410 | |||||||
chr5:64274479 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1228-50707A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274479 | |||||||
chr5:64274522 | T | C | 11 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0207 others(8): Show |
11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1228-50664T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274522 | |||||||
chr5:64274731 | TG | T | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-50454delG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274731 | |||||||
chr5:64274756 | C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-50430C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274756 | |||||||
chr5:64274953 | T | C | 13 | a0001c0001t0005g0232 a0001c0001t0005g0233 a0001c0001t0005g0234 others(10): Show |
13 | HG00597.hp1 NA18942.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.1228-50233T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274953 | |||||||
chr5:64275029 | A | G | 53 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(50): Show |
53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1228-50157A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275029 | |||||||
chr5:64275122 | A | T | 61 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1228-50064A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275122 | |||||||
chr5:64275210 | G | T | 1 | a0001c0001t0002g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1228-49976G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275210 | |||||||
chr5:64275312 | AGAATTCT others(15): Show |
A | 1 | a0001c0001t0007g0034 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1228-49873_1228-49 others(28): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275312 | |||||||
chr5:64275314 | AATTCTCT others(7): Show |
A | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1228-49852_1228-49 others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64275314 | ||||||
chr5:64275643 | C | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-49543C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275643 | |||||||
chr5:64275697 | A | T | 1 | a0001c0001t0002g0217 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1228-49489A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275697 | |||||||
chr5:64275908 | T | C | 2 | a0001c0001t0005g0235 a0001c0001t0029g0236 |
2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1228-49278T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275908 | |||||||
chr5:64275964 | C | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-49222C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275964 | |||||||
chr5:64276165 | T | C | 18 | a0001c0001t0004g0078 a0001c0001t0004g0089 a0001c0001t0004g0090 others(15): Show |
18 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1228-49021T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276165 | |||||||
chr5:64276167 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-49019G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276167 | |||||||
chr5:64276318 | T | TGG | 5 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0240 others(2): Show |
5 | HG02895.hp1 NA18906.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-48867_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276318 | ||||||
chr5:64276319 | G | GGGGT | 4 | a0001c0001t0005g0234 a0001c0001t0005g0243 a0001c0001t0024g0192 others(1): Show |
4 | HG02559.hp1 HG02896.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-48866_1228-48 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | G | GGT | 31 | a0001c0001t0001g0113 a0001c0001t0001g0141 a0001c0001t0001g0164 others(28): Show |
31 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1228-48828_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | G | GGTGT | 45 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(42): Show |
46 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1228-48830_1228-48 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | G | GGTGTGT | 25 | a0001c0001t0001g0085 a0001c0001t0001g0115 a0001c0001t0001g0116 others(22): Show |
25 | HG00408.hp2 HG01433.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.1228-48832_1228-48 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | G | GGTGTGTG others(1): Show |
11 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0114 others(8): Show |
11 | HG00639.hp2 HG00738.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-48834_1228-48 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | G | GGTGTGTG others(3): Show |
7 | a0001c0001t0001g0120 a0001c0001t0001g0131 a0001c0001t0001g0142 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1228-48836_1228-48 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | G | GGTGTGTG others(5): Show |
5 | a0001c0001t0001g0088 a0001c0001t0001g0129 a0001c0001t0001g0135 others(2): Show |
5 | HG00733.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-48838_1228-48 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | G | GGTGTGTG others(7): Show |
2 | a0001c0001t0001g0117 a0001c0001t0001g0130 |
2 | HG01256.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1228-48840_1228-48 others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | GGT | G | 31 | a0001c0001t0002g0027 a0001c0001t0003g0004 a0001c0001t0003g0005 others(28): Show |
32 | HG00642.hp2 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1228-48828_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | GGTGT | G | 20 | a0001c0001t0003g0050 a0001c0001t0004g0097 a0001c0001t0004g0108 others(17): Show |
20 | HG01256.hp1 HG01258.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-48830_1228-48 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | GGTGTGT | G | 3 | a0001c0001t0005g0233 a0001c0001t0019g0166 a0002c0002t0006g0072 |
3 | HG01175.hp1 HG02886.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1228-48832_1228-48 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276319 | GGTGTGTG others(7): Show |
G | 7 | a0001c0001t0002g0208 a0001c0001t0002g0212 a0001c0001t0002g0213 others(4): Show |
7 | HG01243.hp1 HG01928.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1228-48840_1228-48 others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | ||||||
chr5:64276321 | T | G | 8 | a0001c0001t0005g0232 a0001c0001t0005g0235 a0001c0001t0005g0237 others(5): Show |
8 | HG00597.hp1 HG02818.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1228-48865T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276321 | |||||||
chr5:64276323 | T | G | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1228-48863T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276323 | |||||||
chr5:64276325 | T | G | 6 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-48861T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276325 | |||||||
chr5:64276327 | T | G | 2 | a0001c0001t0005g0233 a0001c0001t0019g0166 |
2 | HG02886.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1228-48859T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276327 | |||||||
chr5:64276374 | G | GGT | 4 | a0001c0001t0001g0156 a0001c0001t0005g0084 a0001c0001t0014g0055 others(1): Show |
4 | HG02257.hp2 HG02273.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-48795_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276374 | ||||||
chr5:64276374 | G | GGTGT | 111 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(108): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1228-48797_1228-48 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276374 | ||||||
chr5:64276374 | G | GGTGTGT | 23 | a0001c0001t0001g0129 a0001c0001t0001g0142 a0001c0001t0005g0167 others(20): Show |
23 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1228-48799_1228-48 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276374 | ||||||
chr5:64276374 | G | GGTGTGTG others(1): Show |
3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-48801_1228-48 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276374 | ||||||
chr5:64276393 | T | G | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1228-48793T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276393 | |||||||
chr5:64276448 | G | A | 8 | a0001c0001t0004g0002 a0001c0001t0004g0086 a0001c0001t0004g0092 others(5): Show |
9 | HG01243.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1228-48738G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276448 | |||||||
chr5:64276520 | C | T | 1 | a0001c0001t0005g0235 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1228-48666C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276520 | |||||||
chr5:64276686 | A | T | 59 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(56): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1228-48500A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276686 | |||||||
chr5:64276704 | A | G | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1228-48482A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276704 | |||||||
chr5:64276850 | G | A | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-48336G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276850 | |||||||
chr5:64277018 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1228-48168C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277018 | |||||||
chr5:64277020 | C | CTG | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-48164_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64277020 | ||||||
chr5:64277046 | T | G | 1 | a0001c0001t0003g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1228-48140T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277046 | |||||||
chr5:64277170 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-48016G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277170 | |||||||
chr5:64277190 | A | AG | 6 | a0001c0001t0001g0113 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-47992dupG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64277190 | ||||||
chr5:64277190 | A | G | 21 | a0001c0001t0001g0134 a0001c0001t0002g0207 a0001c0001t0027g0060 others(18): Show |
21 | HG00408.hp2 HG00741.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1228-47996A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277190 | |||||||
chr5:64277194 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0143 |
2 | HG00408.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1228-47992G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277194 | |||||||
chr5:64277194 | G | GA | 74 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(71): Show |
75 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1228-47979dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64277194 | ||||||
chr5:64277195 | A | G | 23 | a0001c0001t0003g0046 a0001c0001t0005g0167 a0001c0001t0005g0168 others(20): Show |
23 | HG00597.hp1 HG00642.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1228-47991A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277195 | |||||||
chr5:64277196 | A | G | 6 | a0001c0001t0005g0234 a0001c0001t0005g0238 a0001c0001t0005g0240 others(3): Show |
6 | NA18946.hp1 NA18954.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-47990A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277196 | |||||||
chr5:64277540 | T | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-47646T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277540 | |||||||
chr5:64277749 | A | G | 1 | a0001c0001t0003g0015 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1228-47437A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277749 | |||||||
chr5:64277757 | C | T | 1 | a0005c0005t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1228-47429C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277757 | |||||||
chr5:64278419 | A | G | 1 | a0005c0005t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1228-46767A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278419 | |||||||
chr5:64278601 | A | G | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-46585A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278601 | |||||||
chr5:64278657 | G | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1228-46529G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278657 | |||||||
chr5:64278845 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-46341C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278845 | |||||||
chr5:64278909 | T | C | 1 | a0001c0001t0003g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1228-46277T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278909 | |||||||
chr5:64279299 | T | A | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228-45887T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64279299 | |||||||
chr5:64279338 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1228-45848A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64279338 | |||||||
chr5:64279457 | T | C | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-45729T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64279457 | |||||||
chr5:64279984 | G | A | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-45202G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64279984 | |||||||
chr5:64280248 | C | A | 1 | a0002c0002t0006g0069 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1228-44938C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280248 | |||||||
chr5:64280484 | A | G | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-44702A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280484 | |||||||
chr5:64280573 | A | C | 1 | a0001c0001t0007g0034 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1228-44613A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280573 | |||||||
chr5:64280622 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1228-44564G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280622 | |||||||
chr5:64280911 | T | C | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228-44275T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280911 | |||||||
chr5:64281349 | T | C | 1 | a0001c0001t0015g0033 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1228-43837T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281349 | |||||||
chr5:64281422 | A | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1228-43764A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281422 | |||||||
chr5:64281453 | C | T | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1228-43733C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281453 | |||||||
chr5:64281677 | C | T | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-43509C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281677 | |||||||
chr5:64281705 | C | A | 2 | a0001c0001t0003g0048 a0001c0001t0003g0049 |
2 | HG00408.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1228-43481C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281705 | |||||||
chr5:64281718 | G | A | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | NA18966.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1228-43468G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281718 | |||||||
chr5:64281743 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-43443G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281743 | |||||||
chr5:64281776 | C | G | 117 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-43410C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281776 | |||||||
chr5:64281932 | C | T | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-43254C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281932 | |||||||
chr5:64282123 | G | T | 3 | a0001c0001t0002g0226 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | NA18989.hp1 NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1228-43063G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282123 | |||||||
chr5:64282132 | C | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-43054C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282132 | |||||||
chr5:64282238 | T | C | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1228-42948T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282238 | |||||||
chr5:64282305 | A | G | 1 | a0001c0001t0015g0033 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1228-42881A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282305 | |||||||
chr5:64282358 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-42828G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282358 | |||||||
chr5:64282894 | C | T | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1228-42292C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282894 | |||||||
chr5:64283002 | A | C | 1 | a0001c0001t0002g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1228-42184A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283002 | |||||||
chr5:64283111 | G | A | 1 | a0001c0001t0005g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1228-42075G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283111 | |||||||
chr5:64283209 | G | A | 1 | a0001c0001t0004g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1228-41977G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283209 | |||||||
chr5:64283589 | T | C | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-41597T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283589 | |||||||
chr5:64283667 | A | G | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-41519A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283667 | |||||||
chr5:64283942 | C | A | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-41244C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283942 | |||||||
chr5:64284020 | C | G | 1 | a0001c0001t0003g0014 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1228-41166C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284020 | |||||||
chr5:64284236 | A | T | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-40950A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284236 | |||||||
chr5:64284486 | C | T | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-40700C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284486 | |||||||
chr5:64284537 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1228-40649G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284537 | |||||||
chr5:64284835 | A | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1228-40351A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284835 | |||||||
chr5:64284848 | A | G | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-40338A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284848 | |||||||
chr5:64284866 | G | A | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-40320G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284866 | |||||||
chr5:64285006 | G | A | 4 | a0001c0001t0004g0098 a0001c0001t0004g0102 a0001c0001t0004g0103 others(1): Show |
4 | HG01993.hp1 NA18943.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-40180G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285006 | |||||||
chr5:64285117 | C | T | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1228-40069C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285117 | |||||||
chr5:64285456 | TTTGGCTG others(36): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1228-39726_1228-39 others(49): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64285456 | ||||||
chr5:64285590 | T | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-39596T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285590 | |||||||
chr5:64285654 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1228-39532G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285654 | |||||||
chr5:64285659 | C | T | 1 | a0001c0001t0017g0020 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1228-39527C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285659 | |||||||
chr5:64285799 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG03491.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1228-39387G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285799 | |||||||
chr5:64285890 | G | A | 1 | a0001c0001t0022g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1228-39296G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285890 | |||||||
chr5:64286149 | A | G | 1 | a0002c0002t0006g0069 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1228-39037A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286149 | |||||||
chr5:64286430 | C | G | 1 | a0001c0001t0003g0040 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1228-38756C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286430 | |||||||
chr5:64286474 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1228-38712C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286474 | |||||||
chr5:64286587 | A | T | 1 | a0001c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1228-38599A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286587 | |||||||
chr5:64286743 | A | G | 5 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0097 others(2): Show |
5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-38443A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286743 | |||||||
chr5:64287049 | C | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-38137C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287049 | |||||||
chr5:64287092 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1228-38094G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287092 | |||||||
chr5:64287216 | C | T | 18 | a0001c0001t0004g0078 a0001c0001t0004g0089 a0001c0001t0004g0090 others(15): Show |
18 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1228-37970C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287216 | |||||||
chr5:64287255 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1228-37931G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287255 | |||||||
chr5:64287744 | T | A | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228-37442T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287744 | |||||||
chr5:64287853 | C | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1228-37333C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287853 | |||||||
chr5:64288349 | G | T | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-36837G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288349 | |||||||
chr5:64288441 | C | T | 1 | a0002c0002t0008g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1228-36745C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288441 | |||||||
chr5:64288486 | C | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1228-36700C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288486 | |||||||
chr5:64288554 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-36632G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288554 | |||||||
chr5:64288597 | G | A | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1228-36589G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288597 | |||||||
chr5:64288811 | A | T | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1228-36375A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288811 | |||||||
chr5:64288915 | T | C | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-36271T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288915 | |||||||
chr5:64289190 | C | T | 1 | a0001c0001t0012g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1228-35996C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289190 | |||||||
chr5:64289297 | A | G | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1228-35889A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289297 | |||||||
chr5:64289644 | T | C | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1228-35542T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289644 | |||||||
chr5:64289870 | T | C | 51 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(48): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1228-35316T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289870 | |||||||
chr5:64289910 | T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-35276T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289910 | |||||||
chr5:64290005 | T | G | 2 | a0001c0001t0003g0048 a0001c0001t0003g0049 |
2 | HG00408.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1228-35181T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290005 | |||||||
chr5:64290026 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-35160A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290026 | |||||||
chr5:64290182 | A | G | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-35004A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290182 | |||||||
chr5:64290462 | T | C | 1 | a0001c0001t0012g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1228-34724T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290462 | |||||||
chr5:64290700 | T | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-34486T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290700 | |||||||
chr5:64290869 | T | C | 2 | a0001c0001t0002g0027 a0001c0001t0003g0031 |
2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1228-34317T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290869 | |||||||
chr5:64291184 | T | C | 58 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(55): Show |
58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1228-34002T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291184 | |||||||
chr5:64291416 | C | CT | 42 | a0001c0001t0002g0039 a0001c0001t0002g0174 a0001c0001t0002g0203 others(39): Show |
42 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1228-33744dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | ||||||
chr5:64291416 | C | CTT | 6 | a0001c0001t0001g0118 a0001c0001t0005g0186 a0001c0001t0005g0189 others(3): Show |
6 | HG02622.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-33745_1228-33 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | ||||||
chr5:64291416 | CT | C | 29 | a0001c0001t0001g0141 a0001c0001t0001g0163 a0001c0001t0002g0183 others(26): Show |
30 | HG00099.hp1 HG01243.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-33744delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | ||||||
chr5:64291416 | CTT | C | 50 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(47): Show |
50 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1228-33745_1228-33 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | ||||||
chr5:64291416 | CTTT | C | 7 | a0001c0001t0001g0085 a0001c0001t0001g0112 a0001c0001t0001g0122 others(4): Show |
7 | HG01109.hp2 HG01515.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1228-33746_1228-33 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | ||||||
chr5:64291520 | G | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1228-33666G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291520 | |||||||
chr5:64291532 | C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-33654C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291532 | |||||||
chr5:64291565 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1228-33621C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291565 | |||||||
chr5:64291591 | A | AT | 85 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(82): Show |
86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1228-33586dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291591 | ||||||
chr5:64291717 | G | A | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-33469G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291717 | |||||||
chr5:64291723 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1228-33463G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291723 | |||||||
chr5:64291939 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1228-33247G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291939 | |||||||
chr5:64291971 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1228-33215A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291971 | |||||||
chr5:64292186 | G | A | 1 | a0001c0001t0011g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1228-33000G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292186 | |||||||
chr5:64292247 | C | G | 1 | a0005c0005t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1228-32939C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292247 | |||||||
chr5:64292384 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1228-32802G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292384 | |||||||
chr5:64292648 | G | C | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1228-32538G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292648 | |||||||
chr5:64292788 | A | G | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1228-32398A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292788 | |||||||
chr5:64293010 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1228-32176C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293010 | |||||||
chr5:64293071 | C | G | 1 | a0002c0002t0008g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1228-32115C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293071 | |||||||
chr5:64293171 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1228-32015G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293171 | |||||||
chr5:64293232 | G | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0161 |
2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1228-31954G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293232 | |||||||
chr5:64293394 | G | A | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228-31792G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293394 | |||||||
chr5:64293397 | C | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-31789C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293397 | |||||||
chr5:64293668 | G | A | 11 | a0001c0001t0001g0088 a0001c0001t0001g0135 a0001c0001t0001g0137 others(8): Show |
11 | HG00099.hp1 HG00733.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-31518G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293668 | |||||||
chr5:64293787 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-31399G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293787 | |||||||
chr5:64293788 | C | T | 2 | a0001c0001t0019g0166 a0001c0001t0026g0247 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1228-31398C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293788 | |||||||
chr5:64294012 | G | A | 2 | a0001c0001t0005g0235 a0001c0001t0029g0236 |
2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1228-31174G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294012 | |||||||
chr5:64294086 | C | A | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-31100C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294086 | |||||||
chr5:64294122 | G | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-31064G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294122 | |||||||
chr5:64294203 | G | T | 1 | a0001c0001t0003g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1228-30983G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294203 | |||||||
chr5:64294241 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1228-30945G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294241 | |||||||
chr5:64294324 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1228-30862A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294324 | |||||||
chr5:64294749 | A | G | 2 | a0001c0001t0002g0027 a0001c0001t0003g0031 |
2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1228-30437A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294749 | |||||||
chr5:64294807 | A | G | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-30379A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294807 | |||||||
chr5:64295295 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1228-29891G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295295 | |||||||
chr5:64295440 | G | A | 1 | a0001c0001t0003g0044 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1228-29746G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295440 | |||||||
chr5:64295510 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1228-29676G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295510 | |||||||
chr5:64295572 | T | C | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1228-29614T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295572 | |||||||
chr5:64295776 | T | C | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1228-29410T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295776 | |||||||
chr5:64295809 | C | A | 1 | a0001c0001t0003g0044 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1228-29377C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295809 | |||||||
chr5:64295851 | G | T | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-29335G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295851 | |||||||
chr5:64296084 | T | G | 1 | a0001c0001t0002g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1228-29102T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296084 | |||||||
chr5:64296296 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1228-28890G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296296 | |||||||
chr5:64296534 | A | T | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1228-28652A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296534 | |||||||
chr5:64296545 | A | G | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-28641A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296545 | |||||||
chr5:64296657 | C | CA | 59 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(56): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1228-28517dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64296657 | ||||||
chr5:64296657 | CA | C | 23 | a0001c0001t0002g0207 a0001c0001t0011g0053 a0001c0001t0011g0054 others(20): Show |
23 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1228-28517delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64296657 | ||||||
chr5:64296740 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-28446G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296740 | |||||||
chr5:64296786 | T | G | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-28400T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296786 | |||||||
chr5:64296877 | G | C | 1 | a0001c0001t0007g0023 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1228-28309G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296877 | |||||||
chr5:64297080 | G | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-28106G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297080 | |||||||
chr5:64297293 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1228-27893G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297293 | |||||||
chr5:64297445 | TAGA | T | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-27735_1228-27 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64297445 | ||||||
chr5:64297455 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1228-27731G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297455 | |||||||
chr5:64297473 | T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-27713T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297473 | |||||||
chr5:64297614 | G | A | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228-27572G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297614 | |||||||
chr5:64297684 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1228-27502A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297684 | |||||||
chr5:64297976 | G | A | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1228-27210G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297976 | |||||||
chr5:64298136 | A | C | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1228-27050A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298136 | |||||||
chr5:64298172 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1228-27014G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298172 | |||||||
chr5:64298330 | G | C | 1 | a0001c0001t0003g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1228-26856G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298330 | |||||||
chr5:64298481 | T | C | 2 | a0001c0001t0003g0012 a0001c0001t0003g0045 |
2 | NA18964.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1228-26705T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298481 | |||||||
chr5:64298520 | C | T | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228-26666C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298520 | |||||||
chr5:64298595 | G | A | 2 | a0001c0001t0012g0195 a0001c0001t0012g0196 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1228-26591G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298595 | |||||||
chr5:64298746 | G | C | 1 | a0001c0001t0021g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1228-26440G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298746 | |||||||
chr5:64299843 | A | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-25343A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64299843 | |||||||
chr5:64299869 | T | G | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-25317T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64299869 | |||||||
chr5:64300209 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1228-24977T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300209 | |||||||
chr5:64300323 | A | G | 1 | a0001c0001t0005g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1228-24863A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300323 | |||||||
chr5:64300436 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1228-24750G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300436 | |||||||
chr5:64300491 | C | T | 6 | a0001c0001t0003g0012 a0001c0001t0003g0022 a0001c0001t0003g0045 others(3): Show |
6 | HG00408.hp1 HG02074.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-24695C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300491 | |||||||
chr5:64300520 | A | T | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1228-24666A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300520 | |||||||
chr5:64301091 | TA | T | 121 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(118): Show |
122 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1228-24093delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301091 | ||||||
chr5:64301254 | G | C | 1 | a0001c0001t0003g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1228-23932G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64301254 | |||||||
chr5:64301300 | A | T | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-23886A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64301300 | |||||||
chr5:64301701 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0005g0167 a0001c0001t0005g0168 |
2 | HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1228-23473_1228-23 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | ||||||
chr5:64301701 | A | ATGTGTGT others(7): Show |
18 | a0001c0001t0005g0169 a0001c0001t0005g0170 a0001c0001t0005g0171 others(15): Show |
18 | HG00597.hp1 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1228-23475_1228-23 others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | ||||||
chr5:64301701 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-23477_1228-23 others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | ||||||
chr5:64301701 | A | ATGTGTGT others(11): Show |
4 | a0001c0001t0005g0189 a0001c0001t0005g0190 a0001c0001t0014g0055 others(1): Show |
4 | HG01891.hp2 HG02895.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-23479_1228-23 others(24): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | ||||||
chr5:64301701 | A | ATGTGTGT others(13): Show |
2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-23481_1228-23 others(26): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | ||||||
chr5:64301701 | A | ATGTGTGT others(15): Show |
2 | a0001c0001t0005g0191 a0001c0001t0026g0247 |
2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1228-23483_1228-23 others(28): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | ||||||
chr5:64301701 | A | ATGTGTGT others(19): Show |
6 | a0001c0001t0005g0188 a0001c0001t0011g0052 a0001c0001t0011g0053 others(3): Show |
6 | HG02559.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-23462_1228-23 others(32): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | ||||||
chr5:64301701 | ATGTG | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-23465_1228-23 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | ||||||
chr5:64301763 | G | A | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1228-23423G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64301763 | |||||||
chr5:64301904 | C | T | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1228-23282C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64301904 | |||||||
chr5:64302228 | A | G | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1228-22958A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302228 | |||||||
chr5:64302250 | A | G | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-22936A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302250 | |||||||
chr5:64302298 | A | G | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-22888A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302298 | |||||||
chr5:64302340 | T | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0135 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1228-22846T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302340 | |||||||
chr5:64302349 | G | A | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-22837G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302349 | |||||||
chr5:64302512 | A | T | 1 | a0001c0001t0003g0041 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1228-22674A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302512 | |||||||
chr5:64303154 | A | C | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-22032A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64303154 | |||||||
chr5:64303550 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1228-21636A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64303550 | |||||||
chr5:64303682 | T | C | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-21504T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64303682 | |||||||
chr5:64304160 | CAG | C | 58 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(55): Show |
58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1228-21025_1228-21 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304160 | |||||||
chr5:64304184 | G | C | 3 | a0001c0001t0002g0226 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | NA18989.hp1 NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1228-21002G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304184 | |||||||
chr5:64304191 | G | A | 141 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(138): Show |
142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1228-20995G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304191 | |||||||
chr5:64304348 | G | A | 1 | a0001c0001t0007g0034 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1228-20838G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304348 | |||||||
chr5:64304406 | A | T | 141 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(138): Show |
142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1228-20780A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304406 | |||||||
chr5:64304836 | G | A | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-20350G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304836 | |||||||
chr5:64305026 | C | T | 143 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(140): Show |
144 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1228-20160C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305026 | |||||||
chr5:64305084 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-20102G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305084 | |||||||
chr5:64305298 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1228-19888C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305298 | |||||||
chr5:64305397 | C | G | 52 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(49): Show |
52 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.1228-19789C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305397 | |||||||
chr5:64305430 | G | C | 2 | a0002c0002t0006g0074 a0002c0002t0006g0075 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1228-19756G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305430 | |||||||
chr5:64305478 | AT | A | 6 | a0001c0001t0001g0155 a0001c0001t0003g0012 a0001c0001t0003g0045 others(3): Show |
6 | HG01433.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-19697delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64305478 | ||||||
chr5:64305600 | AAC | A | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-19584_1228-19 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64305600 | ||||||
chr5:64305698 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1228-19488A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305698 | |||||||
chr5:64306179 | C | G | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1228-19007C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306179 | |||||||
chr5:64306209 | T | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-18977T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306209 | |||||||
chr5:64306264 | A | G | 1 | a0001c0001t0021g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1228-18922A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306264 | |||||||
chr5:64306601 | T | G | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1228-18585T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306601 | |||||||
chr5:64306631 | A | C | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-18555A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306631 | |||||||
chr5:64306773 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1228-18413A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306773 | |||||||
chr5:64306806 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1228-18380A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306806 | |||||||
chr5:64306830 | G | C | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228-18356G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306830 | |||||||
chr5:64306977 | TAATAA | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-18201_1228-18 others(11): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64306977 | ||||||
chr5:64307006 | TA | T | 16 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1228-18171delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64307006 | ||||||
chr5:64307111 | GCTTT | G | 86 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(83): Show |
87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1228-18072_1228-18 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64307111 | ||||||
chr5:64307391 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0142 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1228-17795G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307391 | |||||||
chr5:64307420 | G | A | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-17766G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307420 | |||||||
chr5:64307696 | T | C | 117 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-17490T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307696 | |||||||
chr5:64307713 | T | C | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-17473T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307713 | |||||||
chr5:64307933 | G | A | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1228-17253G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307933 | |||||||
chr5:64307983 | C | T | 121 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(118): Show |
122 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1228-17203C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307983 | |||||||
chr5:64308063 | A | G | 117 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-17123A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308063 | |||||||
chr5:64308237 | C | T | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1228-16949C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308237 | |||||||
chr5:64308302 | A | C | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-16884A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308302 | |||||||
chr5:64308399 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-16787C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308399 | |||||||
chr5:64308431 | G | A | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-16755G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308431 | |||||||
chr5:64308793 | A | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-16393A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308793 | |||||||
chr5:64309142 | G | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1228-16044G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64309142 | |||||||
chr5:64309589 | G | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-15597G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64309589 | |||||||
chr5:64309764 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1228-15422T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64309764 | |||||||
chr5:64309925 | C | T | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1228-15261C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64309925 | |||||||
chr5:64310279 | T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-14907T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64310279 | |||||||
chr5:64310516 | C | CA | 5 | a0001c0001t0001g0088 a0001c0001t0001g0135 a0002c0002t0008g0061 others(2): Show |
5 | HG01516.hp1 HG01517.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1228-14656dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64310516 | ||||||
chr5:64310518 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1228-14668A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64310518 | |||||||
chr5:64310623 | C | T | 141 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(138): Show |
142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1228-14563C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64310623 | |||||||
chr5:64310665 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1228-14521T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64310665 | |||||||
chr5:64311071 | G | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-14115G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311071 | |||||||
chr5:64311196 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1228-13990G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311196 | |||||||
chr5:64311217 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1228-13969T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311217 | |||||||
chr5:64311417 | G | A | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1228-13769G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311417 | |||||||
chr5:64311444 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-13742G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311444 | |||||||
chr5:64311498 | T | G | 3 | a0001c0001t0004g0097 a0001c0001t0004g0108 a0001c0001t0004g0109 |
3 | HG01256.hp1 HG01258.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1228-13688T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311498 | |||||||
chr5:64311705 | A | G | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-13481A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311705 | |||||||
chr5:64311774 | A | C | 1 | a0001c0001t0013g0013 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1228-13412A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311774 | |||||||
chr5:64311861 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1228-13325A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311861 | |||||||
chr5:64312026 | C | G | 59 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(56): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1228-13160C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64312026 | |||||||
chr5:64312255 | A | G | 6 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0002c0002t0008g0061 others(3): Show |
6 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-12931A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64312255 | |||||||
chr5:64312538 | TCAGA | T | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-12645_1228-12 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64312538 | ||||||
chr5:64312709 | C | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-12477C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64312709 | |||||||
chr5:64313029 | A | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-12157A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313029 | |||||||
chr5:64313102 | A | C | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1228-12084A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313102 | |||||||
chr5:64313205 | T | C | 1 | a0001c0001t0003g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1228-11981T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313205 | |||||||
chr5:64313466 | G | A | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1228-11720G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313466 | |||||||
chr5:64313604 | C | T | 1 | a0001c0001t0003g0022 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1228-11582C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313604 | |||||||
chr5:64313984 | T | C | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1228-11202T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313984 | |||||||
chr5:64314079 | T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-11107T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314079 | |||||||
chr5:64314152 | G | T | 1 | a0002c0002t0006g0069 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1228-11034G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314152 | |||||||
chr5:64314288 | AT | A | 114 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(111): Show |
115 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1228-10889delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64314288 | ||||||
chr5:64314332 | G | C | 9 | a0001c0001t0002g0027 a0001c0001t0003g0004 a0001c0001t0003g0005 others(6): Show |
9 | HG00642.hp2 HG00741.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1228-10854G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314332 | |||||||
chr5:64314628 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1228-10558C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314628 | |||||||
chr5:64314793 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1228-10393A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314793 | |||||||
chr5:64314799 | A | G | 11 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0207 others(8): Show |
11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1228-10387A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314799 | |||||||
chr5:64315290 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1228-9896G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315290 | |||||||
chr5:64315482 | C | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-9704C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315482 | |||||||
chr5:64315533 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1228-9653T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315533 | |||||||
chr5:64315546 | A | G | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-9640A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315546 | |||||||
chr5:64315628 | C | CAGCTATT others(1): Show |
30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-9555_1228-954 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64315628 | ||||||
chr5:64315664 | G | A | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1228-9522G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315664 | |||||||
chr5:64315691 | G | A | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-9495G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315691 | |||||||
chr5:64315734 | C | CA | 18 | a0001c0001t0001g0082 a0001c0001t0001g0120 a0001c0001t0001g0150 others(15): Show |
18 | HG01361.hp1 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1228-9432dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64315734 | ||||||
chr5:64315734 | CA | C | 21 | a0001c0001t0001g0119 a0001c0001t0001g0154 a0001c0001t0001g0155 others(18): Show |
21 | HG00408.hp1 HG01433.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1228-9432delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64315734 | ||||||
chr5:64315807 | A | C | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-9379A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315807 | |||||||
chr5:64316015 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1228-9171C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64316015 | |||||||
chr5:64316043 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1228-9143G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64316043 | |||||||
chr5:64316494 | C | A | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228-8692C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64316494 | |||||||
chr5:64316759 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1228-8427G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64316759 | |||||||
chr5:64317100 | A | G | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-8086A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317100 | |||||||
chr5:64317147 | T | C | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-8039T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317147 | |||||||
chr5:64317149 | C | T | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-8037C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317149 | |||||||
chr5:64317246 | G | T | 1 | a0002c0002t0018g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1228-7940G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317246 | |||||||
chr5:64317330 | A | C | 4 | a0002c0002t0008g0061 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-7856A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317330 | |||||||
chr5:64317491 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-7695G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317491 | |||||||
chr5:64317561 | C | T | 117 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-7625C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317561 | |||||||
chr5:64317563 | C | CATACATA others(3): Show |
86 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(83): Show |
87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1228-7617_1228-760 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317563 | ||||||
chr5:64317563 | C | CATACATA others(13): Show |
1 | a0001c0001t0004g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1228-7608_1228-760 others(24): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317563 | ||||||
chr5:64317594 | T | TTA | 25 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(22): Show |
25 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1228-7589_1228-758 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317594 | ||||||
chr5:64317599 | C | T | 117 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-7587C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317599 | |||||||
chr5:64317600 | A | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1228-7586A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317600 | |||||||
chr5:64317617 | C | T | 4 | a0001c0001t0002g0181 a0001c0001t0002g0184 a0001c0001t0002g0187 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-7569C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317617 | |||||||
chr5:64317619 | T | C | 8 | a0001c0001t0001g0134 a0001c0001t0005g0235 a0001c0001t0005g0239 others(5): Show |
8 | HG00408.hp2 HG00741.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-7567T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317619 | |||||||
chr5:64317621 | TATACAC | T | 4 | a0001c0001t0002g0181 a0001c0001t0002g0184 a0001c0001t0002g0187 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-7563_1228-755 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317621 | ||||||
chr5:64317623 | T | TAC | 12 | a0001c0001t0001g0160 a0001c0001t0003g0011 a0001c0001t0003g0014 others(9): Show |
12 | HG00642.hp2 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1228-7537_1228-753 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317623 | ||||||
chr5:64317623 | T | TACAC | 17 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(14): Show |
17 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1228-7539_1228-753 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317623 | ||||||
chr5:64317623 | TAC | T | 77 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(74): Show |
78 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.1228-7537_1228-753 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317623 | ||||||
chr5:64317623 | TACAC | T | 61 | a0001c0001t0001g0115 a0001c0001t0002g0003 a0001c0001t0002g0039 others(58): Show |
61 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1228-7539_1228-753 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317623 | ||||||
chr5:64317625 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0005g0235 a0001c0001t0005g0239 others(1): Show |
4 | HG00408.hp2 NA18966.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-7561C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317625 | |||||||
chr5:64317627 | C | T | 4 | a0002c0002t0006g0072 a0002c0002t0008g0062 a0002c0002t0008g0063 others(1): Show |
4 | HG00741.hp2 HG01175.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-7559C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317627 | |||||||
chr5:64317629 | C | T | 4 | a0002c0002t0006g0065 a0002c0002t0006g0069 a0002c0002t0006g0070 others(1): Show |
4 | HG01081.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-7557C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317629 | |||||||
chr5:64317758 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1228-7428T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317758 | |||||||
chr5:64317775 | G | T | 33 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(30): Show |
33 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1228-7411G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317775 | |||||||
chr5:64317796 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1228-7390T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317796 | |||||||
chr5:64317805 | GA | G | 117 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-7376delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317805 | ||||||
chr5:64317812 | G | A | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-7374G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317812 | |||||||
chr5:64317893 | G | A | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-7293G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317893 | |||||||
chr5:64318238 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1228-6948A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318238 | |||||||
chr5:64318246 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1228-6940T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318246 | |||||||
chr5:64318269 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1228-6917C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318269 | |||||||
chr5:64318403 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1228-6783A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318403 | |||||||
chr5:64318482 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1228-6704A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318482 | |||||||
chr5:64318700 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1228-6486A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318700 | |||||||
chr5:64319102 | G | A | 1 | a0002c0002t0006g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1228-6084G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64319102 | |||||||
chr5:64319174 | T | TA | 30 | a0001c0001t0003g0050 a0001c0001t0004g0002 a0001c0001t0004g0078 others(27): Show |
31 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1228-5995dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64319174 | ||||||
chr5:64319174 | TA | T | 30 | a0001c0001t0001g0130 a0001c0001t0002g0027 a0001c0001t0002g0206 others(27): Show |
30 | HG00642.hp2 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1228-5995delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64319174 | ||||||
chr5:64319482 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1228-5704G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64319482 | |||||||
chr5:64320090 | C | G | 4 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-5096C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320090 | |||||||
chr5:64320234 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0142 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1228-4952C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320234 | |||||||
chr5:64320250 | A | T | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-4936A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320250 | |||||||
chr5:64320419 | A | G | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-4767A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320419 | |||||||
chr5:64320732 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1228-4454G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320732 | |||||||
chr5:64320897 | G | C | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-4289G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320897 | |||||||
chr5:64321027 | G | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1228-4159G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321027 | |||||||
chr5:64321037 | CA | C | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-4138delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64321037 | ||||||
chr5:64321193 | A | G | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-3993A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321193 | |||||||
chr5:64321245 | A | G | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-3941A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321245 | |||||||
chr5:64321359 | A | G | 20 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-3827A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321359 | |||||||
chr5:64321375 | A | G | 1 | a0001c0001t0002g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1228-3811A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321375 | |||||||
chr5:64321597 | G | A | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-3589G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321597 | |||||||
chr5:64321628 | T | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-3558T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321628 | |||||||
chr5:64321674 | C | T | 4 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0010g0076 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-3512C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321674 | |||||||
chr5:64321721 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1228-3465A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321721 | |||||||
chr5:64321738 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1228-3448G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321738 | |||||||
chr5:64321879 | C | T | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1228-3307C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321879 | |||||||
chr5:64322602 | C | CGT | 23 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0004g0078 others(20): Show |
23 | HG00642.hp2 HG01255.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1228-2549_1228-254 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | C | CGTGT | 13 | a0001c0001t0002g0039 a0001c0001t0002g0177 a0001c0001t0002g0180 others(10): Show |
13 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228-2551_1228-254 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | C | CGTGTGT | 19 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0207 others(16): Show |
19 | HG00597.hp2 HG00741.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1228-2553_1228-254 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | C | CGTGTGTG others(1): Show |
24 | a0001c0001t0002g0003 a0001c0001t0002g0080 a0001c0001t0002g0176 others(21): Show |
25 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1228-2555_1228-254 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | C | CGTGTGTG others(3): Show |
11 | a0001c0001t0002g0174 a0001c0001t0002g0206 a0001c0001t0002g0215 others(8): Show |
11 | HG00738.hp2 HG01243.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1228-2557_1228-254 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | C | CGTGTGTG others(5): Show |
11 | a0001c0001t0002g0183 a0001c0001t0002g0208 a0001c0001t0002g0214 others(8): Show |
11 | HG01243.hp1 HG02004.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-2559_1228-254 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | C | CGTGTGTG others(7): Show |
5 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0217 others(2): Show |
5 | HG00642.hp1 HG01928.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-2561_1228-254 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | CGT | C | 6 | a0001c0001t0002g0184 a0001c0001t0002g0187 a0001c0001t0003g0028 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-2549_1228-254 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | CGTGTGT | C | 9 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(6): Show |
9 | HG02055.hp2 HG02622.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1228-2553_1228-254 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | CGTGTGTG others(1): Show |
C | 49 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(46): Show |
49 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1228-2555_1228-254 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0019g0166 |
3 | HG02886.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-2557_1228-254 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322602 | CGTGTGTG others(5): Show |
C | 27 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(24): Show |
27 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1228-2559_1228-254 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | ||||||
chr5:64322656 | A | G | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-2530A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64322656 | |||||||
chr5:64322672 | G | A | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-2514G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64322672 | |||||||
chr5:64323286 | A | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-1900A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323286 | |||||||
chr5:64323396 | T | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-1790T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323396 | |||||||
chr5:64323539 | A | AAATAAT | 4 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-1633_1228-162 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64323539 | ||||||
chr5:64323583 | T | C | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1228-1603T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323583 | |||||||
chr5:64323640 | C | T | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1228-1546C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323640 | |||||||
chr5:64323948 | G | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-1238G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323948 | |||||||
chr5:64324137 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1228-1049A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324137 | |||||||
chr5:64324426 | G | A | 4 | a0001c0001t0002g0176 a0001c0001t0002g0180 a0001c0001t0020g0024 others(1): Show |
4 | HG00733.hp2 HG01168.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-760G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324426 | |||||||
chr5:64324489 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-697G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324489 | |||||||
chr5:64324508 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-678G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324508 | |||||||
chr5:64324563 | T | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1228-623T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324563 | |||||||
chr5:64324742 | G | A | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1228-444G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324742 | |||||||
chr5:64324815 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1228-371A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324815 | |||||||
chr5:64324832 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1228-354A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324832 | |||||||
chr5:64325419 | T | G | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | splice_region_variant&intron_variant | LOW | c.1453+8T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325419 | |||||||
chr5:64325673 | G | C | 6 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453+262G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325673 | |||||||
chr5:64325713 | T | C | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1453+302T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325713 | |||||||
chr5:64325790 | C | A | 1 | a0001c0001t0005g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1453+379C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325790 | |||||||
chr5:64325791 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1453+380C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325791 | |||||||
chr5:64326049 | A | G | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1453+638A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326049 | |||||||
chr5:64326091 | A | G | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1453+680A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326091 | |||||||
chr5:64326164 | G | A | 117 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1453+753G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326164 | |||||||
chr5:64326190 | G | A | 3 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 |
3 | HG00408.hp1 HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1453+779G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326190 | |||||||
chr5:64326206 | T | G | 245 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1453+795T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326206 | |||||||
chr5:64326246 | C | G | 1 | a0001c0001t0004g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1453+835C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326246 | |||||||
chr5:64326283 | T | C | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1453+872T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326283 | |||||||
chr5:64326354 | T | C | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1453+943T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326354 | |||||||
chr5:64326360 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1453+949A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326360 | |||||||
chr5:64326593 | A | C | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1453+1182A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326593 | |||||||
chr5:64326674 | G | T | 7 | a0001c0001t0004g0002 a0001c0001t0004g0099 a0001c0001t0004g0100 others(4): Show |
8 | HG01243.hp2 HG01978.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453+1263G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326674 | |||||||
chr5:64326784 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1453+1373T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326784 | |||||||
chr5:64326913 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1453+1502G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326913 | |||||||
chr5:64327084 | G | A | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0198 others(3): Show |
6 | HG02559.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+1673G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327084 | |||||||
chr5:64327448 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1453+2037T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327448 | |||||||
chr5:64327547 | G | A | 1 | a0001c0001t0004g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1453+2136G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327547 | |||||||
chr5:64327794 | T | C | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1453+2383T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327794 | |||||||
chr5:64327882 | T | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1454-2399T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327882 | |||||||
chr5:64328171 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1454-2110C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64328171 | |||||||
chr5:64328206 | TG | T | 8 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1454-2068delG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 64328206 | ||||||
chr5:64328599 | G | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0039 a0001c0001t0002g0174 others(18): Show |
21 | HG00733.hp2 HG00738.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1454-1682G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64328599 | |||||||
chr5:64328752 | A | G | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1454-1529A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64328752 | |||||||
chr5:64329018 | A | G | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1454-1263A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329018 | |||||||
chr5:64329274 | T | C | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1454-1007T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329274 | |||||||
chr5:64329292 | C | T | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1454-989C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329292 | |||||||
chr5:64329372 | A | G | 1 | a0001c0001t0012g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1454-909A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329372 | |||||||
chr5:64329383 | G | A | 2 | a0002c0002t0006g0074 a0002c0002t0006g0075 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1454-898G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329383 | |||||||
chr5:64329457 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1454-824C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329457 | |||||||
chr5:64329457 | CT | C | 7 | a0001c0001t0004g0091 a0001c0001t0007g0030 a0001c0001t0007g0051 others(4): Show |
7 | HG01123.hp2 HG02280.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-809delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 64329457 | ||||||
chr5:64329472 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1454-809T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329472 | |||||||
chr5:64329479 | A | G | 1 | a0001c0001t0003g0016 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1454-802A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329479 | |||||||
chr5:64329526 | C | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1454-755C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329526 | |||||||
chr5:64329657 | C | T | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1454-624C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329657 | |||||||
chr5:64329787 | C | T | 5 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0191 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1454-494C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329787 | |||||||
chr5:64329949 | G | C | 59 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(56): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1454-332G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329949 | |||||||
chr5:64330190 | A | G | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1454-91A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64330190 | |||||||
chr5:64330466 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1579+60A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64330466 | |||||||
chr5:64330663 | T | C | 1 | a0001c0001t0004g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1579+257T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64330663 | |||||||
chr5:64331187 | G | A | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1579+781G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331187 | |||||||
chr5:64331291 | G | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1579+885G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331291 | |||||||
chr5:64331344 | G | A | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1579+938G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331344 | |||||||
chr5:64331400 | A | G | 1 | a0001c0001t0003g0044 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1579+994A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331400 | |||||||
chr5:64331406 | A | T | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+1000A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331406 | |||||||
chr5:64331550 | G | A | 2 | a0001c0001t0004g0248 a0001c0001t0005g0189 |
2 | HG01978.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1579+1144G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331550 | |||||||
chr5:64331591 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1579+1185T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331591 | |||||||
chr5:64331753 | G | A | 1 | a0001c0001t0003g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1579+1347G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331753 | |||||||
chr5:64331796 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0128 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+1390G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331796 | |||||||
chr5:64331852 | C | T | 2 | a0001c0001t0007g0030 a0001c0001t0007g0051 |
2 | HG01123.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1579+1446C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331852 | |||||||
chr5:64332005 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1579+1599G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332005 | |||||||
chr5:64332532 | T | C | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1579+2126T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332532 | |||||||
chr5:64332750 | G | A | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1579+2344G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332750 | |||||||
chr5:64332850 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1579+2444A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332850 | |||||||
chr5:64332859 | A | G | 1 | a0001c0001t0005g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1579+2453A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332859 | |||||||
chr5:64333364 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1579+2958G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64333364 | |||||||
chr5:64333912 | G | A | 105 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(102): Show |
106 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1579+3506G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64333912 | |||||||
chr5:64334274 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+3868C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334274 | |||||||
chr5:64334547 | GTTC | G | 23 | a0001c0001t0002g0204 a0001c0001t0004g0086 a0001c0001t0004g0092 others(20): Show |
23 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1579+4147_1579+414 others(7): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64334547 | ||||||
chr5:64334672 | A | G | 18 | a0001c0001t0004g0086 a0001c0001t0004g0092 a0001c0001t0027g0060 others(15): Show |
18 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1579+4266A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334672 | |||||||
chr5:64334713 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1579+4307C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334713 | |||||||
chr5:64334746 | T | C | 3 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0025 |
3 | HG00639.hp1 HG01433.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1579+4340T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334746 | |||||||
chr5:64334853 | C | G | 58 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(55): Show |
58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1579+4447C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334853 | |||||||
chr5:64334921 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1579+4515G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334921 | |||||||
chr5:64334924 | T | C | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1579+4518T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334924 | |||||||
chr5:64335013 | T | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+4607T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335013 | |||||||
chr5:64335127 | T | G | 115 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(112): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1579+4721T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335127 | |||||||
chr5:64335177 | T | A | 4 | a0001c0001t0007g0001 a0001c0001t0007g0032 a0001c0001t0007g0034 others(1): Show |
5 | HG01255.hp2 HG01346.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+4771T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335177 | |||||||
chr5:64335256 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1579+4850A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335256 | |||||||
chr5:64335501 | G | T | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1579+5095G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335501 | |||||||
chr5:64335508 | TG | T | 22 | a0001c0001t0004g0086 a0001c0001t0004g0092 a0001c0001t0027g0060 others(19): Show |
22 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1579+5104delG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64335508 | ||||||
chr5:64335844 | A | G | 25 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0089 others(22): Show |
26 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1579+5438A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335844 | |||||||
chr5:64335936 | T | C | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1579+5530T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335936 | |||||||
chr5:64335970 | G | A | 1 | a0001c0001t0003g0040 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1579+5564G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335970 | |||||||
chr5:64335999 | G | A | 1 | a0001c0001t0007g0032 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1579+5593G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335999 | |||||||
chr5:64336042 | G | C | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1579+5636G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336042 | |||||||
chr5:64336345 | T | C | 1 | a0001c0001t0021g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1579+5939T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336345 | |||||||
chr5:64336377 | A | G | 3 | a0001c0001t0003g0011 a0001c0001t0003g0014 a0001c0001t0003g0017 |
3 | HG02602.hp1 HG03491.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1579+5971A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336377 | |||||||
chr5:64336384 | G | A | 1 | a0001c0001t0005g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1579+5978G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336384 | |||||||
chr5:64336390 | CTATT | C | 33 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(30): Show |
33 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1579+5985_1579+598 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336390 | |||||||
chr5:64336451 | C | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+6045C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336451 | |||||||
chr5:64336453 | A | G | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1579+6047A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336453 | |||||||
chr5:64336758 | C | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+6352C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336758 | |||||||
chr5:64336997 | TG | T | 82 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0087 others(79): Show |
82 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1579+6592delG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336997 | |||||||
chr5:64336998 | G | T | 49 | a0001c0001t0004g0002 a0001c0001t0004g0086 a0001c0001t0004g0092 others(46): Show |
50 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.1579+6592G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336998 | |||||||
chr5:64337001 | G | GTT | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1579+6596_1579+659 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64337001 | ||||||
chr5:64337009 | T | G | 12 | a0001c0001t0001g0111 a0001c0001t0001g0116 a0001c0001t0001g0117 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+6603T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337009 | |||||||
chr5:64337009 | T | TG | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1579+6603_1579+660 others(5): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337009 | |||||||
chr5:64337092 | G | T | 4 | a0001c0001t0009g0036 a0001c0001t0009g0037 a0001c0001t0009g0043 others(1): Show |
4 | HG00323.hp2 HG01175.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1579+6686G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337092 | |||||||
chr5:64337130 | C | T | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+6724C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337130 | |||||||
chr5:64337176 | G | T | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+6770G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337176 | |||||||
chr5:64337420 | A | G | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+7014A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337420 | |||||||
chr5:64337583 | G | A | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1579+7177G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337583 | |||||||
chr5:64337753 | G | A | 5 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+7347G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337753 | |||||||
chr5:64338114 | T | C | 85 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(82): Show |
86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1579+7708T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338114 | |||||||
chr5:64338272 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+7866A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338272 | |||||||
chr5:64338402 | A | T | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1579+7996A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338402 | |||||||
chr5:64338451 | G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+8045G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338451 | |||||||
chr5:64338452 | G | T | 18 | a0001c0001t0004g0078 a0001c0001t0004g0089 a0001c0001t0004g0090 others(15): Show |
18 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1579+8046G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338452 | |||||||
chr5:64338493 | G | T | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1579+8087G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338493 | |||||||
chr5:64338504 | G | A | 3 | a0001c0001t0002g0180 a0001c0001t0020g0024 a0003c0006t0002g0175 |
3 | HG00733.hp2 HG01168.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1579+8098G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338504 | |||||||
chr5:64338506 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1579+8100G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338506 | |||||||
chr5:64338591 | C | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+8185C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338591 | |||||||
chr5:64338634 | C | CA | 23 | a0001c0001t0003g0026 a0001c0001t0005g0167 a0001c0001t0005g0168 others(20): Show |
23 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1579+8244dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64338634 | ||||||
chr5:64338634 | CA | C | 11 | a0001c0001t0001g0136 a0001c0001t0002g0204 a0001c0001t0004g0086 others(8): Show |
11 | HG01516.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1579+8244delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64338634 | ||||||
chr5:64338797 | T | A | 22 | a0001c0001t0002g0080 a0001c0001t0002g0202 a0001c0001t0002g0203 others(19): Show |
22 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1579+8391T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338797 | |||||||
chr5:64338831 | C | T | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1579+8425C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338831 | |||||||
chr5:64338909 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1579+8503C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338909 | |||||||
chr5:64339089 | G | A | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1579+8683G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339089 | |||||||
chr5:64339139 | G | A | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1579+8733G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339139 | |||||||
chr5:64339407 | AT | A | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+9007delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64339407 | ||||||
chr5:64339694 | T | G | 1 | a0001c0001t0004g0002 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1579+9288T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339694 | |||||||
chr5:64339797 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1579+9391A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339797 | |||||||
chr5:64339988 | T | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1579+9582T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339988 | |||||||
chr5:64340054 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0143 |
3 | HG01256.hp2 HG02148.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1579+9648A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64340054 | |||||||
chr5:64340500 | T | C | 1 | a0006c0007t0002g0205 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1579+10094T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64340500 | |||||||
chr5:64340753 | G | T | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1579+10347G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64340753 | |||||||
chr5:64341379 | G | A | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1579+10973G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341379 | |||||||
chr5:64341481 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+11075G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341481 | |||||||
chr5:64341526 | G | A | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+11120G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341526 | |||||||
chr5:64341538 | C | T | 5 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0191 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+11132C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341538 | |||||||
chr5:64341621 | G | A | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+11215G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341621 | |||||||
chr5:64342078 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+11672C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342078 | |||||||
chr5:64342213 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1579+11807C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342213 | |||||||
chr5:64342348 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1579+11942T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342348 | |||||||
chr5:64342431 | G | T | 3 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0018g0059 |
3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1579+12025G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342431 | |||||||
chr5:64342505 | G | C | 5 | a0001c0001t0007g0038 a0001c0001t0009g0036 a0001c0001t0009g0037 others(2): Show |
5 | HG00323.hp2 HG01175.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+12099G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342505 | |||||||
chr5:64342823 | T | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1579+12417T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342823 | |||||||
chr5:64343462 | AATTTTCC others(485): Show |
A | 1 | a0001c0001t0002g0217 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1579+13218_1579+13 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64343462 | ||||||
chr5:64343533 | GA | G | 5 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+13130delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64343533 | ||||||
chr5:64343772 | A | G | 5 | a0001c0001t0007g0038 a0001c0001t0009g0036 a0001c0001t0009g0037 others(2): Show |
5 | HG00323.hp2 HG01175.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+13366A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64343772 | |||||||
chr5:64343870 | A | T | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+13464A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64343870 | |||||||
chr5:64343956 | T | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1579+13550T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64343956 | |||||||
chr5:64344144 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1579+13738C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344144 | |||||||
chr5:64344183 | C | A | 85 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(82): Show |
86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1579+13777C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344183 | |||||||
chr5:64344235 | G | A | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+13829G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344235 | |||||||
chr5:64344362 | C | T | 198 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1579+13956C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344362 | |||||||
chr5:64344368 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1579+13962A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344368 | |||||||
chr5:64344374 | C | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1579+13968C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344374 | |||||||
chr5:64344435 | G | A | 244 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(241): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1579+14029G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344435 | |||||||
chr5:64344444 | G | A | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+14038G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344444 | |||||||
chr5:64344530 | A | AAAAG | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1579+14127_1579+14 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64344530 | ||||||
chr5:64344822 | G | A | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1579+14416G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344822 | |||||||
chr5:64344944 | C | A | 1 | a0001c0001t0005g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+14538C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344944 | |||||||
chr5:64345320 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1579+14914A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345320 | |||||||
chr5:64345568 | T | G | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1579+15162T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345568 | |||||||
chr5:64345651 | C | T | 1 | a0001c0001t0003g0015 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1579+15245C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345651 | |||||||
chr5:64345698 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+15292A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345698 | |||||||
chr5:64345724 | G | T | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1579+15318G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345724 | |||||||
chr5:64345779 | C | G | 11 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0207 others(8): Show |
11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1579+15373C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345779 | |||||||
chr5:64345848 | C | CA | 4 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579+15449dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64345848 | ||||||
chr5:64345978 | C | A | 2 | a0001c0001t0002g0222 a0001c0003t0002g0246 |
2 | HG02040.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1579+15572C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345978 | |||||||
chr5:64345987 | A | ATCT | 141 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(138): Show |
142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1579+15582_1579+15 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64345987 | ||||||
chr5:64346097 | T | G | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1579+15691T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346097 | |||||||
chr5:64346106 | G | A | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1579+15700G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346106 | |||||||
chr5:64346135 | G | A | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1579+15729G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346135 | |||||||
chr5:64346198 | CATCTT | C | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+15798_1579+15 others(11): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346198 | ||||||
chr5:64346219 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1579+15813A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346219 | |||||||
chr5:64346296 | G | GT | 37 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(34): Show |
37 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1579+15899dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346296 | ||||||
chr5:64346359 | C | CT | 54 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0155 others(51): Show |
54 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1579+15980dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346359 | ||||||
chr5:64346359 | C | CTT | 5 | a0001c0001t0002g0177 a0002c0002t0006g0065 a0002c0002t0006g0070 others(2): Show |
5 | HG00741.hp2 HG01109.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+15979_1579+15 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346359 | ||||||
chr5:64346359 | CT | C | 29 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0130 others(26): Show |
29 | HG00323.hp1 HG01256.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.1579+15980delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346359 | ||||||
chr5:64346359 | CTT | C | 9 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0198 others(6): Show |
9 | HG02109.hp1 HG02559.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579+15979_1579+15 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346359 | ||||||
chr5:64346961 | T | C | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1579+16555T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346961 | |||||||
chr5:64347012 | C | T | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1579+16606C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347012 | |||||||
chr5:64347340 | G | A | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+16934G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347340 | |||||||
chr5:64347374 | G | A | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1579+16968G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347374 | |||||||
chr5:64347406 | A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1579+17000A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347406 | |||||||
chr5:64347428 | G | A | 1 | a0001c0001t0004g0097 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1579+17022G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347428 | |||||||
chr5:64347435 | C | G | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1579+17029C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347435 | |||||||
chr5:64347462 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1579+17056G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347462 | |||||||
chr5:64347544 | T | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1579+17138T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347544 | |||||||
chr5:64347554 | G | A | 28 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(25): Show |
28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+17148G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347554 | |||||||
chr5:64347830 | C | G | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1579+17424C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347830 | |||||||
chr5:64347880 | G | T | 1 | a0001c0001t0003g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1579+17474G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347880 | |||||||
chr5:64348223 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1579+17817G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64348223 | |||||||
chr5:64348490 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+18084A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64348490 | |||||||
chr5:64348495 | A | AT | 5 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0097 others(2): Show |
5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+18094dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64348495 | ||||||
chr5:64348710 | C | A | 1 | a0001c0001t0002g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1579+18304C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64348710 | |||||||
chr5:64348753 | C | A | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1579+18347C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64348753 | |||||||
chr5:64349096 | T | G | 12 | a0001c0001t0027g0060 a0002c0002t0006g0065 a0002c0002t0006g0066 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+18690T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349096 | |||||||
chr5:64349283 | C | T | 1 | a0001c0001t0005g0237 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1579+18877C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349283 | |||||||
chr5:64349410 | C | CT | 86 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0085 others(83): Show |
87 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1579+19016dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64349410 | ||||||
chr5:64349410 | C | CTT | 16 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0128 others(13): Show |
16 | HG01081.hp2 HG01106.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1579+19015_1579+19 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64349410 | ||||||
chr5:64349673 | T | G | 31 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(28): Show |
31 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1579+19267T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349673 | |||||||
chr5:64349702 | C | T | 1 | a0002c0002t0006g0068 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1579+19296C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349702 | |||||||
chr5:64349795 | C | G | 1 | a0001c0001t0003g0016 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1579+19389C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349795 | |||||||
chr5:64349929 | T | G | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1579+19523T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349929 | |||||||
chr5:64349935 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1579+19529T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349935 | |||||||
chr5:64350187 | T | C | 15 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(12): Show |
15 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1580-19428T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350187 | |||||||
chr5:64350322 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1580-19293C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350322 | |||||||
chr5:64350352 | G | A | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1580-19263G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350352 | |||||||
chr5:64350435 | C | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0142 a0001c0001t0005g0084 |
3 | HG02257.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1580-19180C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350435 | |||||||
chr5:64350436 | G | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-19179G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350436 | |||||||
chr5:64350456 | T | C | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-19159T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350456 | |||||||
chr5:64350465 | A | G | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1580-19150A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350465 | |||||||
chr5:64350513 | A | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
6 | HG00738.hp1 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-19102A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350513 | |||||||
chr5:64350761 | G | C | 29 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(26): Show |
29 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1580-18854G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350761 | |||||||
chr5:64350766 | A | G | 4 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-18849A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350766 | |||||||
chr5:64350821 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1580-18794A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350821 | |||||||
chr5:64350906 | C | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1580-18709C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350906 | |||||||
chr5:64350964 | A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-18651A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350964 | |||||||
chr5:64351081 | T | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1580-18534T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351081 | |||||||
chr5:64351189 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1580-18426C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351189 | |||||||
chr5:64351354 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1580-18261G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351354 | |||||||
chr5:64351548 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-18067A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351548 | |||||||
chr5:64351571 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-18044A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351571 | |||||||
chr5:64351614 | T | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-18001T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351614 | |||||||
chr5:64351620 | T | C | 3 | a0001c0001t0002g0180 a0001c0001t0020g0024 a0003c0006t0002g0175 |
3 | HG00733.hp2 HG01168.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1580-17995T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351620 | |||||||
chr5:64351659 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17956T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351659 | |||||||
chr5:64351665 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17950A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351665 | |||||||
chr5:64351677 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17938T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351677 | |||||||
chr5:64351716 | T | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17899T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351716 | |||||||
chr5:64351718 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17897G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351718 | |||||||
chr5:64351722 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17893G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351722 | |||||||
chr5:64351724 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17891T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351724 | |||||||
chr5:64351725 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17890G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351725 | |||||||
chr5:64351747 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17868A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351747 | |||||||
chr5:64351768 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17847T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351768 | |||||||
chr5:64351799 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17816A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351799 | |||||||
chr5:64351924 | G | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1580-17691G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351924 | |||||||
chr5:64351940 | C | T | 19 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(16): Show |
19 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1580-17675C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351940 | |||||||
chr5:64351954 | T | G | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1580-17661T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351954 | |||||||
chr5:64352217 | T | G | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1580-17398T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352217 | |||||||
chr5:64352218 | A | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1580-17397A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352218 | |||||||
chr5:64352495 | G | A | 118 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(115): Show |
119 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1580-17120G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352495 | |||||||
chr5:64352705 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1580-16910T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352705 | |||||||
chr5:64352952 | G | C | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1580-16663G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352952 | |||||||
chr5:64353251 | T | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-16364T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353251 | |||||||
chr5:64353518 | G | A | 198 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1580-16097G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353518 | |||||||
chr5:64353632 | G | A | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1580-15983G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353632 | |||||||
chr5:64353682 | T | C | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1580-15933T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353682 | |||||||
chr5:64353740 | T | C | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG01433.hp2 HG01928.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-15875T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353740 | |||||||
chr5:64353754 | T | C | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1580-15861T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353754 | |||||||
chr5:64353784 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1580-15831G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353784 | |||||||
chr5:64353997 | T | G | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1580-15618T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353997 | |||||||
chr5:64354115 | C | A | 6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1580-15500C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354115 | |||||||
chr5:64354218 | A | G | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1580-15397A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354218 | |||||||
chr5:64354283 | C | A | 187 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1580-15332C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354283 | |||||||
chr5:64354434 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1580-15181G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354434 | |||||||
chr5:64354443 | T | C | 1 | a0001c0001t0004g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1580-15172T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354443 | |||||||
chr5:64354543 | T | C | 1 | a0001c0001t0003g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1580-15072T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354543 | |||||||
chr5:64354606 | C | A | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1580-15009C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354606 | |||||||
chr5:64354744 | C | T | 27 | a0001c0001t0004g0002 a0001c0001t0004g0078 a0001c0001t0004g0086 others(24): Show |
28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1580-14871C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354744 | |||||||
chr5:64354783 | TA | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1580-14824delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64354783 | ||||||
chr5:64354794 | T | G | 245 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1580-14821T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354794 | |||||||
chr5:64354858 | G | A | 1 | a0002c0002t0008g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1580-14757G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354858 | |||||||
chr5:64354960 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1580-14655A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354960 | |||||||
chr5:64355056 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1580-14559G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64355056 | |||||||
chr5:64355609 | A | G | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1580-14006A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64355609 | |||||||
chr5:64355931 | G | C | 1 | a0001c0001t0004g0098 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1580-13684G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64355931 | |||||||
chr5:64356043 | G | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1580-13572G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64356043 | |||||||
chr5:64356255 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1580-13360A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64356255 | |||||||
chr5:64356259 | C | CA | 11 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0207 others(8): Show |
11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1580-13345dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64356259 | ||||||
chr5:64357400 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1580-12215C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64357400 | |||||||
chr5:64357711 | G | A | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1580-11904G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64357711 | |||||||
chr5:64357788 | G | A | 1 | a0001c0001t0013g0013 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1580-11827G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64357788 | |||||||
chr5:64357800 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1580-11815G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64357800 | |||||||
chr5:64358230 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1580-11385G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358230 | |||||||
chr5:64358361 | C | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1580-11254C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358361 | |||||||
chr5:64358431 | G | C | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1580-11184G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358431 | |||||||
chr5:64358558 | G | A | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1580-11057G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358558 | |||||||
chr5:64358644 | A | AT | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1580-10962dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64358644 | ||||||
chr5:64358644 | AT | A | 21 | a0001c0001t0002g0215 a0001c0001t0005g0167 a0001c0001t0005g0168 others(18): Show |
21 | HG00597.hp1 HG01993.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1580-10962delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64358644 | ||||||
chr5:64358688 | T | A | 2 | a0001c0001t0026g0247 a0001c0001t0027g0060 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1580-10927T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358688 | |||||||
chr5:64358765 | A | G | 2 | a0001c0001t0004g0089 a0001c0001t0004g0090 |
2 | NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1580-10850A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358765 | |||||||
chr5:64358790 | C | G | 5 | a0001c0001t0002g0225 a0001c0001t0002g0226 a0001c0001t0002g0227 others(2): Show |
5 | NA18950.hp1 NA18984.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-10825C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358790 | |||||||
chr5:64358853 | C | T | 30 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(27): Show |
30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1580-10762C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358853 | |||||||
chr5:64358980 | C | A | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-10635C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358980 | |||||||
chr5:64359231 | A | C | 29 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(26): Show |
29 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1580-10384A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359231 | |||||||
chr5:64359238 | T | G | 29 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(26): Show |
29 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1580-10377T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359238 | |||||||
chr5:64359244 | C | T | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1580-10371C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359244 | |||||||
chr5:64359287 | C | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1580-10328C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359287 | |||||||
chr5:64359319 | T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-10296T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359319 | |||||||
chr5:64359461 | C | T | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1580-10154C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359461 | |||||||
chr5:64359830 | A | G | 1 | a0001c0001t0015g0033 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1580-9785A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359830 | |||||||
chr5:64359882 | T | C | 1 | a0001c0001t0003g0025 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1580-9733T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359882 | |||||||
chr5:64360018 | G | A | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1580-9597G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360018 | |||||||
chr5:64360058 | T | C | 19 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(16): Show |
19 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1580-9557T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360058 | |||||||
chr5:64360115 | C | G | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1580-9500C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360115 | |||||||
chr5:64360226 | A | G | 3 | a0001c0001t0003g0011 a0001c0001t0003g0014 a0001c0001t0003g0017 |
3 | HG02602.hp1 HG03491.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1580-9389A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360226 | |||||||
chr5:64360264 | G | A | 5 | a0001c0001t0004g0089 a0002c0002t0008g0061 a0002c0002t0008g0062 others(2): Show |
5 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-9351G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360264 | |||||||
chr5:64360290 | A | G | 9 | a0001c0001t0002g0027 a0001c0001t0003g0004 a0001c0001t0003g0005 others(6): Show |
9 | HG00642.hp2 HG00741.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1580-9325A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360290 | |||||||
chr5:64360319 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1580-9296G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360319 | |||||||
chr5:64360447 | T | C | 245 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1580-9168T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360447 | |||||||
chr5:64360495 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0187 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1580-9120C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360495 | |||||||
chr5:64360585 | G | T | 11 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0207 others(8): Show |
11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1580-9030G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360585 | |||||||
chr5:64360751 | G | T | 31 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(28): Show |
31 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1580-8864G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360751 | |||||||
chr5:64360882 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1580-8733G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360882 | |||||||
chr5:64361018 | G | A | 144 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1580-8597G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361018 | |||||||
chr5:64361068 | G | C | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1580-8547G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361068 | |||||||
chr5:64361165 | G | A | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1580-8450G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361165 | |||||||
chr5:64361236 | A | C | 1 | a0001c0001t0005g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1580-8379A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361236 | |||||||
chr5:64361282 | A | G | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-8333A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361282 | |||||||
chr5:64361283 | GAC | G | 31 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(28): Show |
31 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1580-8330_1580-832 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64361283 | ||||||
chr5:64361713 | A | C | 2 | a0002c0002t0006g0068 a0002c0002t0006g0072 |
2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1580-7902A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361713 | |||||||
chr5:64361914 | T | C | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1580-7701T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361914 | |||||||
chr5:64361984 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1580-7631C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361984 | |||||||
chr5:64362057 | ATTAAAC | A | 4 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0010g0076 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-7552_1580-754 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362057 | ||||||
chr5:64362262 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0003g0031 |
2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1580-7353C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362262 | |||||||
chr5:64362510 | C | G | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1580-7105C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362510 | |||||||
chr5:64362514 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1580-7101G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362514 | |||||||
chr5:64362690 | A | G | 1 | a0001c0001t0002g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1580-6925A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362690 | |||||||
chr5:64362775 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1580-6840A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362775 | |||||||
chr5:64362873 | T | C | 4 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0010g0076 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-6742T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362873 | |||||||
chr5:64362908 | T | TCCTTTGC others(300): Show |
14 | a0001c0001t0005g0234 a0001c0001t0005g0235 a0001c0001t0005g0237 others(11): Show |
14 | HG00597.hp1 HG02818.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1580-6691_1580-669 others(311): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | ||||||
chr5:64362908 | T | TCCTTTGC others(300): Show |
5 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0191 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-6691_1580-669 others(311): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | ||||||
chr5:64362908 | T | TCCTTTGC others(300): Show |
2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1580-6691_1580-669 others(311): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | ||||||
chr5:64362908 | T | TCCTTTGC others(301): Show |
1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1580-6691_1580-669 others(312): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | ||||||
chr5:64362908 | T | TCCTTTGC others(314): Show |
1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1580-6691_1580-669 others(325): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | ||||||
chr5:64362908 | T | TCCTTTGC others(326): Show |
1 | a0001c0001t0005g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1580-6691_1580-669 others(337): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | ||||||
chr5:64362908 | T | TCCTTTGC others(327): Show |
4 | a0001c0001t0005g0168 a0001c0001t0005g0169 a0001c0001t0005g0170 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-6691_1580-669 others(338): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | ||||||
chr5:64362908 | T | TCCTTTGC others(329): Show |
1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1580-6691_1580-669 others(340): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | ||||||
chr5:64363406 | T | C | 1 | a0001c0001t0003g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1580-6209T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64363406 | |||||||
chr5:64363665 | C | A | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-5950C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64363665 | |||||||
chr5:64363720 | A | C | 15 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(12): Show |
15 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1580-5895A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64363720 | |||||||
chr5:64364090 | C | G | 1 | a0001c0001t0003g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1580-5525C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364090 | |||||||
chr5:64364223 | A | G | 5 | a0001c0001t0004g0086 a0001c0001t0004g0092 a0001c0001t0004g0099 others(2): Show |
5 | HG02615.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-5392A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364223 | |||||||
chr5:64364426 | T | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-5189T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364426 | |||||||
chr5:64364468 | A | G | 11 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(8): Show |
11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1580-5147A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364468 | |||||||
chr5:64364597 | G | A | 2 | a0001c0001t0019g0166 a0001c0001t0024g0192 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1580-5018G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364597 | |||||||
chr5:64364619 | A | G | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-4996A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364619 | |||||||
chr5:64364866 | G | A | 1 | a0001c0001t0004g0095 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1580-4749G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364866 | |||||||
chr5:64364917 | TC | T | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1580-4694delC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64364917 | ||||||
chr5:64365000 | C | CA | 31 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(28): Show |
32 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.1580-4604dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64365000 | ||||||
chr5:64365213 | T | G | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1580-4402T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365213 | |||||||
chr5:64365325 | C | A | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1580-4290C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365325 | |||||||
chr5:64365722 | G | A | 4 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0010g0076 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-3893G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365722 | |||||||
chr5:64365742 | G | A | 2 | a0001c0001t0026g0247 a0001c0001t0027g0060 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1580-3873G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365742 | |||||||
chr5:64365773 | T | G | 1 | a0001c0001t0022g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1580-3842T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365773 | |||||||
chr5:64365825 | T | C | 20 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(17): Show |
20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1580-3790T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365825 | |||||||
chr5:64365867 | T | C | 11 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(8): Show |
11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1580-3748T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365867 | |||||||
chr5:64365999 | A | AT | 10 | a0001c0001t0005g0084 a0001c0001t0005g0188 a0001c0001t0005g0189 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1580-3613dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64365999 | ||||||
chr5:64366488 | C | T | 1 | a0001c0001t0005g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1580-3127C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64366488 | |||||||
chr5:64366629 | A | T | 3 | a0002c0002t0008g0062 a0002c0002t0008g0063 a0002c0002t0008g0064 |
3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1580-2986A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64366629 | |||||||
chr5:64366643 | C | A | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1580-2972C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64366643 | |||||||
chr5:64366787 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1580-2828G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64366787 | |||||||
chr5:64367054 | T | A | 1 | a0001c0001t0004g0098 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1580-2561T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367054 | |||||||
chr5:64367204 | G | A | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-2411G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367204 | |||||||
chr5:64367262 | T | C | 15 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(12): Show |
15 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1580-2353T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367262 | |||||||
chr5:64367266 | A | G | 4 | a0002c0002t0010g0057 a0002c0002t0010g0058 a0002c0002t0010g0076 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-2349A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367266 | |||||||
chr5:64367347 | A | G | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1580-2268A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367347 | |||||||
chr5:64367407 | A | C | 1 | a0001c0001t0004g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1580-2208A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367407 | |||||||
chr5:64367503 | G | T | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-2112G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367503 | |||||||
chr5:64367564 | TA | T | 5 | a0001c0001t0005g0189 a0001c0001t0005g0190 a0001c0001t0005g0191 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-2048delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64367564 | ||||||
chr5:64367848 | T | A | 1 | a0001c0001t0004g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1580-1767T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367848 | |||||||
chr5:64368076 | G | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1580-1539G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368076 | |||||||
chr5:64368419 | T | C | 2 | a0001c0001t0014g0055 a0001c0001t0014g0056 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-1196T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368419 | |||||||
chr5:64368424 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1580-1191T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368424 | |||||||
chr5:64368630 | C | T | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1580-985C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368630 | |||||||
chr5:64368655 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1580-960G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368655 | |||||||
chr5:64368865 | C | G | 3 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 |
3 | HG02109.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1580-750C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368865 | |||||||
chr5:64368887 | T | C | 3 | a0001c0001t0003g0025 a0001c0001t0003g0041 a0001c0001t0003g0124 |
3 | HG01168.hp1 HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1580-728T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368887 | |||||||
chr5:64368908 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1580-707C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368908 | |||||||
chr5:64368984 | C | A | 2 | a0001c0001t0004g0086 a0001c0001t0004g0092 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1580-631C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368984 | |||||||
chr5:64369058 | C | T | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1580-557C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369058 | |||||||
chr5:64369081 | T | C | 2 | a0001c0001t0026g0247 a0001c0001t0027g0060 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1580-534T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369081 | |||||||
chr5:64369097 | T | C | 1 | a0001c0001t0002g0223 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1580-518T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369097 | |||||||
chr5:64369148 | A | T | 1 | a0001c0001t0002g0223 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1580-467A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369148 | |||||||
chr5:64369159 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-456G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369159 | |||||||
chr5:64369176 | A | T | 11 | a0002c0002t0006g0065 a0002c0002t0006g0066 a0002c0002t0006g0068 others(8): Show |
11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1580-439A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369176 | |||||||
chr5:64369204 | G | A | 59 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(56): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1580-411G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369204 | |||||||
chr5:64369361 | A | T | 2 | a0002c0002t0006g0074 a0002c0002t0006g0075 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1580-254A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369361 | |||||||
chr5:64369449 | TTAAAG | T | 4 | a0001c0001t0005g0190 a0001c0001t0005g0191 a0001c0001t0024g0192 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-163_1580-159d others(7): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64369449 | ||||||
chr5:64369466 | TA | T | 139 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(136): Show |
140 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1580-139delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64369466 | ||||||
chr5:64369476 | A | G | 3 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0188 |
3 | HG03098.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1580-139A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369476 | |||||||
chr5:64369477 | G | A | 3 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0001t0005g0188 |
3 | HG03098.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1580-138G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369477 | |||||||
chr5:64369508 | G | A | 142 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(139): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-107G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369508 |