Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 254225 |
| ensemblid | ENSG00000166439.6 |
| hgncid | 26961 |
| symbol | RNF169 |
| name | ring finger protein 169 |
| refseq_nuc | NM_001098638.2 |
| refseq_prot | NP_001092108.1 |
| ensembl_nuc | ENST00000299563.5 |
| ensembl_prot | ENSP00000299563.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 74748849 |
| end | 74842413 |
| strand | + |
| ver | v1.2 |
| region | chr11:74748849-74842413 |
| region5000 | chr11:74743849-74847413 |
| regionname0 | RNF169_chr11_74748849_74842413 |
| regionname5000 | RNF169_chr11_74743849_74847413 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 708 | 337 | 81 | 54 | 148 | 18 | 34 | 119 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAG others(703): Show |
chr11 | 74743849 | 74847413 |
| a0002 | 0/0 | 708 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAG others(703): Show |
chr11 | 74743849 | 74847413 |
| a0003 | 0/0 | 708 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAG others(703): Show |
chr11 | 74743849 | 74847413 |
| a0004 | 0/0 | 708 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAG others(703): Show |
chr11 | 74743849 | 74847413 |
| a0005 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAG others(703): Show |
chr11 | 74743849 | 74847413 |
| a0006 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAG others(703): Show |
chr11 | 74743849 | 74847413 |
| a0007 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAG others(703): Show |
chr11 | 74743849 | 74847413 |
| a0008 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAG others(703): Show |
chr11 | 74743849 | 74847413 |
| a0009 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | MAAAD others(703): Show |
chr11 | 74743849 | 74847413 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2124 | 233 | 63 | 41 | 97 | 9 | 21 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0001c0002 | 0/0 | 2124 | 98 | 16 | 13 | 49 | 8 | 12 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0001c0006 | 0/0 | 2124 | 2 | 1 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0001c0008 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0001c0010 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0001c0012 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0001c0014 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0002c0003 | 0/0 | 2124 | 8 | 8 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0003c0004 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0004c0005 | 0/0 | 2124 | 2 | 0 | 0 | 0 | 0 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0005c0013 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0006c0015 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0007c0009 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0008c0011 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 | ||
| a0009c0007 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | ATGGC others(2119): Show |
chr11 | 74743849 | 74847413 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7841 | 5 | 2 | 3 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0002 | 0/0 | 7842 | 69 | 3 | 10 | 52 | 2 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0003 | 1/0 | 7842 | 64 | 6 | 13 | 28 | 5 | 11 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0004 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0005 | 0/0 | 7842 | 3 | 1 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0006 | 0/0 | 7841 | 9 | 9 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0007 | 0/0 | 7841 | 9 | 1 | 1 | 4 | 1 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0008 | 0/0 | 7840 | 7 | 7 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0009 | 0/0 | 7841 | 7 | 0 | 3 | 4 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0011 | 0/0 | 7841 | 6 | 6 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0012 | 0/1 | 7842 | 5 | 0 | 2 | 0 | 1 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0013 | 0/0 | 7842 | 4 | 3 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0014 | 0/0 | 7842 | 4 | 4 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0015 | 0/0 | 7842 | 4 | 4 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0018 | 0/0 | 7843 | 3 | 0 | 2 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7838): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0019 | 0/0 | 7841 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0022 | 0/0 | 7841 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0024 | 0/0 | 7840 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0025 | 0/0 | 7842 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0026 | 0/0 | 7842 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0028 | 0/0 | 7863 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7858): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0030 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0031 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0033 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0037 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0044 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0045 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0046 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0047 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0048 | 0/0 | 7842 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0049 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0050 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0051 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0052 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0053 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0054 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0055 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0056 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0057 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0058 | 0/0 | 7843 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7838): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0059 | 0/0 | 7842 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0060 | 0/0 | 7842 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0001t0062 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0001 | 0/0 | 7841 | 64 | 8 | 12 | 35 | 3 | 6 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0004 | 0/0 | 7840 | 8 | 2 | 0 | 2 | 3 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0005 | 0/0 | 7842 | 7 | 2 | 0 | 5 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0010 | 0/0 | 7842 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0017 | 0/0 | 7841 | 3 | 0 | 0 | 3 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0020 | 0/0 | 7841 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0021 | 0/0 | 7841 | 2 | 0 | 0 | 0 | 0 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0027 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0029 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0032 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0034 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0035 | 0/0 | 7842 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0036 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7838): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0038 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0039 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0040 | 0/0 | 7840 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0042 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0002t0061 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0006t0002 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0006t0043 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7838): Show |
chr11 | 74743849 | 74847413 |
| a0001c0008t0001 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0010t0003 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0001c0012t0001 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0001c0014t0001 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0002c0003t0010 | 0/0 | 7842 | 5 | 5 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0002c0003t0016 | 0/0 | 7841 | 3 | 3 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0003c0004t0023 | 0/0 | 7841 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0004c0005t0001 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0004c0005t0004 | 0/0 | 7840 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7835): Show |
chr11 | 74743849 | 74847413 |
| a0005c0013t0002 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7837): Show |
chr11 | 74743849 | 74847413 |
| a0006c0015t0001 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0007c0009t0001 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0008c0011t0041 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| a0009c0007t0001 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | GCAAC others(7836): Show |
chr11 | 74743849 | 74847413 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0006g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0007g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0009g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0009g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0009g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0009g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0011g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0012g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0012g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0012g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0012g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0013g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0013g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0013g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0013g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0014g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0014g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0015g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0015g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0015g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0015g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0018g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0018g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0019g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0019g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0022g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0022g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0024g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0024g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0025g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0025g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0026g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0026g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0028g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0030g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0031g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0033g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0037g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0044g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0045g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0046g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0047g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0048g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0049g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0050g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0051g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0052g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0053g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0054g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0055g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0056g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0057g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0058g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0059g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0060g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0001t0062g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0004g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0010g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0017g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0017g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0017g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0020g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0020g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0021g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0021g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0027g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0029g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0032g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0034g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0035g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0036g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0038g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0039g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0040g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0042g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0002t0061g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0006t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0006t0043g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0008t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0010t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0012t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0001c0014t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0002c0003t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0002c0003t0010g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0002c0003t0010g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0002c0003t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0002c0003t0010g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0002c0003t0016g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0002c0003t0016g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0003c0004t0023g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0003c0004t0023g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0004c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0004c0005t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0005c0013t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0006c0015t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0007c0009t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0008c0011t0041g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| a0009c0007t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0012 | g0183 | EUR | GBR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0230 | EUR | GBR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0237 | EUR | GBR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0064 | EUR | GBR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0194 | EUR | FIN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | FIN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0021 | EUR | FIN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0062 | EUR | FIN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00408 | hp1 | a0001 | c0002 | t0005 | g0116 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00621 | hp2 | a0005 | c0013 | t0002 | g0220 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00642 | hp2 | a0001 | c0001 | t0018 | g0001 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0202 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01071 | hp1 | a0001 | c0001 | t0060 | g0231 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01099 | hp1 | a0001 | c0001 | t0013 | g0311 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0251 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01167 | hp1 | a0001 | c0001 | t0012 | g0214 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01167 | hp2 | a0001 | c0002 | t0040 | g0073 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0325 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01169 | hp1 | a0001 | c0001 | t0018 | g0222 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0205 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01256 | hp2 | a0001 | c0001 | t0019 | g0020 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01258 | hp1 | a0001 | c0001 | t0012 | g0171 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01258 | hp2 | a0001 | c0001 | t0019 | g0025 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01361 | hp1 | a0001 | c0001 | t0059 | g0333 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0024 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0324 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0207 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0250 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0097 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0005 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01517 | hp2 | a0001 | c0002 | t0004 | g0054 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0330 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02040 | hp2 | a0001 | c0001 | t0051 | g0226 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02055 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0217 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02145 | hp1 | a0001 | c0001 | t0022 | g0150 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02145 | hp2 | a0001 | c0002 | t0038 | g0004 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0321 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | CDX | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | CDX | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | CDX | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | CDX | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02257 | hp2 | a0001 | c0001 | t0057 | g0209 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02258 | hp1 | a0002 | c0003 | t0016 | g0014 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0146 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02280 | hp2 | a0006 | c0015 | t0001 | g0152 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02451 | hp1 | a0002 | c0003 | t0016 | g0014 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02572 | hp1 | a0001 | c0001 | t0014 | g0122 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0136 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0180 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02615 | hp2 | a0001 | c0002 | t0039 | g0037 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0163 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02622 | hp2 | a0001 | c0001 | t0030 | g0148 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0314 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02647 | hp1 | a0001 | c0001 | t0026 | g0272 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02647 | hp2 | a0003 | c0004 | t0023 | g0128 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02683 | hp1 | a0001 | c0002 | t0010 | g0080 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0232 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02723 | hp1 | a0001 | c0001 | t0022 | g0147 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0125 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0156 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0115 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02809 | hp2 | a0002 | c0003 | t0010 | g0015 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02886 | hp1 | a0003 | c0004 | t0023 | g0124 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0087 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02895 | hp1 | a0001 | c0001 | t0053 | g0164 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02895 | hp2 | a0001 | c0001 | t0037 | g0313 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02896 | hp2 | a0002 | c0003 | t0016 | g0015 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02897 | hp1 | a0002 | c0003 | t0010 | g0306 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02897 | hp2 | a0001 | c0001 | t0015 | g0316 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02922 | hp2 | a0001 | c0001 | t0044 | g0137 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0169 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0140 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0161 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03041 | hp2 | a0001 | c0001 | t0015 | g0315 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0086 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03098 | hp2 | a0001 | c0002 | t0032 | g0085 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03130 | hp1 | a0001 | c0001 | t0050 | g0244 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0138 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0004 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0158 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03453 | hp1 | a0002 | c0003 | t0010 | g0308 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03453 | hp2 | a0007 | c0009 | t0001 | g0028 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03490 | hp2 | a0004 | c0005 | t0004 | g0046 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03492 | hp1 | a0004 | c0005 | t0001 | g0093 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03516 | hp1 | a0001 | c0001 | t0026 | g0271 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0041 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03540 | hp1 | a0002 | c0003 | t0010 | g0307 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0310 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0105 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03831 | hp1 | a0001 | c0001 | t0018 | g0192 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0023 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03927 | hp1 | a0001 | c0002 | t0061 | g0112 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03942 | hp1 | a0001 | c0001 | t0058 | g0001 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03942 | hp2 | a0001 | c0002 | t0035 | g0104 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0277 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04115 | hp2 | a0001 | c0001 | t0049 | g0022 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0102 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0301 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04199 | hp1 | a0001 | c0002 | t0004 | g0107 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04204 | hp1 | a0001 | c0001 | t0048 | g0236 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04204 | hp2 | a0001 | c0002 | t0021 | g0063 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04228 | hp1 | a0001 | c0002 | t0021 | g0052 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0287 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0162 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18612 | hp1 | a0001 | c0002 | t0005 | g0043 | EAS | CHB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18906 | hp1 | a0001 | c0002 | t0042 | g0026 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0160 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18940 | hp1 | a0001 | c0001 | t0055 | g0265 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18942 | hp2 | a0001 | c0002 | t0034 | g0286 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18946 | hp1 | a0001 | c0001 | t0009 | g0157 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0281 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18951 | hp2 | a0001 | c0001 | t0046 | g0283 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18961 | hp1 | a0001 | c0002 | t0020 | g0053 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18964 | hp1 | a0001 | c0001 | t0025 | g0256 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18965 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18966 | hp2 | a0001 | c0002 | t0020 | g0051 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18971 | hp1 | a0008 | c0011 | t0041 | g0066 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18973 | hp2 | a0001 | c0002 | t0005 | g0045 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18979 | hp1 | a0001 | c0001 | t0009 | g0296 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0241 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18987 | hp1 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18993 | hp1 | a0001 | c0001 | t0025 | g0191 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18994 | hp2 | a0001 | c0001 | t0024 | g0013 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18998 | hp1 | a0001 | c0002 | t0017 | g0057 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19005 | hp1 | a0001 | c0006 | t0002 | g0001 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19030 | hp1 | a0001 | c0006 | t0043 | g0123 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19030 | hp2 | a0001 | c0014 | t0001 | g0291 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19043 | hp2 | a0001 | c0001 | t0031 | g0142 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19054 | hp2 | a0001 | c0002 | t0036 | g0089 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0240 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19057 | hp2 | a0001 | c0002 | t0004 | g0069 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19060 | hp1 | a0001 | c0002 | t0005 | g0094 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19062 | hp1 | a0001 | c0002 | t0017 | g0095 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19064 | hp2 | a0001 | c0001 | t0054 | g0274 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19065 | hp1 | a0001 | c0002 | t0005 | g0048 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19074 | hp1 | a0001 | c0002 | t0017 | g0061 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19075 | hp2 | a0001 | c0010 | t0003 | g0320 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19081 | hp1 | a0001 | c0001 | t0024 | g0298 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19090 | hp2 | a0001 | c0001 | t0052 | g0278 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ASW | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20129 | hp2 | a0001 | c0001 | t0062 | g0243 | AFR | ASW | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20752 | hp1 | a0001 | c0008 | t0001 | g0106 | EUR | TSI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20752 | hp2 | a0001 | c0002 | t0027 | g0114 | EUR | TSI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20805 | hp1 | a0001 | c0002 | t0029 | g0076 | EUR | TSI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0206 | EUR | TSI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20905 | hp1 | a0001 | c0012 | t0001 | g0047 | SAS | GIH | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | GIH | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02486 | hp1 | a0001 | c0001 | t0033 | g0033 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02559 | hp1 | a0001 | c0001 | t0056 | g0165 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG02559 | hp2 | a0001 | c0001 | t0047 | g0195 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG03471 | hp2 | a0002 | c0003 | t0010 | g0309 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0318 | AFR | USA | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0312 | AFR | USA | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20300 | hp1 | a0001 | c0001 | t0045 | g0159 | AFR | USA | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA20300 | hp2 | a0009 | c0007 | t0001 | g0151 | AFR | USA | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0317 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0012 | g0254 | REF | REF | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0167 | REF | REF | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74748894 | G | A | 1 | a0009 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.14G>A | p.Gly5Asp | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 46/7842 | 14/2127 | 5/708 | chr11 | 74748894 | |||
| chr11:74749001 | C | T | 1 | a0002 | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
missense_variant | MODERATE | c.121C>T | p.Pro41Ser | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 153/7842 | 121/2127 | 41/708 | chr11 | 74749001 | |||
| chr11:74749184 | G | A | 1 | a0007 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.304G>A | p.Gly102Ser | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 336/7842 | 304/2127 | 102/708 | chr11 | 74749184 | |||
| chr11:74789673 | C | T | 1 | a0006 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.550C>T | p.Arg184Cys | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/6 | 582/7842 | 550/2127 | 184/708 | chr11 | 74789673 | |||
| chr11:74835637 | T | C | 1 | a0003 | 2 | HG02647.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.1034T>C | p.Ile345Thr | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1066/7842 | 1034/2127 | 345/708 | chr11 | 74835637 | |||
| chr11:74836329 | G | T | 1 | a0004 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1726G>T | p.Val576Leu | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1758/7842 | 1726/2127 | 576/708 | chr11 | 74836329 | |||
| chr11:74836612 | G | A | 1 | a0005 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.2009G>A | p.Arg670Gln | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2041/7842 | 2009/2127 | 670/708 | chr11 | 74836612 | |||
| chr11:74836636 | G | A | 1 | a0008 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.2033G>A | p.Arg678His | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2065/7842 | 2033/2127 | 678/708 | chr11 | 74836636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74748946 | G | A | 1 | a0001c0008 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.66G>A | p.Arg22Arg | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 98/7842 | 66/2127 | 22/708 | chr11 | 74748946 | |||
| chr11:74749120 | C | T | 1 | a0001c0006 | 2 | NA19005.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.240C>T | p.Ala80Ala | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 272/7842 | 240/2127 | 80/708 | chr11 | 74749120 | |||
| chr11:74810186 | G | C | 1 | a0001c0010 | 1 | NA19075.hp2 | splice_region_variant&synonymous_variant | LOW | c.579G>C | p.Leu193Leu | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/6 | 611/7842 | 579/2127 | 193/708 | chr11 | 74810186 | |||
| chr11:74835860 | G | A | 5 | a0001c0002 a0001c0008 a0001c0012 others(2): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
synonymous_variant | LOW | c.1257G>A | p.Gln419Gln | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1289/7842 | 1257/2127 | 419/708 | chr11 | 74835860 | |||
| chr11:74836187 | C | T | 1 | a0001c0012 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1584C>T | p.Thr528Thr | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1616/7842 | 1584/2127 | 528/708 | chr11 | 74836187 | |||
| chr11:74836274 | C | T | 1 | a0001c0014 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1671C>T | p.Ala557Ala | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1703/7842 | 1671/2127 | 557/708 | chr11 | 74836274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74748859 | C | G | 1 | a0001c0001t0062 | 1 | NA20129.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-22C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | chr11 | 74748859 | |||||||
| chr11:74836843 | T | C | 1 | a0001c0002t0027 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 113 | chr11 | 74836843 | ||||||
| chr11:74836869 | G | C | 1 | a0001c0001t0019 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 139 | chr11 | 74836869 | ||||||
| chr11:74836954 | G | A | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*224G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 224 | chr11 | 74836954 | ||||||
| chr11:74836959 | A | T | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*229A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 229 | chr11 | 74836959 | ||||||
| chr11:74836963 | G | A | 1 | a0001c0002t0029 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*233G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 233 | chr11 | 74836963 | ||||||
| chr11:74836966 | A | T | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 236 | chr11 | 74836966 | ||||||
| chr11:74836967 | G | T | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*237G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 237 | chr11 | 74836967 | ||||||
| chr11:74836969 | A | G | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 239 | chr11 | 74836969 | ||||||
| chr11:74836970 | C | G | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 240 | chr11 | 74836970 | ||||||
| chr11:74836980 | A | T | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 250 | chr11 | 74836980 | ||||||
| chr11:74837001 | G | GAGTAATA others(14): Show |
1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271_*272insAGTAAT others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 272 | chr11 | 74837001 | ||||||
| chr11:74837002 | G | T | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*272G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 272 | chr11 | 74837002 | ||||||
| chr11:74837005 | C | G | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*275C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 275 | chr11 | 74837005 | ||||||
| chr11:74837013 | C | T | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 283 | chr11 | 74837013 | ||||||
| chr11:74837014 | C | A | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 284 | chr11 | 74837014 | ||||||
| chr11:74837016 | C | G | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*286C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 286 | chr11 | 74837016 | ||||||
| chr11:74837019 | T | G | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*289T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 289 | chr11 | 74837019 | ||||||
| chr11:74837044 | T | G | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*314T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 314 | chr11 | 74837044 | ||||||
| chr11:74837045 | T | A | 1 | a0001c0001t0028 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 315 | chr11 | 74837045 | ||||||
| chr11:74837081 | G | A | 1 | a0001c0001t0030 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 351 | chr11 | 74837081 | ||||||
| chr11:74837187 | C | T | 1 | a0001c0002t0061 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*457C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 457 | chr11 | 74837187 | ||||||
| chr11:74837216 | G | A | 46 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(43): Show |
162 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*486G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 486 | chr11 | 74837216 | ||||||
| chr11:74837246 | C | T | 1 | a0001c0001t0060 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 516 | chr11 | 74837246 | ||||||
| chr11:74837442 | T | C | 3 | a0001c0001t0006 a0001c0001t0030 a0001c0001t0031 |
11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*712T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 712 | chr11 | 74837442 | ||||||
| chr11:74837546 | A | G | 4 | a0001c0001t0011 a0001c0001t0044 a0001c0001t0045 others(1): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*816A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 816 | chr11 | 74837546 | ||||||
| chr11:74837553 | C | G | 1 | a0001c0006t0043 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*823C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 823 | chr11 | 74837553 | ||||||
| chr11:74837666 | A | G | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 936 | chr11 | 74837666 | ||||||
| chr11:74837702 | T | G | 1 | a0001c0001t0046 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 972 | chr11 | 74837702 | ||||||
| chr11:74838186 | T | C | 1 | a0001c0001t0047 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1456 | chr11 | 74838186 | ||||||
| chr11:74838346 | G | A | 44 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(41): Show |
160 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1616G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1616 | chr11 | 74838346 | ||||||
| chr11:74838475 | G | T | 4 | a0001c0001t0006 a0001c0001t0022 a0001c0001t0030 others(1): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1745G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1745 | chr11 | 74838475 | ||||||
| chr11:74838575 | G | A | 1 | a0001c0002t0032 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1845G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1845 | chr11 | 74838575 | ||||||
| chr11:74838714 | T | C | 1 | a0001c0001t0033 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1984T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1984 | chr11 | 74838714 | ||||||
| chr11:74838986 | T | C | 2 | a0001c0001t0013 a0001c0001t0014 |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2256T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2256 | chr11 | 74838986 | ||||||
| chr11:74839074 | T | C | 2 | a0001c0002t0020 a0001c0002t0034 |
3 | NA18942.hp2 NA18961.hp1 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2344T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2344 | chr11 | 74839074 | ||||||
| chr11:74839365 | A | G | 1 | a0001c0002t0029 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2635A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2635 | chr11 | 74839365 | ||||||
| chr11:74839412 | T | C | 2 | a0001c0001t0013 a0001c0001t0014 |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2682T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2682 | chr11 | 74839412 | ||||||
| chr11:74839502 | G | T | 1 | a0001c0001t0059 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2772G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2772 | chr11 | 74839502 | ||||||
| chr11:74839571 | T | C | 4 | a0001c0001t0006 a0001c0001t0022 a0001c0001t0030 others(1): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2841T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2841 | chr11 | 74839571 | ||||||
| chr11:74839626 | G | GT | 3 | a0001c0001t0012 a0001c0001t0018 a0001c0001t0058 |
8 | HG00099.hp1 HG00642.hp2 HG01167.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2903dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2904 | INFO_REALIGN_3_PRIME | chr11 | 74839626 | |||||
| chr11:74839706 | A | G | 1 | a0001c0002t0021 | 2 | HG04204.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2976A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2976 | chr11 | 74839706 | ||||||
| chr11:74839911 | A | G | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(61): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*3181A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3181 | chr11 | 74839911 | ||||||
| chr11:74839980 | C | A | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(59): Show |
264 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*3250C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3250 | chr11 | 74839980 | ||||||
| chr11:74840054 | T | C | 1 | a0001c0001t0048 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3324T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3324 | chr11 | 74840054 | ||||||
| chr11:74840078 | A | G | 2 | a0001c0001t0013 a0001c0001t0014 |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3348A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3348 | chr11 | 74840078 | ||||||
| chr11:74840138 | C | T | 1 | a0001c0001t0014 | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3408C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3408 | chr11 | 74840138 | ||||||
| chr11:74840249 | A | G | 1 | a0001c0001t0025 | 2 | NA18964.hp1 NA18993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3519A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3519 | chr11 | 74840249 | ||||||
| chr11:74840387 | A | T | 1 | a0001c0002t0040 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3657A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3657 | chr11 | 74840387 | ||||||
| chr11:74840475 | C | G | 1 | a0001c0001t0051 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3745C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3745 | chr11 | 74840475 | ||||||
| chr11:74840478 | T | C | 1 | a0001c0001t0058 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3748T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3748 | chr11 | 74840478 | ||||||
| chr11:74840717 | A | G | 5 | a0001c0001t0056 a0001c0001t0057 a0001c0002t0038 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3987A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3987 | chr11 | 74840717 | ||||||
| chr11:74840776 | C | T | 2 | a0001c0001t0015 a0001c0001t0037 |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4046C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4046 | chr11 | 74840776 | ||||||
| chr11:74840787 | CT | C | 40 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(37): Show |
157 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*4077delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4077 | INFO_REALIGN_3_PRIME | chr11 | 74840787 | |||||
| chr11:74840787 | CTT | C | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0024 others(8): Show |
27 | HG00323.hp2 HG01167.hp2 HG01517.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4076_*4077delTT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4076 | INFO_REALIGN_3_PRIME | chr11 | 74840787 | |||||
| chr11:74840854 | T | C | 3 | a0001c0001t0008 a0001c0001t0053 a0001c0001t0056 |
9 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4124T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4124 | chr11 | 74840854 | ||||||
| chr11:74840860 | G | T | 1 | a0001c0001t0045 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4130G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4130 | chr11 | 74840860 | ||||||
| chr11:74840885 | T | C | 1 | a0001c0001t0049 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4155T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4155 | chr11 | 74840885 | ||||||
| chr11:74841169 | T | C | 1 | a0001c0001t0054 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4439T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4439 | chr11 | 74841169 | ||||||
| chr11:74841414 | T | C | 2 | a0001c0001t0013 a0001c0001t0014 |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4684T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4684 | chr11 | 74841414 | ||||||
| chr11:74841428 | C | T | 1 | a0001c0001t0055 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4698C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4698 | chr11 | 74841428 | ||||||
| chr11:74841476 | A | C | 1 | a0001c0002t0039 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4746A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4746 | chr11 | 74841476 | ||||||
| chr11:74841614 | T | G | 1 | a0001c0002t0017 | 3 | NA18998.hp1 NA19062.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4884T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4884 | chr11 | 74841614 | ||||||
| chr11:74841876 | T | C | 1 | a0001c0001t0058 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5146T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5146 | chr11 | 74841876 | ||||||
| chr11:74841886 | G | C | 1 | a0001c0002t0035 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5156G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5156 | chr11 | 74841886 | ||||||
| chr11:74841904 | A | T | 3 | a0001c0001t0011 a0001c0001t0044 a0001c0001t0045 |
8 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5174A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5174 | chr11 | 74841904 | ||||||
| chr11:74841921 | G | A | 1 | a0001c0001t0060 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5191G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5191 | chr11 | 74841921 | ||||||
| chr11:74841955 | T | A | 1 | a0001c0001t0050 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5225T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5225 | chr11 | 74841955 | ||||||
| chr11:74842005 | G | GT | 10 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0015 others(7): Show |
25 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5288dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5289 | INFO_REALIGN_3_PRIME | chr11 | 74842005 | |||||
| chr11:74842029 | C | T | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(60): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*5299C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5299 | chr11 | 74842029 | ||||||
| chr11:74842032 | T | C | 2 | a0001c0001t0002 a0001c0001t0009 |
14 | HG00733.hp1 HG01123.hp1 HG01358.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5302T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5302 | chr11 | 74842032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74749451 | G | C | 1 | a0001c0002t0001g0018 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.502+69G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749451 | |||||||
| chr11:74749468 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.502+86G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749468 | |||||||
| chr11:74749472 | T | C | 6 | a0001c0001t0007g0021 a0001c0001t0007g0023 a0001c0001t0007g0024 others(3): Show |
6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+90T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749472 | |||||||
| chr11:74749472 | T | TA | 138 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(135): Show |
142 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.502+91dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74749472 | ||||||
| chr11:74749716 | G | C | 1 | a0001c0002t0042g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+334G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749716 | |||||||
| chr11:74749720 | T | C | 1 | a0001c0002t0001g0027 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.502+338T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749720 | |||||||
| chr11:74750117 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+735G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750117 | |||||||
| chr11:74750122 | TAA | T | 18 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0319 others(15): Show |
20 | HG01168.hp1 HG01169.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.502+743_502+744del others(2): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750122 | ||||||
| chr11:74750208 | C | G | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+826C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750208 | |||||||
| chr11:74750244 | A | C | 1 | a0001c0001t0003g0305 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.502+862A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750244 | |||||||
| chr11:74750588 | C | CT | 110 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0019 others(107): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.502+1233dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | ||||||
| chr11:74750588 | C | CTT | 48 | a0001c0001t0002g0002 a0001c0001t0002g0252 a0001c0001t0002g0253 others(45): Show |
50 | HG00597.hp2 HG01109.hp1 HG01258.hp2 others(47): Show |
intron_variant | MODIFIER | c.502+1232_502+1233d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | ||||||
| chr11:74750588 | C | CTTT | 13 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 others(10): Show |
13 | HG00423.hp2 HG02280.hp1 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.502+1231_502+1233d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | ||||||
| chr11:74750588 | CT | C | 23 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(20): Show |
24 | HG01074.hp2 HG01243.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.502+1233delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | ||||||
| chr11:74750588 | CTT | C | 9 | a0001c0001t0011g0007 a0001c0001t0011g0136 a0001c0001t0011g0138 others(6): Show |
10 | HG01099.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+1232_502+1233d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | ||||||
| chr11:74750588 | CTTT | C | 20 | a0001c0001t0011g0125 a0001c0002t0001g0126 a0001c0002t0001g0127 others(17): Show |
21 | HG02258.hp1 HG02451.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.502+1231_502+1233d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | ||||||
| chr11:74750588 | CTTTT | C | 96 | a0001c0001t0003g0035 a0001c0001t0014g0006 a0001c0001t0014g0041 others(93): Show |
97 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.502+1230_502+1233d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | ||||||
| chr11:74750673 | C | T | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+1291C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750673 | |||||||
| chr11:74750695 | C | G | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+1313C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750695 | |||||||
| chr11:74750730 | C | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+1348C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750730 | |||||||
| chr11:74750865 | G | GT | 92 | a0001c0001t0002g0246 a0001c0001t0003g0012 a0001c0001t0003g0035 others(89): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.502+1509dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750865 | ||||||
| chr11:74750865 | G | GTT | 50 | a0001c0001t0003g0250 a0001c0001t0003g0331 a0001c0001t0006g0149 others(47): Show |
51 | HG00408.hp1 HG01109.hp2 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.502+1508_502+1509d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750865 | ||||||
| chr11:74750865 | GT | G | 78 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(75): Show |
82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.502+1509delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750865 | ||||||
| chr11:74750869 | T | G | 3 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 |
3 | HG01099.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.502+1487T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750869 | |||||||
| chr11:74751143 | TTACAG | T | 12 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(9): Show |
13 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+1762_502+1766d others(7): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751143 | |||||||
| chr11:74751149 | G | A | 5 | a0001c0002t0001g0036 a0001c0002t0004g0004 a0001c0002t0038g0004 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+1767G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751149 | |||||||
| chr11:74751194 | C | T | 3 | a0001c0001t0014g0006 a0001c0001t0014g0041 a0001c0001t0014g0122 |
4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+1812C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751194 | |||||||
| chr11:74751421 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.502+2039G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751421 | |||||||
| chr11:74751459 | G | A | 1 | a0001c0001t0012g0171 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.502+2077G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751459 | |||||||
| chr11:74751590 | A | G | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+2208A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751590 | |||||||
| chr11:74751674 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.502+2292T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751674 | |||||||
| chr11:74751778 | T | C | 98 | a0001c0001t0003g0035 a0001c0001t0014g0006 a0001c0001t0014g0041 others(95): Show |
99 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.502+2396T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751778 | |||||||
| chr11:74751810 | G | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+2428G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751810 | |||||||
| chr11:74752184 | A | T | 7 | a0001c0001t0003g0170 a0001c0001t0003g0289 a0001c0001t0003g0290 others(4): Show |
7 | HG00423.hp2 NA18965.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+2802A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752184 | |||||||
| chr11:74752228 | T | TA | 74 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0263 others(71): Show |
75 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.502+2870dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752228 | ||||||
| chr11:74752228 | T | TAA | 79 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0019 others(76): Show |
82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.502+2869_502+2870d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752228 | ||||||
| chr11:74752228 | T | TAAA | 20 | a0001c0001t0002g0009 a0001c0001t0002g0155 a0001c0001t0002g0172 others(17): Show |
21 | HG00423.hp1 HG01109.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.502+2868_502+2870d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752228 | ||||||
| chr11:74752228 | TA | T | 34 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(31): Show |
36 | HG01074.hp2 HG01099.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+2870delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752228 | ||||||
| chr11:74752253 | G | A | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | NA18994.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.502+2871G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752253 | |||||||
| chr11:74752254 | G | A | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | NA18994.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.502+2872G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752254 | |||||||
| chr11:74752275 | C | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+2893C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752275 | |||||||
| chr11:74752367 | C | T | 154 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(151): Show |
159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.502+2985C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752367 | |||||||
| chr11:74752459 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.502+3077C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752459 | |||||||
| chr11:74752469 | C | T | 5 | a0001c0001t0003g0213 a0001c0001t0003g0285 a0001c0001t0007g0169 others(2): Show |
5 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+3087C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752469 | |||||||
| chr11:74752595 | C | CA | 124 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.502+3229dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752595 | ||||||
| chr11:74752595 | C | CAA | 6 | a0001c0002t0001g0092 a0001c0002t0001g0101 a0001c0002t0001g0102 others(3): Show |
6 | HG01255.hp2 HG01496.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+3228_502+3229d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752595 | ||||||
| chr11:74752994 | A | C | 1 | a0001c0001t0030g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.502+3612A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752994 | |||||||
| chr11:74753068 | A | G | 6 | a0001c0001t0003g0225 a0001c0001t0003g0242 a0001c0001t0003g0249 others(3): Show |
6 | NA18940.hp2 NA18980.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+3686A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753068 | |||||||
| chr11:74753157 | G | A | 12 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(9): Show |
13 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+3775G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753157 | |||||||
| chr11:74753260 | C | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+3878C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753260 | |||||||
| chr11:74753671 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.502+4289G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753671 | |||||||
| chr11:74753753 | C | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+4371C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753753 | |||||||
| chr11:74753878 | G | A | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502+4496G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753878 | |||||||
| chr11:74753965 | C | A | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+4583C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753965 | |||||||
| chr11:74754023 | A | G | 107 | a0001c0001t0003g0035 a0001c0001t0014g0006 a0001c0001t0014g0041 others(104): Show |
108 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.502+4641A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754023 | |||||||
| chr11:74754531 | A | G | 21 | a0001c0001t0002g0019 a0001c0001t0002g0155 a0001c0001t0002g0176 others(18): Show |
21 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.502+5149A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754531 | |||||||
| chr11:74754546 | C | T | 4 | a0001c0001t0002g0175 a0001c0001t0002g0196 a0001c0001t0002g0197 others(1): Show |
4 | HG01261.hp1 NA18978.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+5164C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754546 | |||||||
| chr11:74754567 | T | C | 1 | a0001c0002t0042g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+5185T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754567 | |||||||
| chr11:74754593 | G | T | 2 | a0001c0002t0001g0119 a0001c0002t0001g0120 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.502+5211G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754593 | |||||||
| chr11:74754734 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+5352C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754734 | |||||||
| chr11:74754788 | C | T | 101 | a0001c0001t0003g0035 a0001c0001t0014g0006 a0001c0001t0014g0041 others(98): Show |
102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.502+5406C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754788 | |||||||
| chr11:74754926 | A | G | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+5544A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754926 | |||||||
| chr11:74754931 | T | C | 106 | a0001c0001t0003g0035 a0001c0001t0014g0006 a0001c0001t0014g0041 others(103): Show |
107 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.502+5549T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754931 | |||||||
| chr11:74755430 | G | A | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+6048G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755430 | |||||||
| chr11:74755572 | C | T | 1 | a0008c0011t0041g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.502+6190C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755572 | |||||||
| chr11:74755576 | C | T | 1 | a0001c0001t0022g0147 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.502+6194C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755576 | |||||||
| chr11:74755871 | G | A | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+6489G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755871 | |||||||
| chr11:74755904 | C | T | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+6522C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755904 | |||||||
| chr11:74756368 | T | C | 1 | a0001c0001t0003g0322 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.502+6986T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756368 | |||||||
| chr11:74756368 | T | G | 138 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(135): Show |
142 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.502+6986T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756368 | |||||||
| chr11:74756462 | C | A | 1 | a0002c0003t0016g0014 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.502+7080C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756462 | |||||||
| chr11:74756499 | A | G | 1 | a0001c0001t0008g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.502+7117A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756499 | |||||||
| chr11:74756582 | G | A | 2 | a0001c0002t0001g0103 a0001c0002t0001g0134 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.502+7200G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756582 | |||||||
| chr11:74756647 | G | A | 2 | a0001c0002t0001g0103 a0001c0002t0001g0134 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.502+7265G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756647 | |||||||
| chr11:74756827 | T | A | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+7445T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756827 | |||||||
| chr11:74756907 | T | G | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+7525T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756907 | |||||||
| chr11:74756969 | T | C | 1 | a0001c0001t0022g0147 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.502+7587T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756969 | |||||||
| chr11:74756986 | C | T | 1 | a0001c0001t0006g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.502+7604C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756986 | |||||||
| chr11:74757000 | A | ATTTATTT others(5): Show |
153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+7619_502+7630d others(14): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74757000 | ||||||
| chr11:74757063 | T | C | 2 | a0001c0001t0007g0024 a0001c0001t0049g0022 |
2 | HG01433.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.502+7681T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757063 | |||||||
| chr11:74757148 | T | C | 1 | a0001c0001t0003g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.502+7766T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757148 | |||||||
| chr11:74757218 | A | G | 5 | a0001c0002t0001g0036 a0001c0002t0004g0004 a0001c0002t0038g0004 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+7836A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757218 | |||||||
| chr11:74757243 | C | T | 2 | a0001c0002t0001g0083 a0001c0002t0001g0099 |
2 | HG02165.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.502+7861C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757243 | |||||||
| chr11:74757265 | G | A | 7 | a0001c0001t0003g0170 a0001c0001t0003g0289 a0001c0001t0003g0290 others(4): Show |
7 | HG00423.hp2 NA18965.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+7883G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757265 | |||||||
| chr11:74757267 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.502+7885G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757267 | |||||||
| chr11:74757286 | T | C | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+7904T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757286 | |||||||
| chr11:74757412 | G | C | 8 | a0001c0002t0001g0036 a0002c0003t0010g0015 a0002c0003t0010g0306 others(5): Show |
9 | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.502+8030G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757412 | |||||||
| chr11:74757602 | A | G | 1 | a0001c0001t0002g0293 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.502+8220A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757602 | |||||||
| chr11:74757683 | T | C | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.502+8301T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757683 | |||||||
| chr11:74757684 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.502+8302G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757684 | |||||||
| chr11:74757716 | A | T | 2 | a0001c0001t0003g0213 a0001c0001t0050g0244 |
2 | HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.502+8334A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757716 | |||||||
| chr11:74757825 | G | A | 1 | a0001c0001t0012g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.502+8443G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757825 | |||||||
| chr11:74757920 | T | C | 7 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(4): Show |
8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.502+8538T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757920 | |||||||
| chr11:74757939 | T | G | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+8557T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757939 | |||||||
| chr11:74757944 | G | A | 159 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(156): Show |
164 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.502+8562G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757944 | |||||||
| chr11:74757944 | G | C | 98 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(95): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.502+8562G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757944 | |||||||
| chr11:74757945 | T | G | 257 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(254): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.502+8563T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757945 | |||||||
| chr11:74758020 | A | T | 2 | a0004c0005t0001g0093 a0004c0005t0004g0046 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.502+8638A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758020 | |||||||
| chr11:74758027 | CTTT | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+8647_502+8649d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74758027 | ||||||
| chr11:74758047 | G | A | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+8665G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758047 | |||||||
| chr11:74758075 | C | T | 5 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0117 others(2): Show |
5 | HG00408.hp1 HG01952.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+8693C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758075 | |||||||
| chr11:74758200 | T | G | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+8818T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758200 | |||||||
| chr11:74758219 | C | T | 127 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(124): Show |
130 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.502+8837C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758219 | |||||||
| chr11:74758223 | C | T | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+8841C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758223 | |||||||
| chr11:74758311 | G | A | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+8929G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758311 | |||||||
| chr11:74758312 | T | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+8930T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758312 | |||||||
| chr11:74758352 | A | G | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+8970A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758352 | |||||||
| chr11:74758361 | TCTGTTTT others(15): Show |
T | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502+8990_502+9011d others(24): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74758361 | ||||||
| chr11:74758448 | G | GT | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+9073dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74758448 | ||||||
| chr11:74758451 | T | A | 9 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(6): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+9069T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758451 | |||||||
| chr11:74758532 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.502+9150C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758532 | |||||||
| chr11:74758570 | C | T | 1 | a0001c0002t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.502+9188C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758570 | |||||||
| chr11:74758594 | C | T | 8 | a0001c0002t0005g0086 a0002c0003t0010g0015 a0002c0003t0010g0306 others(5): Show |
9 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+9212C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758594 | |||||||
| chr11:74758616 | C | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+9234C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758616 | |||||||
| chr11:74758621 | C | G | 1 | a0001c0001t0013g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502+9239C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758621 | |||||||
| chr11:74758662 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.502+9280C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758662 | |||||||
| chr11:74758663 | G | A | 1 | a0009c0007t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.502+9281G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758663 | |||||||
| chr11:74758691 | A | G | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+9309A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758691 | |||||||
| chr11:74758726 | G | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+9344G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758726 | |||||||
| chr11:74758746 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+9364C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758746 | |||||||
| chr11:74758751 | A | G | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+9369A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758751 | |||||||
| chr11:74758794 | G | A | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+9412G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758794 | |||||||
| chr11:74758803 | C | T | 1 | a0001c0001t0003g0303 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.502+9421C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758803 | |||||||
| chr11:74758843 | A | G | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+9461A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758843 | |||||||
| chr11:74758898 | G | T | 3 | a0001c0002t0004g0004 a0001c0002t0038g0004 a0001c0002t0039g0037 |
3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.502+9516G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758898 | |||||||
| chr11:74758921 | T | C | 1 | a0001c0002t0035g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.502+9539T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758921 | |||||||
| chr11:74759028 | C | G | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+9646C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759028 | |||||||
| chr11:74759119 | T | C | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.502+9737T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759119 | |||||||
| chr11:74759218 | A | C | 1 | a0001c0002t0010g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502+9836A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759218 | |||||||
| chr11:74759218 | A | T | 1 | a0001c0001t0052g0278 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.502+9836A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759218 | |||||||
| chr11:74759227 | TC | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+9846delC | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759227 | |||||||
| chr11:74759247 | G | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.502+9865G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759247 | |||||||
| chr11:74759318 | T | G | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+9936T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759318 | |||||||
| chr11:74759404 | G | T | 1 | a0001c0001t0013g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502+10022G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759404 | |||||||
| chr11:74759479 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+10097G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759479 | |||||||
| chr11:74759497 | T | G | 1 | a0001c0001t0015g0315 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.502+10115T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759497 | |||||||
| chr11:74759624 | G | A | 1 | a0001c0002t0001g0018 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.502+10242G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759624 | |||||||
| chr11:74759625 | G | T | 8 | a0001c0002t0001g0018 a0002c0003t0010g0015 a0002c0003t0010g0306 others(5): Show |
9 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+10243G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759625 | |||||||
| chr11:74759710 | G | A | 6 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0101 others(3): Show |
6 | HG01109.hp2 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+10328G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759710 | |||||||
| chr11:74759734 | G | A | 1 | a0001c0002t0004g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.502+10352G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759734 | |||||||
| chr11:74759892 | T | C | 1 | a0002c0003t0016g0014 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.502+10510T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759892 | |||||||
| chr11:74759913 | G | A | 1 | a0001c0001t0022g0147 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.502+10531G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759913 | |||||||
| chr11:74759990 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.502+10608C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759990 | |||||||
| chr11:74760016 | G | A | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+10634G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760016 | |||||||
| chr11:74760053 | C | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+10671C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760053 | |||||||
| chr11:74760058 | A | T | 1 | a0001c0001t0002g0216 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.502+10676A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760058 | |||||||
| chr11:74760061 | G | T | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+10679G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760061 | |||||||
| chr11:74760074 | C | G | 1 | a0008c0011t0041g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.502+10692C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760074 | |||||||
| chr11:74760095 | T | C | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+10713T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760095 | |||||||
| chr11:74760108 | G | A | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+10726G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760108 | |||||||
| chr11:74760175 | A | T | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+10793A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760175 | |||||||
| chr11:74760211 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.502+10829A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760211 | |||||||
| chr11:74760258 | C | G | 1 | a0001c0001t0004g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.502+10876C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760258 | |||||||
| chr11:74760449 | G | A | 1 | a0001c0001t0013g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502+11067G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760449 | |||||||
| chr11:74760507 | T | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+11125T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760507 | |||||||
| chr11:74760546 | G | T | 2 | a0001c0001t0003g0249 a0001c0001t0003g0305 |
2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.502+11164G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760546 | |||||||
| chr11:74760676 | T | G | 3 | a0001c0001t0006g0144 a0001c0001t0006g0145 a0001c0001t0006g0146 |
3 | HG02258.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.502+11294T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760676 | |||||||
| chr11:74760679 | T | A | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+11297T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760679 | |||||||
| chr11:74760694 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.502+11312G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760694 | |||||||
| chr11:74760751 | T | C | 1 | a0001c0002t0001g0018 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.502+11369T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760751 | |||||||
| chr11:74760792 | T | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+11410T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760792 | |||||||
| chr11:74760829 | G | A | 6 | a0001c0001t0002g0019 a0001c0001t0002g0155 a0001c0001t0002g0198 others(3): Show |
6 | HG00621.hp1 HG03704.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.502+11447G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760829 | |||||||
| chr11:74760859 | G | A | 3 | a0001c0002t0004g0004 a0001c0002t0038g0004 a0001c0002t0039g0037 |
3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.502+11477G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760859 | |||||||
| chr11:74760920 | C | T | 128 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(125): Show |
131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.502+11538C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760920 | |||||||
| chr11:74760936 | G | A | 1 | a0001c0014t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.502+11554G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760936 | |||||||
| chr11:74760987 | G | T | 2 | a0001c0001t0003g0248 a0001c0002t0001g0121 |
2 | HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.502+11605G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760987 | |||||||
| chr11:74761008 | A | G | 1 | a0001c0002t0005g0087 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502+11626A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761008 | |||||||
| chr11:74761062 | G | T | 161 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(158): Show |
166 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.502+11680G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761062 | |||||||
| chr11:74761069 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.502+11687C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761069 | |||||||
| chr11:74761097 | G | T | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+11715G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761097 | |||||||
| chr11:74761197 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502+11815A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761197 | |||||||
| chr11:74761276 | C | T | 2 | a0001c0001t0009g0251 a0001c0001t0047g0195 |
2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.502+11894C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761276 | |||||||
| chr11:74761401 | T | C | 2 | a0001c0001t0002g0264 a0001c0001t0009g0296 |
2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.502+12019T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761401 | |||||||
| chr11:74761428 | A | G | 1 | a0001c0001t0006g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.502+12046A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761428 | |||||||
| chr11:74761451 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(6): Show |
10 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+12069G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761451 | |||||||
| chr11:74761473 | C | T | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+12091C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761473 | |||||||
| chr11:74761615 | C | T | 2 | a0001c0001t0007g0021 a0001c0001t0007g0023 |
2 | HG00323.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.502+12233C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761615 | |||||||
| chr11:74761735 | C | G | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+12353C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761735 | |||||||
| chr11:74761799 | G | A | 2 | a0001c0001t0015g0315 a0001c0002t0001g0081 |
2 | HG02129.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.502+12417G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761799 | |||||||
| chr11:74761852 | C | A | 1 | a0001c0001t0002g0246 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.502+12470C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761852 | |||||||
| chr11:74761979 | A | G | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502+12597A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761979 | |||||||
| chr11:74762065 | C | T | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+12683C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762065 | |||||||
| chr11:74762082 | C | A | 1 | a0001c0002t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.502+12700C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762082 | |||||||
| chr11:74762091 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+12709C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762091 | |||||||
| chr11:74762123 | T | C | 258 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(255): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.502+12741T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762123 | |||||||
| chr11:74762148 | G | T | 1 | a0001c0002t0001g0079 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.502+12766G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762148 | |||||||
| chr11:74762218 | A | G | 1 | a0001c0001t0002g0263 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.502+12836A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762218 | |||||||
| chr11:74762237 | C | A | 1 | a0001c0001t0007g0240 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.502+12855C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762237 | |||||||
| chr11:74762259 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.502+12877G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762259 | |||||||
| chr11:74762269 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.502+12887G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762269 | |||||||
| chr11:74762305 | G | A | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+12923G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762305 | |||||||
| chr11:74762335 | C | T | 1 | a0001c0002t0001g0078 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.502+12953C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762335 | |||||||
| chr11:74762367 | G | GA | 129 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(126): Show |
132 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.502+12986dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74762367 | ||||||
| chr11:74762376 | C | T | 10 | a0001c0001t0002g0255 a0001c0001t0002g0257 a0001c0001t0002g0258 others(7): Show |
10 | NA18951.hp1 NA18961.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+12994C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762376 | |||||||
| chr11:74762473 | T | A | 2 | a0001c0001t0003g0280 a0001c0001t0051g0226 |
2 | HG02027.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.502+13091T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762473 | |||||||
| chr11:74762588 | C | T | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+13206C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762588 | |||||||
| chr11:74762629 | C | T | 1 | a0001c0002t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.502+13247C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762629 | |||||||
| chr11:74762630 | G | A | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+13248G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762630 | |||||||
| chr11:74762634 | A | G | 2 | a0001c0002t0001g0064 a0001c0002t0001g0065 |
2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.502+13252A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762634 | |||||||
| chr11:74762648 | A | T | 39 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(36): Show |
39 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.502+13266A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762648 | |||||||
| chr11:74762781 | C | T | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+13399C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762781 | |||||||
| chr11:74762801 | C | T | 100 | a0001c0001t0014g0006 a0001c0001t0014g0041 a0001c0001t0014g0122 others(97): Show |
101 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.502+13419C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762801 | |||||||
| chr11:74762897 | G | A | 1 | a0001c0001t0007g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.502+13515G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762897 | |||||||
| chr11:74762984 | T | A | 1 | a0001c0001t0002g0199 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.502+13602T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762984 | |||||||
| chr11:74763055 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.502+13673C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763055 | |||||||
| chr11:74763079 | G | T | 21 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(18): Show |
23 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.502+13697G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763079 | |||||||
| chr11:74763148 | T | G | 4 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0318 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+13766T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763148 | |||||||
| chr11:74763221 | G | A | 105 | a0001c0001t0014g0006 a0001c0001t0014g0041 a0001c0001t0014g0122 others(102): Show |
106 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.502+13839G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763221 | |||||||
| chr11:74763416 | A | G | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+14034A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763416 | |||||||
| chr11:74763489 | A | G | 1 | a0001c0002t0021g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.502+14107A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763489 | |||||||
| chr11:74763581 | A | G | 1 | a0001c0001t0047g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502+14199A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763581 | |||||||
| chr11:74763625 | C | G | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+14243C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763625 | |||||||
| chr11:74763669 | A | C | 1 | a0001c0001t0022g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.502+14287A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763669 | |||||||
| chr11:74763718 | G | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+14336G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763718 | |||||||
| chr11:74763827 | T | C | 1 | a0001c0001t0002g0177 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.502+14445T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763827 | |||||||
| chr11:74763953 | C | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+14571C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763953 | |||||||
| chr11:74763992 | G | C | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+14610G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763992 | |||||||
| chr11:74764006 | C | G | 1 | a0009c0007t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.502+14624C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764006 | |||||||
| chr11:74764148 | A | G | 10 | a0001c0001t0007g0021 a0001c0001t0007g0023 a0001c0001t0007g0024 others(7): Show |
10 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+14766A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764148 | |||||||
| chr11:74764159 | C | A | 1 | a0001c0001t0002g0268 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.502+14777C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764159 | |||||||
| chr11:74764197 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.502+14815C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764197 | |||||||
| chr11:74764226 | T | C | 128 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(125): Show |
131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.502+14844T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764226 | |||||||
| chr11:74764267 | C | T | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+14885C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764267 | |||||||
| chr11:74764271 | C | T | 1 | a0001c0002t0005g0087 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502+14889C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764271 | |||||||
| chr11:74764299 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+14917C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764299 | |||||||
| chr11:74764308 | C | T | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+14926C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764308 | |||||||
| chr11:74764352 | G | C | 1 | a0002c0003t0010g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.502+14970G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764352 | |||||||
| chr11:74764390 | G | A | 1 | a0001c0001t0003g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.502+15008G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764390 | |||||||
| chr11:74764403 | C | T | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+15021C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764403 | |||||||
| chr11:74764447 | C | T | 2 | a0001c0002t0001g0077 a0001c0002t0001g0133 |
2 | HG00558.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.502+15065C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764447 | |||||||
| chr11:74764456 | C | T | 6 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(3): Show |
7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+15074C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764456 | |||||||
| chr11:74764457 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(3): Show |
7 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+15075G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764457 | |||||||
| chr11:74764469 | T | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+15087T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764469 | |||||||
| chr11:74764506 | A | G | 10 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(7): Show |
11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+15124A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764506 | |||||||
| chr11:74764519 | A | G | 1 | a0001c0002t0010g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502+15137A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764519 | |||||||
| chr11:74764711 | G | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+15329G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764711 | |||||||
| chr11:74764716 | G | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+15334G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764716 | |||||||
| chr11:74764803 | C | T | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+15421C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764803 | |||||||
| chr11:74764991 | C | G | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+15609C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764991 | |||||||
| chr11:74765096 | C | T | 1 | a0001c0001t0022g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.502+15714C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765096 | |||||||
| chr11:74765163 | C | T | 2 | a0001c0001t0022g0147 a0001c0001t0022g0150 |
2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.502+15781C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765163 | |||||||
| chr11:74765196 | G | A | 33 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0040 others(30): Show |
33 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.502+15814G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765196 | |||||||
| chr11:74765312 | T | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+15930T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765312 | |||||||
| chr11:74765329 | G | A | 5 | a0001c0001t0007g0013 a0001c0001t0007g0281 a0001c0001t0024g0013 others(2): Show |
5 | NA18942.hp2 NA18949.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+15947G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765329 | |||||||
| chr11:74765385 | T | C | 10 | a0001c0001t0003g0035 a0001c0002t0001g0070 a0001c0002t0001g0071 others(7): Show |
10 | HG00558.hp2 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+16003T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765385 | |||||||
| chr11:74765405 | C | A | 1 | a0001c0002t0001g0036 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.502+16023C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765405 | |||||||
| chr11:74765529 | G | A | 1 | a0001c0001t0003g0302 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.502+16147G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765529 | |||||||
| chr11:74765606 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.502+16224G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765606 | |||||||
| chr11:74765654 | T | C | 2 | a0003c0004t0023g0124 a0003c0004t0023g0128 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.502+16272T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765654 | |||||||
| chr11:74765684 | C | T | 1 | a0001c0014t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.502+16302C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765684 | |||||||
| chr11:74765770 | C | CCAGCCTG others(11): Show |
1 | a0001c0002t0032g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.502+16403_502+1642 others(22): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74765770 | ||||||
| chr11:74765806 | C | CA | 10 | a0001c0001t0003g0299 a0001c0001t0003g0321 a0001c0001t0003g0323 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+16437dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74765806 | ||||||
| chr11:74765838 | A | T | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+16456A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765838 | |||||||
| chr11:74765912 | A | G | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+16530A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765912 | |||||||
| chr11:74766041 | A | C | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.502+16659A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766041 | |||||||
| chr11:74766169 | G | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+16787G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766169 | |||||||
| chr11:74766197 | T | C | 3 | a0001c0002t0004g0004 a0001c0002t0038g0004 a0001c0002t0039g0037 |
3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.502+16815T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766197 | |||||||
| chr11:74766248 | A | G | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+16866A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766248 | |||||||
| chr11:74766263 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+16881C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766263 | |||||||
| chr11:74766264 | G | A | 2 | a0001c0001t0003g0249 a0001c0001t0003g0305 |
2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.502+16882G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766264 | |||||||
| chr11:74766265 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.502+16883C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766265 | |||||||
| chr11:74766375 | A | G | 9 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(6): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+16993A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766375 | |||||||
| chr11:74766383 | C | G | 6 | a0001c0001t0007g0021 a0001c0001t0007g0023 a0001c0001t0007g0024 others(3): Show |
6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+17001C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766383 | |||||||
| chr11:74766574 | A | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+17192A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766574 | |||||||
| chr11:74766723 | G | T | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+17341G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766723 | |||||||
| chr11:74766883 | G | C | 2 | a0001c0001t0022g0147 a0001c0001t0022g0150 |
2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.502+17501G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766883 | |||||||
| chr11:74766897 | G | A | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+17515G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766897 | |||||||
| chr11:74766898 | A | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+17516A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766898 | |||||||
| chr11:74766910 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+17528C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766910 | |||||||
| chr11:74767007 | T | C | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.502+17625T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767007 | |||||||
| chr11:74767067 | T | C | 1 | a0001c0002t0001g0129 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.502+17685T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767067 | |||||||
| chr11:74767079 | A | G | 1 | a0001c0001t0003g0168 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.502+17697A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767079 | |||||||
| chr11:74767183 | C | T | 1 | a0003c0004t0023g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.502+17801C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767183 | |||||||
| chr11:74767255 | G | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+17873G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767255 | |||||||
| chr11:74767414 | TA | T | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+18033delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767414 | |||||||
| chr11:74767417 | T | A | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+18035T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767417 | |||||||
| chr11:74767460 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.502+18078C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767460 | |||||||
| chr11:74767466 | C | T | 1 | a0001c0002t0029g0076 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.502+18084C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767466 | |||||||
| chr11:74767605 | T | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(3): Show |
7 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+18223T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767605 | |||||||
| chr11:74767633 | G | A | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+18251G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767633 | |||||||
| chr11:74767640 | G | A | 1 | a0001c0001t0003g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.502+18258G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767640 | |||||||
| chr11:74767694 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.502+18312C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767694 | |||||||
| chr11:74767701 | C | G | 1 | a0001c0001t0003g0301 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.502+18319C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767701 | |||||||
| chr11:74767829 | G | A | 2 | a0001c0001t0003g0228 a0001c0001t0003g0229 |
2 | HG02109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.502+18447G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767829 | |||||||
| chr11:74767875 | A | T | 1 | a0001c0002t0001g0088 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.502+18493A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767875 | |||||||
| chr11:74768133 | A | G | 3 | a0001c0001t0014g0006 a0001c0001t0014g0041 a0001c0001t0014g0122 |
4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+18751A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768133 | |||||||
| chr11:74768161 | T | C | 134 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(131): Show |
137 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.502+18779T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768161 | |||||||
| chr11:74768347 | C | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+18965C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768347 | |||||||
| chr11:74768445 | G | A | 154 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(151): Show |
159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.502+19063G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768445 | |||||||
| chr11:74768461 | G | T | 1 | a0001c0002t0004g0062 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.502+19079G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768461 | |||||||
| chr11:74768494 | C | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+19112C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768494 | |||||||
| chr11:74768496 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502+19114A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768496 | |||||||
| chr11:74768538 | C | A | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+19156C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768538 | |||||||
| chr11:74768606 | T | TA | 26 | a0001c0001t0002g0275 a0001c0001t0006g0008 a0001c0001t0006g0141 others(23): Show |
27 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.502+19240dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74768606 | ||||||
| chr11:74768606 | TA | T | 7 | a0001c0001t0003g0289 a0001c0001t0003g0290 a0001c0001t0003g0299 others(4): Show |
7 | HG01243.hp2 HG02896.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.502+19240delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74768606 | ||||||
| chr11:74768754 | T | C | 9 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(6): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+19372T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768754 | |||||||
| chr11:74768776 | G | T | 1 | a0001c0002t0001g0036 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.502+19394G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768776 | |||||||
| chr11:74768780 | C | T | 2 | a0001c0002t0005g0086 a0001c0002t0005g0087 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.502+19398C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768780 | |||||||
| chr11:74768781 | A | C | 104 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(101): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.502+19399A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768781 | |||||||
| chr11:74768816 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502+19434G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768816 | |||||||
| chr11:74769032 | A | G | 2 | a0001c0002t0001g0059 a0001c0002t0001g0060 |
2 | HG00597.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.502+19650A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769032 | |||||||
| chr11:74769133 | A | G | 1 | a0001c0001t0002g0273 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.502+19751A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769133 | |||||||
| chr11:74769161 | T | C | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+19779T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769161 | |||||||
| chr11:74769273 | A | G | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.502+19891A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769273 | |||||||
| chr11:74769331 | A | G | 1 | a0001c0001t0003g0302 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.502+19949A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769331 | |||||||
| chr11:74769448 | T | G | 2 | a0001c0001t0002g0260 a0001c0006t0043g0123 |
2 | HG00597.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.502+20066T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769448 | |||||||
| chr11:74769503 | T | C | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.502+20121T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769503 | |||||||
| chr11:74769606 | C | T | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-20020C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769606 | |||||||
| chr11:74769701 | C | T | 1 | a0001c0001t0013g0311 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.503-19925C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769701 | |||||||
| chr11:74769743 | G | A | 1 | a0001c0001t0053g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.503-19883G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769743 | |||||||
| chr11:74769821 | G | C | 1 | a0001c0001t0003g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.503-19805G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769821 | |||||||
| chr11:74769870 | A | C | 1 | a0001c0001t0003g0280 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.503-19756A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769870 | |||||||
| chr11:74769871 | T | A | 1 | a0003c0004t0023g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.503-19755T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769871 | |||||||
| chr11:74769994 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.503-19632G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769994 | |||||||
| chr11:74770019 | T | C | 1 | a0001c0002t0004g0069 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.503-19607T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770019 | |||||||
| chr11:74770086 | C | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0208 a0001c0001t0003g0224 others(2): Show |
6 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-19540C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770086 | |||||||
| chr11:74770243 | C | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-19383C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770243 | |||||||
| chr11:74770273 | G | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-19353G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770273 | |||||||
| chr11:74770459 | T | G | 1 | a0001c0001t0054g0274 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.503-19167T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770459 | |||||||
| chr11:74770548 | C | T | 1 | a0001c0001t0003g0279 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.503-19078C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770548 | |||||||
| chr11:74770586 | T | C | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.503-19040T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770586 | |||||||
| chr11:74770670 | A | C | 2 | a0001c0001t0003g0284 a0001c0001t0046g0283 |
2 | HG02165.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.503-18956A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770670 | |||||||
| chr11:74770700 | TAATA | T | 6 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0101 others(3): Show |
6 | HG01109.hp2 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-18922_503-1891 others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74770700 | ||||||
| chr11:74770718 | A | G | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-18908A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770718 | |||||||
| chr11:74770798 | C | T | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-18828C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770798 | |||||||
| chr11:74770897 | C | G | 3 | a0001c0002t0004g0004 a0001c0002t0038g0004 a0001c0002t0039g0037 |
3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.503-18729C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770897 | |||||||
| chr11:74770956 | C | T | 3 | a0001c0002t0001g0027 a0001c0002t0001g0058 a0001c0002t0001g0110 |
3 | NA18975.hp2 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.503-18670C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770956 | |||||||
| chr11:74771111 | A | G | 1 | a0001c0001t0002g0275 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.503-18515A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771111 | |||||||
| chr11:74771368 | A | G | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-18258A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771368 | |||||||
| chr11:74771483 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.503-18143C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771483 | |||||||
| chr11:74771547 | T | TA | 125 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(122): Show |
127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.503-18072dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74771547 | ||||||
| chr11:74771578 | C | T | 4 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0318 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-18048C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771578 | |||||||
| chr11:74771718 | T | C | 1 | a0001c0001t0011g0125 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.503-17908T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771718 | |||||||
| chr11:74771923 | G | A | 8 | a0001c0001t0002g0175 a0001c0001t0002g0196 a0001c0001t0002g0197 others(5): Show |
8 | HG01109.hp1 HG01261.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-17703G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771923 | |||||||
| chr11:74771998 | G | A | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-17628G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771998 | |||||||
| chr11:74772111 | T | C | 1 | a0001c0001t0011g0136 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.503-17515T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74772111 | |||||||
| chr11:74772127 | ATTAG | A | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-17496_503-1749 others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772127 | ||||||
| chr11:74772181 | TA | T | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-17438delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772181 | ||||||
| chr11:74772187 | A | G | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-17439A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74772187 | |||||||
| chr11:74772263 | C | G | 1 | a0001c0001t0048g0236 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.503-17363C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74772263 | |||||||
| chr11:74772472 | GT | G | 123 | a0001c0001t0002g0212 a0001c0001t0002g0273 a0001c0001t0002g0275 others(120): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.503-17133delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772472 | ||||||
| chr11:74772472 | GTT | G | 123 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(120): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.503-17134_503-1713 others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772472 | ||||||
| chr11:74772472 | GTTT | G | 90 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(87): Show |
93 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.503-17135_503-1713 others(7): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772472 | ||||||
| chr11:74772529 | G | A | 11 | a0001c0002t0001g0067 a0001c0002t0001g0079 a0001c0002t0001g0092 others(8): Show |
11 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-17097G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74772529 | |||||||
| chr11:74773260 | A | T | 3 | a0001c0001t0014g0006 a0001c0001t0014g0041 a0001c0001t0014g0122 |
4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.503-16366A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773260 | |||||||
| chr11:74773304 | A | G | 39 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0040 others(36): Show |
39 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.503-16322A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773304 | |||||||
| chr11:74773471 | C | T | 5 | a0001c0001t0002g0175 a0001c0001t0002g0196 a0001c0001t0002g0197 others(2): Show |
5 | HG01261.hp1 HG02602.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-16155C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773471 | |||||||
| chr11:74773595 | T | C | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-16031T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773595 | |||||||
| chr11:74773925 | T | G | 1 | a0001c0001t0002g0181 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.503-15701T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773925 | |||||||
| chr11:74774002 | G | A | 5 | a0001c0001t0007g0013 a0001c0001t0007g0281 a0001c0001t0024g0013 others(2): Show |
5 | NA18942.hp2 NA18949.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-15624G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774002 | |||||||
| chr11:74774052 | A | G | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503-15574A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774052 | |||||||
| chr11:74774071 | C | G | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-15555C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774071 | |||||||
| chr11:74774076 | A | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-15550A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774076 | |||||||
| chr11:74774168 | T | C | 2 | a0001c0002t0005g0086 a0001c0002t0005g0087 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.503-15458T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774168 | |||||||
| chr11:74774230 | C | T | 4 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0318 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-15396C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774230 | |||||||
| chr11:74774345 | C | CA | 112 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(109): Show |
113 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.503-15269dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74774345 | ||||||
| chr11:74774345 | CA | C | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-15269delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74774345 | ||||||
| chr11:74774379 | C | CA | 10 | a0001c0001t0002g0210 a0001c0001t0003g0334 a0001c0001t0007g0021 others(7): Show |
10 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-15238dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74774379 | ||||||
| chr11:74774388 | A | C | 1 | a0001c0002t0017g0057 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.503-15238A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774388 | |||||||
| chr11:74774568 | C | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-15058C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774568 | |||||||
| chr11:74774689 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.503-14937T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774689 | |||||||
| chr11:74774881 | T | C | 257 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(254): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.503-14745T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774881 | |||||||
| chr11:74774967 | C | G | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.503-14659C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774967 | |||||||
| chr11:74775049 | G | A | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-14577G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775049 | |||||||
| chr11:74775076 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.503-14550C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775076 | |||||||
| chr11:74775111 | A | G | 2 | a0001c0001t0002g0193 a0001c0001t0009g0157 |
2 | NA18946.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.503-14515A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775111 | |||||||
| chr11:74775232 | TAAAGG | T | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-14391_503-1438 others(9): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74775232 | ||||||
| chr11:74775267 | T | C | 1 | a0001c0001t0014g0122 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.503-14359T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775267 | |||||||
| chr11:74775347 | C | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-14279C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775347 | |||||||
| chr11:74775872 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503-13754G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775872 | |||||||
| chr11:74775888 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.503-13738A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775888 | |||||||
| chr11:74775910 | C | A | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-13716C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775910 | |||||||
| chr11:74775910 | C | T | 1 | a0001c0002t0001g0056 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.503-13716C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775910 | |||||||
| chr11:74775923 | C | T | 258 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(255): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.503-13703C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775923 | |||||||
| chr11:74775998 | T | C | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-13628T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775998 | |||||||
| chr11:74776005 | A | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-13621A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74776005 | |||||||
| chr11:74776061 | GACTT | G | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-13561_503-1355 others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74776061 | ||||||
| chr11:74776139 | G | T | 1 | a0001c0001t0003g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.503-13487G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74776139 | |||||||
| chr11:74776511 | C | CA | 145 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(142): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.503-13092dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74776511 | ||||||
| chr11:74776511 | C | CAA | 13 | a0001c0001t0002g0261 a0001c0001t0002g0269 a0001c0001t0002g0275 others(10): Show |
14 | HG01109.hp1 HG01358.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.503-13093_503-1309 others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74776511 | ||||||
| chr11:74776511 | CA | C | 10 | a0001c0001t0003g0325 a0001c0001t0004g0304 a0001c0001t0024g0298 others(7): Show |
10 | HG01099.hp2 HG01168.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-13092delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74776511 | ||||||
| chr11:74776563 | A | C | 2 | a0001c0001t0003g0280 a0001c0001t0051g0226 |
2 | HG02027.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.503-13063A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74776563 | |||||||
| chr11:74776861 | G | A | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-12765G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74776861 | |||||||
| chr11:74777324 | G | A | 165 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(162): Show |
170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.503-12302G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777324 | |||||||
| chr11:74777359 | A | T | 132 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(129): Show |
135 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.503-12267A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777359 | |||||||
| chr11:74777407 | G | A | 1 | a0001c0001t0008g0217 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.503-12219G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777407 | |||||||
| chr11:74777483 | T | G | 1 | a0001c0001t0002g0259 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.503-12143T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777483 | |||||||
| chr11:74777492 | A | G | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-12134A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777492 | |||||||
| chr11:74777551 | T | C | 1 | a0001c0001t0003g0326 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.503-12075T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777551 | |||||||
| chr11:74777556 | G | A | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-12070G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777556 | |||||||
| chr11:74777652 | AT | A | 152 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(149): Show |
157 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.503-11961delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74777652 | ||||||
| chr11:74777671 | A | G | 1 | a0001c0002t0001g0072 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.503-11955A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777671 | |||||||
| chr11:74777740 | C | T | 1 | a0001c0002t0001g0055 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.503-11886C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777740 | |||||||
| chr11:74777819 | A | T | 1 | a0001c0002t0001g0091 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.503-11807A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777819 | |||||||
| chr11:74777918 | C | A | 1 | a0001c0001t0003g0322 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.503-11708C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777918 | |||||||
| chr11:74777976 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.503-11650C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777976 | |||||||
| chr11:74778024 | C | T | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.503-11602C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778024 | |||||||
| chr11:74778364 | G | T | 1 | a0001c0001t0028g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.503-11262G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778364 | |||||||
| chr11:74778434 | C | T | 1 | a0001c0001t0003g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.503-11192C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778434 | |||||||
| chr11:74778501 | C | T | 154 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(151): Show |
159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.503-11125C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778501 | |||||||
| chr11:74778504 | A | G | 9 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(6): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-11122A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778504 | |||||||
| chr11:74778594 | C | T | 51 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(48): Show |
51 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.503-11032C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778594 | |||||||
| chr11:74778716 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.503-10910C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778716 | |||||||
| chr11:74778730 | C | G | 1 | a0001c0001t0018g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.503-10896C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778730 | |||||||
| chr11:74778817 | G | C | 1 | a0001c0002t0001g0044 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.503-10809G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778817 | |||||||
| chr11:74778822 | G | C | 3 | a0001c0002t0001g0103 a0001c0002t0001g0127 a0001c0002t0001g0134 |
3 | HG02896.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.503-10804G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778822 | |||||||
| chr11:74779063 | A | G | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-10563A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779063 | |||||||
| chr11:74779160 | T | A | 1 | a0001c0001t0003g0327 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.503-10466T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779160 | |||||||
| chr11:74779183 | A | C | 264 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(261): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.503-10443A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779183 | |||||||
| chr11:74779381 | A | G | 126 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(123): Show |
128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-10245A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779381 | |||||||
| chr11:74779490 | G | T | 2 | a0001c0001t0025g0191 a0001c0001t0025g0256 |
2 | NA18964.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.503-10136G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779490 | |||||||
| chr11:74779491 | T | C | 6 | a0001c0002t0001g0078 a0001c0002t0001g0088 a0001c0002t0005g0043 others(3): Show |
6 | NA18612.hp1 NA18954.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.503-10135T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779491 | |||||||
| chr11:74779548 | G | C | 126 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(123): Show |
128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-10078G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779548 | |||||||
| chr11:74779778 | T | C | 1 | a0001c0002t0001g0049 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.503-9848T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779778 | |||||||
| chr11:74779914 | G | T | 2 | a0001c0002t0001g0097 a0001c0002t0004g0054 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.503-9712G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779914 | |||||||
| chr11:74780151 | A | G | 1 | a0001c0001t0003g0303 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.503-9475A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74780151 | |||||||
| chr11:74780250 | C | G | 1 | a0001c0002t0004g0062 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.503-9376C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74780250 | |||||||
| chr11:74780418 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.503-9208C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74780418 | |||||||
| chr11:74780971 | C | T | 1 | a0001c0001t0003g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.503-8655C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74780971 | |||||||
| chr11:74781035 | C | T | 2 | a0001c0002t0001g0068 a0001c0006t0043g0123 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.503-8591C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781035 | |||||||
| chr11:74781161 | C | G | 1 | a0001c0002t0001g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.503-8465C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781161 | |||||||
| chr11:74781522 | C | G | 5 | a0001c0002t0001g0036 a0001c0002t0004g0004 a0001c0002t0038g0004 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-8104C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781522 | |||||||
| chr11:74781525 | G | A | 1 | a0001c0002t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.503-8101G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781525 | |||||||
| chr11:74781566 | C | T | 118 | a0001c0001t0003g0035 a0001c0001t0005g0139 a0001c0001t0006g0008 others(115): Show |
119 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.503-8060C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781566 | |||||||
| chr11:74781622 | T | C | 98 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(95): Show |
98 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.503-8004T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781622 | |||||||
| chr11:74781731 | C | T | 154 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(151): Show |
159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.503-7895C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781731 | |||||||
| chr11:74781787 | A | G | 3 | a0001c0001t0002g0155 a0001c0001t0002g0219 a0001c0001t0002g0259 |
3 | HG03704.hp2 NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.503-7839A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781787 | |||||||
| chr11:74781797 | T | G | 103 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.503-7829T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781797 | |||||||
| chr11:74782087 | C | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503-7539C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782087 | |||||||
| chr11:74782314 | C | T | 1 | a0001c0002t0032g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.503-7312C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782314 | |||||||
| chr11:74782338 | G | A | 2 | a0001c0002t0001g0059 a0001c0002t0001g0060 |
2 | HG00597.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.503-7288G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782338 | |||||||
| chr11:74782419 | A | T | 1 | a0001c0001t0003g0288 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.503-7207A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782419 | |||||||
| chr11:74782438 | C | T | 1 | a0001c0002t0001g0091 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.503-7188C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782438 | |||||||
| chr11:74782673 | A | G | 6 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(3): Show |
7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.503-6953A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782673 | |||||||
| chr11:74782907 | G | GT | 9 | a0001c0001t0002g0198 a0001c0001t0002g0255 a0001c0001t0004g0304 others(6): Show |
10 | HG01167.hp1 HG01175.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-6701dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74782907 | ||||||
| chr11:74782907 | GT | G | 20 | a0001c0001t0003g0035 a0001c0001t0011g0007 a0001c0001t0011g0125 others(17): Show |
21 | HG00558.hp2 HG00609.hp1 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.503-6701delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74782907 | ||||||
| chr11:74782941 | A | G | 126 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(123): Show |
128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-6685A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782941 | |||||||
| chr11:74783027 | CAT | C | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.503-6597_503-6596d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74783027 | ||||||
| chr11:74783045 | A | G | 1 | a0001c0002t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.503-6581A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74783045 | |||||||
| chr11:74783060 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-6566C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74783060 | |||||||
| chr11:74783242 | G | GT | 23 | a0001c0001t0003g0321 a0001c0001t0003g0323 a0001c0001t0003g0324 others(20): Show |
24 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.503-6373dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74783242 | ||||||
| chr11:74783768 | G | C | 1 | a0001c0001t0002g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.503-5858G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74783768 | |||||||
| chr11:74784155 | T | C | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-5471T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784155 | |||||||
| chr11:74784395 | CAA | C | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-5230_503-5229d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784395 | |||||||
| chr11:74784397 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.503-5229A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784397 | |||||||
| chr11:74784401 | G | A | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503-5225G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784401 | |||||||
| chr11:74784463 | G | T | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-5163G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784463 | |||||||
| chr11:74784470 | T | G | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-5156T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784470 | |||||||
| chr11:74784527 | G | T | 1 | a0001c0002t0001g0071 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.503-5099G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784527 | |||||||
| chr11:74784577 | A | G | 264 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(261): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.503-5049A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784577 | |||||||
| chr11:74784638 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-4988G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784638 | |||||||
| chr11:74784818 | G | C | 1 | a0001c0002t0001g0091 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.503-4808G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784818 | |||||||
| chr11:74784992 | C | T | 6 | a0001c0001t0007g0021 a0001c0001t0007g0023 a0001c0001t0007g0024 others(3): Show |
6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-4634C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784992 | |||||||
| chr11:74785037 | A | G | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-4589A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785037 | |||||||
| chr11:74785068 | C | T | 126 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(123): Show |
128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-4558C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785068 | |||||||
| chr11:74785158 | T | TATATATA others(21): Show |
1 | a0001c0001t0002g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.503-4457_503-4430d others(30): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785158 | ||||||
| chr11:74785158 | TATATATA others(45): Show |
T | 12 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(9): Show |
13 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-4457_503-4406d others(54): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785158 | ||||||
| chr11:74785160 | T | TATATATA others(6): Show |
1 | a0001c0001t0008g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.503-4442_503-4430d others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785160 | ||||||
| chr11:74785160 | TATATATA others(6): Show |
T | 2 | a0001c0001t0025g0191 a0001c0001t0025g0256 |
2 | NA18964.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.503-4442_503-4430d others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785160 | ||||||
| chr11:74785160 | TATATATA others(30): Show |
T | 9 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(6): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-4442_503-4406d others(39): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785160 | ||||||
| chr11:74785162 | T | TATATATA others(17): Show |
3 | a0001c0001t0002g0188 a0001c0001t0003g0324 a0001c0001t0009g0010 |
3 | HG01433.hp2 NA18952.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.503-4428_503-4405d others(26): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785162 | ||||||
| chr11:74785162 | T | TATATATA others(135): Show |
1 | a0001c0001t0008g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.503-4430_503-4429i others(144): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785162 | ||||||
| chr11:74785162 | T | TATATATA others(41): Show |
1 | a0001c0001t0026g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.503-4452_503-4405d others(50): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785162 | ||||||
| chr11:74785162 | TATATATA others(17): Show |
T | 128 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(125): Show |
131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.503-4428_503-4405d others(26): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785162 | ||||||
| chr11:74785164 | TATATATA others(15): Show |
T | 1 | a0001c0001t0022g0147 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.503-4453_503-4432d others(24): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785164 | ||||||
| chr11:74785173 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.503-4453G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785173 | |||||||
| chr11:74785174 | A | ATATATAT others(205): Show |
1 | a0001c0001t0008g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.503-4443_503-4442i others(214): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785174 | ||||||
| chr11:74785175 | TATATATA others(15): Show |
T | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-4440_503-4419d others(24): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785175 | ||||||
| chr11:74785186 | G | GATATATA others(6): Show |
2 | a0001c0001t0026g0271 a0001c0001t0057g0209 |
2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.503-4418_503-4406d others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785186 | ||||||
| chr11:74785186 | GATATATA others(6): Show |
G | 6 | a0001c0001t0002g0184 a0001c0001t0002g0201 a0001c0001t0002g0212 others(3): Show |
6 | HG00423.hp1 HG02129.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-4418_503-4406d others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785186 | ||||||
| chr11:74785197 | G | A | 7 | a0001c0001t0008g0158 a0001c0001t0008g0162 a0001c0001t0008g0163 others(4): Show |
7 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.503-4429G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785197 | |||||||
| chr11:74785197 | G | T | 1 | a0001c0001t0003g0280 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.503-4429G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785197 | |||||||
| chr11:74785197 | GAT | G | 4 | a0001c0001t0003g0228 a0001c0001t0004g0304 a0001c0001t0055g0265 others(1): Show |
4 | HG02109.hp2 HG03209.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.503-4418_503-4417d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785197 | ||||||
| chr11:74785198 | A | T | 12 | a0001c0001t0008g0158 a0001c0001t0008g0161 a0001c0001t0008g0162 others(9): Show |
12 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.503-4428A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785198 | |||||||
| chr11:74785199 | T | G | 7 | a0001c0001t0008g0158 a0001c0001t0008g0162 a0001c0001t0008g0163 others(4): Show |
7 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.503-4427T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785199 | |||||||
| chr11:74785207 | TATGA | T | 4 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0020g0051 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.503-4418_503-4415d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785207 | |||||||
| chr11:74785211 | A | ATATATAT others(205): Show |
1 | a0001c0001t0008g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.503-4405_503-4404i others(214): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | ||||||
| chr11:74785211 | A | ATATATAT others(181): Show |
5 | a0001c0001t0008g0158 a0001c0001t0008g0217 a0001c0001t0045g0159 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-4405_503-4404i others(190): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | ||||||
| chr11:74785211 | A | ATATATAT others(179): Show |
1 | a0001c0001t0008g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.503-4405_503-4404i others(188): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | ||||||
| chr11:74785211 | A | ATATATAT others(192): Show |
1 | a0001c0001t0008g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.503-4405_503-4404i others(201): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | ||||||
| chr11:74785211 | A | ATATATAT others(15): Show |
1 | a0001c0001t0008g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.503-4395_503-4394i others(24): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | ||||||
| chr11:74785217 | A | G | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-4409A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785217 | |||||||
| chr11:74785222 | T | A | 1 | a0001c0001t0003g0334 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-4404T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785222 | |||||||
| chr11:74785230 | A | G | 3 | a0001c0001t0003g0280 a0001c0002t0001g0074 a0001c0002t0001g0075 |
3 | HG01069.hp1 HG01071.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.503-4396A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785230 | |||||||
| chr11:74785231 | T | TATGATAT others(19): Show |
1 | a0001c0001t0003g0334 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-4395_503-4394i others(28): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785231 | |||||||
| chr11:74785231 | TTA | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-4387_503-4386d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785231 | ||||||
| chr11:74785232 | T | C | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503-4394T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785232 | |||||||
| chr11:74785232 | T | G | 1 | a0001c0001t0003g0334 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-4394T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785232 | |||||||
| chr11:74785234 | T | G | 3 | a0001c0001t0003g0280 a0001c0002t0001g0074 a0001c0002t0001g0075 |
3 | HG01069.hp1 HG01071.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.503-4392T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785234 | |||||||
| chr11:74785238 | TATGTTAT others(9): Show |
T | 2 | a0001c0002t0001g0074 a0001c0002t0001g0075 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.503-4385_503-4370d others(18): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785238 | ||||||
| chr11:74785252 | TAG | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-4372_503-4371d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785252 | ||||||
| chr11:74785254 | G | GAT | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
162 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.503-4365_503-4364d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785254 | ||||||
| chr11:74785254 | G | GATAT | 93 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(90): Show |
93 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.503-4367_503-4364d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785254 | ||||||
| chr11:74785254 | G | T | 5 | a0001c0002t0001g0036 a0001c0002t0004g0004 a0001c0002t0038g0004 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-4372G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785254 | |||||||
| chr11:74785272 | A | G | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-4354A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785272 | |||||||
| chr11:74785304 | T | G | 2 | a0001c0001t0003g0319 a0001c0001t0003g0328 |
2 | NA18968.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.503-4322T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785304 | |||||||
| chr11:74785506 | G | A | 2 | a0001c0002t0001g0119 a0001c0002t0001g0120 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.503-4120G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785506 | |||||||
| chr11:74785690 | C | G | 1 | a0001c0002t0001g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.503-3936C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785690 | |||||||
| chr11:74785835 | C | A | 126 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(123): Show |
128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-3791C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785835 | |||||||
| chr11:74785941 | C | CT | 6 | a0001c0001t0002g0260 a0001c0001t0003g0213 a0001c0001t0003g0238 others(3): Show |
6 | HG00597.hp2 HG01255.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.503-3667dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785941 | ||||||
| chr11:74785941 | CT | C | 116 | a0001c0001t0002g0175 a0001c0001t0002g0199 a0001c0001t0003g0035 others(113): Show |
118 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.503-3667delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785941 | ||||||
| chr11:74785946 | T | C | 8 | a0001c0001t0002g0182 a0001c0001t0013g0310 a0001c0001t0013g0311 others(5): Show |
9 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.503-3680T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785946 | |||||||
| chr11:74785948 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.503-3678T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785948 | |||||||
| chr11:74786083 | G | GGCACCTG others(5): Show |
2 | a0002c0003t0010g0307 a0002c0003t0010g0309 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.503-3542_503-3531d others(14): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74786083 | ||||||
| chr11:74786119 | T | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-3507T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786119 | |||||||
| chr11:74786218 | C | T | 1 | a0001c0001t0002g0293 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.503-3408C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786218 | |||||||
| chr11:74786244 | C | CT | 92 | a0001c0001t0003g0324 a0001c0002t0001g0005 a0001c0002t0001g0018 others(89): Show |
92 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.503-3364dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74786244 | ||||||
| chr11:74786244 | CT | C | 24 | a0001c0001t0001g0029 a0001c0001t0002g0179 a0001c0001t0002g0181 others(21): Show |
25 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.503-3364delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74786244 | ||||||
| chr11:74786382 | A | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-3244A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786382 | |||||||
| chr11:74786408 | G | T | 1 | a0001c0002t0004g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.503-3218G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786408 | |||||||
| chr11:74786410 | G | T | 14 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(11): Show |
16 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.503-3216G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786410 | |||||||
| chr11:74786469 | C | G | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.503-3157C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786469 | |||||||
| chr11:74786744 | T | C | 1 | a0001c0001t0006g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.503-2882T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786744 | |||||||
| chr11:74786829 | G | C | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-2797G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786829 | |||||||
| chr11:74786830 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.503-2796G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786830 | |||||||
| chr11:74786989 | G | C | 1 | a0001c0001t0005g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.503-2637G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786989 | |||||||
| chr11:74787006 | A | G | 1 | a0001c0001t0003g0225 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.503-2620A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787006 | |||||||
| chr11:74787612 | C | T | 3 | a0001c0002t0004g0004 a0001c0002t0038g0004 a0001c0002t0039g0037 |
3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.503-2014C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787612 | |||||||
| chr11:74787716 | T | C | 6 | a0001c0001t0007g0021 a0001c0001t0007g0023 a0001c0001t0007g0024 others(3): Show |
6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-1910T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787716 | |||||||
| chr11:74787723 | C | G | 1 | a0001c0002t0061g0112 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.503-1903C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787723 | |||||||
| chr11:74787796 | A | G | 2 | a0001c0001t0003g0319 a0001c0001t0003g0328 |
2 | NA18968.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.503-1830A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787796 | |||||||
| chr11:74788189 | CTTTGAAA others(3): Show |
C | 1 | a0001c0001t0048g0236 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.503-1430_503-1421d others(12): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788189 | ||||||
| chr11:74788302 | A | AAC | 122 | a0001c0001t0002g0019 a0001c0001t0003g0035 a0001c0001t0003g0248 others(119): Show |
123 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.503-1303_503-1302d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788302 | ||||||
| chr11:74788302 | A | AACAC | 14 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(11): Show |
16 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.503-1305_503-1302d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788302 | ||||||
| chr11:74788302 | A | AACACAC | 11 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(8): Show |
12 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.503-1307_503-1302d others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788302 | ||||||
| chr11:74788302 | AACACAC | A | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-1307_503-1302d others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788302 | ||||||
| chr11:74788779 | G | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.503-847G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74788779 | |||||||
| chr11:74788785 | G | A | 1 | a0001c0002t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.503-841G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74788785 | |||||||
| chr11:74788987 | C | T | 1 | a0001c0001t0003g0284 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.503-639C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74788987 | |||||||
| chr11:74789128 | C | T | 70 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(67): Show |
72 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.503-498C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789128 | |||||||
| chr11:74789129 | G | A | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-497G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789129 | |||||||
| chr11:74789203 | C | T | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-423C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789203 | |||||||
| chr11:74789318 | C | G | 3 | a0001c0002t0004g0004 a0001c0002t0038g0004 a0001c0002t0039g0037 |
3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.503-308C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789318 | |||||||
| chr11:74789347 | G | A | 4 | a0001c0001t0002g0257 a0001c0001t0002g0263 a0001c0001t0002g0266 others(1): Show |
4 | NA18951.hp1 NA18972.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-279G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789347 | |||||||
| chr11:74789505 | G | T | 3 | a0001c0002t0001g0097 a0001c0002t0001g0126 a0001c0002t0004g0054 |
3 | HG01516.hp2 HG01517.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.503-121G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789505 | |||||||
| chr11:74789792 | A | C | 1 | a0001c0002t0001g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.576+93A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74789792 | |||||||
| chr11:74789998 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.576+299C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74789998 | |||||||
| chr11:74790108 | G | T | 1 | a0001c0001t0030g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.576+409G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790108 | |||||||
| chr11:74790226 | C | G | 3 | a0001c0002t0004g0004 a0001c0002t0038g0004 a0001c0002t0039g0037 |
3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.576+527C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790226 | |||||||
| chr11:74790476 | G | A | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.576+777G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790476 | |||||||
| chr11:74790572 | G | A | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.576+873G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790572 | |||||||
| chr11:74790583 | G | A | 1 | a0001c0002t0042g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.576+884G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790583 | |||||||
| chr11:74790638 | G | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+939G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790638 | |||||||
| chr11:74790790 | G | A | 5 | a0001c0001t0002g0179 a0001c0001t0002g0184 a0001c0001t0002g0185 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+1091G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790790 | |||||||
| chr11:74790954 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(3): Show |
7 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.576+1255G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790954 | |||||||
| chr11:74790975 | G | A | 257 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(254): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.576+1276G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790975 | |||||||
| chr11:74791008 | C | G | 1 | a0001c0002t0035g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.576+1309C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791008 | |||||||
| chr11:74791076 | G | A | 7 | a0001c0002t0001g0078 a0001c0002t0001g0088 a0001c0002t0001g0096 others(4): Show |
7 | HG02074.hp1 NA18612.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.576+1377G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791076 | |||||||
| chr11:74791163 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.576+1464G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791163 | |||||||
| chr11:74791216 | C | T | 1 | a0001c0002t0042g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.576+1517C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791216 | |||||||
| chr11:74791325 | T | TGCAGAAC others(14): Show |
10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+1627_576+1647d others(23): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74791325 | ||||||
| chr11:74791340 | C | G | 1 | a0001c0001t0026g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.576+1641C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791340 | |||||||
| chr11:74791391 | C | T | 2 | a0003c0004t0023g0124 a0003c0004t0023g0128 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.576+1692C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791391 | |||||||
| chr11:74791455 | G | A | 335 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(332): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.576+1756G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791455 | |||||||
| chr11:74791555 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.576+1856C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791555 | |||||||
| chr11:74791647 | T | A | 9 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(6): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.576+1948T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791647 | |||||||
| chr11:74791691 | T | C | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.576+1992T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791691 | |||||||
| chr11:74791724 | G | T | 1 | a0001c0001t0006g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.576+2025G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791724 | |||||||
| chr11:74791735 | A | G | 164 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(161): Show |
169 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.576+2036A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791735 | |||||||
| chr11:74791809 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.576+2110A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791809 | |||||||
| chr11:74792123 | C | T | 96 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0027 others(93): Show |
96 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.576+2424C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792123 | |||||||
| chr11:74792357 | G | A | 3 | a0001c0002t0017g0057 a0001c0002t0017g0061 a0001c0002t0017g0095 |
3 | NA18998.hp1 NA19062.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.576+2658G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792357 | |||||||
| chr11:74792388 | G | C | 1 | a0001c0001t0002g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.576+2689G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792388 | |||||||
| chr11:74792424 | C | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+2725C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792424 | |||||||
| chr11:74792622 | C | T | 1 | a0001c0002t0021g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.576+2923C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792622 | |||||||
| chr11:74792739 | A | C | 3 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0040g0073 |
3 | HG01069.hp1 HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.576+3040A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792739 | |||||||
| chr11:74792821 | T | G | 1 | a0001c0001t0046g0283 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.576+3122T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792821 | |||||||
| chr11:74793585 | A | G | 1 | a0001c0002t0021g0052 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.576+3886A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793585 | |||||||
| chr11:74793645 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.576+3946T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793645 | |||||||
| chr11:74793708 | A | G | 1 | a0001c0001t0009g0205 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.576+4009A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793708 | |||||||
| chr11:74793801 | A | G | 3 | a0001c0001t0002g0294 a0001c0001t0002g0295 a0001c0001t0054g0274 |
3 | NA18994.hp1 NA19010.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.576+4102A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793801 | |||||||
| chr11:74793963 | A | G | 6 | a0001c0001t0007g0021 a0001c0001t0007g0023 a0001c0001t0007g0024 others(3): Show |
6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+4264A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793963 | |||||||
| chr11:74794024 | G | A | 1 | a0001c0014t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.576+4325G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74794024 | |||||||
| chr11:74794166 | T | G | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+4467T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74794166 | |||||||
| chr11:74794209 | T | C | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+4510T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74794209 | |||||||
| chr11:74794919 | C | T | 1 | a0001c0001t0005g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.576+5220C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74794919 | |||||||
| chr11:74795068 | A | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+5369A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795068 | |||||||
| chr11:74795219 | CT | C | 178 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(175): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.576+5538delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795219 | ||||||
| chr11:74795219 | CTT | C | 51 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): Show |
55 | HG00558.hp2 HG01074.hp2 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.576+5537_576+5538d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795219 | ||||||
| chr11:74795219 | CTTT | C | 96 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0027 others(93): Show |
96 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.576+5536_576+5538d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795219 | ||||||
| chr11:74795220 | T | TTC | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+5522_576+5523i others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795220 | ||||||
| chr11:74795234 | T | C | 1 | a0001c0001t0002g0273 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.576+5535T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795234 | |||||||
| chr11:74795524 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.576+5825G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795524 | |||||||
| chr11:74795591 | T | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+5892T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795591 | |||||||
| chr11:74795592 | G | A | 2 | a0001c0001t0005g0139 a0009c0007t0001g0151 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.576+5893G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795592 | |||||||
| chr11:74795682 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.576+5983G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795682 | |||||||
| chr11:74795740 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+6041C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795740 | |||||||
| chr11:74795749 | C | T | 6 | a0001c0001t0002g0212 a0001c0001t0002g0270 a0001c0001t0009g0010 others(3): Show |
7 | HG00423.hp1 HG02027.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.576+6050C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795749 | |||||||
| chr11:74795857 | C | CA | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+6166dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795857 | ||||||
| chr11:74795866 | T | A | 1 | a0001c0001t0046g0283 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.576+6167T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795866 | |||||||
| chr11:74796312 | C | T | 152 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(149): Show |
157 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.576+6613C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796312 | |||||||
| chr11:74796421 | T | C | 3 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 |
3 | HG01099.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.576+6722T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796421 | |||||||
| chr11:74796663 | CTGAAGGT others(12): Show |
C | 1 | a0001c0002t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.576+6982_576+7000d others(21): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74796663 | ||||||
| chr11:74796676 | A | G | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+6977A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796676 | |||||||
| chr11:74796700 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+7001C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796700 | |||||||
| chr11:74796814 | C | G | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.576+7115C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796814 | |||||||
| chr11:74796873 | T | C | 1 | a0001c0001t0003g0322 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.576+7174T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796873 | |||||||
| chr11:74796901 | A | G | 1 | a0009c0007t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.576+7202A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796901 | |||||||
| chr11:74796990 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.576+7291C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796990 | |||||||
| chr11:74797236 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.576+7537A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797236 | |||||||
| chr11:74797319 | T | G | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.576+7620T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797319 | |||||||
| chr11:74797331 | G | A | 1 | a0001c0001t0003g0330 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.576+7632G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797331 | |||||||
| chr11:74797564 | C | G | 125 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(122): Show |
127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.576+7865C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797564 | |||||||
| chr11:74797828 | C | T | 1 | a0001c0001t0002g0215 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.576+8129C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797828 | |||||||
| chr11:74797938 | T | C | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.576+8239T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797938 | |||||||
| chr11:74798070 | C | T | 125 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(122): Show |
127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.576+8371C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798070 | |||||||
| chr11:74798130 | A | G | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+8431A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798130 | |||||||
| chr11:74798221 | G | A | 115 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(112): Show |
116 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.576+8522G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798221 | |||||||
| chr11:74798282 | C | A | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.576+8583C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798282 | |||||||
| chr11:74798344 | C | G | 7 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(4): Show |
8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+8645C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798344 | |||||||
| chr11:74798377 | C | T | 3 | a0001c0001t0014g0006 a0001c0001t0014g0041 a0001c0001t0014g0122 |
4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+8678C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798377 | |||||||
| chr11:74798417 | G | A | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.576+8718G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798417 | |||||||
| chr11:74798469 | A | G | 1 | a0001c0002t0001g0055 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.576+8770A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798469 | |||||||
| chr11:74798512 | A | G | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.576+8813A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798512 | |||||||
| chr11:74798518 | G | A | 257 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(254): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.576+8819G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798518 | |||||||
| chr11:74798527 | G | A | 1 | a0001c0001t0003g0326 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.576+8828G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798527 | |||||||
| chr11:74798680 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.576+8981C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798680 | |||||||
| chr11:74798706 | G | T | 2 | a0001c0001t0003g0284 a0001c0001t0046g0283 |
2 | HG02165.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.576+9007G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798706 | |||||||
| chr11:74798739 | G | A | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+9040G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798739 | |||||||
| chr11:74798878 | C | T | 1 | a0001c0002t0005g0043 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.576+9179C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798878 | |||||||
| chr11:74799070 | A | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+9371A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74799070 | |||||||
| chr11:74799086 | G | GT | 314 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(311): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.576+9399dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74799086 | ||||||
| chr11:74799086 | G | GTT | 18 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0003g0017 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.576+9398_576+9399d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74799086 | ||||||
| chr11:74799843 | C | T | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.576+10144C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74799843 | |||||||
| chr11:74800597 | A | G | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-9587A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74800597 | |||||||
| chr11:74800815 | GAGCTCTT others(9): Show |
G | 1 | a0001c0001t0002g0175 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.577-9368_577-9353d others(18): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74800815 | |||||||
| chr11:74800849 | CT | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-9334delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74800849 | |||||||
| chr11:74801048 | T | C | 154 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(151): Show |
159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.577-9136T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801048 | |||||||
| chr11:74801062 | G | T | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-9122G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801062 | |||||||
| chr11:74801597 | A | G | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-8587A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801597 | |||||||
| chr11:74801640 | C | A | 1 | a0001c0008t0001g0106 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.577-8544C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801640 | |||||||
| chr11:74801742 | A | T | 1 | a0001c0001t0002g0201 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.577-8442A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801742 | |||||||
| chr11:74801753 | C | T | 2 | a0001c0002t0005g0086 a0001c0002t0005g0087 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.577-8431C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801753 | |||||||
| chr11:74801808 | A | G | 2 | a0001c0001t0003g0249 a0001c0001t0003g0305 |
2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.577-8376A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801808 | |||||||
| chr11:74801841 | C | T | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577-8343C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801841 | |||||||
| chr11:74801907 | A | G | 3 | a0001c0002t0004g0004 a0001c0002t0038g0004 a0001c0002t0039g0037 |
3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.577-8277A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801907 | |||||||
| chr11:74801981 | G | T | 125 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(122): Show |
127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.577-8203G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801981 | |||||||
| chr11:74802165 | C | T | 4 | a0001c0001t0002g0257 a0001c0001t0002g0263 a0001c0001t0002g0266 others(1): Show |
4 | NA18951.hp1 NA18972.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-8019C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802165 | |||||||
| chr11:74802383 | C | T | 103 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0027 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.577-7801C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802383 | |||||||
| chr11:74802404 | G | T | 86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(83): Show |
90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.577-7780G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802404 | |||||||
| chr11:74802438 | G | A | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.577-7746G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802438 | |||||||
| chr11:74802880 | G | A | 1 | a0001c0001t0033g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.577-7304G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802880 | |||||||
| chr11:74802927 | T | G | 2 | a0001c0001t0009g0251 a0001c0001t0047g0195 |
2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.577-7257T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802927 | |||||||
| chr11:74802933 | G | C | 4 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0149 others(1): Show |
5 | HG01891.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-7251G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802933 | |||||||
| chr11:74802977 | T | C | 8 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(5): Show |
9 | HG01099.hp1 HG01255.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-7207T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802977 | |||||||
| chr11:74802997 | C | T | 2 | a0001c0001t0022g0147 a0001c0001t0022g0150 |
2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.577-7187C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802997 | |||||||
| chr11:74803022 | A | G | 1 | a0001c0002t0004g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.577-7162A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803022 | |||||||
| chr11:74803024 | CATTCTCC others(158): Show |
C | 2 | a0001c0001t0022g0147 a0001c0001t0022g0150 |
2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.577-7139_577-6975d others(2): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74803024 | ||||||
| chr11:74803120 | C | T | 3 | a0001c0001t0014g0006 a0001c0001t0014g0041 a0001c0001t0014g0122 |
4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-7064C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803120 | |||||||
| chr11:74803171 | C | T | 1 | a0009c0007t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.577-7013C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803171 | |||||||
| chr11:74803176 | C | G | 3 | a0001c0001t0014g0006 a0001c0001t0014g0041 a0001c0001t0014g0122 |
4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-7008C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803176 | |||||||
| chr11:74803178 | T | C | 262 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(259): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.577-7006T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803178 | |||||||
| chr11:74803239 | C | T | 1 | a0001c0001t0022g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.577-6945C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803239 | |||||||
| chr11:74803242 | C | T | 3 | a0001c0002t0001g0027 a0001c0002t0001g0058 a0001c0002t0001g0110 |
3 | NA18975.hp2 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.577-6942C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803242 | |||||||
| chr11:74803293 | G | A | 10 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(7): Show |
11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.577-6891G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803293 | |||||||
| chr11:74803315 | G | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0117 |
2 | NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.577-6869G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803315 | |||||||
| chr11:74803336 | C | T | 1 | a0001c0001t0003g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.577-6848C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803336 | |||||||
| chr11:74803558 | C | T | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.577-6626C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803558 | |||||||
| chr11:74803577 | T | C | 1 | a0001c0002t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.577-6607T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803577 | |||||||
| chr11:74803790 | T | G | 1 | a0001c0002t0042g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.577-6394T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803790 | |||||||
| chr11:74803837 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.577-6347G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803837 | |||||||
| chr11:74803905 | G | A | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-6279G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803905 | |||||||
| chr11:74803997 | G | A | 1 | a0001c0001t0007g0281 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.577-6187G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803997 | |||||||
| chr11:74804048 | A | T | 2 | a0001c0002t0001g0101 a0001c0002t0001g0102 |
2 | HG01255.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.577-6136A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804048 | |||||||
| chr11:74804129 | C | T | 4 | a0001c0001t0002g0172 a0001c0001t0026g0271 a0001c0001t0026g0272 others(1): Show |
4 | HG02257.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-6055C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804129 | |||||||
| chr11:74804140 | G | T | 2 | a0001c0001t0003g0279 a0001c0001t0003g0282 |
2 | HG02132.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.577-6044G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804140 | |||||||
| chr11:74804261 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.577-5923C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804261 | |||||||
| chr11:74804314 | G | A | 2 | a0001c0002t0001g0103 a0001c0002t0001g0134 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.577-5870G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804314 | |||||||
| chr11:74804325 | G | A | 1 | a0001c0001t0008g0217 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.577-5859G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804325 | |||||||
| chr11:74804358 | A | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.577-5826A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804358 | |||||||
| chr11:74804425 | T | C | 258 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(255): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.577-5759T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804425 | |||||||
| chr11:74804807 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577-5377G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804807 | |||||||
| chr11:74804920 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.577-5264C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804920 | |||||||
| chr11:74804963 | T | C | 2 | a0001c0002t0005g0086 a0001c0002t0005g0087 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.577-5221T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804963 | |||||||
| chr11:74805382 | A | G | 1 | a0001c0001t0009g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.577-4802A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74805382 | |||||||
| chr11:74805969 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.577-4215G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74805969 | |||||||
| chr11:74806034 | T | C | 2 | a0001c0001t0009g0251 a0001c0001t0047g0195 |
2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.577-4150T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806034 | |||||||
| chr11:74806058 | A | G | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577-4126A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806058 | |||||||
| chr11:74806146 | A | G | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-4038A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806146 | |||||||
| chr11:74806265 | G | C | 1 | a0001c0002t0032g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.577-3919G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806265 | |||||||
| chr11:74806421 | G | A | 4 | a0001c0001t0002g0175 a0001c0001t0002g0196 a0001c0001t0002g0197 others(1): Show |
4 | HG01261.hp1 NA18978.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-3763G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806421 | |||||||
| chr11:74806459 | T | A | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.577-3725T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806459 | |||||||
| chr11:74806461 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-3723C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806461 | |||||||
| chr11:74806522 | T | A | 1 | a0001c0001t0002g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.577-3662T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806522 | |||||||
| chr11:74806569 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.577-3615G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806569 | |||||||
| chr11:74806717 | T | C | 5 | a0001c0001t0002g0172 a0001c0001t0002g0174 a0001c0001t0026g0271 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.577-3467T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806717 | |||||||
| chr11:74806762 | G | T | 2 | a0001c0001t0003g0284 a0001c0001t0046g0283 |
2 | HG02165.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.577-3422G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806762 | |||||||
| chr11:74806887 | A | T | 6 | a0001c0002t0001g0078 a0001c0002t0001g0088 a0001c0002t0005g0043 others(3): Show |
6 | NA18612.hp1 NA18954.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.577-3297A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806887 | |||||||
| chr11:74806983 | G | A | 10 | a0001c0002t0001g0067 a0001c0002t0001g0079 a0001c0002t0001g0092 others(7): Show |
10 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-3201G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806983 | |||||||
| chr11:74807212 | C | T | 1 | a0001c0002t0005g0048 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.577-2972C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807212 | |||||||
| chr11:74807296 | C | G | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.577-2888C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807296 | |||||||
| chr11:74807320 | A | C | 1 | a0001c0002t0001g0126 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.577-2864A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807320 | |||||||
| chr11:74807353 | T | C | 1 | a0001c0001t0005g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.577-2831T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807353 | |||||||
| chr11:74807391 | A | G | 8 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(5): Show |
9 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-2793A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807391 | |||||||
| chr11:74807743 | A | G | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-2441A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807743 | |||||||
| chr11:74807746 | G | T | 1 | a0001c0002t0001g0088 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.577-2438G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807746 | |||||||
| chr11:74807888 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.577-2296G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807888 | |||||||
| chr11:74807981 | A | G | 4 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0308 others(1): Show |
4 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-2203A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807981 | |||||||
| chr11:74808009 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.577-2175C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808009 | |||||||
| chr11:74808088 | G | T | 4 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-2096G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808088 | |||||||
| chr11:74808113 | A | C | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.577-2071A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808113 | |||||||
| chr11:74808117 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.577-2067G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808117 | |||||||
| chr11:74808223 | T | G | 1 | a0001c0002t0010g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.577-1961T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808223 | |||||||
| chr11:74808402 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.577-1782G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808402 | |||||||
| chr11:74808598 | C | T | 1 | a0001c0001t0003g0324 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.577-1586C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808598 | |||||||
| chr11:74808765 | A | T | 1 | a0001c0001t0022g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.577-1419A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808765 | |||||||
| chr11:74809075 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.577-1109T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809075 | |||||||
| chr11:74809095 | G | GT | 9 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(6): Show |
10 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-1080dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74809095 | ||||||
| chr11:74809153 | C | A | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-1031C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809153 | |||||||
| chr11:74809291 | A | C | 98 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(95): Show |
98 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.577-893A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809291 | |||||||
| chr11:74809340 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.577-844T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809340 | |||||||
| chr11:74809404 | T | C | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-780T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809404 | |||||||
| chr11:74809441 | C | T | 104 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(101): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.577-743C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809441 | |||||||
| chr11:74809622 | C | G | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.577-562C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809622 | |||||||
| chr11:74809795 | C | T | 1 | a0001c0001t0003g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.577-389C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809795 | |||||||
| chr11:74809948 | G | C | 2 | a0001c0001t0003g0228 a0001c0001t0003g0229 |
2 | HG02109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.577-236G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809948 | |||||||
| chr11:74810085 | G | T | 9 | a0001c0002t0001g0070 a0001c0002t0001g0071 a0001c0002t0001g0072 others(6): Show |
9 | HG00558.hp2 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-99G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74810085 | |||||||
| chr11:74811196 | T | A | 126 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(123): Show |
128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.723+866T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811196 | |||||||
| chr11:74811281 | G | C | 1 | a0001c0014t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723+951G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811281 | |||||||
| chr11:74811323 | C | A | 2 | a0001c0002t0001g0103 a0001c0002t0001g0134 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.723+993C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811323 | |||||||
| chr11:74811326 | T | C | 263 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(260): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.723+996T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811326 | |||||||
| chr11:74811328 | G | A | 263 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(260): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.723+998G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811328 | |||||||
| chr11:74811442 | C | T | 1 | a0001c0001t0008g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.723+1112C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811442 | |||||||
| chr11:74811527 | C | T | 1 | a0001c0001t0022g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.723+1197C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811527 | |||||||
| chr11:74811910 | C | T | 1 | a0001c0001t0022g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.723+1580C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811910 | |||||||
| chr11:74812420 | A | G | 2 | a0001c0001t0003g0017 a0001c0001t0003g0326 |
3 | NA18941.hp2 NA18945.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.723+2090A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812420 | |||||||
| chr11:74812506 | A | G | 1 | a0001c0002t0001g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.723+2176A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812506 | |||||||
| chr11:74812662 | G | A | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.723+2332G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812662 | |||||||
| chr11:74812672 | T | G | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+2342T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812672 | |||||||
| chr11:74812719 | G | T | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+2389G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812719 | |||||||
| chr11:74812744 | A | T | 1 | a0001c0002t0001g0127 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.723+2414A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812744 | |||||||
| chr11:74812778 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+2448C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812778 | |||||||
| chr11:74812803 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.723+2473T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812803 | |||||||
| chr11:74812906 | T | G | 5 | a0001c0001t0003g0321 a0001c0001t0003g0323 a0001c0001t0003g0324 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+2576T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812906 | |||||||
| chr11:74812943 | T | G | 9 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(6): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+2613T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812943 | |||||||
| chr11:74813023 | A | C | 15 | a0001c0002t0001g0039 a0001c0002t0001g0042 a0001c0002t0001g0044 others(12): Show |
15 | NA18971.hp1 NA18973.hp2 NA18974.hp1 others(12): Show |
intron_variant | MODIFIER | c.723+2693A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813023 | |||||||
| chr11:74813125 | A | G | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.723+2795A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813125 | |||||||
| chr11:74813469 | G | T | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.723+3139G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813469 | |||||||
| chr11:74813759 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+3429C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813759 | |||||||
| chr11:74813890 | C | G | 134 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(131): Show |
137 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.723+3560C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813890 | |||||||
| chr11:74813932 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+3602C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813932 | |||||||
| chr11:74813933 | G | A | 1 | a0001c0001t0011g0125 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.723+3603G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813933 | |||||||
| chr11:74814062 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.724-3534C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814062 | |||||||
| chr11:74814291 | C | T | 1 | a0001c0001t0003g0234 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.724-3305C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814291 | |||||||
| chr11:74814347 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.724-3249A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814347 | |||||||
| chr11:74814380 | C | CT | 183 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(180): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.724-3197dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 74814380 | ||||||
| chr11:74814380 | C | CTT | 23 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(20): Show |
23 | HG01074.hp2 HG01099.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-3198_724-3197d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 74814380 | ||||||
| chr11:74814380 | CT | C | 22 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(19): Show |
25 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.724-3197delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 74814380 | ||||||
| chr11:74814470 | C | G | 2 | a0001c0001t0005g0139 a0009c0007t0001g0151 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.724-3126C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814470 | |||||||
| chr11:74814500 | G | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.724-3096G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814500 | |||||||
| chr11:74814617 | C | T | 1 | a0001c0001t0015g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.724-2979C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814617 | |||||||
| chr11:74814784 | A | G | 4 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0308 others(1): Show |
4 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-2812A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814784 | |||||||
| chr11:74814807 | T | C | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.724-2789T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814807 | |||||||
| chr11:74814808 | T | C | 7 | a0001c0001t0004g0304 a0001c0001t0015g0315 a0001c0001t0015g0316 others(4): Show |
7 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-2788T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814808 | |||||||
| chr11:74815072 | A | G | 14 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(11): Show |
16 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.724-2524A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815072 | |||||||
| chr11:74815235 | G | T | 1 | a0001c0006t0043g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.724-2361G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815235 | |||||||
| chr11:74815274 | C | T | 40 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(37): Show |
40 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.724-2322C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815274 | |||||||
| chr11:74815293 | C | T | 1 | a0001c0002t0061g0112 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.724-2303C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815293 | |||||||
| chr11:74815574 | G | T | 3 | a0001c0001t0006g0144 a0001c0001t0006g0145 a0001c0001t0006g0146 |
3 | HG02258.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.724-2022G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815574 | |||||||
| chr11:74815593 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.724-2003C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815593 | |||||||
| chr11:74816052 | CTG | C | 44 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0042 others(41): Show |
44 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.724-1542_724-1541d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 74816052 | ||||||
| chr11:74816090 | G | A | 28 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(25): Show |
31 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.724-1506G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816090 | |||||||
| chr11:74816098 | C | G | 335 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(332): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.724-1498C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816098 | |||||||
| chr11:74816519 | T | C | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.724-1077T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816519 | |||||||
| chr11:74816646 | T | C | 1 | a0001c0002t0035g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.724-950T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816646 | |||||||
| chr11:74816781 | G | A | 1 | a0001c0001t0013g0311 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.724-815G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816781 | |||||||
| chr11:74816867 | T | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.724-729T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816867 | |||||||
| chr11:74816894 | A | C | 2 | a0001c0001t0008g0161 a0001c0001t0008g0162 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.724-702A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816894 | |||||||
| chr11:74817276 | T | C | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.724-320T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74817276 | |||||||
| chr11:74818491 | C | T | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.842+777C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818491 | |||||||
| chr11:74818494 | AT | A | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+781delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818494 | |||||||
| chr11:74818583 | G | A | 6 | a0001c0001t0007g0021 a0001c0001t0007g0023 a0001c0001t0007g0024 others(3): Show |
6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.842+869G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818583 | |||||||
| chr11:74818802 | ATCTC | A | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+1096_842+1099d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74818802 | ||||||
| chr11:74818939 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.842+1225C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818939 | |||||||
| chr11:74818987 | G | T | 257 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(254): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.842+1273G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818987 | |||||||
| chr11:74819068 | G | GT | 6 | a0001c0002t0001g0036 a0001c0002t0004g0004 a0001c0002t0038g0004 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.842+1368dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74819068 | ||||||
| chr11:74819170 | A | C | 1 | a0001c0001t0005g0003 | 2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.842+1456A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819170 | |||||||
| chr11:74819581 | T | C | 1 | a0001c0002t0004g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.842+1867T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819581 | |||||||
| chr11:74819750 | T | C | 14 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(11): Show |
16 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.842+2036T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819750 | |||||||
| chr11:74819819 | A | G | 1 | a0001c0002t0001g0072 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.842+2105A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819819 | |||||||
| chr11:74819927 | C | T | 4 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0318 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.842+2213C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819927 | |||||||
| chr11:74819974 | G | A | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.842+2260G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819974 | |||||||
| chr11:74820097 | G | C | 12 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(9): Show |
13 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+2383G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74820097 | |||||||
| chr11:74820098 | G | A | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.842+2384G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74820098 | |||||||
| chr11:74820131 | A | G | 335 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(332): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.842+2417A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74820131 | |||||||
| chr11:74820472 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.842+2758C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74820472 | |||||||
| chr11:74820526 | C | CA | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+2815dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74820526 | ||||||
| chr11:74820916 | A | AC | 103 | a0001c0001t0003g0035 a0001c0002t0001g0005 a0001c0002t0001g0018 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.842+3204dupC | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74820916 | ||||||
| chr11:74821012 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.842+3298C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821012 | |||||||
| chr11:74821048 | A | T | 264 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(261): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.842+3334A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821048 | |||||||
| chr11:74821183 | T | A | 1 | a0001c0002t0001g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.842+3469T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821183 | |||||||
| chr11:74821359 | TAAAAGAA others(312): Show |
T | 153 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(150): Show |
158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.842+3665_842+3983d others(2): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821359 | ||||||
| chr11:74821460 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.842+3746C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821460 | |||||||
| chr11:74821549 | C | T | 110 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(107): Show |
114 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.842+3835C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821549 | |||||||
| chr11:74821657 | C | CA | 13 | a0001c0001t0002g0198 a0001c0001t0002g0218 a0001c0001t0003g0230 others(10): Show |
13 | HG00099.hp2 HG00621.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+3968dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821657 | ||||||
| chr11:74821657 | C | CAA | 7 | a0001c0001t0002g0019 a0001c0001t0002g0155 a0001c0001t0002g0219 others(4): Show |
7 | HG00621.hp2 HG01358.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+3967_842+3968d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821657 | ||||||
| chr11:74821657 | CA | C | 79 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(76): Show |
82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.842+3968delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821657 | ||||||
| chr11:74821657 | CAA | C | 17 | a0001c0001t0002g0179 a0001c0001t0002g0194 a0001c0001t0002g0199 others(14): Show |
17 | HG00280.hp1 HG00558.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.842+3967_842+3968d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821657 | ||||||
| chr11:74821869 | T | G | 1 | a0001c0002t0001g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.842+4155T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821869 | |||||||
| chr11:74821876 | G | A | 135 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(132): Show |
138 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.842+4162G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821876 | |||||||
| chr11:74822028 | T | TGA | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+4328_842+4329d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822028 | ||||||
| chr11:74822043 | G | GGT | 11 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(8): Show |
12 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.842+4343_842+4344d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822043 | ||||||
| chr11:74822182 | T | C | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.842+4468T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822182 | |||||||
| chr11:74822266 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.842+4552C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822266 | |||||||
| chr11:74822287 | T | G | 1 | a0001c0001t0007g0241 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.842+4573T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822287 | |||||||
| chr11:74822407 | G | A | 126 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(123): Show |
128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.842+4693G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822407 | |||||||
| chr11:74822479 | C | CT | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+4767dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822479 | ||||||
| chr11:74822556 | A | T | 5 | a0001c0001t0002g0270 a0001c0001t0009g0010 a0001c0001t0025g0191 others(2): Show |
6 | HG02027.hp2 HG02155.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.842+4842A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822556 | |||||||
| chr11:74822606 | A | G | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+4892A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822606 | |||||||
| chr11:74822627 | C | G | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.842+4913C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822627 | |||||||
| chr11:74822677 | A | G | 1 | a0008c0011t0041g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.842+4963A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822677 | |||||||
| chr11:74822683 | TG | T | 4 | a0001c0001t0002g0172 a0001c0001t0026g0271 a0001c0001t0026g0272 others(1): Show |
4 | HG02257.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.842+4973delG | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822683 | ||||||
| chr11:74822798 | TTTTC | T | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+5092_842+5095d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822798 | ||||||
| chr11:74822808 | T | C | 1 | a0001c0002t0010g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.842+5094T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822808 | |||||||
| chr11:74823019 | A | G | 2 | a0001c0002t0001g0005 a0001c0002t0004g0005 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.842+5305A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823019 | |||||||
| chr11:74823207 | C | G | 2 | a0001c0002t0001g0050 a0001c0002t0001g0130 |
2 | HG00609.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.842+5493C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823207 | |||||||
| chr11:74823244 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.842+5530G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823244 | |||||||
| chr11:74823310 | T | C | 1 | a0001c0001t0002g0019 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.842+5596T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823310 | |||||||
| chr11:74823501 | T | C | 2 | a0003c0004t0023g0124 a0003c0004t0023g0128 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.842+5787T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823501 | |||||||
| chr11:74823639 | T | A | 154 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(151): Show |
159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.842+5925T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823639 | |||||||
| chr11:74823715 | C | T | 1 | a0001c0012t0001g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.842+6001C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823715 | |||||||
| chr11:74823729 | C | A | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.842+6015C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823729 | |||||||
| chr11:74823738 | GA | G | 296 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(293): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.842+6044delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74823738 | ||||||
| chr11:74823738 | GAA | G | 21 | a0001c0001t0003g0325 a0001c0001t0005g0139 a0001c0001t0006g0144 others(18): Show |
22 | HG01099.hp1 HG01168.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.842+6043_842+6044d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74823738 | ||||||
| chr11:74823842 | C | G | 1 | a0001c0014t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842+6128C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823842 | |||||||
| chr11:74823855 | T | C | 3 | a0001c0002t0001g0044 a0001c0002t0001g0049 a0001c0002t0001g0132 |
3 | NA18974.hp1 NA18978.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.842+6141T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823855 | |||||||
| chr11:74824832 | T | TA | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+7120dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74824832 | ||||||
| chr11:74824932 | C | T | 335 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(332): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.842+7218C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74824932 | |||||||
| chr11:74824950 | G | C | 154 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(151): Show |
159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.842+7236G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74824950 | |||||||
| chr11:74825155 | ATTC | A | 44 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0042 others(41): Show |
44 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.842+7446_842+7448d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74825155 | ||||||
| chr11:74825166 | G | A | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.842+7452G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825166 | |||||||
| chr11:74825222 | A | G | 9 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(6): Show |
10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.842+7508A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825222 | |||||||
| chr11:74825414 | C | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+7700C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825414 | |||||||
| chr11:74825648 | A | G | 1 | a0001c0001t0022g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.842+7934A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825648 | |||||||
| chr11:74825776 | C | G | 1 | a0001c0001t0002g0275 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.842+8062C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825776 | |||||||
| chr11:74825809 | G | A | 1 | a0001c0001t0003g0237 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.842+8095G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825809 | |||||||
| chr11:74825858 | G | T | 150 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(147): Show |
154 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.842+8144G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825858 | |||||||
| chr11:74826075 | C | T | 5 | a0001c0001t0002g0172 a0001c0001t0002g0174 a0001c0001t0026g0271 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.842+8361C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826075 | |||||||
| chr11:74826119 | A | G | 10 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(7): Show |
11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+8405A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826119 | |||||||
| chr11:74826184 | G | T | 1 | a0006c0015t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.842+8470G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826184 | |||||||
| chr11:74826269 | C | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(6): Show |
10 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.843-8407C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826269 | |||||||
| chr11:74826512 | CT | C | 104 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0027 others(101): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.843-8163delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826512 | |||||||
| chr11:74826736 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(3): Show |
7 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-7940C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826736 | |||||||
| chr11:74826865 | C | T | 9 | a0001c0001t0002g0009 a0001c0001t0002g0177 a0001c0001t0002g0178 others(6): Show |
10 | HG00733.hp1 HG01123.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.843-7811C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826865 | |||||||
| chr11:74826945 | C | A | 9 | a0001c0001t0002g0009 a0001c0001t0002g0177 a0001c0001t0002g0178 others(6): Show |
10 | HG00733.hp1 HG01123.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.843-7731C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826945 | |||||||
| chr11:74827021 | C | G | 2 | a0001c0001t0003g0213 a0001c0001t0050g0244 |
2 | HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.843-7655C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827021 | |||||||
| chr11:74827023 | G | A | 1 | a0001c0002t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843-7653G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827023 | |||||||
| chr11:74827045 | T | C | 15 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(12): Show |
17 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.843-7631T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827045 | |||||||
| chr11:74827123 | C | T | 102 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0027 others(99): Show |
102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.843-7553C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827123 | |||||||
| chr11:74827262 | T | G | 2 | a0001c0002t0001g0103 a0001c0002t0001g0134 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.843-7414T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827262 | |||||||
| chr11:74827285 | C | T | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.843-7391C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827285 | |||||||
| chr11:74827344 | C | T | 2 | a0001c0002t0001g0005 a0001c0002t0004g0005 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.843-7332C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827344 | |||||||
| chr11:74827433 | A | G | 2 | a0001c0001t0003g0213 a0001c0001t0050g0244 |
2 | HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.843-7243A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827433 | |||||||
| chr11:74827471 | T | C | 2 | a0003c0004t0023g0124 a0003c0004t0023g0128 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.843-7205T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827471 | |||||||
| chr11:74827648 | G | A | 3 | a0001c0001t0003g0230 a0001c0001t0003g0239 a0001c0001t0003g0247 |
3 | HG00099.hp2 HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.843-7028G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827648 | |||||||
| chr11:74827654 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.843-7022C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827654 | |||||||
| chr11:74827675 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.843-7001C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827675 | |||||||
| chr11:74827944 | A | G | 6 | a0001c0001t0003g0225 a0001c0001t0003g0242 a0001c0001t0003g0249 others(3): Show |
6 | NA18940.hp2 NA18980.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-6732A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827944 | |||||||
| chr11:74827955 | T | G | 1 | a0009c0007t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.843-6721T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827955 | |||||||
| chr11:74828286 | C | T | 1 | a0001c0001t0003g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.843-6390C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828286 | |||||||
| chr11:74828383 | T | C | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.843-6293T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828383 | |||||||
| chr11:74828391 | A | G | 2 | a0001c0001t0022g0147 a0001c0001t0022g0150 |
2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.843-6285A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828391 | |||||||
| chr11:74828519 | A | G | 1 | a0003c0004t0023g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.843-6157A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828519 | |||||||
| chr11:74828593 | C | G | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.843-6083C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828593 | |||||||
| chr11:74828626 | C | T | 6 | a0001c0001t0007g0021 a0001c0001t0007g0023 a0001c0001t0007g0024 others(3): Show |
6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-6050C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828626 | |||||||
| chr11:74828648 | C | G | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-6028C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828648 | |||||||
| chr11:74828855 | A | C | 1 | a0001c0001t0012g0171 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.843-5821A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828855 | |||||||
| chr11:74829190 | T | C | 1 | a0001c0001t0007g0023 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.843-5486T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829190 | |||||||
| chr11:74829318 | C | T | 1 | a0001c0002t0040g0073 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.843-5358C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829318 | |||||||
| chr11:74829514 | A | G | 3 | a0001c0001t0006g0144 a0001c0001t0006g0145 a0001c0001t0006g0146 |
3 | HG02258.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.843-5162A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829514 | |||||||
| chr11:74829530 | AATACACG others(3): Show |
A | 2 | a0003c0004t0023g0124 a0003c0004t0023g0128 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.843-5143_843-5134d others(12): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74829530 | ||||||
| chr11:74829645 | A | G | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-5031A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829645 | |||||||
| chr11:74829723 | C | T | 1 | a0001c0001t0003g0285 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843-4953C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829723 | |||||||
| chr11:74829726 | A | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-4950A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829726 | |||||||
| chr11:74829789 | A | G | 1 | a0001c0001t0003g0329 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.843-4887A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829789 | |||||||
| chr11:74829952 | T | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-4724T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829952 | |||||||
| chr11:74830020 | G | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-4656G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830020 | |||||||
| chr11:74830120 | A | G | 1 | a0001c0001t0007g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.843-4556A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830120 | |||||||
| chr11:74830225 | A | G | 1 | a0001c0001t0003g0322 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.843-4451A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830225 | |||||||
| chr11:74830542 | A | G | 1 | a0001c0001t0003g0242 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.843-4134A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830542 | |||||||
| chr11:74830546 | TA | T | 109 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(106): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.843-4117delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74830546 | ||||||
| chr11:74830546 | TAA | T | 150 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(147): Show |
155 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.843-4118_843-4117d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74830546 | ||||||
| chr11:74830576 | G | A | 2 | a0001c0001t0004g0304 a0001c0014t0001g0291 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.843-4100G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830576 | |||||||
| chr11:74830674 | T | C | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-4002T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830674 | |||||||
| chr11:74830807 | T | A | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.843-3869T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830807 | |||||||
| chr11:74830833 | C | T | 8 | a0001c0001t0011g0007 a0001c0001t0011g0125 a0001c0001t0011g0136 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-3843C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830833 | |||||||
| chr11:74830890 | C | G | 10 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(7): Show |
11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-3786C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830890 | |||||||
| chr11:74831010 | A | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-3666A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831010 | |||||||
| chr11:74831330 | T | C | 7 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(4): Show |
8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-3346T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831330 | |||||||
| chr11:74831434 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0186 |
2 | NA18981.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.843-3242C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831434 | |||||||
| chr11:74831694 | G | GA | 14 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(11): Show |
15 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.843-2967dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74831694 | ||||||
| chr11:74831785 | T | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-2891T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831785 | |||||||
| chr11:74831821 | G | T | 10 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(7): Show |
11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-2855G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831821 | |||||||
| chr11:74832135 | G | A | 4 | a0001c0001t0007g0013 a0001c0001t0007g0281 a0001c0001t0024g0013 others(1): Show |
4 | NA18949.hp1 NA18971.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-2541G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832135 | |||||||
| chr11:74832166 | A | G | 2 | a0001c0001t0014g0006 a0001c0001t0014g0041 |
3 | HG01884.hp2 HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.843-2510A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832166 | |||||||
| chr11:74832186 | A | G | 1 | a0001c0002t0021g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.843-2490A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832186 | |||||||
| chr11:74832290 | AT | A | 7 | a0001c0001t0002g0184 a0001c0001t0002g0186 a0001c0001t0002g0273 others(4): Show |
7 | HG02897.hp2 HG03041.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-2369delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74832290 | ||||||
| chr11:74832317 | A | C | 1 | a0001c0002t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843-2359A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832317 | |||||||
| chr11:74832784 | A | C | 1 | a0001c0001t0002g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.843-1892A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832784 | |||||||
| chr11:74833093 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.843-1583A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833093 | |||||||
| chr11:74833193 | T | C | 12 | a0001c0001t0006g0008 a0001c0001t0006g0141 a0001c0001t0006g0143 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.843-1483T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833193 | |||||||
| chr11:74833324 | A | G | 1 | a0001c0001t0002g0293 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-1352A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833324 | |||||||
| chr11:74833505 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.843-1171G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833505 | |||||||
| chr11:74833549 | A | G | 5 | a0001c0001t0003g0321 a0001c0001t0003g0323 a0001c0001t0003g0324 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1127A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833549 | |||||||
| chr11:74833626 | T | G | 1 | a0001c0001t0022g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.843-1050T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833626 | |||||||
| chr11:74833735 | C | G | 2 | a0001c0001t0003g0245 a0001c0001t0003g0250 |
2 | HG01516.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.843-941C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833735 | |||||||
| chr11:74833838 | C | T | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-838C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833838 | |||||||
| chr11:74833940 | T | G | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-736T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833940 | |||||||
| chr11:74834173 | T | A | 1 | a0001c0014t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843-503T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834173 | |||||||
| chr11:74834333 | T | G | 265 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(262): Show |
274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.843-343T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834333 | |||||||
| chr11:74834364 | C | T | 7 | a0002c0003t0010g0015 a0002c0003t0010g0306 a0002c0003t0010g0307 others(4): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-312C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834364 | |||||||
| chr11:74834377 | G | T | 1 | a0001c0001t0004g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.843-299G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834377 | |||||||
| chr11:74834431 | C | T | 6 | a0001c0002t0001g0078 a0001c0002t0001g0088 a0001c0002t0005g0043 others(3): Show |
6 | NA18612.hp1 NA18954.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.843-245C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834431 | |||||||
| chr11:74834503 | AATTTCTA others(10): Show |
A | 1 | a0001c0001t0028g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.843-168_843-152del others(17): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74834503 | ||||||
| chr11:74834837 | T | C | 5 | a0001c0001t0015g0315 a0001c0001t0015g0316 a0001c0001t0015g0317 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+62T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74834837 | |||||||
| chr11:74834843 | T | G | 10 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0161 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.942+68T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74834843 | |||||||
| chr11:74835019 | G | T | 102 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0027 others(99): Show |
102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.942+244G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74835019 | |||||||
| chr11:74835212 | T | C | 7 | a0001c0001t0013g0310 a0001c0001t0013g0311 a0001c0001t0013g0312 others(4): Show |
8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-334T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74835212 | |||||||
| chr11:74835400 | G | A | 5 | a0001c0001t0002g0175 a0001c0001t0002g0196 a0001c0001t0002g0197 others(2): Show |
5 | HG01261.hp1 HG02602.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.943-146G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74835400 | |||||||
| chr11:74835422 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.943-124C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74835422 |